ClinVar Miner

List of variants in gene MUTYH studied for Carcinoma of colon

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Total variants: 47
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1105del (p.Ala371fs) rs587778536
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.1442G>A (p.Arg481His) rs144111588
NM_001048171.1(MUTYH):c.270C>A (p.Tyr90Ter) rs121908380
NM_001048171.1(MUTYH):c.306+11G>A rs139977567
NM_001048171.1(MUTYH):c.425G>A (p.Trp142Ter) rs762307622
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.648+14C>G rs752537118
NM_001048171.1(MUTYH):c.697C>T (p.Arg233Ter) rs587782885
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.1087C>T (p.Gln363Ter) rs587783057
NM_001048174.2(MUTYH):c.1103-2A>G rs587781628
NM_001048174.2(MUTYH):c.1103G>A (p.Gly368Asp) rs36053993
NM_001048174.2(MUTYH):c.1143_1144dup (p.Glu382fs) rs587780078
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.1347G>C (p.Thr449=) rs74318065
NM_001048174.2(MUTYH):c.1354G>T (p.Glu452Ter) rs121908381
NM_001048174.2(MUTYH):c.206G>A (p.Arg69Gln) rs755653922
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=) rs121908380
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) rs765123255
NM_001048174.2(MUTYH):c.305-1G>C rs372267274
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys) rs34612342
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.849+3A>C rs587780751
NM_001048174.2(MUTYH):c.850-2A>G rs77542170
NM_001048174.2(MUTYH):c.930G>C (p.Gln310His) rs3219489
NM_001128425.1(MUTYH):c.1090C>T (p.Arg364Cys) rs151316420
NM_001128425.1(MUTYH):c.1464C>T (p.Thr488=) rs373973053
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.37G>A (p.Ala13Thr) rs375349172
NM_001128425.1(MUTYH):c.55C>T (p.Arg19Ter) rs587780088
NM_001128425.1(MUTYH):c.713A>G (p.Asn238Ser) rs1057517765
NM_001128425.1(MUTYH):c.847A>G (p.Met283Val) rs876659676
NM_001128425.1(MUTYH):c.859del (p.Ala287fs) rs761468459
NM_012222.2(MUTYH):c.1205C>T (p.Pro402Leu) rs529008617
NM_012222.2(MUTYH):c.1576C>A (p.Leu526Met) rs3219496
NM_012222.2(MUTYH):c.1592G>A (p.Arg531Gln) rs3219497
NM_012222.2(MUTYH):c.64G>A (p.Val22Met) rs3219484
NM_012222.2(MUTYH):c.725G>A (p.Arg242His) rs140342925
NM_012222.2(MUTYH):c.875C>T (p.Pro292Leu) rs374950566
NM_012222.2(MUTYH):c.881G>T (p.Cys294Phe) rs879254257

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