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

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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.977T>C (p.Ile326Thr)	rs368435578	0.00003
NM_004333.6(BRAF):c.1205C>A (p.Pro402His)	rs199927105
NM_004333.6(BRAF):c.1205C>G (p.Pro402Arg)	rs199927105
NM_004333.6(BRAF):c.1409C>G (p.Thr470Arg)	rs397516891
NM_004333.6(BRAF):c.1455G>T (p.Leu485Phe)	rs180177036
NM_004333.6(BRAF):c.1502A>C (p.Glu501Ala)	rs180177039
NM_004333.6(BRAF):c.1699T>G (p.Leu567Val)
NM_004333.6(BRAF):c.1740T>C (p.Asn580=)
NM_004333.6(BRAF):c.1796C>T (p.Thr599Ile)	rs121913375
NM_004333.6(BRAF):c.2128-16_2128-15del	rs886062015
NM_004333.6(BRAF):c.2128-27_2128-16delinsTCT	rs886062016
NM_004333.6(BRAF):c.2128-28dup	rs60814637
NM_004333.6(BRAF):c.2128-4del	rs886062014
NM_004333.6(BRAF):c.2128-5dup	rs373442098
NM_004333.6(BRAF):c.2161T>G (p.Leu721Val)
NM_004333.6(BRAF):c.793G>C (p.Gly265Arg)	rs397516905

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