List of variants reported as likely pathogenic for Noonan syndrome 7

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Total variants: 5

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HGVS	dbSNP
NM_004333.6(BRAF):c.1387A>G (p.Ile463Val)	rs1562957000
NM_004333.6(BRAF):c.1743T>A (p.Asn581Lys)	rs397516895
NM_004333.6(BRAF):c.1914T>A (p.Asp638Glu)	rs180177042
NM_004333.6(BRAF):c.722C>T (p.Thr241Met)	rs387906660
NM_004333.6(BRAF):c.735A>C (p.Leu245Phe)	rs397507466

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