ClinVar Miner

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

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Total variants: 67
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1030T>C (p.Phe344Leu) rs587781601
NM_001048171.1(MUTYH):c.1033C>A (p.Pro345Thr) rs587782773
NM_001048171.1(MUTYH):c.1213G>A (p.Ala405Thr) rs587780744
NM_001048171.1(MUTYH):c.1214C>A (p.Ala405Asp) rs369299948
NM_001048171.1(MUTYH):c.1235G>T (p.Arg412Leu) rs748700385
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.1264C>G (p.Leu422Val) rs587782043
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.1388C>T (p.Thr463Met) rs767747402
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.1444G>A (p.Val482Met) rs587781385
NM_001048171.1(MUTYH):c.1452G>C (p.Gln484His) rs587782794
NM_001048171.1(MUTYH):c.1495G>T (p.Val499Leu) rs780209880
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.1546G>C (p.Asp516His) rs147923905
NM_001048171.1(MUTYH):c.158-33G>A rs587781374
NM_001048171.1(MUTYH):c.158-33G>T rs587781374
NM_001048171.1(MUTYH):c.158-54C>T rs367908623
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.509G>A (p.Arg170Gln) rs758567247
NM_001048171.1(MUTYH):c.529C>T (p.Arg177Trp) rs761101420
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.62C>T (p.Ala21Val) rs1057517460
NM_001048171.1(MUTYH):c.634A>G (p.Ile212Val) rs200965879
NM_001048171.1(MUTYH):c.637G>A (p.Ala213Thr) rs369854269
NM_001048171.1(MUTYH):c.648+14C>G rs752537118
NM_001048171.1(MUTYH):c.673G>A (p.Val225Ile) rs759295912
NM_001048171.1(MUTYH):c.772C>T (p.Pro258Ser) rs786201772
NM_001048171.1(MUTYH):c.794A>C (p.Asn265Thr) rs587778534
NM_001048171.1(MUTYH):c.803C>T (p.Ala268Val) rs587782764
NM_001048171.1(MUTYH):c.80G>A (p.Arg27Lys) rs587782693
NM_001048171.1(MUTYH):c.838C>T (p.Arg280Cys) rs199840380
NM_001048171.1(MUTYH):c.875G>A (p.Cys292Tyr) rs786204112
NM_001048171.1(MUTYH):c.924C>G (p.Ser308Arg) rs138833473
NM_001048171.1(MUTYH):c.929C>T (p.Ser310Leu) rs558173961
NM_001048171.1(MUTYH):c.958C>A (p.Pro320Thr) rs587778537
NM_001048171.1(MUTYH):c.995C>G (p.Ser332Trp) rs587778538
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.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.14G>A (p.Arg5Gln) rs587780081
NM_001048174.2(MUTYH):c.167A>G (p.Tyr56Cys) rs200747973
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.493-5A>G rs758377868
NM_001048174.2(MUTYH):c.565C>T (p.Arg189Cys) rs537292657
NM_001048174.2(MUTYH):c.566G>A (p.Arg189His) rs147754007
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.848G>A (p.Arg283Lys) rs149342980
NM_001048174.2(MUTYH):c.901G>A (p.Val301Met) rs147718169
NM_001128425.1(MUTYH):c.1640del (p.Ala547fs) rs587780086
NM_001293192.1(MUTYH):c.-83_-78del rs1553130269

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