Variant · Snv
BRD9 NM_023924.5(BRD9):c.816G>A (p.Pro272=)
CI-VAR-00127489Explore in graph →p.Pro272=NM_023924.5:c.816G>AClinVar 708816 rs74984870
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 |
|---|---|---|---|---|---|---|---|---|
| 708816 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Cholangiocarcinoma; Ovarian serous cystadenocarcinoma; Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Clear cell carcinoma of kidney; Thyroid cancer, nonmedullary, 1; Lung cancer | germline | 3 | Oct 19, 2017 | clinvar |