Variant · Snv
BAG3 NM_004281.4(BAG3):c.463G>A (p.Ala155Thr)
CI-VAR-00008575Explore in graph →p.Ala155ThrNM_004281.4:c.463G>AClinVar 44784 rs61756328
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 |
|---|---|---|---|---|---|---|---|---|
| 44784 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Cardiovascular phenotype; Dilated cardiomyopathy 1HH; Myofibrillar myopathy 6; Hypertrophic cardiomyopathy; Cardiomyopathy; Clear cell carcinoma of kidney; Gastric cancer; Uterine carcinosarcoma; Nonpapillary renal cell carcinoma; Sarcoma; Ovarian serous cystadenocarcinoma; Lung cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma | germline | 16 | Jun 01, 2026 | clinvar |