Variant #0000334273 (NC_000023.10:g.54359884A>C, NM_020922.4:c.223T>G (WNK3))
| Chromosome |
X |
| 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.54359884A>C |
| DNA change (hg38) |
g.54333451A>C |
| Published as |
WNK3(NM_001002838.3):c.223T>G (p.(Ser75Ala)), WNK3(NM_020922.4):c.223T>G (p.S75A) |
| ISCN |
- |
| DB-ID |
WNK3_000033 See all 2 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) |
0.00046 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
|