67645095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 106412763-G-A

67645095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 106412763-G-T

http://identifiers.org/hco/16/GRCh38#67645118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106412786-C-A

67645118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 106412786-C-G

67645118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 106412786-C-T

http://identifiers.org/hco/16/GRCh38#67645195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106412862-C-A

67645195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 106412862-C-G

67645195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 106412862-C-T

http://identifiers.org/hco/16/GRCh38#67645232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106412899-C-A

67645232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 106412899-C-T

67645265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106412924-G-A

67645265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106412924-G-T

http://identifiers.org/hco/16/GRCh38#67645405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106413053-C-A

67645405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413053-C-T

67645488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413140-C-G

67645507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413159-A-G

67645507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413159-A-T

http://identifiers.org/hco/16/GRCh38#67645515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106413167-C-A

67645515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413167-C-T

http://identifiers.org/hco/16/GRCh38#67645526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106413178-C-A

67645526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106413178-C-T

67645635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106413287-T-C

http://identifiers.org/hco/16/GRCh38#67645650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106413304-A-C

http://identifiers.org/hco/16/GRCh38#67646026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#106414009-C-A

http://identifiers.org/hco/16/GRCh38#67646134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106414123-C-A

67646134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106414123-C-G

http://identifiers.org/hco/16/GRCh38#67646242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106414241-C-A

67646242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106414241-C-T

67646484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 106414474-C-G

67646525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 106414515-T-A

67646626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 106414618-C-T

67646684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 106414672-T-C

67646827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 106414818-C-T

67647013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 106415001-G-A

67647093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 106415076-C-T

67647110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 106415091-C-G

67647110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 106415091-C-T

67647173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 106415154-C-T

67647382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 106415339-G-C

67647382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 106415339-G-T

67647454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106415383-G-C

67647454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106415383-G-T

67647490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106415408-C-G

67647490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106415408-C-T

http://identifiers.org/hco/16/GRCh38#67647612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106415531-A-C

67647640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415559-G-T

67647642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415561-A-T

67647669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415588-C-T

http://identifiers.org/hco/16/GRCh38#67647700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106415616-C-A

67647700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106415616-C-T

67647753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106415669-G-A

67647753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106415669-G-T

67647768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 106415684-T-G

67647780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415696-G-A

67647780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415696-G-C

67647780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415696-G-T

http://identifiers.org/hco/16/GRCh38#67647796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106415712-A-C

67647796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415712-A-G

67647796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415712-A-T

67647797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415713-G-A

67647797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415713-G-C

67647804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415720-G-A

67647804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415720-G-T

67647809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415728-T-A

67647809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415728-T-C

67647809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415728-T-G

http://identifiers.org/hco/16/GRCh38#67647810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106415729-C-A

67647854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106415776-G-A

http://identifiers.org/hco/16/GRCh38#67648042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106415964-C-A

67648042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106415964-C-T

67648123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416047-G-A

67648156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416078-G-T

67648217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416162-G-A

67648245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416191-C-T

67648337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416283-G-A

67648337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416283-G-C

67648337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416283-G-T

http://identifiers.org/hco/16/GRCh38#67648366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416316-C-A

67648366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416316-C-T

http://identifiers.org/hco/16/GRCh38#67648369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416319-C-A

67648369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416319-C-T

67648390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106416345-T-C

67648390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106416345-T-G

http://identifiers.org/hco/16/GRCh38#67648409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416367-C-A

67648409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416367-C-T

67648413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416371-G-A

67648413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416371-G-T

http://identifiers.org/hco/16/GRCh38#67648419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416377-C-A

67648419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416377-C-G

67648419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416377-C-T

http://identifiers.org/hco/16/GRCh38#67648429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416387-C-A

http://identifiers.org/hco/16/GRCh38#67648441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416399-C-A

67648441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416399-C-G

67648441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416399-C-T

http://identifiers.org/hco/16/GRCh38#67648456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416414-C-A

67648456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416414-C-G

67648456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416414-C-T

67648457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416415-G-A

67648457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416415-G-C

67648457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416415-G-T

67648625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106416573-G-A

67648625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106416573-G-T

http://identifiers.org/hco/16/GRCh38#67648628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416576-C-A

67648628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106416576-C-T

http://identifiers.org/hco/16/GRCh38#67648643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106416588-C-A

67648643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106416588-C-G

67648805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106416765-G-C

67648937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106416859-C-G

67648937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416859-C-T

67648940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106416862-A-G

67648983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416905-G-T

67649011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416933-C-T

67649056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106416990-G-A

67649186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417120-C-T

http://identifiers.org/hco/16/GRCh38#67649189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106417123-C-A

67649204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417138-G-A

67649241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417176-C-T

http://identifiers.org/hco/16/GRCh38#67649351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106417289-C-A

67649414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417343-C-T

http://identifiers.org/hco/16/GRCh38#67649560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106417492-C-A

67649636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417572-G-A

67649636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417572-G-T

http://identifiers.org/hco/16/GRCh38#67649683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106417625-C-A

67649683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417625-C-G

67649759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417679-G-A

67649759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417679-G-T

67649791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417700-C-T

67649910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106417819-A-G

http://identifiers.org/hco/16/GRCh38#67649914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106417823-C-A

67649914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106417823-C-T

67649947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 106417856-G-A

67649974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417883-C-G

67649974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417883-C-T

67650001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417910-G-C

67650015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417924-T-G

67650033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106417942-T-C

67650078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106417988-C-G

67650078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106417988-C-T

67650080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106417990-C-T

http://identifiers.org/hco/16/GRCh38#67650167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418075-C-A

67650167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418075-C-T

http://identifiers.org/hco/16/GRCh38#67650443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418258-C-A

67650443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418258-C-G

67650443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418258-C-T

67650466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418280-C-G

http://identifiers.org/hco/16/GRCh38#67650484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418299-C-A

67650484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418299-C-G

67650484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418299-C-T

http://identifiers.org/hco/16/GRCh38#67650516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418332-C-A

67650519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418335-C-T

67650759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418598-G-C

http://identifiers.org/hco/16/GRCh38#67650775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418614-C-A

67650789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418637-G-A

67650789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418637-G-C

67650789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418637-G-T

http://identifiers.org/hco/16/GRCh38#67650909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418708-A-C

http://identifiers.org/hco/16/GRCh38#67650976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106418777-C-A

67651019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106418799-A-G

67651195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106418941-T-A

67651222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106418968-T-C

67651285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106419031-T-C

67651321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106419067-C-T

67651393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106419139-G-A

67651422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106419170-G-T

http://identifiers.org/hco/16/GRCh38#67651430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106419178-C-A

67651430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106419178-C-T

67651620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106419372-A-T

67651732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106419482-G-A

67651732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106419482-G-T

67651743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106419493-G-T

67651819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106419569-G-A

67651819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106419569-G-T

67651843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 106419593-C-G

67651843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 106419593-C-T

67651946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106419695-A-G

67652016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106419765-G-A

67652031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106419781-C-T

67652052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106419787-G-A

67652321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106420010-G-T

67652361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420050-G-A

http://identifiers.org/hco/16/GRCh38#67652368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420057-C-A

67652622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420290-T-A

67652622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420290-T-C

http://identifiers.org/hco/16/GRCh38#67652631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420299-C-A

http://identifiers.org/hco/16/GRCh38#67652748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420403-C-A

67652794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420447-C-T

67652923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420550-T-A

67652923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420550-T-C

67652923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420550-T-G

http://identifiers.org/hco/16/GRCh38#67652947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420573-C-A

67652947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420573-C-G

67652947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420573-C-T

http://identifiers.org/hco/16/GRCh38#67652954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420580-C-A

67652954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420580-C-G

67652954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420580-C-T

http://identifiers.org/hco/16/GRCh38#67652978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420605-C-A

67652978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420605-C-G

67652978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420605-C-T

67652985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420612-G-A

67652985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420612-G-C

67652985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106420612-G-T

http://identifiers.org/hco/16/GRCh38#67653022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420649-C-A

67653022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106420649-C-G

67653022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106420649-C-T

http://identifiers.org/hco/16/GRCh38#67653131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420758-C-A

67653131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106420758-C-G

67653131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106420758-C-T

http://identifiers.org/hco/16/GRCh38#67653137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420764-C-A

67653137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106420764-C-T

http://identifiers.org/hco/16/GRCh38#67653159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420786-C-A

67653159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106420786-C-T

67653370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: 106420990-T-C

67653375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: 106420995-G-A

67653375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: 106420995-G-T

http://identifiers.org/hco/16/GRCh38#67653393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106420999-C-A

67653393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: 106420999-C-G

67653393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron variant
orthologous variants: 106420999-C-T

67653492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421098-C-T

67653612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421210-G-A

67653711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421296-G-A

67653746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421329-G-A

67653771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421356-G-A

67653771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421356-G-T

67654029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421556-T-C

67654029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421556-T-G

67654181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421689-G-A

67654181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421689-G-C

67654181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421689-G-T

67654244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106421752-T-A

67654244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421752-T-C

67654263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421771-A-G

http://identifiers.org/hco/16/GRCh38#67654268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106421777-C-A

67654268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421777-C-G

67654268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421777-C-T

http://identifiers.org/hco/16/GRCh38#67654279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106421788-A-C

67654279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421788-A-G

67654279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421788-A-T

67654410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421918-C-T

67654459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106421967-C-T

67654515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422023-A-T

http://identifiers.org/hco/16/GRCh38#67654526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106422034-C-A

67654526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106422034-C-T

67654541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106422049-G-A

67654569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422077-G-A

67654569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422077-G-T

67654678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106422186-G-A

67654678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106422186-G-C

http://identifiers.org/hco/16/GRCh38#67654757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106422263-C-A

67654757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106422263-C-T

67654837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422343-A-G

67654882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422388-C-G

67654882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106422388-C-T

67655791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423086-T-A

http://identifiers.org/hco/16/GRCh38#67655840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106423119-A-C

http://identifiers.org/hco/16/GRCh38#67655881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106423166-A-C

67655881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423166-A-G

http://identifiers.org/hco/16/GRCh38#67655901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106423368-C-A

67655994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423456-G-A

67655994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423456-G-C

67656008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423470-T-C

67656039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106423501-T-C

67656039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106423501-T-G

67656188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106423616-T-C

http://identifiers.org/hco/16/GRCh38#67656256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106423684-C-A

67656317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423745-T-C

http://identifiers.org/hco/16/GRCh38#67656409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106423832-C-A

67656479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106423904-G-A

http://identifiers.org/hco/16/GRCh38#67656713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106424104-C-A

67656732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424123-G-T

http://identifiers.org/hco/16/GRCh38#67656901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106424292-C-A

67656901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106424292-C-T

67656908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106424299-T-C

67657154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106424437-G-A

67657352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424613-G-C

67657380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424641-C-G

http://identifiers.org/hco/16/GRCh38#67657390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106424651-C-A

67657391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424652-T-C

http://identifiers.org/hco/16/GRCh38#67657436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106424693-C-A

67657436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106424693-C-G

67657436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27089
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106424693-C-T