Variant #0000623000 (NC_000012.11:g.971317A>G, NM_018979.3:c.2020A>G (WNK1))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.971317A>G |
| DNA change (hg38) |
g.862151A>G |
| Published as |
WNK1(NM_001184985.1):c.2020A>G (p.T674A), WNK1(NM_001184985.2):c.2020A>G (p.T674A) |
| ISCN |
- |
| DB-ID |
WNK1_000105 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) |
0.00227 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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