125186460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5 prime UTR variant
orthologous variants: 125609505-G-C

125186830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense variant
orthologous variants: 125609718-G-A

125186830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense variant
orthologous variants: 125609718-G-T

http://identifiers.org/hco/12/GRCh38#125186873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125609761-C-A

125186873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 125609761-C-T

http://identifiers.org/hco/12/GRCh38#125187384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125610133-C-A

125187505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125610270-G-A

125188517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611257-A-G

125188552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611274-C-T

125188786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611457-C-G

125188886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611524-T-A

http://identifiers.org/hco/12/GRCh38#125189293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125611896-C-A

125189293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611896-C-T

125189330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125611938-A-G

125189413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125612024-C-T

125189883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125612478-T-C

125190368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125613185-T-C

125190378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125613195-G-A

125193651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125615960-T-C

125194096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125616337-C-T

http://identifiers.org/hco/12/GRCh38#125202932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125621400-C-A

125203053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125621537-A-T

125203180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125621657-C-T

125203201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125621676-C-T

http://identifiers.org/hco/12/GRCh38#125203664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125622638-C-A

125206574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125623331-T-C

http://identifiers.org/hco/12/GRCh38#125206653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125623421-C-A

125206653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125623421-C-G

125206653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125623421-C-T

125207201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125623902-C-G

125207201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125623902-C-T

125208748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625140-C-T

125208777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625167-C-T

125208935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625277-G-A

125209400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625615-A-G

125209520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625749-C-T

125209673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625889-G-A

125209673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125625889-G-C

125217075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125626403-T-C

125222601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125628670-T-G

http://identifiers.org/hco/12/GRCh38#125222655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125628724-A-C

125222655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125628724-A-G

125222923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125628932-C-T

125223062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629055-A-G

125223242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629244-A-G

125223250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629252-A-G

http://identifiers.org/hco/12/GRCh38#125223258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125629260-A-C

125223258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629260-A-T

125223306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629309-G-A

125223330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629333-G-C

125223369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125629373-T-C

125230390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125631309-G-A

125230456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125631373-C-T

125234965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125633668-C-G

125234965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125633668-C-T

125236850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635053-G-A

125236850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635053-G-C

125237257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, undefined
orthologous variants: 125635296-G-A

125237257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, undefined
orthologous variants: 125635296-G-C

125237258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, undefined
orthologous variants: 125635297-C-T

125237311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, undefined
orthologous variants: 125635350-C-T

125237884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635726-G-A

125237894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635736-A-G

125237987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635830-T-C

125238108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125635913-T-G

125238285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125636034-G-A

125238498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125636116-G-A

125238508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125636126-G-A

125239240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125636927-A-G

125239314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125637003-T-G

125239531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125637193-C-T

125245753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125639380-T-C

125246002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125639606-A-T

125246559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640465-G-A

125246608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640515-G-C

125246689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640595-C-T

125246730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640644-G-A

125246742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640661-C-T

125246879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640798-C-G

125246912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640821-G-A

125246926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640835-G-A

125246926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640835-G-C

125247035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125640943-C-T

125248000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125642360-G-T

125248207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125642550-C-G

125248278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125642614-A-G

125248278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125642614-A-T

125248824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125643114-G-C

125248896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125643188-T-C

125249249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125643660-C-T

125249368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125643774-C-T

125249685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125644008-G-C

http://identifiers.org/hco/12/GRCh38#125253905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125645244-C-A

125253938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645277-G-A

http://identifiers.org/hco/12/GRCh38#125254368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125645407-C-A

125254420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645459-C-G

125254420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645459-C-T

125255075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645726-C-T

125255248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645876-T-A

125255299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125645921-C-T

125255528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646141-C-T

125255574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646187-T-C

125255601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646218-T-C

125255668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646277-C-T

125255862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646476-C-T

125255898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646514-G-A

125255898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646514-G-T

125255944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125646559-T-C

http://identifiers.org/hco/12/GRCh38#125258261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125648178-C-A

125258431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648327-A-G

125258593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648472-C-T

125258630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648514-C-T

125258651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648653-G-T

125258733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648943-G-A

125258733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125648943-G-T

125259309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125649561-G-A

125259325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125649577-G-A

125259405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125649647-G-T

125259543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125649781-G-A

125259789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125650025-G-A

125259789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125650025-G-T

125259873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125650083-C-T

125259922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125650132-G-A

125262384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125651596-G-T

125262424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125651636-G-T

125262454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125651667-A-G

125262575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125651778-C-T

http://identifiers.org/hco/12/GRCh38#125262787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125651942-C-A

125262831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125651977-T-A

125263073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125652207-C-G

125263073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125652207-C-T

125266621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125652502-G-C

125266629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125652510-T-G

125268843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125653672-G-A

125268843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125653672-G-T

125268857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125653686-C-T

125268968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125653810-G-A

125269199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125654021-T-G

125269284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125654118-C-T

125269530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125654375-G-A

125272636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125661059-G-C

125273091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125661505-A-G

125273116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125661531-T-C

125276175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125663734-C-T

125276446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125663958-C-T

125276742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125664200-C-T

125276760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125664218-C-T

125280788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125666227-C-T

125283177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667360-G-A

125283192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667375-A-G

http://identifiers.org/hco/12/GRCh38#125283369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125667517-A-C

125283461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667606-G-A

125283515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667659-A-G

125283564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667707-A-G

125283610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125667753-A-G

125283983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125668048-C-T

125284016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125668100-C-T

125284030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125668119-C-T

125284109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125668182-A-G

125284162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125668237-T-G

http://identifiers.org/hco/12/GRCh38#125287555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125669918-C-A

125287645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125669987-A-G

125287653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125669994-C-G

125289635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125670993-G-T

125289692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125671055-A-G

125290036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671339-C-T

125290122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671409-G-A

125290167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671455-T-A

125290167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671455-T-C

125290288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671563-A-T

125290328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125671603-A-G

125290407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125671690-T-C

125290463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125671747-T-G

125292237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125675435-A-G

125292347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125675543-G-A

125292566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125676561-C-T

125292682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125676683-C-G

125292777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125676781-C-T

125292896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125676873-A-T

125293048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125677019-C-T

125305343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125678880-G-A

125305392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125678919-G-A

125305415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125678931-G-A

125305597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125679112-T-C

125305637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125679159-G-A

125310707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125679691-G-A

125310944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125679901-G-A

125311021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125681078-A-G

125311110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125681162-G-A

125311114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125681166-G-A

125311989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682290-C-T

125312027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682329-G-A

125312163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682432-G-T

125312307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682551-T-G

125312479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682734-C-T

125312536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682796-G-A

125312544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682804-G-A

125312544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682804-G-T

125312547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682807-C-G

125312609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682860-C-G

125312609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682860-C-T

125312648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125682903-G-A

125314238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125683979-G-A

125314238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125683979-G-T

125314261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684002-C-G

125314261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684002-C-T

125314278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684018-G-C

125314389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684125-C-T

125314550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684292-G-T

125314596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684339-C-T

125314597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684340-G-A

125314597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684340-G-C

125314629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684362-G-A

125314760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125684492-T-C

125319660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686131-C-T

125320187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686317-G-A

125320202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686332-C-T

125320284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686392-C-G

125320284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686392-C-T

125320578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686679-T-G

125320579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125686680-G-T

125325096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125689530-C-T

125325102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125689536-G-A

125325194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125689620-T-C

125325227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125689650-A-G

http://identifiers.org/hco/12/GRCh38#125325274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125689693-A-C

125325365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125689771-G-A

125326317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690265-A-G

125326422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690371-T-A

125326422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690371-T-C

125326422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690371-T-G

http://identifiers.org/hco/12/GRCh38#125326432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125690381-C-A

125326432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690381-C-G

125326432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690381-C-T

http://identifiers.org/hco/12/GRCh38#125326485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125690430-A-C

125326485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690430-A-G

125326485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690430-A-T

125326506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690450-G-A

125326506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690450-G-C

125326506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690450-G-T

125326524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690468-T-G

http://identifiers.org/hco/12/GRCh38#125326525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125690469-A-C

125326525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125690469-A-T

125326563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125690511-G-C

125326664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125690613-G-A

125326664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125690613-G-T

125326665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125690614-C-T

125329697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125690659-G-A

125329743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125690704-G-C

125329747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125690708-C-T

125331065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125691583-C-G

125331081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125691599-C-T

125331217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125691685-C-G

125331217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125691685-C-T

125331284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125691744-C-T

125331316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125691777-G-T

125331318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125691779-C-T

125331516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125691962-G-A

125332897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125693222-T-C

125332993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125693327-C-G

125332993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125693327-C-T

125336706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125694599-T-G

125336716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125694609-T-A

125336963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125694824-G-T

125338801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125696324-A-G

125339294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125696803-G-C

125345566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697106-C-T

125345591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697131-A-T

125345865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697351-C-T

125345866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697352-G-A

125345880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697364-A-G

125345957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697456-A-G

125345977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697474-G-A

125346018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697514-G-T

http://identifiers.org/hco/12/GRCh38#125346075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125697571-C-A

http://identifiers.org/hco/12/GRCh38#125346082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125697578-A-C

125346082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697578-A-T

125346134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697630-G-T

125346258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697752-T-C

125346298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125697789-T-C

125346647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125698127-C-T

125347909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125698402-T-A

125347942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125698433-A-T

http://identifiers.org/hco/12/GRCh38#125349255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125699337-C-A

http://identifiers.org/hco/12/GRCh38#125349350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125699419-C-A

125349350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125699419-C-T

125349624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125699697-C-G

125349870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125699943-C-T

125349936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700009-C-G

125349936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700009-C-T

125349942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700015-G-A

125350080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700153-T-C

125350163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125700236-C-T

125350182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700255-T-C

125350200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700273-C-G

125350200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700273-C-T

125350320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125700393-T-C

125350339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125700412-C-G

125350339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125700412-C-T

http://identifiers.org/hco/12/GRCh38#125350409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125700479-A-C

125350451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125700528-G-C

125350451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125700528-G-T

http://identifiers.org/hco/12/GRCh38#125350464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125700544-C-A

125350482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125700562-A-G

125350482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125700562-A-T

125350545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125700623-T-C

125375099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125703254-C-T

125375432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125704544-C-G

125375433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125704545-T-A

125375726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125704816-G-A

125375908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125704976-C-G

125391409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707701-T-G

125391410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707702-G-A

125391424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707712-C-G

125391607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707889-A-T

125391619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707901-T-A

125391712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707992-A-G

125391714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125707994-A-G

125394571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125708329-G-A

http://identifiers.org/hco/12/GRCh38#125395736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125709357-A-C

125395736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125709357-A-G

125395761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125709383-A-G

125400344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125711556-C-T

http://identifiers.org/hco/12/GRCh38#125400582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125711765-C-A

125400613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125711803-G-A

125400647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125711846-G-A

125403596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125712376-G-A

125403692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125712470-T-C

125404472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713048-G-A

125404506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713079-C-T

125413000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713665-G-A

125413153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713794-G-A

125413153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713794-G-T

125413265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125713853-T-A

http://identifiers.org/hco/12/GRCh38#125415560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125715275-C-A

125415560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125715275-C-T

125415618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125715333-C-T

125415648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125715363-C-T

125415912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125715620-C-T

http://identifiers.org/hco/12/GRCh38#125416649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125716538-C-A

125416777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125716632-T-C

125417163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125716932-G-T

125417182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125716951-T-C

125417277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717025-A-G

125417396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717136-G-A

125417808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717731-G-T

125417823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717746-C-T

125417826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717749-T-C

125417828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717751-C-T

http://identifiers.org/hco/12/GRCh38#125418021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125717966-C-A

125418021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125717966-C-G

125418217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718392-C-T

125418265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718434-A-T

125418406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718542-C-T

125418409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718545-T-C

125418412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718548-G-C

http://identifiers.org/hco/12/GRCh38#125418448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125718578-C-A

125418571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718729-C-T

125418845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125718996-C-T

125418926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125719073-A-G

125431806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125722919-A-T

125431874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125722961-C-T

125432082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125723108-G-A

125432115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125723135-T-A

125432383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125723336-A-G

125432409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125723362-G-A

125432409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125723362-G-C

125437609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125724813-G-A

125440277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125725613-A-G

125440289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125725625-C-T

125440333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125725670-C-G

125440333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125725670-C-T

125440403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125725757-C-G

125441440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727247-A-T

125441473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727285-G-A

125441691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727394-G-C

125441761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727438-T-C

125442433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727959-C-G

125442460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125727986-G-T

125442501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125728029-G-A

125443146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125728591-G-C

125443622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730464-G-A

125443704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730544-A-G

125443744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730637-G-T

125443882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730772-G-A

125443915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730804-C-T

http://identifiers.org/hco/12/GRCh38#125443927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125730816-A-C

125443949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730837-T-C

125443976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730864-A-G

125444028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125730913-T-C

http://identifiers.org/hco/12/GRCh38#125453751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125735078-C-A

125454407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125735683-T-A

125460625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125739428-G-A

http://identifiers.org/hco/12/GRCh38#125461287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125740081-A-C

125463419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125740664-C-T

125463758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125740973-T-G

125464197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741024-T-A

125464390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741171-T-C

125464745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741456-C-T

125464979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741663-G-A

125465046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741693-A-G

125465065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125741714-A-G

125466366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125746093-C-T

125466449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125746176-T-C

125476853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747128-G-T

125477083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747348-G-A

125477122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747387-C-G

125477122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747387-C-T

125477303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747663-T-C

125477315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747675-T-A

125477402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747763-C-T

125477514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747877-T-C

125477623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747981-G-C

125477634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125747992-G-C

125485464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125750040-T-C

125485592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125750156-T-C

125485592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125750156-T-G

125485612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125750177-C-T

125486603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125751806-A-G

http://identifiers.org/hco/12/GRCh38#125486826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125751986-C-A

125486853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125752012-T-A

125486998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125752142-C-T

125487558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125752857-T-G

125487655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125752953-C-T

125487877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125753182-G-A

125487877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125753182-G-T

125487907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125753212-A-G

125489830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125755543-A-G

125492130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125758018-G-A

125492148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125758030-T-C

125492380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125758264-T-C

125496073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125759552-A-G

http://identifiers.org/hco/12/GRCh38#125496375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125759800-C-A

125496386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125759811-T-C

125496823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125760578-G-A

125496842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125760599-C-T

125496864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125760621-C-T

125497142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125760847-G-C

125502684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125762567-C-T

http://identifiers.org/hco/12/GRCh38#125502712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125762593-A-C

125502999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125762835-A-G

125503234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763062-C-T

125503488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763316-A-G

125503721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763513-G-A

125503833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763638-C-G

125503833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763638-C-T

http://identifiers.org/hco/12/GRCh38#125503997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125763937-C-A

125503997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125763937-C-T

125504202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125764141-G-T

125504385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125764309-T-C

125508532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125767986-C-G

125508765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768212-T-C

125508861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768243-C-G

125509035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768275-C-T

125509111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768299-C-G

125509198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768391-A-G

125509323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125768504-G-T

125509780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769289-G-A

125509791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769299-C-T

http://identifiers.org/hco/12/GRCh38#125509815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125769324-A-C

125509961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769459-T-C

125510039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769560-G-A

125510301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769820-T-C

125510452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769926-G-A

125510466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125769940-T-C

125510579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125770030-G-C

125511013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125770427-A-G

125511021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125770435-C-T

http://identifiers.org/hco/12/GRCh38#125511069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125770480-C-A

http://identifiers.org/hco/12/GRCh38#125511077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125770488-A-C

125511077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125770488-A-G

125513212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125770780-T-G

125513450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125771006-G-A

125513739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125771305-A-G

125514507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125772774-C-T

125514508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125772775-C-T

125514726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125772971-C-T

125514733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125772978-C-G

http://identifiers.org/hco/12/GRCh38#125514806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125773033-A-C

125514834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773062-C-T

http://identifiers.org/hco/12/GRCh38#125514868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125773079-C-A

125516040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773264-C-T

125516063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773287-A-G

125516076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773300-C-T

125516125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773346-G-A

125516130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773351-C-T

125516187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773434-G-A

125516187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773434-G-T

125516247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773479-T-A

125516294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773526-G-A

125516314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773545-C-G

125516314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773545-C-T

http://identifiers.org/hco/12/GRCh38#125516473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125773698-C-A

125516473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125773698-C-T

125518207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125774122-A-T

125518223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125774142-C-G

125518323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125774250-A-G

125518464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125774388-G-C

125518597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125774520-C-T

125518742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125774630-C-T

125518761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125774646-C-T

125518902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125774787-C-T

125518936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125774821-A-T

125519215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775393-T-C

125519215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775393-T-G

125519300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775517-A-G

125519300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775517-A-T

125519348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775536-G-T

125519359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775547-A-G

125519425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775614-T-A

125519541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125775730-G-A

125519541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125775730-G-T

125519610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125775799-C-T

125519663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125775850-G-A

125519708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125776298-A-G

125519750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125776342-T-A

125519872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125776462-T-G

125520316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125776866-A-T

http://identifiers.org/hco/12/GRCh38#125520400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125776942-A-C

125525770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780381-G-A

http://identifiers.org/hco/12/GRCh38#125525771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125780382-C-A

125525804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780407-C-T

125525851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780463-G-A

125525961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780585-A-G

125525968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780592-G-A

125525968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780592-G-T

http://identifiers.org/hco/12/GRCh38#125526016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125780644-C-A

125526016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780644-C-T

125526030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780658-G-A

125526036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780664-G-A

125526082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780711-C-T

125526150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780762-C-T

125526179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780790-C-G

125526179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780790-C-T

125526248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125780848-G-A

125526535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781048-C-G

125526545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781058-G-A

125526594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781104-G-A

125526711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781219-G-T

125526717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781225-A-G

125526866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781364-C-T

125527035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781394-C-T

125527051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781410-C-T

125527145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781430-T-A

125527145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781430-T-C

125527156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781441-A-T

125527174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781459-C-T

125527187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781472-C-T

125527225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781510-T-C

125527225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781510-T-G

http://identifiers.org/hco/12/GRCh38#125527243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125781528-C-A

125527243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781528-C-T

125527264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781549-G-A

125527264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781549-G-C

125527264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781549-G-T

http://identifiers.org/hco/12/GRCh38#125527268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125781553-A-C

125527320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781590-C-T

125527352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781622-T-G

125527411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781660-T-A

125527586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781782-G-A

125527586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781782-G-C

125527586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125781782-G-T

125528276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125782399-C-T

125528441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125782567-A-T

125528585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125782708-C-T

125531615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125783905-G-C

http://identifiers.org/hco/12/GRCh38#125531691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125783992-A-C

125531691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125783992-A-G

125531738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125784039-C-T

125531765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125784066-T-C

125532050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125784318-A-G

125532055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125784323-A-T

125532165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125784426-C-T

125533505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125786115-T-C

http://identifiers.org/hco/12/GRCh38#125533555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#125786165-C-A

125533555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125786165-C-T

125533556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125786166-G-A

125533559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125786169-A-G

125533571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125786181-T-C

125535222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125788490-T-C

125535222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125788490-T-G

http://identifiers.org/hco/12/GRCh38#125535485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125788747-A-C

125535626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125788960-T-A

http://identifiers.org/hco/12/GRCh38#125535670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125789004-C-A

125535670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125789004-C-G

125535685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125789019-C-T

125535688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125789022-G-A

http://identifiers.org/hco/12/GRCh38#125535742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125789103-C-A

125536226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125789610-T-C

125537290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125790816-A-T

125537344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125790870-A-G

http://identifiers.org/hco/12/GRCh38#125537448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125790948-C-A

125537448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125790948-C-T

http://identifiers.org/hco/12/GRCh38#125537488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125790986-C-A

125537488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125790986-C-T

125537520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125790996-T-C

125537574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791042-C-G

125537574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791042-C-T

125537663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791131-G-A

125538035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791390-T-G

125538210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791555-A-G

http://identifiers.org/hco/12/GRCh38#125538346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125791689-C-A

125538374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125791717-C-T

125538709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125792033-T-C

125538717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125792041-G-T

125539001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125792294-C-T

125539115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125792407-T-C

125549177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803115-C-G

125549235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803174-C-T

125549292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803229-C-T

125549303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803240-C-T

125549317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803254-C-T

125549704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803829-T-C

http://identifiers.org/hco/12/GRCh38#125549797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125803899-A-C

125549901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125803994-A-G

125549948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125804047-C-G

125550228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125804227-G-A

125550269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125804267-G-C

125550272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125804270-G-A

125550378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125804391-T-C

125551133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125805404-G-A

125551308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125805554-G-A

125552522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125807034-G-A

125552719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807225-A-G

125552739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807245-C-G

125552788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807290-T-C

125552839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807734-G-A

125552874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807769-G-C

125552877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807772-C-T

125552903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807802-C-T

125552943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807842-C-G

125552951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807850-T-C

125552975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807873-G-C

125553068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807948-C-T

125553113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125807997-T-C

125553223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125808119-A-G

125555968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125810350-A-T

125556142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125810522-A-G

125558710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125813525-G-C

125558761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125813573-A-G

125558763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125813575-T-G

125559511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125814185-G-A

125563848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125815959-C-T

125563957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816059-C-T

125564108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816201-A-G

125564294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816373-A-G

125564534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816606-C-T

125564535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816607-G-A

125564535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816607-G-C

125564536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125816608-T-C

125567229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125817193-C-T

125567512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125817535-C-T

125567867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125817856-T-C

125567979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125817972-G-C

125568544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125818286-C-G

125568604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125818343-G-A

125568613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125818352-C-T

125568618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125818357-C-T

125569640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820430-T-C

125569672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820457-A-G

125569734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820507-G-A

125569761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820538-C-T

125569763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820540-C-T

125569878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820657-A-G

125570010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820770-T-C

http://identifiers.org/hco/12/GRCh38#125570145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125820906-C-A

125570281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125820979-C-T

125570363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821044-G-A

125570421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821100-C-G

125570777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821454-G-A

125570958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821597-C-T

125570975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821614-C-T

125570994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125821633-G-T

125571147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125822170-T-C

125571573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125822501-C-T

125571680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125822612-C-T

http://identifiers.org/hco/12/GRCh38#125580764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125825022-C-A

125580764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125825022-C-G

125583788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125826214-C-T

125583830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125826278-G-A

125583830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125826278-G-C

125583955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125826403-G-A

125583961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125826409-G-A

125584005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826473-A-G

125584013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826481-A-G

125584013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826481-A-T

125584154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826629-C-T

125584156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826631-T-C

125584168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826643-G-A

125584227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826672-A-G

125584245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826688-T-C

125584262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826712-T-C

125584266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826716-C-T

125584279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826729-C-G

125584279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826729-C-T

125584324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826779-T-A

125584324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125826779-T-C

http://identifiers.org/hco/12/GRCh38#125584336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125826788-C-A

125584713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827182-G-T

125584729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827201-T-C

125584782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827260-T-C

125584836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827315-G-T

125584923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827378-A-G

125584935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827389-A-G

125584951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827406-T-C

125584955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827410-A-G

125585054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827680-A-G

125585096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827722-G-A

125585170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827791-A-G

125585209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827830-T-C

125585210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827831-C-T

125585239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827859-A-T

125585285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827911-G-T

125585286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827912-G-A

125585286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827912-G-T

125585287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827913-G-A

125585287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827913-G-T

125585295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827921-G-T

125585339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827964-T-C

125585341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125827966-A-G

125585494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828263-C-G

125585494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828263-C-T

http://identifiers.org/hco/12/GRCh38#125585553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125828331-C-A

125585553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828331-C-T

125585642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828416-C-G

125585657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828431-A-G

125585691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828465-A-G

125585736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828505-G-T

125585760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828528-G-A

125585760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828528-G-T

http://identifiers.org/hco/12/GRCh38#125585784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125828552-C-A

125585889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828654-T-C

125586018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828749-A-G

125586018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828749-A-T

125586054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828790-T-A

125586064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828800-A-G

125586147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125828872-C-T

125591727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125832527-G-A

125591736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125832536-G-A

125591751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125832550-G-A

125591790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125832584-C-T

125592081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125832853-C-T

125592266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125833397-C-G

125592738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125833836-A-G

125592790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125833887-C-T

125592800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125833897-T-C

125592966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125834053-C-G

125592966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125834053-C-T

125593459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125834588-A-G

125593798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125834838-A-G

125593811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125834851-A-G

125593964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125835005-G-A

125594984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836406-T-C

125595112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836518-G-A

125595112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836518-G-C

125595136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836542-G-A

125595147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836553-T-C

125595148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836554-G-A

125595167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836573-G-T

125595252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836671-T-C

125595252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836671-T-G

125595407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125836835-G-A

125595635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125837450-T-C

http://identifiers.org/hco/12/GRCh38#125595994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125837746-C-A

125596232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125837936-C-G

125596284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125837988-G-A

125596354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125838057-C-G

125596675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125838495-G-A

http://identifiers.org/hco/12/GRCh38#125596697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125838517-C-A

125596907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125838711-G-A

125597003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125838791-C-T

125597262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125839653-C-G

125597605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125839971-G-A

125597605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125839971-G-T

http://identifiers.org/hco/12/GRCh38#125597614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125839980-A-C

http://identifiers.org/hco/12/GRCh38#125597622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125839984-A-C

125597875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125840180-C-T

125598324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125840905-G-A

125598433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841023-A-G

125598486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841055-G-T

125598620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841188-A-G

125598638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841205-A-G

125598712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841253-T-G

125598750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841292-G-T

125599099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841521-T-A

125599145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841548-C-T

125599165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841563-A-G

125599175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841573-G-C

125599414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125841803-G-A

125599879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842196-A-G

125600396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842586-G-A

125600501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842658-A-G

125600560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842727-A-G

125600661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842862-A-G

125600661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842862-A-T

125604739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125842945-G-T

125604808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843012-T-C

125604812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843016-G-C

http://identifiers.org/hco/12/GRCh38#125604991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125843199-C-A

125605319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843530-A-G

125605385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843603-G-C

125605436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843663-T-A

125605455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: 125843682-A-T

http://identifiers.org/hco/12/GRCh38#125605605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125843789-A-C

http://identifiers.org/hco/12/GRCh38#125622619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125844153-C-A

125622619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125844153-C-T

125622834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125844343-G-A

125622834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125844343-G-T

125622837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125844346-C-T

125622844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125844353-C-T

125623002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125845865-A-G

125623091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125845957-T-C

125623331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125846185-A-G

125623755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125846484-G-A

125623786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125846513-C-T

125623877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125846590-A-G

125638455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851109-A-T

125638475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851129-G-A

125638573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851202-T-C

125638583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851212-A-T

125638590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851219-C-T

125638791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851366-G-A

125639024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125851599-A-G

125641796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853196-T-G

125641873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853273-C-T

125641887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853287-G-T

125641968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853356-C-T

125642000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853377-T-C

125642112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853429-T-G

125642204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853521-C-T

125642277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125853591-T-C

http://identifiers.org/hco/12/GRCh38#125643583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125855214-A-C

125643641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125855275-G-T

125643810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125855445-A-G

http://identifiers.org/hco/12/GRCh38#125644208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125855833-C-A

125644208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125855833-C-G

125644264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125855889-G-A

125644264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125855889-G-T

http://identifiers.org/hco/12/GRCh38#125644276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125855901-C-A

125644276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125855901-C-G

125644276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125855901-C-T

125644299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125855924-A-G

125644300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125855925-G-A

125644300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125855925-G-T

125644330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125855959-A-T

http://identifiers.org/hco/12/GRCh38#125644391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125856028-C-A

125644391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856028-C-T

125644492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856129-T-C

125644647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856286-C-T

125644674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856299-C-T

125644701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856328-C-G

125644701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856328-C-T

125644716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856343-A-G

125644901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856465-C-T

125645174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856866-T-A

125645174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856866-T-C

125645175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856867-G-A

http://identifiers.org/hco/12/GRCh38#125645217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125856912-C-A

125645309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125856974-T-C

125645430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857094-G-A

125645539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857185-G-A

125645745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857363-G-A

http://identifiers.org/hco/12/GRCh38#125645827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125857445-A-C

125645842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857460-C-T

125645931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857543-G-A

http://identifiers.org/hco/12/GRCh38#125645981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125857576-C-A

125645981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857576-C-T

125646041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125857630-A-G

125646500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858047-T-G

125646608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858134-C-T

125646681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858215-A-G

125646771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858282-A-G

125646995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858386-A-G

125647149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858489-T-A

125647278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858606-G-A

125647278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858606-G-T

125647279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858607-T-C

125647280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858608-C-T

125647408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125858692-A-G

125649050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125859399-A-G

125649166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125859511-A-G

http://identifiers.org/hco/12/GRCh38#125649450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125859747-C-A

125649450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125859747-C-T

125649476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125859773-C-T

125649697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860025-C-T

http://identifiers.org/hco/12/GRCh38#125649763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125860086-A-C

125649797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860120-G-A

125649805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860128-A-G

125649868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860196-G-T

125649887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860211-G-A

http://identifiers.org/hco/12/GRCh38#125650579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125860298-C-A

http://identifiers.org/hco/12/GRCh38#125650612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125860323-C-A

125650612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860323-C-T

http://identifiers.org/hco/12/GRCh38#125650635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125860344-C-A

125650704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125860415-C-T

125650828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125860539-C-T

125650857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125860568-T-A

125650906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125860617-G-A

125650906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125860617-G-T

125650928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125860639-G-A

125650928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125860639-G-T

125650935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125860646-G-A

125650981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860714-G-A

125650981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860714-G-T

125651016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860737-T-C

125651046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860777-G-A

125651046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860777-G-C

http://identifiers.org/hco/12/GRCh38#125651081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125860799-C-A

125651081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125860799-C-T

125651448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861715-T-A

125651463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861731-A-T

125651647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861903-G-A

125651714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861958-C-T

125651738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861982-G-A

125651738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125861982-G-T

125651861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125862094-T-A

125651861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125862094-T-C

125651934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125862144-G-A

125652093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125862341-G-A

125652420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125862887-G-A

125652651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863114-C-T

125652660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863123-T-G

125652669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863130-G-A

125652669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863130-G-T

http://identifiers.org/hco/12/GRCh38#125652693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125863154-A-C

125652693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863154-A-G

125652708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863169-G-A

125652708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863169-G-T

125652722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863182-T-C

125652729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863189-T-A

http://identifiers.org/hco/12/GRCh38#125652730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125863190-A-C

125652730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863190-A-G

125652746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863206-G-A

125653001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863446-C-T

125653069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863513-T-C

125653188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863642-T-G

125653189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863643-G-A

125653189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863643-G-T

125653206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863661-A-T

125653224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863679-G-A

125653245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863698-A-G

http://identifiers.org/hco/12/GRCh38#125653413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125863850-C-A

125653413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863850-C-T

125653443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863876-G-T

125653554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125863985-A-G

125653561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125863992-T-C

125653627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125864058-C-T

http://identifiers.org/hco/12/GRCh38#125653893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125864324-A-C

125653893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125864324-A-T

125653933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125864364-C-T

125654061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125864486-G-A

http://identifiers.org/hco/12/GRCh38#125654083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125864505-A-C

http://identifiers.org/hco/12/GRCh38#125654290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125864712-C-A

125654290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125864712-C-T

125654569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125864991-C-T

125654819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865244-G-A

125654819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865244-G-C

125654819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865244-G-T

125654937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865351-A-G

http://identifiers.org/hco/12/GRCh38#125654992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125865375-C-A

125654992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865375-C-T

125655029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865412-C-T

http://identifiers.org/hco/12/GRCh38#125655107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125865495-C-A

http://identifiers.org/hco/12/GRCh38#125655540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125865881-A-C

125655540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865881-A-G

125655652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125865989-A-G

125655859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866425-T-A

125655934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866491-G-T

http://identifiers.org/hco/12/GRCh38#125655961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125866513-A-C

http://identifiers.org/hco/12/GRCh38#125656053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125866585-C-A

125656053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866585-C-T

125656096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866607-A-T

125656226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866742-G-A

http://identifiers.org/hco/12/GRCh38#125656407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125866914-C-A

125656458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866965-T-C

125656467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866974-G-A

125656467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125866974-G-T

125656535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867043-G-A

125656617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867101-G-T

http://identifiers.org/hco/12/GRCh38#125656671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125867141-C-A

125656691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867162-G-A

125656691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867162-G-T

125656705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867176-T-G

125656716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867186-T-C

125656826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867276-G-A

125657107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867463-C-T

125657118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867473-T-A

125657118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867473-T-C

http://identifiers.org/hco/12/GRCh38#125657188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125867541-C-A

125657280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867631-C-T

125657316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867674-C-T

125657365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125867721-G-A

125657673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868040-G-T

http://identifiers.org/hco/12/GRCh38#125657806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125868168-C-A

125657849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868211-T-C

125657853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868215-C-T

125657854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868216-G-A

125657854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868216-G-T

125657891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868259-C-T

125657893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868261-C-T

125657895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868263-G-T

http://identifiers.org/hco/12/GRCh38#125657974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125868343-C-A

125658171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868495-A-G

http://identifiers.org/hco/12/GRCh38#125658263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125868597-C-A

125658395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868981-G-A

125658395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125868981-G-T

125658541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125869118-A-G

125658689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125869260-T-A

125658793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125869382-A-G

125659624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125870202-T-G

125659918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125870422-G-A

125659930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125870434-G-T

125660206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125870476-A-G

125661042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125871460-T-C

125661768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873447-C-G

125661768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873447-C-T

125661785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873464-G-A

125661835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873497-A-T

http://identifiers.org/hco/12/GRCh38#125661842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125873504-C-A

125661842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873504-C-T

125661915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873554-G-T

125662047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873687-G-A

125662047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873687-G-T

125662048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873688-C-T

http://identifiers.org/hco/12/GRCh38#125662050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125873690-C-A

125662122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: 125873762-A-G

http://identifiers.org/hco/12/GRCh38#125662149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125873789-C-A