List of variants in gene BRAF reported as likely pathogenic for RASopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1388_1408dup (p.Ile463_Gly469dup)	rs1562956929
NM_004333.6(BRAF):c.1454T>C (p.Leu485Ser)	rs397507475
NM_004333.6(BRAF):c.1495A>G (p.Lys499Glu)	rs180177037
NM_004333.6(BRAF):c.1505_1507dup (p.Val502dup)	rs1562955153
NM_004333.6(BRAF):c.1595G>A (p.Cys532Tyr)	rs397507479
NM_004333.6(BRAF):c.1695T>A (p.Asp565Glu)
NM_004333.6(BRAF):c.1699T>G (p.Leu567Val)
NM_004333.6(BRAF):c.1786G>T (p.Gly596Cys)	rs121913361
NM_004333.6(BRAF):c.1802A>T (p.Lys601Ile)	rs397507484
NM_004333.6(BRAF):c.722C>A (p.Thr241Lys)	rs387906660
NM_004333.6(BRAF):c.735A>T (p.Leu245Phe)	rs397507466
NM_004333.6(BRAF):c.739T>G (p.Phe247Val)	rs397516903
NM_004333.6(BRAF):c.740T>C (p.Phe247Ser)	rs397507467
NM_004333.6(BRAF):c.784C>A (p.Gln262Lys)	rs397507470
NM_004333.6(BRAF):c.785A>G (p.Gln262Arg)	rs397516904
NM_004333.6(BRAF):c.793G>C (p.Gly265Arg)	rs397516905

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