Variant · Snv
BRAF G468A
CI-VAR-00001748Explore in graph →CIViC 3441
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.
civicProvenance
- 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
- 15035987
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Neoplasm1 | ||||||||
| BRAF G468A | (oncogenic) | Oncogenic | D | Supports Oncogenicity | 3 | submitted | EID9558By expressing B-RAF G468A protein in COS cells and measuring its direct MEK phosphorylation activity, these experiments showed that B-RAF G468A had a basal kinase activity 266 times higher than that o… (full text at CIViC) PMID 15035987 · Wan et al., 2004 · 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
No ClinVar interpretation attached to this variant.