ClinVar Miner

List of variants in gene MUTYH reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
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.63C>T (p.Ala21=) rs201982344
NM_001048171.1(MUTYH):c.956-9C>T rs3219488
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=) rs121908380
NM_001128425.1(MUTYH):c.1013A>G (p.Gln338Arg) rs199742231
NM_001128425.1(MUTYH):c.1215G>A (p.Pro405=) rs876659935
NM_001128425.1(MUTYH):c.1218C>T (p.Ser406=) rs759460243
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.1593T>C (p.Asn531=) rs876659054
NM_001128425.1(MUTYH):c.267C>T (p.Asp89=) rs538419476
NM_001128425.1(MUTYH):c.450C>T (p.Thr150=) rs368383907
NM_001128425.1(MUTYH):c.576+8G>C rs190500741
NM_001128425.1(MUTYH):c.788+9T>C rs143091801
NM_001128425.1(MUTYH):c.78C>T (p.His26=) rs776396492
NM_012222.2(MUTYH):c.129C>T (p.Asn43=) rs141679570
NM_012222.2(MUTYH):c.1576C>A (p.Leu526Met) rs3219496
NM_012222.2(MUTYH):c.1592G>A (p.Arg531Gln) rs3219497

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