ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by GeneDx

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Total variants: 99
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1213G>A (p.Ala405Thr) rs587780744
NM_001048171.1(MUTYH):c.1259C>T (p.Thr420Met) rs587780084
NM_001048171.1(MUTYH):c.1261C>T (p.His421Tyr) rs141432759
NM_001048171.1(MUTYH):c.1351C>G (p.Pro451Ala) rs375597447
NM_001048171.1(MUTYH):c.1363G>A (p.Val455Ile) rs779701238
NM_001048171.1(MUTYH):c.1378C>T (p.Arg460Cys) rs200229669
NM_001048171.1(MUTYH):c.1423G>A (p.Ala475Thr) rs587782263
NM_001048171.1(MUTYH):c.1442G>A (p.Arg481His) rs144111588
NM_001048171.1(MUTYH):c.1514G>A (p.Arg505Gln) rs369410616
NM_001048171.1(MUTYH):c.1528A>T (p.Met510Leu) rs587780080
NM_001048171.1(MUTYH):c.158-33G>A rs587781374
NM_001048171.1(MUTYH):c.170A>G (p.Gln57Arg) rs767237971
NM_001048171.1(MUTYH):c.347-7C>A rs863224698
NM_001048171.1(MUTYH):c.38C>T (p.Ala13Val) rs587780747
NM_001048171.1(MUTYH):c.509G>A (p.Arg170Gln) rs758567247
NM_001048171.1(MUTYH):c.530G>A (p.Arg177Gln) rs369677603
NM_001048171.1(MUTYH):c.565C>T (p.Arg189Cys) rs587780748
NM_001048171.1(MUTYH):c.637G>A (p.Ala213Thr) rs369854269
NM_001048171.1(MUTYH):c.838C>T (p.Arg280Cys) rs199840380
NM_001048171.1(MUTYH):c.929C>T (p.Ser310Leu) rs558173961
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.1205C>T (p.Pro402Leu) rs587780079
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.1424G>A (p.Gly475Glu) rs3219494
NM_001048174.2(MUTYH):c.1463C>T (p.Pro488Leu) rs587778542
NM_001048174.2(MUTYH):c.14G>A (p.Arg5Gln) rs587780081
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.397G>C (p.Asp133His) rs564930066
NM_001048174.2(MUTYH):c.466C>T (p.Arg156Trp) rs779997419
NM_001048174.2(MUTYH):c.504G>C (p.Glu168Asp) rs587781645
NM_001048174.2(MUTYH):c.524G>C (p.Arg175Pro) rs538383136
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.616G>A (p.Val206Met) rs200165598
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.901G>A (p.Val301Met) rs147718169
NM_001048174.2(MUTYH):c.954G>A (p.Ser318=) rs372673338
NM_001048174.2(MUTYH):c.986A>G (p.Asn329Ser) rs754178539
NM_001128425.1(MUTYH):c.1043C>T (p.Pro348Leu) rs780178101
NM_001128425.1(MUTYH):c.1076C>T (p.Pro359Leu) rs1060501323
NM_001128425.1(MUTYH):c.1247A>G (p.Gln416Arg) rs730881835
NM_001128425.1(MUTYH):c.1249C>T (p.Arg417Cys) rs773370513
NM_001128425.1(MUTYH):c.1316T>C (p.Leu439Pro) rs587780745
NM_001128425.1(MUTYH):c.1323G>A (p.Glu441=) rs587782564
NM_001128425.1(MUTYH):c.1346T>G (p.Ile449Ser) rs767996570
NM_001128425.1(MUTYH):c.1430C>A (p.Thr477Lys) rs767747402
NM_001128425.1(MUTYH):c.1435G>A (p.Glu479Lys) rs376790729
NM_001128425.1(MUTYH):c.1476+3A>G rs1064796189
NM_001128425.1(MUTYH):c.1477G>A (p.Val493Ile) rs587782228
NM_001128425.1(MUTYH):c.1493A>G (p.Gln498Arg) rs587780085
NM_001128425.1(MUTYH):c.1514G>A (p.Cys505Tyr) rs1064793656
NM_001128425.1(MUTYH):c.1519-11T>G rs1064793775
NM_001128425.1(MUTYH):c.1588G>T (p.Asp530Tyr) rs147923905
NM_001128425.1(MUTYH):c.1615A>G (p.Thr539Ala) rs151196169
NM_001128425.1(MUTYH):c.1640del (p.Ala547fs) rs587780086
NM_001128425.1(MUTYH):c.196G>A (p.Ala66Thr) rs1064793421
NM_001128425.1(MUTYH):c.217G>A (p.Glu73Lys) rs1064794128
NM_001128425.1(MUTYH):c.244T>C (p.Ser82Pro) rs773198648
NM_001128425.1(MUTYH):c.299T>A (p.Leu100Gln) rs730881831
NM_001128425.1(MUTYH):c.346C>T (p.Arg116Trp) rs373766973
NM_001128425.1(MUTYH):c.347G>A (p.Arg116Gln) rs587782683
NM_001128425.1(MUTYH):c.37-5T>G rs876660715
NM_001128425.1(MUTYH):c.379G>A (p.Ala127Thr) rs746112825
NM_001128425.1(MUTYH):c.390G>A (p.Val130=) rs774780021
NM_001128425.1(MUTYH):c.44T>C (p.Met15Thr) rs201163858
NM_001128425.1(MUTYH):c.462+3G>A rs373939052
NM_001128425.1(MUTYH):c.475C>A (p.Leu159Met) rs199862273
NM_001128425.1(MUTYH):c.497C>T (p.Ser166Phe) rs587780087
NM_001128425.1(MUTYH):c.505-12T>G rs890418965
NM_001128425.1(MUTYH):c.560A>G (p.Gln187Arg) rs757503642
NM_001128425.1(MUTYH):c.576+4A>C rs1064796369
NM_001128425.1(MUTYH):c.578T>C (p.Val193Ala) rs879254293
NM_001128425.1(MUTYH):c.662G>C (p.Gly221Ala) rs1064793779
NM_001128425.1(MUTYH):c.698G>A (p.Gly233Asp) rs147487160
NM_001128425.1(MUTYH):c.713A>C (p.Asn238Thr) rs1057517765
NM_001128425.1(MUTYH):c.719C>T (p.Ala240Val) rs369120013
NM_001128425.1(MUTYH):c.724G>A (p.Val242Met) rs769766446
NM_001128425.1(MUTYH):c.724G>C (p.Val242Leu) rs769766446
NM_001128425.1(MUTYH):c.724G>T (p.Val242Leu) rs769766446
NM_001128425.1(MUTYH):c.736G>A (p.Val246Ile) rs587780749
NM_001128425.1(MUTYH):c.812A>G (p.Asp271Gly) rs879254255
NM_001128425.1(MUTYH):c.869G>A (p.Cys290Tyr) rs1064795466
NM_001128425.1(MUTYH):c.881G>A (p.Arg294His) rs146044717
NM_001128425.1(MUTYH):c.893G>A (p.Ser298Asn) rs757080586
NM_001128425.1(MUTYH):c.918C>G (p.Cys306Trp) rs730881834
NM_001128425.1(MUTYH):c.920G>A (p.Arg307Gln) rs140156029
NM_001128425.1(MUTYH):c.930G>C (p.Gln310His) rs1064793522
NM_001128425.1(MUTYH):c.933+10C>T rs1060504205
NM_001128425.1(MUTYH):c.965G>C (p.Ser322Thr) rs587781810
NM_001128425.1(MUTYH):c.984C>A (p.Asp328Glu) rs587780752
NM_012222.2(MUTYH):c.1064_1066delinsACA (p.Phe355_Pro356delinsTyrThr) rs1064793199
NM_012222.2(MUTYH):c.1547_1595del (p.Arg516fs) rs1064794411
NM_012222.2(MUTYH):c.1591C>T (p.Arg531Trp) rs144616312

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