97849851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5 prime UTR variant
orthologous variants: 42244162-A-G

97849890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5 prime UTR variant
orthologous variants: 42244203-C-T

97849920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5 prime UTR variant
orthologous variants: 42244233-T-C

97849925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5 prime UTR variant
orthologous variants: 42244238-G-A

http://identifiers.org/hco/10/GRCh38#97850148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42244449-C-A

97850148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244449-C-G

97850148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244449-C-T

http://identifiers.org/hco/10/GRCh38#97850157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42244458-C-A

97850157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244458-C-T

97850170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244475-G-A

97850170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244475-G-T

http://identifiers.org/hco/10/GRCh38#97850219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42244523-C-A

97850219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42244523-C-T

http://identifiers.org/hco/10/GRCh38#97850333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42244641-A-C

97850333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron_variant, undefined
orthologous variants: 42244641-A-G

97850333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron_variant, undefined
orthologous variants: 42244641-A-T

http://identifiers.org/hco/10/GRCh38#97850349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42244657-C-A

97850349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244657-C-G

97850349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244657-C-T

97850408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron_variant, undefined
orthologous variants: 42244711-T-C

97850408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron_variant, undefined
orthologous variants: 42244711-T-G

97850415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244718-G-A

97850415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244718-G-T

97850444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244756-G-A

97850444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244756-G-T

97850480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42244800-C-G

http://identifiers.org/hco/10/GRCh38#97850778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42245083-C-A

97851182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42245425-C-T

97851313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42245552-G-A

97851329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42245568-A-G

97851351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42245589-G-C

97851893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42245929-G-A

97852452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42246609-C-T

97852506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42246661-G-A

97852737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42246848-T-G

97853300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42247366-C-G

97853660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42247733-G-A

97853672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42247745-A-G

97853800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42247844-C-T

97854105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248122-G-A

97854241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248261-G-A

97854241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248261-G-C

97854260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248276-G-C

97854261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248277-T-A

97854496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248491-T-C

97854497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248492-A-G

97854740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42248687-A-T

97855146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249023-G-A

97855524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249771-A-G

97855545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249789-C-G

97855726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249908-A-G

97855739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249925-T-G

97855754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42249936-T-C

97856028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250472-T-C

97857998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250588-C-T

97858027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250616-C-T

97858051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250640-C-T

97858202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250775-C-T

97858213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250786-G-A

97858396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42250975-G-T

97858443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251021-G-A

97858443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251021-G-T

97858693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251267-G-C

97858705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251277-C-T

97858874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251427-G-A

http://identifiers.org/hco/10/GRCh38#97859278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42251617-C-A

97859278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251617-C-T

97859299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251639-G-A

97859299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251639-G-C

97859299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251639-G-T

http://identifiers.org/hco/10/GRCh38#97859324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42251662-C-A

97859324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251662-C-T

97859331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251669-G-T

97859410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251722-C-T

97859424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251735-A-G

97859438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42251748-C-T

97859532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42251842-T-C

http://identifiers.org/hco/10/GRCh38#97859565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42251875-C-A

97859565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42251875-C-G

97859565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42251875-C-T

97859720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252029-G-A

97859720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252029-G-T

97860006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252317-G-A

http://identifiers.org/hco/10/GRCh38#97860042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42252344-C-A

97860060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252362-C-G

http://identifiers.org/hco/10/GRCh38#97860759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42252551-C-A

97860917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252701-C-G

97860917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252701-C-T

97861050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252836-A-G

97861113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42252891-G-A

http://identifiers.org/hco/10/GRCh38#97861370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42253152-C-A

97861370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253152-C-G

97861541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253309-T-C

97861721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253446-G-C

97861723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253448-G-T

97863191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253575-G-A

97863302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42253648-C-T

http://identifiers.org/hco/10/GRCh38#97863883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42255150-A-C

http://identifiers.org/hco/10/GRCh38#97863897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42255164-C-A

97863914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255178-C-G

97863914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255178-C-T

97863956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42255216-T-G

97864013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42255273-C-T

97864086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255346-G-A

97864248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: synonymous variant
orthologous variants: 42255496-T-C

97864279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255527-T-C

97864292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255540-G-A

97864292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255540-G-T

97864331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255578-G-A

http://identifiers.org/hco/10/GRCh38#97864351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42255599-C-A

97864351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255599-C-T

97864504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255736-A-G

97864508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42255740-T-C

97864635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42256037-A-G

97864637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42256039-C-G

97864978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: intron variant
orthologous variants: 42256319-A-G

97865146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256460-G-T

97865148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256462-G-T

97865179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256493-G-C

97865179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256493-G-T

97865219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256530-T-G

97865229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256533-G-A

97865229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256533-G-T

http://identifiers.org/hco/10/GRCh38#97865272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42256566-C-A

97865272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256566-C-T

http://identifiers.org/hco/10/GRCh38#97865480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42256697-C-A

97865480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256697-C-T

97865484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256704-A-T

97865492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256712-C-T

97865518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256738-T-C

http://identifiers.org/hco/10/GRCh38#97865519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42256739-C-A

97865519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42256739-C-T

97865566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 42256768-G-A

97865652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 42256853-C-T

http://identifiers.org/hco/10/GRCh38#97865808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257009-C-A

97865808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257009-C-G

97865808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257009-C-T

97865825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257026-G-A

97865825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257026-G-T

http://identifiers.org/hco/10/GRCh38#97865874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257071-C-A

97865874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257071-C-T

97865918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257101-G-A

97865918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257101-G-T

97865950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257147-G-A

97865950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257147-G-T

97865969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257165-T-A

97866067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257251-T-A

97866067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257251-T-G

http://identifiers.org/hco/10/GRCh38#97866068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257252-A-C

97866068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257252-A-G

97866068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257252-A-T

http://identifiers.org/hco/10/GRCh38#97866092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257276-C-A

http://identifiers.org/hco/10/GRCh38#97866098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257282-C-A

97866098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257282-C-T

http://identifiers.org/hco/10/GRCh38#97866099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257283-C-A

97866099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42257283-C-T

http://identifiers.org/hco/10/GRCh38#97866215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257346-C-A

97866242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42257370-G-A

97866242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42257370-G-T

97866262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42257386-T-C

http://identifiers.org/hco/10/GRCh38#97866278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257391-C-A

http://identifiers.org/hco/10/GRCh38#97866295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42257408-C-A

97866295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42257408-C-T

97866373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 42257482-C-T

97866444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42257551-G-T

97866548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42257633-T-C

97866784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42257859-G-T

97866841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42257958-T-C

97866938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258048-C-T

97867014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258136-G-A

97867025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258147-A-G

97867037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258159-G-T

http://identifiers.org/hco/10/GRCh38#97867046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258168-C-A

97867050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258172-G-T

97867056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258178-A-G

http://identifiers.org/hco/10/GRCh38#97867074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258197-C-A

97867074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258197-C-G

97867090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258214-T-C

http://identifiers.org/hco/10/GRCh38#97867166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258285-C-A

97867187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258306-G-T

97867268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258350-C-T

http://identifiers.org/hco/10/GRCh38#97867270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258352-C-A

97867270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258352-C-T

97867293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258371-A-G

97867317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258394-G-A

97867334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258404-T-C

97867391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258461-A-G

http://identifiers.org/hco/10/GRCh38#97867477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258521-C-A

97867477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258521-C-T

97867529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258573-C-T

http://identifiers.org/hco/10/GRCh38#97867592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258624-C-A

97867592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258624-C-T

97867594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258626-C-T

97867629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258661-C-G

97867629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258661-C-T

http://identifiers.org/hco/10/GRCh38#97867643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258675-C-A

97867647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258679-G-T

97867691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258725-G-A

97867736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258770-T-C

97867837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258836-G-T

97867853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258853-G-C

97867853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258853-G-T

97867898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258900-G-A

97867898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258900-G-T

97867922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42258929-T-C

http://identifiers.org/hco/10/GRCh38#97867981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42258989-C-A

97867998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259006-A-G

97868038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259045-G-T

97868120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259172-T-C

97868139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259190-T-C

97868243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259411-A-G

97868261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259429-A-G

97868261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259429-A-T

97868271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259439-T-C

97868306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259473-A-G

http://identifiers.org/hco/10/GRCh38#97868403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42259514-C-A

97868423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259534-T-C

97868427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259538-G-A

97868427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259538-G-T

97868465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259588-C-G

97868465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259588-C-T

http://identifiers.org/hco/10/GRCh38#97868533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42259649-C-A

97868555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259674-T-C

97868570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259689-A-G

97868588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259719-G-A

97868596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259727-T-A

97868596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259727-T-C

97868614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42259744-T-C

97868634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259764-G-T

97868768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42259901-T-C

97868853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260003-A-G

97868921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260283-A-G

97868958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260321-G-A

97868958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260321-G-T

97869128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260496-G-A

97869158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260507-G-A

97869158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260507-G-T

97869172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260521-G-T

97869203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260558-C-T

http://identifiers.org/hco/10/GRCh38#97869262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42260616-C-A

97869265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260619-G-A

97869291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260646-G-A

97869379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260733-G-A

97869379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260733-G-T

97869382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260736-G-A

97869382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260736-G-T

http://identifiers.org/hco/10/GRCh38#97869401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42260751-C-A

97869438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260779-G-A

97869438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260779-G-T

97869481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260805-G-A

97869481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260805-G-T

97869487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260811-A-G

97869487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42260811-A-T

97869509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260833-A-G

97869581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260876-G-A

http://identifiers.org/hco/10/GRCh38#97869636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42260934-A-C

97869636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260934-A-G

97869717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260992-C-T

http://identifiers.org/hco/10/GRCh38#97869724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42260997-C-A

97869724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42260997-C-T

97869824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261103-G-C

97869824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261103-G-T

http://identifiers.org/hco/10/GRCh38#97869845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42261124-C-A

97869845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261124-C-T

http://identifiers.org/hco/10/GRCh38#97869853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42261132-C-A

97869853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42261132-C-T

97869860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42261139-A-G

97869896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42261159-C-T

http://identifiers.org/hco/10/GRCh38#97870337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42261367-C-A

http://identifiers.org/hco/10/GRCh38#97870400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42261404-C-A

97870486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261451-G-A

97870486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261451-G-T

97870527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261457-G-A

97870527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261457-G-T

97870700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261626-A-G

97870733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261662-C-G

97870733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42261662-C-T

97870784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263045-T-C

97870785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263046-G-T

97870811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263071-A-G

97870813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263073-G-A

97870813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263073-G-T

97870814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263074-C-G

97870814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42263074-C-T

97871194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42263727-C-T

http://identifiers.org/hco/10/GRCh38#97871226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42263968-C-A

97871226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42263968-C-T

97871232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42263975-A-G

97871236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42263979-A-G

97871236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42263979-A-T

97871348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42264192-A-G