Variant · Snv
BRWD3 NM_153252.5(BRWD3):c.3865-293G>C
CI-VAR-00199581Explore in graph →NM_153252.5:c.3865-293G>CClinVar 1247577 rs73225394
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 |
|---|---|---|---|---|---|---|---|---|
| 1247577 | Benign | criteria provided, single submitter | 1 | Uterine corpus endometrial carcinoma; Familial pancreatic carcinoma; Cervical cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Nonpapillary renal cell carcinoma | germline | 2 | Oct 09, 2018 | clinvar |