94021432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15023338-G-A

http://identifiers.org/hco/11/GRCh38#94021556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15023214-C-A

94021672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15023105-G-A

94021672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15023105-G-T

http://identifiers.org/hco/11/GRCh38#94021673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15023104-C-A

94021673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15023104-C-T

94021765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15023013-G-A

94021765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15023013-G-C

94021816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022968-C-T

94021919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022881-T-C

94021971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022833-T-C

94021981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022825-T-C

94022065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022738-C-T

94022383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022447-C-T

94022600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022236-G-T

94022763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15022054-T-C

http://identifiers.org/hco/11/GRCh38#94022944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15021913-C-A

94023124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021790-G-T

94023402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021488-T-C

94023505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021387-C-G

94023652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021241-C-T

94023732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021167-C-T

94023922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15021034-G-A

94024186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15020746-G-C

94024235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15020699-A-T

94024318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15020641-A-T

94024835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15020036-C-G

94024878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019993-G-A

94025041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019826-A-T

94025621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019364-G-T

94025725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019275-A-G

94025747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019254-G-A

94025823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15019177-C-G

94026240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15018515-T-C

94026481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15018224-T-C

94026608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15018125-G-C

94027051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017818-G-A

94027051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017818-G-T

94027055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017814-T-A

http://identifiers.org/hco/11/GRCh38#94027725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15017375-C-A

94027810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017286-A-G

94027914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017178-A-G

94028153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15017003-A-G

94028247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016911-G-A

94028792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016403-G-T

94028823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016376-T-C

94028908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016313-A-G

94029011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016233-A-G

94029029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15016210-G-A

94029446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015667-T-C

94029452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015661-A-T

94029630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015517-A-G

94029789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015385-G-A

http://identifiers.org/hco/11/GRCh38#94030194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15015077-A-C

94030194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015077-A-G

94030235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15015035-T-C

94030358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15014924-C-G

http://identifiers.org/hco/11/GRCh38#94031171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15014685-C-A

94031171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15014685-C-T

http://identifiers.org/hco/11/GRCh38#94031787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15014197-C-A

94031831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15014139-A-G

94031915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15014027-T-A

94033638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15013072-T-A

94033638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15013072-T-C

94033843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15012839-A-G

http://identifiers.org/hco/11/GRCh38#94033846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15012836-C-A

94034337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15011940-C-T

94044466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15011671-C-G

94044632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15011513-C-T

94045578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009512-A-G

94045581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009509-T-A

94045581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009509-T-C

94045581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009509-T-G

94045584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009506-T-C

94045613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009481-G-A

94045613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009481-G-T

94045625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009469-G-A

94045911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15009183-T-A

94045957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009138-T-C

94046009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009086-T-C

http://identifiers.org/hco/11/GRCh38#94046011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15009084-C-A

94046011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009084-C-T

94046018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009077-A-G

http://identifiers.org/hco/11/GRCh38#94046040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15009054-C-A

94046040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009054-C-G

http://identifiers.org/hco/11/GRCh38#94046063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15009031-C-A

94046063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009031-C-T

94046085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15009018-T-G

94046175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15008965-A-G

94058277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005722-G-A

94058458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005468-G-T

94058548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005366-G-A

94059777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005263-T-C

94059806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005233-C-T

94059892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005166-T-C

94059929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15005129-A-G

94060119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004952-T-C

94060119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004952-T-G

http://identifiers.org/hco/11/GRCh38#94060153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15004945-C-A

94060153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004945-C-T

http://identifiers.org/hco/11/GRCh38#94060156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15004942-A-C

94060156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004942-A-G

94060156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004942-A-T

94060215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004893-T-C

94060533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004680-C-T

94060611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004614-G-A

94060617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004608-A-T

94061129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004192-G-C

94061227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15004110-A-T

94061586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003807-T-C

94061628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003766-A-G

94061648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003746-C-T

94061714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003694-C-G

94061936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003533-G-A

94061936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003533-G-C

94061997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003474-T-C

94062218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003246-C-G

94062291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003186-G-A

94062373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003056-A-G

94062398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003035-C-G

94062398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003035-C-T

94062405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15003028-A-G

94062622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002836-C-T

94062660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002803-A-G

94062660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002803-A-T

94062664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002799-G-T

94062766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002668-G-A

94062777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002656-C-G

94062890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002540-C-T

http://identifiers.org/hco/11/GRCh38#94062944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15002461-C-A

94062944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002461-C-T

94062972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002434-T-A

http://identifiers.org/hco/11/GRCh38#94063012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15002393-C-A

94063012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002393-C-T

http://identifiers.org/hco/11/GRCh38#94063032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15002373-C-A

94063054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002351-C-T

94063066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002339-A-G

94063248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002191-G-T

94063361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002089-A-T

http://identifiers.org/hco/11/GRCh38#94063385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15002064-C-A

94063386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15002063-A-G

94063454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001996-A-G

94063483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001951-T-C

94064204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001617-A-G

94064235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001598-T-C

94064263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001575-T-G

94064288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001550-T-G

94064363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15001464-G-T

94064420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15001407-T-C

94064462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15001365-T-C

94064545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001289-G-A

94064588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001248-G-C

94064588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001248-G-T

94064625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001213-G-T

94064629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001209-T-A

94064724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15001118-T-C

94067573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 15000366-G-A

94067843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15000083-G-A

94067843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15000083-G-C

94067843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 15000083-G-T

http://identifiers.org/hco/11/GRCh38#94067983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14999973-C-A

94068201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999838-C-T

94068281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999759-G-A

http://identifiers.org/hco/11/GRCh38#94068320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14999720-C-A

94068320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999720-C-T

94068490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999555-C-T

94068497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999548-T-C

94068829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999252-A-G

http://identifiers.org/hco/11/GRCh38#94068867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14999210-A-C

94068867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999210-A-G

94068868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999209-A-G

http://identifiers.org/hco/11/GRCh38#94068916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14999165-C-A

94068934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14999147-G-C

94069081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14998795-A-T

94069087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14998789-A-G

94069150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14998705-T-C

94069172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14998680-C-T

94070347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14997628-A-G

94070432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: synonymous variant
orthologous variants: 14997544-G-A

94070432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14997544-G-C

94070451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14997525-C-T

94070581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14997397-G-C

94070581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14997397-G-T

94070641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14997358-A-G

94072638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14996269-G-C

94072850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14996053-T-C

94072966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995945-T-C

94073013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995903-A-G

94073186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995734-T-A

94073186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995734-T-C

94073190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995730-T-C

http://identifiers.org/hco/11/GRCh38#94073227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14995711-C-A

http://identifiers.org/hco/11/GRCh38#94073231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14995707-A-C

94073336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: synonymous variant
orthologous variants: 14995627-T-C

94073394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14995569-G-A

94073394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14995569-G-T

http://identifiers.org/hco/11/GRCh38#94073443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14995520-A-C

94073466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14995498-G-A

94073537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994818-T-A

94073537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994818-T-C

94073538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994817-G-A

94073538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994817-G-T

http://identifiers.org/hco/11/GRCh38#94073582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14994780-C-A

94073582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994780-C-T

94073647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994713-T-G

94073867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994512-G-A

94073976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994412-A-G

94073987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994401-A-T

94074063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994342-G-A

94074070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994335-T-A

94074070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994335-T-C

94074135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14994270-G-T

http://identifiers.org/hco/11/GRCh38#94074255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14994169-C-A

94075041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993451-A-G

http://identifiers.org/hco/11/GRCh38#94075095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14993401-C-A

94075127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993371-A-G

94075236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14993267-C-T

http://identifiers.org/hco/11/GRCh38#94075266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14993237-C-A

94075266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14993237-C-T

94075462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993054-A-G

94075463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993053-A-T

94075484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993038-T-G

94075515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14993015-A-G

94075611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14992967-G-T

94075647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14992929-T-A

94075660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14992916-G-A

94082322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991593-G-A

94082322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991593-G-T

http://identifiers.org/hco/11/GRCh38#94082380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14991559-C-A

94082380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991559-C-T

94082463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14991476-G-A

94082496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: stop gained
orthologous variants: 14991443-C-T

94082638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991338-G-A

94082638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991338-G-T

94082667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991309-G-C

94082691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991284-G-T

94083042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991063-C-T

94083046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14991059-C-T

94083377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14990837-G-C

94083842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14990359-A-G

94085717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988530-A-T

94085891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988372-G-A

94085891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988372-G-T

94085895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988368-T-A

94085925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988340-C-T

94086162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14988055-A-T

http://identifiers.org/hco/11/GRCh38#94086205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14988012-C-A

94086205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14988012-C-T

http://identifiers.org/hco/11/GRCh38#94086243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14987982-C-A

94086243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987982-C-T

94086269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987956-T-C

94086273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987952-T-A

94086273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987952-T-C

94086274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987951-A-G

http://identifiers.org/hco/11/GRCh38#94086284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14987942-C-A

94086284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987942-C-T

94086287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987939-T-C

http://identifiers.org/hco/11/GRCh38#94086289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14987937-C-A

94086289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987937-C-T

94086297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987929-G-A

94086309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987917-A-G

94086309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987917-A-T

94086355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987872-C-G

94086355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987872-C-T

94086642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987379-G-A

94086869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987154-G-A

94086885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987138-C-T

94086897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14987128-T-G

94087056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14986767-T-C

94087703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14986622-G-A

94087854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14986458-C-T

94087991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14986338-A-G

94087999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14986330-T-C

94088413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14985986-G-C

94088781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14985549-A-G

94088783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14985547-G-A

94088783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14985547-G-T

http://identifiers.org/hco/11/GRCh38#94088818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14985512-A-C

94089242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14985064-A-T

94089248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14985052-G-A

94089319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14984971-G-T

94089358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14984932-G-A

94089664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14984638-A-G

94089722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14984585-T-G

94089767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14984539-G-A

94090844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14983492-T-A

http://identifiers.org/hco/11/GRCh38#94090850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14983486-C-A

94090850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14983486-C-G

94091643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14982868-A-G

94091729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14982820-T-C

94092357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14982140-T-A

94092376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14982032-T-C

94092735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981784-T-C

94092910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981672-A-G

94092999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981593-A-G

94093024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981548-G-A

94093035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981537-T-C

94093038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981534-C-T

94093249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981364-T-A

94093330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981284-T-A

94093330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981284-T-C

94093354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981263-A-G

http://identifiers.org/hco/11/GRCh38#94093384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14981234-A-C

94093384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981234-A-G

94093401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981222-T-A

94093401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981222-T-C

94093401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981222-T-G

94093466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14981172-T-C

94093571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14981067-G-A

http://identifiers.org/hco/11/GRCh38#94093648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14980992-A-C

94093682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14980964-T-C

94093682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14980964-T-G

94093683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14980963-G-A

94101255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14978411-G-A

94101298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14978368-T-G

94101356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14978311-G-C

94101356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14978311-G-T

94101436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14978240-G-T

94102579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973781-T-A

94102654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973682-T-C

94102670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973670-C-T

94102709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973632-G-A

94102709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973632-G-C

94102844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973509-A-G

94102844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973509-A-T

94102884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973476-A-G

94102919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14973451-G-C

94102919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14973451-G-T

http://identifiers.org/hco/11/GRCh38#94102943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14973427-C-A

94102943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14973427-C-G

94102943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14973427-C-T

94102961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14973409-G-C

http://identifiers.org/hco/11/GRCh38#94102985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14973385-C-A

94103079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973305-G-T

94103095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973289-G-A

94103095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973289-G-T

94103133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973253-G-T

94103164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973223-T-A

94103178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973214-G-A

http://identifiers.org/hco/11/GRCh38#94103252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14973132-A-C

94103259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14973125-G-T

94103712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972566-G-A

94103874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972438-A-T

94104477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972302-A-G

94104477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972302-A-T

http://identifiers.org/hco/11/GRCh38#94104493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14972292-A-C

94104493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972292-A-G

94104495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14972290-G-C

94104585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14972200-G-A

94104703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14972082-G-A

http://identifiers.org/hco/11/GRCh38#94104850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14971951-C-A

94104851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971950-T-A

94104851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971950-T-C

94104964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971865-G-A

94104966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971863-G-A

94104966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971863-G-C

94105153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971679-A-T

94105201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971618-T-A

94105275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971556-C-T

94105327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971509-C-T

94105329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971507-C-G

94105415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971436-C-G

94105629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14971087-T-C

94105795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970780-C-T

http://identifiers.org/hco/11/GRCh38#94105856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14970719-C-A

94105864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970711-G-T

94105892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970685-A-G

94105892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970685-A-T

94105955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970629-A-G

94105958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970626-A-G

94106023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14970556-G-A

94106187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970400-A-T

94106236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970356-G-A

94106236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970356-G-C

94106776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14970058-T-C

http://identifiers.org/hco/11/GRCh38#94106856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14969976-C-A

94107024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969858-A-G

94107085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969813-C-T

94107161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969741-T-C

94107333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969634-C-G

94107333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969634-C-T

94107567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14969409-C-T

94110158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14966552-G-T

94110559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14966116-T-C

http://identifiers.org/hco/11/GRCh38#94110615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14966062-A-C

94110615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14966062-A-G

94110896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 14965914-T-A

94111104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965709-A-G

94111163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965650-A-T

94111190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965623-A-G

94111191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965622-T-A

94111191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965622-T-C

94111207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965606-T-C

94111408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965419-G-T

94111427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965402-T-A

http://identifiers.org/hco/11/GRCh38#94111451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14965378-C-A

94111473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965359-T-G

94111474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965354-A-G

94111618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965191-T-G

94111645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: intron variant
orthologous variants: 14965164-C-T

94111748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: missense variant
orthologous variants: 14965058-G-A

http://identifiers.org/hco/11/GRCh38#94111911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964893-C-A

94111920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964884-A-G

94111922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964882-G-C

94111922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964882-G-T

94111962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964844-A-G

http://identifiers.org/hco/11/GRCh38#94111969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964837-C-A

http://identifiers.org/hco/11/GRCh38#94112106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964699-C-A

94112106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964699-C-T

http://identifiers.org/hco/11/GRCh38#94112112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964692-A-C

94112112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964692-A-G

http://identifiers.org/hco/11/GRCh38#94112168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964642-C-A

94112168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964642-C-T

94112239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964582-A-G

94112287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964537-G-A

94112287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964537-G-C

94112289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964535-G-A

94112289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964535-G-T

http://identifiers.org/hco/11/GRCh38#94112400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964419-C-A

94112431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964387-A-T

94112467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964353-T-A

94112519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964302-T-C

http://identifiers.org/hco/11/GRCh38#94112717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14964111-C-A

94112717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14964111-C-T

94113299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14963607-A-G

94113305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: 14963601-G-C

http://identifiers.org/hco/11/GRCh38#94113561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30477
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14963339-C-A