List of variants studied for Noonan syndrome by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.392A>G (p.Lys131Arg)	rs397516805	0.00006
NM_005633.4(SOS1):c.3392G>A (p.Arg1131Lys)	rs768113420	0.00004
NM_002834.5(PTPN11):c.1403C>T (p.Thr468Met)	rs121918457	0.00001
NM_144670.6(A2ML1):c.3397A>C (p.Asn1133His)	rs1466413438	0.00001
NM_002834.5(PTPN11):c.1472C>T (p.Pro491Leu)	rs397507540
NM_002834.5(PTPN11):c.172A>C (p.Asn58His)	rs397507505
NM_002834.5(PTPN11):c.209A>G (p.Lys70Arg)	rs397516801
NM_002834.5(PTPN11):c.215C>G (p.Ala72Gly)	rs121918454
NM_002834.5(PTPN11):c.236A>G (p.Gln79Arg)	rs121918466
NM_002834.5(PTPN11):c.317A>C (p.Asp106Ala)	rs397507517
NM_002834.5(PTPN11):c.923A>G (p.Asn308Ser)	rs121918455
NM_004333.6(BRAF):c.1205C>G (p.Pro402Arg)	rs199927105
NM_004333.6(BRAF):c.736G>C (p.Ala246Pro)	rs180177034
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_006912.6(RIT1):c.233G>A (p.Gly78Glu)	rs1557960268
NM_006912.6(RIT1):c.284G>C (p.Gly95Ala)	rs672601335

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