http://identifiers.org/hco/1/GRCh38#245155078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178356793-C-A

245155078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5 prime UTR variant
orthologous variants: 178356793-C-T

245155127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5 prime UTR variant
orthologous variants: 178356847-G-A

245155127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5 prime UTR variant
orthologous variants: 178356847-G-T

245155402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5 prime UTR variant
orthologous variants: 178357105-T-C

245155463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178357166-C-T

http://identifiers.org/hco/1/GRCh38#245155509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178357213-C-A

245155509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357213-C-G

245155509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357213-C-T

245155620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357328-T-C

245155620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357328-T-G

245155813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357506-T-C

245155827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357520-C-G

245156143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357851-G-T

245156227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357906-G-A

245156233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357912-T-A

245156233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357912-T-C

http://identifiers.org/hco/1/GRCh38#245156235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178357914-C-A

245156235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178357914-C-T

http://identifiers.org/hco/1/GRCh38#245156277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178357949-C-A

245156277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 178357949-C-G

245156277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 178357949-C-T

245156317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178357989-G-T

245156530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178358202-G-A

245156530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178358202-G-C

245156530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178358202-G-T

245156660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense variant
orthologous variants: 178358332-C-G

245156660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense variant
orthologous variants: 178358332-C-T

http://identifiers.org/hco/1/GRCh38#245156705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#178358378-C-A

245156705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178358378-C-G

245156705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178358378-C-T

245156707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178358380-G-A

245156885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178358427-G-A

245156885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178358427-G-C

245156885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178358427-G-T

245157580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359043-G-A

245157587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359050-G-T

245158230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359649-G-A

245158269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359689-T-C

245158301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359720-A-G

http://identifiers.org/hco/1/GRCh38#245158340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178359766-C-A

245158340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178359766-C-T

245158884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178360211-G-T

245159195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178360533-T-C

245159476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178360853-A-G

245159816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361234-T-A

245159921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361360-T-C

245160001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361393-T-G

245160006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361398-C-T

245160069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361468-T-C

245160315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361684-T-C

245160322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361691-T-C

245160403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361770-C-T

245160410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361777-A-G

245160440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361808-C-G

245160454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361822-G-A

http://identifiers.org/hco/1/GRCh38#245160518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178361888-C-A

245160518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361888-C-T

245160544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178361914-C-T

http://identifiers.org/hco/1/GRCh38#245160853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178362224-A-C

http://identifiers.org/hco/1/GRCh38#245161085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178362442-A-C

http://identifiers.org/hco/1/GRCh38#245161145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178363138-A-C

245161316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178363285-G-C

245161621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178363560-G-A

245165976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367154-C-T

245166064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367238-C-T

245166181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367353-A-G

245166249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367419-C-T

245166276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367449-T-C

245166381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367544-G-A

245166503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367672-G-C

245166698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367866-A-T

http://identifiers.org/hco/1/GRCh38#245166774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178367942-A-C

245166775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178367943-T-C

245166902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178368069-A-G

http://identifiers.org/hco/1/GRCh38#245167076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178368210-A-C

245167397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178368464-G-A

245167397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178368464-G-T

245167478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178368540-C-T

245168521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178369589-G-T

245169167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178370230-C-T

245169253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178370334-A-G

245169290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178370365-C-T

245169433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178370905-G-A

245169468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178370940-A-G

245169614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371137-G-T

245169714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371234-G-A

245169787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371297-C-T

245169824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371332-T-C

245170030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371583-T-C

245170312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371823-C-G

245170370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371880-T-C

245170411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178371937-C-T

245170475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178372017-G-T

245170655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178372171-T-C

http://identifiers.org/hco/1/GRCh38#245173602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178374181-C-A

245173602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374181-C-T

http://identifiers.org/hco/1/GRCh38#245173604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178374183-C-A

245173604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374183-C-T

245173627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374223-G-A

245173628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374224-C-T

245173786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374364-C-G

245173862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374418-C-T

245173921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374468-G-C

245174344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178374880-G-C

245174898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178375557-G-C

245175048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178375762-T-C

245175078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178375780-C-T

245175331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178375948-G-A

245175456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178376355-T-G

245175483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178376381-A-G

245175524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178376421-T-C

245176597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178377416-A-G

245176598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178377417-G-A

245176825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178377640-C-T

245177505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178378036-G-A

245177659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378176-C-G

245177659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378176-C-T

245177787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378279-G-C

245177787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378279-G-T

245177848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378339-A-G

http://identifiers.org/hco/1/GRCh38#245177890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178378384-C-A

245177890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378384-C-T

245177891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378385-G-A

245177891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178378385-G-C

245178665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381280-C-T

245180230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178380512-T-C

245180775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381018-A-G

245180898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381042-C-T

245180980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381092-T-G

245181089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381186-C-T

http://identifiers.org/hco/1/GRCh38#245181194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178381291-C-A

245181194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381291-C-T

245181309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381422-C-T

245181371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381537-T-C

245181395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381561-C-T

245181597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381765-T-C

245181857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381927-G-A

245181861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381931-G-A

245181869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381935-G-A

245181892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178381958-A-T

245181997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178382059-T-A

245182309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178382169-T-C

245182612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178382434-A-G

245183498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383677-C-T

245183532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383711-A-G

245183769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383914-G-T

245183810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383952-A-G

245183812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383954-T-G

245183834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178383974-C-T

245184221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178384307-T-G

245184367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178384460-A-G

245184445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178384538-C-T

245184448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178384541-C-T

245184772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178386437-A-G

245184880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178386539-A-G

245184880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178386539-A-T

245185000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178386635-T-C

245185000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178386635-T-G

245193920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178389945-C-T

245193944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178389972-C-T

245194815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178390551-A-G

http://identifiers.org/hco/1/GRCh38#245194872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178390600-A-C

245194874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178390602-G-A

245194874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178390602-G-T

245194886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178390614-G-C

245197819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178392522-A-G

245197901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178392587-T-C

245198019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178392703-G-A

245198090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178392865-C-T

245198250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393005-G-A

http://identifiers.org/hco/1/GRCh38#245198300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178393056-A-C

245198937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393416-C-G

245198937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393416-C-T

245198945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393424-T-C

245198945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393424-T-G

245198980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393449-G-T

245199163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393780-G-A

245199192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178393838-A-T

245200234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178394812-C-T

http://identifiers.org/hco/1/GRCh38#245200299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178394877-C-A

245200742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178395337-G-A

245200901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178395499-G-A

http://identifiers.org/hco/1/GRCh38#245201192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178395743-A-C

245201980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178396818-T-C

245202321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178397135-C-T

245205302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178398908-A-G

245205368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178398974-T-A

245205546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178399139-C-T

http://identifiers.org/hco/1/GRCh38#245206348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178399533-C-A

245206568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178399754-G-T

245206576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178399762-A-T

245206581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178399767-T-C

245206746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178399905-G-A

245206774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178399927-T-C

245208086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401134-G-C

245208099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401147-G-A

245208353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401402-T-C

245208458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401502-G-A

245208486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401524-A-G

245208505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401543-C-T

245208752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178401719-G-A

245211015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178404553-G-A

245211015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178404553-G-C

245211458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405027-G-T

245211795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405546-A-G

http://identifiers.org/hco/1/GRCh38#245211958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178405684-C-A

245211995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405716-G-A

245211998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405717-G-T

245212036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405753-G-T

245212042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178405756-C-G

245212268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406593-G-A

245212394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406712-G-T

245212439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406736-A-G

245212476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406763-C-T

245212562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406847-G-A

245212595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406887-G-A

245212623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406912-C-T

245212647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178406932-G-C

http://identifiers.org/hco/1/GRCh38#245212782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178407068-C-A

245212782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178407068-C-T

245213050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178407334-A-G

245213376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178407713-G-A

245216282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178409794-C-T

http://identifiers.org/hco/1/GRCh38#245216389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178409862-C-A

245216389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178409862-C-G

245216389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178409862-C-T

http://identifiers.org/hco/1/GRCh38#245216400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178409873-C-A

http://identifiers.org/hco/1/GRCh38#245216403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178409876-A-C

245216903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178410362-C-G

245216903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178410362-C-T

245216925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178410383-T-C

http://identifiers.org/hco/1/GRCh38#245217501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178410773-A-C

245217697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178410827-A-G

245217945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411092-G-A

http://identifiers.org/hco/1/GRCh38#245217975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178411124-C-A

245218085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411303-A-G

245218212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411447-G-C

245218465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411687-G-A

245218488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411694-G-A

245218565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411764-G-A

245218609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411812-C-G

245218621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411824-C-T

245218694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178411913-C-T

245221164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178413564-C-T

245221878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178413994-G-C

245222722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178414834-T-A

245222769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178414887-G-A

245222919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178415083-C-T

245223269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178415483-G-A

245225197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178417898-G-C

245225261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178417959-G-C

245225493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418144-G-A

http://identifiers.org/hco/1/GRCh38#245225684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178418334-A-C

245225780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418425-A-G

245226004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418633-G-T

245226053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178418685-T-C

245226059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178418691-C-T

245226104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 178418748-G-A

245226104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 178418748-G-T

245226118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178418762-G-T

245226120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178418764-G-T

http://identifiers.org/hco/1/GRCh38#245226121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178418765-C-A

245226165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418798-G-A

245226165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418798-G-T

http://identifiers.org/hco/1/GRCh38#245226173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178418806-C-A

245226195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418821-C-T

245226210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418836-G-A

245226210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418836-G-T

245226273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418895-G-T

245226280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418902-G-A

245226281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178418903-T-C

245226921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178419153-G-C

245226921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178419153-G-T

245232038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178419505-T-C

245232149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178419648-G-A

245232343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178419935-G-A

245234556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178420513-G-T

245234647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178420601-T-C

http://identifiers.org/hco/1/GRCh38#245234806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178420758-A-C

http://identifiers.org/hco/1/GRCh38#245234873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178420826-C-A

245235151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178421087-G-A

245235164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178421100-T-C

245241685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178421518-G-A

245241805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178421616-G-A

http://identifiers.org/hco/1/GRCh38#245241838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178421649-C-A

245242499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178422396-A-T

245243200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178422839-T-C

245243204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178422848-C-T

245243211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178422855-T-G

245243242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178422886-C-T

245253065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178423811-A-G

245253424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424234-G-A

245253424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424234-G-C

245253484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424300-T-G

245253811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424625-T-C

245253811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424625-T-G

245253848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178424662-T-C

http://identifiers.org/hco/1/GRCh38#245254385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178425515-A-C

245255384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178426263-A-G

245255648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178426673-C-T

245255859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178426836-C-G

245256470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178427602-C-T

245258370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428219-A-G

245258374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428223-G-A

245258374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428223-G-C

245258693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428534-C-T

245258828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428670-T-C

http://identifiers.org/hco/1/GRCh38#245258892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178428734-C-A

245258892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428734-C-T

245259111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178428989-G-A

245259306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178429198-A-G

245259379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178429277-T-A

245259409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178429310-G-C

245260710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430136-G-A

245260742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430163-T-C

245262027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430441-A-G

245262056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430474-T-G

245262799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430913-G-A

245262864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178430957-A-G

245263112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178431941-C-T

http://identifiers.org/hco/1/GRCh38#245263419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178432223-A-C

245263887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433068-G-A

245264107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433295-A-G

245264298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433450-A-T

245264481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433620-T-C

245264528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433667-G-A

245264572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178433710-G-T

245276687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178436655-A-G

http://identifiers.org/hco/1/GRCh38#245276705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178436673-C-A

245277030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178436930-C-T

245277133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437011-C-G

245277209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437086-T-C

245277209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437086-T-G

245277305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437190-G-A

245277511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437350-T-C

245277724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437695-G-A

245277741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437731-C-T

245277819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437839-G-A

245277892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178437914-G-A

http://identifiers.org/hco/1/GRCh38#245277993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178438008-C-A

245277993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438008-C-G

245278104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438117-G-T

245278146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438159-A-G

245278168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438183-A-G

245278168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438183-A-T

245278225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178438240-T-C

http://identifiers.org/hco/1/GRCh38#245278320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178438329-A-C

245278817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178439337-T-C

http://identifiers.org/hco/1/GRCh38#245278933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178439456-C-A

http://identifiers.org/hco/1/GRCh38#245278985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178439512-C-A

245278985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178439512-C-G

245279238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178439695-T-C

245279256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178439705-C-T

245287655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178441964-C-T

245287745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442044-C-G

245287745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442044-C-T

245287909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442188-T-G

245287937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442216-G-A

245287953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442234-G-A

245287953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442234-G-T

245287988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442253-A-G

245288038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442307-C-T

http://identifiers.org/hco/1/GRCh38#245288051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178442320-A-C

245288574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178442816-T-A

245289196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444038-T-C

245289196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444038-T-G

245289205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444047-T-C

245289331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444199-T-C

245289350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444218-C-T

245289688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444733-G-A

245289688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444733-G-C

245289688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444733-G-T

245289770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444822-A-G

245289988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178444998-A-G

245290005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445015-G-A

245290070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445077-C-G

245290091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445098-G-A

245291098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445491-G-T

245291112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445505-C-T

245291313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445589-A-G

245292030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445782-G-T

245292285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178445998-G-C

245292468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446179-G-A

245292659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446303-T-G

245292746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446380-G-C

245292746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446380-G-T

245292771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446404-T-C

245292774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446407-G-A

245292774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446407-G-T

245292844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446478-G-C

245293255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446883-T-C

245293289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446904-G-A

245293319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446928-G-C

245293384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178446993-G-C

245293533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447141-T-G

245294185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447481-G-T

245294222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447517-G-A

245294254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447549-A-G

245294292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447582-C-G

245294292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178447582-C-T

245295314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448144-C-G

245295522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448306-C-T

245295561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448342-G-A

245295585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448367-A-G

245295757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448548-G-A

245295785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448577-A-G

245295997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448884-T-G

245296007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448891-G-A

245296037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448917-A-G

245296071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178448950-C-T

245296126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178449011-T-A

245296126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178449011-T-C

245296176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178449057-T-C

245296235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178449124-C-T

245296710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178449870-T-C

245297360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178450280-A-G

245297493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178450544-C-G

245297507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178450558-A-T

245298505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451164-G-A

245298551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451216-A-G

http://identifiers.org/hco/1/GRCh38#245298788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178451437-A-C

245298877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451530-T-C

245299016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451666-G-A

245299355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451996-G-A

245299355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451996-G-C

245299355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178451996-G-T

245299368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452009-G-A

245299398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452032-G-A

245299401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452035-G-A

245299401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452035-G-C

245299416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452050-C-G

245299443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178452077-G-T

http://identifiers.org/hco/1/GRCh38#245299557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178452189-C-A

http://identifiers.org/hco/1/GRCh38#245299572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178452205-C-A

245300021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178453832-T-A

245300021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178453832-T-C

245301300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178454684-G-C

245301435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178454819-T-C

245301446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178454830-C-G

http://identifiers.org/hco/1/GRCh38#245301475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178454858-C-A

245301475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178454858-C-T

245301669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455016-G-T

245301724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455071-C-T

245301767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455115-G-A

245301896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455226-C-T

http://identifiers.org/hco/1/GRCh38#245303571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178455564-A-C

245303635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455628-C-G

245303635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455628-C-T

245303913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455853-A-G

245303995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455931-T-C

245304042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178455983-G-C

245304111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178456049-C-T

245304277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178456939-A-G

http://identifiers.org/hco/1/GRCh38#245304439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178457100-C-A

245304657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178457341-C-G

245304665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178457349-C-G

245306364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178458882-T-G

245306390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178458905-A-G

245306425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178458940-G-A

245306570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459086-A-G

245306673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459159-G-T

245306785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459253-G-A

245306802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459270-A-G

245306903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459374-G-T

245307145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459612-A-G

http://identifiers.org/hco/1/GRCh38#245307250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178459718-C-A

245307321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459784-T-C

245307458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178459917-A-G

245308162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178461183-G-T

245308218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178461226-G-C

http://identifiers.org/hco/1/GRCh38#245310189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178461614-A-C

245310189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178461614-A-T

245310354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178461770-G-A

245310442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178461841-A-G

245310788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462204-C-T

245310963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462366-T-G

245310966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462369-C-T

245310996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462398-A-G

245311154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462560-C-G

245311169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462575-C-T

245311350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462731-G-C

245311420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462804-C-T

http://identifiers.org/hco/1/GRCh38#245311960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178462832-C-A

245312073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178462942-G-T

245312193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178463044-C-T

245314160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178465180-T-C

245314160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178465180-T-G

245314630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178465477-C-T

245314774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178465612-C-G

245314825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178465671-G-C

245316786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466091-G-C

http://identifiers.org/hco/1/GRCh38#245316828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178466131-C-A

245316828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466131-C-G

245316951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466228-A-G

http://identifiers.org/hco/1/GRCh38#245317014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178466287-C-A

245317014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466287-C-T

245317224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466496-T-C

245317233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466505-T-G

245317291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466553-G-A

245317359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466622-G-A

245317512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466775-T-C

245317661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178466922-C-T

245318023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178467087-T-C

245318259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178467305-G-A

245318264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178467310-C-T

245318310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178467354-C-G

245318310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178467354-C-T

http://identifiers.org/hco/1/GRCh38#245319043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178468575-A-C

245319153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178468703-A-G

http://identifiers.org/hco/1/GRCh38#245319299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178468828-A-C

245319299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178468828-A-G

http://identifiers.org/hco/1/GRCh38#245319345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178468876-C-A

245319346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178468877-C-T

245319799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178469390-G-A

245319799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178469390-G-T

245319837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178469427-G-A

245319853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178469443-G-C

245319948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178469573-T-G

245320978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178470972-T-C

245325885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178470701-T-C

245326056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178470856-C-T

245326169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178470954-G-A

245326174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178470959-A-G

245326286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471072-G-A

245326418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471204-G-A

245326479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471266-G-A

245326819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471597-A-G

245326825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471603-G-A

245326978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471754-C-T

245327062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178471839-G-A

245327277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472059-G-A

http://identifiers.org/hco/1/GRCh38#245327446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178472177-C-A

245327446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472177-C-T

245327504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472267-A-T

http://identifiers.org/hco/1/GRCh38#245327613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178472353-C-A

http://identifiers.org/hco/1/GRCh38#245328235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178472944-C-A

245328235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472944-C-G

245328235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472944-C-T

245328244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178472953-T-G

245328911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178473951-T-G

245328931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178473971-T-C

245329045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474080-C-T

245329077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474111-T-A

245329190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474196-T-C

245329257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474265-G-A

245329383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474379-A-G

245329437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474426-C-T

245329439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474428-C-T

245329586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474572-G-A

245330164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474821-T-C

245330296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474935-G-A

245330331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178474969-T-G

245330370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475008-A-G

245330859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475118-T-C

245331089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475310-G-A

245331225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475459-G-A

245331225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475459-G-T

245331236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475470-T-G

245331363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475642-A-G

245331414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178475692-G-A

245332328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178477939-G-A

245332328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178477939-G-C

245332464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478065-A-G

245332688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478274-G-A

245332721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478303-G-C

245332721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478303-G-T

245332816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478377-C-T

245332856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478418-G-A

245332957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478528-C-T

245333128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478687-G-A

245333165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478718-G-A

245333292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178478796-C-T

http://identifiers.org/hco/1/GRCh38#245333620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178479087-A-C

245333731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178479180-C-T

245334495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178479790-C-T

245334564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178479850-C-T

245334788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178480625-T-A

245334869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178480671-G-A

245334870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178480672-A-T

245335052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178480821-C-T

245335350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481076-T-C

245335388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481104-G-A

245336198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481296-T-C

245336361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481418-G-A

245336411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481468-T-A

245336450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481501-G-C

http://identifiers.org/hco/1/GRCh38#245336527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178481575-C-A

245336730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481739-C-T

245336814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178481822-T-C

245337096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482129-G-A

245337121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482156-G-C

245337123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482158-G-C

245337485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482186-C-G

245337544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482250-G-A

245337546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178482252-G-A

245337869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483049-C-T

245337954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483134-A-G

245337967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483146-A-G

245337972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483151-G-C

245338032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178483211-C-T

245338139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483304-T-A

245338189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483350-C-T

245338231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178483401-G-T

245338342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178483513-C-T

245338824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178483998-C-T

245339064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178484275-G-A

245339897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178484924-C-G

245340011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178485032-A-G

245340033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178485054-G-T

245341821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178485785-G-A

245341821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178485785-G-C

http://identifiers.org/hco/1/GRCh38#245342142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178486082-C-A

245342150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178486090-G-C

245342237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178486184-G-T

245342378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178486379-C-T

245342470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178486516-G-A

http://identifiers.org/hco/1/GRCh38#245342632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178486705-C-A

245343895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178488067-A-G

245343911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178488080-A-G

http://identifiers.org/hco/1/GRCh38#245345148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178489058-A-C

245345148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178489058-A-G

245345148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178489058-A-T

245348282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178489899-C-T

245348315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178489926-A-G

245348714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178490268-A-G

245348922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178490462-G-C

245350351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178491796-C-T

245350393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178491837-C-G

245350415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178491859-T-G

245350621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178491985-C-G

245350621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178491985-C-T

245350674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492044-A-G

245350854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492205-T-C

245350948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492305-C-T

245350997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492353-G-C

245351294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492630-G-A

245351294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492630-G-C

245351454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492679-G-A

245351577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178492794-C-T

245351895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178493563-C-T

245351950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178493616-T-C

245351988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178493653-T-A

245351991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178493656-C-T

245352166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178493803-A-G

http://identifiers.org/hco/1/GRCh38#245354368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178495394-A-C

245354368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178495394-A-G

245354378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178495402-G-A

245354514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178495537-C-T

245354793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178495801-T-A

245355942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178496306-C-T

245356048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178496404-G-T

245359554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178498015-G-C

245361412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499399-T-C

245361468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499458-G-A

245361474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499464-A-G

245361994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499794-G-A

245362097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499898-C-T

245362121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499914-T-C

245362151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499943-C-G

245362172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499989-C-G

245362172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178499989-C-T

245362779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178502635-C-T

245362915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178502783-A-G

245362982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178502847-T-C

245363502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178503059-T-C

245363829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178503392-C-T

245364341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178503888-A-G

245364399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178503948-G-T

245364901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178504531-T-C

245365030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178504625-A-G

245365280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178504884-G-A

245365288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178504891-T-G

245365418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505019-G-C

245365429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505030-A-G

http://identifiers.org/hco/1/GRCh38#245365467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178505068-C-A

http://identifiers.org/hco/1/GRCh38#245365520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178505121-C-A

245365520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505121-C-G

245365520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505121-C-T

http://identifiers.org/hco/1/GRCh38#245365529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178505130-A-C

245365551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505146-G-T

http://identifiers.org/hco/1/GRCh38#245365563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178505157-C-A

245365747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505365-G-A

245365787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505404-A-T

245365888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178505499-A-G

245366622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506215-G-A

http://identifiers.org/hco/1/GRCh38#245366723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178506295-A-C

245366723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506295-A-G

245366974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 178506531-G-C

245367001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 178506558-T-C

http://identifiers.org/hco/1/GRCh38#245367100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178506657-C-A

245367100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 178506657-C-T

http://identifiers.org/hco/1/GRCh38#245367148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178506705-C-A

245367148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 178506705-C-T

http://identifiers.org/hco/1/GRCh38#245367349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178506906-C-A

245367378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506934-T-A

245367378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506934-T-C

245367385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506941-G-A

245367385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506941-G-T

245367395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506951-G-A

245367395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506951-G-T

http://identifiers.org/hco/1/GRCh38#245367401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178506957-C-A

245367401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178506957-C-T

http://identifiers.org/hco/1/GRCh38#245367412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178507017-C-A

245367426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507029-A-G

245367428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507031-G-T

245367510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507105-A-G

245367513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507108-A-G

245367703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507272-A-T

245367706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507275-G-A

245367706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507275-G-C

http://identifiers.org/hco/1/GRCh38#245367900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178507463-A-C

245368065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507646-G-A

245368088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178507669-T-C

245370081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178510111-G-A

http://identifiers.org/hco/1/GRCh38#245370451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178510439-C-A

http://identifiers.org/hco/1/GRCh38#245370473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178510461-C-A

245370473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178510461-C-T

245370474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178510462-T-C

245370609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178510576-C-T

245370632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178510596-G-A

245370632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178510596-G-C

245370805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178510763-C-T

245371146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178511135-C-T

http://identifiers.org/hco/1/GRCh38#245371379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178511386-C-A

245371379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178511386-C-G

245371379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178511386-C-T

245371397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178511404-A-G

245371397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 178511404-A-T

245371437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178511442-A-G

245371499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 178511504-G-A

245371805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178511650-G-T

245374790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178512212-G-A

245374981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178512404-C-T

245375392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178512482-G-A

245375990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178513005-C-T

245376395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178513378-G-C

245377389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178514455-T-C

245377441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178514517-T-C

245377455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178514531-A-T

245377703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178514700-G-A

245377784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178514741-T-C

245378331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178515199-T-G

245378503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178515338-G-A

245378632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178515431-G-A

245378723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178515492-A-G

245378842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178515615-G-A

245378994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178515753-G-A

245378994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178515753-G-T

245379411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178516095-A-G

http://identifiers.org/hco/1/GRCh38#245379625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178516282-C-A

245380179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178516528-A-G

245380212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178516564-G-A

245380260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178516614-A-T

http://identifiers.org/hco/1/GRCh38#245380432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178516773-C-A

245380463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178516804-G-A

http://identifiers.org/hco/1/GRCh38#245380561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178516882-C-A

http://identifiers.org/hco/1/GRCh38#245380574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178516895-C-A

245380719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517037-C-T

245380767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517076-C-T

245381064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517339-A-G

245384815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517814-G-A

245384841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517840-T-C

245385082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178517976-G-T

http://identifiers.org/hco/1/GRCh38#245385137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178518031-C-A

245385538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178518294-T-C

245385607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178518363-G-T

245385869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178518617-A-G

245385995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178518747-G-T

245386522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519418-G-A

245386557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519445-A-G

245386559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519447-G-A

245386657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519547-A-G

245386695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519585-C-T

245386713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519603-A-G

245386819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519696-A-G

245386917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519803-C-T

245386957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178519827-G-T

245389773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178522084-T-G

245390008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178522270-G-A

245390822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523060-A-G

http://identifiers.org/hco/1/GRCh38#245390922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178523177-A-C

245390922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523177-A-T

http://identifiers.org/hco/1/GRCh38#245390934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178523208-A-C

http://identifiers.org/hco/1/GRCh38#245390937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178523310-A-C

245390991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523378-T-A

245391031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523420-T-C

245391053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523442-G-T

245391225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178523623-T-C

245399152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178524598-G-A

245399484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525184-G-T

245399646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525330-G-A

245399666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525357-C-T

245399667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525358-G-A

245399667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525358-G-C

245400000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525678-T-G

245400090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525769-G-C

245400090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525769-G-T

245400137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525810-G-A

245400137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525810-G-T

245400175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525848-T-C

245400244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178525918-A-G

245400451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526153-A-G

245400524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526468-T-A

245400538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526486-C-T

http://identifiers.org/hco/1/GRCh38#245400595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178526577-C-A

245400595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526577-C-T

245400627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526608-G-A

245400875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526837-C-T

245400932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526881-A-T

245400949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526898-A-G

245400955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178526904-G-C

245401125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178527363-T-G

245401175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178527414-A-G

245402086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178527916-C-T

245402239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528070-G-C

245402361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528193-G-A

245402412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528244-C-T

245402555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528388-C-T

http://identifiers.org/hco/1/GRCh38#245402731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178528552-C-A

http://identifiers.org/hco/1/GRCh38#245402734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178528555-C-A

245402851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528674-T-C

245402866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528689-A-G

245402878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178528701-A-G

245403423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178529713-G-A

245403594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178529840-A-G

245403603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178529849-G-C

245403787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178530010-T-C

245403946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178530148-T-C

245403995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178530195-C-T

245404252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178530440-A-T

245404868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531015-G-T

245405013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531178-G-T

245405037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531194-A-G

245405252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531387-G-A

http://identifiers.org/hco/1/GRCh38#245405359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178531494-A-C

245405495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531628-A-G

245405915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178531937-C-T

245406428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178532818-G-A

245406661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533024-T-C

245406764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533128-G-C

245407218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533243-G-A

245407221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533246-A-G

245407298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533320-T-C

http://identifiers.org/hco/1/GRCh38#245407327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178533348-C-A

245407409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533420-A-T

245408870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178533561-T-G

245409462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178535568-G-C

245409814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178535918-G-A

http://identifiers.org/hco/1/GRCh38#245410095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178536192-C-A

245410227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536344-T-C

245410348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536462-A-G

245410370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536484-C-T

245410386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536501-G-A

245410386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536501-G-T

245410390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536504-G-A

245410425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178536538-C-G

245412198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537204-G-A

245412252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537238-T-G

245412443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537425-G-A

245412454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537433-G-T

245412510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537504-T-C

245412740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537674-C-T

245412878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178537859-T-C

245412895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178537924-A-G

245412898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178537927-T-C

245413093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538153-C-T

245413110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538169-G-T

245413146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538190-A-G

245413191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538216-A-G

245413425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538412-G-A

245413561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538466-G-T

245413852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538554-C-T

245413921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538599-T-G

245413965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538640-T-A

245414056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538729-T-C

245414365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178538983-T-C

245414438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539036-G-A

245414443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539041-G-T

245414500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539074-C-G

245414876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539794-T-A

245414876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539794-T-C

245415056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178539945-A-G

http://identifiers.org/hco/1/GRCh38#245415228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178540086-A-C

245415361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178540214-A-G

245415407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178540248-G-C

245415712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178540544-G-A

245418058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541240-C-T

245418381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541513-G-A

245418612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541747-A-G

245418654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541786-C-T

245418699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541844-T-A

245418713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541856-G-A

245418821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178541953-A-G

245418940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178542763-C-T

http://identifiers.org/hco/1/GRCh38#245419089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178542910-C-A

245419089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178542910-C-G

245419222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543030-C-T

245419246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543054-A-G

245419276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543084-G-A

245419457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543260-A-G

http://identifiers.org/hco/1/GRCh38#245419473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178543276-A-C

245419473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543276-A-G

245419473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543276-A-T

http://identifiers.org/hco/1/GRCh38#245419494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178543285-C-A

245419494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543285-C-G

245419494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543285-C-T

245419511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543302-A-T

http://identifiers.org/hco/1/GRCh38#245419706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178543495-C-A

245419710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178543499-C-T

245419740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178543529-T-C

245419740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: missense variant
orthologous variants: 178543529-T-G

245419779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543566-G-A

245419779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543566-G-C

http://identifiers.org/hco/1/GRCh38#245419785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178543572-C-A

245419785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543572-C-T

245419983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543773-G-A

245420175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178543946-G-A

245421991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178545039-G-T

245422210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178545453-G-C

245422285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178545520-C-G

245422285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178545520-C-T

245422449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178545644-C-T

245425030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178546334-G-T

245425042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178546346-C-T

245426327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178546832-A-G

245426353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178546853-C-T

http://identifiers.org/hco/1/GRCh38#245426459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178547389-C-A

245426459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547389-C-T

245426460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547390-G-A

245426511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547442-A-G

245426765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547676-G-T

245426881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547771-C-T

245427059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178547959-C-T

245428224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178548801-C-G

245430324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178550273-C-T

245431882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551736-G-A

245431898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551746-C-T

245431947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551791-T-C

245431952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551799-A-G

245432014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551849-G-T

245432041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551902-A-G

245432115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178551981-G-A

245432159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552019-T-G

245432259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552089-C-T

245432278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552108-A-G

245432279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552109-G-A

245432354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552183-T-C

245432448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552273-A-G

245432504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552328-G-A

http://identifiers.org/hco/1/GRCh38#245432507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178552331-C-A

245432667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552458-T-C

245432791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552568-T-G

245432822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552594-C-G

245433319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552945-T-C

245433415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178552982-C-T

245433606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553042-T-C

245433781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553198-G-A

http://identifiers.org/hco/1/GRCh38#245433860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178553277-C-A

245433869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553286-G-T

245434202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553613-T-A

245434227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553635-A-G

245434420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178553818-C-T

http://identifiers.org/hco/1/GRCh38#245434623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178554042-C-A

245434623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554042-C-T

245434883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554239-C-T

245435002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554344-T-A

245435002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554344-T-C

http://identifiers.org/hco/1/GRCh38#245435030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178554368-C-A

245435030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554368-C-G

245435030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554368-C-T

245435052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554390-T-A

245435052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554390-T-C

245435096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554425-T-A

245435096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554425-T-C

http://identifiers.org/hco/1/GRCh38#245435097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178554426-C-A

245435097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554426-C-T

245435103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554432-C-T

245435393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554637-A-G

245435432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554676-T-C

245435482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554726-G-A

245435589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554811-C-T

245435631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554853-G-A

245435756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554943-A-T

245435784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554964-C-T

245435814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178554988-C-T

245436218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178555066-G-A

245436352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178555163-A-G

245437273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178555709-C-G

245437273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178555709-C-T

245437345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178555781-T-A

245437773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556195-G-A

245437821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556243-A-T

245437938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556377-C-G

245437940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556379-C-T

245437964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556398-C-T

245438055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556489-G-T

http://identifiers.org/hco/1/GRCh38#245438114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178556550-C-A

245438114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556550-C-T

245438134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556570-C-G

245438418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556797-G-T

245438478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556846-A-G

245438492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556860-G-A

245438513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556880-T-C

245438522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556889-G-C

245438560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178556909-C-T

245438775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178557115-G-A

245439466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178557504-C-T

245439516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178557551-T-C

245439594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178557749-T-C

245440611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178559721-C-T

245440810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178559915-G-A

245441000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178560091-G-A

245441606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178560655-C-G

245441606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178560655-C-T

245441790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178560836-G-C

http://identifiers.org/hco/1/GRCh38#245441814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178560860-A-C

245441814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178560860-A-G

245441970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178561018-T-C

245441976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178561024-G-A

http://identifiers.org/hco/1/GRCh38#245442086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178561138-A-C

http://identifiers.org/hco/1/GRCh38#245442381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178561430-A-C

245442432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178561480-T-A

245442513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178561555-C-T

245442602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178561640-G-C

245444536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562438-G-A

245444536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562438-G-C

http://identifiers.org/hco/1/GRCh38#245444666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178562551-C-A

245444666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562551-C-G

245444672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562557-G-T

245444827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562724-A-G

245444849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562746-A-G

245444900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562796-A-T

245445121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178562987-A-G

245445136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178563004-T-C

245445198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178563054-G-A

245445323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178563131-T-A

245445653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178563415-G-A

245445928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178564101-T-C

http://identifiers.org/hco/1/GRCh38#245445959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178564134-C-A

245446540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178564351-G-T

245446873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178564696-A-T

245447003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178564820-G-C

http://identifiers.org/hco/1/GRCh38#245447300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178565114-A-C

245447300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178565114-A-G

245448578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178565569-A-G

245449289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178566493-G-A

245449424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178566619-A-G

245449628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178566813-C-T

245449724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178566906-A-G

245452352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569275-T-C

245452397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569326-G-C

245452452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569376-A-G

245452460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569384-G-A

245452552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569492-C-G

245452562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569502-C-G

245452562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569502-C-T

245452723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569662-T-G

245452826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569772-G-T

http://identifiers.org/hco/1/GRCh38#245452874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178569807-C-A

245452919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178569853-A-G

245453051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570176-T-A

http://identifiers.org/hco/1/GRCh38#245453078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178570202-C-A

245453194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570305-T-A

245453284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570332-A-G

245453327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570375-G-A

245453375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570412-C-T

http://identifiers.org/hco/1/GRCh38#245453385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178570416-C-A

245453385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570416-C-T

http://identifiers.org/hco/1/GRCh38#245453455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178570485-C-A

245453520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570549-G-A

245453520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570549-G-C

245453520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570549-G-T

245453552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570578-T-C

245453593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570625-C-T

245453663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570736-G-C

245453738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570810-G-T

http://identifiers.org/hco/1/GRCh38#245453749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178570821-A-C

245453857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570932-T-C

245453929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178570972-A-G

245453989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178571057-G-A

245453998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178571066-G-A

245454238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178571314-T-C

245454412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178571972-C-G

245454412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178571972-C-T

http://identifiers.org/hco/1/GRCh38#245454466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178572027-A-C

245454466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572027-A-G

245454573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572133-T-A

http://identifiers.org/hco/1/GRCh38#245454622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178572182-A-C

245454684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572244-G-A

245455157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572581-G-A

245455157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572581-G-T

245455621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572916-C-G

245455684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178572973-T-C

245456197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573370-C-T

245456198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573371-T-C

245456214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573387-G-A

245456215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573388-T-A

245456432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573605-A-G

245456453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573622-C-G

245456478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573647-C-T

245456539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573707-C-T

245456801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573925-C-T

245456819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178573943-A-G

245457229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574015-T-C

245457245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574030-G-C

245457604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574498-C-T

245457630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574521-G-A

245457630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574521-G-C

245457728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574621-A-G

245457730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574623-T-C

245457801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574703-T-C

245457880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178574777-C-T

245458335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575203-C-T

245458479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575336-G-T

245458481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575338-T-C

245458643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575472-T-C

http://identifiers.org/hco/1/GRCh38#245458913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178575742-C-A

245458913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575742-C-T

245458917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575746-G-T

http://identifiers.org/hco/1/GRCh38#245458963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178575790-A-C

245458963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575790-A-G

245459015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575831-T-C

245459139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575939-A-G

245459163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178575961-C-T

245459777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178577921-G-A

245459899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178578041-T-C

245459902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178578044-T-G

245459906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178578048-T-G

245462314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178579291-G-A

245462433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178579620-C-T

245462436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178579623-T-A

245462697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178579848-C-G

245462919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178580078-A-G

245462922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178580081-G-C

245463233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178580664-A-G

http://identifiers.org/hco/1/GRCh38#245463271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178580700-C-A

http://identifiers.org/hco/1/GRCh38#245463669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178581134-C-A

245463669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178581134-C-T

245463688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178581158-T-C

245464056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178581526-C-T

245464083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178581551-T-C

http://identifiers.org/hco/1/GRCh38#245465379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178584953-C-A

245465900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585793-A-G

245465924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585837-G-A

245465953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585894-C-T

245465954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585895-G-A

245465955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585896-T-A

245465958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178585899-G-C

245466178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586100-G-A

245466178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586100-G-C

245466178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586100-G-T

245466232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586135-C-T

245467018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586599-C-T

245467259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586878-A-G

245467279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178586935-T-C

245467416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178587082-C-G

245468552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178589150-G-A

245468666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178589254-C-T

245469302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178589895-G-A

245469461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590044-T-G

245469633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590430-G-A

245469736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590528-G-A

245469801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590599-C-G

245469817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590614-A-G

245469884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590737-A-G

245469920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178590773-A-G

245470088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591020-C-T

245470136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591069-G-A

245470232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591156-G-A

245470389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591296-A-G

245470392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591299-G-A

245471129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591904-G-A

245471129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178591904-G-T

245471522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178592463-G-A

245472626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178593019-T-C

245477935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178594991-G-A

245477960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178595031-A-G

245478004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178595076-C-T

245478137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178595206-T-G

http://identifiers.org/hco/1/GRCh38#245478772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178595534-A-C

245479011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178595770-G-C

245479302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178596053-C-T

245479366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178596119-G-A

http://identifiers.org/hco/1/GRCh38#245481227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178597758-A-C

245481289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178597786-G-A

245481393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178597892-A-G

245481429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178597926-T-G

245481852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598356-C-G

245481878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598382-G-A

245481878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598382-G-T

245482632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598753-G-A

245482763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598888-C-T

http://identifiers.org/hco/1/GRCh38#245482801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178598907-A-C

245482873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178598947-G-A

http://identifiers.org/hco/1/GRCh38#245483014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178599024-C-A

245483014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178599024-C-G

245483205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178599223-C-G

245483297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178599317-C-T

245484112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600324-A-G

245484118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600330-G-A

245484200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600421-G-A

245484226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600447-C-T

245484245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600460-T-G

245484376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600584-G-A

http://identifiers.org/hco/1/GRCh38#245484453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178600660-C-A

245484711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600945-T-C

245484720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600954-C-G

245484734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600969-C-T

245484743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600978-T-C

245484746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600981-C-T

245484752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600987-T-C

245484761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600996-T-A

245484764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178600999-T-A

245484767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601002-A-G

245484767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601002-A-T

245484770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601005-T-A

245484785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601020-T-C

245484789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601024-T-G

245485159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601273-G-A

http://identifiers.org/hco/1/GRCh38#245485768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178601816-C-A

245485768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178601816-C-T

245486170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178602206-A-G

245486301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178602340-G-A

http://identifiers.org/hco/1/GRCh38#245487188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178602789-C-A

245487377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178602947-T-C

245487394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178602964-A-G

http://identifiers.org/hco/1/GRCh38#245488762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178603951-C-A

245488819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178604007-G-A

245488990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178604117-C-T

http://identifiers.org/hco/1/GRCh38#245489051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178604185-C-A

245489076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178604214-C-T

http://identifiers.org/hco/1/GRCh38#245489155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178604291-A-C

http://identifiers.org/hco/1/GRCh38#245489158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178604294-A-C

245489259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605051-C-T

245489260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605052-T-G

245489317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605093-A-G

http://identifiers.org/hco/1/GRCh38#245489558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178605332-C-A

245489658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605354-G-A

245489864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605534-A-G

http://identifiers.org/hco/1/GRCh38#245489873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178605543-C-A

245490006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605647-G-A

245490018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605659-A-G

245490141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605787-A-G

245490260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178605903-G-A

245490739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606058-T-A

245490771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606089-A-G

245490817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606135-G-A

http://identifiers.org/hco/1/GRCh38#245490822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178606140-C-A

245490822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606140-C-T

245490823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606141-G-A

245490823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606141-G-T

245490943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606633-G-A

245490971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606661-T-C

245491056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606744-G-T

245491065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606752-C-G

245491137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178606823-T-C

245491520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178607170-T-C

245491568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178607218-G-A

245491569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178607219-G-A

245491582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178607232-G-A

245492232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178607645-A-G

245492762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178608208-A-T

245497527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178613082-T-C

http://identifiers.org/hco/1/GRCh38#245497629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178613172-C-A

245497629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178613172-C-T

245497720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178613258-A-G

http://identifiers.org/hco/1/GRCh38#245498231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178614608-C-A

245498238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178614615-T-G

245498259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178614636-G-A

245498513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178614883-G-T

245498669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178614969-T-C

245498875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615161-C-T

245498972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615260-C-T

245499009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615297-A-G

245499125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615383-A-G

245499127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615385-C-T

245499199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615458-C-T

245499207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615466-C-T

245499224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178615480-G-C

245499602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178616705-G-A

245499602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178616705-G-T

245499712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178616813-T-C

245500021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617232-T-C

245500034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617321-T-G

245500237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617510-G-A

245500331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617608-C-T

245500550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617796-T-C

245500570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617817-T-C

245500580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617827-T-C

245500730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178617977-G-A

245500989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178618311-G-A

http://identifiers.org/hco/1/GRCh38#245501040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178618361-C-A

http://identifiers.org/hco/1/GRCh38#245501391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178618694-A-C

245501595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178618900-G-A

http://identifiers.org/hco/1/GRCh38#245501725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178619024-C-A

245501819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178619118-C-G

245501844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178619143-A-G

245501857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178619156-A-G

245502000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178619292-G-A

http://identifiers.org/hco/1/GRCh38#245503283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178619716-A-C

245503902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620341-G-A

245503946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620384-T-G

245504016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620445-T-C

245504037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620467-G-A

245504113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620535-G-T

245504808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620758-C-T

245504880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620829-T-C

245504881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178620830-A-G

245505710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178621179-T-C

245505855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178621315-A-G

245506265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178621691-G-C

245506484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178621928-A-T

245506949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622181-G-A

245506949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622181-G-C

http://identifiers.org/hco/1/GRCh38#245507038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178622218-C-A

245507121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622295-C-G

245507192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622366-T-A

245507219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622388-G-A

245507608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622698-G-A

245507721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622804-A-G

245507896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178622933-C-T

http://identifiers.org/hco/1/GRCh38#245507935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178622970-C-A

245508015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178623050-G-A

245509019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178623828-A-G

245509023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178623832-G-A

245509286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178624102-T-C

245509474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178624648-C-G

245509600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178624762-G-A

245509757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178624965-T-G

245510142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178625310-A-G

245510555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178625702-G-A

245510638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron_variant, undefined
orthologous variants: 178625803-C-T

245511069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 178626361-T-C

245511290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178626592-C-G

245511675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178626954-C-T

245511813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627069-C-G

245511852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627087-T-C

245512006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627221-A-T

245512063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627282-G-T

245512072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627307-G-A

http://identifiers.org/hco/1/GRCh38#245512107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178627343-A-C

245512116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627352-C-T

245512117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627353-G-A

245512634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178627825-T-C

245513167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628367-T-C

245513167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628367-T-G

245513176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628376-T-C

http://identifiers.org/hco/1/GRCh38#245513219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178628430-A-C

245513219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628430-A-G

245513294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628521-G-A

245513344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628569-T-C

245513344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628569-T-G

245513420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628632-C-T

245513470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628689-G-T

http://identifiers.org/hco/1/GRCh38#245513588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178628804-C-A

245513597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178628813-C-T

245513857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178629039-G-A

245514637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178629479-C-T

245514678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178629522-T-G

http://identifiers.org/hco/1/GRCh38#245516310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178630383-C-A

245516322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630395-G-A

245516322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630395-G-C

http://identifiers.org/hco/1/GRCh38#245516350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178630423-C-A

245516385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630458-G-A

245516406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630476-C-T

245516444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630514-A-G

245516445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630515-T-C

http://identifiers.org/hco/1/GRCh38#245516545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178630583-C-A

245516545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630583-C-T

245516657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630695-C-G

245516892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630890-G-A

245516905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630902-G-A

245516905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630902-G-T

245516949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178630946-T-C

245517643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178631362-T-C

245517682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178631395-A-G

245517715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178631453-G-A

245517715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178631453-G-C

245518291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178631700-C-T

245518414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178632240-G-A

245518774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178632572-A-T

245518914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178632665-C-T

245519040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633241-G-A

245519050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633251-C-G

245519092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633296-T-C

245520147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633960-G-A

245520147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633960-G-T

245520152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633964-T-A

245520152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178633964-T-C

245521488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178635327-C-G

245522305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178635819-T-C

http://identifiers.org/hco/1/GRCh38#245522364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178635879-A-C

245522364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178635879-A-G

245522409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178635924-C-T

245522697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178636184-A-G

245522699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178636186-C-G

245522711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178636197-C-T

http://identifiers.org/hco/1/GRCh38#245525834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178637055-A-C

245526394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178639433-A-T

245526720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178639751-A-T

245526814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178639845-A-G

245526958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178639948-C-T

245527011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178640000-A-G

245527060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178640050-G-C

245527152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178640110-T-C

245527455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178640810-C-T

245527941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178640963-C-T

245532524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178641899-C-T

245532858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178642237-A-G

245533411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178642782-A-G

245534530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178643953-A-G

245534722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178644137-A-G

245535534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178644620-C-T

245535611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178644692-A-G

245535611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178644692-A-T

245535726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178644809-T-C

245539982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648289-C-T

245540006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648313-T-G

245540205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648511-G-A

245540205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648511-G-T

245540277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648587-G-A

245540431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648740-G-T

245540534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648843-A-G

245540534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178648843-A-T

245540824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178649105-T-C

245540890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: synonymous variant
orthologous variants: 178649171-A-G

245540978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178649260-T-C

245540979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178649261-G-C

245541018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178649298-G-C

245541078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178649362-G-A

245541185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178649701-G-A

245541528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650020-T-G

245541576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650066-G-T

245541657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650146-T-G

245541758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650224-G-A

245541898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650324-C-T

245541935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650359-T-C

245542417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650533-T-C

245542538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178650636-G-A

245542971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651001-G-A

245543247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651227-A-T

245543277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651257-G-C

245543458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651437-G-A

http://identifiers.org/hco/1/GRCh38#245544083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#178651641-C-A

245544083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651641-C-T

245544109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651665-C-G

245544330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178651882-A-G

245545778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178652696-G-A

245546058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178653729-G-A

245546123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178653784-T-C

245546615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178654120-T-G

245546827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178654310-G-A

245547575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655111-G-A

245547575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655111-G-C

245547668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655241-G-A

245548300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655743-A-G

245548322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655772-A-T

245548323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655773-T-G

245548328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655778-C-T

245548346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655794-G-T

245548396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655842-A-G

245548468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655924-T-C

245548503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178655959-C-T

245549126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25484
most severe consequence: intron variant
orthologous variants: 178656314-C-T