20560753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8464151-G-T

http://identifiers.org/hco/2/GRCh38#20560828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8464093-C-A

20560828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8464093-C-T

20560862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8464067-G-A

20560981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8463951-A-G

20561076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8463857-C-G

20561076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8463857-C-T

20561532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8462397-A-G

20561641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8462338-G-C

http://identifiers.org/hco/2/GRCh38#20561801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8462167-C-A

20561801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8462167-C-T

20562540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8461390-T-G

20562563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8461365-G-A

http://identifiers.org/hco/2/GRCh38#20562622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8461307-C-A

20562628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8461301-C-T

20562808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8461118-C-T

20563030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8460981-C-T

20563184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8460841-C-T

20563185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8460840-A-G

20566037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8460284-A-T

20566129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8460179-C-T

20566593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8459739-G-T

20567210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452628-G-A

20567251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452590-G-A

20567423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452478-G-A

20567591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8452318-C-T

20567657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452252-A-T

20567751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452158-C-G

20567770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452141-G-A

20567805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452103-T-A

20567875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8452047-A-G

http://identifiers.org/hco/2/GRCh38#20568588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8451026-C-A

20568667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450961-G-A

20568676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450955-G-T

20568986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450711-A-G

20569020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450676-T-C

20569526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450317-G-A

http://identifiers.org/hco/2/GRCh38#20569557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8450283-A-C

http://identifiers.org/hco/2/GRCh38#20569686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8450152-C-A

http://identifiers.org/hco/2/GRCh38#20569812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8450042-C-A

20569812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450042-C-T

20569848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8450006-T-G

http://identifiers.org/hco/2/GRCh38#20570055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8449168-C-A

20570059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8449164-C-T

20570116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8449102-T-C

20570153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8449075-C-T

20570343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448917-C-G

20570343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448917-C-T

20570344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448916-G-A

20570399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448887-T-C

20570586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448782-A-T

20570722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448655-G-A

http://identifiers.org/hco/2/GRCh38#20570759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8448617-C-A

20571414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448508-G-A

20571414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448508-G-C

http://identifiers.org/hco/2/GRCh38#20571416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8448506-C-A

20571548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448375-G-A

20571591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8448341-G-T

20572711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8447469-C-T

20572804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8447397-T-G

20572857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8447344-T-G

20572943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8447275-G-A

20573174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8447060-G-A

http://identifiers.org/hco/2/GRCh38#20573316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8446820-C-A

20573333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8446803-G-T

20573805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8446406-A-G

20573864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8446329-A-G

20573864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8446329-A-T

20574231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445977-C-T

20574395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445809-G-A

20574423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445782-C-T

20574514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445704-T-C

20574558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445665-G-A

20574710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445537-G-A

20574922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445305-G-A

20574954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8445272-A-G

20576780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8443212-G-T

20577126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8440240-T-C

20577198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8440168-A-G

http://identifiers.org/hco/2/GRCh38#20577338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8440036-A-C

20577338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8440036-A-G

20577351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8440012-C-T

20577353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8440010-G-T

20578027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8438914-G-A

20578218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437740-C-T

20578629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437349-C-G

20578632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437347-A-G

20578779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437202-C-G

20578779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437202-C-T

http://identifiers.org/hco/2/GRCh38#20578810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8437171-A-C

20578981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437070-G-A

20579020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437031-A-G

20579029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8437023-G-A

20579451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8436597-G-C

20579496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8436553-A-T

20579519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8436530-G-A

20579914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435780-G-A

20579914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435780-G-T

20580055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435663-A-G

20580091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435626-C-T

20580273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435461-C-G

20580378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8435357-G-T

20580914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8434352-G-C

20581224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8434105-G-A

20581256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8434077-C-G

20581256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8434077-C-T

20583554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8432304-C-T

20584034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8431792-A-T

20584248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8430393-T-C

20584743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429920-G-C

20584759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429905-C-T

20584798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429866-C-T

20584865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429799-C-T

20584992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429470-G-A

20584993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429469-A-G

20585049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429429-C-T

20585071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429414-G-A

20585123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429356-C-T

http://identifiers.org/hco/2/GRCh38#20585220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8429261-C-A

20585243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8429236-G-A

20585530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8428464-C-T

20585581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8428411-T-C

http://identifiers.org/hco/2/GRCh38#20585805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8428209-C-A

20585805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8428209-C-T

20585987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8428078-G-A

20586075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427989-G-A

20586093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427972-T-C

20586124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427929-G-T

20586133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427920-C-T

20586156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427896-T-C

20586168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427883-G-A

20586216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427859-T-C

20586310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427767-G-A

20586310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427767-G-T

20586312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427765-C-G

20586386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427682-C-G

20586414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427664-A-G

20586454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427626-A-G

20586523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8427558-A-G

20586896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427326-C-T

20587061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8427186-T-G

20587819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8426192-A-T

http://identifiers.org/hco/2/GRCh38#20587995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8426061-C-A

20587995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8426061-C-T

20588076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8425979-C-G

20591153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8423111-G-T

20591357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8422928-T-C

http://identifiers.org/hco/2/GRCh38#20591381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8422894-C-A

20591381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8422894-C-T

20593973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8422303-G-T

20594112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8422145-T-C

20594195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8422064-G-A

20594631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421645-T-C

20594677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421599-T-C

20594705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421571-T-A

http://identifiers.org/hco/2/GRCh38#20594804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8421475-C-A

20594804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421475-C-T

20594864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421437-G-A

20594919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421380-C-T

20595122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421194-C-T

20595149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8421169-A-T

20595421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8419537-T-A

20595423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8419535-C-T

20595571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8419425-G-A

20595571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8419425-G-C

http://identifiers.org/hco/2/GRCh38#20595721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8419290-C-A

20595910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8419111-C-T

20595919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: 8419104-C-T

http://identifiers.org/hco/2/GRCh38#20595967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8419063-C-A

20596670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8417322-T-C

20596686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8417317-C-G

20597458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8416546-C-T

20597473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8416542-T-C

http://identifiers.org/hco/2/GRCh38#20597628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8416392-A-C

20597628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8416392-A-G

20597707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8416317-G-T

http://identifiers.org/hco/2/GRCh38#20597901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8416144-C-A

20597901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8416144-C-T

20598958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415909-T-G

20599000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415856-G-A

20599000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415856-G-T

20599072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415799-C-T

20599217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415655-G-A

20599369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415495-C-T

20599370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415494-G-A

20599399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415465-A-G

20599651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8415158-C-T

20600190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414580-G-A

20600229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414541-G-T

20600289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414476-G-A

20600408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414357-A-G

20600433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414332-G-A

20600462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414303-A-G

20600574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8414188-C-T

20600791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8413994-T-C

20602401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8412610-G-A

20602401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8412610-G-T

20602406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8412601-A-T

20602456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8412517-C-T

http://identifiers.org/hco/2/GRCh38#20602556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8412400-C-A

20602628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8412324-T-A

20604970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407775-A-G

20605052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407694-A-G

20605150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407596-C-T

20605209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407528-C-T

20605287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407435-G-A

20605291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407431-T-A

20605489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8407226-A-G

http://identifiers.org/hco/2/GRCh38#20605582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8407117-C-A

20605851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8406892-T-C

20605859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8406884-G-T

20608153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8404468-C-T

20608812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8403650-T-G

http://identifiers.org/hco/2/GRCh38#20608871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8403591-C-A

20608871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8403591-C-T

20609684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8400884-A-T

20609826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8400764-G-C

20610373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8400038-C-G

20610868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399581-T-A

20611150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399303-A-G

20611189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399262-A-G

20611196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399255-G-A

20611287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399174-G-A

20611287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8399174-G-T

20611576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8398897-G-A

20611694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8398793-C-T

20611925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: intron variant
orthologous variants: 8398585-C-T

20612942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8398552-T-C

20613206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8398307-C-T

20613460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8398058-C-G

20613503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8398028-G-A

20613503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8398028-G-C

20613767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8397870-G-C

20614163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8397499-A-G

http://identifiers.org/hco/2/GRCh38#20614276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8397399-A-C

20614289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8397381-A-G

20614289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8397381-A-T

20614530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8397198-T-A

http://identifiers.org/hco/2/GRCh38#20614662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8396808-C-A

20614662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8396808-C-T

20614790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8396677-G-A

20614813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8396656-G-C

20614874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8396594-G-T

20614992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8396481-T-C

20615472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395585-T-C

20615594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395463-A-T

20615709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395347-G-A

20615731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395339-G-C

20615864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395226-G-A

20616024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395103-A-G

20616114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8395016-G-A

20616209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8394927-T-C

20616842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393808-C-G

20616862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393790-C-T

20617042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393602-C-T

20617094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393550-T-C

20617180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393450-A-G

20617211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393411-G-A

20617252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393389-G-A

20617252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393389-G-C

20617305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393327-C-T

20617322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393298-G-A

20617413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393239-A-G

20617425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8393227-T-C

20617705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392981-G-A

20617785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392917-G-A

20617785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392917-G-T

20617824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392892-G-T

20617937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392846-T-C

20617937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392846-T-G

20617970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392824-G-A

20617970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392824-G-T

20617972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392822-A-G

20617988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392806-G-A

20618006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392788-G-T

http://identifiers.org/hco/2/GRCh38#20618104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392750-C-A

20618104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392750-C-T

20618105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392747-A-G

20618105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392747-A-T

20618195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392688-G-A

20618195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392688-G-C

20618195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8392688-G-T

20618307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392575-A-G

http://identifiers.org/hco/2/GRCh38#20618348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392538-C-A

20618357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392529-G-A

20618357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392529-G-T

http://identifiers.org/hco/2/GRCh38#20618409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392498-C-A

20618409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392498-C-G

20618409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392498-C-T

http://identifiers.org/hco/2/GRCh38#20618428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392480-C-A

20618428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392480-C-G

20618428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392480-C-T

20618446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392462-T-A

20618446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392462-T-C

20618446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392462-T-G

http://identifiers.org/hco/2/GRCh38#20618674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392359-C-A

20618674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392359-C-T

http://identifiers.org/hco/2/GRCh38#20618719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392314-C-A

20618719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392314-C-G

20618719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392314-C-T

http://identifiers.org/hco/2/GRCh38#20618720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392313-C-A

20618720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392313-C-G

20618720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392313-C-T

20618735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392297-T-A

20618735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392297-T-C

20618735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392297-T-G

20618745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392287-G-A

20618745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392287-G-C

20618745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392287-G-T

20618759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392276-G-A

20618759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392276-G-T

20618760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392275-G-A

20618760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392275-G-T

20618790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392246-C-G

20618790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392246-C-T

20618791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392245-G-A

20618791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392245-G-C

20618792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392244-C-G

20618792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392244-C-T

http://identifiers.org/hco/2/GRCh38#20618795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8392241-C-A

20618810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392225-T-C

20618888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392185-G-T

20618911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392164-G-A

20618911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8392164-G-T

20618994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8392078-A-G

http://identifiers.org/hco/2/GRCh38#20619110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391965-C-A

20619110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 8391965-C-T

20619123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391952-G-A

20619123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391952-G-C

20619123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391952-G-T

20619171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391904-G-A

http://identifiers.org/hco/2/GRCh38#20619208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391867-C-A

20619208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391867-C-T

20619223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8391852-T-A

20619264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391811-G-A

20619264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391811-G-T

http://identifiers.org/hco/2/GRCh38#20619325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391756-C-A

20619325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391756-C-T

http://identifiers.org/hco/2/GRCh38#20619326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391755-C-A

20619326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391755-C-T

http://identifiers.org/hco/2/GRCh38#20619387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391739-C-A

http://identifiers.org/hco/2/GRCh38#20619393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391733-C-A

20619613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391555-C-T

20619707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391457-C-G

20619707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391457-C-T

20619798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391378-G-A

http://identifiers.org/hco/2/GRCh38#20619902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8391260-C-A

20619902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391260-C-T

20619940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391194-C-T

20619977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8391145-G-C

20620169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390779-C-T

20620297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390652-G-C

20620434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390511-G-A

20620434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390511-G-T

20620512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390443-G-A

20620535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390420-G-A

http://identifiers.org/hco/2/GRCh38#20620649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8390346-C-A

20620737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390251-T-C

20620797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390191-A-G

20620815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390171-T-C

20620848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390137-G-T

20620858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390126-A-T

20620911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390074-G-T

20620927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8390058-T-C

20621088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389918-C-G

20621088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389918-C-T

20621142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389841-G-A

20621142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389841-G-T

20621148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389835-G-C

20621209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389761-G-T

20621426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389604-G-A

20622093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389361-A-G

http://identifiers.org/hco/2/GRCh38#20622108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8389350-A-C

20622108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389350-A-G

20622108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389350-A-T

http://identifiers.org/hco/2/GRCh38#20622116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8389342-C-A

20622116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389342-C-T

20622120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389328-A-G

20622175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8389293-T-C

20622216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389280-A-T

20622394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389160-G-C

20622394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389160-G-T

20622395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389159-A-T

http://identifiers.org/hco/2/GRCh38#20622492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8389063-C-A

20622495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389060-T-C

20622503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8389049-T-C

http://identifiers.org/hco/2/GRCh38#20622523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8389030-C-A

20622562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388999-G-A

20622754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388854-T-A

20622754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388854-T-C

20622754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388854-T-G

20622772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388835-T-C

http://identifiers.org/hco/2/GRCh38#20622774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388833-A-C

http://identifiers.org/hco/2/GRCh38#20622910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388693-C-A

20622910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388693-C-G

20622910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388693-C-T

http://identifiers.org/hco/2/GRCh38#20622978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388625-C-A

20622978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388625-C-T

20622981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388622-G-A

http://identifiers.org/hco/2/GRCh38#20623048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388565-C-A

20623048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388565-C-T

20623059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388559-G-T

20623060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388558-A-G

20623062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388556-C-T

http://identifiers.org/hco/2/GRCh38#20623099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388521-C-A

20623100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388520-T-C

20623100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388520-T-G

20623106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388514-G-T

20623190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388424-T-C

20623205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388409-A-G

20623206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388408-G-T

20623220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388394-G-A

20623220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388394-G-T

20623236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388379-T-C

http://identifiers.org/hco/2/GRCh38#20623239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388376-C-A

20623239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388376-C-T

20623326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388293-C-G

20623326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388293-C-T

20623327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388292-G-A

20623333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388286-G-A

20623345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388274-A-G

20623413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388194-A-G

20623518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388096-G-A

20623518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388096-G-C

20623518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388096-G-T

http://identifiers.org/hco/2/GRCh38#20623549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388065-A-C

20623549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388065-A-T

http://identifiers.org/hco/2/GRCh38#20623557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8388057-C-A

20623557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388057-C-G

20623557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8388057-C-T

20623702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387932-T-C

20623702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387932-T-G

20623725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387920-G-A

20623725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387920-G-T

http://identifiers.org/hco/2/GRCh38#20623728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8387913-C-A

20623728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387913-C-T

http://identifiers.org/hco/2/GRCh38#20623743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8387898-C-A

20623743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387898-C-T

20623765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387876-T-C

http://identifiers.org/hco/2/GRCh38#20623790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8387850-C-A

20623790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8387850-C-T

20623904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8387758-T-C

20623904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8387758-T-G

20623906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8387756-C-T

20623998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8387664-C-T

20624051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387607-G-A

20624051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387607-G-T

20624070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387108-C-G

20624076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387098-T-C

20624079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387095-G-A

20624079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387095-G-T

20624114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387070-G-C

20624114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8387070-G-T

http://identifiers.org/hco/2/GRCh38#20624217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8386963-C-A

20624371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386852-G-A

20624424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386802-T-C

20624433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386795-T-C

20624527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386696-G-A

20624555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386668-C-T

20624595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386611-A-G

20624598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386608-T-C

20624598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386608-T-G

20624724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 8386401-C-G

20624724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 8386401-C-T

20624812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8386316-A-G

20624859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8386269-G-A

http://identifiers.org/hco/2/GRCh38#20624871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8386257-A-C

20624937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386200-T-C

20625004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386136-G-A

20625004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386136-G-T

20625032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8386107-G-T

20625233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8385889-G-A

20625258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8385849-G-A

20625279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8385828-C-T

20625655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384813-G-A

20626207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384310-G-T

20626298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384285-C-T

20626394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384251-T-C

20626499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384168-G-A

20626532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8384140-T-C

http://identifiers.org/hco/2/GRCh38#20626953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8383829-C-A

20627202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383557-C-T

http://identifiers.org/hco/2/GRCh38#20627232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8383525-C-A

20627320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383467-C-T

20627516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383303-G-A

20627516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383303-G-T

20627549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383231-T-C

20627574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8383205-C-T

20629357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8382016-C-T

20629389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8382011-A-T

20629615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381905-C-T

20629697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381824-T-C

20629813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381729-C-T

20629959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381588-G-A

20630003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381545-A-G

20630063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8381484-G-C

20631557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380700-G-C

http://identifiers.org/hco/2/GRCh38#20631559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8380698-C-A

20631571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380686-T-A

20631571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380686-T-C

20631571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380686-T-G

20631850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380432-C-T

20631972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380337-C-T

20632203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380119-C-T

20632257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380065-G-A

20632257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8380065-G-C

20632386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379944-A-T

20632457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379867-G-A

20632635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379597-A-G

20632694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379519-C-T

20632775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379453-A-G

20633118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379084-G-A

20633131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379076-G-A

20633131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379076-G-C

20633215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8379008-T-C

20633255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8378968-G-A

http://identifiers.org/hco/2/GRCh38#20633257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8378966-C-A

20633257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8378966-C-T

http://identifiers.org/hco/2/GRCh38#20633394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8378848-A-C

20633445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8378790-A-T

20634230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8378470-C-T

http://identifiers.org/hco/2/GRCh38#20634633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8378145-C-A

20634671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8378104-T-C

20635018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377824-G-A

20635018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377824-G-T

20635202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377681-A-G

20635202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377681-A-T

20635289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377605-C-T

20635450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377485-T-C

20635519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377416-G-T

20635663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377307-C-T

http://identifiers.org/hco/2/GRCh38#20635836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8377142-C-A

http://identifiers.org/hco/2/GRCh38#20635853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8377125-C-A

20635853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377125-C-T

20635854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8377124-G-A

http://identifiers.org/hco/2/GRCh38#20636047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8376933-C-A

20636453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376263-G-A

http://identifiers.org/hco/2/GRCh38#20636638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8376073-C-A

20636659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376052-G-T

20636692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376024-T-C

20636706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376010-A-G

20636717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376001-G-C

20636717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8376001-G-T

20636805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375923-G-A

20637068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375710-C-T

http://identifiers.org/hco/2/GRCh38#20637074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375684-C-A

20637132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375629-G-A

20637132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375629-G-T

http://identifiers.org/hco/2/GRCh38#20637133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375628-C-A

20637133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375628-C-T

20637231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375534-G-A

20637231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375534-G-C

http://identifiers.org/hco/2/GRCh38#20637281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375484-C-A

20637284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375481-C-T

20637331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375455-G-T

20637332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375454-G-A

20637332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375454-G-T

http://identifiers.org/hco/2/GRCh38#20637333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375453-C-A

20637345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375441-G-A

20637345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375441-G-T

http://identifiers.org/hco/2/GRCh38#20637375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375410-A-C

20637375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375410-A-G

20637377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375408-T-A

20637377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375408-T-C

http://identifiers.org/hco/2/GRCh38#20637441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375357-C-A

20637441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375357-C-T

20637456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375347-G-A

20637456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375347-G-C

20637456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375347-G-T

20637512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375320-G-A

http://identifiers.org/hco/2/GRCh38#20637626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375225-C-A

20637626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375225-C-G

20637626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375225-C-T

20637629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375222-T-C

http://identifiers.org/hco/2/GRCh38#20637693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375158-C-A

http://identifiers.org/hco/2/GRCh38#20637701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8375150-C-A

20637851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375011-G-T

20637852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8375010-A-G

http://identifiers.org/hco/2/GRCh38#20637902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8374958-C-A

20637930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374930-A-G

20637967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374899-A-G

20638040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374396-A-G

20638102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374337-T-C

http://identifiers.org/hco/2/GRCh38#20638107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8374333-C-A

20638135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374304-G-A

20638135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374304-G-T

http://identifiers.org/hco/2/GRCh38#20638140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8374299-A-C

20638140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374299-A-G

20638216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374236-G-T

20638242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374210-A-G

20638242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374210-A-T

20638261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374193-G-A

20638261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374193-G-T

20638300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374152-G-A

20638300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374152-G-C

20638300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8374152-G-T

20638569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8373951-C-G

http://identifiers.org/hco/2/GRCh38#20638628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8373892-C-A

20638677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373845-G-C

20638704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373824-G-A

http://identifiers.org/hco/2/GRCh38#20638730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8373795-C-A

20638730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373795-C-T

http://identifiers.org/hco/2/GRCh38#20638777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8373748-C-A

20638777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373748-C-G

20638777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373748-C-T

http://identifiers.org/hco/2/GRCh38#20638779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8373746-A-C

20638779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373746-A-G

20638961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373128-C-T

20638967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373122-G-A

20639021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373077-G-A

20639023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8373075-G-A

20639156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8372932-T-G

20640091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372465-T-C

20640114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372443-T-G

20640141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372416-T-G

20640152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372403-G-A

20640152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372403-G-T

http://identifiers.org/hco/2/GRCh38#20640155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8372400-A-C

20640166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372386-G-A

20640166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372386-G-T

20640210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372343-T-C

http://identifiers.org/hco/2/GRCh38#20640211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8372342-C-A

20640211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372342-C-G

20640211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372342-C-T

20640235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372314-G-A

http://identifiers.org/hco/2/GRCh38#20640285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8372277-C-A

20640285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372277-C-T

http://identifiers.org/hco/2/GRCh38#20640323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8372242-C-A

20640323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372242-C-T

20640337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372228-G-A

20640337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372228-G-T

http://identifiers.org/hco/2/GRCh38#20640346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8372219-C-A

20640346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372219-C-T

20640366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372201-G-T

20640400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372170-G-A

20640400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372170-G-C

20640405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372165-G-A

20640406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372164-A-G

20640406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372164-A-T

20640410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372160-G-A

20640410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372160-G-C

20640430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372131-G-A

20640430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372131-G-T

20640522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372068-G-T

20640547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372045-G-A

20640547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8372045-G-T

20640802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8371890-C-T

20640918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8371778-G-A

20640918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8371778-G-T

20640945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8371752-G-A

http://identifiers.org/hco/2/GRCh38#20641077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8371620-C-A

20641134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8371563-C-T

20641218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371479-G-T

20641300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371423-C-T

http://identifiers.org/hco/2/GRCh38#20641309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8371414-C-A

20641309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371414-C-T

20641421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371332-G-A

20641459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371300-G-C

20641656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371157-A-G

http://identifiers.org/hco/2/GRCh38#20641696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8371136-C-A

20641743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371089-G-A

20641781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8371051-G-A

20641977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370857-A-G

20642062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370790-C-T

20642400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8370450-G-A

20642609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8370234-C-T

20642663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370200-C-T

20642679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370192-C-G

20642767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370110-A-G

20642892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8370005-C-T

20642945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369896-C-T

http://identifiers.org/hco/2/GRCh38#20642950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8369891-C-A

20642950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369891-C-T

20643347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369433-G-C

20643447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369381-A-G

20643518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369311-T-G

20643526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8369303-G-T

http://identifiers.org/hco/2/GRCh38#20644071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8369162-C-A

http://identifiers.org/hco/2/GRCh38#20644288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8368957-C-A

20644527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368753-G-A

20644581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368735-T-C

20644685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368631-A-G

20644805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368540-C-G

20644961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368387-T-A

20644961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368387-T-G

20644977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368340-C-T

20645235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8368025-A-G

20645319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8367969-T-C

http://identifiers.org/hco/2/GRCh38#20645358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8367930-C-A

20645386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8367902-G-A

http://identifiers.org/hco/2/GRCh38#20645404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8367884-A-C

20645543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8367746-A-G

20645634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8367666-G-T

20648837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8365365-C-T

20649140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8365123-T-G

http://identifiers.org/hco/2/GRCh38#20649238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8365075-A-C

20649389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364937-T-C

20649584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364759-G-A

20649885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364481-C-T

20649980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364391-A-G

20650108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364267-T-C

20650111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364264-G-A

20650261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364146-G-C

20650347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8364054-G-C

20650459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363976-T-C

20650524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363930-C-T

20650601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363851-C-T

20650816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363645-C-T

http://identifiers.org/hco/2/GRCh38#20650885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8363564-A-C

20650885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363564-A-G

20650885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363564-A-T

20650916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363539-G-A

20650916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363539-G-C

20650916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363539-G-T

20650921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363532-G-A

20650921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8363532-G-T

http://identifiers.org/hco/2/GRCh38#20650927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8363526-C-A

20650927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8363526-C-G

http://identifiers.org/hco/2/GRCh38#20650933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8363520-C-A

20650933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24979
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8363520-C-T