158765920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005783-C-T

158765941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005815-A-G

158765941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005815-A-T

158765963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005837-G-T

http://identifiers.org/hco/6/GRCh38#158766066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#7005950-C-A

158766066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 7005950-C-T

158766119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005995-G-A

158766119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7005995-G-T

http://identifiers.org/hco/6/GRCh38#158766138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7006013-A-C

158766415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006270-G-A

158766415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006270-G-T

http://identifiers.org/hco/6/GRCh38#158766508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7006353-C-A

158766688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006482-G-A

158766688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006482-G-C

158766688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006482-G-T

158766732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006529-G-A

158766732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006529-G-T

158766775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006570-T-C

158766775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006570-T-G

158766824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006619-T-A

158766824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006619-T-C

158766891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006679-T-G

158766892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006680-G-A

158766892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006680-G-C

158766892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 3 prime UTR variant
orthologous variants: 7006680-G-T

158766926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7006714-G-A

158766926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: missense variant
orthologous variants: 7006714-G-C

158767067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7006855-G-A

158767106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, undefined
orthologous variants: 7006903-T-G

158767211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7007010-G-A

158767211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7007010-G-C

158767300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007068-A-G

158767300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007068-A-T

158767357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007125-G-A

158767369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007137-G-A

158767435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007203-T-A

158767435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007203-T-G

158767453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7007221-T-C

158768854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7007960-C-T

158768988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008074-T-A

http://identifiers.org/hco/6/GRCh38#158769246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008313-C-A

158769246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008313-C-T

http://identifiers.org/hco/6/GRCh38#158769368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008404-C-A

158769368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7008404-C-T

http://identifiers.org/hco/6/GRCh38#158769484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008514-A-C

158769492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008522-T-C

158769493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008523-G-C

158769493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008523-G-T

158769549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008569-T-A

158769549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008569-T-C

158769595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008619-C-G

158769595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008619-C-T

http://identifiers.org/hco/6/GRCh38#158769643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008663-C-A

158769643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008663-C-G

158769643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008663-C-T

http://identifiers.org/hco/6/GRCh38#158769655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008673-C-A

158769658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008676-C-T

158769660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008678-G-A

158769660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008678-G-T

http://identifiers.org/hco/6/GRCh38#158769661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008679-C-A

158769661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008679-C-T

http://identifiers.org/hco/6/GRCh38#158769669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008716-C-A

158769669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7008716-C-T

158769826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7008862-C-T

http://identifiers.org/hco/6/GRCh38#158769862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7008898-A-C

158769913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: missense variant
orthologous variants: 7008949-C-G

158769913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7008949-C-T

http://identifiers.org/hco/6/GRCh38#158769976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009013-C-A

158769976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009013-C-T

158769982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009019-G-T

158770012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009045-T-A

158770012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009045-T-C

http://identifiers.org/hco/6/GRCh38#158770078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009116-C-A

158770078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009116-C-T

158770156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009190-C-T

http://identifiers.org/hco/6/GRCh38#158770435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009429-C-A

158770662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009645-G-A

158770662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009645-G-T

158770737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009725-T-G

158770740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009728-A-T

http://identifiers.org/hco/6/GRCh38#158770744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009732-C-A

158770744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7009732-C-T

158770766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 7009755-C-T

158770840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7009829-C-T

http://identifiers.org/hco/6/GRCh38#158770846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009835-C-A

158770864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: missense variant
orthologous variants: 7009853-T-A

158770879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: synonymous variant
orthologous variants: 7009868-T-C

http://identifiers.org/hco/6/GRCh38#158771104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7009989-C-A

http://identifiers.org/hco/6/GRCh38#158771157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7010016-A-C

158771157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010016-A-G

158771443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010288-C-G

158771448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010293-G-A

158771450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010295-T-A

158771477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010322-A-G

http://identifiers.org/hco/6/GRCh38#158771552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7010408-C-A

158771552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010408-C-T

158771838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7010617-G-A

158772586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, undefined
orthologous variants: 7011051-C-T

158773023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7011366-C-T

158773076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, undefined
orthologous variants: 7011419-T-C

158773435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7011715-C-T

158773771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7011960-C-T

158773845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012026-A-G

158773850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012031-G-A

158773919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012078-G-A

158774139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012255-C-T

158774222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012340-G-A

158774222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012340-G-C

158774288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012397-G-C

158774441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7012543-G-A

158775604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7013820-T-C

158775960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014147-G-A

158776089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014279-C-T

158776248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014508-T-C

http://identifiers.org/hco/6/GRCh38#158776266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014526-C-A

158776317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014568-T-A

158776317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014568-T-C

http://identifiers.org/hco/6/GRCh38#158776325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014576-C-A

158776325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014576-C-G

158776325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014576-C-T

http://identifiers.org/hco/6/GRCh38#158776351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014613-C-A

158776367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014629-T-A

158776367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014629-T-C

158776368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014630-G-T

http://identifiers.org/hco/6/GRCh38#158776392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014647-A-C

158776509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7014764-G-A

158776557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014825-T-C

http://identifiers.org/hco/6/GRCh38#158776595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014849-C-A

158776595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7014849-C-T

http://identifiers.org/hco/6/GRCh38#158776754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7014971-C-A

158776851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7015041-C-T

158777085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7015218-T-C

158777922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016094-A-G

158777949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016115-A-G

158778000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016189-A-G

158778030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016214-T-C

158778187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016354-C-T

158778243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016414-G-C

158778294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016458-T-C

158778311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016474-T-A

158778311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016474-T-C

158778407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016577-A-G

158778424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016625-G-A

158778516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016774-C-T

158778562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7016833-G-A

158780588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7018141-T-C

158780757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7018294-T-C

158781092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7018595-T-C

158781258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7018743-G-A

158781386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, undefined
orthologous variants: 7018860-T-C

158781500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7018974-G-A

158781555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019028-T-C

158781789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019279-G-A

158781789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019279-G-C

158781789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019279-G-T

158781815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019305-G-A

158782010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019437-C-T

158782020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019446-G-A

158782981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019884-C-T

158783008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019910-G-A

158783081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7019981-C-T

158783199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7020100-G-C

158783229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7020106-T-C

158783469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: 7020313-T-C

http://identifiers.org/hco/6/GRCh38#158783483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7020327-C-A

158783651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7020513-C-T

158783777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020632-T-G

http://identifiers.org/hco/6/GRCh38#158783786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7020641-C-A

158783786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020641-C-T

158783804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020649-G-A

158784260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021002-T-C

158784287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021038-C-T

158784294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021045-C-G

158784361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021116-T-C

158784407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021162-G-T

158784455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021210-C-G

http://identifiers.org/hco/6/GRCh38#158784538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7021297-C-A

158784538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021297-C-G

158784586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021336-A-G

158784664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 7021405-C-T

158784706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 7021447-A-G

http://identifiers.org/hco/6/GRCh38#158784832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#7021576-C-A

http://identifiers.org/hco/6/GRCh38#158784834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#7021578-A-C

158784834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7021578-A-G

158785081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021809-T-C

158785163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021878-T-C

158785191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021905-G-A

158785191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021905-G-C

158785191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021905-G-T

158785237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021953-C-T

http://identifiers.org/hco/6/GRCh38#158785260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7021968-C-A

158785260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021968-C-T

158785264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021972-G-C

158785297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021998-T-G

http://identifiers.org/hco/6/GRCh38#158785329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7022030-A-C

158785350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7022051-G-A

158785392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7022093-G-A

http://identifiers.org/hco/6/GRCh38#158785437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7022138-A-C

http://identifiers.org/hco/6/GRCh38#158785512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7022213-A-C

158785512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7022213-A-G

158785542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7022243-G-C

158785542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7022243-G-T

158785554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7022255-A-G

158786410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022619-C-T

158786433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022642-C-G

158786474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022673-T-C

158786486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022685-T-C

158786525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022734-A-G

http://identifiers.org/hco/6/GRCh38#158786645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7022786-C-A

158786964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023103-C-T

158787007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023146-G-A

158787007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023146-G-T

158787010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023149-A-G

158787036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023176-G-A

158787036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023176-G-C

158787036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023176-G-T

http://identifiers.org/hco/6/GRCh38#158787040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7023180-C-A

158787040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023180-C-T

158787049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023189-T-C

http://identifiers.org/hco/6/GRCh38#158787061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7023201-A-C

158787079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023219-C-G

158787079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023219-C-T

158787125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7023264-G-C

158787165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7023304-A-G

158787261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023382-G-A

158787261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023382-G-T

http://identifiers.org/hco/6/GRCh38#158787298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7023414-C-A

158787343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023449-T-A

158789149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7026722-T-C

http://identifiers.org/hco/6/GRCh38#158789152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7026725-C-A

158789152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7026725-C-T

158789218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7026810-A-G

http://identifiers.org/hco/6/GRCh38#158789969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7027185-C-A

158789987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7027203-A-T

158790043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7027278-G-A

http://identifiers.org/hco/6/GRCh38#158790136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7027373-C-A

http://identifiers.org/hco/6/GRCh38#158790218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7027452-C-A

158790218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7027452-C-T

158790941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7028299-C-T

158791017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7028374-G-A

158791042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7028398-C-T

158794595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031159-T-C

158794760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031404-T-C

158796314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033209-C-T

158796673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033491-G-A

158796705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033513-G-A

158796705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033513-G-C

158796974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033746-T-C

158796986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033758-C-T

158797037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7033810-G-T

158797404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034278-T-G

158797424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034294-T-C

158797562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034405-T-C

158797643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034486-T-C

158797691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034527-G-A

158797795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034611-T-C

158797936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034747-T-C

158798204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035070-T-G

158798205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035071-C-G

158798319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035193-T-C

158798366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035230-A-G

158798436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035314-G-C

158799643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7036023-T-C

158799794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7036173-G-T

158801657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037363-T-G

158802236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037799-C-T

158802312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037892-A-G

158802568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038152-G-A

158802781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038221-T-C

158802790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038230-A-G

158802826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038267-G-A

158802961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038367-A-G

158803073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7038481-C-T

158803305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038656-T-C

http://identifiers.org/hco/6/GRCh38#158803703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7039173-C-A

158803703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039173-C-G

158803703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039173-C-T

158803833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039305-G-A

158803902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039374-C-G

158804112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039561-G-A

158804112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039561-G-T

158804203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039644-A-G

158804303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039723-T-G

158804531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039925-T-C

158804599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039962-G-A

158806800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7041911-A-G

158806828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7041938-G-T

158806846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7041957-T-C

http://identifiers.org/hco/6/GRCh38#158807448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7042173-C-A

158807448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042173-C-T

158807724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042570-T-C

158807772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042652-G-A

http://identifiers.org/hco/6/GRCh38#158807840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7042720-C-A

158807926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042796-A-G

158808493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042999-G-A

158808493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042999-G-C

158808509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043016-G-C

158809399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043604-A-G

http://identifiers.org/hco/6/GRCh38#158809459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7043660-A-C

http://identifiers.org/hco/6/GRCh38#158809538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7043745-C-A

158809923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044103-G-A

http://identifiers.org/hco/6/GRCh38#158809949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7044129-A-C

158810088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044273-T-C

158810231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044423-T-G

158810267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044458-T-A

158810267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044458-T-C

158810315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044518-A-G

158810680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044763-G-C

158810716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044799-C-T

158813507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046743-T-A

158813577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046814-C-T

158813785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047039-A-G

158814031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7047293-G-C

158814046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7047306-G-C

158814378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7047599-T-C

158814451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047667-C-G

158814451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047667-C-T

158815053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047922-G-C

158815901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048426-C-G

158816192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048687-T-G

158816197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048692-T-C

158816476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048849-C-T

158816541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048902-G-A

158817184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049234-T-C

158817367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049403-C-T

158817403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049439-G-A

158817677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049708-G-C

http://identifiers.org/hco/6/GRCh38#158817728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7049763-C-A

158817800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049833-G-C

158818103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 7050052-C-G

158818125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7050075-G-A

http://identifiers.org/hco/6/GRCh38#158819245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7050517-C-A

158819245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 12691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7050517-C-T