136440232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26299559-G-A

136440232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26299559-G-C

136440343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26299664-T-C

136440587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26299872-G-T

http://identifiers.org/hco/9/GRCh38#136440680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26299964-C-A

136440680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26299964-C-T

http://identifiers.org/hco/9/GRCh38#136440826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26300097-C-A

136440957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300156-G-T

http://identifiers.org/hco/9/GRCh38#136441039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26300231-C-A

136441166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300336-T-C

136441385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300544-T-A

136441412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300568-G-T

http://identifiers.org/hco/9/GRCh38#136441438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26300594-A-C

136441703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300841-G-A

136441703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 26300841-G-T

136441858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26301001-C-G

136441858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26301001-C-T

136441932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26301055-G-T

136442179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26301311-G-A

136443845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26302870-T-C

136443860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26302885-C-T

http://identifiers.org/hco/9/GRCh38#136443923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26302947-C-A

http://identifiers.org/hco/9/GRCh38#136443933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26302957-C-A

http://identifiers.org/hco/9/GRCh38#136443996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26303022-C-A

136443996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26303022-C-G

136443996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26303022-C-T

http://identifiers.org/hco/9/GRCh38#136444011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26303033-A-C

136444075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26303088-A-G

136444112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303120-G-T

http://identifiers.org/hco/9/GRCh38#136444194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26303198-C-A

136444194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303198-C-T

136444270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303242-G-A

136444325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303298-G-A

136444403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303381-G-C

136444708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303525-G-A

136444919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303569-G-A

136444919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303569-G-T

136444979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303624-G-A

136444979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303624-G-T

136444981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303626-C-T

136445030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303669-G-A

136445030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303669-G-T

http://identifiers.org/hco/9/GRCh38#136445140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26303779-C-A

136445193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303825-T-C

136445254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26303882-G-T

http://identifiers.org/hco/9/GRCh38#136445476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26304087-A-C

http://identifiers.org/hco/9/GRCh38#136445507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26304120-C-A

136445507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26304120-C-T

136445637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26304375-C-G

http://identifiers.org/hco/9/GRCh38#136445669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26304407-C-A

136445733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26304479-G-C

136445733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26304479-G-T

http://identifiers.org/hco/9/GRCh38#136445775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26304519-A-C

http://identifiers.org/hco/9/GRCh38#136445892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26304630-C-A

136446352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26305023-G-A

136446361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26305032-A-G

136446916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26305380-C-T

136447187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26305622-T-A

136447187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26305622-T-C

http://identifiers.org/hco/9/GRCh38#136447399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26305818-C-A

136447399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26305818-C-T

136447636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26306196-C-T

136447781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26306325-A-G

136447943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26306475-G-A

136447943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26306475-G-T

136448013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26306545-G-A

136448043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26306598-A-G

http://identifiers.org/hco/9/GRCh38#136448178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26306737-C-A

136448178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26306737-C-T

http://identifiers.org/hco/9/GRCh38#136448231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26306788-C-A

136448231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26306788-C-T

136451318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26309695-G-T

136451370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26309744-T-C

136451395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26309769-G-A

http://identifiers.org/hco/9/GRCh38#136451430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26309806-C-A

136451430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26309806-C-G

http://identifiers.org/hco/9/GRCh38#136451458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26309834-C-A

136451458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26309834-C-G

136451493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26309866-G-T

136453117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26310914-A-G

136453118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26310915-G-A

136453329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311288-G-A

136453329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311288-G-T

136453368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311330-G-C

136453368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311330-G-T

136453401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311362-A-G

136453470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 26311428-G-A

136453625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311595-T-C

136453809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311762-G-A

136453960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26311906-G-T

http://identifiers.org/hco/9/GRCh38#136454100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26312011-C-A

136454100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26312011-C-T

136454135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26312046-A-G

136454135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26312046-A-T

136454198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26312136-A-G

136454372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26312310-G-T

http://identifiers.org/hco/9/GRCh38#136454414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26312350-C-A

136454414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26312350-C-T

http://identifiers.org/hco/9/GRCh38#136455159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26313074-A-C

http://identifiers.org/hco/9/GRCh38#136455462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26313368-C-A

136455462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313368-C-T

http://identifiers.org/hco/9/GRCh38#136455493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26313385-C-A

136455493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313385-C-G

136455493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313385-C-T

136455592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313457-T-C

http://identifiers.org/hco/9/GRCh38#136455608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26313473-C-A

http://identifiers.org/hco/9/GRCh38#136455713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26313569-C-A

136455713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 26313569-C-T

136456028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313853-G-A

136456028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313853-G-C

136456028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313853-G-T

136456047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26313874-C-T

136456216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26314055-A-G

136456217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26314056-G-C

http://identifiers.org/hco/9/GRCh38#136457468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26314453-C-A

136457468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26314453-C-T

136457528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26314513-G-A

136457537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26314522-G-T

136457617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26314605-T-C

136459012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315106-T-C

http://identifiers.org/hco/9/GRCh38#136459040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26315136-C-A

136459040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315136-C-G

136459040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315136-C-T

136459251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315323-G-A

136459251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315323-G-C

http://identifiers.org/hco/9/GRCh38#136459349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26315396-C-A

136459349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315396-C-T

136459363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315410-T-C

136459374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315421-A-G

http://identifiers.org/hco/9/GRCh38#136459409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26315453-A-C

136459409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315453-A-G

136459439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315483-T-C

136459439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315483-T-G

http://identifiers.org/hco/9/GRCh38#136459637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26315659-C-A

136459637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315659-C-G

136459637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315659-C-T

http://identifiers.org/hco/9/GRCh38#136459721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26315743-C-A

136459721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26315743-C-T

136459802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26315824-T-A

136459802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26315824-T-C

136459802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26315824-T-G

136459866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26315888-T-C

136459987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316034-G-A

136461085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316383-T-A

136461085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316383-T-G

http://identifiers.org/hco/9/GRCh38#136461120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26316401-C-A

136461120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316401-C-T

http://identifiers.org/hco/9/GRCh38#136461285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26316569-C-A

136461544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316772-G-A

http://identifiers.org/hco/9/GRCh38#136461677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26316871-C-A

136461699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316884-G-A

136461719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26316904-G-C

136461904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26317084-C-T

136462068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26317229-A-G

http://identifiers.org/hco/9/GRCh38#136462941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26318206-C-A

136462941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26318206-C-T

136462944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26318209-G-T

136463046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26318311-G-A

136463046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26318311-G-T

136463049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26318314-T-C

136463179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318497-G-A

136463179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318497-G-T

136463182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318519-G-T

136463338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318681-G-A

136463338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318681-G-T

http://identifiers.org/hco/9/GRCh38#136463643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26319020-C-A

136463643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26319020-C-T

136463748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26319143-G-A

http://identifiers.org/hco/9/GRCh38#136463784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26319174-C-A

136463903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319267-A-T

136465600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319781-G-A

136465616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319797-G-C

http://identifiers.org/hco/9/GRCh38#136465797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26319970-C-A

136465797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319970-C-T

136465911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320061-G-A

136465911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320061-G-T

136465958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320085-A-G

136466273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26320415-G-A

136466342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26320484-G-A

136466342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26320484-G-T

136466514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320647-G-A

136466514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320647-G-T

http://identifiers.org/hco/9/GRCh38#136466530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26320664-C-A

136466530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320664-C-T

136466554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320691-G-A

136466562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320729-G-C

136466562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320729-G-T

http://identifiers.org/hco/9/GRCh38#136466595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26320777-A-C

136466595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320777-A-G

136466616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320819-T-C

http://identifiers.org/hco/9/GRCh38#136466788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26320970-C-A

136466788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320970-C-T

136466789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26320971-C-G

http://identifiers.org/hco/9/GRCh38#136466828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26321007-C-A

136466828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321007-C-T

136466843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321022-G-A

136466843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321022-G-T

136466865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321039-G-T

136467111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321268-C-G

136467111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26321268-C-T

http://identifiers.org/hco/9/GRCh38#136468306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26323246-C-A

136468306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26323246-C-T

136468396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26323324-T-C

136468431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26323359-G-T

http://identifiers.org/hco/9/GRCh38#136468549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26323473-C-A

136468549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26323473-C-T

http://identifiers.org/hco/9/GRCh38#136468589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26323491-C-A

136468606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26323511-T-C

http://identifiers.org/hco/9/GRCh38#136471512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26325497-C-A

136471639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26325621-T-C

136472117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26326066-G-A

136473246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26327263-C-T

136473247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26327264-G-A

136473270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26327287-C-T

136473364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26327354-T-C

136474088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328438-C-G

136474088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328438-C-T

136474113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26328463-G-A

136474113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26328463-G-C

136474130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328480-G-A

136474136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328486-G-A

136474200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26328550-G-A

http://identifiers.org/hco/9/GRCh38#136474247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26328597-A-C

136474355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328702-C-T

136474379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26328726-C-T

136474387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26328734-T-C

136474387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26328734-T-G

http://identifiers.org/hco/9/GRCh38#136474514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26328858-C-A

136474514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26328858-C-T

136474594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, missense_variant
orthologous variants: 26328938-C-T

136474805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, missense_variant
orthologous variants: 26329131-C-G

136474840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, missense_variant
orthologous variants: 26329166-C-T

136474931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, missense_variant
orthologous variants: 26329257-G-T

136475004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, missense_variant
orthologous variants: 26329330-C-T

136475379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26329711-G-A

136475545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26329877-G-A

136475696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26330028-G-A

136475700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330032-C-T

136475701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330033-A-G

136475701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330033-A-T

136476278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26330631-T-C

http://identifiers.org/hco/9/GRCh38#136476317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26330748-A-C

136476317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26330748-A-G

136476333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330764-A-G

136476393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330815-C-T

136476523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330936-C-G

136476539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26330952-A-G

136476556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330963-C-T

136476576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26330983-G-A

136476713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26331120-T-C

http://identifiers.org/hco/9/GRCh38#136476751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#26331158-C-A

136476764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331171-G-C

136476773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26331180-G-A

136476773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331180-G-C

136476773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331180-G-T

136476795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331202-G-A

136476795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331202-G-C

136476795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331202-G-T

http://identifiers.org/hco/9/GRCh38#136477031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26331432-C-A

136477031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26331432-C-T

http://identifiers.org/hco/9/GRCh38#136477059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26331460-A-C

136477059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331460-A-G

136477300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: missense variant
orthologous variants: 26331701-G-A

136477415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: synonymous variant
orthologous variants: 26331816-C-T

136477617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5 prime UTR variant
orthologous variants: 26332015-A-T

http://identifiers.org/hco/9/GRCh38#136477629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26332028-C-A

136477629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5 prime UTR variant
orthologous variants: 26332028-C-T

136477717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26332114-T-C

136478036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26332270-C-T

136478047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26332282-A-T

136481023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26333685-A-G

136481049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26333712-T-C

136481076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26333736-G-A

136482218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26334343-T-C

136482793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26334966-C-T

http://identifiers.org/hco/9/GRCh38#136482823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26334999-C-A

136482849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335020-G-A

136482849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335020-G-C

136482849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335020-G-T

136482992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26335141-T-C

136483111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335265-G-C

136483149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335283-T-A

136483239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335353-C-G

136483239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335353-C-T

136483304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335420-C-T

136483359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335468-C-T

136483371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335480-T-C

http://identifiers.org/hco/9/GRCh38#136483390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26335500-C-A

136483390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335500-C-T

http://identifiers.org/hco/9/GRCh38#136483478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26335559-C-A

136483478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, undefined
orthologous variants: 26335559-C-T

136483490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335569-G-A

136483490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron variant
orthologous variants: 26335569-G-T

136483551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335634-C-G

136483551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335634-C-T

136483584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335667-T-A

136483610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335691-T-C

136483624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335705-A-G

136483654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335733-A-G

http://identifiers.org/hco/9/GRCh38#136483668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26335747-C-A

136483668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335747-C-T

136483741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335800-A-G

http://identifiers.org/hco/9/GRCh38#136483774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26335831-C-A

136483787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335840-G-T

136483799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335852-G-A

136483845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335890-G-T

136483896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335923-C-G

136483896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26335923-C-T

136483909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29006
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26335936-G-A