Variant · Snv
WRN NM_000553.6(WRN):c.95A>G (p.Lys32Arg)
CI-VAR-00021599Explore in graph →p.Lys32ArgNM_000553.6:c.95A>GClinVar 135423 rs34477820
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 135423 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Werner syndrome; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Cervical cancer; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Familial cancer of breast; Colon adenocarcinoma; Colorectal cancer; Gastric cancer; Ovarian serous cystadenocarcinoma | germline | 12 | Apr 01, 2026 | clinvar |