ClinVar Miner

List of variants in gene MUTYH reported by Mendelics

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Total variants: 70
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
NM_001048171.1(MUTYH):c.1105del (p.Ala371fs) rs587778536
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1269G>A (p.Arg423=) rs199575659
NM_001048171.1(MUTYH):c.1434+2C>T rs140288388
NM_001048171.1(MUTYH):c.37-7G>A rs780029247
NM_001048171.1(MUTYH):c.534G>A (p.Lys178=) rs876660092
NM_001048171.1(MUTYH):c.565C>T (p.Arg189Cys) rs587780748
NM_001048171.1(MUTYH):c.672C>T (p.Asn224=) rs767327888
NM_001048171.1(MUTYH):c.673G>A (p.Val225Ile) rs759295912
NM_001048171.1(MUTYH):c.929C>T (p.Ser310Leu) rs558173961
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.1057G>T (p.Gly353Trp) rs587778539
NM_001048174.2(MUTYH):c.1072C>G (p.Gln358Glu) rs878854183
NM_001048174.2(MUTYH):c.1087C>T (p.Gln363Ter) rs587783057
NM_001048174.2(MUTYH):c.1102+42_1102+43del rs775033999
NM_001048174.2(MUTYH):c.1103-27C>T rs3219490
NM_001048174.2(MUTYH):c.1103G>A (p.Gly368Asp) rs36053993
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met) rs144079536
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.11C>T (p.Pro4Leu) rs79777494
NM_001048174.2(MUTYH):c.1205C>T (p.Pro402Leu) rs587780079
NM_001048174.2(MUTYH):c.1226G>A (p.Arg409Gln) rs587782120
NM_001048174.2(MUTYH):c.1350GGA[1] (p.Glu452del) rs587778541
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu) rs3219494
NM_001048174.2(MUTYH):c.1434+3A>T rs1553123967
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.14G>C (p.Arg5Pro) rs587780081
NM_001048174.2(MUTYH):c.1515T>A (p.Phe505Leu) rs1557444106
NM_001048174.2(MUTYH):c.167A>G (p.Tyr56Cys) rs200747973
NM_001048174.2(MUTYH):c.181G>C (p.Asp61His) rs1557486724
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) rs765123255
NM_001048174.2(MUTYH):c.278T>C (p.Met93Thr) rs1557484437
NM_001048174.2(MUTYH):c.305-1G>C rs372267274
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.395A>G (p.Gln132Arg) rs1212933615
NM_001048174.2(MUTYH):c.397G>C (p.Asp133His) rs564930066
NM_001048174.2(MUTYH):c.421-2A>C rs786203161
NM_001048174.2(MUTYH):c.421-2A>G rs786203161
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys) rs34612342
NM_001048174.2(MUTYH):c.461G>A (p.Arg154His) rs143353451
NM_001048174.2(MUTYH):c.484G>T (p.Ala162Ser) rs764458059
NM_001048174.2(MUTYH):c.493-5A>G rs758377868
NM_001048174.2(MUTYH):c.493-5A>T rs758377868
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.566G>A (p.Arg189His) rs147754007
NM_001048174.2(MUTYH):c.571A>G (p.Thr191Ala) rs771064557
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val) rs200872702
NM_001048174.2(MUTYH):c.606+21C>A rs148552450
NM_001048174.2(MUTYH):c.606+3G>C rs1553128340
NM_001048174.2(MUTYH):c.610A>G (p.Thr204Ala) rs587782351
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.743G>A (p.Gly248Glu) rs1557471507
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.849+3A>C rs587780751
NM_001048174.2(MUTYH):c.850-2A>G rs77542170
NM_001048174.2(MUTYH):c.901G>A (p.Val301Met) rs147718169
NM_001048174.2(MUTYH):c.986A>G (p.Asn329Ser) rs754178539
NM_001128425.1(MUTYH):c.1617T>C (p.Thr539=) rs756708148
NM_001128425.1(MUTYH):c.161G>A (p.Cys54Tyr) rs560905645
NM_001128425.1(MUTYH):c.694A>T (p.Thr232Ser) rs587782351
NM_001128425.1(MUTYH):c.987G>C (p.Val329=) rs749048388
NM_001350650.1(MUTYH):c.33+147del rs1553129638
NM_012222.2(MUTYH):c.1576C>A (p.Leu526Met) rs3219496
NM_012222.2(MUTYH):c.682-18_682-17del rs765157527

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