Variant · Snv
RAD51D NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)
CI-VAR-00023338Explore in graph →p.Arg266CysNM_002878.4:c.796C>TClinVar 141519 rs587781813
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 |
|---|---|---|---|---|---|---|---|---|
| 141519 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Hereditary cancer-predisposing syndrome; Breast-ovarian cancer, familial, susceptibility to, 4; Malignant tumor of breast; Hereditary site-specific ovarian cancer syndrome; Breast and/or ovarian cancer; RAD51D-related disorder; Hereditary breast ovarian cancer syndrome; Cancer or benign tumor | germline | 28 | Jun 09, 2026 | clinvar |