ClinVar Miner

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

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Total variants: 27
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
NM_001048171.1(MUTYH):c.1353A>C (p.Pro451=) rs768239149
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.37-7G>A rs780029247
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.771C>T (p.Asp257=) rs730881838
NM_001048171.1(MUTYH):c.942C>T (p.Asp314=) rs587780752
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.1161T>C (p.Leu387=)
NM_001048174.2(MUTYH):c.1463C>T (p.Pro488Leu) rs587778542
NM_001048174.2(MUTYH):c.1518G>A (p.Arg506=)
NM_001048174.2(MUTYH):c.690T>C (p.Val230=)
NM_001128425.1(MUTYH):c.1086C>T (p.Ala362=) rs878854182
NM_001128425.1(MUTYH):c.1218C>T (p.Ser406=) rs759460243
NM_001128425.1(MUTYH):c.1371G>A (p.Gly457=) rs1553125186
NM_001128425.1(MUTYH):c.1464C>T (p.Thr488=) rs373973053
NM_001128425.1(MUTYH):c.1477-9_1477-7del rs763940868
NM_001128425.1(MUTYH):c.1548G>C (p.Pro516=) rs143796254
NM_001128425.1(MUTYH):c.267C>T (p.Asp89=) rs538419476
NM_001128425.1(MUTYH):c.409C>T (p.Leu137=) rs368963039
NM_001128425.1(MUTYH):c.576+8G>C rs190500741
NM_001128425.1(MUTYH):c.657A>C (p.Thr219=) rs778014929
NM_001128425.1(MUTYH):c.873C>A (p.Thr291=) rs1557470723
NM_001128425.1(MUTYH):c.972G>A (p.Ser324=) rs771683103
NM_001128425.1(MUTYH):c.981T>C (p.Pro327=) rs149334084
NM_012222.2(MUTYH):c.129C>T (p.Asn43=) rs141679570

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