8126299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25589028-A-G

http://identifiers.org/hco/2/GRCh38#8126466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25588833-A-C

8126674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25588522-A-T

8126726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25588466-T-C

8126890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25588300-C-G

8127142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25588095-T-C

8132838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25586335-C-T

8132993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25586163-T-C

8133004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25586152-C-T

8133008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25586148-A-G

8133139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25586041-C-T

8133322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585799-G-A

8133332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585789-G-T

8133400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585668-T-C

http://identifiers.org/hco/2/GRCh38#8133437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25585625-C-A

8133437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585625-C-G

8133446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585599-G-C

http://identifiers.org/hco/2/GRCh38#8133461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25585584-A-C

8133519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585537-T-C

8133656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585362-C-G

http://identifiers.org/hco/2/GRCh38#8133796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25585201-A-C

8133796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585201-A-G

8133796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25585201-A-T

8134437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25584907-G-A

8134905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25584446-G-A

8134928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25584425-C-T

8135261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25584052-T-C

8135413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583910-A-T

8135455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583867-C-T

http://identifiers.org/hco/2/GRCh38#8135617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25583709-A-C

8135846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583484-A-G

8135953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583378-C-T

8136014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583308-G-A

8136191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25583096-G-T

http://identifiers.org/hco/2/GRCh38#8136419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25582853-A-C

8136419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582853-A-G

8136419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582853-A-T

8136917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582408-T-C

8136980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582342-C-G

8137030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582303-T-C

8137102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582248-T-G

http://identifiers.org/hco/2/GRCh38#8137118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25582234-A-C

8137118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582234-A-G

8137237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582142-A-G

8137332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25582050-T-C

8137449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581933-A-T

http://identifiers.org/hco/2/GRCh38#8137639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25581721-A-C

8138074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581224-A-G

8138162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25581137-T-C

8138387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580932-T-C

8138424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580903-A-G

8138511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580812-T-C

8138550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580784-C-T

8138702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25580645-G-A

8139207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25580232-A-G

http://identifiers.org/hco/2/GRCh38#8139359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25580077-C-A

8139379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25580058-A-G

8139405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25580032-G-T

8139410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25580027-T-A

8139410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25580027-T-C

http://identifiers.org/hco/2/GRCh38#8139431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25580002-C-A

8139431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25580002-C-G

8139431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25580002-C-T

8139526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579914-G-A

8139526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579914-G-T

8139543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579895-G-A

8139543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579895-G-T

8139549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579889-A-G

8139549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579889-A-T

8139568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579874-A-G

8139570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579872-G-A

8139570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579872-G-C

8139570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25579872-G-T

8139736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25579740-G-A

8139888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25579589-T-C

8139982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25579513-G-A

8140019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25579476-G-A

8140147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25579281-T-A

http://identifiers.org/hco/2/GRCh38#8140667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25578084-C-A

8140667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25578084-C-T

8140877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577905-C-T

8141153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577645-A-G

8141256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577558-T-C

8141578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577243-G-A

8141608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577216-C-T

8141728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25577108-C-G

8141827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25577013-C-G

8142337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25576506-T-C

8142403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25576428-G-T

http://identifiers.org/hco/2/GRCh38#8143193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25574333-C-A

8143278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25574268-A-G

http://identifiers.org/hco/2/GRCh38#8143360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25574222-C-A

8143414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25574169-G-A

8143508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25574074-A-T

8143800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25573668-C-T

8144035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25568878-A-G

8144137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25568779-T-C

8144504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25568444-A-G

8144685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25568290-T-C

8144759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25568214-A-G

8144930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25568067-C-G

8145004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25568001-A-G

8145005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25568000-T-G

8145125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567877-A-G

8145245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567779-G-A

8145417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567709-G-A

8145576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567569-T-G

8145638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567504-C-G

8145743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25567336-C-T

8146269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25566809-C-T

8146298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25566770-T-C

http://identifiers.org/hco/2/GRCh38#8146721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25566387-C-A

8146837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25566279-T-C

8148826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25564215-G-A

8148830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25564211-G-A

8148838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25564203-G-A

8148850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25564191-G-A

8148956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25564058-C-T

8149119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25563908-G-C

8149119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25563908-G-T

8150382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25562538-G-A

8150482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25562452-A-G

8150578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25562352-C-T

8150908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25562037-C-T

8151015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561946-T-G

8151072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561890-C-G

8151072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561890-C-T

8151082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561882-C-T

8151123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561856-A-T

8151233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25561746-T-C

http://identifiers.org/hco/2/GRCh38#8153632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25558900-A-C

8153797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25558738-C-T

http://identifiers.org/hco/2/GRCh38#8153984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25558560-C-A

8154001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25558543-C-G

http://identifiers.org/hco/2/GRCh38#8154022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25558525-C-A

8154093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25558440-T-C

8154206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25558333-A-G

8154430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25557719-A-G

8154667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25557509-G-A

8154667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25557509-G-C

8155655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25554219-A-T

8156046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553764-G-A

8156085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553715-G-A

8156104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553697-G-A

8156352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553526-G-T

8156568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553341-C-G

8156591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553321-C-T

8156727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25553193-G-A

8157788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25551017-G-A

http://identifiers.org/hco/2/GRCh38#8157801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25551002-C-A

8157838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550965-A-G

8158510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550290-C-T

8158563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550222-A-T

8158651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25550152-C-T

8158980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549866-G-A

8159026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549821-C-T

http://identifiers.org/hco/2/GRCh38#8159054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25549794-C-A

8159096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549754-G-A

http://identifiers.org/hco/2/GRCh38#8159220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25549609-C-A

8159297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549512-A-G

8159298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549511-G-A

8159327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549483-C-T

8159405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549418-G-T

8159494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25549373-C-G

8159920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25547375-T-C

8159971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25547325-C-T

8159997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25547307-T-A

8160012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25547294-G-A

8160361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25546955-C-T

8160614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25546760-G-C

8160909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25546039-G-T

http://identifiers.org/hco/2/GRCh38#8161122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25545877-A-C

8161148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545849-C-G

8161148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545849-C-T

8162290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545759-A-G

8162334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545715-T-A

8162344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545704-A-T

8162370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25545678-A-G

8162485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25543733-C-T

8162526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25543696-C-T

8162566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25543651-G-A

8162577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25543643-C-T

8162752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25543468-A-T

8163845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542922-T-A

8163845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542922-T-C

8164059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542709-A-T

8164393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542419-C-T

8164480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542345-T-C

8164663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25542174-T-C

8164989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25541868-T-A

8164989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25541868-T-C

8165043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25541804-C-T

8167088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25539297-G-A

8167830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25538867-T-C

8167832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25538865-T-C

8168120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25537048-C-T

http://identifiers.org/hco/2/GRCh38#8170489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25536135-A-C

8170585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25536044-T-C

8170596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25536032-T-C

8170639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25535990-C-T

8170811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25535814-G-A

8170921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25535707-C-T

8171006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25535622-T-C

8171103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25535525-G-A

8171861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25534224-A-G

8171965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25534129-G-A

8171968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25534126-T-C

8172238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533834-G-A

8172238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533834-G-C

8172238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25533834-G-T

8190217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25528374-G-A

8190380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25528188-A-G

http://identifiers.org/hco/2/GRCh38#8190417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25528141-A-C

8190481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25528073-T-C

8190608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25527912-G-T

8190694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25527814-G-A

8193445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25526027-T-C

8193543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525902-A-G

8194022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525479-G-A

8194227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25525287-G-T

8195064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524366-G-A

8195343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524086-G-A

8195403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524052-A-G

8195403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25524052-A-T

http://identifiers.org/hco/2/GRCh38#8195421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25524034-C-A

8195522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25523889-G-A

8195834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522852-T-G

8195883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522805-A-G

8195937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522756-C-T

8196251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522479-C-T

8196339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522375-C-G

8196431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522287-G-A

8196531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522195-A-G

8196817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521937-C-T

8197001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521764-G-A

8197106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521660-G-T

8197320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521525-C-T

8197449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521399-C-T

8197804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521088-A-G

8197874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521037-C-T

8197919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520988-C-T

8197938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520969-A-T

8198331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520602-C-T

8201183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520364-C-G

8201207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520339-T-C

8201224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520322-G-C

8201239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520307-C-G

8201359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520183-A-G

8201396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520148-T-C

8201632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519927-T-C

8201657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519903-A-G

8201720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519841-G-A

8201784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519770-C-T

8202316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519308-A-G

8202321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519303-T-C

8202337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519287-C-T

8202494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519137-G-A

8202750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518936-C-T

8202926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518797-G-A

8202977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518744-G-T

8202991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518731-T-A

8202991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518731-T-G

8203207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518501-T-G

8203307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518280-G-T

8203526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25518055-G-C

8203619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517978-G-A

8204280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517378-G-A

8204294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517364-G-A

8204294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517364-G-C

8204294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517364-G-T

8204305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517353-A-G

8204321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25517337-C-T

8212574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509297-G-T

8212620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509232-A-T

8212814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509076-C-T

8213269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508921-C-T

http://identifiers.org/hco/2/GRCh38#8213342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25508852-A-C

8213403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508800-A-T

http://identifiers.org/hco/2/GRCh38#8213445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25508761-C-A

8213445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508761-C-T

8213566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508646-G-A

8213588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508633-C-T

8213767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508472-C-G

8213767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508472-C-T

8213773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508466-C-T

8213906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508341-T-C

8213924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508323-A-G

8213969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25508283-G-T

8214618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507336-C-T

8214638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507317-C-G

8214638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507317-C-T

8214657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507298-T-G

8214698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507257-A-T

8214812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507172-T-A

8214889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507111-G-A

8214927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507072-T-C

8214950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507050-C-G

8214986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506986-G-T

http://identifiers.org/hco/2/GRCh38#8215183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25506851-C-A

8215536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506506-A-G

8215557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506482-T-A

8215557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506482-T-C

8215760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505899-G-A

8216108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505544-G-T

8216316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505103-G-T

8216575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504871-A-T

http://identifiers.org/hco/2/GRCh38#8216730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25504742-A-C

8216750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504723-T-C

8216788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504683-A-T

8216854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504609-A-G

8216879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504587-G-A

8216880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504586-T-C

http://identifiers.org/hco/2/GRCh38#8217107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25504365-A-C

8217146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504322-G-C

8217369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504109-G-A

8217378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504100-G-C

8217599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503875-C-T

8217676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503796-G-A

http://identifiers.org/hco/2/GRCh38#8220647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25502593-C-A

8220647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502593-C-T

8220714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502501-T-A

8220718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502497-C-T

8221319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502199-T-C

http://identifiers.org/hco/2/GRCh38#8221342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25502170-C-A

8221415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502097-A-G

8221415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502097-A-T

8221447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502076-A-G

8221682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501852-A-T

8221753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501797-C-T

8221856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501706-C-T

8222283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501264-G-C

8222289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501257-G-A

8222498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501102-C-T

8222582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25501045-G-A

8222672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500967-G-T

http://identifiers.org/hco/2/GRCh38#8222681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25500958-C-A

http://identifiers.org/hco/2/GRCh38#8222701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25500939-C-A

8222725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500917-T-C

8222762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500885-C-T

8222885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500798-C-T

8222946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500749-T-C

8223091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500657-C-T

8223140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500605-T-C

8223222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500520-G-A

8223607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500162-G-A

8223839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499961-T-C

http://identifiers.org/hco/2/GRCh38#8224857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25499007-C-A

8224857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25499007-C-T

8224954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498906-A-T

http://identifiers.org/hco/2/GRCh38#8225401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25498483-A-C

8225405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498479-C-T

8225603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498289-C-T

8225806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498145-T-C

8225990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497938-C-G

http://identifiers.org/hco/2/GRCh38#8226009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25497919-C-A

8226054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497849-A-G

8226286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497624-C-T

8226362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497548-C-T

8226363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497547-T-A

8226363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497547-T-C

8226500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497414-G-A

8226588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497327-A-G

8226596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497319-A-G

8226723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497208-C-T

8227175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496815-T-A

8227175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496815-T-C

8227295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496669-T-C

8227401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496569-G-A

8227401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496569-G-C

http://identifiers.org/hco/2/GRCh38#8227524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25496474-C-A

8227602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496397-T-C

8227698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496304-A-G

8227698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496304-A-T

8227845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25496166-T-C

http://identifiers.org/hco/2/GRCh38#8228286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25495705-A-C

8228304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495687-C-G

http://identifiers.org/hco/2/GRCh38#8228344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25495644-C-A

8228344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25495644-C-T

http://identifiers.org/hco/2/GRCh38#8230820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25493418-A-C

8231026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493224-G-C

http://identifiers.org/hco/2/GRCh38#8231106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25493161-C-A

8231106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493161-C-T

8231149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493123-T-C

8231244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493023-A-T

8231264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25493003-G-A

8231298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492965-G-T

8231412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492868-G-A

8234110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489693-G-A

8234243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489566-T-A

8234540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489275-T-C

8234815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25489060-G-T

http://identifiers.org/hco/2/GRCh38#8234858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25489017-C-A

8234923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25488957-C-T

8234935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25488945-G-A

8235124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25488725-T-C

8235389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25488474-A-G

8235441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25488403-C-T

8235644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25488285-C-G

8235652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25488278-G-A

8239899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25486352-T-C

8239964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486287-T-C

8239983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486268-T-C

8239983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486268-T-G

8240967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25485076-C-T

8241113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25484919-C-T

8241237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25484801-T-A

8241289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25484747-G-A

8241339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25484697-T-G

8241523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25484517-G-A

8242020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483954-C-T

http://identifiers.org/hco/2/GRCh38#8242037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25483937-A-C

http://identifiers.org/hco/2/GRCh38#8242090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25483886-C-A

8242363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483611-C-G

8242363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483611-C-T

8242416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483558-A-G

8242475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483499-C-G

http://identifiers.org/hco/2/GRCh38#8242549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25483425-C-A

8242863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25483135-T-C

8243187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25482815-G-C

8243345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25482651-G-A

8243763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25482001-G-T

8244148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481455-A-G

8244261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481373-C-G

8244326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481302-C-T

8244333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481295-G-A

http://identifiers.org/hco/2/GRCh38#8244338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25481290-C-A

8244339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25481289-T-G

8246797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479629-T-G

8246849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479577-C-T

8247004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479424-T-C

8247157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479297-G-C

8247281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25479192-C-G

8247563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478959-G-T

8248960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478495-T-C

8249067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478398-G-A

8249067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478398-G-T

8249211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25478266-G-T

8249822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472013-G-A

8249822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472013-G-C

8249835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25472000-G-T

8249857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471988-A-G

8249868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471975-T-A

8250665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25471687-C-T

8255329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467708-C-T

8255363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467685-G-A

8255549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25467561-T-C

8256327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466915-T-C

8256396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466842-C-G

8256472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466768-T-C

8256577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466665-C-T

8256603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466642-T-C

http://identifiers.org/hco/2/GRCh38#8257045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25466517-A-C

8257238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25466324-C-T

8257721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465826-G-A

http://identifiers.org/hco/2/GRCh38#8257833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25465725-A-C

8257833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465725-A-G

http://identifiers.org/hco/2/GRCh38#8258002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25465573-A-C

8258096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465508-C-T

8258403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465240-A-T

8258424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465219-A-G

8258479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465145-C-T

8258605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465029-A-T

8258607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465027-C-T

8258619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465016-T-G

8258633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25465002-G-A

8258654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464981-G-A

8259179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464451-G-A

8259273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464372-C-G

8259592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25464100-C-T

8259804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463109-T-A

8259926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463017-G-A

8259927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25463016-T-C

8260031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462938-C-G

8260031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462938-C-T

8260446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25462513-T-C

8260549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25462411-A-T

http://identifiers.org/hco/2/GRCh38#8260838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25461377-C-A

8260838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461377-C-T

http://identifiers.org/hco/2/GRCh38#8260884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25461332-A-C

8261123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25461122-G-A

8261463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25460844-C-T

8262142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25460134-C-T

8262286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25459991-T-C

8266405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458756-C-T

8266427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458734-A-G

http://identifiers.org/hco/2/GRCh38#8266545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25458637-C-A

8266547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458635-T-C

http://identifiers.org/hco/2/GRCh38#8266549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25458633-C-A

8266630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458546-T-C

8266653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458523-A-G

8266692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458482-C-T

8266755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458422-A-G

8266838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25458343-T-C

8267350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457847-G-A

8267350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457847-G-C

8267619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457621-T-G

8267695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457570-T-C

8267695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457570-T-G

8267745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457530-G-A

8268689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455544-C-T

8268776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455463-C-T

8276473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25452311-C-T

8277217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451646-G-A

8277225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451638-A-G

8277276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451589-C-G

8277276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451589-C-T

8277285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451580-T-C

8277694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451134-C-T

8277857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25451090-T-A

8277857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25451090-T-G

http://identifiers.org/hco/2/GRCh38#8277990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25450981-C-A

8278006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25450965-A-G

http://identifiers.org/hco/2/GRCh38#8278073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25450897-C-A

8278073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25450897-C-T

http://identifiers.org/hco/2/GRCh38#8278122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25450852-C-A

8278135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25450837-A-T

8278250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450761-C-T

8278336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450685-C-T

8278447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450584-A-T

8278527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450520-G-A

8278568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450483-C-T

8278641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25450398-G-C

http://identifiers.org/hco/2/GRCh38#8282705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25449903-C-A

8282747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449865-C-G

8283105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449498-T-C

8283188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449421-G-A

8283275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449335-A-G

8294994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447674-G-A

8295156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447475-T-C

8295356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447280-C-T

8303360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439732-T-G

8303501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439613-G-A

8303616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25439502-G-A

8303789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439329-C-G

8303789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439329-C-T

8303930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439214-C-T

8304149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439051-G-A

8304149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439051-G-T

8304228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438942-C-T

http://identifiers.org/hco/2/GRCh38#8304274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25438898-C-A

8304671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438375-T-C

8304714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438313-A-G

8304835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438191-G-A

8304987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25438067-C-T

8305063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437993-C-G

8305604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25437627-T-C

8305751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25436981-A-T

8305794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25436933-A-G

8306255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435893-C-T

8306305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25435839-G-A

8306781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25435368-A-G

8306879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25435270-T-C

8307229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434988-G-A

8307229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434988-G-C

8307335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434874-T-A

8307358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434851-C-T

8307453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434803-C-T

8308276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434340-C-T

8308608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25434144-G-A

8308856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25433733-G-A

8309385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25433167-G-A

8309385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25433167-G-C

8309517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25433061-G-A

8309659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432942-T-A

8309883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432721-G-A

8310181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432497-G-A

8310181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432497-G-T

8310212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432471-G-A

8310329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432348-T-C

8310424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432248-G-A

http://identifiers.org/hco/2/GRCh38#8310470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25432202-A-C

8310496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432162-T-C

8310676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431975-G-C

8310680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431971-A-G

8310712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431946-T-G

8310746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431909-C-T

8310754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431901-T-G

8310763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431898-G-A

8310763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431898-G-C

8310989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431668-T-C

8311158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431483-A-T

8311299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431366-C-T

8311436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431215-G-A

8311905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430808-T-C

http://identifiers.org/hco/2/GRCh38#8311908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25430805-C-A

8312000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430722-T-C

8312044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430678-G-A

8312064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430658-C-T

8312192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430562-A-G

8312490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430281-G-A

8312490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430281-G-C

8312584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430201-C-T

http://identifiers.org/hco/2/GRCh38#8312629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25430167-C-A

http://identifiers.org/hco/2/GRCh38#8312630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25430166-C-A

8312630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430166-C-T

8312665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25430133-T-C

http://identifiers.org/hco/2/GRCh38#8312784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25430015-C-A

8312802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25429997-T-C

http://identifiers.org/hco/2/GRCh38#8312941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25429734-C-A

8313040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25429529-A-G

8313069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25429510-G-A

8313839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428727-G-A

8313839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428727-G-T

8313860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428706-T-C

8313992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428580-G-A

8313992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428580-G-T

8314211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428360-T-A

8314427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428177-A-G

http://identifiers.org/hco/2/GRCh38#8314543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25428108-C-A

8314727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427940-G-A

8314748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427919-G-A

8314857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427804-A-T

8314887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427666-G-A

8314887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427666-G-C

8314937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427589-A-G

8314993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427536-C-T

http://identifiers.org/hco/2/GRCh38#8315052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25427476-A-C

8315124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427347-A-T

8315201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427266-C-T

8315242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427226-T-C

8315322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427159-A-G

8315402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25427076-A-T

8315872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426591-C-T

8315955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426504-G-A

8315955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426504-G-T

8316217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426279-G-T

8316789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426066-G-C

8316799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426056-T-C

8316886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425970-T-C

8317130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425802-T-C

8317222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425764-G-A

8317361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425653-T-A

8317654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425377-C-T

8317774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425276-T-C

8318645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425080-T-A

8318696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425015-C-G

8318696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425015-C-T

8318887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424800-T-C

8318911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424777-A-T

8319073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424618-T-A

http://identifiers.org/hco/2/GRCh38#8319158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25424540-A-C

http://identifiers.org/hco/2/GRCh38#8319197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25424499-A-C

8319450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424237-C-T

8319557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424146-A-G

8320760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423753-G-A

8320966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423534-A-G

8321063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423429-A-T

8321322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25422634-T-A

8322349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421364-C-T

8323045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420697-T-C

8323157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420597-T-C

8323347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420417-G-A

8323347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420417-G-T

8323390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420375-T-C

8323405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420364-G-A

8323415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420352-T-G

8323499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420268-G-A

8323529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420238-T-C

8323712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420069-A-G

8323773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419974-G-C

8324027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419779-C-T

8327856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419490-C-T

8327896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419447-G-A

8327896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419447-G-T

8328007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419318-C-T

8328098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419165-G-A

8328098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419165-G-C

8328098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419165-G-T

8328099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419164-G-C

8328119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419144-A-G

http://identifiers.org/hco/2/GRCh38#8328135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25419128-C-A

8328135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419128-C-T

8328157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419107-A-G

8328532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418565-G-C

8328532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418565-G-T

8328533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418564-G-A

8328536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418561-G-A

8328536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418561-G-T

8328642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418462-G-C

8328915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418203-G-A

8329002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418127-A-G

8329242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417891-T-C

8329249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417884-T-C

8329257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417876-A-G

8329292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417844-C-T

http://identifiers.org/hco/2/GRCh38#8329305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25417835-A-C

8329305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417835-A-G

8329724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417144-A-G

8329868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415561-C-T

8330130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415295-G-T

8330236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415188-C-G

8330251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415172-G-A

8330356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25415082-C-T

8332597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25414270-G-A

8332597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25414270-G-T

8332628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25414240-G-C

http://identifiers.org/hco/2/GRCh38#8332863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25414021-C-A

8332931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413958-C-T

8333270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413661-T-C

8333334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413615-C-T

8333388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413563-G-A

8333423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413534-C-T

8333483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413475-G-A

8334938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413239-G-A

8334958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413219-A-G

8335115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25413058-G-A

8335342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412926-T-C

8335342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412926-T-G

8335755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412264-G-T

8335819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412197-G-C

8336245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411853-G-A

8336280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411818-T-C

http://identifiers.org/hco/2/GRCh38#8336344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25411753-C-A

8336367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411733-G-A

8336774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411316-T-C

8336774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411316-T-G

8336947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410875-T-G

8337830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409749-T-C

8338009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409581-A-G

8338073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409522-T-G

8338671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408937-G-A

8338725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408884-C-G

8338769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408838-A-T

8338995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408622-A-G

http://identifiers.org/hco/2/GRCh38#8341237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25406724-C-A

8341237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406724-C-T

8341240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406721-A-G

8341326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406647-T-C

http://identifiers.org/hco/2/GRCh38#8341388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25406585-A-C

8341499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406441-G-A

8341720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406231-G-A

8343336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404728-G-A

8343376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404698-A-G

8343557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404011-A-G

http://identifiers.org/hco/2/GRCh38#8344394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25403634-A-C

8344415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403613-T-C

http://identifiers.org/hco/2/GRCh38#8344536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25403493-C-A

8344562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403467-C-G

8344562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403467-C-T

8344667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403362-T-C

8344919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403141-T-G

8346399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400989-C-T

8346551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25400839-T-C

8346572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400818-C-T

8346691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25400728-T-C

8346832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400597-G-A

8346835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400594-T-G

8347369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400119-C-T

8347452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400044-C-G

8347880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399653-A-G

8347902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399631-A-T

8347903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399630-A-G

8348383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398802-G-A

8348383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398802-G-C

http://identifiers.org/hco/2/GRCh38#8348403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25398771-A-C

8348406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398768-A-G

http://identifiers.org/hco/2/GRCh38#8355379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25398131-C-A

8355462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398055-G-A

8355462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398055-G-T

8357170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25397121-C-T

8357189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25397102-G-A

8357397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396930-T-A

8357507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396825-G-C

8357528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396809-G-C

8357591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396754-T-C

8357702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396609-A-G

8357759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396556-G-A

8357760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396555-G-A

8358102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396273-T-A

8358102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396273-T-G

8358187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396184-T-G

http://identifiers.org/hco/2/GRCh38#8358414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25395982-C-A

http://identifiers.org/hco/2/GRCh38#8358551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25395874-C-A

8358551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395874-C-T

http://identifiers.org/hco/2/GRCh38#8359595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25395128-C-A

8359595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395128-C-T

8359603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395120-G-A

8359607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395116-T-A

8359607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395116-T-C

8359618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395105-A-G

8359797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394913-T-C

8359830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394879-C-T

8360076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394653-G-A

8360082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394647-G-A

8360111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394618-G-C

8360371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394362-C-T

8360396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394338-C-T

8360448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25394302-T-C

http://identifiers.org/hco/2/GRCh38#8360802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25393788-A-C

http://identifiers.org/hco/2/GRCh38#8360813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25393765-A-C

8360813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393765-A-G

8360813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393765-A-T

8360940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25393603-C-G

8361011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25393528-G-A

8361011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25393528-G-T

8361079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25393463-C-G

http://identifiers.org/hco/2/GRCh38#8361118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25393434-A-C

8361257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25393304-T-A

8361943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389653-G-A

8362914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389177-G-T

8363069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389036-G-A

http://identifiers.org/hco/2/GRCh38#8363110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25388994-C-A

http://identifiers.org/hco/2/GRCh38#8363125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25388979-C-A

8363272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388861-A-G

8363807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387303-C-T

8363854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387257-A-G

8363881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387230-C-T

8364274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386883-A-G

http://identifiers.org/hco/2/GRCh38#8364656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25386548-C-A

http://identifiers.org/hco/2/GRCh38#8364684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25386520-C-A

8364762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386443-T-C

8364762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386443-T-G

8364809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386395-T-G

8364812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386392-T-C

8364878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386326-G-A

8365023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385036-G-A

8365272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384812-C-G

8365272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384812-C-T

8365284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384800-C-T

8365477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384632-C-T

8365555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384548-A-G

8368099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382561-A-G

8368334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382382-G-A

http://identifiers.org/hco/2/GRCh38#8368489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25382210-C-A

8369878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380192-T-C

8370037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380083-G-T

8370269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379821-T-C

http://identifiers.org/hco/2/GRCh38#8370391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25379743-A-C

http://identifiers.org/hco/2/GRCh38#8370672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25379501-C-A

8370698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379483-T-C

8371120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379107-G-A

8371236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379009-C-T

8371563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378686-T-C

8372020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378236-A-G

8372055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378201-G-T

8372291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377769-T-C

http://identifiers.org/hco/2/GRCh38#8372314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25377747-A-C

8372323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377738-T-A

8372518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377305-T-C

8372857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376877-G-T

8372906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376825-G-A

8372916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376815-C-T

8373048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376696-C-T

8373080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376660-G-C

http://identifiers.org/hco/2/GRCh38#8373113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25376626-A-C

8373120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376619-C-T

8373319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376427-T-C

8373320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376426-G-A

8373435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376306-C-G

8373451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376291-G-A

8373451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376291-G-T

8373463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376280-C-T

8373525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376218-A-G

8373525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376218-A-T

8373538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376205-G-A

8373608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376144-G-A

http://identifiers.org/hco/2/GRCh38#8373818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25375893-C-A

8373952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375716-C-T

8373989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375670-C-T

8374601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25375065-T-A

8374601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25375065-T-C

8375488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25371961-G-C

8377126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371888-T-C

8377156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371866-G-A

8377163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371859-T-C

8377166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371856-T-C

8377193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371830-T-C

8377297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371732-A-T

8377557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371453-G-A

8377676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371334-A-G

8377683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371327-C-G

8377903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25371114-T-A

8378162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370906-T-C

8378215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370858-T-C

8378232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370843-T-A

8378294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370768-T-C

8378490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370584-G-A

8378563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25370508-A-G

8378581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370490-A-T

8378750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25370309-T-C

http://identifiers.org/hco/2/GRCh38#8378992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25369378-A-C

8379444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25368911-G-A

8379530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25368843-G-A

8380007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25368380-C-T

http://identifiers.org/hco/2/GRCh38#8380058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25368337-C-A

8380058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25368337-C-T

8380195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25368218-G-A

8380195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25368218-G-T

8380391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25368047-C-T

8380550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367881-G-A

8380649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367779-G-A

8380649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367779-G-C

8380649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367779-G-T

8380674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367757-A-G

8381208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367215-A-T

8381402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367051-G-A

http://identifiers.org/hco/2/GRCh38#8382388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25366801-C-A

http://identifiers.org/hco/2/GRCh38#8382437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25366757-C-A

8382622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366555-C-T

http://identifiers.org/hco/2/GRCh38#8386418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25364030-A-C

8386465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363974-A-G

8386698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363657-T-C

8387605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363427-T-G

8387659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363355-T-C

8387787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363261-C-T

8387856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363194-G-T

8387940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363143-G-T

8387958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363102-A-T

http://identifiers.org/hco/2/GRCh38#8387989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25363072-C-A

8388270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362771-G-A

8388339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362616-G-A

8388741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362139-T-C

8389432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25360950-T-C

8395978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357702-T-C

8395994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357686-T-G

8396124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357535-C-G

8396576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357100-T-C

8408658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356579-G-C

8408658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356579-G-T

8408958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356263-C-T

8409275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355955-C-T

8409381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355864-G-A

8409382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355863-T-C

8409580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355665-T-A

8409871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355325-A-T

8410480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354726-T-A

8410521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354688-G-A

8410687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354597-G-A

8410781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354536-A-T

8410856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354462-A-G

8412444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25353753-G-A

8412586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25353608-A-G

8412880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25353312-T-C

http://identifiers.org/hco/2/GRCh38#8414288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25350922-A-C

8414288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350922-A-G

8414342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350887-C-T

8414428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350799-A-T

8414438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350788-T-A

8414438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350788-T-G

http://identifiers.org/hco/2/GRCh38#8414460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25350776-C-A

8415410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350443-C-T

8415486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350373-A-T

8415600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25350265-T-C

8415673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25349794-C-T

8416036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25349482-C-T

8416051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25349464-T-C

8417442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25349040-G-A

8417442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25349040-G-C

8417573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348934-C-T

8417612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348894-A-G

8417679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348832-C-T

http://identifiers.org/hco/2/GRCh38#8417726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25348779-C-A

8417759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348747-G-A

8417800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348707-T-G

8417801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348706-G-A

8417890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348615-C-T

8417938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348551-G-A

8418325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348207-T-G

8418388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25348147-G-C

8418751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25347975-G-T

http://identifiers.org/hco/2/GRCh38#8418808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25347912-A-C

http://identifiers.org/hco/2/GRCh38#8418854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25347866-A-C

8423047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345292-T-A

8423096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345243-A-G

8423146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345199-C-T

8423253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345040-C-T

8423284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25345013-T-C

8423302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344998-G-C

8424824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344311-C-T

8424963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344173-G-T

8424972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25344164-T-C

8425579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25343514-T-C

8425598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25343495-T-C

8426360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342810-G-C

8426360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342810-G-T

8426414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342754-C-T

8426680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342569-C-G

8426680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342569-C-T

8426775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342505-G-A

8426775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342505-G-T

8427022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342302-C-T

8427149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342179-G-A

8427149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342179-G-T

8427188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25342140-T-C

8427590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25341819-C-T

8429851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25334504-C-T

http://identifiers.org/hco/2/GRCh38#8430036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25334308-C-A

8430086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25334269-C-T

http://identifiers.org/hco/2/GRCh38#8430208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25334177-A-C

8430381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333993-C-T

8430392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333982-A-T

http://identifiers.org/hco/2/GRCh38#8430443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25333929-C-A

8430443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333929-C-T

8430551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333826-C-T

8430603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333774-A-G

8430606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333771-T-C

8430658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333719-T-C

http://identifiers.org/hco/2/GRCh38#8430675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25333703-C-A

8430675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333703-C-T

8430714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333665-G-C

8430959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333470-G-T

8431010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333414-G-A

8431136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25333279-T-A

8435820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331121-A-G

8435851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331090-G-A

8435925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331020-G-A

8435925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25331020-G-C

8436054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25330884-G-A

8436855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329422-T-G

8436861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329416-G-A

8436935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329340-C-T

http://identifiers.org/hco/2/GRCh38#8437090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25329203-C-A

8437090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25329203-C-T

8437327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25328954-C-G

8437329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25328952-G-C

8437382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25328895-T-C

8437467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25328801-A-G

8437615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25328670-C-G

8443297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25326056-T-C

8444869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25325418-A-G

http://identifiers.org/hco/2/GRCh38#8445299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25325017-C-A

8445843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324418-C-G

8445843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324418-C-T

8445927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324346-C-T

8447053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324161-C-G

8447056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324158-T-C

8447124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25324097-T-C

8447250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323971-A-G

8447591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323671-C-T

8447895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323362-C-T

8448664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323232-G-A

8448825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323073-T-C

8448831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25323067-A-T

8449500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25322402-A-G

8449530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25322372-T-G

http://identifiers.org/hco/2/GRCh38#8452882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25320592-C-A

8453377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319989-G-A

http://identifiers.org/hco/2/GRCh38#8453489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25319869-C-A

8453518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319840-T-G

8453568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319785-G-A

8453742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319619-A-G

8453770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319590-G-A

8453834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319531-G-A

8453835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319530-C-T

8454006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319382-A-G

8454084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319303-C-G

8454139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319248-T-C

8454161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319229-C-T

8454177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319213-C-G

8454177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319213-C-T

8454240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319144-G-A

8454240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319144-G-C

8454251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319133-T-C

8454251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25319133-T-G

8454307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25319077-C-G

8454412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25318997-C-G

8454512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25318923-C-T

http://identifiers.org/hco/2/GRCh38#8454530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25318905-C-A

8454660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25318749-C-T

http://identifiers.org/hco/2/GRCh38#8454702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25318705-C-A

http://identifiers.org/hco/2/GRCh38#8454760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25318653-C-A

8454760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25318653-C-T

8455165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25318442-G-A

8455165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25318442-G-T

8455177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25318429-C-T

8455280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25318340-A-G

8456232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317804-G-A

8456241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317795-A-G

8456249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317787-A-G

8456367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317682-G-C

8456372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317677-G-T

8456467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317591-G-C

8456559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317560-C-T

8456873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317328-T-A

8457110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317197-G-A

8457121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317186-G-C

8457121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317186-G-T

http://identifiers.org/hco/2/GRCh38#8457139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25317168-C-A

8457139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317168-C-T

8457191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317114-T-C

8457198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317107-C-T

8457266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317017-G-A

8457266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25317017-G-T

http://identifiers.org/hco/2/GRCh38#8457346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25316929-A-C

http://identifiers.org/hco/2/GRCh38#8457378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25316855-C-A

8457378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25316855-C-G

8457381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25316852-T-G

8457870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25316114-A-G

8457968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315997-T-C

8458013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315952-C-T

8458014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315951-G-A

8458227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315700-G-A

8458524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315401-C-G

8458524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315401-C-T

8458614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315312-T-A

8458649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315272-C-G

8458665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315256-C-T

8458747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315204-T-A

8458747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315204-T-C

8458887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25315050-G-T

http://identifiers.org/hco/2/GRCh38#8458965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25314997-C-A

8458974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25314988-T-C

8459601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25314415-G-C

8459708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25314324-T-C

8460004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25313606-A-G

8460085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25313524-C-T

8460232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25313420-A-G

8460652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25312986-A-G

8461034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25312604-A-G

8461034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25312604-A-T

8461302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25312353-G-A

8461328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25312326-C-T

8461776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25311568-C-G

8461789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25311555-T-C

http://identifiers.org/hco/2/GRCh38#8461802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25311544-C-A

8461849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25311497-T-C

http://identifiers.org/hco/2/GRCh38#8462321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25311023-C-A

8462441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25310902-T-C

http://identifiers.org/hco/2/GRCh38#8464921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25310121-C-A

8469126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25308001-T-C

8469450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25307658-T-C

http://identifiers.org/hco/2/GRCh38#8469591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25307548-A-C

8469689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25307481-G-C

8470008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25307152-G-A

8470040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25307115-A-G

8470115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25307050-G-A

8470220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25306947-T-C

8471251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25305677-G-A

8471400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25305450-T-C

8471519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25305322-T-C

8473227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25304521-G-A

8473585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25303417-G-A

8473585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25303417-G-C

8473821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25303258-T-C

http://identifiers.org/hco/2/GRCh38#8474039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25303074-A-C

8474151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302975-A-G

8474245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302906-G-A

8474245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302906-G-C

8474422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302730-T-C

8474449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302703-G-A

8474537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25302634-T-C

8475231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25301897-A-G

8476676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25300484-T-A

8476676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25300484-T-G

8476694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25300464-G-A

8476694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25300464-G-C

8477286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25299801-G-A

8477485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25299600-G-A

8477766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25299314-C-T

8477887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25299200-G-A

8478170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25298923-C-T

http://identifiers.org/hco/2/GRCh38#8478213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25298878-C-A

8478213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25298878-C-T

8478809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25298365-T-C

http://identifiers.org/hco/2/GRCh38#8479791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25298045-C-A

8479791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25298045-C-G

8479791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25298045-C-T

8479855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25297984-C-T

8481924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25297163-C-T

8482443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25296652-G-A

8482443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25296652-G-C

http://identifiers.org/hco/2/GRCh38#8482692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25296439-C-A

8482708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25296423-C-T

8482829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25296171-G-A

http://identifiers.org/hco/2/GRCh38#8483058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#25295805-A-C

8485444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292726-C-T

8485670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292528-G-A

8485670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292528-G-C

8485732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292471-G-T

8485865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292345-T-C

8485985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25292024-C-G

8486034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25291979-C-T

8486291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25291749-G-A

8486343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25291714-T-C

http://identifiers.org/hco/2/GRCh38#8486769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25291313-C-A

8487656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25290882-G-C

8487660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25290878-G-T

8487836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25290717-C-G

8487958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25290642-G-A

http://identifiers.org/hco/2/GRCh38#8488098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#25290507-C-A

8488210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25290404-C-T

8488252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25290371-G-A

8488253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25290370-C-T