23940194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55708501-T-C

http://identifiers.org/hco/14/GRCh38#23940219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55708525-C-A

23940327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55708632-G-T

23940743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55708749-G-A

23940743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55708749-G-T

23940795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55708826-T-C

23941005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: non coding transcript exon variant
orthologous variants: 55709003-G-T

23942039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55709327-C-T

23942208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55709457-C-T

23942262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55709504-G-A

23949694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55711672-G-A

23951223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55712794-A-G

23951623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55712858-A-G

http://identifiers.org/hco/14/GRCh38#23951681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55712919-A-C

http://identifiers.org/hco/14/GRCh38#23951993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713145-A-C

23952225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713355-C-T

23953042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714650-A-T

23953096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714703-G-C

23953096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714703-G-T

23953098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714705-G-A

23953098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714705-G-C

23953109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714719-G-T

23953155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714868-T-G

23953212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714984-T-A

23953212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55714984-T-G

23953245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715035-G-A

23953245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715035-G-T

23953250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715040-G-C

http://identifiers.org/hco/14/GRCh38#23953335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55715128-C-A

23953335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715128-C-T

23953349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715142-G-A

23953349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715142-G-C

23953365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55715166-T-C

http://identifiers.org/hco/14/GRCh38#23953449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716000-C-A

23953449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716000-C-T

23953497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716065-A-G

http://identifiers.org/hco/14/GRCh38#23953519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716097-C-A

23953519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716097-C-T

23953534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716110-G-T

23953589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716147-G-A

23953589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716147-G-C

23953589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716147-G-T

23953644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716190-G-A

23953644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716190-G-T

http://identifiers.org/hco/14/GRCh38#23953678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716240-C-A

23953678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716240-C-G

23953678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716240-C-T

http://identifiers.org/hco/14/GRCh38#23953690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716252-C-A

23953690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716252-C-G

23953690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716252-C-T

http://identifiers.org/hco/14/GRCh38#23953711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716280-C-A

23953711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716280-C-G

23953711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716280-C-T

http://identifiers.org/hco/14/GRCh38#23953715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716284-C-A

23953715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716284-C-G

23953715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716284-C-T

23953815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716389-C-T

http://identifiers.org/hco/14/GRCh38#23953881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716455-A-C

23953881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716455-A-G

23953894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716468-C-G

23953992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716543-G-A

23953992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716543-G-C

23953992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716543-G-T

23954030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716581-G-C

http://identifiers.org/hco/14/GRCh38#23954059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716614-C-A

23954059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716614-C-T

23954063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716618-T-A

23954063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716618-T-C

http://identifiers.org/hco/14/GRCh38#23954070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716625-A-C

http://identifiers.org/hco/14/GRCh38#23954118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716672-C-A

23954118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55716672-C-T

http://identifiers.org/hco/14/GRCh38#23954121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716675-C-A

23954121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716675-C-T

23954160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716711-T-C

23954160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716711-T-G

http://identifiers.org/hco/14/GRCh38#23954176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716725-A-C

23954176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716725-A-G

23954176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716725-A-T

23954334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716828-G-A

23954334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716828-G-T

23954536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717011-A-G

23954724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717173-C-T

23954738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717186-C-T

23954765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717213-G-A

23954765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717213-G-T

23954876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717320-C-T

http://identifiers.org/hco/14/GRCh38#23954890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717336-C-A

23954916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717360-A-G

23954983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717429-G-A

23954983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717429-G-C

23954984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717430-A-G

23954994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717442-C-T

23955056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717504-G-A

23955211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717659-C-G

23955211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717659-C-T

23955212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717660-G-A

23955212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717660-G-C

23955220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717668-G-T

23955225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717673-G-A

23955231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717679-G-C

23955231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717679-G-T

http://identifiers.org/hco/14/GRCh38#23955233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717681-C-A

23955233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717681-C-G

23955233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717681-C-T

23955278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717732-C-T

23955361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718113-C-T

23955411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718163-T-G

http://identifiers.org/hco/14/GRCh38#23956192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55719186-A-C

23956192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55719186-A-G

http://identifiers.org/hco/14/GRCh38#23956274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55719248-C-A

23956362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55719791-C-T

23957076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721299-G-A

23957333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721613-A-G

23957334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721614-T-C

23957408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721663-G-A

http://identifiers.org/hco/14/GRCh38#23957528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55721766-C-A

23958037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722116-C-T

23958310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722390-G-A

23958310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722390-G-T

23958347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722426-G-A

23958749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722940-T-G

23958843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723032-C-G

23958971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723157-T-C

23959203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723338-G-A

23959203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723338-G-C

23959824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723496-G-A

23959832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723504-T-C

http://identifiers.org/hco/14/GRCh38#23959869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55723543-C-A

23959869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723543-C-T

23959883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723557-A-T

23959918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55723590-G-A

23959918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55723590-G-C

23965442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724255-C-T

23965485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724303-T-G

http://identifiers.org/hco/14/GRCh38#23965547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724365-A-C

23965602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724423-C-T

23965611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724436-A-G

23965611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724436-A-T

23965623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724448-T-A

23965677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724480-A-T

http://identifiers.org/hco/14/GRCh38#23965698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724498-A-C

23965715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724508-C-T

http://identifiers.org/hco/14/GRCh38#23965723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724516-C-A

23965723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724516-C-G

http://identifiers.org/hco/14/GRCh38#23965851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724639-A-C

23965919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724704-C-G

http://identifiers.org/hco/14/GRCh38#23966130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724888-C-A

23966130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724888-C-T

http://identifiers.org/hco/14/GRCh38#23966160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724911-A-C

23966160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55724911-A-G

http://identifiers.org/hco/14/GRCh38#23966209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724962-C-A

23966405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725163-C-G

http://identifiers.org/hco/14/GRCh38#23966443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725198-A-C

23966446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725201-G-C

http://identifiers.org/hco/14/GRCh38#23966550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725290-C-A

23966550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725290-C-G

23966550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725290-C-T

http://identifiers.org/hco/14/GRCh38#23966573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725313-C-A

23966617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725366-A-G

23966623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725372-G-A

23966816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725542-G-A

23966816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725542-G-T

23966839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725569-G-A

23966839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725569-G-C

23966839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725569-G-T

23967196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725602-C-T

23967327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725719-G-A

23967487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725850-G-A

23967487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725850-G-T

23967636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725937-G-T

23967672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725974-C-T

23967698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725996-G-A

23967698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725996-G-C

23967698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725996-G-T

http://identifiers.org/hco/14/GRCh38#23967767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726065-A-C

23967792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726090-G-T

23967892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726216-G-A

23967892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726216-G-T

23967896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726220-C-T

http://identifiers.org/hco/14/GRCh38#23967953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726259-C-A

23967953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726259-C-T

http://identifiers.org/hco/14/GRCh38#23967978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726285-C-A

23967978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726285-C-T

http://identifiers.org/hco/14/GRCh38#23967979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726286-A-C

23967979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726286-A-G

23967993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726301-G-A

23967993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726301-G-C

23967993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55726301-G-T

23968561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726783-A-G

23968684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727202-C-T

23968730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727252-T-C

23968730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727252-T-G

23968864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727383-G-A

http://identifiers.org/hco/14/GRCh38#23968948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727461-C-A

http://identifiers.org/hco/14/GRCh38#23968985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727498-C-A

23968985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727498-C-T

23969076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727586-G-A

23969076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727586-G-T

http://identifiers.org/hco/14/GRCh38#23969223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727746-A-C

23969258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727781-G-T

23969305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727825-G-A

23969305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727825-G-T

23969336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727851-T-G

23969386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727904-T-A

23969401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727919-C-G

http://identifiers.org/hco/14/GRCh38#23969437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727967-A-C

23969437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727967-A-T

23969497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728094-A-G

23969714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728317-C-G

23969766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728372-G-A

23969766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728372-G-T

23970048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728637-T-C

23970050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728639-T-C

23970050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728639-T-G

http://identifiers.org/hco/14/GRCh38#23970183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728785-C-A

23970183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728785-C-G

http://identifiers.org/hco/14/GRCh38#23977216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55709793-C-A

23985682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55712794-A-G

23986606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713001-C-T

23986830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713146-G-A

23986903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713217-T-G

23986931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713246-G-A

http://identifiers.org/hco/14/GRCh38#23987197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713547-C-A

http://identifiers.org/hco/14/GRCh38#23987206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713556-C-A

23987206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713556-C-T

http://identifiers.org/hco/14/GRCh38#23987229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713579-C-A

23987229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713579-C-T

http://identifiers.org/hco/14/GRCh38#23987230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713580-A-C

23987230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713580-A-G

23987230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713580-A-T

http://identifiers.org/hco/14/GRCh38#23987268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713624-C-A

23987268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713624-C-G

23987268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55713624-C-T

23987702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714176-A-G

23987804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714279-T-G

23987972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714451-A-T

http://identifiers.org/hco/14/GRCh38#23988062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55714543-A-C

23988099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714580-T-C

23988145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714626-A-G

23988218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714682-C-G

23988267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714733-A-T

23988312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714941-G-A

23988312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714941-G-C

23988394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55715040-G-A

http://identifiers.org/hco/14/GRCh38#23988593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716000-C-A

23988593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716000-C-G

23988593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716000-C-T

23988607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716023-A-G

http://identifiers.org/hco/14/GRCh38#23988663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716097-C-A

23988678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716110-G-A

23988678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716110-G-T

23988735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716147-G-A

23988735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716147-G-C

23988735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716147-G-T

23988803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716190-G-A

23988803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716190-G-T

23988833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716219-G-A

23988833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716219-G-T

23988838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716224-A-G

23988848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716252-G-A

23988848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716252-G-C

23988848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716252-G-T

23988864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716284-G-A

23988864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716284-G-T

23988974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716389-C-G

23988974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716389-C-T

23989053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716468-C-T

23989151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716543-G-C

23989189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716581-G-A

23989189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716581-G-T

http://identifiers.org/hco/14/GRCh38#23989218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716614-C-A

23989218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716614-C-T

23989222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716618-T-A

23989222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716618-T-C

23989222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716618-T-G

23989229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716625-C-T

23989312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716711-T-G

23989554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716882-G-T

23989700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717028-A-G

http://identifiers.org/hco/14/GRCh38#23989771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717085-A-C

23989885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717186-C-G

23990023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717320-C-T

http://identifiers.org/hco/14/GRCh38#23990037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717336-C-A

23990037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717336-C-G

23990063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717360-A-G

23990127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717426-G-C

23990130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717429-G-A

23990130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717429-G-C

23990130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717429-G-T

http://identifiers.org/hco/14/GRCh38#23990131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717430-A-C

23990141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717442-C-G

23990203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717504-G-A

23990203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717504-G-T

23990358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717659-T-C

23990358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717659-T-G

23990359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55717660-G-A

23990367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717668-G-A

23990367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717668-G-C

23990367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717668-G-T

23990378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717679-G-A

http://identifiers.org/hco/14/GRCh38#23990380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717681-C-A

23990380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717681-C-T

http://identifiers.org/hco/14/GRCh38#23990425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717732-C-A

23990425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717732-C-G

23990425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717732-C-T

http://identifiers.org/hco/14/GRCh38#23990508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718113-C-A

23990665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718222-G-A

23990665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718222-G-C

23990676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718233-T-G

23990806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718466-A-G

23990846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718520-A-T

http://identifiers.org/hco/14/GRCh38#23990882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718532-C-A

23990882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718532-C-T

23990896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718547-G-A

23990896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718547-G-C

23990896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718547-G-T

23990901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718552-G-A

23990948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718624-A-G

23990948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55718624-A-T

http://identifiers.org/hco/14/GRCh38#23991024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718682-C-A

23991057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718715-A-T

23991418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55719257-C-G

23992189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721280-G-C

23992208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721299-G-A

23992225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721316-G-A

23992361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721513-A-G

23992660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721766-C-G

23993230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722174-C-T

http://identifiers.org/hco/14/GRCh38#23993477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55722426-A-C

23993477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722426-A-G

23993916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722975-C-G

23994132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723167-A-G

http://identifiers.org/hco/14/GRCh38#23994222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55723243-A-C

http://identifiers.org/hco/14/GRCh38#23994226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55723247-A-C

23994271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723278-G-A

23994954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723496-G-A

23994962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723504-T-C

http://identifiers.org/hco/14/GRCh38#23995013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55723557-A-C

23995048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55723590-G-A

23995048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55723590-G-T

24000712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724436-A-G

24000712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724436-A-T

24000769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724468-A-G

24000799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724498-A-G

24000816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724508-C-G

24000816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724508-C-T

http://identifiers.org/hco/14/GRCh38#24000824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724516-C-A

http://identifiers.org/hco/14/GRCh38#24000952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724639-A-C

24001180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724837-A-T

24001231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724888-C-G

http://identifiers.org/hco/14/GRCh38#24001260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724911-C-A

24001260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724911-C-G

http://identifiers.org/hco/14/GRCh38#24001306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724958-A-C

24001306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724958-A-G

24001310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724962-C-T

24001504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725162-G-A

24001504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725162-G-C

http://identifiers.org/hco/14/GRCh38#24001543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725198-A-C

24001543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725198-A-G

24001546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725201-G-A

http://identifiers.org/hco/14/GRCh38#24001650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725290-C-A

http://identifiers.org/hco/14/GRCh38#24001673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725313-C-A

24001677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725317-C-G

24001717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725366-A-G

24001775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725424-G-A

24001833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725481-G-A

24001916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725542-G-A

24001938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725564-C-T

24004322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725602-C-G

24004322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725602-C-T

24004613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725850-G-A

24004613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725850-G-T

24004762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725937-G-A

http://identifiers.org/hco/14/GRCh38#24004798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55725974-C-A

24004824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725996-G-A

http://identifiers.org/hco/14/GRCh38#24004893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726065-A-C

24004917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726089-T-C

24005022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726220-C-T

24005228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726392-T-C

24005455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726565-C-T

24005525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726637-C-T

24005737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726830-A-G

24005813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727202-C-T

24005823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727212-C-T

24005859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727252-T-C

24005910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727300-T-G

24005973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727363-G-A

24005973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727363-G-T

24005993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727383-G-A

24005993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727383-G-T

24006034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727426-C-T

24006071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727455-G-A

24006071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727455-G-C

http://identifiers.org/hco/14/GRCh38#24006114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727498-C-A

24006205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727586-G-A

24006205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727586-G-T

http://identifiers.org/hco/14/GRCh38#24006352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727746-A-C

24006352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727746-A-T

24006387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55727781-G-C

24006432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727823-T-G

24006434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727825-G-A

24006465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727851-T-G

24006482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727869-G-T

http://identifiers.org/hco/14/GRCh38#24006566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727967-A-C

24006609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728050-G-A

24006626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728094-A-G

24006843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728317-C-G

24006843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728317-C-T

24007356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55728825-C-G

24033279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55712633-G-A

24034175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713001-C-T

24034473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713217-T-G

24034501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713246-A-G

24034651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713335-G-A

http://identifiers.org/hco/14/GRCh38#24034672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713347-A-C

http://identifiers.org/hco/14/GRCh38#24034677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55713352-A-C

24034680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713355-G-A

24035071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713683-A-G

24035083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713695-T-C

24035136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713733-C-G

24035136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713733-C-T

24035145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713742-G-T

24035170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55713770-A-G

24035264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714177-T-A

http://identifiers.org/hco/14/GRCh38#24035356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55714270-A-C

24035666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714581-G-A

24035764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714662-G-A

24035825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714725-T-C

24035833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55714733-A-T

24035941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55715040-G-A

24036140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716000-C-G

24036140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716000-C-T

24036282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716147-G-A

24036387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716219-G-A

24036387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716219-G-T

24036392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716224-A-G

24036398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716252-G-A

24036398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716252-G-C

24036398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716252-G-T

24036418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716284-G-C

24036418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55716284-G-T

24036527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716389-C-G

24036527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716389-C-T

24036593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716455-A-G

24036606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716468-C-G

24036606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716468-C-T

24036742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716581-G-A

24036742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716581-G-T

http://identifiers.org/hco/14/GRCh38#24036771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716614-C-A

24036771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716614-C-T

http://identifiers.org/hco/14/GRCh38#24036775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55716618-C-A

24036775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716618-C-G

24036775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716618-C-T

24036782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716625-C-G

24036833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55716675-C-T

24037166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55716926-G-A

24037309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717053-A-G

http://identifiers.org/hco/14/GRCh38#24037603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717336-C-A

24037603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717336-C-T

24037625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717356-A-G

24037629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717360-G-A

24037629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717360-G-C

24037629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717360-G-T

24037692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717426-G-A

24037692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717426-G-C

24037692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717426-G-T

24037695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55717429-C-G

24037706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717442-C-T

24037764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717504-G-A

24037764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717504-G-C

24037767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717507-T-C

24037919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717659-C-T

24037920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717660-A-G

24037939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717679-G-A

24037939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717679-G-C

http://identifiers.org/hco/14/GRCh38#24037941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717681-C-A

24038005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55717751-T-C

24038012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717758-G-A

24038012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717758-G-T

http://identifiers.org/hco/14/GRCh38#24038015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55717761-C-A

24038031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55717823-A-G

http://identifiers.org/hco/14/GRCh38#24038140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718113-C-A

24038140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718113-C-T

24038190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718163-T-C

24038297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718222-G-A

24038297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718222-G-T

24038308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718233-T-G

http://identifiers.org/hco/14/GRCh38#24038438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718466-A-C

http://identifiers.org/hco/14/GRCh38#24038478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718520-A-C

24038514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55718532-C-G

24038514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55718532-C-T

http://identifiers.org/hco/14/GRCh38#24038656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55718682-C-A

24038656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718682-C-T

24038689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718715-A-G

24038831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718854-G-A

24038933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55719162-A-T

http://identifiers.org/hco/14/GRCh38#24039048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55719257-A-C

24039862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721299-A-G

24039879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721316-G-T

24040015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721513-A-G

24040120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721614-T-C

24040574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721907-C-T

24040883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722174-C-T

24041085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722390-G-A

24041122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722426-G-A

24041122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55722426-G-C

http://identifiers.org/hco/14/GRCh38#24041561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55722975-C-A

24042610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723496-G-A

24042655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723543-C-T

24042669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55723557-A-T

24042704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55723590-G-A

24047821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724255-C-G

24047901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724327-G-A

http://identifiers.org/hco/14/GRCh38#24047933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724355-A-C

24047976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724397-A-G

http://identifiers.org/hco/14/GRCh38#24047998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724423-C-A

24048011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724436-G-A

24048011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724436-G-C

24048011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724436-G-T

24048061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724465-G-A

24048061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724465-G-C

http://identifiers.org/hco/14/GRCh38#24048094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724498-A-C

24048094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724498-A-G

24048100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724508-A-G

http://identifiers.org/hco/14/GRCh38#24048245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724639-A-C

24048473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724837-A-G

http://identifiers.org/hco/14/GRCh38#24048524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724888-C-A

24048524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724888-C-T

24048554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724911-A-G

24048599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724958-A-G

http://identifiers.org/hco/14/GRCh38#24048603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55724962-C-A

24048603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55724962-C-T

24048798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725162-G-A

24048798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725162-G-C

24048799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55725163-C-T

24048834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725198-C-T

24048944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725290-C-T

24049069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725424-G-A

24049161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55725515-G-A

24049210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725542-G-A

24049210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725542-G-T

24049232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725564-T-C

24049237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725569-C-T

24049270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725602-C-T

24049561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725850-G-A

24049746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725974-C-T

24049772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55725996-G-C

24049841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726065-A-G

24049999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726216-A-G

http://identifiers.org/hco/14/GRCh38#24050060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55726259-C-A

24050428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726565-C-T

24050444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726579-C-G

24050658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55726782-G-A

24050781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727202-T-C

http://identifiers.org/hco/14/GRCh38#24050827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727252-C-A

24050827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727252-C-G

24050827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727252-C-T

24050941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727363-G-A

24050941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727363-G-C

24050961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727383-G-A

http://identifiers.org/hco/14/GRCh38#24051002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727426-C-A

http://identifiers.org/hco/14/GRCh38#24051045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727461-C-A

http://identifiers.org/hco/14/GRCh38#24051082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727498-C-A

24051173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727586-G-A

24051173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727586-G-T

http://identifiers.org/hco/14/GRCh38#24051321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727746-A-C

24051321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727746-A-G

24051356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727781-G-A

24051356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55727781-G-T

24051396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727823-G-A

24051396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727823-G-T

24051398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727825-G-A

24051398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727825-G-T

24051429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727851-G-A

24051429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727851-G-T

24051446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727869-G-A

24051479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727904-T-A

24051479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727904-T-C

24051494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727919-G-A

24051494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727919-G-C

24051494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727919-G-T

http://identifiers.org/hco/14/GRCh38#24051526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55727963-A-C

24051526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727963-A-G

24051526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55727963-A-T

24051589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728094-G-A

24051641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728129-A-T

24051646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728134-G-C

24051795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728317-G-A

24051847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55728372-G-C

http://identifiers.org/hco/14/GRCh38#24052105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728637-C-A

24052105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728637-C-T

24052107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728639-G-T

http://identifiers.org/hco/14/GRCh38#24052240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728785-C-A

24052240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728785-C-G

http://identifiers.org/hco/14/GRCh38#24052284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728825-C-A