29920130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54482897-G-T

29920329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483069-A-G

29920329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483069-A-T

29920413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483153-C-T

29920470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483209-G-T

http://identifiers.org/hco/7/GRCh38#29920473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54483212-A-C

http://identifiers.org/hco/7/GRCh38#29920474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54483213-C-A

29920474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483213-C-T

29920486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483225-G-A

29920489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483228-T-C

29920678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483351-G-T

http://identifiers.org/hco/7/GRCh38#29920834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54483476-C-A

29920842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483484-T-C

http://identifiers.org/hco/7/GRCh38#29920903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54483542-C-A

29920985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483614-T-C

29921152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483777-T-A

29921152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483777-T-C

29921152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483777-T-G

29921312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483922-T-A

http://identifiers.org/hco/7/GRCh38#29921358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54483968-A-C

29921386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54483996-C-T

29921459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484060-C-T

http://identifiers.org/hco/7/GRCh38#29921497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484097-C-A

29921500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484100-T-C

29921521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484121-C-T

http://identifiers.org/hco/7/GRCh38#29921552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484156-A-C

29921552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484156-A-G

29921561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484165-A-G

29921611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 54484192-A-G

29921611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 54484192-A-T

29921656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484234-G-A

29921656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484234-G-T

http://identifiers.org/hco/7/GRCh38#29921689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484255-C-A

29921689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484255-C-G

http://identifiers.org/hco/7/GRCh38#29921769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484328-C-A

29921769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484328-C-T

29921842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484394-A-G

29921992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484535-A-G

http://identifiers.org/hco/7/GRCh38#29922035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484573-C-A

29922092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484626-T-A

29922092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484626-T-C

29922300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484797-T-G

29922303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484800-G-A

29922303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484800-G-T

29922347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484852-A-G

29922376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484872-G-A

29922380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484876-G-A

29922380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484876-G-C

29922381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484877-G-A

29922381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484877-G-T

http://identifiers.org/hco/7/GRCh38#29922428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54484890-C-A

29922428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484890-C-G

29922431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54484895-G-A

29922565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485026-T-C

29922581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485042-A-G

29922585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485046-G-C

29922585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485046-G-T

http://identifiers.org/hco/7/GRCh38#29922642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485093-C-A

29922645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485096-G-A

29922645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485096-G-T

29922656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485102-G-T

29922715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485160-G-A

29922715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485160-G-T

http://identifiers.org/hco/7/GRCh38#29922766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485207-C-A

29922766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485207-C-T

29922775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485216-G-A

29922775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485216-G-T

29922908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485312-C-T

http://identifiers.org/hco/7/GRCh38#29922911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485315-C-A

http://identifiers.org/hco/7/GRCh38#29923127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485518-C-A

29923127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485518-C-T

29923267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485584-A-G

http://identifiers.org/hco/7/GRCh38#29923310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485625-A-C

29923310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485625-A-G

http://identifiers.org/hco/7/GRCh38#29923353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485661-C-A

29923362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485670-A-G

29923439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485725-C-T

29923451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485739-C-G

29923453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485741-G-T

http://identifiers.org/hco/7/GRCh38#29923474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485766-A-C

29923474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485766-A-G

29923474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485766-A-T

29923488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485780-T-A

29923488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485780-T-G

29923572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485860-A-G

http://identifiers.org/hco/7/GRCh38#29923630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54485914-C-A

29923631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485915-T-C

29923642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54485926-T-C

http://identifiers.org/hco/7/GRCh38#29923739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54486019-C-A

29923739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54486019-C-T

29923748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54486028-T-A

29923748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54486028-T-C

29923749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54486029-G-A

29923749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3 prime UTR variant
orthologous variants: 54486029-G-T

29924014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54486246-C-T

29924148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54486370-C-T

29924159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, undefined
orthologous variants: 54486375-G-T

29924160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, undefined
orthologous variants: 54486376-G-A

29924197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54486410-A-G

http://identifiers.org/hco/7/GRCh38#29924403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54486603-A-C

29924575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54486758-T-G

29924589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54486771-C-T

29925456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488322-C-T

29925841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488525-T-C

29925846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488530-T-A

29925846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488530-T-C

29925995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488659-C-T

http://identifiers.org/hco/7/GRCh38#29926337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54488939-C-A

29926337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488939-C-G

29926337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488939-C-T

29926369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54488970-G-T

http://identifiers.org/hco/7/GRCh38#29926374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54488975-C-A

http://identifiers.org/hco/7/GRCh38#29926506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54489088-C-A

29926599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54489181-G-A

29926677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489257-C-T

29926692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489272-G-A

29926692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489272-G-T

29927168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489624-G-A

29927168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489624-G-T

29927300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489759-G-C

29927314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489773-A-G

http://identifiers.org/hco/7/GRCh38#29927345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54489804-A-C

29927432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54489860-G-A

29927690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490074-A-G

29928232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490278-A-G

29928404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490439-C-T

29928431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490466-C-T

29928543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490563-G-A

29928543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54490563-G-T

29928803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491041-T-G

29928848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491071-C-T

http://identifiers.org/hco/7/GRCh38#29928868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54491091-A-C

29928868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491091-A-G

29928983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491142-A-G

29929023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491172-C-T

http://identifiers.org/hco/7/GRCh38#29929114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54491253-C-A

http://identifiers.org/hco/7/GRCh38#29929195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54491321-C-A

29929195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491321-C-G

29929195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491321-C-T

29929247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491327-G-A

29929367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491424-T-C

29929378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491433-C-T

29929394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491447-T-C

http://identifiers.org/hco/7/GRCh38#29929420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54491471-A-C

29929420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491471-A-G

29929509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491553-T-C

29929534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491587-C-T

29929616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491634-G-A

29929776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491790-G-A

29929791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54491805-G-T

http://identifiers.org/hco/7/GRCh38#29929834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54491848-C-A

29929988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54492000-C-T

http://identifiers.org/hco/7/GRCh38#29930114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54492147-A-C

29931427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54493041-T-C

29933217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494358-T-C

29933255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494396-T-C

29933427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494558-T-C

29933487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494621-A-G

29933487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494621-A-T

29933582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54494718-T-C

http://identifiers.org/hco/7/GRCh38#29933618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54494765-A-C

29933802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495103-A-T

29933876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495165-G-A

29933880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495169-T-C

29934031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495330-T-C

29934168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495443-T-C

29934441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495706-G-A

29934634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495857-C-T

29934635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495858-G-A

29934768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495951-G-C

29934819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54495998-G-C

29934824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496003-G-T

29935069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496332-C-T

29935210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496459-C-T

29935211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496460-G-A

29935334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496561-G-A

29935360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496569-C-G

29935360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496569-C-T

29935482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496685-C-T

http://identifiers.org/hco/7/GRCh38#29935495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54496689-A-C

http://identifiers.org/hco/7/GRCh38#29935622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54496790-A-C

29935626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496794-G-C

29935679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496833-C-G

29935718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54496865-C-T

29935881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497019-A-T

29936175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497279-T-A

29936187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497291-G-A

29936187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497291-G-T

http://identifiers.org/hco/7/GRCh38#29936517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54497647-C-A

29936517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497647-C-T

29936518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497648-A-G

29936529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497659-G-A

http://identifiers.org/hco/7/GRCh38#29936594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54497723-C-A

29936594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54497723-C-G

29936594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54497723-C-T

29936597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54497726-A-G

29936676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54497805-G-A

29936714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54497843-G-A

29936735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497864-A-G

29936905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497908-G-C

29937022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497912-G-A

29937140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54497991-T-C

http://identifiers.org/hco/7/GRCh38#29937146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54497997-A-C

29937167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498018-G-A

29937190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498043-C-G

29937358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498206-G-A

29937492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498338-C-T

29937515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498360-A-G

29937515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498360-A-T

29937602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498444-G-A

29937607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498449-G-T

29937653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498495-T-C

29937653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498495-T-G

http://identifiers.org/hco/7/GRCh38#29937667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54498505-C-A

29937771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54498600-G-T

http://identifiers.org/hco/7/GRCh38#29939676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54499168-A-C

29939771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499254-G-A

29939779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499262-G-A

29939796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499282-G-A

29939828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499314-T-A

29939828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499314-T-C

29939852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499338-T-C

29940275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499437-A-G

29940366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499506-T-C

29940566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499681-A-G

http://identifiers.org/hco/7/GRCh38#29940602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54499720-C-A

29940602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499720-C-G

29940602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499720-C-T

29940726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499789-T-C

29940770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499833-C-G

29940770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54499833-C-T

29940777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499840-G-A

29940777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499840-G-T

29940806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499869-C-G

29940825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499888-G-A

29940825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499888-G-T

29940840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499903-G-C

29940841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense variant
orthologous variants: 54499904-T-C

29940889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499952-C-G

29940889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499952-C-T

http://identifiers.org/hco/7/GRCh38#29940894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54499957-C-A

29940894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499957-C-T

29940963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499977-T-C

29940987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54499989-G-T

29941047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500049-A-G

29941127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500126-G-A

29941191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500179-G-A

29941193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500181-T-A

29941286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500242-T-C

29941294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500250-C-T

http://identifiers.org/hco/7/GRCh38#29941343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54500295-C-A

http://identifiers.org/hco/7/GRCh38#29941375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54500329-C-A

29941917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500488-A-G

29941991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500578-G-A

29942172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500788-T-C

29942317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54500983-G-A

29942460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501124-G-A

29942504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501168-C-T

29942535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501199-G-T

29942706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501364-T-C

29942716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501374-A-G

29942970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54501583-T-C

29943537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502084-G-A

29943774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502285-T-C

29943847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502370-A-G

29943865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502387-G-A

29943865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502387-G-C

29943865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502387-G-T

29943872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron variant
orthologous variants: 54502394-T-C

29944011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54502528-G-A

29944011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: synonymous variant
orthologous variants: 54502528-G-T

29944053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54502570-T-C

http://identifiers.org/hco/7/GRCh38#29944083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54502600-A-C

29944083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54502600-A-G

29944098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54502615-C-G

29944098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54502615-C-T

http://identifiers.org/hco/7/GRCh38#29944261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54502775-C-A

http://identifiers.org/hco/7/GRCh38#29944278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54502792-C-A

29944278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54502792-C-T

29944292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54502806-C-T

http://identifiers.org/hco/7/GRCh38#29944309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54502823-A-C

29944316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54502830-G-A

29944316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54502830-G-T

29945447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54503723-C-G

29945590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54503853-G-A

http://identifiers.org/hco/7/GRCh38#29945605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54503868-A-C

29945661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54503917-C-G

29945698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54503953-T-G

29945765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504018-A-G

29946462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504672-A-G

29946469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504679-C-G

29946470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504680-G-A

29946565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504762-T-C

29946728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504873-T-A

29946842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54504991-T-C

http://identifiers.org/hco/7/GRCh38#29946872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54505021-C-A

29946872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54505021-C-T

29946914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54505041-A-G

29947071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505196-T-C

http://identifiers.org/hco/7/GRCh38#29947182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54505278-C-A

29947208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54505304-G-T

29947212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54505308-C-T

29947395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505420-T-G

29947423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505448-G-A

29947520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505532-C-G

29947738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505728-T-C

29947897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505845-G-A

29947968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505896-A-G

29948019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505946-A-G

29948033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54505960-A-G

29948239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54506559-A-G

29948387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54506711-T-C

http://identifiers.org/hco/7/GRCh38#29948458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54506758-C-A

29948472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54506774-C-T

29948492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54506799-A-G

http://identifiers.org/hco/7/GRCh38#29948503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54506807-A-C

29948522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54506824-C-T

29948687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507266-A-G

29948774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507359-C-G

29948789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507373-T-C

29948890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507450-C-T

29948921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507483-T-C

29951539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507608-G-A

29951572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507648-G-A

http://identifiers.org/hco/7/GRCh38#29951590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54507666-A-C

29951727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507922-C-T

29951760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507953-A-T

29951804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54507997-C-G

29951849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508042-C-T

29951891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508072-C-T

29951901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508082-G-C

29951915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508096-G-A

29952051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508230-G-C

29952232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508412-C-T

29952289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508468-G-A

29952293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508472-A-G

29952339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508506-T-C

29952741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508554-A-G

29952839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508646-G-T

29953036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508846-T-C

29953036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508846-T-G

29953127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508950-C-T

29953130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54508953-C-T

29953235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54509060-A-G

29953798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510352-T-C

29954083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510663-T-C

29954204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510748-G-T

http://identifiers.org/hco/7/GRCh38#29954237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54510780-A-C

29954237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510780-A-G

29954266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510808-G-C

29954278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510820-G-A

29954382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54510925-G-A

http://identifiers.org/hco/7/GRCh38#29954430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54511034-C-A

29954498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511092-C-T

29954574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511148-T-C

http://identifiers.org/hco/7/GRCh38#29955056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54511310-C-A

29955056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511310-C-T

29955074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511324-T-A

29955120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511352-T-C

29955145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511364-T-C

29955322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54511541-A-G

29955322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 54511541-A-T

29955343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54511562-G-A

29955385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511603-A-G

29955385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511603-A-T

29955432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511650-T-C

29955462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511675-G-A

29955462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511675-G-T

29955495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511704-T-A

29955495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511704-T-C

29955516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511724-G-C

29955520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511728-A-G

29955585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511791-T-C

29955598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511801-T-C

29955764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511975-G-A

http://identifiers.org/hco/7/GRCh38#29955768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54511979-A-C

29955770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54511982-C-G

29955860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54512077-A-G

29956030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54512276-C-T

29956541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54512953-A-G

29956672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54513081-T-A

29956676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54513085-G-A

29956700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54513109-T-C

29956862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54513475-T-C

29957648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515563-G-A

29957648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515563-G-T

29957713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515629-A-G

29957793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515698-C-G

http://identifiers.org/hco/7/GRCh38#29957892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54515784-A-C

29957956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515845-A-T

29957997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54515884-A-G

29958229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54516110-A-G

http://identifiers.org/hco/7/GRCh38#29958312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54516191-C-A

http://identifiers.org/hco/7/GRCh38#29958509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54516389-C-A

29958954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517101-A-T

29958987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517140-G-A

29958987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517140-G-C

29959014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517170-A-G

http://identifiers.org/hco/7/GRCh38#29959016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54517172-C-A

29959199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517349-G-A

29959548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517538-G-A

29959700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54517618-T-C

29960451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54518805-G-T

29960673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54519001-G-A

29960673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54519001-G-C

29962942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54520648-G-T

29962948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54520654-G-A

29963013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54520714-G-C

29963198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521005-G-C

29963325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521173-G-A

29963325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521173-G-T

29963550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521378-G-A

29963562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521390-G-A

29963589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521417-G-A

29965315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521617-C-G

29965579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521851-A-G

29965588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521861-T-C

29965650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54521917-G-A

29966231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54522712-T-A

29966318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54522809-T-C

29966494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523000-G-C

29966503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523009-G-A

29966576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523075-T-A

29966576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523075-T-G

29966586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523085-A-G

29966806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523292-T-A

29967291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523629-G-A

29967291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523629-G-T

http://identifiers.org/hco/7/GRCh38#29967591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54523771-C-A

29967811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523928-T-C

29967838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523954-G-C

29967876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54523992-A-G

29968203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524325-T-C

29968205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524327-G-C

29968276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524404-T-C

29968289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524419-A-G

29968321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524472-C-T

http://identifiers.org/hco/7/GRCh38#29968325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54524476-A-C

29968369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524542-T-C

29968656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54524969-T-A

29968761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525066-A-G

http://identifiers.org/hco/7/GRCh38#29968787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525090-A-C

29968787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525090-A-G

http://identifiers.org/hco/7/GRCh38#29968806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525108-C-A

29968806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525108-C-T

29968814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525116-T-C

29968817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525119-G-A

29968874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525171-G-A

29968874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525171-G-C

29968927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54525227-T-G

http://identifiers.org/hco/7/GRCh38#29968969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525269-A-C

29968969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54525269-A-G

http://identifiers.org/hco/7/GRCh38#29969056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525356-A-C

29969056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54525356-A-T

29969125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525428-G-C

29969144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525447-T-C

http://identifiers.org/hco/7/GRCh38#29969152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525455-C-A

http://identifiers.org/hco/7/GRCh38#29969157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525460-A-C

29969178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525481-G-A

29969178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525481-G-C

29969178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525481-G-T

http://identifiers.org/hco/7/GRCh38#29969179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525482-C-A

29969179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525482-C-G

29969179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525482-C-T

http://identifiers.org/hco/7/GRCh38#29969184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525487-C-A

29969207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525509-T-C

http://identifiers.org/hco/7/GRCh38#29969232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525532-A-C

29969232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525532-A-G

29969232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54525532-A-T

http://identifiers.org/hco/7/GRCh38#29969305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525603-C-A

29969305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525603-C-T

29969343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525642-G-A

29969343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525642-G-T

http://identifiers.org/hco/7/GRCh38#29969443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54525896-A-C

29969466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54525976-G-T

29969571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54526131-A-G

29969711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54526214-C-G

29969737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54526247-T-C

29969738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54526248-G-A

29969770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54526280-T-G

29970868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54527344-A-G

29971712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54527876-C-T

29972535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54528154-G-C

29972797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54528436-G-A

29975626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529747-T-A

29975626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529747-T-C

29975665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529782-T-C

29975688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529807-C-T

29975705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529824-A-G

29975843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54529957-T-A

29976107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54530199-C-T

29976113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54530205-C-T

29976147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54530239-G-A

http://identifiers.org/hco/7/GRCh38#29976809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54531404-C-A

29976809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54531404-C-G

29977499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532061-T-G

29977665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532189-A-G

29978107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532754-C-T

29978282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532887-A-G

29978314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532919-A-G

29978320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54532925-A-G

29978352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54532955-T-C

29978483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54533077-G-C

29978487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54533081-C-T

29978524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54533118-C-G

29978524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54533118-C-T

29979949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54535293-C-T

29980114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54535452-G-T

http://identifiers.org/hco/7/GRCh38#29980160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54535477-A-C

29980160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54535477-A-T

http://identifiers.org/hco/7/GRCh38#29980220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54535523-A-C

http://identifiers.org/hco/7/GRCh38#29980443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54535723-C-A

29980672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54535959-T-G

29980697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54535984-T-G

29980746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536019-C-T

29980923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536214-A-G

29980937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536228-A-G

29981054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536336-C-T

29981113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536392-G-T

29981207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536488-T-G

29981393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536641-A-G

29981394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536642-G-A

http://identifiers.org/hco/7/GRCh38#29981422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54536663-A-C

29981521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536755-G-T

http://identifiers.org/hco/7/GRCh38#29981567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54536790-C-A

29981683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536877-A-G

http://identifiers.org/hco/7/GRCh38#29981715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54536900-C-A

29981736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54536916-C-T

29981867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54537033-T-C

29981903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54537069-G-A

29981903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54537069-G-C

29981903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54537069-G-T

29986331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540200-T-C

29986836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540729-T-C

29986886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540775-G-A

29987015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540827-C-T

http://identifiers.org/hco/7/GRCh38#29987212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54540968-C-A

29987212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540968-C-T

29987217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54540973-T-G

29987254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541016-G-C

29987354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541109-C-T

29987501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541232-T-C

29987527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541258-T-C

29987699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541435-C-T

29987741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541463-C-T

29987772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54541494-C-G

29987772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54541494-C-T

29987798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541516-G-C

29987916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541623-C-G

29987917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541624-T-G

http://identifiers.org/hco/7/GRCh38#29987951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54541660-C-A

29988043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541762-G-A

29988043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54541762-G-C

http://identifiers.org/hco/7/GRCh38#29988121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54541842-C-A

29988299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542005-C-T

29988514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54542202-A-G

29988528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542218-G-A

29988528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542218-G-T

29988529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542219-G-T

http://identifiers.org/hco/7/GRCh38#29988549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542239-C-A

29988549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54542239-C-T

29988609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542300-G-A

29988609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542300-G-T

http://identifiers.org/hco/7/GRCh38#29988764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542433-C-A

29988764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542433-C-T

29988869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542538-A-G

29988874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542543-C-T

http://identifiers.org/hco/7/GRCh38#29988990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542687-C-A

29988990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542687-C-T

29988996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542693-C-T

29989040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542733-G-A

29989040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542733-G-T

http://identifiers.org/hco/7/GRCh38#29989090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542790-C-A

29989090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542790-C-T

29989218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542877-G-A

http://identifiers.org/hco/7/GRCh38#29989220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542879-A-C

http://identifiers.org/hco/7/GRCh38#29989296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542928-C-A

http://identifiers.org/hco/7/GRCh38#29989319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542951-C-A

29989319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542951-C-T

29989320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542952-T-C

29989340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542972-G-A

29989340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542972-G-T

29989423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543072-G-C

29989494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543124-G-A

29989545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543130-G-A

29989545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543130-G-T

29989554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543139-T-C

29989670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543247-T-C

29989693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543270-C-T

29989726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543302-G-A

29989726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543302-G-C

29989761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543325-T-C

29989763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543327-G-T

http://identifiers.org/hco/7/GRCh38#29989787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543346-C-A

29989787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543346-C-T

29989790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543349-C-T

http://identifiers.org/hco/7/GRCh38#29989793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543352-C-A

29989793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543352-C-T

29989849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543401-T-A

29989849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543401-T-G

29989884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-A

29989884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-C

29989884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-T

http://identifiers.org/hco/7/GRCh38#29990053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543596-A-C

http://identifiers.org/hco/7/GRCh38#29990135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543675-C-A

29990135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543675-C-T

http://identifiers.org/hco/7/GRCh38#29990194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543734-C-A

29990194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54543734-C-T

29990277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543809-T-C

29990277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22192
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54543809-T-G