Variant · Snv
SMURF1 NM_181349.3(SMURF1):c.1128A>G (p.Glu376=)
CI-VAR-00306304Explore in graph →p.Glu376=NM_181349.3:c.1128A>GClinVar 2657718 rs141532197
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 |
|---|---|---|---|---|---|---|---|---|
| 2657718 | Likely benign | criteria provided, single submitter | 1 | Ovarian serous cystadenocarcinoma; Melanoma; Lung cancer; Familial cancer of breast; Colon adenocarcinoma; Thyroid cancer, nonmedullary, 1; Cervical cancer; Clear cell carcinoma of kidney; Uveal melanoma; Acute myeloid leukemia; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma | germline | 2 | Jul 01, 2022 | clinvar |