57092639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95259703-G-A

57092639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95259703-G-T

57092714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95259773-C-T

57092791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: splice donor variant
orthologous variants: 95259838-G-T

http://identifiers.org/hco/16/GRCh38#57092913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95259920-C-A

57092913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95259920-C-T

57092919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95259927-A-G

57093179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95260132-C-T

57093215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95260148-T-A

57093215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95260148-T-C

http://identifiers.org/hco/16/GRCh38#57093453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95260366-C-A

57093453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95260366-C-T

57093713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95260628-A-G

http://identifiers.org/hco/16/GRCh38#57093836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95261160-C-A

57093836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261160-C-G

57093999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95261319-G-A

http://identifiers.org/hco/16/GRCh38#57094018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95261338-C-A

57094018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95261338-C-G

57094018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95261338-C-T

http://identifiers.org/hco/16/GRCh38#57094185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95261511-C-A

57094238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261604-G-T

57094276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261643-T-A

57094294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261661-A-G

57094381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261733-G-A

57094643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261963-C-G

57094643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95261963-C-T

57094835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262192-T-C

57094976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262298-T-C

57095007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262316-C-T

57095211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262469-A-G

57095513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262629-C-T

57095520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262636-C-T

57095799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262702-T-C

57095929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95262811-C-T

57096202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95263045-G-T

57098246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95264152-C-G

57098246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95264152-C-T

57098516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95264428-T-C

57098567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95264479-G-A

57098668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95264572-C-T

57099125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95265750-C-T

57099552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95266051-A-G

57100307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95266217-G-A

57100473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95266383-G-A

57100473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95266383-G-T

57100922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95267053-A-T

57101396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95267512-C-G

57101409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95267527-A-G

57101614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95267685-C-T

57101828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95267808-G-T

57104502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95269449-A-T

57104518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95269459-G-A

http://identifiers.org/hco/16/GRCh38#57104545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95269482-A-C

57105012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95269914-G-A

57105192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270045-G-A

57105192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270045-G-T

57105198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270051-G-T

57105468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270306-C-T

57105551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270350-T-C

57105929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270691-G-A

57105988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270741-A-G

http://identifiers.org/hco/16/GRCh38#57106005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95270755-C-A

57106068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95270820-G-T

57106102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95270853-T-C

57106103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95270854-T-C

57106187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95270938-T-C

http://identifiers.org/hco/16/GRCh38#57106263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95271025-C-A

57106263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271025-C-T

57106268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271030-C-T

57106273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271035-G-T

57106478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271182-G-A

57106478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271182-G-T

57106526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271224-G-A

57106526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271224-G-T

57106668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271338-G-A

57106928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271887-G-C

57106986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95271948-A-G

57107081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95272040-T-C

57107389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95272334-T-C

57108599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95273964-G-A

57108730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95274087-C-T

57110230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95274672-T-C

57110342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95274705-A-G

57110656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95274904-G-A

57110656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95274904-G-T

57110664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95274912-G-T

http://identifiers.org/hco/16/GRCh38#57110672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95274922-C-A

57110672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95274922-C-T

57110925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275176-G-A

57110985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275213-T-A

57110985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275213-T-C

57110985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275213-T-G

http://identifiers.org/hco/16/GRCh38#57110995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95275219-C-A

57110995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275219-C-G

57110995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275219-C-T

57111007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275231-A-G

57111038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275259-G-A

57111038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275259-G-T

57111039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275260-G-T

57111526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95275751-G-A

57112025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95276231-G-A

57112125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95276432-C-T

http://identifiers.org/hco/16/GRCh38#57112580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95276865-C-A

http://identifiers.org/hco/16/GRCh38#57112668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95276939-C-A

57112668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95276939-C-T

57112675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95276946-C-T

57112676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95276947-A-G

http://identifiers.org/hco/16/GRCh38#57112728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95277000-C-A

http://identifiers.org/hco/16/GRCh38#57112878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95277432-C-A

http://identifiers.org/hco/16/GRCh38#57112900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95277454-C-A

57112976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95277526-G-C

57112976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95277526-G-T

57113065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95277592-T-C

http://identifiers.org/hco/16/GRCh38#57113130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95277637-C-A

57113130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95277637-C-G

57113167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 95277674-G-T

57113281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 95277791-C-T

http://identifiers.org/hco/16/GRCh38#57113392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95277902-C-A

57113392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95277902-C-G

57113392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95277902-C-T

57113458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: synonymous variant
orthologous variants: 95277968-C-T

57113485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95277995-G-A

57113485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95277995-G-T

http://identifiers.org/hco/16/GRCh38#57113517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95278053-C-A

http://identifiers.org/hco/16/GRCh38#57113518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95278054-C-A

http://identifiers.org/hco/16/GRCh38#57115592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95278489-A-C

57115802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95278759-C-T

57116071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279000-C-T

57116290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279175-G-T

57116619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279358-C-T

57117196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279736-G-A

57117386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279883-T-A

57117453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95279927-G-C

http://identifiers.org/hco/16/GRCh38#57117498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95280020-C-A

57117498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 95280020-C-T

57117734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95280236-G-A

57118952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281084-G-A

57118957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281091-A-G

http://identifiers.org/hco/16/GRCh38#57119055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281165-C-A

57119055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281165-C-G

57119067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281181-G-T

57119068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281182-G-A

57119068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281182-G-T

http://identifiers.org/hco/16/GRCh38#57119102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281213-C-A

http://identifiers.org/hco/16/GRCh38#57119104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281215-C-A

57119142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281253-C-T

57119156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281267-G-A

57119349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281434-A-G

57119396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281452-G-A

57119396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281452-G-C

57119396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281452-G-T

http://identifiers.org/hco/16/GRCh38#57119397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281453-C-A

57119397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281453-C-T

57119457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281483-G-A

57119457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281483-G-T

57119465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281491-G-T

57119468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281494-T-C

http://identifiers.org/hco/16/GRCh38#57119546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281543-C-A

57119584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: synonymous variant
orthologous variants: 95281581-T-A

57119584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: synonymous variant
orthologous variants: 95281581-T-C

57119620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: synonymous variant
orthologous variants: 95281617-G-A

57119666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281662-G-A

57119666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281662-G-T

57119675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281670-T-C

http://identifiers.org/hco/16/GRCh38#57119676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281671-C-A

57119676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281671-C-G

57119676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281671-C-T

57119749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281744-T-A

57119749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281744-T-G

57119789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281775-T-A

57119789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281775-T-C

http://identifiers.org/hco/16/GRCh38#57119802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95281788-C-A

57119802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281788-C-T

57120879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281933-C-T

57120912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281962-C-G

57120912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95281962-C-T

http://identifiers.org/hco/16/GRCh38#57120967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282018-C-A

57120969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282020-A-G

57120969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282020-A-T

57121002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282051-G-A

57121002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282051-G-T

http://identifiers.org/hco/16/GRCh38#57121073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282117-C-A

57121073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282117-C-G

57121077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282121-G-T

http://identifiers.org/hco/16/GRCh38#57121085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282129-C-A

57121178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: missense variant
orthologous variants: 95282222-G-A

http://identifiers.org/hco/16/GRCh38#57121210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282256-C-A

57121210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282256-C-G

57121210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282256-C-T

57121247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282292-G-A

57121247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282292-G-T

57121259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282304-G-A

57121259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282304-G-T

http://identifiers.org/hco/16/GRCh38#57121295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282342-C-A

http://identifiers.org/hco/16/GRCh38#57121303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95282350-C-A

57121303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282350-C-T

57121322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282370-T-C

57121532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282457-G-A

57121532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282457-G-C

57121532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282457-G-T

57121559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282484-G-T

57121597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282520-G-A

57121597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282520-G-C

57121960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282765-A-G

57122019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282822-C-T

57122086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95282901-T-C

57122396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283207-C-T

http://identifiers.org/hco/16/GRCh38#57122553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95283313-A-C

http://identifiers.org/hco/16/GRCh38#57122675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95283396-C-A

57122728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283445-G-A

57122762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283480-T-G

57122797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283499-C-T

57122952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283613-T-G

57123160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283857-A-G

57123246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283901-G-A

57123246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283901-G-C

57123246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283901-G-T

57123277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283931-G-C

57123277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron variant
orthologous variants: 95283931-G-T

57123364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284001-G-T

http://identifiers.org/hco/16/GRCh38#57123505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95284125-C-A

57123505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284125-C-G

57123533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284158-G-A

57123533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284158-G-T

57123600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284213-G-A

57123600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284213-G-T

57123610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284223-G-A

57123655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284264-G-A

57123655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284264-G-T

57123692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95284297-G-T

57125988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95284881-C-T

57126044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284938-G-A

57126070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284964-G-A

57126111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284989-G-T

57126132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285010-A-G

57126187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285065-G-A

http://identifiers.org/hco/16/GRCh38#57126219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95285097-A-C

57126300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285188-A-T

57126349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285253-C-G

57126899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285690-C-T

57126991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285766-C-T

57127300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286044-G-C

57127300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286044-G-T

57127421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286208-T-C

57127450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286246-G-T

57127456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95286253-A-G

57127708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286572-C-T

57127732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286582-G-A

57127732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286582-G-T

57127760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286603-T-C

57127797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286689-G-A

57127797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286689-G-T

57127804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286697-G-A

http://identifiers.org/hco/16/GRCh38#57127915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95286802-C-A

57127915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286802-C-T

57127916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286803-G-A

57127916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286803-G-T

http://identifiers.org/hco/16/GRCh38#57127971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95286845-C-A

57127988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286857-T-C

57128041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286908-A-G

57128041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286908-A-T

57130444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287077-C-T

57130649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287277-G-C

57130819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287403-G-A

57130879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287457-G-A

57130890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287465-G-A

57130986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287536-G-A

57130988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287538-T-A

57131011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287559-G-A

57131122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287680-C-T

57131318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287847-C-T

57131473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288000-G-A

57131512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288037-G-A

57131724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288263-C-T

57131950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288447-C-T

57132034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288528-G-A

57134192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288873-G-C

57134244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288923-C-T

57134270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288949-G-C

57134274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288953-T-A

57134291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95288969-C-T

57134326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289003-C-G

57134504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289179-G-C

57134629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289259-G-A

57134629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289259-G-T

57134635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289261-T-A

57134635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289261-T-G

57134653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289279-G-A

http://identifiers.org/hco/16/GRCh38#57134725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95289316-C-A

57134725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289316-C-T

57134738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289329-C-T

57134739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289330-G-A

57134739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289330-G-C

57134837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289428-G-A

57134837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289428-G-T

57134886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289446-G-C

57134886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289446-G-T

57134990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289552-G-C

57135143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289716-A-G

http://identifiers.org/hco/16/GRCh38#57135272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95289824-C-A

57135272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289824-C-G

57135272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95289824-C-T

57136958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95290417-A-G

http://identifiers.org/hco/16/GRCh38#57137062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95290508-A-C

57137062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95290508-A-G

http://identifiers.org/hco/16/GRCh38#57137071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95290517-A-C

57137097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95290538-T-A

57137097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95290538-T-C

57137139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95290579-C-T

57137228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95290664-C-T

57137234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95290670-C-T

57141483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95291463-A-G

57141535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95291511-A-G

57141542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95291518-G-T

57141564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95291539-A-G

57141690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95291648-A-G

57142014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95292024-C-T

http://identifiers.org/hco/16/GRCh38#57142036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95292046-C-A

57142037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292047-A-T

57142044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292054-G-A

57142044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292054-G-T

57142115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292108-G-A

57142115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292108-G-T

http://identifiers.org/hco/16/GRCh38#57142155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95292139-C-A

57142155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292139-C-T

57142157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292141-G-A

57142178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292154-T-C

57142281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292263-G-A

http://identifiers.org/hco/16/GRCh38#57142318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95292303-C-A

57142347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292334-A-G

57142401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292403-T-C

57142406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292408-G-T

57142439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292439-G-T

57142443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292443-T-A

57142443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292443-T-C

http://identifiers.org/hco/16/GRCh38#57142509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95292510-C-A

57142509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292510-C-T

http://identifiers.org/hco/16/GRCh38#57142521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95292522-C-A

57142521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292522-C-G

57142521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292522-C-T

57142629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292628-G-A

57142629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292628-G-T

57142826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292786-T-C

57142883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292837-A-G

57142909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292861-G-T

57142960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95292918-G-T

http://identifiers.org/hco/16/GRCh38#57143017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293009-C-A

http://identifiers.org/hco/16/GRCh38#57143064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293042-C-A

57143064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293042-C-T

http://identifiers.org/hco/16/GRCh38#57143111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293070-C-A

57143144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293107-G-T

57143187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293148-T-A

57143187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293148-T-C

57143370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293207-G-A

http://identifiers.org/hco/16/GRCh38#57143450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293285-C-A

57143450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293285-C-T

http://identifiers.org/hco/16/GRCh38#57143554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293372-C-A

57143612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293421-G-A

57143652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293452-C-T

57143683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293479-T-A

57143683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293479-T-C

http://identifiers.org/hco/16/GRCh38#57143704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293501-C-A

57143704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293501-C-T

57143748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293555-G-T

http://identifiers.org/hco/16/GRCh38#57143774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293580-C-A

57143775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293581-T-C

57143844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293594-A-G

http://identifiers.org/hco/16/GRCh38#57143892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293636-C-A

57143892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293636-C-T

57143938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293664-A-G

57143956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293682-T-C

http://identifiers.org/hco/16/GRCh38#57143966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293692-C-A

57143966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293692-C-T

57143985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293711-G-A

57143985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293711-G-T

57144001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293727-G-T

57144049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293775-A-G

57144090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293812-C-T

57144113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293837-G-A

http://identifiers.org/hco/16/GRCh38#57144248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95293961-C-A

57144248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293961-C-T

57144294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293986-G-A

57144294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95293986-G-T

http://identifiers.org/hco/16/GRCh38#57144384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294074-C-A

57144432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294103-G-T

57144460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294131-G-A

http://identifiers.org/hco/16/GRCh38#57144469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294133-C-A

http://identifiers.org/hco/16/GRCh38#57144498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294163-C-A

57144498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294163-C-G

57144541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294211-G-T

57144548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294218-A-G

http://identifiers.org/hco/16/GRCh38#57144567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294232-C-A

57144567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294232-C-G

http://identifiers.org/hco/16/GRCh38#57144573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294237-C-A

http://identifiers.org/hco/16/GRCh38#57144627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294294-C-A

57144627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294294-C-T

57145003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294414-A-G

57145466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294783-A-G

57145531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294845-T-C

57145585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294896-G-A

57145585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294896-G-T

57145650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294957-G-A

57145650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294957-G-T

http://identifiers.org/hco/16/GRCh38#57145669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294960-C-A

57145669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294960-C-T

57145679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294970-G-A

57145707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95294993-A-T

http://identifiers.org/hco/16/GRCh38#57145708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95294994-C-A

57145796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295082-T-C

57145799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295085-A-G

57145799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295085-A-T

57146029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95295165-G-A

57146066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295197-G-A

57146066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295197-G-C

57146066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295197-G-T

57146111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 95295245-G-A

57146114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 95295248-C-T

http://identifiers.org/hco/16/GRCh38#57146142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295276-C-A

57146142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95295276-C-G

57146142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95295276-C-T

57146195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95295329-C-T

57146204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 95295338-T-C

57146234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95295368-T-A

57146234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95295368-T-C

57146455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295538-G-T

http://identifiers.org/hco/16/GRCh38#57146458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295541-C-A

57146458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295541-C-T

http://identifiers.org/hco/16/GRCh38#57146462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295545-C-A

57146462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295545-C-G

57146462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295545-C-T

http://identifiers.org/hco/16/GRCh38#57146463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295546-C-A

57146516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295596-G-C

57146516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295596-G-T

57146517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295597-T-A

57146517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295597-T-G

57146543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295623-G-T

http://identifiers.org/hco/16/GRCh38#57146553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295633-C-A

57146553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295633-C-T

57146585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295667-G-C

57146593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295675-G-C

57146593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295675-G-T

57146660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295728-G-A

57146660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295728-G-C

57146660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295728-G-T

57146671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295742-T-G

57146805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295889-G-A

57146805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295889-G-T

http://identifiers.org/hco/16/GRCh38#57146827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95295909-C-A

57146827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295909-C-G

57146827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95295909-C-T

http://identifiers.org/hco/16/GRCh38#57147045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95296167-A-C

57147045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296167-A-G

57147246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296320-T-C

57147273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296358-A-G

57147273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296358-A-T

57147275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296360-A-G

http://identifiers.org/hco/16/GRCh38#57147282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95296367-C-A

57147282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296367-C-T

57147357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296428-G-A

57147357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296428-G-T

57147399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296466-A-G

57147510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296561-T-C

57147510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95296561-T-G

57147686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95296732-G-A

57147686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95296732-G-T

57147833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95296886-G-A

57147833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95296886-G-T

57147876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95296929-C-T

http://identifiers.org/hco/16/GRCh38#57147980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95297032-A-C

http://identifiers.org/hco/16/GRCh38#57148079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95297109-C-A

57148222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: 95297257-G-C

57148222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: 95297257-G-T

http://identifiers.org/hco/16/GRCh38#57148291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95297301-C-A

57148298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: 95297308-A-G

57148319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2315
most severe consequence: 3 prime UTR variant
orthologous variants: 95297331-A-G