148791119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 5 prime UTR variant
orthologous variants: 20353634-G-T

148791207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 5 prime UTR variant
orthologous variants: 20353536-G-A

148791324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353409-G-T

148791409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353337-T-C

148791417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353329-C-G

148791441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353305-G-C

148791523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353231-G-A

148791760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20353055-G-A

148791827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352986-T-A

148791860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352955-G-C

148791972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352865-G-T

http://identifiers.org/hco/3/GRCh38#148792069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20352724-A-C

148792160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352644-A-G

148792295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352519-A-G

148792298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352516-A-G

148792309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352506-G-A

148792432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352399-C-G

148792432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352399-C-T

148792714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352161-G-A

148792739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352135-G-A

148792761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20352113-A-G

http://identifiers.org/hco/3/GRCh38#148793027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20350507-C-A

148793057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20350477-T-C

http://identifiers.org/hco/3/GRCh38#148793867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20350154-C-A

148793867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20350154-C-G

148794388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20350035-G-A

http://identifiers.org/hco/3/GRCh38#148794518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20349889-A-C

148794550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20349858-A-G

148796902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20344456-T-C

148797117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20344125-A-G

http://identifiers.org/hco/3/GRCh38#148797781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20343315-C-A

148797964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20343141-T-G

148801270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20342643-A-G

148801277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20342636-C-T

148823436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20335768-T-G

148823790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20335368-A-G

148823814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20335339-T-A

148824165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20332091-A-G

148824231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20332035-G-A

148824360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20331892-A-T

http://identifiers.org/hco/3/GRCh38#148827517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20330109-A-C

148827535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20330091-T-G

http://identifiers.org/hco/3/GRCh38#148827539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20330087-A-C

148827637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20330001-T-A

http://identifiers.org/hco/3/GRCh38#148827684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20329957-C-A

148827773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 5 prime UTR variant
orthologous variants: 20329867-T-C

148827799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 5 prime UTR variant
orthologous variants: 20329841-T-C

148827881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20329761-G-A

148828039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20329620-C-T

148828118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329544-T-A

http://identifiers.org/hco/3/GRCh38#148828119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20329543-C-A

148828119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329543-C-T

http://identifiers.org/hco/3/GRCh38#148828138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20329526-C-A

148828195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329471-A-G

148828195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329471-A-T

http://identifiers.org/hco/3/GRCh38#148828209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20329458-C-A

148828209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329458-C-T

148828221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329446-T-A

148828221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329446-T-C

148828221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20329446-T-G

148828735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328947-G-A

148828789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328861-C-T

148828880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328703-T-C

148828897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328687-G-A

148828991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328592-C-T

148829046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328552-T-C

148829046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328552-T-G

148829176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20328431-T-G

148830261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20327655-T-C

148830417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20327447-C-G

148830805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20327176-A-T

148830838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20327148-T-A

148831000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326981-A-G

148831218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326764-G-A

148831241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326741-T-C

148831369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326628-T-C

148831377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326620-T-C

http://identifiers.org/hco/3/GRCh38#148831408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20326597-A-C

148831421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326584-T-A

148831488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326520-A-G

148831503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326505-A-G

148833305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20326028-G-A

148833378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325955-G-T

http://identifiers.org/hco/3/GRCh38#148833563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20325753-C-A

148833563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325753-C-G

148833743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325580-A-T

148833805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325511-C-T

148833849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325474-G-C

148833911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20325420-G-A

http://identifiers.org/hco/3/GRCh38#148834087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20325160-A-C

148834251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324766-G-A

148834338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324682-T-G

148834398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324628-A-G

148834425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324601-G-A

148834643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324384-T-C

148834685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324349-A-T

148834695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324339-G-T

148834786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324257-C-T

148834955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324127-C-T

148835041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324059-A-G

148835090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20324028-G-T

148835546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20323570-A-G

http://identifiers.org/hco/3/GRCh38#148836265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20322661-C-A

148837062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321931-A-T

148837250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321718-G-A

http://identifiers.org/hco/3/GRCh38#148837454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20321370-C-A

148837454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321370-C-T

148837467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321357-T-A

http://identifiers.org/hco/3/GRCh38#148837523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20321308-C-A

148837523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321308-C-T

148837596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321226-A-G

148840314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20321031-A-G

148840450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320911-C-T

148840544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320822-A-G

148840571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320795-T-A

148840571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320795-T-G

148840577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320789-G-A

148840577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320789-G-T

148840587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320779-T-C

148840644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320725-T-A

148840674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320697-G-A

148840674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320697-G-C

148840679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20320692-G-A

148840679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20320692-G-C

148840709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20320662-A-G

148840819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20320547-T-C

148840898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20320465-G-A

148840898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20320465-G-T

148840923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20320440-C-G

http://identifiers.org/hco/3/GRCh38#148841027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20320346-A-C

148841037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320336-C-G

148841037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320336-C-T

148841039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320334-T-C

148841057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320316-A-G

http://identifiers.org/hco/3/GRCh38#148841060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20320313-C-A

148841060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320313-C-T

148841082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320290-A-G

148841098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320283-C-T

148841124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320267-G-T

148841126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320265-T-C

148841338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320042-A-G

148841359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20320022-T-C

148841428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319955-G-T

148841543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319846-G-A

148841553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319836-A-G

http://identifiers.org/hco/3/GRCh38#148841704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20319722-C-A

148841704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319722-C-T

148841782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319653-A-G

148841787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319648-G-A

148841859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20319576-A-G

148841859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20319576-A-T

148841883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20319552-G-A

148841883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20319552-G-C

http://identifiers.org/hco/3/GRCh38#148841918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20319517-A-C

148841939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319496-T-C

148841969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319466-A-G

148841973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319462-T-C

148841973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319462-T-G

148841982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319453-T-A

http://identifiers.org/hco/3/GRCh38#148841989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20319446-A-C

http://identifiers.org/hco/3/GRCh38#148842031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20319416-C-A

148842394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20319104-A-G

148842609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318979-A-G

148842781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318800-T-G

148842783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318798-A-G

148842883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318723-A-G

148843020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318648-T-A

148843063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318603-G-A

148843269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318271-A-G

148843303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318227-A-G

148843367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318178-A-G

148844419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20318008-T-C

148844448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20317978-A-G

148844514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20317914-G-C

148844562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20317866-G-T

148844642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317793-A-G

148844768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: splice donor variant
orthologous variants: 20317667-G-C

148844789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317642-T-G

148844804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317628-G-A

148844804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317628-G-T

148844861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317559-G-A

148844861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317559-G-T

148845287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20317001-T-C

http://identifiers.org/hco/3/GRCh38#148845303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20316944-A-C

148845348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20316882-T-A

148845459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20316739-T-C

148845474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20316724-G-A

148845474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20316724-G-T

148845579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20316619-T-C

148845621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: missense variant
orthologous variants: 20316577-G-A

http://identifiers.org/hco/3/GRCh38#148845692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20316504-A-C

148845778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20316358-G-A

http://identifiers.org/hco/3/GRCh38#148845827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20316306-C-A

148849478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20316050-G-A

148849479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20316049-G-A

148849828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20315736-G-A

148849873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20315692-T-C

148849978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311668-C-T

148849995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311651-T-A

148850082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311572-T-C

148850111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311545-C-G

148850154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311500-T-C

148850154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20311500-T-G

148850666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20310965-T-A

148850720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20310918-G-A

148850837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron variant
orthologous variants: 20310813-G-T

http://identifiers.org/hco/3/GRCh38#148850935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20310719-C-A

148850968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310686-G-A

148850968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310686-G-T

148851045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310609-A-G

148851050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310604-A-G

148851085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310548-G-A

148851085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310548-G-C

148851085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310548-G-T

148851106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310527-G-T

148851222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310397-T-A

148851222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310397-T-C

http://identifiers.org/hco/3/GRCh38#148851223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20310396-C-A

148851227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310392-G-A

148851227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310392-G-T

148851230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310389-A-G

148851254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310365-G-C

http://identifiers.org/hco/3/GRCh38#148851283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20310333-C-A

148851283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310333-C-T

148851347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310285-A-G

148851359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310273-A-G

148851368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310265-A-G

148851368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310265-A-T

148851378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310255-A-G

148851411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310222-G-A

148851411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310222-G-T

148851618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310085-A-T

http://identifiers.org/hco/3/GRCh38#148851657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20310025-A-C

148851665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310017-A-G

148851672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20310010-G-T

148851695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309988-G-T

148851698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309985-G-T

http://identifiers.org/hco/3/GRCh38#148851731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20309960-C-A

http://identifiers.org/hco/3/GRCh38#148851742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20309949-A-C

148851804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309917-G-A

148851924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309836-A-G

148851925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309835-G-A

148851925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20309835-G-T

148851938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 20309822-A-G

http://identifiers.org/hco/3/GRCh38#148851998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20309762-C-A

148852006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309754-T-C

148852016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309744-T-A

148852016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309744-T-G

148852069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309688-G-C

148852080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309677-C-G

http://identifiers.org/hco/3/GRCh38#148852237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20309560-A-C

148852259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309553-C-T

148852404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309417-A-G

148852446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20309373-G-A

148852804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308929-G-A

148852834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308892-C-G

148852835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308891-T-G

148852942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308786-G-A

148853041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308695-G-A

148853220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308548-C-T

148853298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308480-A-G

148853314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308464-A-G

148853364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308414-T-G

148853491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308286-A-T

148853605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308188-G-A

148853651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308147-C-T

148853724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308063-T-C

148853787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20308009-A-T

148853972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20307879-C-T

148854024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20307831-T-C

http://identifiers.org/hco/3/GRCh38#148854040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307817-C-A

148854040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20307817-C-T

http://identifiers.org/hco/3/GRCh38#148854202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307728-C-A

148854217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20307713-C-T

148854245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20307685-A-T

148854272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20307659-A-G

148854292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20307639-G-T

148854384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307557-T-C

148854410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307531-T-C

http://identifiers.org/hco/3/GRCh38#148854553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307415-C-A

148854553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307415-C-G

148854610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307354-A-G

http://identifiers.org/hco/3/GRCh38#148854616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307348-C-A

148854660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307319-C-T

148854669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307310-G-C

148854669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307310-G-T

148854715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307272-C-T

148854720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307267-G-A

148854720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307267-G-T

148854728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307261-A-G

148854737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307252-A-G

148854760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307220-G-T

148854790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307186-A-T

148854809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307156-C-G

http://identifiers.org/hco/3/GRCh38#148854838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307127-C-A

148854845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307120-G-T

148854876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307094-A-G

http://identifiers.org/hco/3/GRCh38#148854900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20307070-A-C

148854900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307070-A-G

148854908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307062-T-C

148854950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20307024-G-C

148854977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306996-A-G

148854981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306992-T-C

http://identifiers.org/hco/3/GRCh38#148854991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306985-C-A

http://identifiers.org/hco/3/GRCh38#148855000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306976-C-A

148855042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306939-A-G

http://identifiers.org/hco/3/GRCh38#148855145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306861-C-A

148855160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306846-G-A

148855272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306735-C-T

148857015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306606-C-T

148857018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306603-T-C

148857047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306576-G-A

148857047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306576-G-T

148857067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306556-T-G

148857241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306422-G-A

148857241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306422-G-T

148857249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306414-A-G

148857255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306400-T-C

148857255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306400-T-G

148857257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306398-A-G

148857257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306398-A-T

148857266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306389-A-G

http://identifiers.org/hco/3/GRCh38#148857327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306327-C-A

148857338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306316-A-G

148857366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306288-A-G

148857366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306288-A-T

148857420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306234-T-G

148857452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20306206-T-C

http://identifiers.org/hco/3/GRCh38#148857461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306197-C-A

http://identifiers.org/hco/3/GRCh38#148857475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306183-A-C

148857475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306183-A-G

148857542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 20306116-G-A

http://identifiers.org/hco/3/GRCh38#148857573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306084-C-A

148857573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20306084-C-T

148857621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20306038-G-A

148857621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20306038-G-C

148857621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20306038-G-T

http://identifiers.org/hco/3/GRCh38#148857720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20306001-A-C

148857724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305997-T-A

148857724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305997-T-G

148858001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305885-A-G

148858005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305881-A-T

148858178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305739-C-G

148858178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20305739-C-T

148858897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304895-G-A

148859074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304736-T-C

148859189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304621-A-G

148859199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304611-C-G

148859312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304533-T-C

148859448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304329-G-T

148859484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304300-C-T

148859628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304175-G-A

148859687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304125-A-G

148859687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304125-A-T

http://identifiers.org/hco/3/GRCh38#148859704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20304111-C-A

148859746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304068-A-G

http://identifiers.org/hco/3/GRCh38#148859766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20304047-C-A

148859766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304047-C-T

148859792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304021-T-C

148859792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20304021-T-G

148859847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303968-T-C

148860014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303801-G-A

148860056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303759-T-C

148860063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303752-T-A

148860108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303716-T-C

http://identifiers.org/hco/3/GRCh38#148860130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20303695-A-C

148860139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303686-G-T

148860151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303676-T-C

148860166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303661-G-A

148860166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303661-G-T

148860168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303659-G-A

148860168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303659-G-C

148860168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20303659-G-T