vabase

BRAF V600E

c.1799T>ANM_004333.67-140753336-A-T
RAS-MAPK gain of function transversion Cancer hotspot ClinVar: Conflicting classifications of pathogenicity AlphaMissense: likely pathogenic LMGLAKLACCLA

Reports 4 in LM · GLA · KLA · CCLA

ISSVA entityAllele fractionSources
LM 0.1-3.6% (ddPCR; Zenner Table 1)
GLA 0.2-8%
KLA 0.2-2.2%
CCLA Li 2023: 0.91% (CLA060); Fox 2025: 2.2-2.6% (Patient 1)

Bars show the reported allele-fraction range on a 0 to 50 percent axis.

Position in BRAF 1 catalogued variant in this gene

RBD (155–227)RBDProtein kinase (457–717)Protein kina…1766 aaV600E

Pathway and targeted therapy

Variant in the RAS-MAPK pathway. Repurposed drugs already used in the clinic for this pathway: trametinib and other MEK inhibitors.

Open and recent trials (3 in vascular / lymphatic anomalies for trametinib)

Primary sources 3

  1. Expansion of the Phenotype of Lymphatic Anomalies Caused by Somatic Activating BRAF Variant.
    Fox MD, Kumar S, Britt AD, Srinivasan AS, Surrey LF, Vatsky SE, Borst AJ, Hakonarson H, Li D, Sheppard SE, Snyder KM, Adams DM. · Pediatr Blood Cancer · 2025
  2. Genomic profiling informs diagnoses and treatment in vascular anomalies.
    Li D, Sheppard SE, March ME, Battig MR, Surrey LF, Srinivasan AS, Matsuoka LS, Tian L, Wang F, Seiler C, Dayneka J, Borst AJ, Matos MC, Paulissen SM, Krishnamurthy G, Nriagu B, Sikder T, Casey M, Williams L, Rangu S, O'Connor N, Thomas A, Pinto E, Hou C, Nguyen K, Pellegrino da Silva R, Chehimi SN, Kao C, Biroc L, Britt AD, Queenan M, Reid JR, Napoli JA, Low DM, Vatsky S, Treat J, Smith CL, Cahill AM, Snyder KM, Adams DM, Dori Y, Hakonarson H. · Nat Med · 2023
  3. Somatic activating BRAF variants cause isolated lymphatic malformations.
    Zenner K, Jensen DM, Dmyterko V, Shivaram GM, Myers CT, Paschal CR, Rudzinski ER, Pham MM, Cheng VC, Manning SC, Bly RA, Ganti S, Perkins JA, Bennett JT. · HGG Adv · 2022

Mentioned in 30,966 publications indexed by Europe PMC.

Annotations refreshed 2026-10-09 from Europe PMC, ClinVar, ClinicalTrials.gov, gnomAD, and Genome Nexus. Coordinates handled per assembly (gnomAD GRCh38, Genome Nexus GRCh37).