Variant · Snv
NDUFV3 NM_021075.4(NDUFV3):c.168A>C (p.Lys56Asn)
CI-VAR-00058689Explore in graph →p.Lys56AsnNM_021075.4:c.168A>CClinVar 403223 rs141922962
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 |
|---|---|---|---|---|---|---|---|---|
| 403223 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | NDUFV3-related disorder; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Clear cell carcinoma of kidney; Sarcoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer; Cervical cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Gastric cancer; Thymoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary | germline | 5 | Aug 01, 2025 | clinvar |