183797696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: missense variant
orthologous variants: 47866347-C-T

183797746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: missense variant
orthologous variants: 47866296-G-T

http://identifiers.org/hco/4/GRCh38#183797797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47866245-C-A

183797797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: missense variant
orthologous variants: 47866245-C-T

183797805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: synonymous variant
orthologous variants: 47866237-C-T

183797959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: synonymous variant
orthologous variants: 47866077-C-T

183798007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: missense variant
orthologous variants: 47866029-A-G

http://identifiers.org/hco/4/GRCh38#183798078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865945-C-A

183798078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865945-C-G

183798078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865945-C-T

183798104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865919-G-A

183798104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865919-G-T

183798127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865907-G-A

http://identifiers.org/hco/4/GRCh38#183798130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865904-C-A

183798130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865904-C-T

183798153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865883-G-A

http://identifiers.org/hco/4/GRCh38#183798179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865866-C-A

183798179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865866-C-T

http://identifiers.org/hco/4/GRCh38#183798185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865860-C-A

183798185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865860-C-T

http://identifiers.org/hco/4/GRCh38#183798190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865855-C-A

http://identifiers.org/hco/4/GRCh38#183798203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865842-C-A

183798454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865586-A-G

183798496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865549-G-T

http://identifiers.org/hco/4/GRCh38#183798503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47865542-C-A

183798503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865542-C-G

183798503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865542-C-T

183798504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865541-A-G

183798504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865541-A-T

183798505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865540-G-A

183798505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865540-G-T

183798553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865483-C-G

183798553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865483-C-T

183798570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865462-G-A

183798678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865366-G-A

183798688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865356-C-T

183798779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865254-C-T

183798886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865150-T-A

183798886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865150-T-G

183799121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864939-C-T

183799734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864334-T-C

183799772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864291-T-A

183800083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863977-A-G

183800279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863806-A-G

183800288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863794-A-G

183800572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863491-G-A

http://identifiers.org/hco/4/GRCh38#183800618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47863447-C-A

183800905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863168-C-T

183801617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862322-A-T

183801748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862211-G-A

183801775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862177-G-A

183801787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862165-G-C

183801831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862110-G-A

183801950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862014-C-G

183802003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47861958-G-A

183804346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47859804-T-C

183804599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47859608-G-A

183804675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47859534-G-A

183809334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855441-C-T

183809368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855408-G-A

183809368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855408-G-C

183809480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855266-C-T

183809524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855235-G-T

183809741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47855113-C-T

183809935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47854341-T-C

183810096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47854181-G-A

183810362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47853932-G-C

183811073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47853005-A-G

183811148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852877-C-T

183811182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852843-G-A

183811310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852699-A-T

183811400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852605-C-T

183811455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852551-C-T

183811664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47852356-T-A

183812360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851781-C-G

183812360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851781-C-T

183812478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851675-A-T

183812535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851617-C-T

183812590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851564-G-A

183812940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851259-A-G

183813644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851131-T-C

183813678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47851097-C-T

183813821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850976-G-T

http://identifiers.org/hco/4/GRCh38#183813824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47850973-C-A

183813824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850973-C-T

183814094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850780-C-T

183814128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850744-T-C

183814273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850475-A-G

183814488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850306-T-C

183814488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850306-T-G

183814713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47850167-T-A

183814927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849921-G-C

183814927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849921-G-T

183815008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849860-A-T

183815068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849794-T-C

183815326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849612-T-C

183815344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849592-G-C

183815765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47849193-G-A

183820267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47846480-G-A

183820379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47846339-T-G

183820622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47846021-C-T

183820708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845935-T-C

183820749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845907-C-T

183820764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845892-T-C

183821151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845818-C-T

183821276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845690-G-A

183821276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845690-G-T

http://identifiers.org/hco/4/GRCh38#183821282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47845684-C-A

183821528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47845446-G-A

183823934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47843228-T-G

183823988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47843174-T-C

183824680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47841835-T-G

183824739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47841779-A-T

183824761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47841757-G-A

183824774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47841744-C-T

183828099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47838525-T-G

183828295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47838335-T-C

183828374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47838261-G-A

183828512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47838117-T-C

183828590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47838031-G-T

183828647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47837735-A-G

183828829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47837535-T-C

183828914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47837424-G-A

183828928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47837410-G-T

183829291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47836947-C-T

183829332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47836906-T-A

183829334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47836904-G-A

183829821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834978-A-G

183830060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834868-T-C

183830134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834839-T-G

183830164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834812-C-T

183830252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834722-G-T

183830306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834235-C-T

183830309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47834232-G-A

183830642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833920-G-C

183830702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833859-T-C

183830871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833666-A-G

http://identifiers.org/hco/4/GRCh38#183830940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47833605-C-A

183831029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833553-G-A

183831045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833537-C-T

183831130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833446-G-C

183831245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833328-C-T

183831284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833287-T-C

183831446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47833116-T-C

http://identifiers.org/hco/4/GRCh38#183833065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47831890-C-A

183835611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47828630-A-G

183835670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47828567-A-G

183835687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47828541-T-C

183835757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47828474-T-A

183836842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47827249-A-G

183837066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47827063-T-C

183837224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47826916-A-G

http://identifiers.org/hco/4/GRCh38#183837279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47826843-A-C

183837279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47826843-A-G

183837348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47826768-T-G

183837414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47826701-C-T

183838022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47825840-T-C

183839058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47825329-C-T

183839070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47825317-C-G

183839105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47825277-T-A

http://identifiers.org/hco/4/GRCh38#183839127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47825259-A-C

183839541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47824802-T-A

183839599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47824751-A-G

183840244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47824151-A-G

183840343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47824048-G-A

183840413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47823977-G-A

183840420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47823954-A-T

http://identifiers.org/hco/4/GRCh38#183840506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#47823899-A-C

183840656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47823767-A-G

183841547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47823218-G-A

183841626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47823136-A-G

http://identifiers.org/hco/4/GRCh38#183841649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47823113-A-C

183841745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47823026-A-G

183841764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47823005-A-G

183842146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47822654-T-A

183842220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47822579-A-G

183842221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47822578-T-G

http://identifiers.org/hco/4/GRCh38#183842266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47822545-C-A

183842274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47822537-G-A

http://identifiers.org/hco/4/GRCh38#183842455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47822355-C-A

183842561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47822249-T-C

183843565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47820244-C-G

183843565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47820244-C-T

183843705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47820124-T-C

http://identifiers.org/hco/4/GRCh38#183844305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47810615-C-A

183844334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47810586-C-G

183848812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47808321-T-C

183848888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47808248-G-C

183848953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47808174-G-A

183849034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47808094-C-G

183849151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47807971-G-A

http://identifiers.org/hco/4/GRCh38#183849395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47807726-C-A

183852816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47806054-G-A

183852826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47806044-A-G

183852921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47805963-G-T

183853137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47805758-G-A

183853638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47805267-T-G

183853756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47805151-A-G

183854562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47804357-A-T

183854716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47804207-T-C

183854857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47804065-T-C

183854957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803993-C-T

183855110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803846-G-A

http://identifiers.org/hco/4/GRCh38#183855120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47803836-A-C

183855273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803712-G-A

183855354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803631-G-T

183855820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803202-T-A

183855862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47803160-C-T

http://identifiers.org/hco/4/GRCh38#183856003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47803056-A-C

183856582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47802842-G-A

183856897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47802399-C-T

183857016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47802302-T-G

183857062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47802267-G-T

183857097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47802233-T-A

http://identifiers.org/hco/4/GRCh38#183857803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47801488-A-C

183857810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801481-T-G

183858143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801188-G-A

183858162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801167-A-G

183858164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801165-C-T

http://identifiers.org/hco/4/GRCh38#183858223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47801114-C-A

183858321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801040-G-A

183858321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47801040-G-C

http://identifiers.org/hco/4/GRCh38#183858393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47800978-C-A

183858414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47800957-G-A

183858428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47800943-C-T

183858523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47800846-C-T

183858582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47800772-T-C

183858582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47800772-T-G

183859649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47799249-G-A

183859649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47799249-G-T

183859809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47799096-T-C

183860026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47798865-T-C

183860483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47798454-G-A

http://identifiers.org/hco/4/GRCh38#183860787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47798155-A-C

183860952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47798006-T-C

183863187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47795024-T-A

183863368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47794846-A-G

183863767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47794470-G-A

183863805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47794436-T-C

183864073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47794177-T-C

183864187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47794075-G-A

http://identifiers.org/hco/4/GRCh38#183864851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47793849-C-A

183864851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47793849-C-T

183865488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47793127-C-T

183865965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47792677-C-T

183866224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47792222-C-T

183866273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47792173-G-A

183866390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47792025-T-C

183866391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47792024-G-T

183866501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47791916-G-C

183866517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47791900-A-G

183866608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47791813-G-T

183867157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786888-G-A

183867166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786879-G-A

183867166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786879-G-T

183867480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786488-C-T

http://identifiers.org/hco/4/GRCh38#183867619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47786358-A-C

183867664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786313-A-G

183867796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786196-G-A

183867796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47786196-G-T

183868020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47785590-A-G

183868020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47785590-A-T

183868146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47785499-T-C

183870206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47784298-A-G

183870211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47784293-G-A

183870445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47784054-A-G

183871032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782686-G-A

183871032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782686-G-T

183871083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782643-A-G

183871130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782597-C-T

183871321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782140-G-C

183871353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782110-C-G

183871420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47782042-G-A

183871954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781494-T-A

183871956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781492-A-G

183871956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781492-A-T

183871979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781469-A-G

183872576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781168-T-C

183872671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781072-T-C

183872691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781053-G-A

183872691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47781053-G-C

183873929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47780064-G-A

183874011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47779970-T-C

183874086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47779895-T-C

183875471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47779295-A-G

183876034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778735-T-C

183876153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778625-G-T

183876268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778507-G-A

183876293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778490-A-G

183876317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778467-G-A

183876317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778467-G-C

183876317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778467-G-T

183876552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778251-C-G

183876552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778251-C-T

183876708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778117-C-G

183876732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778092-C-G

183876732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47778092-C-T

http://identifiers.org/hco/4/GRCh38#183877269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47775237-C-A

183877269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47775237-C-T

183877516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774972-G-T

183877569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774932-A-G

183877980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774855-G-A

183877987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774848-G-A

183878040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774798-T-G

183878151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774693-G-A

183878248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774593-A-T

183878610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47774175-T-C

183878779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773970-A-G

183878831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773918-G-A

183878831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773918-G-C

183878932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773816-A-T

183878951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773797-G-A

183878951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773797-G-T

183878955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773793-A-T

183878975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773778-C-T

183879139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773625-G-A

183879139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773625-G-C

183879216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773539-T-C

183879242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773511-C-G

183879242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47773511-C-T

183879513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47771824-G-A

183879651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47771705-T-C

183880480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47770773-G-A

183880480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47770773-G-T

183880675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47770579-G-C

183881043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47770073-C-G

183881043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47770073-C-T

183881249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47769830-T-G

http://identifiers.org/hco/4/GRCh38#183881326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47769715-C-A

183881761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47769120-G-A

183881805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47769074-C-T

183882232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768681-T-C

183882303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768611-C-G

183882333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768581-G-A

183882345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768569-C-T

183882371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768543-A-G

183882652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47768258-T-C

183883014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47767920-T-C

183883016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47767918-T-C

183883095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47767835-A-G

183883127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47767799-C-T

183884329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47766100-G-A

183884329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47766100-G-T

183884516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47766029-A-G

183884557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47765989-A-G

http://identifiers.org/hco/4/GRCh38#183884884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47765007-A-C

183884947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47764953-C-T

183884951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47764949-G-A

http://identifiers.org/hco/4/GRCh38#183885208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47764709-A-C

183885391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47764507-G-A

183885693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47762630-T-C

183886260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47762183-A-T

183886433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47762015-A-T

183886592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47761870-T-C

183886640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47761823-C-T

183887405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47760952-G-A

http://identifiers.org/hco/4/GRCh38#183887517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47760823-C-A

183887517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47760823-C-T

183887562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47760776-G-A

183887715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47760623-A-G

183887983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47760215-G-A

183888284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759717-T-C

183888298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759703-C-G

183888298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759703-C-T

183888376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759626-C-T

183888377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759622-G-A

183888505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759509-G-A

183888703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759318-C-T

183888728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47759294-G-A

183889112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758779-C-T

183889148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758744-A-G

183889184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758708-A-G

183889240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758652-G-C

183889334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758556-G-A

183889334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758556-G-T

183889627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47758308-G-T

183892679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47757115-A-G

183892682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47757112-C-T

183893218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47756389-C-T

183893555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47756101-G-A

183893555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47756101-G-C

183893634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47756047-T-C

183893684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47756008-C-G

183893702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47755990-G-T

183894263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47755351-G-A

183894276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47755318-C-T

183894292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47755302-T-C

183894582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47754924-A-G

183894709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47754813-C-G

183895063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47754468-G-T

183895093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47754440-C-T

183895247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47754290-A-G

183897066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47753088-C-G

183897174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47752985-A-G

183897284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47752884-A-G

183897649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47751810-C-T

183898029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47751470-G-C

183898253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47751079-G-A

183898362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47750960-T-C

183898388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47750934-G-T

183902466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47744417-A-G

183902590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47744287-T-A

183902593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47744284-G-A

183902782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47744129-G-A

183903527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47743407-G-A

183903590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47743386-G-A

183904469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47743181-G-A

183904469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47743181-G-C

183905269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47742476-G-A

183905269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47742476-G-T

183905309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742436-A-G

183905309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742436-A-T

183905392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742351-T-C

183905392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742351-T-G

http://identifiers.org/hco/4/GRCh38#183905453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47742308-C-A

183905453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742308-C-G

183905453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742308-C-T

183905500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742280-C-T

http://identifiers.org/hco/4/GRCh38#183905563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47742234-C-A

183905563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742234-C-T

183905591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742206-T-C

http://identifiers.org/hco/4/GRCh38#183905668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47742118-C-A

183905668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742118-C-T

http://identifiers.org/hco/4/GRCh38#183905679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47742106-C-A

183905679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742106-C-G

183905679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47742106-C-T

http://identifiers.org/hco/4/GRCh38#183906008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47741832-C-A

183906008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741832-C-G

183906008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741832-C-T

183906172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741697-A-G

183906212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741657-G-A

183906212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741657-G-T

183906283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741584-G-A

183906283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741584-G-C

183906283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741584-G-T

http://identifiers.org/hco/4/GRCh38#183906290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47741576-C-A

183906290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741576-C-T

http://identifiers.org/hco/4/GRCh38#183906306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47741560-C-A

183906306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741560-C-T

http://identifiers.org/hco/4/GRCh38#183906518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47741358-C-A

183906518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741358-C-G

183906518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741358-C-T

183906704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741166-T-G

183906754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741116-G-A

183906754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741116-G-C

183906754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741116-G-T

183906783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741087-T-C

183906783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47741087-T-G

183906998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47740888-G-A

http://identifiers.org/hco/4/GRCh38#183907006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47740880-C-A

183907006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47740880-C-G

183907344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47740539-G-A

183907451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47740430-G-T

http://identifiers.org/hco/4/GRCh38#183907628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47740260-A-C

183908140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739843-G-A

183908144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739839-C-T

183908253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739728-A-G

183908265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739716-T-C

183908290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739691-G-A

183908315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739666-T-C

183908374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739609-T-C

183908512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739473-T-C

183908833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739180-A-G

183908911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739110-G-A

183908994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47739030-G-A

183909235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47738778-T-A

http://identifiers.org/hco/4/GRCh38#183909517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47738505-C-A

183909785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47738233-C-T

183909890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47738136-C-G

183910295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737738-T-A

183910356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737686-T-A

http://identifiers.org/hco/4/GRCh38#183910361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47737681-A-C

183910552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737522-A-G

183910791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737272-A-G

183910791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737272-A-T

183910929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737116-T-C

183911036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737022-T-C

183911036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737022-T-G

183911037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47737021-G-A

183911478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47736684-C-T

183911726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47736405-A-G

183911964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47736161-G-A

183912754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47735298-A-G

183912826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47735240-A-G

183913134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734873-G-A

183913172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734845-A-G

183913234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734800-T-C

183914833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732884-T-C

183914952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732763-C-T

183915108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732594-G-A

http://identifiers.org/hco/4/GRCh38#183915116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47732586-C-A

183915439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732285-T-C

183915440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732284-T-G

183915473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732251-C-T

183915715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47732036-A-G

183915755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731988-C-T

183915924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731836-G-A

183915976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731790-G-T

183915990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731776-G-C

183916142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731575-G-A

183916142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731575-G-T

183916165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731558-G-A

183916167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731556-C-T

183916398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731314-C-T

183916431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731283-G-T

183916726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47731011-A-T

183916847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47730894-C-T

183917136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47730458-A-G

183917250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47730345-C-T

183917261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47730334-G-C

183917286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47730316-C-G

http://identifiers.org/hco/4/GRCh38#183917623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47729948-C-A

183917818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47729388-C-G

183918327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47728919-C-G

http://identifiers.org/hco/4/GRCh38#183918653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47728518-C-A

183920530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47726297-C-T

183920653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47726175-C-T

183921216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47725053-T-C

183921541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47724710-C-T

183921687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47724573-C-T

183921917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47724383-T-C

183921918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47724382-A-G

http://identifiers.org/hco/4/GRCh38#183922027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47724285-A-C

183923629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47722025-A-G

183923704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47721936-G-A

183923797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47721838-G-C

183923946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47721683-T-C

183924301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47721347-G-A

183924487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47721124-C-T

183924649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47720886-T-C

183925293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47720344-T-C

183925549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47720243-A-G

183925915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47719893-T-G

183925933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47719875-A-T

http://identifiers.org/hco/4/GRCh38#183926022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47719786-A-C

183926137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47719689-T-C

183927009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718890-A-G

183927195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718702-C-T

183927250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718642-G-C

183927261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718631-C-T

183927353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718583-A-G

http://identifiers.org/hco/4/GRCh38#183927443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47718504-A-C

183927637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718326-G-T

183927641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718322-A-G

http://identifiers.org/hco/4/GRCh38#183927924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47718059-C-A

183927924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47718059-C-T

183928059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717939-G-A

183928059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717939-G-T

183928148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717852-T-G

183928317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717675-G-A

http://identifiers.org/hco/4/GRCh38#183928352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47717642-A-C

183928352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717642-A-G

183928664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47717439-C-T

183929662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47716595-A-G

183929735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47715952-A-G

183929735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47715952-A-T

183929793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47715903-A-G

183930916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47715260-A-G

183931260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47715094-C-T

183931425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714943-C-T

183931518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714828-G-A

183931584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714763-T-C

183931641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714743-G-A

183931717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714716-T-A

183931939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714545-G-A

183932018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714468-G-A

183932131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714404-G-A

183932140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714395-A-G

183932224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47714296-A-T

183932786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47713981-C-T

183932796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47713971-G-T

183934501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47712764-A-T

183934763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47712501-G-A

183934808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47712457-A-G

http://identifiers.org/hco/4/GRCh38#183934965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47712307-C-A

183934965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47712307-C-T

183935405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47711820-G-C

183936047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47711349-A-G

183940900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47710161-T-C

http://identifiers.org/hco/4/GRCh38#183941095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47709973-A-C

183941325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47709477-T-C

183941529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47709390-C-T

183941696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47709271-G-A

http://identifiers.org/hco/4/GRCh38#183941779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47709197-A-C

183941895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47709088-T-C

183942465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47708539-G-A

183942807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47708219-T-C

183942810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47708216-T-C

183942928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47708115-T-C

183943132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47707702-A-G

183943986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706953-G-A

183944006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706943-C-G

183944047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706900-A-G

183944119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706833-G-A

183944154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706797-G-A

183944273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706667-A-G

183944273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706667-A-T

183944287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706651-G-C

183944937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706296-A-T

183944950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706283-A-G

183944992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47706240-A-G

http://identifiers.org/hco/4/GRCh38#183945041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47706186-C-A

http://identifiers.org/hco/4/GRCh38#183945217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47706025-C-A

183945389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705882-G-A

183945394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705877-G-A

183945822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705458-T-G

183945844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705436-C-G

183945844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705436-C-T

183945854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705425-G-A

183945862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705417-C-G

183946111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705154-G-A

183946115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47705150-C-T

183948339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703650-C-G

183948339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703650-C-T

183948340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703649-G-A

http://identifiers.org/hco/4/GRCh38#183948501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47703337-C-A

183948501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703337-C-T

183948522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703316-A-T

183948884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703255-T-C

183948918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703222-T-C

http://identifiers.org/hco/4/GRCh38#183949056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47703081-C-A

183949056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703081-C-G

183949072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703065-A-G

183949131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47703006-G-A

183949196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47702938-A-G

http://identifiers.org/hco/4/GRCh38#183949365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47702689-C-A

183949365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47702689-C-T

183950103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47702339-T-C

183950105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47702337-T-C

183950645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47701913-G-A

183950691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47701882-G-A

183950781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47701795-A-G

183952058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47701390-A-G

183952620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47700810-T-G

183952728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47700729-G-A

183956343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47698873-T-A

183956524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47698798-A-G

183957235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47698342-A-G

183957354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47698226-C-T

183957402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47698174-A-T

183957578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697993-G-A

183957578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697993-G-T

183957680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697907-A-G

http://identifiers.org/hco/4/GRCh38#183957729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47697848-A-C

183957729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697848-A-G

183958437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697558-T-G

183958688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697314-T-C

183958794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697212-C-G

183958958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47697040-T-C

183960140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47695867-G-T

183960176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47695831-A-G

183960330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695677-T-C

183960330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695677-T-G

183960380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695627-C-T

183960576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695412-A-G

183960697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695290-G-T

183960903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695094-T-C

183960904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47695093-G-A

183961028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694983-C-G

183961153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694858-G-C

183961192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694828-C-T

183961438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694605-C-T

183961439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694604-G-A

183961456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694586-G-C

183961523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694526-C-G

183962057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47694134-C-T

183962204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47693987-A-G

183962283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47693904-C-G

183962425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47693767-T-C

183962630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47693562-A-G

http://identifiers.org/hco/4/GRCh38#183963171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47693001-A-C

http://identifiers.org/hco/4/GRCh38#183963239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47692931-C-A

183964116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47692605-G-C

183964403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47692308-T-C

183964771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47692096-A-T

183965177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47691806-G-A

183965271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47691727-G-C

183965312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47691688-C-T

183965334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47691659-G-A

183965464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47691558-C-T

183966103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690681-G-A

183966105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690679-G-A

183966353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690439-T-C

183966472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690319-A-G

183966529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690260-G-A

183966530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47690259-G-A

http://identifiers.org/hco/4/GRCh38#183968509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47689668-C-A

183968819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47689322-A-G

183969098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47689093-C-T

183970210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47688005-G-T

183970300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687925-T-C

183970619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687606-C-T

183970635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687583-C-T

183970678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687515-C-G

183970836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687191-T-C

183970891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47687134-T-A

183971097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686915-G-A

183971138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686854-A-G

183971143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686849-A-G

183971168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686788-G-A

183971499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686385-C-T

183971552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686334-C-G

183971583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686303-A-G

183971621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686270-G-A

183971621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686270-G-T

183971684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686210-G-A

183971684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47686210-G-T

183971892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47685925-G-A

183971935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47685875-G-A

183971935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47685875-G-T

183972010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47685783-G-A

183979463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47680233-T-C

183979481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47680215-G-C

183979544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47680167-C-T

183979564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47680148-T-A

183979564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47680148-T-G

183980592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47678704-G-A

183980686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47678619-C-T

183980834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47678476-T-C

http://identifiers.org/hco/4/GRCh38#183980968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47678340-A-C

http://identifiers.org/hco/4/GRCh38#183981164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47678172-A-C

183981408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677692-A-G

183981513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677584-T-G

183981698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677305-G-A

183981722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677279-A-G

183982079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677136-G-A

183982140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47677079-A-G

183982546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47676643-G-A

183982546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47676643-G-T

183982696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47676388-G-A

183982710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47676274-G-C

183982948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47676053-C-T

183983088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675940-C-G

183983188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675840-G-A

183983370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675678-C-T

183983395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675654-C-T

183983589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675477-G-A

183983981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675079-C-G

http://identifiers.org/hco/4/GRCh38#183984068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47675010-C-A

183984069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47675009-A-G

183984322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47674832-C-T

183984461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47674696-C-G

183984482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47674664-G-A

183985904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673570-C-T

183985959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673520-A-G

183986060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673435-C-T

http://identifiers.org/hco/4/GRCh38#183986143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47673383-A-C

183986233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673330-A-G

183986595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672954-A-G

183986709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672834-G-A

183986784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672762-G-C

183986787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672759-C-T

183986788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672758-C-T

183986868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672680-G-A

183986922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672549-G-A

183987090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672380-A-G

183987156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672316-C-T

183987167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672305-G-A

183987240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672240-C-G

183987240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672240-C-T

183987371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672126-A-G

183987371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672126-A-T

183987432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672045-A-T

183987692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671792-T-C

183987714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671770-G-T

183987738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671759-G-T

183987843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671654-C-T

183987886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671606-T-C

183987927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671551-A-G

183987975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671504-T-A

183988010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671469-T-C

183988129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671367-C-T

http://identifiers.org/hco/4/GRCh38#183988356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47671148-C-A

183988356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47671148-C-T

183988773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47670613-G-T

183988904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670477-G-A

183989184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670236-T-G

183989654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670088-T-C

183989923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669820-C-T

183989968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669778-G-A

183989969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669777-T-G

183990026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47669712-C-T

183990034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47669704-C-T

183990736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667429-C-T

183990971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667187-C-G

183991024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667140-G-C

183991071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667120-G-C

183991141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667042-T-C

183991156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667027-T-G

183992100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666145-A-G

183992147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666098-G-A

183992494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665769-G-A

183992709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665563-C-T

183993282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665037-T-G

183993390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47664936-T-C

183993409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47664916-G-A

183993854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47664469-T-C

183993970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47664349-G-A

183994110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47664213-G-T

183994377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663949-A-G

183995289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47663009-G-T

183995357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662938-A-T

183995364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662931-G-A

183995509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662802-A-G

183995523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662788-C-T

183995817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662494-G-A

183995885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662457-C-G

183996076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662264-A-G

183996120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662217-T-G

183996269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47662060-A-G

http://identifiers.org/hco/4/GRCh38#183996293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47662036-A-C

183996342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47661991-G-A

183996342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47661991-G-C

183996533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47661379-C-T

183996714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47661215-T-C

183996938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47661076-T-A

183997500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47660034-G-A

183997570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47659961-G-C

183997771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47659709-T-A

183997902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47659570-C-G

183998248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47659265-C-G

183998285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47659229-A-T

183999305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47658939-C-T

183999606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47658670-G-C

183999706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47658575-C-T

183999779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47658512-C-T

184000270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47657374-G-C

184000405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47657232-C-T

184000484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47657157-C-T

http://identifiers.org/hco/4/GRCh38#184000922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656714-C-A

184000922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656714-C-T

184000923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656713-G-A

184001134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656497-G-A

184001134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656497-G-C

http://identifiers.org/hco/4/GRCh38#184001213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656439-C-A

184001213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656439-C-T

184001281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656352-G-A

184001281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656352-G-C

184001402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47656229-A-G

184001487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656145-C-T

http://identifiers.org/hco/4/GRCh38#184001512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656120-C-A

184001512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656120-C-T

184001527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656108-G-A

184001527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656108-G-T

http://identifiers.org/hco/4/GRCh38#184001528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656107-C-A

184001528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656107-C-T

http://identifiers.org/hco/4/GRCh38#184001536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656099-C-A

http://identifiers.org/hco/4/GRCh38#184001538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47656097-C-A

184001538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47656097-C-T

http://identifiers.org/hco/4/GRCh38#184001579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47655991-C-A

184001579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47655991-C-T

http://identifiers.org/hco/4/GRCh38#184001588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47655982-C-A

184001588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47655982-C-T

184001761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47655761-A-G

184001962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47655549-C-T

184002248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47655110-A-G

184002386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47654978-A-T

184002720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47654706-C-G

184002722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47654704-A-G

184002793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47654598-G-A

184002876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47654498-T-C

184003730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653619-T-A

184003865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653350-A-G

184003955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653286-T-G

184004022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653239-T-C

184004041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653220-G-A

184004239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47653022-A-G

184004688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47652127-G-A

184004765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47651867-T-C

http://identifiers.org/hco/4/GRCh38#184004866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47651768-A-C

184004866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47651768-A-G

184005753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47651059-C-T

184005805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47651011-C-T

http://identifiers.org/hco/4/GRCh38#184007283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47650314-A-C

184007364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47650226-C-G

184007482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47650109-C-T

184007516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47650078-G-C

184007615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47650013-A-G

184007759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649849-G-A

184007759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649849-G-T

184007949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649343-A-T

184008032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649241-G-A

184008032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649241-G-T

184008035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47649238-C-T

184009700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47646595-G-T

184009742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47646553-A-G

184009758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47646537-C-T

184009823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47646472-C-T

184010210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47646085-C-T

184010290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47646005-C-T

http://identifiers.org/hco/4/GRCh38#184010411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47645884-C-A

184010630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645665-G-T

184010666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645629-G-C

184010678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645617-C-T

184010873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645422-C-T

184011104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645191-G-A

http://identifiers.org/hco/4/GRCh38#184011110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47645185-C-A

184011176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47645119-G-A

184011500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644806-C-G

184011526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644781-A-G

184011542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644765-G-A

184011542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644765-G-C

184011783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644518-G-A

184011783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644518-G-C

184011783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644518-G-T

184012056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644254-A-G

184012135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47644178-G-A

184012466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643810-G-A

184012488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643788-C-G

184012778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643521-C-G

184012778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643521-C-T

184012840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643466-T-A

184012904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643406-T-A

184012915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47643394-T-C

184013120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643204-C-T

184013177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47643151-T-A

184013177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47643151-T-G

184013324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643017-G-A

184013324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47643017-G-T

184013461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47642882-A-G

184013474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47642869-T-C

184013544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47642803-A-G

184013756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47642603-G-A

184014176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47642475-G-A

184014176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47642475-G-T

184014323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47642325-G-A

184014399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47642242-G-T

184014475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47642094-G-A

http://identifiers.org/hco/4/GRCh38#184014557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47641979-C-A

184014776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641799-T-G

184014939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641624-C-G

184014996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641572-T-C

184015130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641445-T-A

184015156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641420-T-C

184015162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641414-A-G

184015195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641381-C-T

http://identifiers.org/hco/4/GRCh38#184015274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47641136-C-A

184015274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641136-C-T

http://identifiers.org/hco/4/GRCh38#184015283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47641127-C-A

184015283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641127-C-T

184015297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641113-G-T

184015321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641090-G-A

184015321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641090-G-C

184015321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47641090-G-T

http://identifiers.org/hco/4/GRCh38#184015434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47640969-C-A

184015496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640918-G-A

184015530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640895-T-A

184015745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640728-A-G

184015745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640728-A-T

184015794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640682-T-C

184015934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47640540-C-T

184016449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47640198-T-C

184016548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47640099-T-G

http://identifiers.org/hco/4/GRCh38#184016649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47640002-A-C

184017207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47639487-G-A

184017207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47639487-G-C

184017316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47639378-T-A

184017342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47639351-G-A

http://identifiers.org/hco/4/GRCh38#184017376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47639317-C-A

184017376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47639317-C-G

http://identifiers.org/hco/4/GRCh38#184017681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47638999-A-C

http://identifiers.org/hco/4/GRCh38#184017683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47638997-A-C

184017683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638997-A-G

184017776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638948-G-A

184017902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638817-T-C

184018116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638598-G-A

184018150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638564-A-G

http://identifiers.org/hco/4/GRCh38#184018167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47638547-C-A

184018564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638149-G-A

184018564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638149-G-T

184018633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47638079-T-C

http://identifiers.org/hco/4/GRCh38#184018797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47637924-A-C

http://identifiers.org/hco/4/GRCh38#184018850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47637869-C-A

184018850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47637869-C-T

http://identifiers.org/hco/4/GRCh38#184019040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47637683-A-C

184019048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47637675-G-T

184019126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47637613-G-T

184019406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47637314-T-C

184019785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636918-G-A

184019785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636918-G-T

184019801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636902-G-A

http://identifiers.org/hco/4/GRCh38#184019911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47636765-C-A

184019938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636738-G-A

184020095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636565-T-C

184020172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636483-T-A

184020172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636483-T-C

184020198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636457-C-T

http://identifiers.org/hco/4/GRCh38#184020300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47636342-C-A

184020358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636285-T-C

184020385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636258-T-A

184020385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636258-T-C

184020396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636236-G-T

184020473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47636161-A-G

http://identifiers.org/hco/4/GRCh38#184020657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47635982-C-A

184020657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635982-C-G

184020657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635982-C-T

184020682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635959-A-G

184020710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635930-A-G

184020755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635885-A-G

184020780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635860-A-G

184020818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635822-G-T

184020840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635800-A-G

http://identifiers.org/hco/4/GRCh38#184020842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47635798-C-A

184020981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635658-G-T

184021145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635524-A-G

184021160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635515-T-C

184021185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635490-T-C

http://identifiers.org/hco/4/GRCh38#184021198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47635477-C-A

184021203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635472-G-T

184021250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635431-C-T

184021258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635423-T-C

184021388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635268-T-C

184021388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635268-T-G

184021548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635120-C-T

184021611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635055-G-A

184021611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635055-G-T

184021651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635017-C-G

184021651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47635017-C-T

184021883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634782-T-G

184021884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634781-G-A

184021884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634781-G-T

184021925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634736-T-C

http://identifiers.org/hco/4/GRCh38#184021929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634732-C-A

184021929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634732-C-T

http://identifiers.org/hco/4/GRCh38#184021931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634730-C-A

184021931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634730-C-G

184021931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634730-C-T

184021934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634727-T-A

184021934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634727-T-C

184021939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634722-C-T

http://identifiers.org/hco/4/GRCh38#184021946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634715-C-A

184021946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634715-C-T

184021953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634708-G-A

184021953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634708-G-C

184021953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634708-G-T

184021976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634678-G-A

184021976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634678-G-T

184022005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634649-A-G

http://identifiers.org/hco/4/GRCh38#184022323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634338-C-A

184022357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634302-T-G

184022365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634294-A-T

http://identifiers.org/hco/4/GRCh38#184022553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634116-C-A

http://identifiers.org/hco/4/GRCh38#184022580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47634089-C-A

184022580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47634089-C-G

184022646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633985-G-C

184022776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633856-G-A

184022776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633856-G-C

184022826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633791-T-C

184022839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633778-G-T

184023009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47633612-A-G

http://identifiers.org/hco/4/GRCh38#184023081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25450
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47633540-C-A