Variant · Snv
NDUFS4 NM_002495.4(NDUFS4):c.425-174G>A
CI-VAR-00122763Explore in graph →NM_002495.4:c.425-174G>AClinVar 669918 rs2290696
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 |
|---|---|---|---|---|---|---|---|---|
| 669918 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Familial cancer of breast; Malignant tumor of esophagus | germline | 3 | Jun 14, 2018 | clinvar |