List of variants in gene BRAF reported as pathogenic for Melanoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1574T>C (p.Leu525Pro)	rs869025340
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004333.6(BRAF):c.1914T>G (p.Asp638Glu)	rs180177042

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