Variant · Snv
BAG1 NM_004323.6(BAG1):c.910A>G (p.Ser304Gly)
CI-VAR-00127069Explore in graph →p.Ser304GlyNM_004323.6:c.910A>GClinVar 785282 rs114225550
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 |
|---|---|---|---|---|---|---|---|---|
| 785282 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Lung cancer; Clear cell carcinoma of kidney; Thymoma; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Cervical cancer | germline | 3 | May 18, 2018 | clinvar |