ClinVar Miner

List of variants in gene MUTYH reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 59
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
NM_001048171.1(MUTYH):c.1095G>A (p.Gln365=) rs886046366
NM_001048171.1(MUTYH):c.1105del (p.Ala371fs) rs587778536
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1149G>T (p.Leu383=) rs201412035
NM_001048171.1(MUTYH):c.1213G>A (p.Ala405Thr) rs587780744
NM_001048171.1(MUTYH):c.1434+2C>T rs140288388
NM_001048171.1(MUTYH):c.1435-11T>G rs868701952
NM_001048171.1(MUTYH):c.1452G>C (p.Gln484His) rs587782794
NM_001048171.1(MUTYH):c.1477-5C>A rs886046365
NM_001048171.1(MUTYH):c.1506G>A (p.Pro502=) rs143796254
NM_001048171.1(MUTYH):c.158-8C>T rs760321509
NM_001048171.1(MUTYH):c.170A>G (p.Gln57Arg) rs767237971
NM_001048171.1(MUTYH):c.247C>T (p.Arg83Ter) rs138775799
NM_001048171.1(MUTYH):c.267G>A (p.Trp89Ter) rs748170941
NM_001048171.1(MUTYH):c.306+11G>A rs139977567
NM_001048171.1(MUTYH):c.347-13C>G rs201207780
NM_001048171.1(MUTYH):c.347-4C>G rs767717597
NM_001048171.1(MUTYH):c.347-7C>A rs863224698
NM_001048171.1(MUTYH):c.37-14T>A rs587781284
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.534G>A (p.Lys178=) rs876660092
NM_001048171.1(MUTYH):c.637G>A (p.Ala213Thr) rs369854269
NM_001048171.1(MUTYH):c.771C>T (p.Asp257=) rs730881838
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048171.1(MUTYH):c.97C>T (p.Gln33Ter) rs886046367
NM_001048174.2(MUTYH):c.1103-2A>G rs587781628
NM_001048174.2(MUTYH):c.1143_1144dup (p.Glu382fs) rs587780078
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met) rs144079536
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys) rs150792276
NM_001048174.2(MUTYH):c.11C>T (p.Pro4Leu) rs79777494
NM_001048174.2(MUTYH):c.1225C>T (p.Arg409Trp) rs587778540
NM_001048174.2(MUTYH):c.1226G>A (p.Arg409Gln) rs587782120
NM_001048174.2(MUTYH):c.1333G>A (p.Ala445Thr) rs192816572
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=) rs74318065
NM_001048174.2(MUTYH):c.1350GGA[1] (p.Glu452del) rs587778541
NM_001048174.2(MUTYH):c.1354G>T (p.Glu452Ter) rs121908381
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu) rs3219494
NM_001048174.2(MUTYH):c.167A>G (p.Tyr56Cys) rs200747973
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=) rs121908380
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys) rs34612342
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val) rs200872702
NM_001048174.2(MUTYH):c.637C>T (p.Arg213Trp) rs34126013
NM_001048174.2(MUTYH):c.652G>T (p.Val218Phe) rs587780749
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.848G>A (p.Arg283Lys) rs149342980
NM_001048174.2(MUTYH):c.850-2A>G rs77542170
NM_001048174.2(MUTYH):c.930G>C (p.Gln310His) rs3219489
NM_001293192.1(MUTYH):c.-3del rs786203213
NM_012222.2(MUTYH):c.*34_*36GTT[1] rs373507005
NM_012222.2(MUTYH):c.1205C>T (p.Pro402Leu) rs529008617
NM_012222.2(MUTYH):c.1440C>T (p.Thr480=) rs150269172
NM_012222.2(MUTYH):c.1535C>T (p.Ser512Phe) rs140118273
NM_012222.2(MUTYH):c.1576C>A (p.Leu526Met) rs3219496
NM_012222.2(MUTYH):c.1592G>A (p.Arg531Gln) rs3219497
NM_012222.2(MUTYH):c.496-4A>G rs201678305
NM_012222.2(MUTYH):c.64G>A (p.Val22Met) rs3219484

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