36970402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047494-G-A

36970403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047495-T-G

36970432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047534-C-T

36970438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047540-G-A

36970547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047638-C-T

36971174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047663-G-A

36972250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79047973-C-T

36972343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79048061-G-A

36972348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79048066-G-A

36972435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79048152-T-C

36972443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79048162-T-C

36972773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79049116-C-T

http://identifiers.org/hco/2/GRCh38#36973223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79049980-A-C

36973314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79050187-T-C

36973314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79050187-T-G

36973321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79050194-G-A

36973455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79050313-T-C

36973716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79050570-T-A

36973759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79050611-T-G

36975746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79053434-G-A

http://identifiers.org/hco/2/GRCh38#36978121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79054704-C-A

36978130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79054713-T-A

36978193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79054764-A-G

36978268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79054831-T-C

36978310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79054872-T-C

36980327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055782-A-G

36980332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055787-A-G

36980355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055810-A-T

36980356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055811-A-G

36980359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055814-C-T

http://identifiers.org/hco/2/GRCh38#36980364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79055819-A-C

36980364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79055819-A-G

36980580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79056018-C-T

36980612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79056047-T-C

36980620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79056055-G-A

36980672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79056106-T-C

36980672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79056106-T-G

36980902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79056341-T-A

36980913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79056352-T-C

36981387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79058122-T-C

36981402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79058135-G-A

36981402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79058135-G-T

36981426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79058155-T-C

http://identifiers.org/hco/2/GRCh38#36981436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79058165-A-C

36981444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79058173-T-A

36981574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79060545-C-T

36981715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79060686-T-C

36985104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79061618-T-A

36985104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79061618-T-G

36985322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79061331-T-A

36985869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79061117-G-C

36985896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79061090-A-G

http://identifiers.org/hco/2/GRCh38#36987466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79062156-C-A

36987659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062266-T-A

36987659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062266-T-C

36988135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062403-T-G

36988195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062455-G-A

http://identifiers.org/hco/2/GRCh38#36988560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79062558-C-A

36988560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062558-C-T

36988621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062615-T-C

36988622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79062616-A-G

36988704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 79062698-C-T

http://identifiers.org/hco/2/GRCh38#36988791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79062785-A-C

36989130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063045-G-A

36989130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063045-G-C

36989451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063082-T-C

36989613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063230-A-G

36989720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063469-C-T

http://identifiers.org/hco/2/GRCh38#36989774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79063524-C-A

36989774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063524-C-T

36989835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063584-T-A

http://identifiers.org/hco/2/GRCh38#36989847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79063596-C-A

36990353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063937-T-C

36990361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063945-G-A

36990426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79063979-T-C

36990483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79064034-T-C

36990504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79064055-T-G

36990660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79064304-T-A

36990660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79064304-T-C

36990750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79064394-T-C

36990750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79064394-T-G

36990765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, missense_variant
orthologous variants: 79064409-C-T

http://identifiers.org/hco/2/GRCh38#36993821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79065331-C-A

36994237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79065906-C-T

http://identifiers.org/hco/2/GRCh38#36994345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79066014-A-C

http://identifiers.org/hco/2/GRCh38#36994418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79066080-C-A

36994418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79066080-C-T

36998317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79066347-A-G

36998446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79066389-T-C

36998822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79066671-C-T

36998824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79066673-C-G

36999352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79067246-T-C

http://identifiers.org/hco/2/GRCh38#36999382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79067276-A-C

37000551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79067808-C-G

37000559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79067816-C-G

37000559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79067816-C-T

37000659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79067915-C-G

http://identifiers.org/hco/2/GRCh38#37000797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79068053-C-A

37000797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79068053-C-T

http://identifiers.org/hco/2/GRCh38#37000852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79068108-A-C

37000867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068123-G-A

37000867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068123-G-C

37000867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068123-G-T

37000962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068533-T-C

37001109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068651-G-A

37001256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068775-G-C

37001396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79068845-G-C

37001972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069076-T-A

37002035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069139-T-G

37002071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069179-G-A

37002071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069179-G-C

37002129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069263-A-G

37002153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069288-A-T

http://identifiers.org/hco/2/GRCh38#37002236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79069360-A-C

37002310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79069433-G-A

37002370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79069493-A-G

37002379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79069502-T-C

37002379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79069502-T-G

37002400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, missense_variant
orthologous variants: 79069523-T-C

37002634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069751-G-A

37002649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79069764-T-G

37003152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070124-G-A

http://identifiers.org/hco/2/GRCh38#37003494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79070331-A-C

37003494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070331-A-G

37003495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070332-G-A

37003495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070332-G-C

http://identifiers.org/hco/2/GRCh38#37003512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79070349-C-A

37003512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070349-C-T

37003588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79070408-T-C

37003647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79070467-G-A

37003647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79070467-G-C

37003736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070555-T-C

37003745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070564-A-G

37003745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070564-A-T

37003771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070589-T-C

37003809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070622-G-A

37003809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070622-G-C

37003809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070622-G-T

37003864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070671-C-G

37003864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79070671-C-T

37004617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79071764-C-G

37004696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79071848-A-T

37004770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79071908-A-G

37004798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79071936-T-C

37004811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79071946-C-T

37004976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79072093-C-G

37004976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79072093-C-T

37005292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79072477-C-T

37005372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79072551-T-G

37005413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79072613-G-A

37005609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79072734-T-C

37005609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79072734-T-G

http://identifiers.org/hco/2/GRCh38#37005644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79072769-A-C

37005677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79072802-G-A

37005677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79072802-G-C

37005683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79072808-T-C

37005766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79072891-T-C

37005805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79073136-T-C

37005805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79073136-T-G

37005825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79073156-A-T

37005947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79073256-A-G

37005972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79073281-T-C

37006755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074049-C-T

37006846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074129-A-G

37006886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074163-G-C

37006896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074173-T-A

http://identifiers.org/hco/2/GRCh38#37006942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074216-C-A

37006942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074216-C-T

37006958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074232-T-C

37006961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074235-A-T

37007254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79074513-G-A

37007254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79074513-G-C

37007300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79074559-T-C

37007307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79074566-G-A

37007307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79074566-G-T

http://identifiers.org/hco/2/GRCh38#37007332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074596-C-A

37007332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074596-C-T

37007354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074622-T-A

37007354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074622-T-G

37007356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074624-T-C

http://identifiers.org/hco/2/GRCh38#37007384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074651-C-A

37007384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074651-C-T

37007390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074657-C-G

37007390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074657-C-T

http://identifiers.org/hco/2/GRCh38#37007415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074681-C-A

37007415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074681-C-T

37007425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074687-C-T

http://identifiers.org/hco/2/GRCh38#37007431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074694-C-A

http://identifiers.org/hco/2/GRCh38#37007432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79074695-C-A

37007434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074697-G-A

37007434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074697-G-C

37007434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79074697-G-T

37007740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075052-C-T

37007744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075056-C-G

37007830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075116-C-T

37007831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075117-T-C

37007889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075173-T-C

37007997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075216-C-T

http://identifiers.org/hco/2/GRCh38#37008016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075232-C-A

37008016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075232-C-G

http://identifiers.org/hco/2/GRCh38#37008035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075248-C-A

37008035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075248-C-G

37008046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075259-G-A

37008046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79075259-G-T

http://identifiers.org/hco/2/GRCh38#37008062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075275-A-C

http://identifiers.org/hco/2/GRCh38#37008171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075364-A-C

37008171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075364-A-G

37008171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075364-A-T

37008184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075379-T-A

37008184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075379-T-G

http://identifiers.org/hco/2/GRCh38#37008218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075415-C-A

37008218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075415-C-T

http://identifiers.org/hco/2/GRCh38#37008225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075422-C-A

37008242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075438-A-G

37008248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075444-T-G

37008280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075467-G-T

37008391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075579-T-A

37008391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075579-T-G

http://identifiers.org/hco/2/GRCh38#37008409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075594-C-A

37008409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075594-C-T

37008412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075597-C-T

http://identifiers.org/hco/2/GRCh38#37008435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075624-C-A

37008459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075648-A-G

37008468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075657-T-A

37008468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075657-T-C

37008468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075657-T-G

http://identifiers.org/hco/2/GRCh38#37008495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075685-C-A

37008495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075685-C-G

37008495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075685-C-T

http://identifiers.org/hco/2/GRCh38#37008501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79075690-A-C

37008509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075698-A-G

37008512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075701-G-A

37008512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075701-G-T

37008538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075726-T-C

37008588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075771-A-G

37008592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075775-C-T

37008600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075784-G-T

37008607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075791-T-A

37008607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79075791-T-C

37008657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79075841-T-A

37008657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79075841-T-C

37008684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79075868-C-T

37008696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79075880-T-C

http://identifiers.org/hco/2/GRCh38#37008863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79076047-A-C

37008881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076062-G-A

http://identifiers.org/hco/2/GRCh38#37008883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79076064-C-A

37008883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076064-C-T

37008888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076069-G-A

37008888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076069-G-T

37008928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076107-G-C

37008942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076121-G-A

37008942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076121-G-C

37008951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076129-G-C

37008951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076129-G-T

37008960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076138-T-C

37008961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076139-T-A

37008961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076139-T-C

37009673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076394-C-T

37009809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076479-A-T

http://identifiers.org/hco/2/GRCh38#37009916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79076591-C-A

http://identifiers.org/hco/2/GRCh38#37010012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79076689-A-C

37010070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076749-T-C

37010095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076770-T-A

37010215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076875-C-T

37010243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79076902-C-T

37010516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077102-A-G

37010516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077102-A-T

37010647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077243-G-A

37010715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077292-C-T

37010754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077305-T-C

37010796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077335-T-G

37010853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077385-T-A

37010864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077396-T-C

37010942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077456-C-T

37010970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077477-C-G

37011008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077516-C-T

37011178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077791-C-T

37011191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077811-G-A

37011332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79077971-T-C

37011524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078201-C-T

37011555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078230-G-A

37011555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078230-G-T

http://identifiers.org/hco/2/GRCh38#37011623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79078290-C-A

37011623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078290-C-T

37011772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078414-G-C

37011772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078414-G-T

37011967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79078589-G-A

37013894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79081020-G-A

37013894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79081020-G-C

37014030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081156-G-A

37014030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081156-G-T

37014048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081173-G-A

37014048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081173-G-C

37014048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081173-G-T

37014057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081183-A-T

37014089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081211-G-A

37014089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081211-G-C

37014089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081211-G-T

37014113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081239-A-G

http://identifiers.org/hco/2/GRCh38#37014146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79081269-C-A

37014146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081269-C-G

37014146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081269-C-T

http://identifiers.org/hco/2/GRCh38#37014148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79081271-A-C

37014148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081271-A-G

37014196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081319-C-T

37014559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79081938-T-G

37017842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79090108-G-A

http://identifiers.org/hco/2/GRCh38#37017994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79090256-C-A

37017994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79090256-C-T

37018345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79090601-G-A

37018641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79090877-C-T

37018789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79091191-G-T

37019233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79091316-T-G

37019260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79091343-T-A

37019329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79091411-G-A

37019413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79091820-T-C

37019801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79095626-C-T

37019839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 79095664-T-C

37020366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098612-G-A

37020366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098612-G-C

37020394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098650-C-T

37020458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098714-T-A

37020458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098714-T-C

37020497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098749-G-A

37020497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098749-G-T

37020527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098769-A-G

37020573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098793-G-A

37020573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098793-G-T

37020592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098806-G-A

37020592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098806-G-T

37020629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098840-G-A

37020629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79098840-G-T

37020852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79099061-G-A

37020852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79099061-G-C

37020852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79099061-G-T

37021168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79099321-T-A

37024627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79100340-A-G

37025069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79100754-T-C

http://identifiers.org/hco/2/GRCh38#37025336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79100954-C-A

http://identifiers.org/hco/2/GRCh38#37027786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79102407-A-C

37027786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102407-A-G

37027862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102460-G-C

37027862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102460-G-T

37027910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102511-A-G

37028004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79102605-T-C

37028089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79102690-G-C

37028186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102787-A-G

37028198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102799-G-A

37028198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102799-G-C

37028198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102799-G-T

http://identifiers.org/hco/2/GRCh38#37028273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79102875-C-A

http://identifiers.org/hco/2/GRCh38#37028284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79102886-C-A

37028284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102886-C-T

37028397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79102991-C-T

37028411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103005-C-T

37028539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103124-G-A

37028539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103124-G-C

37028539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103124-G-T

37028612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103182-T-C

37028632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103202-A-G

37028654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103224-T-G

37028739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103309-T-A

37028739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103309-T-C

37028739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103309-T-G

37028829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103399-T-C

http://identifiers.org/hco/2/GRCh38#37028838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79103408-A-C

37028898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103468-C-G

37028927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79103497-G-A

37028962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103533-G-A

37028962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103533-G-C

37028999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103569-T-C

http://identifiers.org/hco/2/GRCh38#37029088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79103641-A-C

37032584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79103773-A-G

37032693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103877-C-T

37032753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79103937-A-G

http://identifiers.org/hco/2/GRCh38#37032789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79103981-A-C

37036229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79108152-T-C

37036342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79108260-T-C

37036503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79108370-T-C

37037002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79108681-T-G

37037274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79108809-T-G

37037834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109021-A-G

http://identifiers.org/hco/2/GRCh38#37037843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79109030-C-A

37037843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109030-C-T

37037888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79109075-A-G

37038032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79109220-A-G

37038042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109230-A-G

37038042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109230-A-T

37038053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109241-T-A

37038137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109324-G-A

37038137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109324-G-C

37038137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79109324-G-T

37040070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110087-G-C

37040184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110652-G-A

37040184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110652-G-C

37040214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110681-A-G

37040214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110681-A-T

37040226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110693-T-C

37040270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110736-G-A

37040270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79110736-G-T

http://identifiers.org/hco/2/GRCh38#37040471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79110943-C-A

37040471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79110943-C-T

http://identifiers.org/hco/2/GRCh38#37040561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79111032-C-A

37040561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111032-C-T

http://identifiers.org/hco/2/GRCh38#37040563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79111034-A-C

37040563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111034-A-T

37040595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111070-A-G

37040607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111082-T-C

37040661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111187-T-G

37040666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111192-A-G

37040917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79111415-A-G

37041007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79113168-A-G

37041034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79113195-G-A

37041034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79113195-G-C

37041034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79113195-G-T

http://identifiers.org/hco/2/GRCh38#37041041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79113202-C-A

37041041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79113202-C-T

37041145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79113388-G-A

37041145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79113388-G-T

37041241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79113484-A-G

37041249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79113492-A-G

37041303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113544-G-C

37041305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113546-T-C

37041308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113549-T-C

37041324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113565-T-A

37041324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113565-T-G

37041366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113607-A-G

37041376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79113617-A-G

http://identifiers.org/hco/2/GRCh38#37041396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79113638-A-C

37048923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115182-T-C

37049218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115401-G-T

37049328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115480-G-A

http://identifiers.org/hco/2/GRCh38#37049507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79115608-A-C

37049507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115608-A-G

37049507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115608-A-T

37049600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115710-T-A

37049610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79115720-C-G

37049685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79115791-A-G

37050299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116091-A-G

37050393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116175-C-T

37050463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116245-T-G

37050658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116287-C-T

37051590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116625-C-G

37052133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116827-G-A

37052152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116846-C-G

37052217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116913-G-C

37052259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79116955-T-C

37053185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117237-G-C

37053231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117283-A-G

37053239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117291-T-C

37053356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117408-G-A

37053356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117408-G-T

37053377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117429-C-G

37053401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117834-G-A

37053401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117834-G-C

http://identifiers.org/hco/2/GRCh38#37053429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79117866-C-A

37053429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117866-C-G

37053476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117907-G-C

37053476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117907-G-T

37053478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79117909-A-G

http://identifiers.org/hco/2/GRCh38#37053670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79118322-C-A

37053670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79118322-C-T

37053705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79118356-T-A

37053705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79118356-T-C

http://identifiers.org/hco/2/GRCh38#37053710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79118361-C-A

37053710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79118361-C-T

37053760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79118406-T-C

37055485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79119787-A-G

37055960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120118-T-C

37055981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120139-C-T

37055983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120140-A-G

37056225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120320-A-G

37056246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120338-T-C

37056317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120412-G-A

37056317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120412-G-C

37056317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120412-G-T

37056368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120457-G-A

37056368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120457-G-T

37056384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120473-T-C

37056384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120473-T-G

37056403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120488-T-C

37056422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79120506-G-T

http://identifiers.org/hco/2/GRCh38#37056428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79120512-C-A

http://identifiers.org/hco/2/GRCh38#37056472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79120556-A-C

http://identifiers.org/hco/2/GRCh38#37056647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79120730-A-C

37056647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120730-A-G

37056648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120731-T-C

37056654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120737-T-C

37056657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120740-G-A

37056729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120795-A-G

37056735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120801-T-C

37056735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120801-T-G

37056751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120817-A-G

37056757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120823-G-A

37056757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120823-G-C

http://identifiers.org/hco/2/GRCh38#37056863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79120934-C-A

37056863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79120934-C-T

http://identifiers.org/hco/2/GRCh38#37057175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79121391-C-A

37057189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121398-T-G

37057207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121411-T-C

http://identifiers.org/hco/2/GRCh38#37057241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79121450-C-A

37057241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121450-C-T

37057265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121471-G-A

37057265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121471-G-C

37057265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121471-G-T

37057329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79121513-T-A

37057329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79121513-T-G

37057422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79121606-T-A

37057494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121678-C-T

37057501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121685-T-A

37057522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79121702-T-C

37058191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122646-T-C

37058321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122785-A-G

37058323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122787-G-A

37058323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122787-G-T

37058338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122802-G-A

37058338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122802-G-T

37058352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122816-G-A

37058352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122816-G-T

37058355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122819-C-G

37058361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122825-G-T

37058365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122829-G-A

37058365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122829-G-T

37058390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122852-A-T

37058422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122892-T-A

http://identifiers.org/hco/2/GRCh38#37058424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79122894-A-C

37058424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122894-A-G

37058426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122896-C-G

37058426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122896-C-T

http://identifiers.org/hco/2/GRCh38#37058431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79122901-A-C

http://identifiers.org/hco/2/GRCh38#37058436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79122906-A-C

37058439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79122909-T-C

37058536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79123004-A-G

37058630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123111-T-C

37058630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123111-T-G

37058634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123115-T-A

37058634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123115-T-C

37058639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123120-G-A

37058639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123120-G-T

37058696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123174-T-C

37058836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123389-A-G

37058836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123389-A-T

http://identifiers.org/hco/2/GRCh38#37058838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79123391-A-C

37058845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123514-A-G

37058876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123616-T-A

37058876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123616-T-C

37058890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79123663-T-C

http://identifiers.org/hco/2/GRCh38#37058938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79123711-C-A

37058938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79123711-C-T

http://identifiers.org/hco/2/GRCh38#37058947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79123720-A-C

37058998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123771-T-C

37059027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123794-T-C

37059031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123798-G-A

37059031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123798-G-C

37059031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123798-G-T

37059158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79123920-C-T

37059832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124252-T-A

37059902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124311-G-C

37059914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124323-G-A

37059954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124361-C-T

37059978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124374-G-A

37060084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124477-A-T

37060097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124490-T-C

http://identifiers.org/hco/2/GRCh38#37060228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79124597-C-A

37060302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124624-T-A

37060470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124776-T-C

37060470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124776-T-G

37060537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124836-A-G

37060537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79124836-A-T

37060729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79125050-T-A

37060729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79125050-T-C

37060747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125068-T-C

37060750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125072-G-A

37060750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125072-G-C

37060750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125072-G-T

37060803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125121-T-C

37060803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125121-T-G

37060944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125423-T-A

37060955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125434-C-T

http://identifiers.org/hco/2/GRCh38#37060957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79125436-A-C

37061096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125552-G-C

37061194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125636-T-C

37061297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125723-G-A

http://identifiers.org/hco/2/GRCh38#37061409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79125816-C-A

37061474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125872-G-A

http://identifiers.org/hco/2/GRCh38#37061560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79125957-C-A

37061560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79125957-C-T

37061787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79126152-T-C

37061905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79126208-G-T

37061976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79126272-T-C

http://identifiers.org/hco/2/GRCh38#37062124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79126424-C-A

37062124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79126424-C-T

37063379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127056-C-T

37063384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127061-A-G

37063434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127114-A-G

37063447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127125-T-C

37063580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127227-G-A

http://identifiers.org/hco/2/GRCh38#37063664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79127295-A-C

37063766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127390-A-G

37064151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127559-A-G

37064564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127867-G-A

37064649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127945-G-A

37064649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127945-G-C

37064649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127945-G-T

http://identifiers.org/hco/2/GRCh38#37064656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79127952-C-A

37064656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127952-C-T

37064675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127971-G-T

http://identifiers.org/hco/2/GRCh38#37064679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79127975-C-A

37064679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127975-C-G

37064679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79127975-C-T

37064729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79128039-C-T

http://identifiers.org/hco/2/GRCh38#37064732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79128042-C-A

37064732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79128042-C-T

http://identifiers.org/hco/2/GRCh38#37065008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79128317-A-C

37065026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79128335-G-T

37065165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79128463-T-A

37065295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79128618-C-T

37065609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79128774-T-C

37065843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79128932-A-G

37065942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129029-G-A

37065942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129029-G-T

37065952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129039-T-A

37065952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129039-T-C

37065954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129041-G-A

37065954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129041-G-T

37065981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129066-T-G

37066009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129094-T-C

http://identifiers.org/hco/2/GRCh38#37066011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79129096-C-A

37066011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129096-C-T

37066081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129347-A-G

37066374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129763-A-T

37066428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129816-T-A

37066428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129816-T-C

37066431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129819-C-T

37066499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129889-A-G

37066509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129899-T-C

37066529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129914-T-A

37066556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79129941-T-A

http://identifiers.org/hco/2/GRCh38#37066661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79130035-C-A

37066888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130170-G-T

37066925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130202-G-A

37066928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130205-G-A

37066945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130222-C-G

37067018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130288-C-T

37067244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130419-T-C

37067466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130607-T-C

http://identifiers.org/hco/2/GRCh38#37067830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79130646-A-C

37067969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130762-T-A

37067991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130772-T-C

37067991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79130772-T-G

37068216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79131244-G-A

37068216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79131244-G-C

37068666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79131906-G-A

37068670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79131910-C-G

37068715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79131959-G-A

37068715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79131959-G-C

37068718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: missense variant
orthologous variants: 79131962-T-G

http://identifiers.org/hco/2/GRCh38#37068766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79132010-A-C

37068778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79132022-G-A

37068817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79132061-A-G

http://identifiers.org/hco/2/GRCh38#37068950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79132195-C-A

37068950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79132195-C-T

37068958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79132203-G-C

37068958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79132203-G-T

37069477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79132954-T-C

37069649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133119-T-C

37069661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133131-C-T

37069674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133148-C-T

37069734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133185-T-C

37070207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133638-T-C

37070213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133644-A-G

37070213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133644-A-T

37070214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133645-C-T

http://identifiers.org/hco/2/GRCh38#37070317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79133748-A-C

37070320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79133751-C-T

37070395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79133826-G-C

37070428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133859-T-C

37070428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133859-T-G

http://identifiers.org/hco/2/GRCh38#37070478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79133925-C-A

37070478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79133925-C-T

37070650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134055-T-G

37070846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134421-C-G

37070846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134421-C-T

37071011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134620-T-C

37071294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134854-G-A

37071294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79134854-G-T

http://identifiers.org/hco/2/GRCh38#37071332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79134888-C-A

37071626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135171-T-A

37071626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135171-T-C

37071628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135173-C-T

37071669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135209-C-T

37072050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135317-G-T

37072083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135331-G-C

37072083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79135331-G-T

37072237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79135488-A-G

37072326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135580-C-T

http://identifiers.org/hco/2/GRCh38#37072363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79135614-C-A

37072363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135614-C-G

37072363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135614-C-T

37072364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135615-T-A

37072364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135615-T-C

37072364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135615-T-G

37072415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135662-A-G

37072415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135662-A-T

37072424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135669-G-C

37072424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79135669-G-T

37075029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136510-A-T

37075136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136599-G-C

37075140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136603-T-C

37075194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136654-T-C

http://identifiers.org/hco/2/GRCh38#37075215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79136675-A-C

37075226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136686-G-T

37075357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136802-T-C

37075380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136825-T-C

37075428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136865-G-A

37075428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136865-G-T

37075437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136874-A-G

37075451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136888-A-G

37075455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136892-A-G

37075455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79136892-A-T

37075569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79137006-T-C

37075572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79137009-T-C

37075640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79137077-C-T

37075642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79137079-T-C

37075642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79137079-T-G

http://identifiers.org/hco/2/GRCh38#37075653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137090-C-A

37075653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137090-C-T

http://identifiers.org/hco/2/GRCh38#37075701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137145-A-C

37075701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137145-A-G

37075726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137168-G-A

37075726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137168-G-T

http://identifiers.org/hco/2/GRCh38#37075735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137177-C-A

37075751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137188-A-T

37075754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137191-T-C

37075823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137252-T-A

37075823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137252-T-C

37075825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137254-T-C

37075846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137274-T-A

37075881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79137289-G-T

37076384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137576-T-A

37076420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137599-T-A

37076420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137599-T-C

http://identifiers.org/hco/2/GRCh38#37076539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137688-C-A

37076594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137729-C-T

37076667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137784-G-A

37076777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137877-A-G

http://identifiers.org/hco/2/GRCh38#37076821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137921-C-A

37076821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137921-C-T

http://identifiers.org/hco/2/GRCh38#37076843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79137946-C-A

37076843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137946-C-T

37076859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137964-T-A

37076859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79137964-T-C

http://identifiers.org/hco/2/GRCh38#37077019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79138096-C-A

http://identifiers.org/hco/2/GRCh38#37077108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79138308-C-A

http://identifiers.org/hco/2/GRCh38#37078999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79138681-C-A

http://identifiers.org/hco/2/GRCh38#37079022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79138704-C-A

37079022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79138704-C-G

37079022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79138704-C-T

http://identifiers.org/hco/2/GRCh38#37079023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79138705-C-A

37079023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79138705-C-T

37079146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 79138829-G-C

37079146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 79138829-G-T

37079341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139024-A-G

37079397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139079-T-A

37079422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139100-C-T

37079537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139211-G-C

http://identifiers.org/hco/2/GRCh38#37079577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79139255-C-A

37079642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139300-T-C

37080131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139721-G-A

37080141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139731-T-A

37080141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139731-T-C

37080197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139787-G-A

37080233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79139809-A-G

37080489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79140075-T-C

37080655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79140163-C-T

37080663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79140171-T-A

37083138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141376-G-A

37083138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141376-G-C

37083138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141376-G-T

37083170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141428-C-T

37083194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141456-T-A

37083194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141456-T-C

37083194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141456-T-G

37083216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141474-G-A

37083274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141511-A-T

37083346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 79141582-T-G

37083382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: synonymous variant
orthologous variants: 79141618-T-C

37083465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141982-G-A

37083465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141982-G-C

37083465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79141982-G-T

37083487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142005-A-T

37083566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142101-G-A

37083650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142181-G-C

37083663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142194-A-G

37083670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142201-G-A

37083670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142201-G-T

37083709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: 79142276-T-C

http://identifiers.org/hco/2/GRCh38#37083892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79142392-C-A

37083906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: intron_variant, undefined
orthologous variants: 79142399-T-C

http://identifiers.org/hco/2/GRCh38#37084294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79142761-C-A

37084316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5 prime UTR variant
orthologous variants: 79142772-G-A

http://identifiers.org/hco/2/GRCh38#37084353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79142809-C-A

37084353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79142809-C-T

http://identifiers.org/hco/2/GRCh38#37084368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79142824-A-C

37084368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29273
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79142824-A-G