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Variant Information

Gene Interpretation
BRAF chr7:140481402 chr7:140781602 c.1406G>C p.G469A Pathogenic
BRAF chr7:140453136 chr7:140753336 c.1799T>A p.V600E Pathogenic
BRAF chr7:140453134 chr7:140753334 c.1801A>G p.K601E Pathogenic