Variant · Snv
NQO1 NM_000903.3(NQO1):c.415C>T (p.Arg139Trp)
CI-VAR-00395783Explore in graph →p.Arg139TrpNM_000903.3:c.415C>TClinVar 4414689 rs1131341
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 |
|---|---|---|---|---|---|---|---|---|
| 4414689 | association | no assertion criteria provided | 0 | Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Adrenocortical carcinoma, hereditary; Colon adenocarcinoma; Sarcoma; Malignant tumor of esophagus; Cervical cancer; Uveal melanoma; Gastric cancer | germline | 2 | Mar 26, 2026 | clinvar |