http://identifiers.org/hco/17/GRCh38#2755712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74501732-C-A

2755712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5 prime UTR variant
orthologous variants: 74501732-C-T

2755736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74501708-C-T

2755791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501660-G-T

2755862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501626-G-A

2755862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501626-G-C

2755862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501626-G-T

2755869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501619-G-A

2755869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501619-G-C

2755869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501619-G-T

2756014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501486-C-T

2756032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501460-C-T

2756049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501443-G-A

http://identifiers.org/hco/17/GRCh38#2756109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74501318-C-A

2756112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501314-C-T

2756255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501161-C-T

http://identifiers.org/hco/17/GRCh38#2756284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74501135-C-A

2756410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74501021-G-T

2756470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74500954-C-T

2763449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492697-G-A

2763468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492677-G-A

2763468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492677-G-C

2763538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492594-A-G

2763927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492089-C-T

2763940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74492076-G-A

2764095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74491940-G-A

2765129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74491321-C-T

2765142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74491305-T-A

http://identifiers.org/hco/17/GRCh38#2770109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74488006-A-C

2770109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74488006-A-T

2770158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487957-T-C

2770230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487890-C-T

http://identifiers.org/hco/17/GRCh38#2770345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74487806-C-A

2770345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74487806-C-G

2770345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74487806-C-T

http://identifiers.org/hco/17/GRCh38#2770429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74487722-C-A

2770429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74487722-C-T

2770430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74487721-T-A

2770430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 74487721-T-C

2770497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487518-C-T

2770502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487485-A-G

2770567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487421-G-T

2770568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487420-T-G

2770672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74487314-A-T

2775443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481875-G-A

2775808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481574-T-C

2775808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481574-T-G

2776269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481425-T-C

2776493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481228-C-T

2776511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481211-C-T

2776619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74481099-G-A

2777025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74480700-G-T

2777081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 74480651-C-T

http://identifiers.org/hco/17/GRCh38#2777129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74480616-C-A

2777129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74480616-C-T

2777213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74480492-C-T

2777219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74480486-T-C

2777224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74480466-T-C

2777227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74480463-G-A

2777941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74479750-G-T

2778176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74479634-C-G

2778261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74479557-T-C

2778320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74479517-G-A

2778679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478987-G-A

2778679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478987-G-C

2778763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478902-G-A

2778828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478844-G-A

2778828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478844-G-C

2778836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478836-A-G

2778865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478796-C-T

2778959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478712-G-T

2779018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478655-A-G

2779018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74478655-A-T

2779298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477798-G-C

2779298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477798-G-T

2779401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477705-G-A

2779401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477705-G-C

2779926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477240-A-T

2780385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74477093-C-T

2780693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74476785-T-C

2780694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74476784-G-A

http://identifiers.org/hco/17/GRCh38#2780977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74476517-A-C

http://identifiers.org/hco/17/GRCh38#2781079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74476411-A-C

http://identifiers.org/hco/17/GRCh38#2781209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74476267-C-A

2782148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74475841-C-T

2782648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74475371-G-T

2783172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74475193-G-A

2783728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474583-C-T

2783762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474545-A-G

2783762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474545-A-T

2783764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474543-G-T

2783856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474462-G-A

2783962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474362-T-G

2784750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74474155-A-T

2784844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74473663-G-A

2786406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472666-C-T

2786430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74472400-C-T

2786479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472351-G-C

2786521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74472310-G-A

2786574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472221-C-T

2786600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472203-C-T

http://identifiers.org/hco/17/GRCh38#2786613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74472190-A-C

2786625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472178-C-G

2786625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472178-C-T

2786643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472160-T-C

http://identifiers.org/hco/17/GRCh38#2786664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74472139-C-A

2786664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74472139-C-T

2786842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74471975-T-G

2789347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74468270-A-G

2789347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74468270-A-T

http://identifiers.org/hco/17/GRCh38#2789474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74468139-C-A

2790501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467858-A-T

2790514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467845-G-A

2790710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467670-G-A

2791221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467412-A-G

http://identifiers.org/hco/17/GRCh38#2791319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74467298-C-A

2791378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467224-G-A

2791378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467224-G-T

2791486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74467120-G-A

2792610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74466472-G-A

2792638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74466444-G-A

2792748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74466205-A-T

2792801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74466164-C-T

http://identifiers.org/hco/17/GRCh38#2792850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74466118-C-A

2793077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74465908-A-G

2793132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74465855-A-T

2793150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74465837-A-G

2793150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74465837-A-T

2794303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464952-G-A

2794313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464939-C-T

2794340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464913-T-C

http://identifiers.org/hco/17/GRCh38#2794407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74464832-C-A

2795709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464258-T-G

2795752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464214-T-A

2795960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74464027-G-C

2796006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463983-G-A

2796092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463887-A-G

2796146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463848-C-G

2796146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463848-C-T

2796406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463588-G-A

2796406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463588-G-C

http://identifiers.org/hco/17/GRCh38#2796427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74463567-C-A

2796445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74463552-C-G

2796515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74463487-T-C

http://identifiers.org/hco/17/GRCh38#2796709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74463291-C-A

2796709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463291-C-G

2796709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463291-C-T

2796816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463202-G-T

2796924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463090-G-A

2796975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463065-C-T

2796981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74463059-A-G

2797062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462958-T-A

2797184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462888-T-A

2797433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462680-G-A

2797433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462680-G-C

2797552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462561-G-A

2797552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462561-G-T

2797560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462553-G-T

http://identifiers.org/hco/17/GRCh38#2797576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74462536-C-A

2797576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462536-C-T

2797714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462399-G-A

2797714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462399-G-C

2797930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74462195-A-G

2798520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460792-G-A

2798520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460792-G-T

2798592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460709-T-A

2798593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460708-C-G

2798593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460708-C-T

2799006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460564-T-G

2799056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460521-T-C

2799056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460521-T-G

2799093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460482-C-G

2799158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460426-G-A

2799463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74460148-C-T

2799897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74459448-A-G

2799926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74459425-C-T

2800438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458151-G-T

http://identifiers.org/hco/17/GRCh38#2800444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74458145-C-A

2800444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458145-C-T

2800445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458144-C-G

2800445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458144-C-T

2800516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 74458074-A-G

2800560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458030-A-G

2800560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74458030-A-T

http://identifiers.org/hco/17/GRCh38#2800595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74457994-A-C

http://identifiers.org/hco/17/GRCh38#2800611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74457970-C-A

2800611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457970-C-T

2800612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457969-T-G

2800701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457883-G-A

2800720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457862-C-T

2801537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457708-T-G

2802841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457167-G-C

2802854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457154-G-T

2802896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457126-G-A

2802896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74457126-G-T

2803081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74455942-A-T

2803115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74455911-G-T

2803219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74455793-A-G

2804065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74454128-G-A

2804117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74454080-C-T

2804273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453926-C-T

2804475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453736-T-C

2804637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453623-C-T

2804703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453547-A-G

2804788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453468-C-G

2804945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74453216-G-A

2805171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74452992-G-T

2805219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74452722-C-T

2807269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74451232-T-C

2807271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74451230-G-T

2807614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74450825-G-A

2808343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74450578-T-G

2808706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74450221-G-C

http://identifiers.org/hco/17/GRCh38#2809169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74449746-C-A

2809338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74449635-G-A

2809492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74449496-A-G

2811986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74448791-A-G

2812007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74448767-G-A

2812562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74448257-A-G

2814469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74447316-C-T

2814780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74447065-G-A

2814781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74447064-C-T

2814827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74447018-G-T

2814852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74447000-G-A

2814912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74446943-G-A

2814958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74446868-G-A

2815592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74446286-C-T

2816247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74445533-T-C

2816289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74445485-C-T

2821333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74442772-A-G

2822166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74441560-G-T

2823601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74440622-G-T

2827234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74438949-G-C

2828474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74438560-G-A

2828499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74438531-T-C

2829602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74437807-G-A

2829602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74437807-G-T

http://identifiers.org/hco/17/GRCh38#2837534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74427355-A-C

http://identifiers.org/hco/17/GRCh38#2838533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74427138-C-A

http://identifiers.org/hco/17/GRCh38#2838587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74427084-A-C

2838709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74426967-G-A

2838739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74426942-C-T

http://identifiers.org/hco/17/GRCh38#2843646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74423474-A-C

2843647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74423473-C-T

2844326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74422331-C-T

2844405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74422251-G-C

2847545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74418613-T-C

http://identifiers.org/hco/17/GRCh38#2848176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74417994-C-A

2848997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74417480-G-T

2849009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74417459-C-G

http://identifiers.org/hco/17/GRCh38#2849084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74417386-C-A

2849084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74417386-C-G

2849442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74416706-A-G

2849525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74416633-G-C

2849528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74416630-C-T

http://identifiers.org/hco/17/GRCh38#2849653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74416523-C-A

2851169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74416007-G-C

2851183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74415994-A-G

2851527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74415664-C-T

2852203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74415169-A-G

2852756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414660-G-C

2852820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414599-A-G

2852891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414525-C-T

2852930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414507-C-T

2853259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414198-G-A

2853355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74414114-T-C

http://identifiers.org/hco/17/GRCh38#2853602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74413826-C-A

http://identifiers.org/hco/17/GRCh38#2853755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74413561-C-A

2853755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74413561-C-T

2853938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74413395-G-T

2854005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, missense_variant
orthologous variants: 74413321-C-T

2854047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, missense_variant
orthologous variants: 74413279-G-A

http://identifiers.org/hco/17/GRCh38#2854289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74413105-C-A

2854295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74413099-C-G

2854388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74413056-C-T

2854518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74412945-G-A

2854518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74412945-G-T

http://identifiers.org/hco/17/GRCh38#2854581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74412881-A-C

2855008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74412494-A-G

2855463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74412086-G-A

2855939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74411698-G-A

2856274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74411138-G-A

2856274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74411138-G-T

2856356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74411016-C-T

http://identifiers.org/hco/17/GRCh38#2856575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74410807-C-A

2856575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410807-C-T

2856650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410759-G-A

2856686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410721-G-A

2856771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410645-A-G

2856815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410603-C-T

2857361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74410069-G-C

2857482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74409948-G-A

2857482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74409948-G-T

2857605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74409631-G-A

2857715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74409556-A-G

2857862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74409418-G-T

2859863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74408849-C-T

2860225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74408523-G-C

http://identifiers.org/hco/17/GRCh38#2860644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74408264-C-A

2860750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74408201-C-T

2861152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407876-A-G

2861166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407862-A-G

2861435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407605-C-T

2862195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407340-C-G

2862532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407010-C-T

2862535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74407007-G-C

http://identifiers.org/hco/17/GRCh38#2862548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74406996-C-A

2862548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406996-C-T

2863223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74405928-C-G

2863269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74405968-G-A

2863269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74405968-G-T

2864084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406331-C-T

2864089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406336-G-A

2864261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406459-C-G

2864263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406461-A-G

2864270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74406468-G-A

2864413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74403687-G-A

2864601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74403537-G-A

http://identifiers.org/hco/17/GRCh38#2864716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74403451-C-A

2864716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74403451-C-T

2864742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74403424-C-T

http://identifiers.org/hco/17/GRCh38#2864836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74403336-C-A

2865118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402944-T-C

2865439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402468-T-C

2865582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402334-A-G

2865588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402328-A-G

2865763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402161-T-C

2865860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402071-C-G

http://identifiers.org/hco/17/GRCh38#2865926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74402009-C-A

2865926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74402009-C-T

2866038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74401868-A-G

2866111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74401803-C-T

2866621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74401336-G-A

http://identifiers.org/hco/17/GRCh38#2866722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74401276-C-A

2866778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74401212-T-G

http://identifiers.org/hco/17/GRCh38#2868103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74399608-C-A

2868158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74399553-A-T

2868283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74399425-A-G

http://identifiers.org/hco/17/GRCh38#2868288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74399420-A-C

2868407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74399284-C-G

2868407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74399284-C-T

2868412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74399279-C-G

2869119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74398426-A-G

2869439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74398184-G-A

http://identifiers.org/hco/17/GRCh38#2869487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74398139-A-C

http://identifiers.org/hco/17/GRCh38#2869734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74397930-C-A

2869734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397930-C-T

2869907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397816-G-T

2869934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397782-G-C

2870008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397718-G-T

2870639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397395-G-A

2870639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74397395-G-T

2873530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74395876-A-G

2882845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74393044-C-T

2882876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74393013-C-T

2883219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74392578-T-G

2883322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74392504-T-C

http://identifiers.org/hco/17/GRCh38#2883533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74392307-A-C

2883761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74392076-G-T

2884150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74391700-G-A

http://identifiers.org/hco/17/GRCh38#2884168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74391682-C-A

2884168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74391682-C-T

2885342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74390665-C-T

2885525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74390503-C-T

2886656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388741-C-T

2886896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388561-G-C

2887064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388423-A-G

2888045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388370-T-C

2889395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388155-G-A

2889556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74388002-G-A

2890161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387775-A-T

2890169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387767-C-T

2890446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387485-G-A

2891502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387201-T-A

http://identifiers.org/hco/17/GRCh38#2891529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74387178-A-C

2891529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387178-A-T

2891554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74387154-T-C

2891776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386913-T-C

2892043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386632-C-T

2892045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386630-G-A

2892065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386616-C-T

2892265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386483-G-A

2892481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386308-C-T

2892507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74386282-G-A

http://identifiers.org/hco/17/GRCh38#2892512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74386268-C-A

2892669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74386084-C-G

2892669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74386084-C-T

2892763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74386050-T-C

2893095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74385729-T-G

2893108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74385716-A-T

2893110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74385714-C-T

2893113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74385711-T-C

2893153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74385657-A-G

2893487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74385249-C-G

2893523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74385213-T-C

2893726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74385016-C-T

2893766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74384980-G-C

2893803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74384943-C-T

2893829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74384921-C-G

2893829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74384921-C-T

2896365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74383705-C-T

2896501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74383564-G-A

2896896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74383212-G-T

2898340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74382665-C-T

2898341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74382664-A-T

2898402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74382612-A-G

2898413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74382601-C-T

2898429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74382590-G-C

2898542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74382486-C-T

2898770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74382277-G-A

2900224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74380169-G-T

2900407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74380028-C-G

2900407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74380028-C-T

2900967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379521-G-A

2900967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379521-G-C

2900967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379521-G-T

2900987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379503-C-G

2900987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379503-C-T

2901030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379460-G-C

2901078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379448-C-T

2901126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379402-G-A

2901126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379402-G-C

2901126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379402-G-T

2901159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379369-T-A

2901555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74379001-T-C

2901582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74378974-G-A

2901688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74378867-G-A

2902585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377958-T-G

2902640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377903-T-C

2902746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377834-A-G

2902812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377796-C-T

2902978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377683-C-T

2903193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377455-C-T

2903638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377107-A-T

2903715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74377056-A-G

2903894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376840-G-A

2904109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376654-T-C

2904138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376625-T-C

2904176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376587-C-T

2904493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376288-C-T

2904616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376131-C-T

2904629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376125-C-T

2904710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74376045-C-T

http://identifiers.org/hco/17/GRCh38#2905206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74375881-C-A

2905206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74375881-C-T

2905530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74375547-G-A

2905533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74375544-A-T

2905770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74375314-T-A

2906488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74374721-T-C

2906779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74374493-T-A

2907053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74374289-G-C

2907089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74374251-G-A

2907089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74374251-G-T

2907429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74373959-T-C

2907451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74373937-A-G

2907570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74373822-G-T

2907753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74373662-G-C

2909847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74372493-G-C

http://identifiers.org/hco/17/GRCh38#2909854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74372485-C-A

2909969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74372415-T-C

2909971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74372413-T-C

2910113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74372320-G-A

2910211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74372228-G-A

2910616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74371075-A-G

2911505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370779-C-T

2911758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370552-C-T

2911816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370498-C-G

http://identifiers.org/hco/17/GRCh38#2911898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74370423-C-A

2911898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370423-C-T

2911908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370406-G-A

2911908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370406-G-T

2912238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74370094-T-C

http://identifiers.org/hco/17/GRCh38#2912278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74370054-C-A

2916089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74369250-T-C

2916184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74369163-A-G

2916549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368814-C-T

2916560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368803-C-G

2916593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368771-G-A

2916667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368703-G-A

2916781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368620-C-T

2916791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368610-T-G

2916798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368603-C-T

2916909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74368499-G-A

2917028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367903-C-T

http://identifiers.org/hco/17/GRCh38#2917051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74367880-C-A

2917057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367874-G-T

2917086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367845-T-G

2917155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367778-G-T

2918909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367538-T-C

2918967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367464-G-A

2919428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74367001-G-A

2919476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74366953-C-G

2920391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74366663-C-T

2920620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74366245-C-G

http://identifiers.org/hco/17/GRCh38#2920908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74365979-A-C

2920922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74365965-C-G

2920941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74365948-C-T

2923867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74364407-A-G

2924000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74364273-T-C

2924150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363994-C-T

2924196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363946-G-A

2924210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363932-T-C

http://identifiers.org/hco/17/GRCh38#2924265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74363883-C-A

2924265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363883-C-G

2924265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363883-C-T

2924279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363868-C-G

2924279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363868-C-T

http://identifiers.org/hco/17/GRCh38#2924319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#74363826-A-C

2924321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74363824-G-A

2924519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363632-T-C

2924675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363487-T-C

2924719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363444-G-T

2924725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363439-G-A

2924869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363365-A-G

2925260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74363017-C-T

2928197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74359648-G-A

2928197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74359648-G-T

2928874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74359087-C-T

2930123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74356249-G-T

2930436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74356007-A-G

2930723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74355721-C-T

2931168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74355667-G-T

2931193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74355642-T-G

http://identifiers.org/hco/17/GRCh38#2931491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74355361-C-A

2931491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74355361-C-T

2931639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74355214-A-G

http://identifiers.org/hco/17/GRCh38#2932012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74354672-C-A

2932012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74354672-C-T

2932352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74354355-C-G

2932880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74353989-T-C

http://identifiers.org/hco/17/GRCh38#2932884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74353986-C-A

2932884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74353986-C-T

2932896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74353974-C-G

2933906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74353293-T-G

2936312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74350328-C-T

2936328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74350306-T-C

2936429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74350220-C-T

2936499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74350154-C-T

2936642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74350028-G-A

2937183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74349995-T-C

2937469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74349746-T-C

2937641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74349616-G-T

http://identifiers.org/hco/17/GRCh38#2937691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74349570-A-C

2938049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74349251-C-T

2938287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74349045-C-G

2938402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74348933-G-C

2938413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74348924-G-A

http://identifiers.org/hco/17/GRCh38#2939788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74348289-C-A

2940372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74347662-T-C

2940497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74347540-C-T

2940754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74347382-C-G

http://identifiers.org/hco/17/GRCh38#2941092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74347104-C-A

2941092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74347104-C-T

http://identifiers.org/hco/17/GRCh38#2946169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74342780-C-A

2946169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74342780-C-T

2946448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74342529-T-G

2946552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74342443-G-A

2947080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74342201-A-G

http://identifiers.org/hco/17/GRCh38#2947098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74342199-A-C

http://identifiers.org/hco/17/GRCh38#2947109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74342188-A-C

2947426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74341894-C-T

2948068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74341003-C-T

2948346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74340718-T-A

2948449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74340610-A-G

2948985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74339808-T-C

2949121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74339661-A-G

2949336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74339451-G-C

2949976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74339014-A-G

2955998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333914-C-T

2956059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333864-G-A

2956189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333751-G-A

2956195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333745-C-T

2956287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333657-A-G

2956402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333540-C-T

http://identifiers.org/hco/17/GRCh38#2956736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74333265-C-A

2956742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333259-G-A

2956742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333259-G-T

2956746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74333255-C-T

2957485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332861-A-G

2957485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332861-A-T

2957595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332766-G-C

2957595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332766-G-T

http://identifiers.org/hco/17/GRCh38#2957660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74332696-C-A

2957660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332696-C-T

2957739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332626-C-T

http://identifiers.org/hco/17/GRCh38#2957830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74332547-C-A

2957830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332547-C-G

2957830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332547-C-T

2957847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332530-T-C

2957848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332529-G-A

2957848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332529-G-T

http://identifiers.org/hco/17/GRCh38#2957863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74332517-C-A

2957863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332517-C-T

2957873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332507-G-A

2957873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332507-G-T

2958134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332308-T-C

2958187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332254-G-A

2958205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332236-C-T

2958341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74332097-A-T

2958492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331673-T-C

2958556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331609-G-T

2958654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331523-G-A

2958963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331232-T-G

2959128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331082-G-A

2959128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74331082-G-T

2959302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330964-G-A

2959302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330964-G-C

2959436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330839-G-A

2959504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330773-C-T

2959608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330659-C-T

2960161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74330425-C-G

2960164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74330422-T-A

2960218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330367-G-A

2960281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330307-C-G

2960281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330307-C-T

2960446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74330150-C-T

2961560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74329879-G-T

2961604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74329837-T-G

2961725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74329748-G-A

2961771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74329710-C-T

2961820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74329635-C-T

2962254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329521-G-A

2962422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329354-T-C

http://identifiers.org/hco/17/GRCh38#2962476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74329296-C-A

2962476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329296-C-T

2962482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329290-G-A

2962482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329290-G-T

2962484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329288-G-A

2962484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329288-G-T

2962534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329236-A-G

2962534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329236-A-T

2962535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329235-T-C

2962535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329235-T-G

2962763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329064-A-G

http://identifiers.org/hco/17/GRCh38#2962791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74329036-C-A

2962791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329036-C-G

2962791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329036-C-T

2962792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329035-G-A

2962792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74329035-G-T

http://identifiers.org/hco/17/GRCh38#2962861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328966-C-A

2962861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328966-C-T

2962892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328935-G-T

http://identifiers.org/hco/17/GRCh38#2962923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328904-C-A

2962923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328904-C-G

2962923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328904-C-T

http://identifiers.org/hco/17/GRCh38#2962956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328873-C-A

2962956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328873-C-G

http://identifiers.org/hco/17/GRCh38#2962963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328866-C-A

2962963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328866-C-T

2962971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328858-T-A

2962971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328858-T-C

2962971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328858-T-G

2963037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328787-G-A

2963037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328787-G-T

2963153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328583-G-A

2963153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328583-G-T

2963154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328582-T-C

2963154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328582-T-G

2963180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74328557-A-G

2963257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328478-G-T

2963286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328445-G-A

http://identifiers.org/hco/17/GRCh38#2963347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328383-C-A

2963388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328329-A-G

2963553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328200-C-T

2963783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328030-A-T

http://identifiers.org/hco/17/GRCh38#2963809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74328013-C-A

2963810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328012-T-A

2963810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328012-T-C

2964348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74327708-G-A

2964363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74327693-G-T

2964547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327602-G-A

2964547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327602-G-T

http://identifiers.org/hco/17/GRCh38#2964574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74327577-C-A

2964574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327577-C-T

http://identifiers.org/hco/17/GRCh38#2964587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74327564-A-C

2964587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327564-A-T

2964611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327540-G-A

2964611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327540-G-T

2964621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327530-G-A

2964621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327530-G-T

2964827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327324-C-T

2964857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327293-G-A

http://identifiers.org/hco/17/GRCh38#2964918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74327235-C-A

2964952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327189-T-A

2964952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327189-T-G

2965023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327130-T-A

2965023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327130-T-C

2965023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327130-T-G

2965098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74327064-G-A

2965098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74327064-G-C

2965098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74327064-G-T

2965134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327030-G-C

2965156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327008-G-T

2965157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74327007-T-G

http://identifiers.org/hco/17/GRCh38#2965190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74326978-C-A

2965190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326978-C-G

2965190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326978-C-T

2965212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326957-T-C

2965290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326920-G-C

2965290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326920-G-T

2965313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326897-G-A

2965313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326897-G-T

http://identifiers.org/hco/17/GRCh38#2965432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74326720-C-A

2965432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326720-C-T

2965471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326677-G-A

2965471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326677-G-T

2965494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326656-G-T

2965521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326647-A-G

http://identifiers.org/hco/17/GRCh38#2965522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74326646-C-A

2965522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74326646-C-T

2965600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74326568-T-C

http://identifiers.org/hco/17/GRCh38#2965650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74326518-C-A

2965650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74326518-C-T

2965709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74326456-G-A

2965709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74326456-G-T

http://identifiers.org/hco/17/GRCh38#2965715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#74326450-A-C

2965929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74326258-A-G

2965945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74326243-A-G

2965970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74326218-A-G

2966247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74325991-A-G

2966472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74325792-T-C

2966606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74325126-G-A

2967072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74324647-A-G

2967210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74324415-T-C

2967510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74324254-C-T

2967747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74324022-C-G

http://identifiers.org/hco/17/GRCh38#2967802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74323967-A-C

2967802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74323967-A-G

2967882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74323902-G-A

2967882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74323902-G-C

2967915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74323864-G-A

2979013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74317476-A-T

2979047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74317438-G-A

2980241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316861-A-G

2980381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316717-G-A

2980476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316645-G-A

2980597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316539-A-G

2980773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316444-C-G

2980825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74316355-A-G

http://identifiers.org/hco/17/GRCh38#2981293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74315955-A-C

2981293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74315955-A-T

2981325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74315926-T-C

http://identifiers.org/hco/17/GRCh38#2981381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74315870-C-A

2981548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74315703-G-C

2981677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74315572-G-T

2982769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74314798-G-A

http://identifiers.org/hco/17/GRCh38#2982797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74314770-C-A

2982812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74314760-G-A

2982972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74314621-G-A

2983000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, undefined
orthologous variants: 74314593-C-T

2984564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313743-C-G

2984564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313743-C-T

2984596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313711-G-C

2984636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313670-T-C

http://identifiers.org/hco/17/GRCh38#2984816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74313491-C-A

2984816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313491-C-T

2984843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313467-T-C

2984865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313445-T-C

http://identifiers.org/hco/17/GRCh38#2984966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74313356-C-A

2984966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313356-C-T

2985077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313243-C-G

2985077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313243-C-T

2985093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313227-C-G

http://identifiers.org/hco/17/GRCh38#2985112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74313208-A-C

2985112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313208-A-G

http://identifiers.org/hco/17/GRCh38#2985120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74313206-C-A

http://identifiers.org/hco/17/GRCh38#2985142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74313184-C-A

2985142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74313184-C-T

2985425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311922-C-T

2985577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311829-A-G

2985605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311791-C-T

2985633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311759-A-G

2985736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311652-G-C

2985844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311564-A-G

http://identifiers.org/hco/17/GRCh38#2985854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74311554-A-C

2985854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311554-A-T

2985894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311516-C-G

2986138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311360-G-T

2986238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74311270-T-A

2986573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310931-T-C

2986575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310929-G-T

2986648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310856-T-C

2986820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310681-T-C

2986864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310639-T-C

2986881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310622-C-T

2986944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310592-G-T

2987187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74310367-G-T

2989717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74308367-T-G

http://identifiers.org/hco/17/GRCh38#2990884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74307589-A-C

2990884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74307589-A-G

2990884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74307589-A-T

2991006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74307478-A-G

http://identifiers.org/hco/17/GRCh38#2991011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74307473-C-A

2991036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74307431-G-C

http://identifiers.org/hco/17/GRCh38#2991120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74307329-A-C

2991272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74307179-G-T

2991348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74307105-G-A

http://identifiers.org/hco/17/GRCh38#2991420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74307034-C-A

http://identifiers.org/hco/17/GRCh38#2991428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74307028-C-A

2991444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307012-T-C

2991444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307012-T-G

2991458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306998-G-A

2991467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306989-G-A

2991467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306989-G-C

http://identifiers.org/hco/17/GRCh38#2991470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74306986-C-A

2991623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306846-C-T

2991705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306759-G-C

2991749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306722-C-T

2995201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305458-A-G

http://identifiers.org/hco/17/GRCh38#2995217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74305442-A-C

2995217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305442-A-G

2995217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305442-A-T

2995237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305424-T-C

2995509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305193-G-A

2995652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305122-C-T

2996037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304823-G-A

2996110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304749-G-A

2996476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304485-G-A

2996745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304232-G-A

2996794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304175-G-A

2996796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304117-G-A

2996796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304117-G-T

2997332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303711-C-T

2997343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303698-T-A

2997404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303641-C-T

2997530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303531-C-T

2997549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303512-T-A

2997573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303491-C-T

2998305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74303192-G-A

2998346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74303151-G-A

2998420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74303077-C-T

http://identifiers.org/hco/17/GRCh38#2998467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74303026-A-C

http://identifiers.org/hco/17/GRCh38#2998478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#74303015-C-A

2998478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74303015-C-G

2998478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74303015-C-T

2998483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74303010-T-G

2998522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74302971-G-A

2998522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74302971-G-C

2999278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74302018-G-A

3002714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74301579-C-T

3002951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74301348-A-T

3002970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74301329-G-A

3003427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74300705-G-A

http://identifiers.org/hco/17/GRCh38#3003437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74300695-C-A

3003437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74300695-C-T

3004019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74300369-G-A

3004039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74300352-G-A

http://identifiers.org/hco/17/GRCh38#3004106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74300214-C-A

3004701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74299584-C-G

3004702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74299583-C-T

3005014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74299107-C-G

3005242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74298882-G-A

3005260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74298868-G-T

3005277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74298851-G-T

3005372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74298780-T-G

http://identifiers.org/hco/17/GRCh38#3005461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74298692-C-A

3005461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74298692-C-T

3005473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74298680-C-T

3005526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74298627-T-A

3005535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74298618-G-A

3005535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74298618-G-T

3006887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297859-G-A

3007094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297663-G-C

3007162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297610-C-T

3007296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297495-G-A

3007332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297467-T-C

3007333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297466-G-A

3007424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74297378-T-C

3007807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296882-T-C

http://identifiers.org/hco/17/GRCh38#3007884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74296807-C-A

3007884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296807-C-G

3007884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296807-C-T

3007888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296804-A-G

http://identifiers.org/hco/17/GRCh38#3007889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74296803-C-A

3007889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296803-C-G

3007889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296803-C-T

http://identifiers.org/hco/17/GRCh38#3007890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74296802-C-A

3007890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296802-C-T

3007950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296740-G-A

3007950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296740-G-T

3008032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74296660-C-T

3008211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296489-A-G

3008276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296432-G-T

3008542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296298-C-G

3008555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296285-G-A

3008804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74296065-G-A

3008889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295971-A-G

3009055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295832-G-A

3009055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295832-G-T

3009087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295800-C-T

3009121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295769-C-T

http://identifiers.org/hco/17/GRCh38#3009184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74295705-A-C

3009295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295593-T-C

3009354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295542-C-T

3009649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74295237-C-G

3009804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294950-A-G

3009863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294885-G-A

3010624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294470-G-A

3010640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294454-G-A

3010640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294454-G-T

3010662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294434-G-A

3010754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294342-A-G

3010907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294189-A-G

3012024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293842-C-T

3012086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293805-T-C

3012103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293797-T-C

3012747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293513-T-C

3012811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293432-G-A

3012818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293421-C-T

3012927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293359-C-T

3012958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293330-C-T

3013028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293259-C-T

3013066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293246-C-G

3013071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293241-A-G

3013170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293142-G-A

3013227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293088-G-A

http://identifiers.org/hco/17/GRCh38#3013423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74292821-C-A

3013423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74292821-C-T

3013531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74291725-C-T

http://identifiers.org/hco/17/GRCh38#3013660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74291630-A-C

3013660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74291630-A-G

3013660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74291630-A-T

3013666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74291625-G-T

3015101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290904-G-A

http://identifiers.org/hco/17/GRCh38#3015203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74290802-A-C

3015223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290782-G-A

http://identifiers.org/hco/17/GRCh38#3015361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74290651-A-C

3015361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290651-A-G

3015955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290441-C-T

3016072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290331-G-A

http://identifiers.org/hco/17/GRCh38#3016091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74290313-C-A

3016132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290275-C-T

3016433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290004-G-A

3016457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289980-G-A

3016593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289859-G-A

3016593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289859-G-T

3016686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289774-C-T

3016689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289771-T-G

3016798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289675-C-T

3016840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289636-C-G

http://identifiers.org/hco/17/GRCh38#3016846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74289630-A-C

3016912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289575-C-T

3017060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289415-G-A

3017328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289106-C-T

3017847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288492-C-G

3017944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288405-T-A

3017944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288405-T-C

3017950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288399-T-C

3017950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288399-T-G

http://identifiers.org/hco/17/GRCh38#3018021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74288357-C-A

3018021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288357-C-G

3018021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288357-C-T

3018124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74288255-A-G

http://identifiers.org/hco/17/GRCh38#3018148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74288231-A-C

3018148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74288231-A-G

3018154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74288225-G-A

http://identifiers.org/hco/17/GRCh38#3018225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74288156-C-A

3018225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288156-C-T

3018287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288106-G-A

3018287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288106-G-C

3018287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288106-G-T

3018342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288045-G-A

3018342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288045-G-T

3019601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74287485-C-T

3019959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74287204-T-C

3020197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286965-A-G

3020231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286923-T-C

3020371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286815-G-T

http://identifiers.org/hco/17/GRCh38#3020392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74286795-C-A

http://identifiers.org/hco/17/GRCh38#3020425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74286770-A-C

3020470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74286728-T-A

3020470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74286728-T-C

3020558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74286640-A-G

3020676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286525-T-G

http://identifiers.org/hco/17/GRCh38#3020677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74286524-A-C

3020677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286524-A-G

3020711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286483-G-A

3020711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286483-G-T

3020719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74286475-T-C

http://identifiers.org/hco/17/GRCh38#3024376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74285821-C-A

3024464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74285736-C-T

3024704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74285508-A-G

3024736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74285484-G-A

3025048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74285201-G-A

3025399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74284869-G-A

3025438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74284837-G-T

3025939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74284375-T-C

3026192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74284133-G-A

3026192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74284133-G-T

http://identifiers.org/hco/17/GRCh38#3026197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74284128-C-A

3026197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74284128-C-T

3026266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74284060-G-A

3026266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74284060-G-T

3026336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74284000-C-G

3026336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74284000-C-T

3026468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283865-G-T

3026506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283820-G-A

3026524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283741-T-G

3026539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283715-A-G

http://identifiers.org/hco/17/GRCh38#3026592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74283663-A-C

3026592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283663-A-T

3026611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283611-G-A

3026611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283611-G-T

3026837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283273-G-A

3026837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283273-G-C

3026866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283245-T-G

3026937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 74283177-T-A

3026937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 74283177-T-C

3027092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283022-G-A

3027092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74283022-G-T

3027129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282984-A-G

3027140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282973-G-T

http://identifiers.org/hco/17/GRCh38#3027149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74282958-C-A

3027217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282889-T-C

3027279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282853-G-A

3027315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282815-C-T

3027556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282639-C-T

3027717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282488-C-T

http://identifiers.org/hco/17/GRCh38#3027752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74282456-A-C

3027758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282450-A-G

3027781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282421-G-T

3027782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282420-A-G

3027799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282409-G-A

3027906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282316-T-G

3027937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74282293-G-T

http://identifiers.org/hco/17/GRCh38#3028151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74282119-A-C

3028651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74281632-C-T

3028751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74281544-A-G

3029364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74281108-C-T

3029449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74281050-G-A

3029500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74280999-G-A

3030087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74280534-T-C

3030097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74280524-C-T

http://identifiers.org/hco/17/GRCh38#3030460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74280123-A-C

3030460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74280123-A-T

3030595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279992-G-C

3030622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279964-A-G

3030806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279778-T-C

3030995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: synonymous variant
orthologous variants: 74279610-T-C

http://identifiers.org/hco/17/GRCh38#3031024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74279555-C-A

3031024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279555-C-T

http://identifiers.org/hco/17/GRCh38#3031046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74279538-C-A

3031046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279538-C-T

http://identifiers.org/hco/17/GRCh38#3031058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74279526-C-A

3031100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279472-C-G

3031100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279472-C-T

3031250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74279302-T-A

http://identifiers.org/hco/17/GRCh38#3032634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278980-C-A

3032634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278980-C-T

3032645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278969-G-A

3032645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278969-G-T

3032648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278967-G-A

3032656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278959-T-C

3032744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278884-T-C

3032824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278810-G-A

3032949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278717-G-T

http://identifiers.org/hco/17/GRCh38#3032963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278703-C-A

3032963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278703-C-T

3032984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278686-G-A

3032984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278686-G-C

3033018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278652-C-T

3033024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron variant
orthologous variants: 74278639-T-C

3033259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278430-T-C

3033260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278429-G-A

3033260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278429-G-T

http://identifiers.org/hco/17/GRCh38#3033311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278409-C-A

3033311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278409-C-G

http://identifiers.org/hco/17/GRCh38#3033321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278399-C-A

3033321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278399-C-T

http://identifiers.org/hco/17/GRCh38#3033364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278363-C-A

3033364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74278363-C-T

http://identifiers.org/hco/17/GRCh38#3033495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278231-C-A

http://identifiers.org/hco/17/GRCh38#3033596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278157-C-A

3033596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278157-C-T

3033598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278155-T-C

3033615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278148-G-A

3033615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278148-G-T

3033704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278051-G-A

3033704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278051-G-T

http://identifiers.org/hco/17/GRCh38#3033726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74278028-C-A

3033726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278028-C-T

3033727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74278027-T-C

http://identifiers.org/hco/17/GRCh38#3033784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277943-C-A

3033784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277943-C-T

3033884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277892-T-C

3033932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277882-A-G

3033961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277875-T-C

3033962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277874-G-A

3033962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277874-G-T

http://identifiers.org/hco/17/GRCh38#3033968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277868-C-A

3033996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277840-G-A

3033996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277840-G-T

3034024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277813-G-A

3034024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277813-G-C

3034024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277813-G-T

http://identifiers.org/hco/17/GRCh38#3034034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277804-C-A

3034034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277804-C-T

http://identifiers.org/hco/17/GRCh38#3034081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277757-C-A

3034081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277757-C-G

3034081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277757-C-T

http://identifiers.org/hco/17/GRCh38#3034147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277688-C-A

3034147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277688-C-T

3034152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277683-G-C

3034152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277683-G-T

3034298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277613-A-G

3034340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277571-T-C

http://identifiers.org/hco/17/GRCh38#3034354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277558-C-A

3034354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277558-C-T

3034405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277506-G-A

3034405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277506-G-C

3034405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277506-G-T

3034409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277502-G-A

3034409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277502-G-C

3034409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277502-G-T

3034413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277498-T-C

3034421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277489-G-A

3034421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277489-G-T

http://identifiers.org/hco/17/GRCh38#3034432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277478-A-C

3034432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277478-A-G

3034434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277476-G-A

3034434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277476-G-C

3034434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277476-G-T

3034506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277387-G-A

3034612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74277308-A-G

3034695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74277232-G-A

3034695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74277232-G-C

http://identifiers.org/hco/17/GRCh38#3034731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277191-C-A

3034731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277191-C-T

3034750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277172-C-T

http://identifiers.org/hco/17/GRCh38#3034768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277154-C-A

3034768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277154-C-T

3034787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277142-G-A

3034787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277142-G-C

3034787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277142-G-T

3034804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277135-G-A

3034804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277135-G-T

3034855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277062-G-A

http://identifiers.org/hco/17/GRCh38#3034896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74277015-C-A

3034896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74277015-C-T

3035118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276816-T-A

3035118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276816-T-C

3035223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276700-C-G

3035223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276700-C-T

3035347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276574-C-T

3035380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276544-C-T

3035395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276529-G-T

http://identifiers.org/hco/17/GRCh38#3035566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74276398-C-A

3035566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276398-C-T

http://identifiers.org/hco/17/GRCh38#3035649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74276315-C-A

3035649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276315-C-T

http://identifiers.org/hco/17/GRCh38#3035691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74276274-A-C

3035697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276268-A-G

3035698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276267-G-A

3035698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276267-G-T

http://identifiers.org/hco/17/GRCh38#3035701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74276264-C-A

3035701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276264-C-T

3035739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276224-T-C

3035925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276087-A-G

3035948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276064-G-T

3035986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276026-G-A

3035986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276026-G-C

3035986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74276026-G-T

3036127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275911-G-T

3036135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275901-G-A

3036135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275901-G-C

http://identifiers.org/hco/17/GRCh38#3036237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74275797-C-A

3036426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275655-A-G

3036581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275526-G-C

3036600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275509-G-A

3036600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275509-G-T

3036687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275375-A-G

3036734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275316-A-G

3036741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275292-A-G

3036741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275292-A-T

3036915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275095-G-C

3036915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74275095-G-T

http://identifiers.org/hco/17/GRCh38#3037107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74274889-C-A

3037107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274889-C-G

3037107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274889-C-T

3037121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274875-G-A

3037121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274875-G-T

3037173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274827-C-T

3037193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274819-C-T

3037213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274803-G-A

3037288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274735-G-C

3037288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274735-G-T

3037311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274713-T-G

3037348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274676-C-T

3037357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274667-G-A

3037357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274667-G-C

3037357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274667-G-T

3037461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274584-G-A

3037461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274584-G-C

3037461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29176
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74274584-G-T