ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 19
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HGVS dbSNP
NM_001048174.2(MUTYH):c.1031C>T (p.Ser344Phe) rs763862261
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys) rs150792276
NM_001048174.2(MUTYH):c.1225C>T (p.Arg409Trp) rs587778540
NM_001048174.2(MUTYH):c.1333G>A (p.Ala445Thr) rs192816572
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu) rs3219494
NM_001048174.2(MUTYH):c.203T>A (p.Phe68Tyr) rs750954949
NM_001048174.2(MUTYH):c.206G>A (p.Arg69Gln) rs755653922
NM_001048174.2(MUTYH):c.229G>A (p.Asp77Asn) rs587780746
NM_001048174.2(MUTYH):c.466C>T (p.Arg156Trp) rs779997419
NM_001048174.2(MUTYH):c.524G>C (p.Arg175Pro) rs538383136
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val) rs200872702
NM_001048174.2(MUTYH):c.610A>G (p.Thr204Ala) rs587782351
NM_001048174.2(MUTYH):c.616G>A (p.Val206Met) rs200165598
NM_001048174.2(MUTYH):c.737G>A (p.Arg246Gln) rs149866955
NM_001048174.2(MUTYH):c.827G>A (p.Ser276Asn) rs1553127574
NM_001048174.2(MUTYH):c.850-2A>G rs77542170
NM_001048174.2(MUTYH):c.901G>T (p.Val301Leu) rs147718169
NM_001048174.2(MUTYH):c.954G>A (p.Ser318=) rs372673338
NM_012222.2(MUTYH):c.157+2_157+3dup rs1553131287

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