Variant · Snv
BAG3 NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)
CI-VAR-00008574Explore in graph →p.Arg71GlnNM_004281.4:c.212G>AClinVar 44780 rs35434411
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 |
|---|---|---|---|---|---|---|---|---|
| 44780 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Myofibrillar myopathy 6; Dilated cardiomyopathy 1HH; Cardiovascular phenotype; Cardiomyopathy; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Uveal melanoma; Uterine carcinosarcoma; Thymoma; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Melanoma; Malignant tumor of esophagus | germline | 21 | Feb 04, 2026 | clinvar |