ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 26
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HGVS dbSNP
NM_000251.2(MSH2):c.128A>G (p.Tyr43Cys) rs17217723
NM_000251.2(MSH2):c.138C>G (p.His46Gln) rs33946261
NM_000251.2(MSH2):c.1511-41G>C rs202215396
NM_000251.2(MSH2):c.166G>A (p.Glu56Lys) rs587779102
NM_000251.2(MSH2):c.1682_1685inv (p.Glu561_Glu562delinsValLeu) rs1553367614
NM_000251.2(MSH2):c.1730T>C (p.Ile577Thr) rs63749910
NM_000251.2(MSH2):c.1765G>A (p.Val589Ile) rs1064793981
NM_000251.2(MSH2):c.1774A>G (p.Met592Val) rs371614039
NM_000251.2(MSH2):c.2053A>G (p.Ile685Val) rs1060499876
NM_000251.2(MSH2):c.2305T>C (p.Tyr769His) rs1114167859
NM_000251.2(MSH2):c.2354A>C (p.His785Pro) rs200252727
NM_000251.2(MSH2):c.2377C>G (p.Gln793Glu) rs730881769
NM_000251.2(MSH2):c.2503A>C (p.Asn835His) rs41295296
NM_000251.2(MSH2):c.2537A>G (p.Gln846Arg) rs140754514
NM_000251.2(MSH2):c.2576_2584del (p.Glu859_Gln861del) rs587781278
NM_000251.2(MSH2):c.2579C>T (p.Ser860Leu) rs63750849
NM_000251.2(MSH2):c.2680dup (p.Met894fs) rs876658211
NM_000251.2(MSH2):c.2732T>G (p.Leu911Arg) rs41295182
NM_000251.2(MSH2):c.2782T>G (p.Ser928Ala) rs587781852
NM_000251.2(MSH2):c.304G>A (p.Val102Ile) rs193922373
NM_000251.2(MSH2):c.435T>G (p.Ile145Met) rs63750124
NM_000251.2(MSH2):c.645+3A>G rs587779168
NM_000251.2(MSH2):c.764G>A (p.Ser255Asn) rs763184168
NM_000251.2(MSH2):c.815C>T (p.Ala272Val) rs34136999
NM_000251.2(MSH2):c.818T>C (p.Val273Ala) rs144288433
NM_000251.2(MSH2):c.97A>C (p.Thr33Pro) rs63751107

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