94618505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283743-T-C

94618506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283742-T-C

94618541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283707-C-T

http://identifiers.org/hco/5/GRCh38#94618560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77283686-C-A

94618680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77283570-G-A

94618680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77283570-G-T

http://identifiers.org/hco/5/GRCh38#94618692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77283558-A-C

94618692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283558-A-G

94618734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283517-C-T

94618747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77283494-C-T

94618909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77283372-C-T

http://identifiers.org/hco/5/GRCh38#94619028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77283299-C-A

94619039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77283288-C-G

94619060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77283269-C-T

94619106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77283223-G-A

94619106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77283223-G-T

94619337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77282995-A-G

94619445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77282907-G-A

94619528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77282843-A-G

http://identifiers.org/hco/5/GRCh38#94619556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77282815-A-C

94619556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77282815-A-G

94621085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77281836-T-A

94621118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77281807-C-T

94621140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77281780-C-T

94621192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77281722-A-G

94621753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77281199-T-C

94622285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77280540-T-C

94622747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77280071-T-A

94623138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77279557-T-G

94623448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77279257-A-G

94623493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77279226-C-T

94623553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77279156-A-G

94623936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77278478-T-C

94624032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77278386-A-G

94624067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77278339-G-A

94624198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77278215-G-C

94624394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77278020-G-C

http://identifiers.org/hco/5/GRCh38#94625237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77277298-C-A

94625849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77277037-T-C

http://identifiers.org/hco/5/GRCh38#94626536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77276689-C-A

94626536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77276689-C-T

http://identifiers.org/hco/5/GRCh38#94626567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77276658-C-A

94626567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77276658-C-G

http://identifiers.org/hco/5/GRCh38#94627294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77275559-A-C

94627514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275394-A-G

94627514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275394-A-T

94627577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275356-G-A

94627577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275356-G-T

http://identifiers.org/hco/5/GRCh38#94627585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77275348-C-A

94627585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275348-C-T

94628505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77275128-T-G

94628803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77274839-T-G

94628954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274683-T-C

94629373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274294-A-G

94629487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274177-G-A

94629845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273966-C-T

94630396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273700-T-G

94630405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273694-T-C

94630405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273694-T-G

94630448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273643-T-C

94630634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 77273456-C-T

http://identifiers.org/hco/5/GRCh38#94630825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77273273-C-A

94630825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77273273-C-T

94631068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77272088-A-G

94631136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77272013-A-G

http://identifiers.org/hco/5/GRCh38#94631422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77271423-A-C

94631427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77271418-C-T

http://identifiers.org/hco/5/GRCh38#94631796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77271079-C-A

94642374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261763-A-G

94642813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261354-A-G

94642833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261306-T-C

94642847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261292-A-G

94642861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261275-T-A

94642875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261248-T-A

94642894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261229-A-G

94642957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261165-A-G

94642957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261165-A-T

94642985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261141-A-G

94643055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261072-A-G

94643073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261054-A-G

94643119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261019-T-A

94643119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77261019-T-G

94643218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260936-G-T

94643312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 77260812-A-G

94643493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260543-A-G

94643501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260344-A-G

94643501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260344-A-T

94643513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260332-A-G

94643523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260322-T-G

94643551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260300-G-A

94643594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260250-T-C

94643673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260141-A-G

94643741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77260066-T-C

94644000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77259837-T-G

http://identifiers.org/hco/5/GRCh38#94644894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77259601-C-A

94644895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77259600-C-T

94645022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77259480-T-C

94645405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77259009-G-A

94645819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77258668-A-T

94646503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77258349-T-C

94646571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77258278-C-T

94647350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77256224-A-G

94647357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77256217-T-G

94647401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77256175-A-G

94647437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77256142-C-T

94647670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77255943-T-C

94647758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77255851-T-G

94649372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77254314-G-C

94649442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77254232-A-G

http://identifiers.org/hco/5/GRCh38#94649486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77254189-C-A

94649541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 77254146-G-A

http://identifiers.org/hco/5/GRCh38#94649737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77253958-C-A

94649737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253958-C-T

94649835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253860-C-G

94650080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253660-C-T

94650714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253352-C-T

94650721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253345-T-C

94651479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77253028-T-C

http://identifiers.org/hco/5/GRCh38#94651525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77252977-A-C

94651571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252927-T-C

94651583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252908-T-C

94651613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252879-G-T

94652418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252364-T-C

94652444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252344-T-C

94652642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77252107-A-G

94653343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 77251676-A-G

94653395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77251624-A-G

94653416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77251603-G-A

94653416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77251603-G-T

94653433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77251587-A-G

94653442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77251581-T-A

94653469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77251554-G-A

94653547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77251468-G-A

94654594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77249194-A-G

94662041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77246776-G-A

94662241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240582-G-T

94662331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 77240495-C-T

94662384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240433-G-A

94662384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240433-G-C

94662470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240404-G-A

94662470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240404-G-T

94662610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240298-A-G

94662804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77240174-C-T

94663040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239918-A-T

94663533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239581-A-G

94663533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239581-A-T

94663683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239524-A-G

94663683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239524-A-T

94663831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 77239379-G-A

94663831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 77239379-G-T

http://identifiers.org/hco/5/GRCh38#94663903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77239307-C-A

94664090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77239173-C-G

94666111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77238351-T-C

94666111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77238351-T-G

http://identifiers.org/hco/5/GRCh38#94666221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77238255-A-C

94666382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77238111-A-G

94666424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77238074-G-T

94666620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237901-C-T

94666632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237889-T-C

94669115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237720-G-A

94669118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237717-G-A

94669161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237678-T-C

94669375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237171-T-C

94669391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237157-T-A

94669391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237157-T-C

94669453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77237095-A-G

94670040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232689-A-T

94670062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232667-A-G

94670097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232632-A-G

http://identifiers.org/hco/5/GRCh38#94670263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77232465-C-A

94670289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232439-A-G

94670290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232438-A-G

94670309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232424-T-C

94670383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232341-A-T

94670473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77232241-C-T

94670869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense variant
orthologous variants: 77231697-A-G

http://identifiers.org/hco/5/GRCh38#94671051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77231513-C-A

94671224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: -T-C

94672802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77222513-G-C

94673122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77222234-T-C

94673141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77222214-C-T

94673281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77222096-G-C

94673495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77221909-T-C

94673509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77221895-C-G

94674134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77220931-G-C

94674369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77220718-G-T

94674812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77220274-G-A

94674927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77220130-T-C

94675224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77219858-G-A

94675399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77219689-A-G

94675903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218458-G-T

94675904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218457-A-T

94675960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218422-G-T

94676066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218328-A-G

94676393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218062-G-T

94676454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77218001-T-G

94676525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77217942-C-T

94676678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77217799-A-G

94676693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron variant
orthologous variants: 77217784-T-A

94678591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77215372-G-C

94678627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77215033-A-T

94678690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77214980-A-T

94678708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77214962-A-G

94678751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77214925-T-C

94679028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214640-G-C

http://identifiers.org/hco/5/GRCh38#94679097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77214600-A-C

94679097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214600-A-G

94679097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214600-A-T

http://identifiers.org/hco/5/GRCh38#94679099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77214598-A-C

94679099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214598-A-T

http://identifiers.org/hco/5/GRCh38#94679104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77214593-C-A

94679104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214593-C-G

94679104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214593-C-T

94679259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214434-A-G

94679827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211487-T-C

94679845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211475-T-A

94679846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211474-C-G

94680009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211349-G-C

94680011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211347-G-A

94680011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211347-G-C

94680069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211287-G-A

94680069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211287-G-T

94680456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210558-T-C

94680489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210533-C-G

94680649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210382-G-T

94680891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210164-G-A

94680949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210103-T-G

94681065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209324-G-A

94681065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209324-G-T

94682451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201856-T-A

94682460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201847-T-G

http://identifiers.org/hco/5/GRCh38#94682637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77201760-A-C

94682703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201690-A-G

94682861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201565-A-G

94682979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201480-T-C

94683298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200997-C-T

94686496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199476-T-G

94686617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77199367-T-C

94687971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198639-T-A

94688383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198273-G-A

94688383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198273-G-C

94688423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198234-T-C

94688530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77198134-G-A

94688530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77198134-G-C

94688565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77198099-G-T

94688719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197945-T-G

94689323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197472-A-G

94689355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197441-G-T

94689568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77197242-T-C

http://identifiers.org/hco/5/GRCh38#94689703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77197107-C-A

94689703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197107-C-G

94689703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197107-C-T

94689709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197101-T-C

94689717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197093-T-A

94690512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196336-G-C

94690520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196328-G-T

94690787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196077-G-T

94690917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195935-C-T

94690921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195931-C-T

94691255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195598-T-A

94691255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195598-T-G

94691301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195553-T-A

94691301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195553-T-C

94691301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195553-T-G

94691316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195539-T-A

94691316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195539-T-C

94691316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195539-T-G

94691335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195522-T-A

94691336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195521-G-T

94691339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195518-G-A

94691339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195518-G-T

94691351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195506-G-A

94691351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195506-G-T

94691366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195493-G-A

94691366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195493-G-T

94691367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195492-G-T

94691379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195480-T-A

94691379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195480-T-C

94691379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195480-T-G

94691388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195471-T-A

94691388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195471-T-C

94691388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195471-T-G

http://identifiers.org/hco/5/GRCh38#94691396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77195463-C-A

94691396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195463-C-G

94691396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195463-C-T

http://identifiers.org/hco/5/GRCh38#94691399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77195460-C-A

94691399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195460-C-G

94691399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195460-C-T

94691411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195444-T-C

94691411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77195444-T-G

http://identifiers.org/hco/5/GRCh38#94691617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77195266-C-A

94691617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77195266-C-G

94691617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77195266-C-T

94691676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195205-G-A

94691676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195205-G-C

94691722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195159-T-A

94691722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195159-T-C

http://identifiers.org/hco/5/GRCh38#94691764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77195117-C-A

94691789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195101-A-G

94691789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195101-A-T

94691923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194966-A-G

94691938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77194951-A-G

http://identifiers.org/hco/5/GRCh38#94691973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77194917-C-A

94692036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77194859-T-C

94692205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77194690-G-A

94692217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77194678-G-A

94692217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77194678-G-C

94692310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194585-A-G

94692803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77194088-G-T

94692915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77193990-T-C

94692982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77193933-A-G

94693438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77193442-G-A

94694088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77192869-A-G

94694138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77192818-A-G

94694250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77192679-G-C

http://identifiers.org/hco/5/GRCh38#94694801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77192178-C-A

94694801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77192178-C-T

94694978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77192000-A-T

94695015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77191963-T-C

http://identifiers.org/hco/5/GRCh38#94695143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77191835-A-C

94695143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191835-A-G

94695329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191652-G-C

94695329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191652-G-T

94695348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191635-G-C

94695364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191619-T-C

94695484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191519-T-C

http://identifiers.org/hco/5/GRCh38#94695525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77191497-A-C

94695702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191300-G-A

94695702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77191300-G-T

94695916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189405-G-A

94695916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189405-G-T

94695959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189363-A-G

http://identifiers.org/hco/5/GRCh38#94695964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77189358-A-C

94695964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189358-A-T

94696020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189311-G-A

94696020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189311-G-T

94696069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77189254-T-G

94697497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77188078-G-A

94697497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77188078-G-T

94697574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77188001-C-G

94698200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187411-A-G

94698405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77187234-T-C

94698451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77187187-T-C

94698511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187139-G-C

94698533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77187122-C-T

94698626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77187029-T-A

94698750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186935-C-G

94698826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186825-T-C

94698847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186798-C-T

94698933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186567-T-C

94699001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186494-T-C

94699182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186324-A-G

94699199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186311-A-G

94699393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77186144-A-G

http://identifiers.org/hco/5/GRCh38#94699430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77186117-A-C

94699843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77185805-A-G

94700110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77185568-T-C

94700112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77185566-T-C

94700147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77185536-G-A

94701554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77183061-T-C

http://identifiers.org/hco/5/GRCh38#94701836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77182902-A-C

94702631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77182347-A-T

http://identifiers.org/hco/5/GRCh38#94703195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77181850-C-A

94703195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77181850-C-T

94703213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77181832-G-A

94703969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77181504-G-A

94703969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77181504-G-C

94704033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77181441-A-G

94704080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77181399-T-C

94704402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77181128-G-T

94704541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77180997-A-G

http://identifiers.org/hco/5/GRCh38#94705367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77180104-C-A

http://identifiers.org/hco/5/GRCh38#94705479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77179989-C-A

94705954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77179533-G-T

94706003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77179486-A-G

94706121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77179388-A-G

http://identifiers.org/hco/5/GRCh38#94706591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77178947-C-A

94706591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178947-C-G

94706591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178947-C-T

94706758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178813-A-G

94706801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178773-G-A

94707203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178360-A-G

http://identifiers.org/hco/5/GRCh38#94707381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77178184-A-C

94707381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178184-A-G

94707426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178132-C-T

94707428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178130-G-T

94707435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178123-C-G

94707439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178116-G-A

94707439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77178116-G-T

94707521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77178043-T-A

94707602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177964-G-A

94707602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177964-G-T

http://identifiers.org/hco/5/GRCh38#94707639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77177927-A-C

94707730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177838-C-G

94707940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177452-A-G

94707945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177447-G-C

94707954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177436-G-A

94707970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177416-A-G

94707970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177416-A-T

http://identifiers.org/hco/5/GRCh38#94707981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77177405-A-C

http://identifiers.org/hco/5/GRCh38#94708121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77177205-A-C

94708121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177205-A-T

http://identifiers.org/hco/5/GRCh38#94708141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77177187-A-C

94708141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177187-A-G

http://identifiers.org/hco/5/GRCh38#94708198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77177146-C-A

94708198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177146-C-G

94708198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77177146-C-T

94708221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77177118-T-A

94708221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77177118-T-C

94708364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77176971-A-G

http://identifiers.org/hco/5/GRCh38#94708414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77176928-C-A

94708414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77176928-C-T

94708698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77176618-G-T

http://identifiers.org/hco/5/GRCh38#94708787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77176545-C-A

94708794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77176538-A-G

94708901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77175090-A-G

94709027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174980-G-A

94709027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174980-G-T

94709226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174795-A-T

94709250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174771-T-C

94709265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174759-T-C

94709309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174713-G-T

94709369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174657-G-A

94709483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174534-G-A

94709484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174533-G-A

http://identifiers.org/hco/5/GRCh38#94709491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77174526-C-A

94709761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174303-A-G

94709820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77174250-G-T

94709893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173950-G-C

94709893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173950-G-T

94710025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173787-C-G

94710025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173787-C-T

94710183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173634-T-C

94710211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173606-G-A

94710212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173605-C-T

94710280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173541-T-C

http://identifiers.org/hco/5/GRCh38#94710437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77173395-C-A

94710437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173395-C-T

http://identifiers.org/hco/5/GRCh38#94710488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77173347-A-C

94710488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173347-A-T

94710667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173163-T-C

94710667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173163-T-G

94710669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173161-G-A

94710669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173161-G-C

94710669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77173161-G-T

94710880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77172947-G-A

94711130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77172764-T-A

94713645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77171034-G-A

94713721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170964-G-A

94713884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170797-G-T

94714014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77170673-G-A

94714401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169335-A-G

http://identifiers.org/hco/5/GRCh38#94714459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77169284-A-C

94714459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169284-A-G

94714637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169108-G-T

94714665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169080-G-A

94714665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169080-G-T

http://identifiers.org/hco/5/GRCh38#94714685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77169063-C-A

94714685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169063-C-T

94714726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77169024-T-A

94714766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77168989-C-T

94714817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77168938-T-A

http://identifiers.org/hco/5/GRCh38#94715036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77168715-C-A

94715175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77168506-A-G

http://identifiers.org/hco/5/GRCh38#94715356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77167441-A-C

http://identifiers.org/hco/5/GRCh38#94715397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77167405-A-C

94715397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77167405-A-T

94716109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77166725-T-G

94716694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77166047-A-G

94716756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165996-T-G

94716921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165810-C-G

94720452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165085-A-G

94720524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165037-T-C

94720541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77165024-C-T

94721089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164520-G-T

94721139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164485-T-C

http://identifiers.org/hco/5/GRCh38#94721303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77164350-C-A

94721303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164350-C-G

94721363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164303-T-G

94721384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164281-T-C

94721384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164281-T-G

94721393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77164272-G-C

94722101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77161524-A-T

94722351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77161296-G-C

94722384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77161264-G-A

94722384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77161264-G-C

94722507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77161140-T-G

94722557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160743-C-G

94722766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160547-T-C

94722892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160451-G-A

94722906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160437-T-C

94722979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160381-C-T

94723140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160214-G-A

94723192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77160163-G-C

94724144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77155600-A-G

94725319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

94725469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

94726561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151593-C-T

94727165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77151010-A-G

http://identifiers.org/hco/5/GRCh38#94727178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77150997-C-A

94727333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150849-T-C

94727448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150738-G-A

94727530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150656-G-A

94727732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150243-G-T

94727883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150123-T-C

94727903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150103-C-T

94728560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149102-G-A

94728672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149013-T-C

94733367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77125568-C-T

94733477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77125467-G-A

94733540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77125425-A-G

94734746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77121057-G-T

94734861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77120977-G-C

94735041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77120794-A-G

94735326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77120558-T-C

94735701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77119194-A-G

94736082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77118816-A-T

http://identifiers.org/hco/5/GRCh38#94736956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77118266-A-C

94736980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77118242-T-C

94737302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77118192-G-A

94737309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77118185-A-T

94737322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77118172-A-G

94738288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77117518-G-T

94738373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77117428-C-T

94738470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77117332-G-A

http://identifiers.org/hco/5/GRCh38#94738477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#77117325-C-A

94738657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77117185-G-A

94738803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77117028-A-G

94739009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77116813-C-T

94739019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77116803-G-T

94739107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77116712-G-T

94739400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77116434-A-G

94739408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77116426-G-T