81489742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366557-T-C

81489781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366519-G-A

81489913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366390-T-A

81489913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366390-T-G

81490116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366190-A-G

81490186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366123-T-C

81490244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366082-A-G

81490266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70366060-A-G

81490391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 3 prime UTR variant
orthologous variants: 70365947-C-G

81490486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365854-G-A

81490486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365854-G-T

81490542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365798-G-T

81490578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365764-T-G

http://identifiers.org/hco/3/GRCh38#81490596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70365746-C-A

81490596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365746-C-T

81490611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365731-T-A

81490611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365731-T-C

81490739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, undefined
orthologous variants: 70365614-A-G

81490976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365451-G-C

81490977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365450-A-G

81491238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365244-T-C

81491270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70365209-C-G

81491390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364946-C-T

81491515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364829-A-T

http://identifiers.org/hco/3/GRCh38#81491578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70364774-C-A

81491578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364774-C-T

81491719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364639-T-C

81492000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364376-T-C

81492074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364303-A-G

81492142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364237-A-G

81492161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364218-C-G

81492190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70364191-T-C

81493215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70363370-T-C

81493351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70363239-C-T

http://identifiers.org/hco/3/GRCh38#81493418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70363151-C-A

81493856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362994-A-G

81493899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362955-C-T

81493988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362866-G-A

81494053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362807-G-T

81494054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362806-T-C

81494102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362767-C-T

81494316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362540-A-G

81494370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362485-G-A

81494370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362485-G-C

81494682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70362210-A-G

http://identifiers.org/hco/3/GRCh38#81494873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70362058-A-C

81495421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70361724-A-G

81495498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70361663-G-T

http://identifiers.org/hco/3/GRCh38#81495681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70361545-A-C

http://identifiers.org/hco/3/GRCh38#81495747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70361477-A-C

81495750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70361474-T-C

81496013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70361227-T-C

81496213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360964-T-C

81496214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360963-T-C

81496331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360849-G-A

http://identifiers.org/hco/3/GRCh38#81496430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70360748-C-A

81496576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360608-C-G

http://identifiers.org/hco/3/GRCh38#81496669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70360522-C-A

81496696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360494-G-T

81496749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360441-G-C

81496793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360381-G-A

81496793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360381-G-C

81496843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360279-T-C

81496867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360259-G-A

81496867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360259-G-T

81496927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360199-C-G

81496966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360159-T-C

81497060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360072-T-C

http://identifiers.org/hco/3/GRCh38#81497074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70360058-C-A

81497126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360009-A-G

81497126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70360009-A-T

81497253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359882-T-C

81497339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359797-C-T

81497434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359701-T-C

81497435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359700-T-C

81497458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359677-C-G

81497483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359651-C-T

81497748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359378-G-T

81497818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359310-C-T

81498110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70359032-C-T

81498235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358935-G-C

81498432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358646-C-T

http://identifiers.org/hco/3/GRCh38#81498438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70358640-A-C

81498483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358594-C-T

81498529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358549-C-G

81498632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358457-C-G

81498844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358265-G-T

http://identifiers.org/hco/3/GRCh38#81499021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70358119-A-C

81499021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358119-A-T

81499049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358091-A-G

81499049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358091-A-T

81499066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358073-G-C

81499066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70358073-G-T

81499158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: synonymous variant
orthologous variants: 70357979-G-A

81499158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense variant
orthologous variants: 70357979-G-T

81499225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 70357912-A-G

81499225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 70357912-A-T

81499537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70357622-T-C

81499680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70357482-A-G

81499681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70357481-T-A

81499681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70357481-T-C

81499932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70357032-C-T

81500036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356917-A-G

81500095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356859-G-A

81500149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356805-A-G

81500176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356779-T-C

81500231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356726-T-C

http://identifiers.org/hco/3/GRCh38#81500370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70356582-A-C

81500373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356579-A-G

81500494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356470-A-G

81500543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356418-T-A

81500543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356418-T-C

81500749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356191-A-G

81500753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356187-T-A

81500753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70356187-T-C

81502525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70349022-A-G

81502653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348900-G-T

81502949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348671-G-A

http://identifiers.org/hco/3/GRCh38#81503114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70348414-C-A

81503217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348319-T-C

81503262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348276-C-T

81503283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348256-T-C

81503286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348253-G-A

81503490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70348093-G-A

81503707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70347912-C-T

81504400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70347624-G-C

81504710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70347316-C-T

http://identifiers.org/hco/3/GRCh38#81505003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70347015-C-A

81505003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70347015-C-T

81505019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346999-T-A

81505067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346954-T-C

81505070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346951-C-T

81505098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346927-C-T

81505192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346834-A-G

81505419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346601-G-A

81505427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346598-C-T

81505473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346554-G-T

81505538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346489-A-G

81505647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346374-T-C

81505697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346323-T-C

81505717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346303-G-C

81505717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346303-G-T

http://identifiers.org/hco/3/GRCh38#81507148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70346184-A-C

81507148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70346184-A-T

81507675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345997-T-C

http://identifiers.org/hco/3/GRCh38#81507754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70345941-A-C

81507786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345909-T-C

81507786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345909-T-G

81508159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345539-T-C

81508305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345396-T-C

81508418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345266-A-G

http://identifiers.org/hco/3/GRCh38#81508451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70345233-C-A

81508468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345218-A-T

81508519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70345169-T-A

81508863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70339167-G-T

81508880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70339150-T-C

81509030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338997-G-A

81509167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338871-T-C

81509251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338784-A-T

81509312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338746-A-G

81509312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338746-A-T

81509320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338736-G-A

81509320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338736-G-T

81509343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338713-G-T

81509417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338635-T-C

http://identifiers.org/hco/3/GRCh38#81509426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70338623-C-A

81509465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338580-A-G

http://identifiers.org/hco/3/GRCh38#81509520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70338557-C-A

81509563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70338537-A-G

81509576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70338524-C-T

81509612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70338485-T-A

81509637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70338468-C-T

81509666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338442-G-T

81509875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338244-A-T

81509915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338209-T-C

81510018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338113-T-C

81510035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70338096-T-C

http://identifiers.org/hco/3/GRCh38#81510073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70338058-C-A

81510251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70337911-G-A

http://identifiers.org/hco/3/GRCh38#81511884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70335233-C-A

81511944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70335184-T-C

81512141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70335011-A-T

http://identifiers.org/hco/3/GRCh38#81512296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70334778-A-C

81512407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334669-G-C

81512450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334628-T-C

81512475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334578-C-T

81512743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334286-T-G

81512951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334162-C-T

81513001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70334113-T-A

81513210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70333892-T-C

81513364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70333734-T-C

81513394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70333704-G-A

81513409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70333689-C-G

81513413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron variant
orthologous variants: 70333685-G-A

81518107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70333197-A-G

81518252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70333057-G-C

http://identifiers.org/hco/3/GRCh38#81518354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70332964-C-A

81518354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332964-C-G

http://identifiers.org/hco/3/GRCh38#81518376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70332952-A-C

81518376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332952-A-G

81518384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332944-T-C

81518795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332667-G-A

81519164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332296-A-G

81519206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332254-A-T

http://identifiers.org/hco/3/GRCh38#81519209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70332251-C-A

81519311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332146-C-G

81519311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70332146-C-T

81519525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331937-A-G

81519613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331851-T-G

81519666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331807-T-A

81519666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331807-T-C

81519666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331807-T-G

81519869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331616-G-C

81519899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331585-T-A

81520102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331375-T-A

81520107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331370-T-C

81520390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331270-T-C

81520396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331264-G-C

81520396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331264-G-T

81520462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331208-T-A

81520462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331208-T-C

81520542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70331131-T-C

http://identifiers.org/hco/3/GRCh38#81520579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70331108-A-C

http://identifiers.org/hco/3/GRCh38#81520687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70330998-C-A

81520734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70330951-C-T

81521121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70330597-T-C

81521315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70330408-T-G

81521344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70330381-T-C

81521576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70330163-A-T

81532414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70327032-C-T

81532416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70327030-C-T

81532494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70326964-G-A

http://identifiers.org/hco/3/GRCh38#81532513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70326945-C-A

81532513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70326945-C-T

81532632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70326839-T-C

81532788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70326675-C-T

81533095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70326423-T-C

81535003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70326063-T-G

81535018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70326048-A-G

81535055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70326020-T-C

81535060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70326015-T-C

81535062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70326013-C-G

81535102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325983-A-T

81535115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325970-G-A

81535115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325970-G-T

81535125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325960-T-A

81535125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325960-T-C

http://identifiers.org/hco/3/GRCh38#81535137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70325946-A-C

81535137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325946-A-G

81535137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70325946-A-T

81535365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325732-T-C

http://identifiers.org/hco/3/GRCh38#81535371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70325726-C-A

81535371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325726-C-T

81535384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325713-A-G

81535410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325664-T-C

81535416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325658-T-A

81535416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325658-T-C

81535460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325619-A-G

81535460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325619-A-T

81535522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325577-G-A

81535546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325553-G-T

81535547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325552-C-T

81535580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325515-G-T

81535621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70325479-T-C

http://identifiers.org/hco/3/GRCh38#81536208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70324909-C-A

81536237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324882-A-G

81536438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324674-A-G

81536478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324634-T-C

81536573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324537-A-G

81536573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324537-A-T

81536714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324387-A-G

81536770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324331-A-G

81536775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324326-A-G

http://identifiers.org/hco/3/GRCh38#81536790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70324309-C-A

81536844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324254-T-C

81536866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324232-A-G

81536866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70324232-A-T

81537127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323957-T-A

81537127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323957-T-C

81537177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323907-T-A

http://identifiers.org/hco/3/GRCh38#81537202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70323882-C-A

81537265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323805-C-G

81537664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323411-C-T

81537788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323324-T-G

81537899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70323236-A-G

81542966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70322583-T-C

81543019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70322524-T-G

81543220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70322090-A-G

81543256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70322052-A-G

81543306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321968-T-C

81543308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321966-G-A

81543363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321909-T-G

81543414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321857-T-C

81543507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321745-T-A

81544179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321098-G-A

81544284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70321004-G-T

81544308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320980-A-G

81544447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320846-A-G

81544553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320741-G-A

81544603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320689-G-A

81544670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320622-T-C

81544953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320338-G-A

81544958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320333-T-C

81544985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320307-A-G

81545042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320250-G-A

81545049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320243-T-A

81545049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320243-T-G

http://identifiers.org/hco/3/GRCh38#81545150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70320151-C-A

81545154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320147-G-A

81545251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320056-C-T

81545279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320030-G-T

81545309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70320000-G-C

81545323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70319986-C-T

81551931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318919-T-A

81551939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318911-T-C

81551973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318877-T-C

http://identifiers.org/hco/3/GRCh38#81551975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70318875-C-A

81551976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318874-C-G

81552003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318847-C-T

81552025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70318824-A-G

http://identifiers.org/hco/3/GRCh38#81553170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70318113-A-C

81554351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316595-A-T

81554353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316593-T-C

81554362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316586-A-G

81554424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316517-C-T

81554555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316377-A-T

http://identifiers.org/hco/3/GRCh38#81554647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70316293-C-A

81554722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316219-G-A

81554865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70316105-A-G

81555000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315960-G-C

81555319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315714-T-G

81555455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315595-G-T

81555479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315572-C-G

81555487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315564-G-A

81555577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315496-G-C

81555712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315378-T-C

http://identifiers.org/hco/3/GRCh38#81555741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70315349-A-C

81555829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315231-T-C

81555975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315110-C-T

81556040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70315025-T-C

81556272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70314820-C-G

81556276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70314816-A-G

81556449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70314624-T-A

81557693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70313067-A-G

81557771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312987-G-A

81557771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312987-G-C

81557896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312878-G-A

81558033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312766-A-G

81558090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312709-G-A

http://identifiers.org/hco/3/GRCh38#81558428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70312445-C-A

81558428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312445-C-G

81558938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70312262-T-C

81559313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70311618-T-C

http://identifiers.org/hco/3/GRCh38#81559458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70311482-C-A

http://identifiers.org/hco/3/GRCh38#81559483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70311459-C-A

81559611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70311336-T-C

81559615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70311332-G-C

81559669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70311288-C-T

81559786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70311203-C-T

81560252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310755-A-T

81560629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310337-G-A

81560630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310336-T-C

81560687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310164-C-T

81560801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310051-C-T

81560839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310014-T-A

81560839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70310014-T-C

81560868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70309988-C-T

81560962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70309889-C-T

81561468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308863-G-A

http://identifiers.org/hco/3/GRCh38#81561522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70308808-C-A

81561614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308716-T-C

81561629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308701-G-A

81561685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308643-T-C

81561755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308571-A-G

81561856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308449-C-T

81562832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308247-C-T

81563078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308002-G-A

81563080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70308000-T-C

81563125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307949-T-C

81563301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307770-A-G

81563374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307710-C-T

81563376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307708-T-C

81563480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307622-C-G

81563507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307601-T-C

81563701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70307375-A-G

http://identifiers.org/hco/3/GRCh38#81564668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70306033-A-C

81564753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70305963-G-T

81564888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70305871-T-G

81564987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70305800-T-G

81565839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304972-G-C

81565839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304972-G-T

http://identifiers.org/hco/3/GRCh38#81565938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70304880-A-C

81565994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304833-G-A

81566046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304782-C-T

81566500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304624-A-G

81566838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304307-T-A

81566838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304307-T-C

81566952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304196-T-C

81566982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304169-C-T

81566984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70304167-A-G

http://identifiers.org/hco/3/GRCh38#81567053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70304124-C-A

http://identifiers.org/hco/3/GRCh38#81567254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70303968-C-A

81567254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303968-C-T

81567383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303838-G-A

81567445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303782-T-C

81567715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303550-C-T

81567790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303475-T-C

81567906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70303382-T-C

81571174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298778-T-C

81571193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298760-A-G

81571398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298565-T-C

81571424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298539-G-A

81571439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298524-T-C

81571551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298391-A-G

81571581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298360-C-T

81571670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70298274-C-T

81573751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296928-C-T

81573784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296889-T-A

81573784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296889-T-G

81573816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296856-G-A

81573816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296856-G-T

81573936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296702-T-C

81573964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296674-G-A

81574003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296638-C-T

81574009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296632-C-G

81577264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292822-A-G

81577286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292800-C-T

81577313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292777-A-T

http://identifiers.org/hco/3/GRCh38#81577479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70292613-C-A

http://identifiers.org/hco/3/GRCh38#81577577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70292518-A-C

81577760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292385-G-A

81577837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292365-A-G

81577877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292331-A-G

81577902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292300-A-G

http://identifiers.org/hco/3/GRCh38#81578140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70292067-C-A

81578140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292067-C-T

81578148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292059-T-A

81578148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292059-T-C

81578169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292038-T-C

81578749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291978-C-T

81579028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291733-T-C

81579087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291677-A-T

http://identifiers.org/hco/3/GRCh38#81579131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70291636-A-C

81579206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291496-T-A

81579606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290527-T-C

81579606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290527-T-G

81579614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290519-T-C

81579799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290335-A-G

81579881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290251-G-A

81580277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289684-C-G

81580305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289656-G-A

81580424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289550-G-A

81580429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289545-A-G

81580461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289519-C-G

81580584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289417-T-C

81580625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289383-C-T

81580726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289287-G-C

http://identifiers.org/hco/3/GRCh38#81580739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70289271-A-C

81580876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289172-A-G

81580876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289172-A-T

81580970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289105-C-T

81580971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289104-A-G

81581017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289069-A-G

http://identifiers.org/hco/3/GRCh38#81581034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70289054-C-A

81581034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289054-C-T

81581080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289014-T-C

81581080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289014-T-G

81581096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288998-T-C

81581096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288998-T-G

81581110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288984-G-A

81581110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288984-G-T

http://identifiers.org/hco/3/GRCh38#81581112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70288982-A-C

81581154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288941-T-A

81581154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288941-T-C

81581294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288794-A-G

http://identifiers.org/hco/3/GRCh38#81581323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70288760-C-A

81581360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288706-T-C

81581400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288659-T-C

81581400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288659-T-G

81581401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288658-A-G

81581422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288626-A-T

81581589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288418-T-C

81581844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288154-C-T

81581887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288115-G-A

81581887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288115-G-C

81582080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287937-T-C

81584101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287183-C-T

http://identifiers.org/hco/3/GRCh38#81584116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70287160-C-A

81584413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286879-C-G

81584433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286805-T-A

81584438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286675-C-T

81585154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286035-T-C

81585243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285957-A-G

81585285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285922-G-A

http://identifiers.org/hco/3/GRCh38#81585347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70285863-C-A

81585395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285817-A-G

81585457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285757-A-G

81585643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285430-T-A

81585643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285430-T-C

81585941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285146-T-C

81585963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285131-G-C

81585963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285131-G-T

http://identifiers.org/hco/3/GRCh38#81585983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70285104-A-C

81585983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285104-A-G

81586059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285031-A-T

81586070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285020-A-G

81586280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284827-G-T

81586306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284802-G-A

81586306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284802-G-T

81586316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284785-A-G

81586335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284767-G-A

81586335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284767-G-T

http://identifiers.org/hco/3/GRCh38#81586336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70284766-C-A

81586336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284766-C-T

81586356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284746-G-A

81586686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284452-G-C

81586715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284424-A-T

81586760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284380-T-C

81586904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284320-T-C

81587260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284205-C-T

81587506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283954-A-G

81587560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283895-A-T

81587587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283863-T-C

81587897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283607-G-C

81588129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283344-A-G

81588153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283320-G-T

81588236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283227-A-G

81588278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283188-A-G

81588372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283062-C-G

http://identifiers.org/hco/3/GRCh38#81589197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70282559-A-C

81589251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282518-G-A

81589413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282377-T-C

81589519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282271-A-G

81589526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282269-A-T

81589598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282197-A-T

81589672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282123-T-C

81589887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281910-A-T

81589906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281899-G-A

81589966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281858-G-T

81590244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281624-C-T

81590618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281251-C-T

http://identifiers.org/hco/3/GRCh38#81590676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70281194-C-A

81590676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281194-C-T

http://identifiers.org/hco/3/GRCh38#81590909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70280963-C-A

81590909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280963-C-G

81590909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280963-C-T

81590963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280909-A-G

81590963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280909-A-T

81591068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70280803-G-A

http://identifiers.org/hco/3/GRCh38#81591149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70280722-C-A

81591168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70280703-A-G

http://identifiers.org/hco/3/GRCh38#81593805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275448-C-A

81593805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275448-C-G

81593813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275440-G-A

81593813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275440-G-C

81593813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275440-G-T

81593823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275430-T-C

81593887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275367-T-C

http://identifiers.org/hco/3/GRCh38#81594015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275200-A-C

81594015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70275200-A-G

http://identifiers.org/hco/3/GRCh38#81594024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275191-C-A

81594024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 70275191-C-T

http://identifiers.org/hco/3/GRCh38#81594068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275147-A-C

81594068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275147-A-G

81594094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275114-G-T

http://identifiers.org/hco/3/GRCh38#81594116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275095-C-A

81594116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275095-C-T

http://identifiers.org/hco/3/GRCh38#81594131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275080-C-A

81594131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275080-C-G

http://identifiers.org/hco/3/GRCh38#81594152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70275064-C-A

81594193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275023-T-C

81594443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274770-A-T

81594710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274526-A-G

http://identifiers.org/hco/3/GRCh38#81594944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70274298-C-A

81594944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274298-C-T

http://identifiers.org/hco/3/GRCh38#81595000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70274243-C-A

81595026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274217-T-C

81595053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274190-T-C

http://identifiers.org/hco/3/GRCh38#81595075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70274168-A-C

81595187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274047-G-C

81595242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273997-T-C

81595744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271782-T-C

81595760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271766-T-A

81595760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271766-T-G

81595788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271738-A-G

81595824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271704-G-A

81595910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271611-C-G

81596052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271495-C-T

81596609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269913-C-T

http://identifiers.org/hco/3/GRCh38#81596614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70269908-C-A

http://identifiers.org/hco/3/GRCh38#81596797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70269756-A-C

81596880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269665-G-T

81596896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269648-C-T

81596992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269555-T-C

81597104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269477-A-G

81597122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269460-G-A

81597126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269456-A-T

81597271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269313-T-C

81597331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269245-T-C

http://identifiers.org/hco/3/GRCh38#81597377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70269204-C-A

81597391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269190-G-A

81597826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268821-A-G

81597919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268728-T-C

http://identifiers.org/hco/3/GRCh38#81598979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70267029-A-C

81599028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70266989-T-C

81599294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70266595-T-C

http://identifiers.org/hco/3/GRCh38#81599881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70265526-C-A

81599973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70265442-C-T

81603297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70264857-T-C

81604124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70264420-T-C

81604714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70264148-C-T

81604732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70264130-T-C

81604791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70264042-T-C

http://identifiers.org/hco/3/GRCh38#81604812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70264023-A-C

81605017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70263673-T-C

http://identifiers.org/hco/3/GRCh38#81605158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70263534-A-C

81605274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70263416-A-T

81605615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70263108-G-A

81605717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70263008-A-G

81605720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70263005-T-C

81605744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70262980-G-T

81605750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70262970-G-A

81605979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70262749-T-A

81606185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70262557-C-G

81606289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70262467-T-G

81606375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261895-T-C

81606408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261858-C-T

81606659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261607-G-A

81606704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261561-T-C

81606714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261551-C-T

81606715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261550-G-A

81606715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261550-G-T

81606867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261410-T-C

81607051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261188-C-T

81607146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70261029-C-T

81609055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70259113-T-A

81609062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70259106-G-C

81609208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258968-T-C

http://identifiers.org/hco/3/GRCh38#81609211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70258965-A-C

81609298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258887-T-C

81609316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258859-T-C

81609386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258770-T-C

81609428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258731-T-A

81609499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258707-A-G

81609561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258651-T-A

81609725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258501-T-G

81609734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258487-T-C

http://identifiers.org/hco/3/GRCh38#81609760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70258459-A-C

81609817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258407-T-C

81609874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258339-A-G

81609875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258338-G-A

81609910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258304-T-C

81610077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258116-G-A

81610078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258115-T-C

81610266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257899-T-C

81610266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257899-T-G

81610435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257729-G-A

81610651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257510-T-C

81610651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257510-T-G

81610899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257301-C-T

81610922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257278-T-C

81611031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257170-C-T

81611219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257018-G-A

http://identifiers.org/hco/3/GRCh38#81611574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70256686-C-A

81611842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70256441-A-G

81619109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70256322-A-T

http://identifiers.org/hco/3/GRCh38#81619374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70256052-A-C

81619391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70256035-A-G

http://identifiers.org/hco/3/GRCh38#81619537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70255873-A-C

81619644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70255759-G-A

81619759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70255646-T-G

http://identifiers.org/hco/3/GRCh38#81619806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70255602-C-A

81619806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70255602-C-T

81620060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70254948-T-C

81621182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253835-A-G

81621404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253617-G-A

http://identifiers.org/hco/3/GRCh38#81621578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70253461-A-C

81621579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253460-T-C

81621798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253306-T-C

81627050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250225-T-A

81627080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250196-G-A

http://identifiers.org/hco/3/GRCh38#81627158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70250118-C-A

81627158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250118-C-T

81627668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249596-T-C

81628044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249455-G-C

81628147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249355-G-T

81628189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249314-G-A

81628330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249186-A-T

http://identifiers.org/hco/3/GRCh38#81628340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70249177-C-A

81628340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249177-C-T

http://identifiers.org/hco/3/GRCh38#81628353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70249161-C-A

81628353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249161-C-T

81628422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249089-G-A

81628423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249088-G-A

81628605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248922-A-T

81628680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248865-A-T

81628714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248831-T-C

81628777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248796-A-G

81628832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248751-A-G

81628940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248646-A-G

81633112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246377-C-T

81633427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246235-G-C

http://identifiers.org/hco/3/GRCh38#81633557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70246106-C-A

81633597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246070-A-G

81633597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246070-A-T

81633614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246053-T-C

81633673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246001-T-C

http://identifiers.org/hco/3/GRCh38#81633977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70245701-C-A

81634084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245605-A-T

81634148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245538-C-T

81634225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245492-T-C

81634286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245438-A-G

81634292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245423-A-G

81634783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244695-T-C

81634789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244688-A-T

81635022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244484-A-T

81635025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244481-G-A

81635084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244446-G-A

81635095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244435-A-G

81635360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243818-C-T

81635484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243700-A-G

81635576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243610-T-A

81635677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243506-T-C

81635718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243456-C-T

81635929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243280-C-T

81636055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243154-T-C

81636319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242891-G-A

81636321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242889-G-A

81636440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242740-C-T

81637864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240814-G-A

81637973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240686-T-C

81638023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240635-A-G

http://identifiers.org/hco/3/GRCh38#81638034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70240626-C-A

http://identifiers.org/hco/3/GRCh38#81638189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70240471-C-A

81638189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240471-C-T

81638526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240148-T-C

81638792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239883-T-C

81638953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239730-T-C

81639262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239429-T-C

81639843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238987-G-C

http://identifiers.org/hco/3/GRCh38#81642396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238564-A-C

http://identifiers.org/hco/3/GRCh38#81642426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238537-C-A

81642426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238537-C-T

http://identifiers.org/hco/3/GRCh38#81642489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238477-A-C

81642494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238472-G-A

81642494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238472-G-T

81642496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238470-C-T

http://identifiers.org/hco/3/GRCh38#81642522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238444-C-A

81642522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238444-C-T

81642533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238433-T-A

81642537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238430-A-G

81642537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238430-A-T

81642542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238425-A-T

81642543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238424-T-G

81642576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238399-T-C

http://identifiers.org/hco/3/GRCh38#81642599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238373-A-C

http://identifiers.org/hco/3/GRCh38#81642606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238366-C-A

81642606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238366-C-T

81642659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238317-A-G

81642659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238317-A-T

81642666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238310-A-G

http://identifiers.org/hco/3/GRCh38#81642674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238302-C-A

81642674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238302-C-T

http://identifiers.org/hco/3/GRCh38#81642696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70238280-A-C

81642696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238280-A-G

81642737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238240-T-C

81642738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238239-A-T

81642742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238238-A-T

81642750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70238230-T-C

81642818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70238168-G-A

81642818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70238168-G-C

http://identifiers.org/hco/3/GRCh38#81643025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70237967-A-C

81643025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237967-A-G

http://identifiers.org/hco/3/GRCh38#81643042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70237950-C-A

81643042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237950-C-G

81643042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237950-C-T

81643376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237613-G-T

81643418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237590-C-G

81643460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237548-T-C

81643460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70237548-T-G

81644057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236254-C-T

81644139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236182-T-C

81644160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236161-C-T

81644244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236079-C-T

81644932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235288-G-T

81644969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235254-T-C

81645010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235215-T-C

81645094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235152-T-C

81645147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235097-A-G

81645147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235097-A-T

81645317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234973-G-A

81645522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234775-T-C

81645522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234775-T-G

81645847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234385-T-A

81645903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234332-A-G

81646225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234040-T-A

81646225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234040-T-C

81646225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234040-T-G

81646234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234027-A-G

81646271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233994-T-C

81646278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233987-A-T

81646286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233981-T-C

81646486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70233810-T-C

81646535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233764-T-A

81646550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233757-G-A

81646550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233757-G-T

81646626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233682-A-T

81646645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233660-T-G

81647382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233255-C-T

81647385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233252-T-C

81647671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232968-A-G

81647747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232833-A-T

81648005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232388-A-G

81648056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232348-T-A

81648106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232292-A-G

81648142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232252-T-C

81648168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232230-A-G

81648329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232058-T-C

81648329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232058-T-G

81648338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232049-C-T

81648453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231943-T-C

81648719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231674-G-A

81648719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231674-G-C

http://identifiers.org/hco/3/GRCh38#81648758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70231635-C-A

81648758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231635-C-T

81648897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70231494-T-A

81648918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70231473-T-C

http://identifiers.org/hco/3/GRCh38#81648954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70231437-C-A

81648954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70231437-C-T

81649111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231279-T-A

81649133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231257-C-T

81649179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231219-C-T

81649320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70231050-A-G

http://identifiers.org/hco/3/GRCh38#81649473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70230861-C-A

81649473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230861-C-T

81649478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230856-C-T

81649530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230808-C-T

81649550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230788-G-A

81649553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230785-A-G

81649640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230706-T-C

81649714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230636-T-A

81649770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230581-T-C

81649803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70230549-G-A

81649988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230362-A-G

81649999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230351-T-C

81650002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230348-A-T

81650012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230341-G-A

81650012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230341-G-T

http://identifiers.org/hco/3/GRCh38#81650203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70230168-C-A

81650203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230168-C-G

81650258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230115-T-C

http://identifiers.org/hco/3/GRCh38#81650318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70230056-C-A

81650318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70230056-C-T

81650383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229995-G-A

81650383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229995-G-T

81650401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229977-G-A

81650401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229977-G-T

81650405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229973-G-A

81650405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229973-G-T

81653963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225903-G-T

81653964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225902-C-T

http://identifiers.org/hco/3/GRCh38#81654143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70225693-A-C

81654506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225327-G-T

81654687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70225121-T-G

81654972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70224865-A-G

81657441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70223295-A-T

http://identifiers.org/hco/3/GRCh38#81657729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70222257-A-C

81657876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70222098-G-A

81657889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70222083-G-C

81657944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70222031-T-C

81657980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221995-T-C

81658035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221941-C-G

http://identifiers.org/hco/3/GRCh38#81658433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70221582-A-C

81658449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221566-T-A

81658517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221499-G-C

81658569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221448-A-G

81658776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221238-G-A

81659203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220808-G-T

81659325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220689-A-G

81659957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220392-T-C

81659957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220392-T-G

81660034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220307-T-C

81660034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220307-T-G

81660096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220247-T-C

81660351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219999-T-C

81660684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219780-T-C

81660860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219596-T-C

http://identifiers.org/hco/3/GRCh38#81661048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70219451-C-A

http://identifiers.org/hco/3/GRCh38#81661062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70219437-C-A

81661390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218894-G-T

81664036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218358-G-A

81664036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218358-G-C

81664101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218290-T-C

81664119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218270-T-C

81664350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218095-G-A

81664509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217984-C-T

81664540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217953-A-G

81664739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217584-A-G

81664751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217572-C-T

81664763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217561-T-C

81664895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217424-T-C

81665083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217264-A-G

81665586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217106-G-C

81665586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217106-G-T

http://identifiers.org/hco/3/GRCh38#81665589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70217103-A-C

81665618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217074-A-T

81666281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216189-G-T

81670812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198760-A-T

81670825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198747-G-A

81670825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198747-G-C

81670825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198747-G-T

81670832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198741-A-G

81670832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198741-A-T

81670857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198716-G-A

81670857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198716-G-C

81670861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198712-C-T

http://identifiers.org/hco/3/GRCh38#81670867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70198706-C-A

81670867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198706-C-T

81670873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198700-T-G

http://identifiers.org/hco/3/GRCh38#81670908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70198665-C-A

81670908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198665-C-T

81670926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198647-T-A

81670926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70198647-T-C

http://identifiers.org/hco/3/GRCh38#81670969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70198604-A-C

81670969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70198604-A-G

81670993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198582-G-A

81670993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198582-G-C

81670993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198582-G-T

http://identifiers.org/hco/3/GRCh38#81671023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70198523-C-A

81671023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198523-C-T

81671081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198433-G-T

81671105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198356-T-C

81671207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198159-T-C

81671442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197925-A-G

81671501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197843-C-T

http://identifiers.org/hco/3/GRCh38#81671502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70197842-A-C

http://identifiers.org/hco/3/GRCh38#81671516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70197809-A-C

81671516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197809-A-G

http://identifiers.org/hco/3/GRCh38#81671677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70197622-A-C

81671702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197597-C-T

81671745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197557-A-G

81671746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197556-T-C

http://identifiers.org/hco/3/GRCh38#81679056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70196938-A-C

81679117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196879-C-T

81679204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196812-G-A

81679229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196787-A-G

81679244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196774-A-G

81679269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196747-T-C

81679269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196747-T-G

81679335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196681-C-T

81679336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196680-T-C

81679505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196509-T-G

81679516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196498-T-C

81679542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196477-G-A

81679972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70196032-T-A

81683247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70195006-C-T

81683611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70194631-G-C

http://identifiers.org/hco/3/GRCh38#81683918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70193912-C-A

81684302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193565-G-A

81684365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193517-C-T

81684427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193462-C-T

81684583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193297-G-A

81684583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193297-G-C

81684817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70193013-A-G

81684881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192967-C-G

81684887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192961-T-C

81685015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192673-T-C

81685088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192523-A-T

81685229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192383-C-T

81685689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70192003-T-G

81685817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191890-A-G

81685820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191887-A-T

81686040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191684-T-C

81687220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191392-T-C

81687222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191390-T-C

81687344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191287-G-A

81687355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70191276-T-C

http://identifiers.org/hco/3/GRCh38#81687494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70191145-A-C

81687821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190813-A-G

81687849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190778-G-A

81688853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70189107-T-C

81688861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70189099-A-G

81688891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70189076-T-A

81688891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70189076-T-C

81688936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70189034-A-T

81689531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70188469-T-A

http://identifiers.org/hco/3/GRCh38#81689560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70188440-C-A

81689621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70188379-G-T

81689640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70188363-A-G

81691303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186422-G-A

81691807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186186-T-C

81691959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186078-G-A

http://identifiers.org/hco/3/GRCh38#81692520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70185544-C-A

81693051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70185018-T-G

81693479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70184127-A-G

81693480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70184126-T-C

81693874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70183884-T-C

81694171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70183641-A-G

http://identifiers.org/hco/3/GRCh38#81696011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70178329-A-C

http://identifiers.org/hco/3/GRCh38#81696018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70178322-C-A

81696030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70178310-T-C

81696638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177186-G-C

81696706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177123-A-G

81698446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70176609-T-C

http://identifiers.org/hco/3/GRCh38#81698583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70176475-A-C

81698719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70176322-G-A

81699250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175870-T-C

http://identifiers.org/hco/3/GRCh38#81699922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70175404-C-A

81699963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175366-T-C

81699964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175365-G-C

81699999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175332-G-C

http://identifiers.org/hco/3/GRCh38#81700000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70175331-A-C

81700000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175331-A-G

81700075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175215-T-C

81700131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175159-G-T

81700140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175150-A-G

81700143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70175146-G-A

81700335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174959-T-C

81700399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174896-C-T

81700445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174855-A-G

81700449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174851-T-C

81701933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70170884-T-A

81702331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162475-A-G

81702434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162175-T-A

81702434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162175-T-C

81702544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162062-C-G

81702562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162047-C-T

81703054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70161315-T-A

81703054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70161315-T-C

81703360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70161072-G-C

81703540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70160844-T-C

81704462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158934-T-C

81704754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158672-T-C

81704760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158666-T-A

81704760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158666-T-C

81704841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158500-C-G

81704969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158375-G-A

81705324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158023-G-A

81705352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70157996-T-G

81705408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70157948-A-G

81705408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70157948-A-T

81705557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70157800-T-A

81705557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70157800-T-C

81705884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70157706-T-C

81706673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156572-C-T

81709472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70155140-T-C

81709550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70155053-T-C

81709649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154951-T-C

81709692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154908-T-C

81709711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154889-T-C

81709743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154857-C-T

81709957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154643-C-T

81710021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154581-T-C

81710222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154396-G-C

81710222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154396-G-T

81710422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154361-T-C

81710543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154307-C-T

81710596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154253-T-C

81710714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70154128-G-A

81710877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153980-C-G

81711070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153778-T-C

81711091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153754-C-T

81711113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153732-G-T

81711151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153694-A-G

81711201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70153653-T-C

81713492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70152418-G-A

81713492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70152418-G-C

81713492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70152418-G-T

81713513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70152398-G-T

81713526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70152385-C-T

81715927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150375-G-A

http://identifiers.org/hco/3/GRCh38#81716547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70149514-C-A

81716980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70149083-A-G

81717345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70148724-G-T

81719678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70147206-T-C

81719916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70147007-A-G

81719920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70147003-A-G

81719960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146915-G-A

81720168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146702-G-A

81720481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146267-C-T

81720719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146061-C-T

81721534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70145348-G-A

81721650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70145279-G-A

81721763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70145155-G-T

http://identifiers.org/hco/3/GRCh38#81721850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70145066-C-A

81721975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70144935-T-C

http://identifiers.org/hco/3/GRCh38#81721988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70144922-A-C

http://identifiers.org/hco/3/GRCh38#81721995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70144915-C-A

81722094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70144809-A-G

81722192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70144711-C-T

81722313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70144576-G-C

81722313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70144576-G-T

81723518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143012-T-C

http://identifiers.org/hco/3/GRCh38#81723561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70142963-C-A

81723655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142859-T-C

81723706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142805-T-C

81723824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142694-G-A

http://identifiers.org/hco/3/GRCh38#81724078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70142456-C-A

81724270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142265-C-G

http://identifiers.org/hco/3/GRCh38#81724555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70141877-A-C

http://identifiers.org/hco/3/GRCh38#81724786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70141692-A-C

http://identifiers.org/hco/3/GRCh38#81724839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70141629-A-C

81725004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70141483-G-A

81725085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70141410-G-A

81725085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70141410-G-C

81726220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142742-T-G

81726242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142764-G-A

81726280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142792-G-A

81726308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70142814-A-G

81726350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142859-T-G

81726367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142876-G-A

http://identifiers.org/hco/3/GRCh38#81726443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70142963-A-C

81727326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70140491-C-T

81727414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70140418-C-T

81727652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70140293-C-T

81728120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139809-C-T

http://identifiers.org/hco/3/GRCh38#81728154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70139774-C-A

81728154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139774-C-T

81728253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139674-A-T

81728282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139645-A-G

81728320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139615-A-G

81728533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139403-T-C

81728578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139358-A-G

81728587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139350-T-C

81728587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139350-T-G

81728593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139344-T-C

81728642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139297-G-A

81730767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139205-T-A

81730781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139191-T-A

81730781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139191-T-C

http://identifiers.org/hco/3/GRCh38#81730930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70138604-A-C

81733937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70137006-G-A

http://identifiers.org/hco/3/GRCh38#81733986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70136969-C-A

81734034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136928-C-T

81734316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136698-G-A

81734454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136591-G-A

81734454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136591-G-C

81734602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136424-T-G

81734646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136377-T-A

81734646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136377-T-C

81740880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70130398-T-C

81740996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70130279-G-A

81741111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70130131-T-A

81741665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70129123-G-A

81741948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70129015-G-A

81742522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128668-G-A

http://identifiers.org/hco/3/GRCh38#81742957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70128234-A-C

81742999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128192-C-T

81743120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128069-C-T

81743413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127802-A-G

http://identifiers.org/hco/3/GRCh38#81743448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70127761-C-A

81743448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127761-C-G

81743448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127761-C-T

81743474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127744-T-G

http://identifiers.org/hco/3/GRCh38#81743513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70127705-A-C

http://identifiers.org/hco/3/GRCh38#81743523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70127697-C-A

81743523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127697-C-T

81743551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127670-A-T

81743575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, start_lost
orthologous variants: 70127643-A-G

81743672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127555-T-A

81743677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127550-T-C

81743677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127550-T-G

81743678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127549-G-T

81743680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70127547-T-C

http://identifiers.org/hco/3/GRCh38#81743697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70127530-A-C

81743910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127311-T-A

81744109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127118-T-C

81744155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127062-G-C

81744349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70126865-G-A

81744510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70126706-C-T

81744973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70126222-C-T

http://identifiers.org/hco/3/GRCh38#81746126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70125400-A-C

81749275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70124070-G-A

81749299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70124046-G-A

81749528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70123833-C-T

81749794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70123577-A-G

81749949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70123448-T-C

http://identifiers.org/hco/3/GRCh38#81750137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70123271-A-C

81750198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70123189-A-G

81751544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121383-G-A

81751660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121279-A-G

81751723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121204-A-G

81751790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121173-T-C

81751822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121141-G-T

81751831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121132-T-A

81751843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121120-A-G

http://identifiers.org/hco/3/GRCh38#81751866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70121097-C-A

81751866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70121097-C-G

http://identifiers.org/hco/3/GRCh38#81751909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70121058-C-A

http://identifiers.org/hco/3/GRCh38#81752295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70120720-C-A

81752719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70120298-T-G

81752826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70120198-T-C

81752843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70120187-T-C

81752960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70120092-T-C

81752974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70120078-T-C

http://identifiers.org/hco/3/GRCh38#81753197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70118806-A-C

81753520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70118033-T-C

81753559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70118002-T-G

81753786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70117777-G-T

81753794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70117769-T-C

81753825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117740-G-A

81753909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117656-G-A

81753924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117641-C-T

81753940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117625-T-G

http://identifiers.org/hco/3/GRCh38#81756776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70117514-C-A

81756867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117416-T-C

81756942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117351-A-G

http://identifiers.org/hco/3/GRCh38#81756970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70117324-C-A

81756970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70117324-C-T

81757338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70116959-G-A

81758508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114444-G-A

http://identifiers.org/hco/3/GRCh38#81758627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#70114345-A-C

81758672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114307-A-G

81758953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114184-T-C

81759064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114128-T-C

81759175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114075-G-A

81759175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114075-G-C

81759289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114001-G-C

81759379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70113909-T-C

81759405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70113890-T-C

81759544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70113068-C-T

81759693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70112917-G-T

81759962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70112646-T-A

81759962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70112646-T-C

81760462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70112045-G-A

81760746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70111707-G-A

81760746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70111707-G-T

81760884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70111586-G-A

81761099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111405-A-G

81761151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111376-A-G

81761172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70111362-T-A

81761219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111328-C-T

http://identifiers.org/hco/3/GRCh38#81761227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#70111325-C-A

81761227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111325-C-G

81761227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111325-C-T

http://identifiers.org/hco/3/GRCh38#81761230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#70111322-A-C

81761230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111322-A-T

http://identifiers.org/hco/3/GRCh38#81761249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#70111303-C-A

81761250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111302-A-T

81761251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70111301-C-T

http://identifiers.org/hco/3/GRCh38#81761475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#70111081-C-A

81761475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70111081-C-G

81761475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70111081-C-T

81761487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70111069-G-A

http://identifiers.org/hco/3/GRCh38#81761522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#70111032-C-A

81761522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70111032-C-T

81761561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70110992-G-A

81761561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4180
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70110992-G-T