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BRAF V600E mutation

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDBIO-BRAF-V600E
TypeBiomarker
Aliases
BRAF V600EМутація BRAF V600E
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-AML DIS-CHOLANGIOCARCINOMA DIS-CLL DIS-CRC DIS-DLBCL-NOS DIS-GBM DIS-HCC DIS-HCL DIS-MELANOMA DIS-MM DIS-NSCLC DIS-OVARIAN DIS-PDAC DIS-THYROID-ANAPLASTIC DIS-THYROID-PAPILLARY
SourcesSRC-NCCN-BCELL-2025

Biomarker Facts

Biomarker typegene_mutation
Mutation details{"functional_impact": "activating", "gene": "BRAF", "hgvs_protein": "p.V600E", "variant_type": "missense"}
Measurement
MethodPCR / sequencing on bone marrow or peripheral blood (HCL); FFPE tumor (melanoma)
Unitscategorical (positive | negative)
Actionability lookup{"gene": "BRAF", "variant": "V600E"}
Related biomarkersNone declared

Notes

Defining feature of HCL (~100%). Targetable with BRAF inhibitors (vemurafenib, dabrafenib) — useful in relapsed/refractory HCL when cladribine fails. Also relevant in melanoma, some thyroid, colorectal cancers (different therapeutic context).

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