63838935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5 prime UTR variant
orthologous variants: 7319158-G-T

http://identifiers.org/hco/11/GRCh38#63839663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7318432-C-A

63839663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7318432-C-G

63839663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7318432-C-T

63840461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7317647-C-T

63840485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7317623-G-A

63840679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7317426-G-A

63840971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7317146-C-G

63840971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7317146-C-T

63842068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7316204-A-G

http://identifiers.org/hco/11/GRCh38#63842568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7315966-A-C

63842601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7315936-C-T

63842869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7315674-A-T

63842946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7315605-T-A

63843027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7315535-A-T

63844150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7314276-T-C

63844523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7314215-G-A

63844554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7314185-T-C

63844953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313788-T-G

63845012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313729-C-T

63845023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313718-C-T

63845148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313592-C-G

63845271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313470-T-C

63845524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313227-A-T

63845689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7313076-C-T

63845803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7312941-A-G

63846166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7312009-A-G

63847278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7311882-A-G

63847288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7311872-T-C

63847289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7311871-T-C

63847307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7311853-A-G

63847788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7311378-C-T

63848268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7310898-C-T

63848558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7310684-T-G

http://identifiers.org/hco/11/GRCh38#63848594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7310638-A-C

63848641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7310599-C-T

63848694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7310555-G-A

http://identifiers.org/hco/11/GRCh38#63849991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7309939-C-A

63850098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7309827-A-G

63856096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7297912-C-G

63856096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7297912-C-T

63856320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7297691-T-G

63856655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7297316-C-T

http://identifiers.org/hco/11/GRCh38#63856818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7297204-C-A

63856818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7297204-C-T

63857030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296963-C-G

63857033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296960-G-A

63857107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296853-G-A

63857107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296853-G-C

63858630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7298086-G-A

63858631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7298085-G-A

63858631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7298085-G-T

63858735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7297964-G-A

63858801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7297906-G-A

63859395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7297343-C-T

63859429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7297316-T-C

63859692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296963-C-T

63859695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296960-G-C

63859779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296867-G-A

63859779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296867-G-T

63859793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7296853-G-A

63862937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7294118-A-T

63863233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7293875-G-A

63865765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7293239-G-A

63865782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7293226-T-C

63865904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7292783-C-T

63865911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7292776-G-A

63868503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7289070-G-T

63868506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7289067-G-T

63868521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7289052-G-A

63868521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7289052-G-T

63868578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7289003-G-T

63868606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7288976-G-C

63868827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, missense_variant
orthologous variants: 7288777-C-T

63868866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, missense_variant
orthologous variants: 7288739-G-A

63869014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7288601-T-C

63869294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7288320-A-G

63869496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7288119-T-C

63869502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7288113-T-A

63869502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7288113-T-C

63869554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7288075-G-A

63869775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7287906-T-C

63869782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7287899-G-A

63870103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7287596-C-T

63870602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7287253-G-T

63870623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7287230-C-T

63871052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7286841-G-A

63871060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7286833-G-A

http://identifiers.org/hco/11/GRCh38#63871068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7286825-C-A

63871071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7286822-C-T

63871923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7286362-G-A

63872101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7286212-G-A

63872135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7286178-A-T

63872142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7286171-C-T

63872181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7286130-C-T

63872310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7286005-A-G

63872397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7285918-G-A

63872659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7285733-G-A

63872863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7285530-T-C

63872958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7285450-C-T

63873194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7285243-A-G

http://identifiers.org/hco/11/GRCh38#63873251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7285194-A-C

63873266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7285179-A-G

http://identifiers.org/hco/11/GRCh38#63873270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7285175-C-A

63873775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284674-A-G

63873925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284530-G-A

63873992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284463-A-G

63874021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284448-C-T

63874071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284421-G-C

63874162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7284343-G-A

63874594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7283636-T-G

63874776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7283434-C-T

63874809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7283401-C-G

63876049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7282625-T-G

63876368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7282316-A-G

63876770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7281455-G-T

http://identifiers.org/hco/11/GRCh38#63876787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7281440-C-A

63877916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7281039-T-G

63878148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7280858-C-G

http://identifiers.org/hco/11/GRCh38#63878275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7280750-A-C

63878357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7280663-G-A

63878357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7280663-G-T

63879866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7279870-C-G

63880029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7279716-A-G

63880158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7279583-T-G

63880171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7279570-G-T

63880337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7279406-G-A

63880337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7279406-G-T

63883120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7276530-C-T

63883390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7276275-C-T

63883931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7275810-C-T

63884217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7275537-A-G

63884468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7275290-C-T

63884735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7275047-C-T

63887050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7274693-C-T

63887162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7274614-T-C

63887166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7274610-G-A

63887254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7274548-C-G

63887326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7274471-G-A

63887704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7273433-C-T

63887963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7273297-T-C

63887971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron variant
orthologous variants: 7273289-G-A

63888143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7273143-G-C

63888146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: intron_variant, undefined
orthologous variants: 7273140-T-C

63888596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7272755-T-C

http://identifiers.org/hco/11/GRCh38#63888604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#7272747-C-A

63888604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7272747-C-T

63889110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7272279-A-G

63889303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7272132-C-T

63889515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271904-C-T

63889603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271844-C-T

63890352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271328-G-A

63890352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271328-G-T

63890391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271291-G-A

63890391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271291-G-C

63890391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7271291-G-T

63890796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7270885-T-A

63894885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268429-A-G

63894956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268360-G-A

63894977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268339-T-C

63895033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268282-A-G

63895058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268254-T-A

63895058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268254-T-C

http://identifiers.org/hco/11/GRCh38#63895102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7268206-A-C

63895102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268206-A-G

63895102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7268206-A-T

http://identifiers.org/hco/11/GRCh38#63895264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7268040-C-A

63895264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7268040-C-T

63895532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7267779-T-A

63895595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7267717-A-T

63896309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7266946-C-G

63896309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7266946-C-T

63896802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7266460-C-T

http://identifiers.org/hco/11/GRCh38#63897763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7265203-C-A

63897900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7265075-A-G

63897906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7265070-G-A

63897929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7265049-A-G

63898032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7264956-G-A

63898221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7264752-T-A

http://identifiers.org/hco/11/GRCh38#63898951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7264081-C-A

63899024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7264015-T-C

63899085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7263955-T-C

http://identifiers.org/hco/11/GRCh38#63899199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7263896-C-A

63899199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263896-C-G

63899199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263896-C-T

63899207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263888-G-A

63899207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263888-G-T

http://identifiers.org/hco/11/GRCh38#63899225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7263871-C-A

63899225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263871-C-T

63899438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263705-C-T

http://identifiers.org/hco/11/GRCh38#63899801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7263403-C-A

63899801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263403-C-T

63900154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263047-G-A

63900154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263047-G-C

63900154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263047-G-T

63900173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7263028-G-T

63900494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7262449-G-C

63900527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7262415-T-C

63900527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7262415-T-G

63900747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7262158-C-T

63900769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7262133-G-T

63901167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7261729-T-A

63901262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7261655-G-A

63902105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7261023-G-A

63902105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7261023-G-T

63902155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260975-A-G

63902243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7260886-C-G

http://identifiers.org/hco/11/GRCh38#63902309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7260820-C-A

63902309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7260820-C-G

63902315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7260814-C-T

63902346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260783-A-G

63902353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260776-G-T

63902386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260744-G-C

63902442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260705-T-A

63902442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260705-T-C

63902442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260705-T-G

63902458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260689-G-A

63902458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7260689-G-T

63902769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7260409-C-G

http://identifiers.org/hco/11/GRCh38#63902858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7260333-C-A

63903824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259467-G-A

63903824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259467-G-T

63904674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258728-G-A

63904692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258708-C-T

63905114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258328-G-A

63905114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258328-G-T

63905187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258274-A-G

63905798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257696-G-A

63905815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257679-C-T

http://identifiers.org/hco/11/GRCh38#63906003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7257533-C-A

63906003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257533-C-G

63906003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257533-C-T

http://identifiers.org/hco/11/GRCh38#63906008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7257528-C-A

63906008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257528-C-T

63906152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257311-T-A

63906152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257311-T-C

http://identifiers.org/hco/11/GRCh38#63906247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7257222-C-A

63906247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7257222-C-T

63906515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7256965-G-A

63906756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7256756-G-A

63907862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7255829-G-A

63908037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7255657-A-G

63908382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7255338-G-A

63908382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7255338-G-T

63908513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7255214-T-G

http://identifiers.org/hco/11/GRCh38#63908751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7254950-C-A

63908751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7254950-C-T

63908863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7254827-T-A

http://identifiers.org/hco/11/GRCh38#63908881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7254809-C-A

63908881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7254809-C-T

63909043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7254647-A-G

63909401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 7254291-G-A

63909401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 7254291-G-C

63909401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 7254291-G-T

63909761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7253931-T-A

63909761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7253931-T-C

63909764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7253928-T-A

63909764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7253928-T-C

63909764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7253928-T-G

http://identifiers.org/hco/11/GRCh38#63910780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7252995-C-A

63910780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7252995-C-T

63910896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3332
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7252882-A-G