40519023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434887-C-T

40519120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434794-G-A

http://identifiers.org/hco/5/GRCh38#40519251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5434654-A-C

40519295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434607-A-G

http://identifiers.org/hco/5/GRCh38#40519472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5434430-C-A

40519472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434430-C-T

40519527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434357-T-C

40519552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434335-T-A

40519552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434335-T-G

40519686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434202-A-T

40519690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5434198-T-G

40519911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433970-G-T

40520027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433858-A-G

40520255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433653-T-C

http://identifiers.org/hco/5/GRCh38#40520346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5433349-A-C

http://identifiers.org/hco/5/GRCh38#40520359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5433331-A-C

40520389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433300-G-A

40520460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433224-A-G

40520558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433154-T-A

40520617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5433096-T-C

http://identifiers.org/hco/5/GRCh38#40520995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5432471-A-C

40520995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5432471-A-G

40521233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431824-A-G

http://identifiers.org/hco/5/GRCh38#40521344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5431701-A-C

40521399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431661-G-T

40521447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431613-T-G

40521448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431612-G-A

40521494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431566-G-A

http://identifiers.org/hco/5/GRCh38#40521789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5431280-C-A

40521789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5431280-C-T

http://identifiers.org/hco/5/GRCh38#40522038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5431041-C-A

40522132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430966-A-G

40522193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430906-G-A

40522262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430856-C-T

40522342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430773-T-C

40522405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430713-T-A

40522438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430678-T-A

40522458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430656-A-G

40527349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430447-G-A

40527349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430447-G-C

40527351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5430445-G-T

40528172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5424590-G-A

http://identifiers.org/hco/5/GRCh38#40528761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5424033-A-C

http://identifiers.org/hco/5/GRCh38#40529026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5423791-C-A

http://identifiers.org/hco/5/GRCh38#40529333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5423503-C-A

40529461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5423303-G-A

http://identifiers.org/hco/5/GRCh38#40530695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5420612-A-C

40531161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5420213-T-G

40531547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419876-A-G

40531579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419843-T-C

40531586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419836-G-A

40531588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419834-G-A

40531588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419834-G-C

40532390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419368-A-G

40532591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5419039-A-G

40532870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5418762-G-C

40532930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5418714-A-G

40548230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5416891-A-G

40548545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5416611-T-C

40549729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415218-T-C

40549755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415192-G-A

40549755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415192-G-C

40549755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415192-G-T

40549762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415185-G-A

40549762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5415185-G-T

40552062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5393753-A-G

40552338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5393497-T-A

40552338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5393497-T-G

40552431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5393406-A-G

40552474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5393364-T-C

40552519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5393319-G-T

40552576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5393256-G-A

http://identifiers.org/hco/5/GRCh38#40552869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5392938-A-C

40554146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5390616-T-C

40554258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5390511-A-T

40554639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5389572-T-C

40554839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5389364-C-T

40554840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5389363-A-G

40554876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5389321-G-A

40556711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5385409-T-G

http://identifiers.org/hco/5/GRCh38#40556974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5385152-C-A

40557663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5384132-A-G

http://identifiers.org/hco/5/GRCh38#40557686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5384109-A-C

40557868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5383920-A-G

40558877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5381510-T-C

40559286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380502-G-A

40559596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380199-T-G

40559650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380150-C-T

40559694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380106-G-A

40559694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380106-G-T

40559739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5380082-C-T

40560311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5379830-T-G

40560314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5379827-A-G

http://identifiers.org/hco/5/GRCh38#40560351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5379791-A-C

40560431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5379712-G-A

40560522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5379622-T-C

40560574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5379569-T-G

40567982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5378877-T-A

http://identifiers.org/hco/5/GRCh38#40569607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5377826-A-C

40569607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377826-A-G

40569607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377826-A-T

40569681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377753-A-G

40570053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377462-T-A

40570086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377430-C-T

40570187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377339-A-T

40570201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377325-T-C

40570365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377133-T-A

40570383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5377118-A-T

40570792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5376763-T-A

40571117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5376447-A-T

40571368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5375953-T-C

40571469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5375853-A-G

40572123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374606-C-T

40572180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374549-C-T

40572269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374461-T-C

40572402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374343-A-G

40572461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374275-C-T

40572519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374212-G-A

40572534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374203-A-T

40572562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5374178-G-A

40572772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373988-T-A

40572819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373802-T-C

http://identifiers.org/hco/5/GRCh38#40573256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5373339-C-A

http://identifiers.org/hco/5/GRCh38#40573278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5373317-A-C

40573298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373298-C-T

40573333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373263-C-T

40573469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373134-A-G

40573528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373079-A-G

40573531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5373076-A-G

40573631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5372970-G-A

40573647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5372959-A-G

40573681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5372935-G-T

40574226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369775-C-T

40574546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369466-G-A

40574582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369430-G-A

40574655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369357-G-A

40574834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369182-T-C

40574942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5369069-A-G

40576032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366467-T-A

40576065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366434-T-C

40576202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366264-C-G

40576352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366120-T-C

40576370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366112-T-C

40576469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366025-A-G

40576469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5366025-A-T

40576626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365863-T-A

40576626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365863-T-C

40576635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365855-C-T

40576675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365815-A-G

40576940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365565-T-C

40577170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365366-C-T

40577192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365344-A-G

40577470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5365067-A-G

40577714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5364823-G-A

40583623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5357300-T-C

40583738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5357201-G-C

40584059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5356873-G-A

40584449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5356521-A-T

40585820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5344421-A-G

40586021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5344234-C-T

40586176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5344050-G-A

40586176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5344050-G-T

http://identifiers.org/hco/5/GRCh38#40589788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: -C-A

40597434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336788-T-C

40597767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336452-G-A

40597775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336444-T-C

40597780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336439-T-C

40597824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336396-G-A

40597890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5336325-G-C

40599571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5335666-T-C

40599701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5335542-C-T

40599861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5335387-A-G

40600066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335162-G-A

40600066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335162-G-C

40600089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335139-T-A

40600089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335139-T-C

40600115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335112-G-A

40600165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335065-C-T

40600188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335042-G-C

40600208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335034-T-C

40600248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334994-A-G

40600274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334968-G-A

40600481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334765-G-A

40600514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334732-G-A

40600658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334587-C-T

40600812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334433-C-T

40600849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334400-A-G

40600849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334400-A-T

http://identifiers.org/hco/5/GRCh38#40600936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5334313-C-A

40601538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333582-C-T

40601601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333518-T-A

40601630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333489-A-G

http://identifiers.org/hco/5/GRCh38#40601775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5332951-A-C

40601811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332918-A-G

40601924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332805-G-T

40601930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332799-C-T

40601974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332745-G-A

40602088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332610-A-G

40602158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332556-C-G

40602225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332498-T-C

40602261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332466-A-G

40602439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332320-C-G

40602439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332320-C-T

40604418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330741-A-G

40604543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330634-A-G

http://identifiers.org/hco/5/GRCh38#40604566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5330611-C-A

40604667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330518-G-T

40604687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330498-A-G

40605421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330125-C-T

40605507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330038-G-T

40605542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330001-A-G

40605542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330001-A-T

40605946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329627-C-T

40606099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329492-C-T

40606758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329296-G-T

40606863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329195-T-C

40607036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328955-C-T

40607126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328869-G-A

http://identifiers.org/hco/5/GRCh38#40607158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5328837-C-A

40607455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327860-T-C

http://identifiers.org/hco/5/GRCh38#40607461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5327854-C-A

40607486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327823-T-C

40607486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327823-T-G

40607805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327372-T-C

40608401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325065-T-C

40608456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325010-A-G

40608459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325004-T-C

40609241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324557-T-C

40609252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324550-C-T

40609447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324356-T-C

40609619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324187-G-A

40609619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324187-G-T

40609685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324127-A-G

40609771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324063-T-A

40610362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323468-G-T

40610450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323345-G-A

40610450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323345-G-C

http://identifiers.org/hco/5/GRCh38#40610547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5323094-C-A

40610603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323033-T-C

40610650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322986-G-T

http://identifiers.org/hco/5/GRCh38#40612401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5322292-A-C

40612401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322292-A-G

http://identifiers.org/hco/5/GRCh38#40612529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5322169-C-A

40612927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322076-T-C

http://identifiers.org/hco/5/GRCh38#40612940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5322063-C-A

40612940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322063-C-T

40612941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322062-A-G

40612941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322062-A-T

http://identifiers.org/hco/5/GRCh38#40612980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5322001-C-A

40612980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5322001-C-T

http://identifiers.org/hco/5/GRCh38#40613031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5321952-C-A

40613136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5321870-A-G

40613174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5321840-A-G

40613265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5321764-T-C

40613298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5321731-A-G

http://identifiers.org/hco/5/GRCh38#40613314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5321716-C-A

40613870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321203-G-A

40614200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320871-A-G

40614220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320851-G-C

40614312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320780-G-A

40614312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320780-G-C

40614803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319867-A-G

40614956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319712-T-A

40615061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319625-T-C

40615122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319580-C-T

40615586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318163-T-A

40615600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318149-T-A

40615762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317986-A-T

40615843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317936-A-G

40616120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317661-T-C

http://identifiers.org/hco/5/GRCh38#40616405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5317133-C-A

40616405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317133-C-T

40616465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317078-A-G

40619946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5313045-G-A

http://identifiers.org/hco/5/GRCh38#40621751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5310345-C-A

40622251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309931-T-C

40622408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309776-G-T

40622814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309372-T-A

40622838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309119-G-A

40623229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5308676-G-A

40623381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5308553-G-C

40623474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5308467-T-C

40624090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5307882-G-A

40625186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305847-C-G

40625259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305799-A-T

40625325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305736-C-T

http://identifiers.org/hco/5/GRCh38#40625521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5304533-C-A

40625525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304529-T-A

40625995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304120-C-T

http://identifiers.org/hco/5/GRCh38#40626100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5304025-C-A

http://identifiers.org/hco/5/GRCh38#40626358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5303802-C-A

40626358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5303802-C-G

40627485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296303-G-A

40627573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296219-A-G

40627826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295767-C-T

40627836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295757-C-T

40628048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295549-T-A

40628048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295549-T-C

40628283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295396-G-C

40631661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5294362-C-T

40631758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5294268-G-C

40631920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5294129-G-A

40631951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5294095-G-A

40632427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293677-A-G

http://identifiers.org/hco/5/GRCh38#40632451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5293653-C-A

40632466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293638-G-A

40632466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293638-G-T

40632638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293334-C-G

40632638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293334-C-T

40632803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293156-A-G

40633813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293085-G-A

40633898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5293009-A-G

40633944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5292954-A-G

40646546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5289828-C-T

40646693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5289683-A-G

40646840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5289546-G-C

40646945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5289424-G-A

40647028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5289351-G-A

40666070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5284740-A-G

40666319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5284494-T-C

40670493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5282491-G-A

http://identifiers.org/hco/5/GRCh38#40670718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5282292-A-C

40670718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5282292-A-G

40670734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5282276-T-C

40671041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5282151-T-C

40671284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5281885-C-T

40674559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5281276-C-T

http://identifiers.org/hco/5/GRCh38#40674824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5281051-C-A

http://identifiers.org/hco/5/GRCh38#40674954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5280939-A-C

http://identifiers.org/hco/5/GRCh38#40675049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5280848-A-C

http://identifiers.org/hco/5/GRCh38#40675396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5280675-A-C

40675396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280675-A-G

40675451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280635-A-G

http://identifiers.org/hco/5/GRCh38#40675501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5280585-C-A

40675501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280585-C-T

40675703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280340-T-C

40675768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280279-T-A

40675768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280279-T-C

40675885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5280155-C-G

40676341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5278366-A-G

http://identifiers.org/hco/5/GRCh38#40676420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5278266-A-C

40676422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5278264-T-C

40676642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5278053-T-A

40676741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277946-T-C

40676782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277911-T-C

40676786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277907-G-C

40676853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277846-A-T

40677041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277638-A-T

40677062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277617-G-T

40677141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5277555-A-G

40677548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5276967-G-A

40677548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5276967-G-T

40678088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5275546-G-C

40678088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5275546-G-T

http://identifiers.org/hco/5/GRCh38#40679369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5274212-A-C

40679386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5274194-C-T

40679474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5274114-T-C

http://identifiers.org/hco/5/GRCh38#40679524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5274063-C-A

40679524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5274063-C-T

40679528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5274059-A-G

40679564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5274024-T-A

40679644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5273947-G-C

40679644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5273947-G-T

40679693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273906-G-A

40679693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273906-G-T

40679695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273904-G-A

40679695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273904-G-C

40679695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273904-G-T

http://identifiers.org/hco/5/GRCh38#40679746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5273844-C-A

40679778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5273808-C-T

40679848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, undefined
orthologous variants: 5273734-G-A

40680099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273482-G-A

40680099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273482-G-T

40680141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273445-G-A

40680141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273445-G-T

40680220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273366-A-G

http://identifiers.org/hco/5/GRCh38#40680254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5273325-C-A

40680254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5273325-C-T

http://identifiers.org/hco/5/GRCh38#40680511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5273077-C-A

40680511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273077-C-T

40680569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273028-G-A

40680810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5272796-G-A

40680810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5272796-G-C

40680810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5272796-G-T

40680814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5272792-A-G

40680930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5272687-T-A

40680976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5272636-G-A

40681189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5272420-C-G

40681249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5272360-C-T

40681681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5271928-G-T

40681687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5271922-G-A

40681687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5271922-G-C

40681687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5271922-G-T

40681699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5271901-G-A

40681760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5271840-G-A

40681760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5271840-G-T

40681951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271657-T-C

40681953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271645-G-A

40681953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271645-G-T

40681959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5271639-G-A

40681959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5271639-G-T

40681979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5271618-G-A

40681979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5271618-G-T

40682097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271494-C-T

40682321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271253-G-T

40682863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270823-T-C

40682944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270741-A-G

40683699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270021-A-G

http://identifiers.org/hco/5/GRCh38#40683934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5269820-A-C

http://identifiers.org/hco/5/GRCh38#40683963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5269791-C-A

40684106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269646-T-C

40684630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269137-A-G

40685081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268714-G-A

40685263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268543-T-C

40685291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268519-A-G

40685471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5268384-G-T

http://identifiers.org/hco/5/GRCh38#40685510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5268346-C-A

40685510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5268346-C-T

40685723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5268139-C-T

40686258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5267638-G-A

40687384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266871-C-T

40687387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266868-A-T

40687895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266600-A-T

40687972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266524-T-C

40688149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266403-C-T

40688316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266224-G-A

40690439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5265273-T-C

40690528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5265187-T-C

40690694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264921-G-C

40691738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264748-G-A

40691738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264748-G-T

40691971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5264509-T-G

40692163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 5264326-G-A

40692220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 5264269-T-C

40692591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263931-G-A

40692591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263931-G-T

40692654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263886-A-G

40692673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263867-G-A

http://identifiers.org/hco/5/GRCh38#40692748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5263796-C-A

40693119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263440-G-C

40693228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263340-T-C

40693303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263267-G-A

40693303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263267-G-C

40693324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263255-A-T

40693341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263238-A-T

40693389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5263190-A-G

40693622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5262996-T-C

40693679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5262939-G-T

http://identifiers.org/hco/5/GRCh38#40693691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5262927-C-A

40693691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5262927-C-T

40694490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5259750-T-C

40694954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5259299-A-G

40696480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5258800-G-C

40696667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant
orthologous variants: 5258590-T-C

40696772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5258498-T-A

http://identifiers.org/hco/5/GRCh38#40696858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5258422-C-A

40711413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5251859-A-G

40711515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5251763-C-T

http://identifiers.org/hco/5/GRCh38#40711520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5251758-A-C

40711520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron variant
orthologous variants: 5251758-A-T

40711710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5251601-G-C

40711819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5251520-T-C

40711991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5251379-G-A

40712216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5251197-T-C

40712270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5251145-T-C

http://identifiers.org/hco/5/GRCh38#40712695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5250789-A-C

40712695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5250789-A-T

40712913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5250537-G-A

40712913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5250537-G-C

40713435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5250051-G-A

40713494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249993-C-T

40713620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249884-T-G

40713820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249688-T-C

40713820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249688-T-G

40713876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249629-T-C

40714040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249480-A-G

40714262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249276-A-G

40714262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249276-A-T

40714376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249189-G-T

40714523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5249064-A-G

40714795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248801-G-T

40714897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248696-G-C

40714932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248502-T-C

40714982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248454-A-G

40715112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248183-T-A

40715112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5248183-T-C

http://identifiers.org/hco/5/GRCh38#40715510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247655-C-A

http://identifiers.org/hco/5/GRCh38#40715593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247553-C-A

http://identifiers.org/hco/5/GRCh38#40715617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247529-A-C

40715617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247529-A-G

http://identifiers.org/hco/5/GRCh38#40715684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247455-A-C

http://identifiers.org/hco/5/GRCh38#40715913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247233-C-A

40715926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247220-A-T

40715937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247209-T-C

http://identifiers.org/hco/5/GRCh38#40715940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247206-C-A

http://identifiers.org/hco/5/GRCh38#40715972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247176-C-A

40715972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247176-C-T

40715978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247170-C-G

http://identifiers.org/hco/5/GRCh38#40715985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247163-C-A

http://identifiers.org/hco/5/GRCh38#40715997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5247151-C-A

40715997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247151-C-T

40716035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5247115-A-G

40716260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5246867-A-G

40716308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5246819-T-A

40716354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5246773-T-A

40716579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246541-T-A

40716607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246510-A-G

40716607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246510-A-T

40728391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 5241563-C-T

40728501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241450-A-G

http://identifiers.org/hco/5/GRCh38#40729168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5240847-A-C

40729271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240737-T-G

40729287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240725-T-C

40729552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238293-A-G

40730181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238006-T-C

40730888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228385-C-T

40730992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228276-G-C

40731020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228246-T-A

40731020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228246-T-C

40731243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228044-G-A

40731243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228044-G-T

40731291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227997-G-A

40733395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226682-T-C

40733433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226645-A-G

40733458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226619-G-A

40733458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226619-G-C

40733520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226570-T-A

40733520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226570-T-G

40733557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226533-C-T

40733741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226321-C-G

40733830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226250-A-G

40734340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225743-C-T

40734604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225482-T-C

40734604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225482-T-G

40734629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225457-C-T

40734779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225361-T-C

40734881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5225276-G-A

40735137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225003-T-C

40735213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5224928-T-C

http://identifiers.org/hco/5/GRCh38#40735231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5224916-A-C

40735301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5224854-G-A

http://identifiers.org/hco/5/GRCh38#40735337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5224821-A-C

40735351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5224807-T-C

40735351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5224807-T-G

40735649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224528-T-C

40735657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224521-C-G

40736031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223945-C-T

40736032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223944-G-A

40736112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223867-G-A

40736296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223679-T-A

40736512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223475-C-T

40736570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223414-T-C

40736759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223261-T-A

40736759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223261-T-G

40736848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223160-A-G

40744007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5221981-G-A

40744009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5221979-G-T

40744056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5221933-T-C

40744106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5221865-A-G

40744213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5221766-T-C

40746132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5220427-T-C

40746132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5220427-T-G

http://identifiers.org/hco/5/GRCh38#40746190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5220372-C-A

40746255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5220320-G-T

http://identifiers.org/hco/5/GRCh38#40746782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5219298-A-C

40746782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5219298-A-G

http://identifiers.org/hco/5/GRCh38#40746784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5219296-C-A

40746784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5219296-C-T

40746912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5219168-T-G

40749361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217834-A-T

40753845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216918-C-G

http://identifiers.org/hco/5/GRCh38#40753928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5216863-A-C

40753942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216859-T-A

40753949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216852-A-G

40753950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216851-T-A

40754105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216724-T-C

40754146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216697-C-T

40754725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216294-G-A

40754889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215936-T-C

http://identifiers.org/hco/5/GRCh38#40754913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#5215906-A-C

40754937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215882-G-C

40755152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215690-T-A

40755583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215357-G-A

40755583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215357-G-C

40755639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215319-G-A

40755760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215237-C-T

http://identifiers.org/hco/5/GRCh38#40755768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5215229-C-A

40755810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215178-G-A

40755810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215178-G-C

40755810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5215178-G-T

40755859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5215119-G-T

http://identifiers.org/hco/5/GRCh38#40755948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29959
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#5215034-C-A