Variant #0001064847 (NC_000007.13:g.143047558A>G, NM_000083.2:c.2497A>G (CLCN1))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.143047558A>G |
| DNA change (hg38) |
- |
| Published as |
CLCN1(NM_000083.3):c.2497A>G (p.(Thr833Ala)) |
| ISCN |
- |
| DB-ID |
CLCN1_000397 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2026-01-20 18:57:21 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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