List of variants in gene BRAF reported as uncertain significance for Cardiofaciocutaneous syndrome 1

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.437G>A (p.Arg146Gln)	rs557241012	0.00001
NM_004333.6(BRAF):c.1146G>C (p.Leu382Phe)	rs1801519948
NM_004333.6(BRAF):c.1382A>G (p.Gln461Arg)	rs1554399925
NM_004333.6(BRAF):c.160A>G (p.Ile54Val)
NM_004333.6(BRAF):c.1820C>T (p.Ser607Phe)	rs1255101216
NM_004333.6(BRAF):c.67A>G (p.Met23Val)	rs1818671266
NM_004333.6(BRAF):c.712-221T>C	rs1803141356
NM_004333.6(BRAF):c.789_790del (p.Cys264fs)	rs1803104915

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