List of variants reported as uncertain significance for Familial adenomatous polyposis 2 by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys)	rs150792276	0.00081
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu)	rs3219494	0.00076
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys)	rs138089183	0.00051
NM_000465.4(BARD1):c.2116A>G (p.Lys706Glu)	rs149262370	0.00009
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val)	rs200872702	0.00009
NM_001048174.2(MUTYH):c.836G>A (p.Arg279Gln)	rs140156029	0.00009
NM_001048174.2(MUTYH):c.1400G>A (p.Arg467His)	rs144111588	0.00008
NM_001048174.2(MUTYH):c.1399C>T (p.Arg467Cys)	rs587781668	0.00003
NM_001048174.2(MUTYH):c.991C>A (p.Pro331Thr)	rs587782773	0.00003
NM_001048174.2(MUTYH):c.683C>T (p.Thr228Ile)	rs766173546	0.00001
NM_001048174.2(MUTYH):c.761C>T (p.Ala254Val)	rs587782764	0.00001
NM_001048174.2(MUTYH):c.1058G>C (p.Gly353Ala)
NM_001048174.2(MUTYH):c.1489G>A (p.Gly497Ser)	rs2149088733
NM_001048174.2(MUTYH):c.1490G>A (p.Gly497Asp)
NM_001048174.2(MUTYH):c.308G>A (p.Trp103Ter)
NM_001048174.2(MUTYH):c.953C>G (p.Ser318Trp)	rs587778538

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