Variant · Snv
FXN NM_000144.5(FXN):c.226A>G (p.Met76Val)
CI-VAR-00047882Explore in graph →p.Met76ValNM_000144.5:c.226A>GClinVar 263542 rs59907886
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 |
|---|---|---|---|---|---|---|---|---|
| 263542 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Sarcoma; Uterine carcinosarcoma; Hepatocellular carcinoma; Malignant tumor of esophagus; Cervical cancer | germline | 7 | Oct 22, 2025 | clinvar |