93448143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 5 prime UTR variant
orthologous variants: 122413312-G-A

93448143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 5 prime UTR variant
orthologous variants: 122413312-G-C

93448230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 5 prime UTR variant
orthologous variants: 122413256-A-G

93448504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122413043-G-C

93448637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122412958-G-T

93448986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122412684-G-T

http://identifiers.org/hco/1/GRCh38#93449214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122412373-C-A

93449258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122412329-G-A

93449594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122412026-C-T

93449633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, undefined
orthologous variants: 122411989-G-T

93449634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, undefined
orthologous variants: 122411988-T-G

93449778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, undefined
orthologous variants: 122411878-T-A

http://identifiers.org/hco/1/GRCh38#93450597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122411152-C-A

93450716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122411036-T-C

93450804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410943-G-A

93450898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410490-A-G

93450902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410486-C-G

93450927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410457-T-C

93451186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410247-A-G

93451202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410233-G-T

93451206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410230-G-A

93451220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410218-A-G

93451220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410218-A-T

93451269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122410174-T-G

93451308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122409914-T-G

93453914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122409086-A-G

93454009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122408986-A-G

93454082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, undefined
orthologous variants: 122408914-A-G

93454089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, undefined
orthologous variants: 122408907-G-A

93454180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122408794-T-C

93456017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122407494-C-T

93456080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122407429-A-G

93456151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122407355-G-A

93456324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122407177-G-A

http://identifiers.org/hco/1/GRCh38#93473685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122400790-A-C

93477242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122399622-G-A

93477245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122399619-G-A

93477249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122399615-A-G

93477999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398702-A-G

93478154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398587-C-G

93478184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398559-A-G

93478190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398553-G-C

93478229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398513-T-C

93478550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398229-G-A

93478667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122398133-T-C

93483530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393908-A-G

93483602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393837-A-G

93483602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393837-A-T

93483663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393779-A-T

http://identifiers.org/hco/1/GRCh38#93483768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122393674-A-C

93483921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393547-C-G

93484457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393312-T-G

93484460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393309-G-T

93484491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393278-T-C

93484701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122393063-G-C

http://identifiers.org/hco/1/GRCh38#93485413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122392379-C-A

93485483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122392317-A-G

93488059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391707-G-T

93488456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391284-G-T

93488512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391228-G-A

93488516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391224-A-G

93488518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391222-G-A

93488640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391106-A-G

93488650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391095-C-T

93488738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122391024-A-G

93488932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122390267-T-C

93489077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122390115-A-G

93489199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122389969-C-T

93489486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122389736-T-A

93489490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122389732-A-G

93489490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122389732-A-T

93489507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122389715-C-T

93490179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122388843-T-G

93490209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122388813-G-A

93490443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122388615-G-T

93490513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122388575-C-G

http://identifiers.org/hco/1/GRCh38#93492300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122387317-A-C

93492315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122387307-A-G

http://identifiers.org/hco/1/GRCh38#93499351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122384009-C-A

93499525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122383833-T-C

93499679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383680-T-C

93499691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383668-A-G

93499725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383645-G-C

93500024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383294-A-T

93500233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383102-C-T

93500250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383084-A-G

93500271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122383063-A-G

93500367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122382994-C-T

93500395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122382968-T-C

93501717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122381852-C-T

93501771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122381811-C-T

http://identifiers.org/hco/1/GRCh38#93501991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122381620-A-C

93502264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122381356-T-C

93502317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122381307-T-G

93502632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122381007-C-T

93502692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122380947-A-G

93502768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122380886-T-G

93502852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122380835-G-A

93502865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122380822-T-C

93502898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122380772-T-G

93503784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122379415-T-C

93503998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122379204-G-T

93504210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122379021-A-T

93504259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122378992-G-A

93504270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122378981-A-G

93518508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122368130-G-T

93518553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122368086-T-G

http://identifiers.org/hco/1/GRCh38#93518558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122368081-A-C

93518579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122368060-G-A

93519201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122367059-T-C

93520004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122366209-A-G

93520111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122366064-G-A

http://identifiers.org/hco/1/GRCh38#93520112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122366063-C-A

93520114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122366061-G-A

93520246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122365931-A-G

93520416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122365831-T-C

93521145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122365236-A-G

93521150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122365231-C-T

93521152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122365229-T-C

http://identifiers.org/hco/1/GRCh38#93521242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122365140-A-C

93521966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364709-T-C

93522173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364502-A-G

93522173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364502-A-T

93522384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364276-T-C

93522570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364160-T-A

93522570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364160-T-C

93522597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364140-A-G

93522652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122364091-A-G

http://identifiers.org/hco/1/GRCh38#93523138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122363594-A-C

93523204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363528-A-G

93523204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363528-A-T

93523237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363496-A-G

93523237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363496-A-T

93523244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363489-A-G

93523244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363489-A-T

93523320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363413-A-G

93523501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363232-A-G

http://identifiers.org/hco/1/GRCh38#93523519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122363214-C-A

93523519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363214-C-T

http://identifiers.org/hco/1/GRCh38#93523579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122363151-A-C

93523579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363151-A-G

93523641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122363046-G-T

93523703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362980-C-G

93523792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362885-A-G

93523933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362788-C-T

http://identifiers.org/hco/1/GRCh38#93524083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122362638-A-C

93524122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362605-A-G

93524122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362605-A-T

93524253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122362470-A-G

93524253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122362470-A-T

93524383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362341-A-G

93524391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362333-G-A

93524391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362333-G-T

93524404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362324-T-C

93524404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362324-T-G

93524479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362240-A-G

93524558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362153-C-T

93524559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122362152-A-G

http://identifiers.org/hco/1/GRCh38#93524849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122361832-C-A

93525171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122361573-T-C

93525255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122361476-A-G

93525551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122361140-G-A

93525653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122361037-C-T

93525759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122360919-C-T

93526490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122360304-T-C

93526538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122360257-C-T

93526574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122360239-G-A

93526575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122360238-C-T

93527513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359918-G-A

93527543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359892-T-C

93527591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359840-T-C

http://identifiers.org/hco/1/GRCh38#93528032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122359423-C-A

93528076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359368-A-T

93528113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359344-A-G

93528164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359317-A-G

93528228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122359223-A-T

93528397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358905-G-T

93528417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358886-T-C

93528444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358860-A-G

93528692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358599-G-A

93528823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358422-G-C

93528950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122358225-T-C

93529177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357863-C-G

93529191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357849-G-A

93529626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357606-G-A

93529709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122357529-G-A

93529709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: stop gained
orthologous variants: 122357529-G-T

93529795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357449-T-A

93529795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357449-T-C

93529811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357440-A-G

93529822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357429-G-A

93529822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357429-G-T

93530042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122357200-G-A

93530507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122354766-A-G

93530779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122354584-A-G

93530857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122354506-T-C

93531857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122353503-G-A

93531917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122353434-T-A

http://identifiers.org/hco/1/GRCh38#93532538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122353160-A-C

93532538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122353160-A-G

93532653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122353044-G-C

93533099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352636-T-C

http://identifiers.org/hco/1/GRCh38#93533118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122352618-C-A

93533118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352618-C-T

93533165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352568-T-A

93533165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352568-T-C

93533203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352530-G-A

93533203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352530-G-C

93533203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352530-G-T

93533208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352525-A-G

93533385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352391-T-C

93533394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352382-G-C

93533412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122352319-C-T

http://identifiers.org/hco/1/GRCh38#93533704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122352044-A-C

93534804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122351654-G-A

93534816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122351642-A-T

93534902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: synonymous variant
orthologous variants: 122351556-G-A

93534902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122351556-G-T

93534969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351491-G-A

93534969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351491-G-C

93534969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351491-G-T

93534991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351469-A-G

http://identifiers.org/hco/1/GRCh38#93535044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122351415-C-A

93535044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351415-C-G

93535202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351291-G-T

93535332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351173-G-A

93535480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122351018-A-G

93535509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122350989-A-G

93535510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122350988-T-C

93535715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122350793-T-G

93535768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122350740-T-A

http://identifiers.org/hco/1/GRCh38#93536640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122349910-A-C

93536669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122349881-C-T

93537228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348958-A-G

http://identifiers.org/hco/1/GRCh38#93537348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122348825-C-A

93537348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348825-C-T

93537727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348669-T-C

93537738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348658-C-T

93538251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348485-G-A

93538251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348485-G-T

93538605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348209-T-A

93538782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122348043-A-G

93539340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122347492-G-A

93539948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346914-T-C

http://identifiers.org/hco/1/GRCh38#93539958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122346904-C-A

93540066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346707-G-A

93540111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346665-T-C

http://identifiers.org/hco/1/GRCh38#93540407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122346441-A-C

93540527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346350-C-T

93540630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346247-T-C

93540668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122346211-C-T

93540910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122345928-T-G

http://identifiers.org/hco/1/GRCh38#93541705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122345170-A-C

93541705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122345170-A-G

93541864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122345022-A-G

93542119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122344789-A-G

93542475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122344625-T-A

93543638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122343327-T-C

93543644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122343321-A-G

http://identifiers.org/hco/1/GRCh38#93543950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122343046-C-A

93544035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122342982-T-A

93544070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122342948-A-G

http://identifiers.org/hco/1/GRCh38#93544071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122342947-A-C

93544074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122342944-T-C

http://identifiers.org/hco/1/GRCh38#93544077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122342941-C-A

93544077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122342941-C-G

93544247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122342771-A-G

93544337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122342598-A-G

93545991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122341626-A-G

93546019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122341605-G-A

http://identifiers.org/hco/1/GRCh38#93546278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122341384-A-C

93546278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122341384-A-G

93546453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122341231-G-A

93546555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122341020-G-A

http://identifiers.org/hco/1/GRCh38#93546775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122340783-A-C

93546775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122340783-A-G

93546867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122340697-G-A

93547055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122340498-T-C

93547087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122340474-A-G

http://identifiers.org/hco/1/GRCh38#93547204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122340306-C-A

93547204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122340306-C-T

93547378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122340010-G-A

93547378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122340010-G-T

93547389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122339999-G-C

93547389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122339999-G-T

93547431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122339957-G-A

93547431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122339957-G-T

93547437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122339951-G-T

93547456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339929-T-C

93547531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339860-A-G

http://identifiers.org/hco/1/GRCh38#93547559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122339844-C-A

93547559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339844-C-G

93547559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339844-C-T

93547591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339813-G-A

93547591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339813-G-T

93547735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339644-A-G

93548034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122339328-C-T

93548540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338996-G-A

93548561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338980-T-G

93548815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338739-A-G

93548978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338615-A-G

93548997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338596-T-C

http://identifiers.org/hco/1/GRCh38#93549134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122338466-C-A

93549134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338466-C-T

93549196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338420-T-C

93549246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122338371-T-C

93549282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122338335-G-T

93549339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122338278-G-T

93549408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: missense variant
orthologous variants: 122338209-G-A

http://identifiers.org/hco/1/GRCh38#93549501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122337402-A-C

93549577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122337321-C-T

http://identifiers.org/hco/1/GRCh38#93549925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122337007-C-A

93549925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122337007-C-T

93550015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122336927-T-C

93550091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122336852-T-C

93550736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122336148-C-T

93550799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122336088-A-T

http://identifiers.org/hco/1/GRCh38#93550817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122336070-C-A

93550840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: intron variant
orthologous variants: 122336037-G-T

http://identifiers.org/hco/1/GRCh38#93551136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122335743-C-A

93551136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335743-C-T

http://identifiers.org/hco/1/GRCh38#93551168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122335727-A-C

93551168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335727-A-G

93551423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335476-G-A

93551423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335476-G-T

93551519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335386-T-A

http://identifiers.org/hco/1/GRCh38#93551535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122335370-C-A

93551535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335370-C-T

93551611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335313-T-C

93551965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122335009-A-G

93552065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122334906-G-A

93552065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122334906-G-T

93552077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122334894-T-G

http://identifiers.org/hco/1/GRCh38#93552300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122334683-C-A

93552300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122334683-C-T

93552775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334212-T-A

93552796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334192-A-G

93552803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334185-G-A

93552803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334185-G-T

93552828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334168-T-C

93552841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334155-C-T

http://identifiers.org/hco/1/GRCh38#93552845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122334151-C-A

93552845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334151-C-T

http://identifiers.org/hco/1/GRCh38#93552858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122334138-C-A

93552874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122334122-T-C

93553015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333980-C-T

93553041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333954-C-T

93553089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333908-T-C

93553097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333900-G-T

93553123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333874-C-T

93553157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333844-A-G

93553176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333825-G-T

93553726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333305-G-T

93553767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333265-T-C

93553822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20851
most severe consequence: 3 prime UTR variant
orthologous variants: 122333210-G-T