Variant · Snv
BRAF G464V
CI-VAR-00001740Explore in graph →NP_004324.2:p.Gly464ValNM_004333.4:c.1391G>TClinVar 40364 CIViC 1106 rs121913348
Curated evidence
Evidence by cancer (2 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
- 18519791
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Breast Neoplasm1 | ||||||||
| BRAF G464V | Sorafenib | Predictive | D | Supports Sensitivity Response | 1 | submitted | EID2811In an attempt to block both MAPK and PI3K/Akt pathways, two signaling inhibitors (sorafenib, a BRAF kinase inhibitor, and ceramide, an agent that dephosphorylates Akt) were used in cell culture and mo… (full text at CIViC) PMID 18519791 · Tran et al., 2008 · Open in CIViC | civic |
| Malignant Neoplasm1 | ||||||||
| BRAF G464V | Vemurafenib | Predictive | C | Does Not Support Sensitivity Response | 2 | accepted | EID5964The phase 2a MyPathway study assigned patients with HER2, EGFR, BRAF or SHH alterations to treatment with pertuzumab plus trastuzumab, erlotinib, vemurafenib, or vismodegib, respectively. Of 26 patien… (full text at CIViC) PMID 29320312 · | |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 40364 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | RASopathy; Non-small cell lung carcinoma; Noonan syndrome and Noonan-related syndrome; Cardiofaciocutaneous syndrome 1; Ovarian Sertoli-Leydig cell tumor | germline/somatic | 8 | Jul 16, 2023 | clinvar |