Variant · Snv
FANCD2 NM_001018115.3(FANCD2):c.836C>T (p.Pro279Leu)
CI-VAR-00180149Explore in graph →p.Pro279LeuNM_001018115.3:c.836C>TClinVar 1057753 rs752880854
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 |
|---|---|---|---|---|---|---|---|---|
| 1057753 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Familial cancer of breast; Inborn genetic diseases; Fanconi anemia | germline | 3 | Jun 16, 2024 | clinvar |