ClinVar Miner

List of variants in gene MSH2 reported as not provided

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Total variants: 35
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HGVS dbSNP
NG_007110.2:g.114289A>G rs2303424
NM_000251.2(MSH2):c.*387C>A rs104895028
NM_000251.2(MSH2):c.*392G>A rs104895029
NM_000251.2(MSH2):c.*61T>A rs104895027
NM_000251.2(MSH2):c.1076+176A>G rs104895023
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.1276+1G>A rs267607950
NM_000251.2(MSH2):c.1387-265A>G rs104895024
NM_000251.2(MSH2):c.1387-9T>A rs587779087
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.1661+176A>G rs104895025
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.181C>T (p.Gln61Ter) rs63750951
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.2164G>A (p.Val722Ile) rs587781996
NM_000251.2(MSH2):c.2179G>T (p.Ala727Ser) rs104895026
NM_000251.2(MSH2):c.220A>C (p.Asn74His) rs150548839
NM_000251.2(MSH2):c.2211-1G>A
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.2510C>G (p.Pro837Arg)
NM_000251.2(MSH2):c.2545C>G (p.Leu849Val) rs587778527
NM_000251.2(MSH2):c.367-108A>C rs104895021
NM_000251.2(MSH2):c.380A>G (p.Asn127Ser) rs17217772
NM_000251.2(MSH2):c.382C>G (p.Leu128Val) rs145649774
NM_000251.2(MSH2):c.5C>T (p.Ala2Val) rs587778521
NM_000251.2(MSH2):c.874A>T (p.Thr292Ser) rs104895022
NM_000251.2(MSH2):c.928del (p.Asn311fs) rs1064793179
NM_000251.2(MSH2):c.965G>A (p.Gly322Asp) rs4987188
Single allele

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