List of variants reported as likely pathogenic for Noonan syndrome 7

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.722C>T (p.Thr241Met)	rs387906660	0.00001
NM_004333.6(BRAF):c.1387A>G (p.Ile463Val)	rs1562957000
NM_004333.6(BRAF):c.1397G>A (p.Gly466Glu)	rs121913351
NM_004333.6(BRAF):c.1454T>C (p.Leu485Ser)	rs397507475
NM_004333.6(BRAF):c.1743T>A (p.Asn581Lys)	rs397516895
NM_004333.6(BRAF):c.1802A>T (p.Lys601Ile)	rs397507484
NM_004333.6(BRAF):c.1914T>A (p.Asp638Glu)	rs180177042
NM_004333.6(BRAF):c.2135C>A (p.Ala712Asp)	rs727502904
NM_004333.6(BRAF):c.735A>C (p.Leu245Phe)	rs397507466
NM_004333.6(BRAF):c.823G>A (p.Glu275Lys)	rs2129044284

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