Variant · Snv
WDR83OS NM_016145.4(WDR83OS):c.14A>G (p.Asn5Ser)
CI-VAR-00285107Explore in graph →p.Asn5SerNM_016145.4:c.14A>GClinVar 2039517 rs117131055
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 |
|---|---|---|---|---|---|---|---|---|
| 2039517 | Benign | criteria provided, single submitter | 1 | Uterine corpus endometrial carcinoma; Thymoma; Melanoma; Nonpapillary renal cell carcinoma; Lung cancer; Cholangiocarcinoma; Acute myeloid leukemia; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Hepatocellular carcinoma; Malignant tumor of esophagus; Uveal melanoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Adrenocortical carcinoma, hereditary; Cervical cancer | germline | 2 | Feb 01, 2026 | clinvar |