Variant · Snv
NDUFAF6 NM_152416.4(NDUFAF6):c.715-3C>A
CI-VAR-00049713Explore in graph →NM_152416.4:c.715-3C>AClinVar 284262 rs200620409
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 284262 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Leigh syndrome; Inborn genetic diseases; Mitochondrial complex I deficiency, nuclear type 17; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Cervical cancer; Familial cancer of breast; Ovarian cancer; Clear cell carcinoma of kidney; Sarcoma | germline | 8 | Mar 01, 2026 | clinvar |