Variant #0000976212 (NC_000004.11:g.170618496C>T, NM_001829.3:c.1174C>T (CLCN3))
| Chromosome |
4 |
| 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.170618496C>T |
| DNA change (hg38) |
g.169697345C>T |
| Published as |
CLCN3(NM_001829.4):c.1174C>T (p.(Pro392Ser)) |
| ISCN |
- |
| DB-ID |
CLCN3_000005 |
| 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 |
2024-04-19 20:27:30 +02:00 (CEST) |
| Date last edited |
2025-10-31 18:58:02 +01:00 (CET) |

Variant on transcripts
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