Variant · Snv
NDUFS2 NM_001377299.1(NDUFS2):c.1354+5G>A
CI-VAR-00022478Explore in graph →NM_001377299.1:c.1354+5G>AClinVar 138487 rs190184430
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 |
|---|---|---|---|---|---|---|---|---|
| 138487 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Mitochondrial complex I deficiency, nuclear type 1; NDUFS2-related disorder; Optic atrophy; Uveal melanoma; Melanoma; Colorectal cancer; Gastric cancer; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Familial cancer of breast | germline | 9 | Sep 05, 2024 | clinvar |