ClinVar Miner

List of variants in gene MSH2 reported by ITMI

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Gene type:
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Total variants: 19
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HGVS dbSNP
NG_007110.2:g.114262C>T rs72888274
NG_007110.2:g.114271G>A rs116117580
NG_007110.2:g.114289A>G rs2303424
NM_000251.2(MSH2):c.1168C>T (p.Leu390Phe) rs17224367
NM_000251.2(MSH2):c.1255C>A (p.Gln419Lys) rs63750006
NM_000251.2(MSH2):c.138C>G (p.His46Gln) rs33946261
NM_000251.2(MSH2):c.1601G>A (p.Arg534His) rs587778523
NM_000251.2(MSH2):c.1631T>C (p.Ile544Thr) rs587778524
NM_000251.2(MSH2):c.1662C>T (p.Ser554=) rs587778525
NM_000251.2(MSH2):c.1798G>T (p.Ala600Ser) rs587778526
NM_000251.2(MSH2):c.1886A>G (p.Gln629Arg) rs61756468
NM_000251.2(MSH2):c.208G>A (p.Ala70Thr) rs587778522
NM_000251.2(MSH2):c.220A>C (p.Asn74His) rs150548839
NM_000251.2(MSH2):c.23C>T (p.Thr8Met) rs17217716
NM_000251.2(MSH2):c.2425G>A (p.Glu809Lys) rs202145681
NM_000251.2(MSH2):c.2545C>G (p.Leu849Val) rs587778527
NM_000251.2(MSH2):c.380A>G (p.Asn127Ser) rs17217772
NM_000251.2(MSH2):c.5C>T (p.Ala2Val) rs587778521
NM_000251.2(MSH2):c.965G>A (p.Gly322Asp) rs4987188

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