ClinVar Miner

List of variants in gene MUTYH reported as likely benign for not provided

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Gene type:
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Total variants: 91
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1435-17C>G rs199664013
NM_001048171.1(MUTYH):c.1477-9T>C rs372815910
NM_001048171.1(MUTYH):c.1506G>A (p.Pro502=) rs143796254
NM_001048171.1(MUTYH):c.174G>A (p.Pro58=) rs144551668
NM_001048171.1(MUTYH):c.347-4C>G rs767717597
NM_001048171.1(MUTYH):c.37-7G>A rs780029247
NM_001048171.1(MUTYH):c.63C>T (p.Ala21=) rs201982344
NM_001048171.1(MUTYH):c.654C>T (p.Thr218=) rs780747266
NM_001048171.1(MUTYH):c.672C>T (p.Asn224=) rs767327888
NM_001048171.1(MUTYH):c.771C>T (p.Asp257=) rs730881838
NM_001048171.1(MUTYH):c.844C>T (p.Leu282=) rs778782508
NM_001048171.1(MUTYH):c.942C>T (p.Asp314=) rs587780752
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.-4C>T rs1570467350
NM_001048174.2(MUTYH):c.1032T>C (p.Ser344=) rs1570383363
NM_001048174.2(MUTYH):c.1095C>G (p.Pro365=) rs1570380575
NM_001048174.2(MUTYH):c.1117C>T (p.Leu373=) rs1060501334
NM_001048174.2(MUTYH):c.1152A>C (p.Ser384=) rs1570375279
NM_001048174.2(MUTYH):c.116-23T>C rs1570447004
NM_001048174.2(MUTYH):c.11C>T (p.Pro4Leu) rs79777494
NM_001048174.2(MUTYH):c.123C>T (p.Ala41=) rs752376615
NM_001048174.2(MUTYH):c.1272A>G (p.Thr424=) rs1570366627
NM_001048174.2(MUTYH):c.1320C>A (p.Thr440=) rs746668146
NM_001048174.2(MUTYH):c.1332T>C (p.Gly444=) rs1477315899
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=) rs74318065
NM_001048174.2(MUTYH):c.1365C>G (p.Thr455=) rs150269172
NM_001048174.2(MUTYH):c.1482C>G (p.Pro494=) rs1553122945
NM_001048174.2(MUTYH):c.1494G>A (p.Gln498=) rs1570312666
NM_001048174.2(MUTYH):c.1518G>C (p.Arg506=) rs1570311414
NM_001048174.2(MUTYH):c.1545C>T (p.Ser515=) rs1570310355
NM_001048174.2(MUTYH):c.174A>T (p.Leu58=) rs786201439
NM_001048174.2(MUTYH):c.198A>G (p.Thr66=) rs1570443483
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=) rs121908380
NM_001048174.2(MUTYH):c.294G>A (p.Arg98=) rs1232031176
NM_001048174.2(MUTYH):c.318G>A (p.Glu106=) rs1277275044
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.39G>A (p.Arg13=) rs1570465755
NM_001048174.2(MUTYH):c.421-10C>T rs1374872761
NM_001048174.2(MUTYH):c.474G>A (p.Leu158=) rs1448426714
NM_001048174.2(MUTYH):c.609A>C (p.Ala203=) rs908344724
NM_001048174.2(MUTYH):c.704+7T>C rs369052315
NM_001048174.2(MUTYH):c.774G>A (p.Gly258=) rs771290019
NM_001048174.2(MUTYH):c.840A>G (p.Ala280=) rs1046870284
NM_001048174.2(MUTYH):c.849+8T>C rs1570398146
NM_001048174.2(MUTYH):c.850-4T>C rs1570396278
NM_001048174.2(MUTYH):c.913+7A>T rs1570393359
NM_001128425.1(MUTYH):c.1008T>C (p.Thr336=) rs924192790
NM_001128425.1(MUTYH):c.1013A>G (p.Gln338Arg) rs199742231
NM_001128425.1(MUTYH):c.1023G>T (p.Leu341=) rs1553126969
NM_001128425.1(MUTYH):c.1186+17C>T rs369034810
NM_001128425.1(MUTYH):c.1200A>G (p.Gly400=) rs1570377075
NM_001128425.1(MUTYH):c.1215G>A (p.Pro405=) rs876659935
NM_001128425.1(MUTYH):c.1263G>A (p.Leu421=) rs878854184
NM_001128425.1(MUTYH):c.1324-4C>G rs1060504206
NM_001128425.1(MUTYH):c.1332C>T (p.His444=) rs764366493
NM_001128425.1(MUTYH):c.1404C>T (p.Thr468=) rs746668146
NM_001128425.1(MUTYH):c.1431G>A (p.Thr477=) rs74318065
NM_001128425.1(MUTYH):c.1461C>T (p.Ser487=) rs876658316
NM_001128425.1(MUTYH):c.1476+228C>T rs3219491
NM_001128425.1(MUTYH):c.1477-9_1477-7del rs763940868
NM_001128425.1(MUTYH):c.1530G>A (p.Arg510=) rs747201171
NM_001128425.1(MUTYH):c.1548G>C (p.Pro516=) rs143796254
NM_001128425.1(MUTYH):c.1593T>C (p.Asn531=) rs876659054
NM_001128425.1(MUTYH):c.256C>T (p.Leu86=) rs781163298
NM_001128425.1(MUTYH):c.267C>T (p.Asp89=) rs538419476
NM_001128425.1(MUTYH):c.324A>G (p.Lys108=) rs876659705
NM_001128425.1(MUTYH):c.346C>A (p.Arg116=) rs373766973
NM_001128425.1(MUTYH):c.36+1936G>A rs115736558
NM_001128425.1(MUTYH):c.367C>T (p.Leu123=) rs764221826
NM_001128425.1(MUTYH):c.389-7C>T rs863224698
NM_001128425.1(MUTYH):c.450C>T (p.Thr150=) rs368383907
NM_001128425.1(MUTYH):c.453A>G (p.Gly151=) rs753538213
NM_001128425.1(MUTYH):c.510G>A (p.Val170=) rs761195246
NM_001128425.1(MUTYH):c.576+7G>A rs756863931
NM_001128425.1(MUTYH):c.576+8G>C rs190500741
NM_001128425.1(MUTYH):c.594G>A (p.Gly198=) rs1475004261
NM_001128425.1(MUTYH):c.634C>T (p.Leu212=) rs1553128497
NM_001128425.1(MUTYH):c.66G>A (p.Val22=) rs370493415
NM_001128425.1(MUTYH):c.691-4C>T rs1557474961
NM_001128425.1(MUTYH):c.732C>T (p.Cys244=) rs776769508
NM_001128425.1(MUTYH):c.747T>C (p.Ile249=) rs577792676
NM_001128425.1(MUTYH):c.788+9T>C rs143091801
NM_001128425.1(MUTYH):c.78C>T (p.His26=) rs776396492
NM_001128425.1(MUTYH):c.921G>A (p.Arg307=) rs1180530486
NM_001128425.1(MUTYH):c.951C>G (p.Leu317=) rs11211096
NM_001128425.1(MUTYH):c.954A>G (p.Leu318=) rs1553127406
NM_012222.2(MUTYH):c.129C>T (p.Asn43=) rs141679570
NM_012222.2(MUTYH):c.1440C>T (p.Thr480=) rs150269172
NM_012222.2(MUTYH):c.720G>A (p.Leu240=) rs1060504204

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