ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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Total variants: 30
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1351C>G (p.Pro451Ala) rs375597447
NM_001048171.1(MUTYH):c.1434+2C>T rs140288388
NM_001048171.1(MUTYH):c.1442G>A (p.Arg481His) rs144111588
NM_001048171.1(MUTYH):c.158-33G>A rs587781374
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.956-27G>A rs188830619
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys) rs150792276
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=) rs74318065
NM_001048174.2(MUTYH):c.206G>A (p.Arg69Gln) rs755653922
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.566G>A (p.Arg189His) rs147754007
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val) rs200872702
NM_001048174.2(MUTYH):c.737G>A (p.Arg246Gln) rs149866955
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys) rs138089183
NM_001048174.2(MUTYH):c.901G>A (p.Val301Met) rs147718169
NM_001128425.1(MUTYH):c.1186+1G>A rs587781337
NM_001128425.1(MUTYH):c.158-13C>T rs1316542179
NM_001128425.1(MUTYH):c.254A>G (p.His85Arg) rs558707786
NM_001128425.1(MUTYH):c.338G>A (p.Trp113Ter) rs888691362
NM_001128425.1(MUTYH):c.346C>T (p.Arg116Trp) rs373766973
NM_001128425.1(MUTYH):c.37G>A (p.Ala13Thr) rs375349172
NM_001128425.1(MUTYH):c.475C>A (p.Leu159Met) rs199862273
NM_001128425.1(MUTYH):c.548G>A (p.Gly183Asp) rs587781864
NM_001128425.1(MUTYH):c.718G>A (p.Ala240Thr) rs774237159
NM_001128425.1(MUTYH):c.791G>T (p.Gly264Val) rs1570404090
NM_012222.2(MUTYH):c.1106C>G (p.Ser369Cys) rs763862261
NM_012222.2(MUTYH):c.129C>T (p.Asn43=) rs141679570
NM_012222.2(MUTYH):c.496-4A>G rs201678305
NM_012222.2(MUTYH):c.724C>T (p.Arg242Cys) rs200495564
NM_012222.2(MUTYH):c.881G>T (p.Cys294Phe) rs879254257

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