ClinVar Miner

List of variants in gene MUTYH reported as benign for not specified

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Total variants: 28
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1506G>A (p.Pro502=) rs143796254
NM_001048171.1(MUTYH):c.158-54C>T rs367908623
NM_001048171.1(MUTYH):c.306+11G>A rs139977567
NM_001048171.1(MUTYH):c.330C>T (p.Asp110=) rs730881836
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.654C>T (p.Thr218=) rs780747266
NM_001048171.1(MUTYH):c.771C>T (p.Asp257=) rs730881838
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met) rs144079536
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.228C>T (p.Tyr76=) rs121908380
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043
NM_001048174.2(MUTYH):c.606+21C>A rs148552450
NM_001048174.2(MUTYH):c.930G>C (p.Gln310His) rs3219489
NM_001128425.1(MUTYH):c.1014G>T (p.Gln338His) rs3219489
NM_001128425.1(MUTYH):c.1186+17C>T rs369034810
NM_001128425.1(MUTYH):c.1290C>T (p.Pro430=) rs752408891
NM_001128425.1(MUTYH):c.157+30A>G rs3219485
NM_001128425.1(MUTYH):c.504+35A>G rs3219487
NM_001128425.1(MUTYH):c.627G>A (p.Gln209=) rs730881837
NM_012222.2(MUTYH):c.1440C>T (p.Thr480=) rs150269172
NM_012222.2(MUTYH):c.1535C>T (p.Ser512Phe) rs140118273
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.496-4A>G rs201678305
NM_012222.2(MUTYH):c.64G>A (p.Val22Met) rs3219484

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