List of variants reported as likely pathogenic for Noonan syndrome by Database of Curated Mutations (DoCM)

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1472C>T (p.Thr491Ile)	rs80338799
NM_002880.4(RAF1):c.1837C>G (p.Leu613Val)	rs80338797
NM_002880.4(RAF1):c.770C>T (p.Ser257Leu)	rs80338796
NM_002880.4(RAF1):c.776C>T (p.Ser259Phe)	rs397516827
NM_002880.4(RAF1):c.781C>G (p.Pro261Ala)	rs121434594
NM_002880.4(RAF1):c.781C>T (p.Pro261Ser)	rs121434594
NM_002880.4(RAF1):c.782C>T (p.Pro261Leu)	rs397516828
NM_002880.4(RAF1):c.788T>C (p.Val263Ala)	rs397516830

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