ClinVar Miner

List of variants in gene MUTYH reported as likely pathogenic by Counsyl

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Total variants: 19
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1005G>A (p.Trp335Ter) rs1060501324
NM_001048171.1(MUTYH):c.1435-1G>A rs1057517459
NM_001048171.1(MUTYH):c.206C>G (p.Ser69Ter) rs370124822
NM_001048171.1(MUTYH):c.267G>A (p.Trp89Ter) rs748170941
NM_001048171.1(MUTYH):c.310G>T (p.Glu104Ter) rs1553129892
NM_001048171.1(MUTYH):c.425G>A (p.Trp142Ter) rs762307622
NM_001048171.1(MUTYH):c.502C>T (p.Arg168Cys) rs747993448
NM_001048171.1(MUTYH):c.517C>T (p.Gln173Ter) rs1553128813
NM_001048171.1(MUTYH):c.85C>T (p.Gln29Ter) rs768386527
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) rs765123255
NM_001048174.2(MUTYH):c.637C>T (p.Arg213Trp) rs34126013
NM_001048174.2(MUTYH):c.652G>T (p.Val218Phe) rs587780749
NM_001128425.1(MUTYH):c.1078del (p.Arg360fs) rs1057517456
NM_001128425.1(MUTYH):c.504+19_504+31del rs781222233
NM_001128425.1(MUTYH):c.526_535del (p.Gly176fs) rs1057517457
NM_012222.2(MUTYH):c.1258_1260delinsC (p.Glu420fs) rs1553125766
NM_012222.2(MUTYH):c.1386dup (p.Val463fs) rs1553125100
NM_012222.2(MUTYH):c.725G>A (p.Arg242His) rs140342925
NM_012222.2(MUTYH):c.875C>T (p.Pro292Leu) rs374950566

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