11370384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12311555-A-G

http://identifiers.org/hco/7/GRCh38#11370412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12311583-A-C

11370433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12311605-G-T

11370927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312101-A-G

http://identifiers.org/hco/7/GRCh38#11371048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12312240-C-A

11371048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312240-C-T

http://identifiers.org/hco/7/GRCh38#11371237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12312407-C-A

11371260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312471-A-G

11371405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312605-G-T

11371611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312810-T-A

11371611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312810-T-C

11371659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12312896-T-C

11371803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313123-T-C

http://identifiers.org/hco/7/GRCh38#11371840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12313160-A-C

11371924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313576-T-G

11371947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313610-G-C

11371947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313610-G-T

11371996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313672-G-T

11372106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313776-G-A

11372106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313776-G-T

11372197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313832-C-T

11372278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313905-G-A

11372332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12313955-A-T

11372398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12314014-G-T

11372808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12314454-T-A

11372978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12314571-T-C

11373163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12314676-A-T

11373249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12314775-T-A

11373655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315152-C-T

11373699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315200-T-C

11373721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315228-C-G

11373721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315228-C-T

11373774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315281-T-G

11373789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315296-T-C

11373823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315351-T-A

11373828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315356-G-A

http://identifiers.org/hco/7/GRCh38#11373886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12315426-C-A

http://identifiers.org/hco/7/GRCh38#11374076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12315631-A-C

http://identifiers.org/hco/7/GRCh38#11374131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12315698-C-A

11374172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315741-G-A

http://identifiers.org/hco/7/GRCh38#11374231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12315796-A-C

11374250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315814-G-A

11374250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315814-G-T

11374317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315880-G-T

11374419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315971-T-A

11374419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12315971-T-G

11374644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316196-G-A

11374644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316196-G-T

11374850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316405-C-T

11374922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316476-T-C

http://identifiers.org/hco/7/GRCh38#11375073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12316623-C-A

http://identifiers.org/hco/7/GRCh38#11375115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12316665-C-A

11375115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316665-C-G

11375131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316681-G-A

11375131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12316681-G-T

http://identifiers.org/hco/7/GRCh38#11375218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12316768-C-A

11375523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12317096-G-A

http://identifiers.org/hco/7/GRCh38#11375613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12317184-A-C

11375613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12317184-A-G

http://identifiers.org/hco/7/GRCh38#11375639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12317210-C-A

11375749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12317322-G-A

11375749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12317322-G-T

11375915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317490-G-A

11375922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317497-A-G

11376031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317592-T-C

11376099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317647-A-T

11376381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12317888-C-T

11376521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318031-G-A

11376521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318031-G-T

11376590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12318133-G-A

11376590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12318133-G-T

http://identifiers.org/hco/7/GRCh38#11376764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12318283-C-A

11376764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318283-C-T

11376848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318359-G-T

11376858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12318369-A-G

11377021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12318521-A-G

http://identifiers.org/hco/7/GRCh38#11377056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12318561-C-A

http://identifiers.org/hco/7/GRCh38#11377141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12318632-A-C

http://identifiers.org/hco/7/GRCh38#11377397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12318876-A-C

11377679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12319631-T-C

11377679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12319631-T-G

http://identifiers.org/hco/7/GRCh38#11378196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12320061-C-A

11378196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320061-C-T

11378372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320193-A-G

11378476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320295-C-T

http://identifiers.org/hco/7/GRCh38#11378525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12320362-C-A

11378547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320385-G-A

11378551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320389-T-C

11378574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320413-G-T

11378581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320420-G-A

11378581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12320420-G-T

http://identifiers.org/hco/7/GRCh38#11378611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12320454-C-A

11378705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320546-A-G

11378741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320582-G-C

http://identifiers.org/hco/7/GRCh38#11378746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12320587-C-A

11378747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320588-A-T

11378786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320632-G-T

11378816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320662-G-T

11378956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320796-G-A

11378956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320796-G-T

11379007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320843-A-T

11379049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12320889-A-G

http://identifiers.org/hco/7/GRCh38#11379074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12320910-C-A

11379074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12320910-C-T

11379191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12321027-T-C

11379215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12321051-T-C

11379328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321165-G-C

http://identifiers.org/hco/7/GRCh38#11379359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12321196-C-A

http://identifiers.org/hco/7/GRCh38#11379460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12321711-A-C

11379460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321711-A-T

11379486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321740-T-A

11379486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321740-T-C

11379486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321740-T-G

11379504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321764-A-G

11379607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321865-T-A

11379607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12321865-T-C

11379649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321907-G-A

11379649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321907-G-T

http://identifiers.org/hco/7/GRCh38#11379683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12321941-C-A

11379683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321941-C-G

11379683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321941-C-T

11379738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12321996-A-G

11379881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322111-T-C

11380035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322290-G-C

11380035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322290-G-T

http://identifiers.org/hco/7/GRCh38#11380049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12322308-A-C

11380095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322360-C-T

11380199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322467-C-G

11380567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12322882-T-C

11380937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323230-G-A

11380981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323270-A-G

11381120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323414-A-G

11381173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323459-G-A

11381222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323514-T-C

11381372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323668-A-G

11381372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323668-A-T

11381389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323685-G-C

11381410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323706-G-C

11381493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323792-C-T

11381527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323826-T-C

11381567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323867-T-A

11381591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12323891-C-G

11381703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12324006-G-A

http://identifiers.org/hco/7/GRCh38#11381772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12324073-A-C

11382073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12324175-A-G

11382488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12324564-T-C

11382488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12324564-T-G

11382533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12324608-T-C

11382558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12324633-T-C

11400486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12324787-G-A

11400805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325103-T-A

11400853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325147-A-G

11400925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325225-G-A

11400925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325225-G-T

11401053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325353-C-T

11401139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325440-G-A

11401139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325440-G-T

11401228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325524-G-A

11401228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12325524-G-T

11401767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327473-G-T

11401773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327479-G-C

11401773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327479-G-T

11402010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327702-G-C

11402010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327702-G-T

11402015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327707-G-A

11402015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327707-G-C

11402015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327707-G-T

11402038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327730-T-C

11402181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12327850-T-C

11402460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12328094-G-C

11402718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12328311-C-T

http://identifiers.org/hco/7/GRCh38#11403076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12328585-A-C

11403076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12328585-A-G

11403183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12328668-A-G

11403302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12328781-A-G

11403567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12329903-T-A

11403801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12330133-G-C

11406140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12330344-G-A

http://identifiers.org/hco/7/GRCh38#11406149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12330352-C-A

11406149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12330352-C-G

11406149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12330352-C-T

11406346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12330983-A-G

11406566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12331205-T-C

11406922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12331556-T-A

11406922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12331556-T-C

11407145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12331777-T-A

11407247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12331869-G-T

11407441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12332063-G-C

11407441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12332063-G-T

11409234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335723-G-A

11409409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12335985-C-T

11410122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336244-T-A

11410271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336388-C-T

11410282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336400-A-G

http://identifiers.org/hco/7/GRCh38#11410508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12336538-A-C

http://identifiers.org/hco/7/GRCh38#11410599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12336641-C-A

11410599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336641-C-G

11410599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336641-C-T

11410636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336681-A-G

11410689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336733-A-G

11410705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336749-T-C

11410811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12336860-T-A

http://identifiers.org/hco/7/GRCh38#11411111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12337156-A-C

11411113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337158-T-C

11411191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337235-C-T

http://identifiers.org/hco/7/GRCh38#11411415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12337457-C-A

11411415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337457-C-G

11411429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337471-G-T

11411623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337665-T-C

11411872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12337895-C-T

http://identifiers.org/hco/7/GRCh38#11411899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12337922-C-A

http://identifiers.org/hco/7/GRCh38#11411933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12337952-C-A

11412010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338028-A-G

11412048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338065-C-T

http://identifiers.org/hco/7/GRCh38#11412184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12338192-A-C

11412423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338349-C-G

11412464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338389-C-T

11412515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338442-A-G

11412515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338442-A-T

http://identifiers.org/hco/7/GRCh38#11412543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12338469-C-A

11412543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338469-C-G

11412543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338469-C-T

11412593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338525-G-A

11412593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338525-G-T

http://identifiers.org/hco/7/GRCh38#11412602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12338534-C-A

11412602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338534-C-T

11412603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12338535-T-C

http://identifiers.org/hco/7/GRCh38#11412713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#12338637-C-A

http://identifiers.org/hco/7/GRCh38#11416482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12340727-C-A

11416482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12340727-C-G

11417141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12342866-T-C

11417166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12342891-G-C

11417206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12342932-T-G

11417217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12342949-G-T

11417300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343025-G-A

11417300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343025-G-T

11417305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343030-A-T

http://identifiers.org/hco/7/GRCh38#11417322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12343047-C-A

11417324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343049-T-C

11417327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343051-C-G

11417327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343051-C-T

http://identifiers.org/hco/7/GRCh38#11417337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12343061-C-A

11417337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343061-C-T

11417409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343071-T-A

11417429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343091-T-C

11417498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12343160-A-G

11417871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343495-G-A

http://identifiers.org/hco/7/GRCh38#11417900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12343534-A-C

11417901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343535-G-C

11417931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343595-C-T

11417958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12343622-A-G

11418566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344293-C-T

11418584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344311-A-G

11418651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344379-C-T

11418708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344437-T-A

11418881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344589-A-T

11419113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344801-T-C

11419113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344801-T-G

11419133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344821-C-G

11419133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344821-C-T

11419160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344848-C-T

11419198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12344884-G-T

11422037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12345220-A-G

11422102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12345274-G-A

http://identifiers.org/hco/7/GRCh38#11422265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12346245-C-A

11422325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12346304-C-T

http://identifiers.org/hco/7/GRCh38#11422394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12346371-C-A

11422394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12346371-C-T

http://identifiers.org/hco/7/GRCh38#11422630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12346582-C-A

11422630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12346582-C-G

11424191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12347178-T-A

11424343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12347337-A-G

11424525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348034-T-C

11424532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348041-A-G

11424534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348043-C-G

http://identifiers.org/hco/7/GRCh38#11424599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12348102-C-A

11424601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348104-G-C

11424613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348116-G-A

11424613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348116-G-T

11424640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348143-G-C

11424640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348143-G-T

11424788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12348288-G-A

11424788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 12348288-G-T

http://identifiers.org/hco/7/GRCh38#11424902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12348406-C-A

11424902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348406-C-T

11425181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348596-G-A

11425326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348722-T-C

11425549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12348951-C-G

11425783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349140-G-A

11425887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349202-A-G

11425935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349212-T-C

11426050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349240-G-A

11426053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349243-T-A

http://identifiers.org/hco/7/GRCh38#11426108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12349253-C-A

11426298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349444-G-A

11426610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349675-G-A

11426629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349694-G-T

11426669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 12349712-T-A

11426669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 12349712-T-C

11426728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349772-T-A

11426728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349772-T-C

11426735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349778-A-G

http://identifiers.org/hco/7/GRCh38#11426738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12349781-C-A

11426738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349781-C-T

11426841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349888-A-T

11426931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12349973-G-C

http://identifiers.org/hco/7/GRCh38#11427071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12350118-C-A

11427398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12350448-A-G

11427401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12350451-C-T

11427580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12350593-C-T

11427889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12350885-C-T

11428165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351113-T-C

11428245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351188-A-G

http://identifiers.org/hco/7/GRCh38#11428442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12351380-C-A

11428442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351380-C-T

11428494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351519-A-G

11428812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351840-A-T

11428878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351906-A-G

11428878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351906-A-T

http://identifiers.org/hco/7/GRCh38#11428907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12351942-A-C

11428907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351942-A-G

http://identifiers.org/hco/7/GRCh38#11428914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12351949-C-A

11428928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351963-T-C

11428928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12351963-T-G

11429052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12352089-G-T

11429140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352177-A-G

11429168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352202-T-C

11429181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352215-A-G

11429181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352215-A-T

http://identifiers.org/hco/7/GRCh38#11429186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12352220-C-A

11429186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352220-C-T

11429211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352245-T-C

http://identifiers.org/hco/7/GRCh38#11429230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12352264-C-A

11429230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352264-C-T

11429458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352495-T-C

11429539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352578-T-C

11429539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352578-T-G

11429630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352669-C-G

11429659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12352704-G-T

http://identifiers.org/hco/7/GRCh38#11430000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12352976-C-A

11430083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353030-G-A

11430253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353183-G-A

11430260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353190-G-C

11430430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353311-T-G

11430813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12353468-T-C

http://identifiers.org/hco/7/GRCh38#11431572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12354223-A-C

11431851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354511-T-C

11431942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354596-A-G

11432080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354739-A-G

11432102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354758-T-C

11432108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354764-A-T

11432132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12354788-A-T

http://identifiers.org/hco/7/GRCh38#11432899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12357799-A-C

11433074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12357958-A-G

http://identifiers.org/hco/7/GRCh38#11433893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12358281-C-A

11434331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358723-T-G

11434380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358790-G-A

11434396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12358821-G-C

http://identifiers.org/hco/7/GRCh38#11434498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12358924-C-A

11434612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12359036-A-G

11434877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12359321-C-G

11434921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12359364-G-A

11435001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12359435-T-A

11436984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360280-A-T

11437050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360341-G-C

11437053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360344-A-G

http://identifiers.org/hco/7/GRCh38#11437130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12360417-C-A

11437143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360430-G-A

11437211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12360498-C-T

11437551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12370888-C-G

http://identifiers.org/hco/7/GRCh38#11437707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12371029-A-C

11438340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371703-T-G

11438380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371738-G-C

11438405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371761-A-G

11438413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371769-T-C

11438420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371776-A-G

11438433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371789-G-T

http://identifiers.org/hco/7/GRCh38#11438459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12371843-C-A

11438489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12371871-C-T

11438756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372162-G-T

11438779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372177-G-A

11438814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372213-C-T

11438927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372324-G-C

11438932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372329-A-T

11439003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372399-G-C

11439003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372399-G-T

http://identifiers.org/hco/7/GRCh38#11439014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12372410-C-A

11439014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372410-C-T

11439035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12372432-C-G

11442601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376574-G-A

11442688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12376655-G-T

http://identifiers.org/hco/7/GRCh38#11443000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12377664-C-A

11443258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378025-C-T

http://identifiers.org/hco/7/GRCh38#11443332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12378096-A-C

11443378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378139-T-A

11443378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378139-T-C

11443573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378301-A-G

11445467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378864-C-T

11445502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378894-G-A

11445502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12378894-G-T

11445715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379070-C-T

http://identifiers.org/hco/7/GRCh38#11445785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12379147-C-A

11445785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379147-C-G

11445785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379147-C-T

11445827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379189-C-T

11445936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379275-G-T

11445986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379319-T-C

11446003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379336-G-A

http://identifiers.org/hco/7/GRCh38#11446188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12379519-C-A

11446188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12379519-C-T

11446200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12379531-T-C

11446239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12379570-A-G

http://identifiers.org/hco/7/GRCh38#11446405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12379725-C-A

11446405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379725-C-T

http://identifiers.org/hco/7/GRCh38#11446418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12379736-C-A

11446418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12379736-C-T

11446620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380586-T-C

http://identifiers.org/hco/7/GRCh38#11446665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12380620-A-C

11446710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380672-C-T

11446784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380771-T-C

11446845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380842-T-C

11446856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12380853-C-T

11447099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12381066-A-T

http://identifiers.org/hco/7/GRCh38#11447345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12381335-A-C

11447345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12381335-A-T

11447665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382336-C-G

11447669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382343-G-A

11447669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382343-G-C

11447973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382611-A-G

11448057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382683-C-T

11448173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12382943-T-A

11448319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383172-G-A

11448506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383364-G-A

11448506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383364-G-T

11448678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383521-T-A

11449030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383811-A-G

http://identifiers.org/hco/7/GRCh38#11449068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12383845-A-C

11449068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383845-A-T

11449172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383951-G-C

11449219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12383980-A-G

11449515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384694-C-T

11449567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384735-T-C

http://identifiers.org/hco/7/GRCh38#11449768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12384910-C-A

11449768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12384910-C-T

11450023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385113-A-G

http://identifiers.org/hco/7/GRCh38#11450052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12385144-C-A

11450052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385144-C-G

11450052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385144-C-T

11450061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385153-A-G

http://identifiers.org/hco/7/GRCh38#11450069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12385161-C-A

11450089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385181-A-G

11450102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385197-C-G

11450107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385215-T-C

11450255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385410-T-A

11450255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385410-T-C

11450324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385481-G-A

11450399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385563-G-A

11450424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385584-T-C

11450648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385809-A-G

11450732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385892-T-A

11450732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12385892-T-C

11450864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386007-C-G

11450864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386007-C-T

11451040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386168-G-A

http://identifiers.org/hco/7/GRCh38#11451194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12386317-A-C

11451322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386765-G-C

11451446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12386898-G-T

11452450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387896-T-C

11452460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387906-G-C

http://identifiers.org/hco/7/GRCh38#11452472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12387918-C-A

11452536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12387978-T-C

http://identifiers.org/hco/7/GRCh38#11452585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12388026-C-A

11452595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388036-A-G

11452621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388060-C-T

11452697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388140-T-C

11452720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388163-C-T

11452863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388311-G-A

11453150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388570-T-G

11453754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388853-G-A

11453754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12388853-G-T

11454001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12389951-G-A

11454072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390022-A-T

11454564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390333-T-A

11454674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390449-T-C

11454792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12390522-T-G

11456238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391430-C-G

11456238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391430-C-T

11456286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391480-C-T

http://identifiers.org/hco/7/GRCh38#11456289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12391483-A-C

http://identifiers.org/hco/7/GRCh38#11456314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12391508-C-A

11456314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391508-C-T

11456416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391608-T-G

11456471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391662-T-C

http://identifiers.org/hco/7/GRCh38#11456587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12391755-A-C

11456600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391767-T-C

11456679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12391844-C-T

11456948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392115-A-T

11457002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392178-C-G

11457164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392339-G-T

11457284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392447-T-A

11457571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392742-C-G

11457592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392763-C-T

11457802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12392967-C-T

11458138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393289-G-T

11458144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393295-T-C

11458408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393577-C-G

11458497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393646-T-C

11458640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393842-T-C

11458706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393909-G-A

11458755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12393960-G-A

11458904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394146-C-G

11458904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394146-C-T

11459070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394709-G-A

11459229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394828-C-T

http://identifiers.org/hco/7/GRCh38#11459272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12394873-A-C

11459316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12394915-C-T

11460028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12395938-T-C

http://identifiers.org/hco/7/GRCh38#11460158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12396059-A-C

11460192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396093-C-G

http://identifiers.org/hco/7/GRCh38#11460342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12396245-C-A

11460342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396245-C-G

11460342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396245-C-T

11460382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396267-G-A

11460425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396314-C-T

11460531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396413-G-A

11460531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396413-G-T

http://identifiers.org/hco/7/GRCh38#11460556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12396437-C-A

11460556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396437-C-G

11460610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396486-G-A

11460610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396486-G-T

http://identifiers.org/hco/7/GRCh38#11460619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12396495-C-A

11460619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396495-C-T

11460638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396533-G-C

11460638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396533-G-T

11460643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396538-G-C

11460688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12396581-C-T

11460705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12396598-G-A

11460705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12396598-G-C

11460734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12396627-A-T

http://identifiers.org/hco/7/GRCh38#11460780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12396673-C-A

11460780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396673-C-G

11460780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396673-C-T

11460900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396776-T-A

11460900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396776-T-G

11461063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12396942-C-T

11461205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397048-C-T

http://identifiers.org/hco/7/GRCh38#11461425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12397273-C-A

11461425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397273-C-T

11461750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397602-C-T

11461788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397640-G-A

11461788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397640-G-C

11461788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397640-G-T

http://identifiers.org/hco/7/GRCh38#11461881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12397736-C-A

11461881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397736-C-T

http://identifiers.org/hco/7/GRCh38#11461882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12397737-C-A

11461882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397737-C-T

11462034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12397861-T-G

11462082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12397909-C-G

11462082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12397909-C-T

11462085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12397912-G-A

11462085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12397912-G-T

11462160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12397987-T-G

11462192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398019-A-G

11462257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398086-T-C

11462260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398093-G-A

11462265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398098-T-A

11462265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398098-T-G

11462312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398144-T-C

http://identifiers.org/hco/7/GRCh38#11462524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12398343-C-A

11462661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398466-T-C

11462690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398486-C-T

11462810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398599-T-C

http://identifiers.org/hco/7/GRCh38#11462864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12398651-C-A

11462936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398732-T-A

11462958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398756-G-C

11462975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398773-C-T

11462978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12398776-T-C

11463398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399212-G-A

11463398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399212-G-T

11463524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399333-T-A

11463524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399333-T-C

11463596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399399-G-A

11463710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399508-A-G

11463710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399508-A-T

11464077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12399854-C-T

11464576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400406-C-G

11464673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400511-C-G

11464815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12400644-A-G

http://identifiers.org/hco/7/GRCh38#11464940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12400741-C-A

11466078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401003-T-A

11466119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401046-T-A

11466260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401186-T-G

11466365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401278-A-G

11466381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401293-T-A

11466421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401333-A-G

11466455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401372-T-A

11466628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401523-C-G

11466628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401523-C-T

11466641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401536-A-G

11466651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401546-T-C

11466784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401678-C-T

11466821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401715-A-G

11466976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401831-G-T

http://identifiers.org/hco/7/GRCh38#11466992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12401847-C-A

11466992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401847-C-T

11467004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12401859-C-G

11469121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404371-T-G

11469248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404482-C-G

11469457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404692-T-G

11469497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404731-C-T

11469678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404908-G-A

11469678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404908-G-T

http://identifiers.org/hco/7/GRCh38#11469685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12404915-C-A

11469739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404971-T-C

11469739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404971-T-G

http://identifiers.org/hco/7/GRCh38#11469753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12404985-A-C

11469753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12404985-A-G

11469806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405038-A-G

11469830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405060-C-T

11469927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12405156-C-T

11469930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12405159-T-C

http://identifiers.org/hco/7/GRCh38#11470004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12405234-C-A

11470004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405234-C-T

11470089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405317-A-G

11470097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405325-C-T

11470149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405367-A-G

http://identifiers.org/hco/7/GRCh38#11470186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12405404-A-C

11470324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12405537-A-G

11471466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406126-C-T

11471479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406139-T-C

11471923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406413-T-C

11471946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12406436-T-C

11472565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407057-C-T

http://identifiers.org/hco/7/GRCh38#11472885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12407335-C-A

11472885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407335-C-T

11473119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407560-T-C

11473162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407603-G-C

11473253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407692-G-C

11473336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407798-G-T

11473416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407877-G-C

http://identifiers.org/hco/7/GRCh38#11473472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12407957-C-A

11473472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12407957-C-T

11473734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408221-G-A

11473767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408241-T-G

11474227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408696-G-A

11474227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408696-G-C

11474227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408696-G-T

11474228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408697-G-A

11474228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408697-G-C

11474228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408697-G-T

http://identifiers.org/hco/7/GRCh38#11474301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12408769-C-A

11474301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408769-C-G

11474301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408769-C-T

11474311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12408779-T-C

11474354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12408822-C-T

11474393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12408861-G-A

11474627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409095-C-T

11474786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412896-A-T

11474833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412957-G-C

11474875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412995-G-A

http://identifiers.org/hco/7/GRCh38#11474886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12413006-A-C

11474963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413080-A-G

11475061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413165-G-C

11475299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413342-T-C

11475300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413343-T-C

11475324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413368-C-T

11475325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413369-C-T

11475330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413374-T-G

11475510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413446-G-A

11475514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413450-G-A

11475514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413450-G-C

11475644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413501-T-G

11475857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413725-G-C

11476031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413838-T-G

11476044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413851-A-G

11476053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413860-G-T

11476421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414262-T-C

11476421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414262-T-G

11479426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415833-G-A

http://identifiers.org/hco/7/GRCh38#11479523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12415917-A-C

http://identifiers.org/hco/7/GRCh38#11479526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12415920-A-C

11479782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416129-T-C

11479963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416189-T-C

11479978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416204-T-C

11479978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416204-T-G

11480108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416246-T-C

11480235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416374-G-A

11480250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416388-C-T

11480275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416413-T-C

11480381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416519-G-A

11480381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416519-G-T

11480572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416706-T-G

11480815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416920-T-C

11480882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416986-G-A

http://identifiers.org/hco/7/GRCh38#11480955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12417057-A-C

11480963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417063-T-G

11481219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417303-T-C

11481439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417889-T-C

11481479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417928-G-A

11481672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418132-T-A

11481672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418132-T-C

http://identifiers.org/hco/7/GRCh38#11481679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418139-A-C

http://identifiers.org/hco/7/GRCh38#11481693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418153-A-C

11481693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418153-A-G

http://identifiers.org/hco/7/GRCh38#11481698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418158-C-A

11481698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418158-C-T

11481710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418170-T-C

11481771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418226-T-C

11481771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418226-T-G

http://identifiers.org/hco/7/GRCh38#11481951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418407-A-C

11481951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12418407-A-G

11481995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418451-T-C

http://identifiers.org/hco/7/GRCh38#11482069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418526-A-C

http://identifiers.org/hco/7/GRCh38#11482107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418561-C-A

11482107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418561-C-T

11482139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418585-T-G

11482380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418823-T-C

http://identifiers.org/hco/7/GRCh38#11482499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12418939-A-C

11482514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418954-G-A

11482689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419125-G-A

11482813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419555-T-A

11482876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419615-T-C

11482914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419653-A-G

11482914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419653-A-T

11483227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419928-T-A

11483227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419928-T-C

11483229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419930-T-C

11483655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420303-C-G

11483655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420303-C-T

11483678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420326-G-A

11483678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420326-G-T

11483728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420354-C-T

11483809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420435-A-G

11483876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420500-A-T

11490088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421556-C-T

11490133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421599-G-C

11490221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421685-C-T

11490222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421686-C-T

11490238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421703-T-A

11490249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421714-G-A

11490269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421734-T-C

11490334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421793-T-G

11490407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421844-T-A

11490554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421979-T-C

http://identifiers.org/hco/7/GRCh38#11490929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12424118-C-A

11490929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424118-C-T

http://identifiers.org/hco/7/GRCh38#11490958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12424145-A-C

http://identifiers.org/hco/7/GRCh38#11491065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12424251-A-C

11491296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424459-T-C

11491463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424715-T-C

11491711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12424945-C-T

11492072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425390-G-A

11492074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425392-A-G

11492086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12425404-C-G

11492514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12426021-T-C

11492720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12426210-T-C

11492774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12426259-C-T

11493129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433053-A-G

11493154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433080-T-C

11493154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433080-T-G

11493216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433132-A-G

11493257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433173-A-G

11493296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433206-C-T

11493464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12433372-G-A

http://identifiers.org/hco/7/GRCh38#11493686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12435298-A-C

11493798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435412-A-T

http://identifiers.org/hco/7/GRCh38#11493858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12435467-C-A

11493858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435467-C-T

11493903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435512-G-A

11493903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435512-G-C

11493965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435576-C-G

11494072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435694-G-A

11494193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435807-T-C

11494781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436406-C-G

11494781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436406-C-T

11494809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436433-G-A

http://identifiers.org/hco/7/GRCh38#11494845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12436464-C-A

http://identifiers.org/hco/7/GRCh38#11494958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12436572-A-C

11494965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436579-T-G

11495167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436790-A-G

11495329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436952-G-T

11495422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437040-G-A

11495422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437040-G-T

11495540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437155-T-A

11495570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437185-T-A

11495644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437259-T-C

11495832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437455-G-T

http://identifiers.org/hco/7/GRCh38#11495845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12437468-C-A

11495845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437468-C-G

11495845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437468-C-T

11496030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437642-A-T

11496056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437668-C-T

11496089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437703-T-C

11505013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438193-G-T

11505384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438550-A-G

11505385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438551-G-A

11505451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438614-T-C

11505540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438700-C-T

11505642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438802-G-A

11505730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438859-T-A

11505769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438898-G-A

http://identifiers.org/hco/7/GRCh38#11505790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12438974-C-A

11505790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438974-C-T

http://identifiers.org/hco/7/GRCh38#11505893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12439075-A-C

11506008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439172-G-C

11506296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439221-T-C

11516475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441163-G-A

11516514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441200-G-C

11516542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441228-T-C

11516652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441317-A-G

11516660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441325-T-C

11516779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441625-A-T

http://identifiers.org/hco/7/GRCh38#11516885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12441729-A-C

http://identifiers.org/hco/7/GRCh38#11516898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12441745-C-A

11516898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441745-C-T

11517003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441860-G-C

11517571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12443467-A-G

http://identifiers.org/hco/7/GRCh38#11517652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12443547-C-A

11517652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12443547-C-T

11517673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12443568-G-T

http://identifiers.org/hco/7/GRCh38#11517809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12443620-C-A

http://identifiers.org/hco/7/GRCh38#11518007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12443793-C-A

11518197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12443931-T-C

11518396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444109-G-A

11518409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444122-T-A

11518409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444122-T-C

11518442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444152-A-T

11518479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444180-T-C

11518990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445567-C-T

11519424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445937-G-A

11519603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446103-G-A

11519658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446162-A-G

http://identifiers.org/hco/7/GRCh38#11519938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12446746-C-A

11519952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446769-T-G

11519961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446778-G-A

11519973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446790-C-T

http://identifiers.org/hco/7/GRCh38#11519976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12446793-C-A

11519976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446793-C-G

11519976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446793-C-T

11519977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446794-T-A

11520002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446819-G-T

11520102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12446917-G-A

11520192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12446997-A-G

11520215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447017-G-T

11520224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447026-A-T

http://identifiers.org/hco/7/GRCh38#11520239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12447040-C-A

11520328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447121-T-C

11520482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447250-C-G

http://identifiers.org/hco/7/GRCh38#11520557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12447345-C-A

11520632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447421-G-A

11520632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447421-G-C

11520748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447514-G-T

11521021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447793-T-C

11521108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447879-T-C

11521108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447879-T-G

11521142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447910-A-G

11521190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447942-T-C

11521348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448088-T-C

http://identifiers.org/hco/7/GRCh38#11521419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12448156-A-C

11521965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448779-T-C

11521966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448780-A-G

http://identifiers.org/hco/7/GRCh38#11522068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12448861-A-C

11522092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448883-T-C

11522102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448893-G-C

11522267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449037-T-C

11522284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449053-T-C

http://identifiers.org/hco/7/GRCh38#11522363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12449134-A-C

11522458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449223-A-T

11522611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449351-G-A

11522639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449383-G-C

11522639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449383-G-T

11522787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449544-T-C

11522894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452816-T-C

11522924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452846-G-C

11522995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452926-A-G

11523132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453072-T-C

11523159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453099-G-T

11523185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453124-T-C

http://identifiers.org/hco/7/GRCh38#11523212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12453151-A-C

11523412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453328-G-A

11523579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453461-T-G

http://identifiers.org/hco/7/GRCh38#11523639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12453510-A-C

11523639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453510-A-G

11523896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455050-A-G

11523944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455099-T-C

http://identifiers.org/hco/7/GRCh38#11524100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12455209-A-C

11524371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455438-A-G

11524414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455463-A-G

11524654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455681-G-A

11524654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455681-G-C

11524758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455774-C-G

11524758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455774-C-T

11524784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455801-G-A

11524801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455818-A-T

11524804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455821-T-G

11524820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455831-G-T

11524826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455837-G-A

11524854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455865-T-C

11524923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455937-T-C

11524952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455970-A-G

http://identifiers.org/hco/7/GRCh38#11525022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12456042-C-A

11525055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456074-T-A

11525069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456088-T-C

11525199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456240-G-C

11525270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456314-T-G

11525279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456323-C-G

11525348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456376-C-T

11525630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456885-T-C

11525630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456885-T-G

11525633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456888-A-G

11525640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456895-T-A

11525663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456917-C-G

11525803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457064-A-T

11525916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457176-A-G

http://identifiers.org/hco/7/GRCh38#11526098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12457370-C-A

http://identifiers.org/hco/7/GRCh38#11526269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12457526-A-C

11526269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457526-A-G

11526355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457596-T-C

11530052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457955-A-T

11530072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457975-G-A

11530072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457975-G-C

11530169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458066-T-C

http://identifiers.org/hco/7/GRCh38#11530180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12458087-A-C

11530210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458116-G-C

11530365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458270-G-A

11530385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458290-T-C

11530511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458408-T-C

http://identifiers.org/hco/7/GRCh38#11530568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12458450-A-C

11531044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458622-T-C

11531102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458656-T-C

11531210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458761-T-C

http://identifiers.org/hco/7/GRCh38#11531297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12458838-C-A

11531297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458838-C-T

11531347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458888-G-A

11531678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459186-G-T

11531831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459349-T-C

11531932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459438-C-T

11531948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459452-G-A

11531948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12459452-G-C

http://identifiers.org/hco/7/GRCh38#11532014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12459518-A-C

11535015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460877-G-A

11535051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460906-G-A

11535223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461062-C-T

11535298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461130-T-C

11535320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461164-T-C

11535375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461230-T-A

11535385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461249-C-T

11535398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461262-G-T

11535462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461326-G-A

11535462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461326-G-T

11535568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461428-G-A

11535749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461614-G-A

11535762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461627-C-G

11535777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461642-G-A

11535894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461764-T-C

11535905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12461775-T-C

11536181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462046-G-A

11536181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462046-G-C

11538395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465465-C-T

http://identifiers.org/hco/7/GRCh38#11538659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12465706-C-A

11538775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465812-G-A

11538778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465815-G-T

11538968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12466008-G-A

11538973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12466013-A-T

11539145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12466185-C-T

http://identifiers.org/hco/7/GRCh38#11539228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12466267-C-A

11539257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12466295-T-G

11539395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466430-G-A

11539395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466430-G-T

11539825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466830-A-G

11540213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467236-C-G

11540268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467291-T-C

11540367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467404-T-C

11540378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467415-G-C

11540384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467421-T-G

11540389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467426-G-A

11540449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467486-G-A

11540803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12467824-G-C

http://identifiers.org/hco/7/GRCh38#11540835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12467855-C-A

11540835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467855-C-T

11540897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467905-G-A

11540902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467910-G-A

http://identifiers.org/hco/7/GRCh38#11540944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12467963-C-A

11540944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467963-C-G

11541244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468676-T-G

11541281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468714-G-A

11541281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468714-G-C

11541281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468714-G-T

11541295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468728-G-A

11541295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468728-G-T

http://identifiers.org/hco/7/GRCh38#11541296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12468729-C-A

11541344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468734-G-A

11541346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468736-A-G

11541346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468736-A-T

http://identifiers.org/hco/7/GRCh38#11541389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12468759-A-C

11541389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468759-A-G

http://identifiers.org/hco/7/GRCh38#11541407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12468776-C-A

11541407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468776-C-G

11541407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468776-C-T

11541673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469043-G-A

11541673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469043-G-T

11541716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469086-T-C

11541719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469089-G-T

11541720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469090-A-G

11541720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469090-A-T

11541755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469127-T-C

http://identifiers.org/hco/7/GRCh38#11541756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12469128-C-A

http://identifiers.org/hco/7/GRCh38#11541768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12469141-C-A

11541768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469141-C-T

http://identifiers.org/hco/7/GRCh38#11541769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12469142-C-A

11541769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469142-C-T

11543061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12471140-G-A

11543061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12471140-G-T

11543219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471291-A-T

http://identifiers.org/hco/7/GRCh38#11543233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12471305-C-A

11543233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471305-C-T

http://identifiers.org/hco/7/GRCh38#11543240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12471312-C-A

11543240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471312-C-G

11543240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471312-C-T

11543499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471528-G-A

11543510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471539-G-T

11543529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471558-A-T

http://identifiers.org/hco/7/GRCh38#11543530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12471559-A-C

11543530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471559-A-T

11543549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471577-C-T

11543584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471611-G-A

11543618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471648-T-C

11543759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471777-A-G

11543844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12471867-T-C

http://identifiers.org/hco/7/GRCh38#11543917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12471926-A-C

11544460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472127-A-G

11544702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472360-T-C

11544702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472360-T-G

11544817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472451-C-G

http://identifiers.org/hco/7/GRCh38#11544819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12472453-C-A

11544906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472530-G-C

11544914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472535-G-A

11544914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472535-G-C

11545002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472622-T-C

11545044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12472664-T-C

11564218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12477714-C-G

11564218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12477714-C-T

11564259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12477763-T-A

11564279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12477778-G-T

11564436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478072-G-A

11564514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478140-T-G

11564812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478381-T-G

11564896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478456-T-C

http://identifiers.org/hco/7/GRCh38#11564922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12478481-A-C

11564922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478481-A-T

11565079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478638-T-C

11565144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478707-C-G

11565235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478795-G-A

11565299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478855-T-A

http://identifiers.org/hco/7/GRCh38#11565311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12478867-A-C

11565311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478867-A-G

11565349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12478901-C-G

11565573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479141-T-C

11565783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479339-T-A

11565853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479387-T-G

11565900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479441-G-T

11565908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479447-G-A

11565908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479447-G-C

http://identifiers.org/hco/7/GRCh38#11566050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12479590-A-C

11566050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479590-A-T

http://identifiers.org/hco/7/GRCh38#11566254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12479760-C-A

11566419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479899-T-C

11566452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479932-T-C

11566457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12479937-T-C

http://identifiers.org/hco/7/GRCh38#11566541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12480016-A-C

11566662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480137-A-G

11566709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480186-A-G

11566723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480200-C-T

11566737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480214-C-T

11566955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480420-T-C

http://identifiers.org/hco/7/GRCh38#11566961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12480426-A-C

11566961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480426-A-G

11566963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480428-A-G

11566989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480446-T-G

http://identifiers.org/hco/7/GRCh38#11567007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12480463-C-A

11567007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480463-C-G

11567525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480578-C-G

11567756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12480806-C-T

11568019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481024-G-A

11568296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481563-C-T

11568297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481564-T-C

11568298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481565-G-T

11570760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481710-C-T

11570792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481724-T-C

11570871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481803-C-T

11570910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12481841-G-C

11571364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482246-T-A

11571578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482471-G-A

11571805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482712-T-A

11571924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482803-G-A

11571950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482828-T-C

11572005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482879-T-G

11572251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12482989-G-T

11572360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483097-C-T

11572467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483168-C-T

11572690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483220-G-T

11572691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483221-G-A

11572811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483279-G-A

11573278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483581-T-G

11573292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483595-C-T

11573328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483630-C-G

http://identifiers.org/hco/7/GRCh38#11573367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12483670-C-A

11573505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12483818-G-A

11573711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12484004-A-T

11573733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12484026-A-T

11577170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12487316-A-G

http://identifiers.org/hco/7/GRCh38#11577868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12487654-A-C

11577868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12487654-A-G

11578202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12487967-C-T

11578204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12487969-A-G

11578839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488567-G-A

11578839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488567-G-C

11578939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488672-C-G

11578980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488710-T-C

11579004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488729-T-A

11579009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488734-T-A

11579094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12488878-T-C

11579401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489192-A-G

11579460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489251-G-A

11579502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489292-T-C

11579529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489319-G-C

11579549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489339-T-C

11579566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489356-G-A

11579622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489413-T-C

11579715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489491-G-T

http://identifiers.org/hco/7/GRCh38#11579767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12489522-C-A

11579767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12489522-C-T

http://identifiers.org/hco/7/GRCh38#11579788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12489543-A-C

11580995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491628-A-T

11581048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491670-T-G

11581057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491679-T-G

11581076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491698-C-T

11581100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491722-C-T

11581155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491781-T-G

11581213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491824-A-G

11581298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491912-A-G

11581308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491921-G-A

11581328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491941-G-A

11581359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12491971-T-G

11581405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12492014-T-C

11581420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12492025-A-G

11581421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12492026-T-C

http://identifiers.org/hco/7/GRCh38#11581425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12492030-C-A

11581425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12492030-C-T

11581510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12492114-T-C

http://identifiers.org/hco/7/GRCh38#11581845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12492370-A-C

http://identifiers.org/hco/7/GRCh38#11583977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12493731-C-A

11583977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 12493731-C-T

11583985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493739-T-C

11584089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493809-T-C

11584102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493822-C-T

11584134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493854-C-T

11584138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493858-T-C

11584141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493861-C-G

http://identifiers.org/hco/7/GRCh38#11584258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12493971-C-A

11584258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12493971-C-T

11584587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12494714-T-C

http://identifiers.org/hco/7/GRCh38#11584626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12494759-C-A

11584626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12494759-C-T

11584714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12494846-A-G

11584830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12494970-A-G

11584880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495019-G-A

11584881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495020-T-C

11584881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495020-T-G

11584978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495088-T-C

11585006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495116-T-C

11585058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495153-C-T

11585088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495183-G-A

http://identifiers.org/hco/7/GRCh38#11585104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12495225-C-A

11585104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495225-C-T

11585112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495233-T-C

11585115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495236-T-C

11585130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495251-T-C

11585245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495371-C-G

11586074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495576-A-G

11586164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495667-T-C

11586314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495831-T-A

11586341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12495858-T-C

11586501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496004-A-T

11586759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496256-A-T

11586786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496269-T-C

11586792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496275-C-T

http://identifiers.org/hco/7/GRCh38#11586846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12496330-C-A

11586846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496330-C-T

11587135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496592-C-T

11587202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12496671-A-T

11587696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497118-A-T

11587709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497131-C-G

11587709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497131-C-T

11587866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497283-G-C

11587866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497283-G-T

11588125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497786-G-A

11588144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497803-C-T

11588215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497873-A-G

11588229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497887-C-T

11588230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497888-G-A

11588241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12497899-C-G

11588413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498039-G-C

http://identifiers.org/hco/7/GRCh38#11588422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12498048-C-A

11588422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498048-C-T

11588556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498213-C-T

11588601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498281-T-C

11588602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498282-T-G

11588612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498292-T-C

11588737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498414-T-A

11588742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498419-C-G

11588875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498551-A-T

11588882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498558-G-C

11588882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498558-G-T

11588917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498593-C-T

11588942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498618-T-C

11589030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498688-T-C

11589057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498714-A-G

11589061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498718-C-T

11589099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498757-G-T

11589106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498764-A-G

11589163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498819-G-C

11589163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498819-G-T

11589165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498821-A-T

11589173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498829-T-C

11589293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498928-A-G

11589298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498933-G-A

11589298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498933-G-T

11589321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498943-A-G

11589349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498971-T-A

11589349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12498971-T-C

11589387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12499007-C-T

11589434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12499056-C-G

11589434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12499056-C-T

11590034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12500528-T-C

http://identifiers.org/hco/7/GRCh38#11590221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12500703-C-A

11590399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12500930-G-C

11590399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12500930-G-T

11590503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12501029-G-A

11590503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12501029-G-C

11590503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12501029-G-T

11590523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12501049-C-G

11590523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12501049-C-T

11590605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12501131-A-G

11590605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12501131-A-T

http://identifiers.org/hco/7/GRCh38#11590688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12501217-C-A

11590688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501217-C-T

11590715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501244-G-C

11590715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501244-G-T

http://identifiers.org/hco/7/GRCh38#11590735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12501261-C-A

11590735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501261-C-G

11590956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501479-G-A

11591008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12501531-C-T

11591210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12501742-A-T

11591300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12501827-A-G

11591705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502226-A-G

11591731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502249-G-A

11591900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502423-G-A

11591900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502423-G-C

11591900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502423-G-T

11591958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502475-G-T

11592031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502564-T-C

11592036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502569-C-T

11592039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502574-T-G

11592046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502581-G-C

http://identifiers.org/hco/7/GRCh38#11592079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12502616-A-C

11592203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502712-A-G

11592376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12502876-C-T

11592975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12503564-C-T

11593041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12503628-T-C

11593232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12503895-A-G

11593313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12503974-T-C

11593337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12503998-G-A

11593613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504260-T-C

11593645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504300-T-A

11593645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504300-T-G

11593649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504304-G-A

11593649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504304-G-C

11593649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12504304-G-T

11600522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12505485-G-A

11600541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12505504-A-G

11600687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12505631-A-G

11600692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12505636-G-T

11601059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12506039-T-A

11601059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12506039-T-C

11601540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12506528-G-A

11602001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507048-T-A

11602167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507476-T-C

11602299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507625-T-C

11602311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507637-T-A

11602468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507797-C-T

11602480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12507809-T-A

11605314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12516920-T-G

11605395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12516946-G-T

11605414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12516966-T-C

11605497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12517046-T-G

11605731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12517324-T-A

http://identifiers.org/hco/7/GRCh38#11605755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12517346-C-A

11605755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12517346-C-T

http://identifiers.org/hco/7/GRCh38#11606568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12518091-C-A

11606568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518091-C-T

11606805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518333-G-A

http://identifiers.org/hco/7/GRCh38#11606844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12518373-A-C

11607048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518458-G-A

11607063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518473-T-C

11607065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518475-C-T

11607097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518504-C-T

11607121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518528-C-T

http://identifiers.org/hco/7/GRCh38#11607188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12518584-C-A

11607238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518623-A-G

11607356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518731-C-T

11607399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518774-T-A

11607497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12518879-T-C

11607890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519250-C-T

11607976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519336-C-T

11608333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519657-A-G

11608358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519682-C-G

11608503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519801-A-G

11608561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12519861-A-G

11608752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520036-G-T

11608775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520059-A-G

11608833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520786-C-G

11608864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520817-G-A

11608883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520834-C-T

11609014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12520933-A-G

11609190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12521101-C-T

11609275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12521187-C-T

11610320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12521828-C-T

11610841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12522345-G-A

11611006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12522521-T-C

11611311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12529108-C-T

11611961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12529595-A-G

11612234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12529819-T-C

http://identifiers.org/hco/7/GRCh38#11612356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12529937-C-A

11612377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12529958-A-T

11612516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530090-T-C

11612516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530090-T-G

11612538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530111-C-T

11612639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530294-T-C

11613146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530787-C-T

11613224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12530857-C-T

11613409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531194-G-T

11613469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531248-G-A

11613571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531341-G-A

11613660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531412-G-C

11613668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531420-C-T

11613723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531473-C-T

http://identifiers.org/hco/7/GRCh38#11613766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12531515-A-C

11613871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531600-G-T

11613914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531643-T-C

11613932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531673-C-T

11613945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531697-G-A

11613946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, undefined
orthologous variants: 12531698-A-G

11614025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531776-G-A

11614122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531852-T-C

11614255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531982-A-G

11614265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12531991-A-G

11614474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532161-T-A

11614493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532180-G-A

11614516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532203-T-G

11614524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532211-C-T

11614592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532272-T-C

11614877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532570-T-C

11615060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532731-A-G

11615192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532879-G-A

11615202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532889-A-G

11615316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12532997-T-C

11615456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12533123-C-G

http://identifiers.org/hco/7/GRCh38#11615489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12533156-C-A

11615666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12533322-G-C

11615666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12533322-G-T

11615692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12533348-C-T

11615783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12534011-T-C

http://identifiers.org/hco/7/GRCh38#11616016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12534437-A-C

11616249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12534631-G-C

http://identifiers.org/hco/7/GRCh38#11616619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12535244-C-A

11616619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12535244-C-T

11617591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12537260-T-C

11621835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12541976-G-A

11621845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12541986-C-T

11621897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542043-T-C

11621982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542111-T-C

11622064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542289-G-C

11622237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542435-C-G

11622249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542444-T-C

11622293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542485-A-G

11622295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542487-G-A

11622314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542507-G-T

11622437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542634-T-A

11622467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542664-G-A

11622467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542664-G-C

11622539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542735-A-G

11622539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542735-A-T

11622786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542932-T-G

11622787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12542933-C-T

11623078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12543164-T-C

11623200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12543286-T-C

11623215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12543300-G-C

11625346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12543651-T-C

http://identifiers.org/hco/7/GRCh38#11625466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12543774-C-A

11625509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12543817-C-T

11625949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12544280-T-C

11625961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12544292-T-C

http://identifiers.org/hco/7/GRCh38#11625991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12544322-C-A

http://identifiers.org/hco/7/GRCh38#11626060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12544384-A-C

11626512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545179-G-A

11626512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545179-G-T

11626581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545233-A-T

11626620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545272-C-T

11626641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545301-G-A

11626740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545588-C-G

11626864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12545728-A-G

11627342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12546038-T-C

11627687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12546245-A-G

11627772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12546326-C-T

11627821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12546395-G-C

11628101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547197-T-C

11628152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547267-T-C

http://identifiers.org/hco/7/GRCh38#11628162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12547276-C-A

11628356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547438-C-T

11628466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547546-C-G

11629076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547931-G-T

11629095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12547950-G-C

11629149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548004-C-T

http://identifiers.org/hco/7/GRCh38#11629272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12548121-A-C

11629355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548207-T-G

11629436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548284-A-T

11629548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548405-G-T

11629684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548549-C-T

http://identifiers.org/hco/7/GRCh38#11629697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12548566-A-C

11629751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548608-T-C

11629883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12548727-T-A

11630388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12549985-A-G

11630642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550222-G-T

11630653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550233-C-G

11630653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550233-C-T

11630774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550355-C-T

11630920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550495-T-C

11633204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550634-G-A

11633300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12550724-T-C

11633923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12552755-G-C

http://identifiers.org/hco/7/GRCh38#11633949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12552777-A-C

11634041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12552855-A-G

http://identifiers.org/hco/7/GRCh38#11634324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12552957-C-A

11634472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553106-T-C

11634484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553118-C-T

11634612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553254-T-C

11634635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553277-T-A

11634932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553674-C-G

11635017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553754-C-T

11635023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553760-G-T

http://identifiers.org/hco/7/GRCh38#11635055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12553790-C-A

11635055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553790-C-T

11635112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12553846-G-A

11635366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554098-G-A

11635462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554194-C-T

11635669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554399-C-T

11635994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554803-G-A

11636009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554818-G-A

11636009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554818-G-T

11636075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron variant
orthologous variants: 12554865-T-C

http://identifiers.org/hco/7/GRCh38#11636143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12554907-C-A

11636143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12554907-C-T

11636166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12554930-A-G

http://identifiers.org/hco/7/GRCh38#11636168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12554932-A-C

11636168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12554932-A-G

11636225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12554989-C-G

11636225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12554989-C-T

http://identifiers.org/hco/7/GRCh38#11636252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12555016-A-C

11636252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555016-A-G

11636254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12555018-T-A

11636282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555046-T-A

11636357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12555121-C-T

http://identifiers.org/hco/7/GRCh38#11636381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12555145-C-A

11636444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555208-C-G

11636444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555208-C-T

11636525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555289-G-C

11636525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555289-G-T

11636573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: synonymous variant
orthologous variants: 12555337-T-C

11636573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense variant
orthologous variants: 12555337-T-G

11636645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12555409-C-T

11636680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12555444-T-A

11636680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12555444-T-C

11636723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12555487-A-G

11636723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12555487-A-T

11636846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12555610-G-A

11636846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12555610-G-T

11636996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555756-A-G

11637034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555793-G-C

11637034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555793-G-T

11637048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555807-T-A

11637048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555807-T-C

11637111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555869-T-C

11637192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555949-G-C

11637209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12555966-C-T

11637352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556108-A-G

11637353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556109-T-C

11637355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556111-G-A

11637475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556231-T-C

11637650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556397-T-C

11637718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556470-A-G

11637753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556494-T-G

11637777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556555-A-G

11637801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12556579-C-T

11638222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557227-C-G

11638264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557269-G-A

11638321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557322-T-C

11638331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557334-T-C

11638433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557433-A-G

11638672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557645-C-T

11638770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557699-G-A

11638843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557776-C-T

11638893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557822-G-T

11639068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12557982-A-T

11639122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12558029-A-T

11639169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12558076-A-G

http://identifiers.org/hco/7/GRCh38#11639192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12558397-C-A

11639284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12558481-A-G

11641490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560298-C-G

11641551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560342-A-G

11641727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560492-A-T

11641843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560566-G-T

11641920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560642-C-G

11641920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560642-C-T

http://identifiers.org/hco/7/GRCh38#11642054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12560739-A-C

11642314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12560998-G-T

11642441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561115-T-C

11642450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561124-A-G

11642478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561152-A-G

11642532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561208-G-A

11642607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561282-A-T

11642741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561419-G-T

11642788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561464-A-G

11642803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561479-A-G

11642839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561508-T-G

http://identifiers.org/hco/7/GRCh38#11642918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12561583-C-A

11643065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561725-G-A

http://identifiers.org/hco/7/GRCh38#11643189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12561848-C-A

11643200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12561859-T-C

http://identifiers.org/hco/7/GRCh38#11643359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12562011-C-A

11643401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562045-A-G

11643431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562066-G-C

http://identifiers.org/hco/7/GRCh38#11643521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12562136-C-A

11643555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562167-C-T

11643560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562172-T-A

11643560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562172-T-C

11643615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562201-A-G

11643699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562271-G-A

11643699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562271-G-T

11643785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562349-T-C

11643949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562488-T-A

11644006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562535-A-T

11644010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562539-C-G

11644010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562539-C-T

11644122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562621-C-T

11644255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562749-G-C

11644272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562766-T-C

11644319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562837-C-G

11644319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562837-C-T

11644321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12562839-A-G

11644481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563180-G-T

11644550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563253-A-G

11644791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563487-G-A

11644827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563524-A-G

11644831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563528-T-G

11644959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563700-G-A

11645036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563777-C-T

11645083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12563823-C-T

11647107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564737-G-A

11647144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564774-A-G

11647180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564804-G-A

11647291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564903-G-A

11647311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564916-G-A

11647313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12564918-G-A

11651193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568289-A-G

11651276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568363-T-C

http://identifiers.org/hco/7/GRCh38#11651462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12568533-C-A

11651462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568533-C-T

11651585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568625-A-G

11651597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568637-T-C

11651629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568666-G-C

http://identifiers.org/hco/7/GRCh38#11651685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12568709-C-A

11651730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12568752-G-T

11652118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569140-A-G

11652134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569156-A-G

11652208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569217-C-T

11652291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569299-C-G

11652317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569325-A-G

11652317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569325-A-T

11652321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569329-A-T

11652540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569534-G-A

11652851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569749-T-G

11652929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569817-G-C

11652986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569875-T-C

11652989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12569878-C-G

11653137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12570001-T-A

11653190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12570049-G-A

11657086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571138-G-A

11657109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571161-A-G

11657237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571265-G-C

11657354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571396-G-A

11657521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571518-C-T

11657523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571520-G-C

11657523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571520-G-T

http://identifiers.org/hco/7/GRCh38#11657739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12571724-C-A

http://identifiers.org/hco/7/GRCh38#11657798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12571769-A-C

11657800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571771-G-T

11657961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571896-G-A

11657961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571896-G-C

11657961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571896-G-T

11658032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12571968-A-G

11658260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12572197-T-A

11658330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12572267-G-A

11658650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12572570-T-C

11658954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12572869-T-G

11659000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12572961-G-A

11659039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573005-T-C

11659071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573020-C-T

11659209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573153-C-T

11659260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573203-A-G

11660067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573335-G-T

11660078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573346-C-T

11660244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573505-G-C

11660249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573510-A-G

11660276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573538-A-G

11660367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573630-T-G

11660414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12573914-T-A

http://identifiers.org/hco/7/GRCh38#11660462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12573957-C-A

11660545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574062-T-C

11660668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574367-T-A

11660702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574399-T-A

http://identifiers.org/hco/7/GRCh38#11660716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12574409-A-C

11660717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574410-G-A

11660717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574410-G-C

11660775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574466-A-G

11660845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574531-C-T

11660945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574617-G-A

11661157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12574831-C-T

http://identifiers.org/hco/7/GRCh38#11664133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12575056-C-A

11664336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575255-T-C

11664479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575405-T-A

http://identifiers.org/hco/7/GRCh38#11664827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12575745-C-A

11664827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575745-C-G

11664827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575745-C-T

11664861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575779-T-C

11664905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12575825-G-A

http://identifiers.org/hco/7/GRCh38#11665316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12576238-C-A

11665316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12576238-C-G

11665437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12576359-G-A

11665839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12576795-G-T

11665886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12576899-G-C

http://identifiers.org/hco/7/GRCh38#11666116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12577138-C-A

11666116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12577138-C-T

11667499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578480-A-G

11667503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578484-T-C

11667503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578484-T-G

11667621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578602-A-G

11667756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578741-C-G

11667792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12578773-C-T

11668033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579029-A-G

11668093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579086-G-A

11668807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579341-A-G

11668807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579341-A-T

11669256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579793-T-G

11669318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579853-G-A

11669318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579853-G-T

11669381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579911-G-A

11669410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579940-C-T

11669441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579969-G-T

11669495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12579995-G-A

11669501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580001-A-G

11669504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580004-G-T

11669526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580026-G-C

11669673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580150-T-A

11669673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580150-T-G

11669995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580430-A-G

11670088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580505-C-G

11670255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580672-G-C

11670255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580672-G-T

11670271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580687-T-A

11670271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580687-T-G

11670291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580707-G-A

11670382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580791-T-A

11670437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12580842-A-G

11670947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581297-T-C

11670948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581298-G-A

11670988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581338-G-C

11671361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581696-C-T

11671401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581733-G-A

11671401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581733-G-T

11671437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581769-T-C

http://identifiers.org/hco/7/GRCh38#11671491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12581821-C-A

11671529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581858-G-A

11671593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581923-T-A

11671593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581923-T-C

11671779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582113-A-G

11671782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582116-C-G

11672138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582453-T-C

11672158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582469-G-A

11672190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582499-C-G

11672199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582508-C-G

11672228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582513-C-T

11672374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582638-T-C

11672397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582661-T-C

11672674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582899-T-G

11687111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583899-C-T

11687602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12584533-T-C

11688897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585188-T-C

11688942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585228-C-G

11688942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585228-C-T

11689074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585348-T-A

11689123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585377-A-G

11689124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585378-G-T

11689167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585404-C-G

11689167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585404-C-T

11689242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585459-T-C

http://identifiers.org/hco/7/GRCh38#11689279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12585496-C-A

11689332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585549-C-G

11689355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585571-T-A

11689489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585765-A-G

11689508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585811-T-G

11689538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585846-T-A

11689578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12585877-G-A

11690077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586375-T-C

11690125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586431-T-G

11690180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586491-A-G

11690445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586773-T-C

11690580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586869-T-C

11690682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12586945-C-T

http://identifiers.org/hco/7/GRCh38#11690746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12587085-A-C

11690891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587343-T-C

11691188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587596-T-C

11691335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587735-A-G

11691359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587759-T-C

11691709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588518-A-G

11691746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588545-A-G

11691902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588677-A-G

11691965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588701-G-A

11692228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588857-G-A

http://identifiers.org/hco/7/GRCh38#11692376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12588958-C-A

11692439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589021-A-T

11692473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589054-G-A

11692720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589621-G-A

11692720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589621-G-T

11692766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589680-T-C

11692873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589786-G-A

11692992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589904-T-A

11693066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589967-C-T

11693684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590429-C-T

11693745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590497-T-C

11693745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590497-T-G

11693828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590589-C-T

11693998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590759-A-G

11694085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590836-A-G

11694089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590840-G-C

11694139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590889-T-G

http://identifiers.org/hco/7/GRCh38#11694224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12590977-C-A

11694470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591222-G-A

11694599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591329-T-G

11694654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591380-T-C

11694661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591387-C-G

11694690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591413-C-T

11694693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591416-T-G

http://identifiers.org/hco/7/GRCh38#11694762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12591490-C-A

http://identifiers.org/hco/7/GRCh38#11694766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12591494-C-A

http://identifiers.org/hco/7/GRCh38#11694896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12591612-C-A

11694896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591612-C-G

11695031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591745-T-C

11695031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591745-T-G

11695218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591931-C-T

11695272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591981-G-A

11695275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12591985-T-C

11696951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594936-A-T

11697466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595288-G-T

11697498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595324-G-C

11697832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595656-C-G

http://identifiers.org/hco/7/GRCh38#11697877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12595705-C-A

11697877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595705-C-T

11697881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595709-T-G

11698387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596229-G-C

11698832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596662-T-A

11698858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596688-G-T

11698937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596766-G-A

http://identifiers.org/hco/7/GRCh38#11698997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12596829-C-A

11698997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596829-C-G

11698997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596829-C-T

http://identifiers.org/hco/7/GRCh38#11699016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12596848-C-A

11699020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596854-G-T

11699195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597028-C-T

11699643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598608-A-G

11699661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598624-T-A

11699661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598624-T-G

11699827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598790-G-A

11700226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599541-C-T

11700248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599563-G-A

11700456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599775-T-C

11700632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599935-G-A

11700723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600024-T-C

11700725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600026-G-A

11701207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600512-T-A

11701253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600557-A-T

11701545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600770-G-T

11701550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600775-G-A

http://identifiers.org/hco/7/GRCh38#11701571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12600796-A-C

11701571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600796-A-G

11701576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600801-G-A

11701576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600801-G-T

11701644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600871-T-C

http://identifiers.org/hco/7/GRCh38#11701666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12600892-C-A

11701855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601004-C-T

11701934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601067-C-G

11701959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601092-A-T

11701990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601130-G-A

11702053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601192-A-G

11702492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601625-C-T

11702679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601943-G-T

11702680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12601944-G-T

11702821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602084-C-G

11702965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602223-A-G

11703041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602296-C-T

11703061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602312-T-G

11703070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602321-T-C

11703170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602427-G-A

11703170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602427-G-C

11703334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602572-G-A

11703775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603001-A-G

11703987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603202-G-C

11703987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603202-G-T

http://identifiers.org/hco/7/GRCh38#11704220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12603441-C-A

11704403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603596-A-G

11704416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603624-G-C

11704419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603627-A-G

http://identifiers.org/hco/7/GRCh38#11704425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12603633-C-A

11704427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603635-C-G

11704433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603641-G-T

11704451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603659-G-T

11704526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603730-A-G

11704686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603876-G-A

11704797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604003-C-T

11704867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604056-G-T

11704939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604123-G-A

11705192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604258-T-A

11705206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604272-T-G

11705274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604341-G-C

11705544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604581-A-T

11705656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604831-C-T

11705728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12604920-A-G

11706627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606116-G-T

11706689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606155-G-C

11706689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606155-G-T

11706882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606346-C-G

11707058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606479-G-C

11707111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606527-T-C

11707143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606559-T-G

11707195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606604-T-C

11707224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606630-G-C

11707244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606650-C-T

11707676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607068-C-T

11707733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607125-A-G

11707739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607131-G-A

11707739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607131-G-T

http://identifiers.org/hco/7/GRCh38#11707801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12607193-C-A

11707912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607295-T-C

11708353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607913-A-G

11708548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608517-C-T

11708588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608556-T-C

11708588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608556-T-G

http://identifiers.org/hco/7/GRCh38#11708832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12608826-A-C

11708913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609269-C-G

11708927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609281-T-C

11709168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609462-A-T

11709561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609854-C-T

11709592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609883-A-G

11709614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609903-G-A

11709614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609903-G-T

11709637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609927-G-A

http://identifiers.org/hco/7/GRCh38#11709694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12609983-C-A

11709951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610222-G-A

11710200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610555-G-A

11710200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610555-G-C

11710264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610621-T-A

11710264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610621-T-C

http://identifiers.org/hco/7/GRCh38#11710365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12610773-C-A

11710479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610884-C-T

11710517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610915-G-A

http://identifiers.org/hco/7/GRCh38#11710541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#12610936-A-C

11710591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610983-C-T

11710651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12611043-G-A