Variant · Snv
RAD51B NM_133510.4(RAD51B):c.728A>G (p.Lys243Arg)
CI-VAR-00239578Explore in graph →p.Lys243ArgNM_133510.4:c.728A>GClinVar 1678952 rs34594234
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 |
|---|---|---|---|---|---|---|---|---|
| 1678952 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Hereditary breast ovarian cancer syndrome; Uveal melanoma; Colon adenocarcinoma; Sarcoma; Gastric cancer; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Cervical cancer; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Melanoma; Thymoma; Lung cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary | germline | 6 | Jun 06, 2025 | clinvar |