List of variants reported as likely benign for Noonan syndrome 5

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1755A>G (p.Val585=)	rs3730296	0.02125
NM_002880.4(RAF1):c.1941C>T (p.Val647=)	rs3730297	0.00729
NM_002880.4(RAF1):c.923C>T (p.Pro308Leu)	rs5746220	0.00523
NM_002880.4(RAF1):c.*495C>T	rs12808	0.00354
NM_002880.4(RAF1):c.*160C>T	rs5746246	0.00295
NM_002880.4(RAF1):c.*110T>C	rs550188508	0.00111
NM_002880.4(RAF1):c.321-14T>A	rs3730270	0.00057
NM_002880.4(RAF1):c.1914G>A (p.Thr638=)	rs144876026	0.00034
NM_002880.4(RAF1):c.*404G>A	rs150460686	0.00023
NM_002880.4(RAF1):c.119G>A (p.Arg40His)	rs192632236	0.00015
NM_002880.4(RAF1):c.*556G>A	rs187286358	0.00014
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys)	rs370242565	0.00013
NM_002880.4(RAF1):c.834+598G>A	rs375404697	0.00009
NM_002880.4(RAF1):c.1150C>G (p.Pro384Ala)	rs140788943	0.00001
NM_002880.4(RAF1):c.*606A>G	rs556460176
NM_002880.4(RAF1):c.-267G>A	rs116247741
NM_002880.4(RAF1):c.1629G>C (p.Thr543=)	rs5746244

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