ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 70
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1033C>A (p.Pro345Thr) rs587782773
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1213G>A (p.Ala405Thr) rs587780744
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.1378C>T (p.Arg460Cys) rs200229669
NM_001048171.1(MUTYH):c.1423G>A (p.Ala475Thr) rs587782263
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.38C>T (p.Ala13Val) rs587780747
NM_001048171.1(MUTYH):c.451G>A (p.Ala151Thr) rs201103359
NM_001048171.1(MUTYH):c.469A>G (p.Asn157Asp) rs773674701
NM_001048171.1(MUTYH):c.530G>A (p.Arg177Gln) rs369677603
NM_001048171.1(MUTYH):c.637G>A (p.Ala213Thr) rs369854269
NM_001048171.1(MUTYH):c.956-8G>A rs757672024
NM_001048171.1(MUTYH):c.995C>T (p.Ser332Leu) rs587778538
NM_001048174.2(MUTYH):c.1174C>G (p.Leu392Val) rs144079536
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.1226G>A (p.Arg409Gln) rs587782120
NM_001048174.2(MUTYH):c.1333G>A (p.Ala445Thr) rs192816572
NM_001048174.2(MUTYH):c.1392+7C>T rs1570361183
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu) rs3219494
NM_001048174.2(MUTYH):c.1434+10C>G
NM_001048174.2(MUTYH):c.14G>A (p.Arg5Gln) rs587780081
NM_001048174.2(MUTYH):c.1525A>C (p.Ile509Leu)
NM_001048174.2(MUTYH):c.206G>A (p.Arg69Gln) rs755653922
NM_001048174.2(MUTYH):c.466C>T (p.Arg156Trp) rs779997419
NM_001048174.2(MUTYH):c.484G>T (p.Ala162Ser) rs764458059
NM_001048174.2(MUTYH):c.504G>C (p.Glu168Asp) rs587781645
NM_001048174.2(MUTYH):c.565C>T (p.Arg189Cys) rs537292657
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.850-2A>G rs77542170
NM_001048174.2(MUTYH):c.854A>T (p.Glu285Val)
NM_001048174.2(MUTYH):c.901G>A (p.Val301Met) rs147718169
NM_001128425.1(MUTYH):c.1000C>G (p.Pro334Ala) rs587778537
NM_001128425.1(MUTYH):c.1139C>G (p.Pro380Arg) rs774441289
NM_001128425.1(MUTYH):c.1249C>T (p.Arg417Cys) rs773370513
NM_001128425.1(MUTYH):c.125A>G (p.Asn42Ser) rs563275223
NM_001128425.1(MUTYH):c.1513T>G (p.Cys505Gly) rs876659488
NM_001128425.1(MUTYH):c.1532C>T (p.Ser511Phe) rs796921537
NM_001128425.1(MUTYH):c.1567C>T (p.Arg523Cys) rs147480076
NM_001128425.1(MUTYH):c.157+3A>G rs1553131280
NM_001128425.1(MUTYH):c.1588G>T (p.Asp530Tyr) rs147923905
NM_001128425.1(MUTYH):c.161G>A (p.Cys54Tyr) rs560905645
NM_001128425.1(MUTYH):c.1622C>T (p.Ala541Val) rs751053826
NM_001128425.1(MUTYH):c.254A>G (p.His85Arg) rs558707786
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.377G>A (p.Arg126Gln) rs587781444
NM_001128425.1(MUTYH):c.389-6C>T rs376600220
NM_001128425.1(MUTYH):c.394G>A (p.Val132Ile) rs763273196
NM_001128425.1(MUTYH):c.449C>T (p.Thr150Ile) rs745507536
NM_001128425.1(MUTYH):c.504G>A (p.Glu168=) rs876658641
NM_001128425.1(MUTYH):c.563_576+1del rs766553845
NM_001128425.1(MUTYH):c.564G>C (p.Glu188Asp) rs1335408660
NM_001128425.1(MUTYH):c.671C>A (p.Ala224Asp) rs1553128391
NM_001128425.1(MUTYH):c.736G>A (p.Val246Ile) rs587780749
NM_001128425.1(MUTYH):c.83A>T (p.Lys28Met) rs1553131499
NM_001128425.1(MUTYH):c.881G>A (p.Arg294His) rs146044717
NM_001128425.1(MUTYH):c.904G>T (p.Val302Leu) rs760889663
NM_001128425.1(MUTYH):c.920G>A (p.Arg307Gln) rs140156029
NM_012222.2(MUTYH):c.1004_1005delinsGC (p.Gln335Arg) rs587780083
NM_012222.2(MUTYH):c.1155_1156delinsAT (p.Leu385_Leu386=) rs1553126326

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