Variant #0000608435 (NC_000003.11:g.184071129C>T, NM_004366.5:c.1937G>A (CLCN2))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.184071129C>T |
| DNA change (hg38) |
g.184353341C>T |
| Published as |
CLCN2(NM_001171087.2):c.1886G>A (p.(Arg629Gln)), CLCN2(NM_004366.5):c.1937G>A (p.R646Q), CLCN2(NM_004366.6):c.1937G>A (p.R646Q) |
| ISCN |
- |
| DB-ID |
FAM131A_000019 See all 3 reported entries |
| 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) |
0.0004 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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