101569614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49661870-G-A

101569617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49661873-A-G

101569658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49661920-G-T

101570016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662242-G-T

http://identifiers.org/hco/9/GRCh38#101570059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49662280-C-A

101570156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662365-C-G

101570221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662445-A-G

101570221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662445-A-T

101570235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662517-G-A

101570299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662584-C-T

http://identifiers.org/hco/9/GRCh38#101570358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49662630-C-A

101570358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662630-C-G

101570358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662630-C-T

101570463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662730-G-A

101570463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662730-G-T

http://identifiers.org/hco/9/GRCh38#101570621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49662895-C-A

101570662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49662923-G-T

101570761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663015-T-C

101570768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663022-T-C

http://identifiers.org/hco/9/GRCh38#101570864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49663114-C-A

101571047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663287-T-C

101571076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663316-A-G

101571140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663374-G-T

101571155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663384-T-C

101571175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663403-G-A

101571175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663403-G-T

http://identifiers.org/hco/9/GRCh38#101571239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49663454-C-A

101571239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663454-C-T

101571453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663653-A-G

101571537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663718-A-G

101571786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663935-G-A

101571825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663970-C-T

101571838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663979-G-A

http://identifiers.org/hco/9/GRCh38#101571852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49663991-C-A

101571852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49663991-C-T

101571871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664010-T-A

101571871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664010-T-C

101571876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664015-T-C

101571919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664067-A-G

http://identifiers.org/hco/9/GRCh38#101571929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49664077-C-A

101571929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664077-C-T

101571975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664122-G-T

101572024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664176-A-G

101572114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664235-A-G

101572166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664281-G-A

101572166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664281-G-T

http://identifiers.org/hco/9/GRCh38#101572244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49664358-C-A

101572256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664370-A-G

http://identifiers.org/hco/9/GRCh38#101572533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49664588-A-C

http://identifiers.org/hco/9/GRCh38#101572623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49664679-C-A

101572623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664679-C-T

http://identifiers.org/hco/9/GRCh38#101572679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49664746-C-A

101572679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664746-C-G

101572679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664746-C-T

101572681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664748-G-A

101572681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664748-G-T

101572858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49664924-C-T

101573095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3 prime UTR variant
orthologous variants: 49665149-A-T

101573195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665247-T-C

101573195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665247-T-G

101573213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665265-C-T

101573300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665352-T-A

101573300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665352-T-C

101573300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665352-T-G

101573347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49665399-G-A

101573347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665399-G-T

101573351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665403-G-A

101573420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665472-T-C

http://identifiers.org/hco/9/GRCh38#101573459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49665511-A-C

101573459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49665511-A-G

101573610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49665646-T-G

http://identifiers.org/hco/9/GRCh38#101573655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49665691-C-A

101573655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49665691-C-G

101573685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49665722-T-A

101574082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49666483-A-G

http://identifiers.org/hco/9/GRCh38#101574118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49666519-A-C

101574219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49666607-A-G

101574239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49666627-A-G

101574378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49666751-T-C

101574845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667325-A-G

101574965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667440-T-C

101575056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667494-G-C

101575086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667518-G-C

101575159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667592-G-C

101575213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667639-G-C

101575620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667860-A-G

101575620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49667860-A-T

101575776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49668003-G-C

101575971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49668196-G-T

http://identifiers.org/hco/9/GRCh38#101576635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49668873-A-C

101576990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669268-G-A

http://identifiers.org/hco/9/GRCh38#101577135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49669389-C-A

101577164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669416-G-T

101577189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669429-A-T

101577325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669561-A-T

101577452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669693-T-C

101577640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669856-T-C

http://identifiers.org/hco/9/GRCh38#101577652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49669884-C-A

101577652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669884-C-G

101577655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669887-T-C

101577694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669932-T-C

101577694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669932-T-G

101577731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49669994-A-G

101577778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49670034-C-T

http://identifiers.org/hco/9/GRCh38#101577780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49670036-C-A

101577780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49670036-C-T

101577796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49670052-G-C

101577877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670128-T-A

101577877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670128-T-C

101577879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670130-T-C

101577879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670130-T-G

101577890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670137-T-A

101577890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670137-T-C

101577909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670155-C-T

101577911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670157-A-G

http://identifiers.org/hco/9/GRCh38#101577912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49670158-C-A

101577912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670158-C-G

101578123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670348-A-G

101578276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670486-C-T

101578344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670545-T-C

101578345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670546-A-G

101578390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49670612-T-G

101578695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672020-T-C

101578713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672038-A-T

101578744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672069-G-A

101578866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672178-G-A

101578932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672245-C-T

101578960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672274-T-C

http://identifiers.org/hco/9/GRCh38#101579053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672356-C-A

http://identifiers.org/hco/9/GRCh38#101579057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672360-C-A

101579057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672360-C-G

101579077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672372-A-T

101579119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672409-C-G

101579119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672409-C-T

http://identifiers.org/hco/9/GRCh38#101579181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672458-A-C

101579181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672458-A-T

http://identifiers.org/hco/9/GRCh38#101579183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672460-C-A

101579186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672463-T-C

http://identifiers.org/hco/9/GRCh38#101579242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672519-C-A

101579242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49672519-C-T

http://identifiers.org/hco/9/GRCh38#101579386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49672655-C-A

101580375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49672844-G-A

101584671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49674998-T-C

101584896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49675221-G-C

http://identifiers.org/hco/9/GRCh38#101584944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49675269-C-A

101584967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49675292-G-C

101585013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49675338-G-A

101585069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49675372-C-T

101585095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49675398-G-T

101589421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49676914-A-G

101589502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677091-T-C

101589541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677127-G-A

http://identifiers.org/hco/9/GRCh38#101589611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49677187-C-A

101589611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677187-C-T

101589652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677219-A-G

http://identifiers.org/hco/9/GRCh38#101589814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49677383-A-C

101589882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677449-T-G

101589977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677508-G-T

101590111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677588-G-A

101590111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677588-G-T

101590139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677611-T-C

101590139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677611-T-G

101591052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49677980-G-A

101591336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49678707-C-G

101591540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49678887-G-A

101591695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679028-G-A

101591695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679028-G-T

101591868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679175-G-T

101591899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679193-C-G

101591921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679215-A-T

http://identifiers.org/hco/9/GRCh38#101592033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49679331-C-A

101592099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679394-G-T

http://identifiers.org/hco/9/GRCh38#101592149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49679444-C-A

101592165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679460-A-G

101592190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679484-A-G

101592222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679516-G-A

101592349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679634-G-T

101592478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679723-A-G

http://identifiers.org/hco/9/GRCh38#101592540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49679774-C-A

101592603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49679854-T-C

101593017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680196-C-T

101593071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680248-G-A

101593081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680258-A-G

101593091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680263-G-A

http://identifiers.org/hco/9/GRCh38#101593193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49680347-C-A

101593393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680549-A-G

101593410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680567-C-T

101593452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680592-C-T

101593490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680629-G-T

101593501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680640-T-C

101593539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680678-T-C

101593705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680801-A-G

101593716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49680812-G-T

101594085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681142-T-C

http://identifiers.org/hco/9/GRCh38#101594182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49681239-C-A

101594188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681245-G-A

101594188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681245-G-T

http://identifiers.org/hco/9/GRCh38#101594189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49681246-C-A

101594189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681246-C-T

101594231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681270-T-C

101594296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681309-C-T

101594306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49681319-T-C

101594451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681478-G-T

101594595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681622-G-A

101594607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681634-G-A

101594607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681634-G-T

101594727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681754-G-A

101594805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49681832-G-A

101594805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, missense_variant
orthologous variants: 49681832-G-T

http://identifiers.org/hco/9/GRCh38#101594844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49681871-C-A

101594896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 49681923-G-A

101594896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 49681923-G-C

101594896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 49681923-G-T

http://identifiers.org/hco/9/GRCh38#101595785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49682639-A-C

101595838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49682691-C-T

101596073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49682895-G-A

101596102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49682924-G-A

101596115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49682937-C-G

101596129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49682962-A-T

http://identifiers.org/hco/9/GRCh38#101596208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49683040-C-A

http://identifiers.org/hco/9/GRCh38#101596224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49683056-C-A

101596235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49683067-G-T

http://identifiers.org/hco/9/GRCh38#101596236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49683068-C-A

101596324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49683723-C-T

101596370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49683772-C-T

101596427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49683829-G-A

101600005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49686615-C-T

101600034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49686648-G-A

101600047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49686661-T-C

101600113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49686726-A-G

http://identifiers.org/hco/9/GRCh38#101600167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49686778-A-C

101600216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49686813-G-A

http://identifiers.org/hco/9/GRCh38#101600349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49686943-C-A

101600757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49687306-T-C

101600945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49687488-G-T

101601016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49687562-G-A

101601016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49687562-G-C

101601119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49687737-G-A

101601154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49687773-A-G

http://identifiers.org/hco/9/GRCh38#101601970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49688464-A-C

101601970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688464-A-G

101601989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688483-A-G

101602020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688516-G-A

101602020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688516-G-C

101602253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688740-C-T

101602304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49688774-T-G

101602603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689051-T-G

101602807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689239-G-A

101602853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689286-G-C

101602869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689302-A-G

101603067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689487-G-C

101603067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689487-G-T

101603119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689537-T-C

101603188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689594-G-A

101603236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689638-A-G

101604011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49691414-G-A

101604320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49691634-C-G

101604740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692041-T-C

http://identifiers.org/hco/9/GRCh38#101604853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49692134-A-C

101604933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692552-C-T

101605199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692850-A-G

101605212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692863-G-C

101605315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692958-A-G

101605617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49693358-A-G

101605707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49693526-G-A

101606079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49693867-C-G

101606079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49693867-C-T

101606116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49693902-G-A

http://identifiers.org/hco/9/GRCh38#101606178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49693952-C-A

101606227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49694001-G-A

101606697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49694572-G-A

http://identifiers.org/hco/9/GRCh38#101606976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49694837-A-C

101607069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49694928-C-T

101607263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695119-G-C

101607365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695222-T-G

101607518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695325-G-A

101607527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695334-C-T

101607549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695356-C-T

101607550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695357-G-A

101607550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695357-G-T

101607730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695477-T-A

http://identifiers.org/hco/9/GRCh38#101607769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49695516-A-C

101607984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695762-A-G

101608100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695880-T-C

101608412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49696440-T-C

101608706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49698009-G-A

101609155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49698462-C-T

101609265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49698564-A-T

101609697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49698890-T-G

http://identifiers.org/hco/9/GRCh38#101610147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49699157-A-C

101611620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49700867-A-G

101611620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49700867-A-T

101611758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701009-G-A

http://identifiers.org/hco/9/GRCh38#101611791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49701041-A-C

101611916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701309-C-T

101612006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701460-G-A

101612417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701833-G-A

101612441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701858-T-G

101612604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49701985-T-C

101612772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702152-G-T

101613103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702425-C-T

http://identifiers.org/hco/9/GRCh38#101613263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49702584-A-C

101613263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702584-A-G

101613296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702610-G-A

101613296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702610-G-T

http://identifiers.org/hco/9/GRCh38#101613623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49702959-A-C

101614213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704320-T-C

101614377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704454-A-G

101614391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704468-C-T

101614410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704487-A-G

101614559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704628-A-G

http://identifiers.org/hco/9/GRCh38#101614987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49704737-C-A

101615096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704841-C-T

101615184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704935-G-A

101615184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49704935-G-T

http://identifiers.org/hco/9/GRCh38#101615323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49705087-A-C

101615781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49706265-A-G

101615844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49706096-G-T

101616449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49705351-G-A

101616459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49705341-T-A

101616605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49705200-A-T

101617405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49707443-C-G

101617587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49707628-A-G

101618780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49707807-A-G

101618873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49707898-C-T

101619167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708193-T-C

101619181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708207-C-T

http://identifiers.org/hco/9/GRCh38#101619285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49708333-C-A

101619507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708541-T-G

101619693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708722-G-C

101619693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708722-G-T

101619723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708751-A-T

101619731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708759-G-A

101619744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708771-A-G

101619870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708900-G-A

101619870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708900-G-T

101619883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49708913-A-G

101620091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49709522-G-A

101620246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49709671-G-A

http://identifiers.org/hco/9/GRCh38#101620344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49709764-A-C

101620611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49710043-T-C

101620623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49710055-T-G

101620725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49710150-T-G

101620911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49710318-A-G

101621585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49712222-T-C

101622321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49712946-C-G

101622348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49712973-T-C

101622646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49713261-T-A

101622969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49713803-T-C

101623322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49714134-T-G

101623502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49714323-G-A

101623502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49714323-G-T

http://identifiers.org/hco/9/GRCh38#101625484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49716501-C-A

http://identifiers.org/hco/9/GRCh38#101625598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49716606-C-A

101625598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49716606-C-T

101625779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49716799-A-G

http://identifiers.org/hco/9/GRCh38#101625854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49716866-C-A

101626170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49716946-A-G

101626177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49716953-C-G

101626269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49717036-A-G

101626953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49717624-G-A

101627281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49717932-G-A

101627511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49718144-T-C

101628009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49718609-C-T

101628122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49718721-A-G

101628122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49718721-A-T

101628141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49719144-C-T

http://identifiers.org/hco/9/GRCh38#101628494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49719477-A-C

101628494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49719477-A-G

101628494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49719477-A-T

101628695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49719951-G-A

101628695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49719951-G-T

http://identifiers.org/hco/9/GRCh38#101628750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49719995-A-C

101629154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49720921-A-G

101629922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49721481-T-G

101630011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49721876-C-G

101630011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49721876-C-T

101630092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49721954-T-C

101630220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722090-T-C

101630225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722095-T-A

101630225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722095-T-G

101630420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722148-T-C

101630469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722199-T-C

101630847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722573-G-A

101630884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49722608-C-T

101631649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49723678-C-G

101631710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49723740-G-A

101631899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49723895-T-G

101631970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49723965-C-G

101632099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49724110-C-G

101632099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49724110-C-T

101632488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49724482-A-G

http://identifiers.org/hco/9/GRCh38#101632713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49724684-A-C

101633118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49725077-G-A

101633165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49725119-T-C

101634972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49726430-T-A

101635248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49726702-T-A

101635474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49726915-T-C

101635567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49727037-A-G

101635818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49727255-C-G

101636878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49728508-G-A

101637669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729028-T-C

http://identifiers.org/hco/9/GRCh38#101637695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49729054-A-C

101637802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729149-C-T

101637886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729222-C-T

101638066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729402-T-C

http://identifiers.org/hco/9/GRCh38#101638257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49729586-C-A

101638318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729647-C-T

101638370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729696-C-G

101638415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729741-A-G

101638468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49729795-T-A

101638786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49739440-T-C

101638886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49739536-G-A

101638886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49739536-G-C

101639028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740521-C-G

101639109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740602-G-C

101639222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740709-A-G

101639350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740839-A-G

101639376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740864-G-C

101639384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740872-A-T

101639415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49740904-C-G

101639798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49741260-T-C

101639799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49741261-A-G

101639839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49741301-A-G

101640430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49741820-G-T

101641006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49742006-C-G

101642296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49742803-C-T

101642388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49742893-A-G

101642532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49743036-G-T

101650523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49744496-A-G

101650856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49744674-G-A

101650895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49744713-C-T

101651390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49745161-A-G

101651518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49745328-A-T

101651540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49745350-T-C

101651686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49746417-T-C

101651794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49746516-A-G

101651809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49746531-C-T

101651890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49746611-A-G

101651966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49747335-A-G

101652097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49747440-A-G

101652302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49747976-T-G

http://identifiers.org/hco/9/GRCh38#101652304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49747978-A-C

101652304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49747978-A-G

101652561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49748221-C-T

101653217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49748899-C-G

101653882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49749502-T-C

101654057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49749678-C-T

101654192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49749801-T-G

101654219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49749828-G-A

101654563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49750325-C-T

101654853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49750861-C-T

101654935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49750943-C-T

http://identifiers.org/hco/9/GRCh38#101655272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49751271-C-A

101655285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751284-T-C

101655383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751380-T-G

101655398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751399-T-C

101655432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751433-A-G

101655432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751433-A-T

http://identifiers.org/hco/9/GRCh38#101655675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49751713-C-A

101655866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49751921-A-T

101656013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752062-G-A

101656165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752214-A-G

101656255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752315-C-T

101656465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752525-C-T

101656565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752625-A-G

101656588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49752650-T-C

101656647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49753585-G-A

http://identifiers.org/hco/9/GRCh38#101656762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49753687-A-C

101656763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49753688-G-A

101656856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49753766-C-T

101656892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49753801-G-A

http://identifiers.org/hco/9/GRCh38#101657076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49753985-C-A

101657076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49753985-C-T

101657093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754002-T-C

101657204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754121-A-G

101658060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754403-A-G

101658111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754454-T-C

101658125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754468-G-C

101658159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754500-T-C

101658179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754520-A-G

http://identifiers.org/hco/9/GRCh38#101658266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49754611-C-A

101658273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754618-A-G

101658395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49754733-G-A

101658871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49755564-G-A

101659107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49755771-A-G

101659406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49756029-A-G

101659952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49756504-T-A

101661168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757032-G-A

101661336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757148-A-G

101661843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757643-C-T

101662061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757838-C-T

101662145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757924-C-T

101662215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49757985-T-C

101663148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49759606-C-T

101663261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49759697-A-G

101663369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49759800-A-G

101663572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49760006-A-G

http://identifiers.org/hco/9/GRCh38#101663600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760034-C-A

http://identifiers.org/hco/9/GRCh38#101663672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760110-A-C

http://identifiers.org/hco/9/GRCh38#101663699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760136-A-C

http://identifiers.org/hco/9/GRCh38#101663713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760150-A-C

http://identifiers.org/hco/9/GRCh38#101663735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760172-A-C

101663806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49760240-G-T

101663903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49760326-G-T

http://identifiers.org/hco/9/GRCh38#101663935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49760358-C-A

101664319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49760686-A-G

101664862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49761232-C-T

101664901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49761271-A-G

http://identifiers.org/hco/9/GRCh38#101664958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49761422-A-C

101664972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49761436-A-G

101669946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49770309-G-A

101669946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49770309-G-T

101670026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49770385-C-T

http://identifiers.org/hco/9/GRCh38#101670557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49770916-C-A

101670557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49770916-C-T

101670933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49771292-A-G

101671133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49771492-A-G

http://identifiers.org/hco/9/GRCh38#101671223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49771596-A-C

101671223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49771596-A-T

101671233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49771660-C-G

http://identifiers.org/hco/9/GRCh38#101671366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49771972-C-A

101671366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49771972-C-T

101671428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49772016-G-T

101671877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49772433-C-G

101672083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49772594-C-G

101672136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49772647-A-G

http://identifiers.org/hco/9/GRCh38#101672414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49772828-A-C

101672922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49773343-A-G

101672943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49773364-A-G

http://identifiers.org/hco/9/GRCh38#101672999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49773422-C-A

101673014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49773440-A-T

101673478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49773901-A-G

101673620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774056-A-G

101673717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774151-C-T

101673729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774169-T-C

101674122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774525-A-G

101674149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774555-T-A

101674162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774567-T-C

101674208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774614-T-C

http://identifiers.org/hco/9/GRCh38#101674231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49774636-A-C

101674231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774636-A-G

101674370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774733-T-C

101674563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774898-A-G

101674563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49774898-A-T

101675075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49775413-C-T

101675276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49775602-T-C

101675292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49775621-C-T

101675441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49775769-T-G

101675787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49781853-A-G

101675832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49781902-G-C

101675883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49781947-A-G

101676296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783292-C-T

101676490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783479-T-C

101676540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783530-G-A

101676558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783763-T-A

101676569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783798-G-A

101676569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49783798-G-T

http://identifiers.org/hco/9/GRCh38#101677641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49784355-C-A

101677641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49784355-C-T

101677877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49784646-C-G

101677877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49784646-C-T

101677989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49784762-C-T

101678406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49785168-T-C

101678636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49785387-T-G

101678828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49785571-G-T

101678836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49785579-G-A

101678836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49785579-G-T

101679405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786169-T-A

101679423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786187-T-G

101679693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786409-G-T

101679707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786423-G-A

101679864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786565-T-C

101680344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786962-T-G

101680375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49786993-C-T

101680801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49787418-G-C

101680814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49787427-C-T

101681401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49787690-T-C

101682975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49788754-C-G

101683479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49789250-G-T

101683628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49789399-A-G

http://identifiers.org/hco/9/GRCh38#101683783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49789573-C-A

101684824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49790449-A-T

101684871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49790491-A-G

101684871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49790491-A-T

http://identifiers.org/hco/9/GRCh38#101685278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49790987-C-A

http://identifiers.org/hco/9/GRCh38#101685303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49791012-C-A

101685303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791012-C-T

101685375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791035-T-C

101685378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791038-G-T

101685461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791107-G-T

101685876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791734-G-T

101685879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791737-C-T

101685916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791791-C-T

101685929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49791804-G-A

101686205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792064-G-T

101686393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792242-A-G

101686393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792242-A-T

http://identifiers.org/hco/9/GRCh38#101686416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49792259-A-C

101686416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792259-A-T

http://identifiers.org/hco/9/GRCh38#101686446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49792289-C-A

101686446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792289-C-G

http://identifiers.org/hco/9/GRCh38#101686467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49792311-C-A

101686517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49792358-G-T

101687258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793089-T-A

101687258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793089-T-C

101687303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793140-T-A

http://identifiers.org/hco/9/GRCh38#101687332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49793168-C-A

http://identifiers.org/hco/9/GRCh38#101687583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49793411-C-A

101687686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793510-T-A

101687686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793510-T-C

101687763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49793572-A-G

101689510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795558-A-G

101689510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795558-A-T

101689732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795816-A-G

101689745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795829-C-T

101689761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795845-C-T

101689778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795862-A-G

101689778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49795862-A-T

101690828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796366-G-T

101690872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796399-T-C

101690876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796403-T-C

http://identifiers.org/hco/9/GRCh38#101691043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49796524-C-A

101691043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796524-C-T

101691385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796919-G-A

101691480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49796996-G-A

101691490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797006-A-G

101691496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797013-C-T

101691497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797014-G-A

101691729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797200-G-A

101691730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797201-T-C

101691754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797225-T-G

http://identifiers.org/hco/9/GRCh38#101691893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49797357-C-A

http://identifiers.org/hco/9/GRCh38#101692020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49797459-C-A

101692064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797505-G-A

101692160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49797594-T-C

101696714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49799133-A-G

101696765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49799184-C-T

101696845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49799261-T-A

101696875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49799291-A-G

101696919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49799334-G-A

101697578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49800253-C-T

101697940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49800584-G-C

101699580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801261-A-G

101699764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801425-G-A

101699874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801533-C-G

101699904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801563-G-A

http://identifiers.org/hco/9/GRCh38#101699908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49801564-A-C

101699917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801573-T-C

101699983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801621-C-T

101700110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801725-A-T

101700233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49801847-G-C

http://identifiers.org/hco/9/GRCh38#101700384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49801998-A-C

http://identifiers.org/hco/9/GRCh38#101700412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49802024-C-A

101700412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802024-C-T

101700418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802030-T-C

101700419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802031-G-T

http://identifiers.org/hco/9/GRCh38#101700493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49802103-C-A

101700576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802186-T-C

101700727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802311-T-C

http://identifiers.org/hco/9/GRCh38#101700789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49802371-C-A

101700891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49802946-T-C

101701071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803098-C-T

101701112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803139-G-A

101701174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803202-G-A

101702332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803453-T-A

http://identifiers.org/hco/9/GRCh38#101702602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49803667-C-A

101702602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803667-C-T

101702710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803761-G-A

101702777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803802-C-T

101702900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803842-C-T

101702908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49803850-C-T

101703573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49804582-G-A

101703625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49804633-A-G

101703641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49804649-G-T

101703681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49804681-T-C

101703695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49804695-T-G

101704141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49805105-C-T

101705938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49805617-C-T

101706554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49806213-G-C

101706554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49806213-G-T

101706714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49806360-T-A

101707293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49806971-G-C

101707499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49807173-C-T

101707593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49807257-A-T

101707765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49807417-T-A

101707765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49807417-T-G

http://identifiers.org/hco/9/GRCh38#101708236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49808182-A-C

101708401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808373-C-G

101708428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808399-G-C

101708429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808400-C-T

http://identifiers.org/hco/9/GRCh38#101708430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49808401-A-C

101708430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808401-A-G

101708517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808490-C-G

101708517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49808490-C-T

http://identifiers.org/hco/9/GRCh38#101708681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49810067-A-C

101708716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810102-T-C

101708797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810181-C-T

101709051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810431-C-T

101709097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810476-G-C

101709097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810476-G-T

101709098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810477-T-G

101709107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810486-T-A

http://identifiers.org/hco/9/GRCh38#101709246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49810623-C-A

101709395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810722-G-A

101709419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810746-G-T

101709476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810790-A-G

101709509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49810822-G-A

101709858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49811533-A-G

101710205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49811867-G-T

http://identifiers.org/hco/9/GRCh38#101710248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49811909-C-A

101710739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49812384-T-C

http://identifiers.org/hco/9/GRCh38#101713373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49814388-C-A

101713373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814388-C-G

101713602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814602-G-T

101713727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814728-G-T

101713762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814762-G-A

101713762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814762-G-C

101713879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49814794-C-G

101714370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815065-G-C

101714542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815224-C-T

http://identifiers.org/hco/9/GRCh38#101714744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49815396-C-A

101714775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815425-A-G

101715082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815732-G-A

101715105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815755-A-T

101715120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815770-C-G

101715120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815770-C-T

101715226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815902-G-A

101715226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815902-G-T

101715331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49815999-C-T

101715480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816046-T-A

101715545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816108-G-C

http://identifiers.org/hco/9/GRCh38#101715602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49816164-A-C

101715602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816164-A-T

101715688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816245-G-A

http://identifiers.org/hco/9/GRCh38#101715730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49816290-A-C

101715730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816290-A-G

101715803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49816367-T-C

101716001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817141-C-G

101716084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817187-T-C

101716267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817398-G-C

101716325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817456-A-G

http://identifiers.org/hco/9/GRCh38#101716691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49817780-C-A

101716691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817780-C-T

101716749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817821-C-G

101716749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817821-C-T

101716811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49817881-T-C

101717048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49825889-G-T

101717384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49826225-A-G

101718173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49826838-C-G

101718199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49826856-T-A

101718199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49826856-T-C

101718223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49826874-C-G

101718423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49827078-A-G

101718970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49827595-T-C

101719756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49828016-A-G

101719856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49828101-T-G

101720039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49828289-T-C

101720042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49828292-C-T

101720522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829111-T-C

101720538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829127-T-C

101720573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829159-A-G

101720629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829215-A-G

101720641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829227-A-G

101720648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829234-A-T

101720688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829273-A-G

101720750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829336-T-A

101720750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829336-T-C

101720770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829355-A-G

http://identifiers.org/hco/9/GRCh38#101724896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49829433-A-C

101725238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49829700-G-A

http://identifiers.org/hco/9/GRCh38#101725680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49830075-C-A

101725680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49830075-C-T

http://identifiers.org/hco/9/GRCh38#101725693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49830090-A-C

101725694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49830091-G-A

101725995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49830395-A-G

http://identifiers.org/hco/9/GRCh38#101726181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49830580-C-A

101726967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49831432-C-G

101727166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49831607-G-A

101727337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49831763-T-A

101727359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49831787-G-A

101727359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49831787-G-T

101727817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49832207-G-A

101727840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, undefined
orthologous variants: 49832230-C-T

101727853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, undefined
orthologous variants: 49832243-T-C

101727854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, undefined
orthologous variants: 49832244-G-A

101728184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49832877-A-G

101728468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49833204-T-C

101728836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49833691-G-A

101728836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49833691-G-T

101729363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49834227-G-A

101729410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49834273-T-G

101729853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835340-G-A

101729907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835371-C-G

101729960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835422-T-G

101729983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835443-G-T

101730001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835461-T-C

101730461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49835975-A-G

101730613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49836203-A-G

101731039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49837348-A-G

101731307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49837603-C-T

101731608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838001-T-A

101731680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838103-C-G

101731684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838107-T-C

http://identifiers.org/hco/9/GRCh38#101731836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49838454-C-A

http://identifiers.org/hco/9/GRCh38#101731914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49838514-C-A

101731914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838514-C-T

101732078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838658-A-G

101732346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49838910-C-T

http://identifiers.org/hco/9/GRCh38#101732388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49838958-C-A

101732956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49839506-G-A

101733234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49839721-G-T

101733414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49839902-T-A

101733494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49839980-C-T

101733595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49840288-T-C

101733809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49840516-G-T

101734297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49841201-G-T

101734362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49841264-G-A

101734629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49841768-G-C

101734680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49841819-G-A

http://identifiers.org/hco/9/GRCh38#101734695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49841834-C-A

101734786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49841926-G-T

101735185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49842332-A-T

101735217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49842364-G-C

101735282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49842427-T-C

http://identifiers.org/hco/9/GRCh38#101735579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49842713-A-C

http://identifiers.org/hco/9/GRCh38#101736046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49843190-A-C

101736293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49843426-T-A

101736546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49843669-C-T

101736561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49843685-C-T

101736562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49843686-T-G

101736983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron_variant, undefined
orthologous variants: 49844069-A-G

101737136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49844246-G-A

101737136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49844246-G-T

101737175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49844282-G-T

http://identifiers.org/hco/9/GRCh38#101737232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49844337-C-A

101737232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49844337-C-G

101737232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: intron variant
orthologous variants: 49844337-C-T

101737302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49844404-G-A

101737419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49844521-G-A

101737565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49844667-C-T

http://identifiers.org/hco/9/GRCh38#101737631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49844733-C-A

101737631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49844733-C-T

101737721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49844823-G-A

101737721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49844823-G-C

101737721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: synonymous variant
orthologous variants: 49844823-G-T

101737768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: missense variant
orthologous variants: 49844870-T-C

http://identifiers.org/hco/9/GRCh38#101738040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49845158-C-A

101738040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845158-C-T

http://identifiers.org/hco/9/GRCh38#101738069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49845187-C-A

101738069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 49845187-C-G

101738100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845218-G-T

101738201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845319-T-A

101738201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845319-T-C

101738201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845319-T-G

101738363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845450-G-A

101738363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845450-G-T

http://identifiers.org/hco/9/GRCh38#101738497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49845594-A-C

101738497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845594-A-G

101738497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845594-A-T

http://identifiers.org/hco/9/GRCh38#101738545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49845642-C-A

http://identifiers.org/hco/9/GRCh38#101738615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49845713-C-A

101738615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16767
most severe consequence: 5 prime UTR variant
orthologous variants: 49845713-C-T