Variant #0001074722 (NC_000023.10:g.49834690G>C, NC_000023.10(NM_001127898.3):c.315+5G>C (CLCN5))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.49834690G>C |
| DNA change (hg38) |
g.50070035G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CLCN5_000184 |
| Variant remarks |
effect on RNA studied using mini-gene splicing assay |
| Reference |
PubMed: Inoue 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2026-04-24 19:32:09 +02:00 (CEST) |
| Date last edited |
2026-04-24 19:33:35 +02:00 (CEST) |

Variant on transcripts
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