Variant · Snv
WNK1 NM_018979.4(WNK1):c.5325C>T (p.Ser1775=)
CI-VAR-00181488Explore in graph →p.Ser1775=NM_018979.4:c.5325C>TClinVar 1057218 rs373370309
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1057218 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Pseudohypoaldosteronism type 2C; Neuropathy, hereditary sensory and autonomic, type 2A; Ovarian serous cystadenocarcinoma | germline | 4 | Nov 09, 2025 | clinvar |