http://identifiers.org/hco/10/GRCh38#30014043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4683331-C-A

http://identifiers.org/hco/10/GRCh38#30014063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4683311-C-A

30014063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4683311-C-T

http://identifiers.org/hco/10/GRCh38#30014176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4683224-C-A

30014264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4683147-T-C

30014345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4683103-G-A

30014518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682987-A-G

30014901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682855-A-G

http://identifiers.org/hco/10/GRCh38#30014923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682832-C-A

30014923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682832-C-T

http://identifiers.org/hco/10/GRCh38#30014959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682795-C-A

30015071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682675-C-T

30015079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682667-G-T

http://identifiers.org/hco/10/GRCh38#30015092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682654-A-C

30015190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682572-C-T

30015201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682561-T-A

http://identifiers.org/hco/10/GRCh38#30015451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682331-A-C

http://identifiers.org/hco/10/GRCh38#30015513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682271-A-C

http://identifiers.org/hco/10/GRCh38#30015659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4682134-C-A

30015659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4682134-C-G

http://identifiers.org/hco/10/GRCh38#30015870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4681988-C-A

30015877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681980-C-T

30016000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681879-C-T

http://identifiers.org/hco/10/GRCh38#30016355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4681607-C-A

30016370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681592-G-A

30016402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681566-G-A

30016407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681561-A-G

30016559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681433-T-C

http://identifiers.org/hco/10/GRCh38#30016691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4681288-C-A

30016917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4681073-G-T

http://identifiers.org/hco/10/GRCh38#30017309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4680705-C-A

30017356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4680663-G-T

http://identifiers.org/hco/10/GRCh38#30017400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4680621-C-A

30017841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 3 prime UTR variant
orthologous variants: 4680298-A-T

30018215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4679957-G-A

30018236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4679936-T-C

30018402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4679513-G-C

30026065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4676203-T-C

30026065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4676203-T-G

30026073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4676195-G-T

30026138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4676130-T-G

30026304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: stop gained
orthologous variants: 4675982-G-A

30026304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4675982-G-T

http://identifiers.org/hco/10/GRCh38#30026428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4675858-A-C

30026717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4675614-G-A

30026717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4675614-G-C

30026717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4675614-G-T

http://identifiers.org/hco/10/GRCh38#30026730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4675601-C-A

30026730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4675601-C-T

30026926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4675405-T-G

30027037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4675297-A-T

30027078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4675250-T-G

30027161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4675167-G-C

30027359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674975-G-T

30027389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674945-A-G

30027410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674924-G-T

30027437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674893-C-T

30027452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674885-G-A

30027452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674885-G-C

30027452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674885-G-T

30027474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674863-G-A

30027511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4674837-C-T

30027537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674812-G-A

30027537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674812-G-C

30027537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense_variant, undefined
orthologous variants: 4674812-G-T

30027752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674612-C-G

30027752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674612-C-T

30027767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674597-T-A

30027795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674587-A-G

30027795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674587-A-T

30027936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674446-T-C

30027937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4674445-A-G

30028000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4674382-T-C

30028288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4674097-T-C

30028293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674092-G-C

30028299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674086-G-A

30028313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4674072-C-T

http://identifiers.org/hco/10/GRCh38#30028577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4673817-C-A

30028579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673815-C-G

30028579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4673815-C-T

http://identifiers.org/hco/10/GRCh38#30028630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4673764-C-A

30028676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673718-A-G

30028696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4673698-C-G

30028696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4673698-C-T

30028760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673634-G-A

30028853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673541-C-T

30029007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673384-C-T

30029308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4673071-G-A

30029308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673071-G-C

30029357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4673022-G-A

30029474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4672896-T-C

30029649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: missense variant
orthologous variants: 4672733-G-C

30029710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: synonymous variant
orthologous variants: 4672672-A-G

30029740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 4672642-G-A

30029747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 4672635-A-G

30029997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4672006-G-A

30029997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4672006-G-T

30030086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4671921-C-G

30032619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4670180-G-A

30033467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4669258-C-G

30033507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4669217-C-T

http://identifiers.org/hco/10/GRCh38#30033687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4669069-C-A

30034645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4668627-C-T

30034964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4668372-T-C

30035472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4667419-T-A

30035472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4667419-T-C

30035863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4667053-G-A

30035863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4667053-G-T

30035888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4667031-A-G

30037114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4665113-C-T

30037115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4665112-G-A

30037336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4664916-C-T

30037795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4657963-G-C

30038058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4657749-G-T

30039783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656933-C-T

30040067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656658-C-T

30040191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656534-G-A

30040221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656506-C-T

30040348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656378-C-T

30040594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656124-T-A

30040696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4656035-A-G

30040807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655952-C-G

30040807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655952-C-T

30040911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655868-T-G

http://identifiers.org/hco/10/GRCh38#30041076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4655689-C-A

30041079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655686-C-T

30041204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655568-G-C

http://identifiers.org/hco/10/GRCh38#30041497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4655308-C-A

30041644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4655167-C-T

30041915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4654708-T-C

30041980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4654646-G-C

30041980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4654646-G-T

30043241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4652045-A-G

30043551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651909-T-C

30043643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651847-C-T

30043754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651762-G-T

http://identifiers.org/hco/10/GRCh38#30044327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4651562-C-A

30044358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651534-C-T

30044450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651434-A-G

30044652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651238-T-C

30044700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651189-A-T

http://identifiers.org/hco/10/GRCh38#30044857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4651050-A-C

30044913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4651018-C-T

http://identifiers.org/hco/10/GRCh38#30045218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4650810-C-A

30045218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4650810-C-T

30045626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4650504-C-T

30045627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4650503-T-G

http://identifiers.org/hco/10/GRCh38#30045700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4650450-C-A

30045700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4650450-C-T

30046347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4649932-G-A

30046422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4649855-G-A

30046422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4649855-G-T

30046516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron variant
orthologous variants: 4649791-C-G

30047673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4649268-T-C

30047715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4649226-G-A

30047753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4649188-T-C

http://identifiers.org/hco/10/GRCh38#30047836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4649108-C-A

30047839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4649105-C-T

30047852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4649092-G-A

30047852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4649092-G-T

30048864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4648677-G-A

http://identifiers.org/hco/10/GRCh38#30048888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4648655-A-C

30049318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4648213-G-A

30049409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4648138-G-A

30049481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4648072-G-A

30049864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4647719-C-T

http://identifiers.org/hco/10/GRCh38#30049913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4647674-A-C

30049985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4647603-G-A

http://identifiers.org/hco/10/GRCh38#30051869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4642222-C-A

30052569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4640647-C-T

30052701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4640556-G-A

30052708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4640549-G-A

30052770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4640483-T-C

30054972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4639132-A-G

30055395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4638731-A-G

30055473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4638660-T-G

30055516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4638619-C-G

30055737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4638386-T-C

30055741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4638382-T-G

30055963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637973-C-T

http://identifiers.org/hco/10/GRCh38#30056165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4637724-A-C

http://identifiers.org/hco/10/GRCh38#30056240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4637655-C-A

30056249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637646-G-C

30056249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637646-G-T

30056452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4637447-A-G

30056543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637382-G-A

30056543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637382-G-T

30056550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637375-A-T

30056868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4637130-G-A

30057530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4636516-C-G

30057530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4636516-C-T

30057573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4636444-C-T

http://identifiers.org/hco/10/GRCh38#30058476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4635669-C-A

30058491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635654-C-T

30059343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635145-A-G

30059415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635077-C-T

30059538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4634974-G-A

30059906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4634581-G-A

30059906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4634581-G-C

30061920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4633454-A-T

30062373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4633078-T-G

30062480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4632958-G-A

http://identifiers.org/hco/10/GRCh38#30063147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4632405-C-A

http://identifiers.org/hco/10/GRCh38#30063168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4632385-C-A

30063168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4632385-C-T

30063176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4632378-T-A

30063176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4632378-T-G

30066675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4630568-T-C

30066719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4630525-A-G

30069998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4627500-T-G

30070013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4627486-T-A

30070030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4627469-G-C

30070081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4627420-C-T

30070105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4627183-G-A

30070108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4627180-T-C

30070157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4627133-G-A

30070336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626963-T-C

30070355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626943-G-A

30070450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626865-A-G

30070601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626725-T-C

30070663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626663-C-G

30070666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4626660-C-T

http://identifiers.org/hco/10/GRCh38#30070704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4626620-C-A

30073931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4623726-T-C

30074182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4623394-C-G

30074306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4623283-G-A

30074556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4622987-C-T

30074557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4622986-G-A

30075173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4622776-C-T

30075366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4622606-T-A

30075608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4622198-G-A

http://identifiers.org/hco/10/GRCh38#30075832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4621973-A-C

30076821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4620870-G-A

30076945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4620759-A-G

http://identifiers.org/hco/10/GRCh38#30077027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4620683-A-C

30077555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4620317-A-G

30077900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619962-T-G

30078185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619687-T-C

http://identifiers.org/hco/10/GRCh38#30078545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4619328-C-A

30078545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619328-C-T

http://identifiers.org/hco/10/GRCh38#30078677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4619181-C-A

30078677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619181-C-G

30078732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619121-T-G

30078746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4619107-A-G

30078886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618960-C-T

30079066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618793-C-G

30079114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618745-C-T

30079179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618680-C-T

30079217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618655-G-T

30079254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618619-A-G

30079282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618593-G-T

http://identifiers.org/hco/10/GRCh38#30079432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4618404-C-A

http://identifiers.org/hco/10/GRCh38#30079555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4618267-C-A

30079789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4618144-G-A

30079944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617991-C-T

30080318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617726-G-A

30080362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617678-C-G

30080493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617547-T-C

30080538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617506-T-A

http://identifiers.org/hco/10/GRCh38#30080673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4617365-C-A

http://identifiers.org/hco/10/GRCh38#30080765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4617290-A-C

30080765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617290-A-G

http://identifiers.org/hco/10/GRCh38#30080768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4617287-A-C

30080902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4617183-T-G

http://identifiers.org/hco/10/GRCh38#30081311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4616756-C-A

30082020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4616430-G-A

30082020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4616430-G-C

30082125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4616322-A-G

30082132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4616306-A-G

30086257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4615454-T-A

30086266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4615445-T-C

30086432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4615311-G-A

30086815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4615033-C-T

30087706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613650-A-G

30087801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613553-G-A

30088314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613326-C-T

30088325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613315-T-C

30088402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613261-T-C

http://identifiers.org/hco/10/GRCh38#30088412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4613251-C-A

30088693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613007-C-T

http://identifiers.org/hco/10/GRCh38#30088695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4613005-C-A

30088695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4613005-C-T

http://identifiers.org/hco/10/GRCh38#30089555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4612476-C-A

30089555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4612476-C-T

30089976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4611573-C-T

30089979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4611570-T-G

http://identifiers.org/hco/10/GRCh38#30090545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4610835-A-C

30090545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4610835-A-T

http://identifiers.org/hco/10/GRCh38#30090609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4610806-A-C

30090713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4610706-C-T

30090923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4610516-A-G

30091152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4610318-T-A

30091219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4610247-T-C

30092286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4609901-T-C

30092690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4609555-G-A

http://identifiers.org/hco/10/GRCh38#30094766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4606561-C-A

30095398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4606062-G-A

30095588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4605883-C-T

http://identifiers.org/hco/10/GRCh38#30096086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4604856-C-A

30096086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604856-C-G

30096362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604728-C-G

30096506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604602-C-G

30096507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604601-T-C

30096642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604473-G-T

30096722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4604422-G-A

30098692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4602858-T-C

30098766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4602786-A-G

30098778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4602774-C-T

30099077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4602468-T-G

30099346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4602234-C-T

http://identifiers.org/hco/10/GRCh38#30105246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4595787-A-C

30105647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4595691-A-G

30105656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4595682-T-G

30105942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4595394-T-G

30106930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4595047-G-A

30114183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591903-A-T

30114272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591810-A-G

30114374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591717-T-C

30114517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591567-G-T

30114609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591515-T-A

30114609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591515-T-G

30115060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591149-A-G

30115118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591134-G-A

30115167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4591085-C-T

30115353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4590924-A-G

30115375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4590848-A-G

http://identifiers.org/hco/10/GRCh38#30115463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29283
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#4590767-C-A