Variant · Snv
SMARCA4 G1162C
CI-VAR-00001582Explore in graph →CIViC 5362
Curated evidence
Evidence by cancer (1 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.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 33144586
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Unmapped disease1unmapped disease | ||||||||
| SMARCA4 G1162C | (functional) | Functional | D | Supports Loss Of Function | 4 | submitted | EID12726In a large retrospective study evaluating SMARCA4 variants from 131,668 solid tumor patients, 9434 patients were identified to have one or more SMARCA4 variants. The G1162 residue was noted to be a re… (full text at CIViC) PMID 33144586 · Fernando et al., 2020 · Open in CIViC | civic |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available