ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by PreventionGenetics,PreventionGenetics

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Total variants: 15
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1423G>A (p.Ala475Thr) rs587782263
NM_001048171.1(MUTYH):c.637G>A (p.Ala213Thr) rs369854269
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.1333G>A (p.Ala445Thr) rs192816572
NM_001048174.2(MUTYH):c.616G>A (p.Val206Met) rs200165598
NM_001048174.2(MUTYH):c.737G>A (p.Arg246Gln) rs149866955
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys) rs138089183
NM_001048174.2(MUTYH):c.848G>A (p.Arg283Lys) rs149342980
NM_001128425.1(MUTYH):c.1153G>T (p.Ala385Ser) rs876659232
NM_001128425.1(MUTYH):c.1567C>T (p.Arg523Cys) rs147480076
NM_001128425.1(MUTYH):c.1588G>T (p.Asp530Tyr) rs147923905
NM_001128425.1(MUTYH):c.37-2A>G rs1383826978
NM_001128425.1(MUTYH):c.491G>A (p.Ser164Asn) rs1557480827
NM_001128425.1(MUTYH):c.596G>A (p.Gly199Asp) rs1263648272

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