ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by University of Washington Department of Laboratory Medicine,University of Washington

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Total variants: 31
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HGVS dbSNP
NM_000251.2(MSH2):c.-12G>A rs1558450937
NM_000251.2(MSH2):c.1033T>G (p.Trp345Gly) rs1558466616
NM_000251.2(MSH2):c.1071G>A (p.Glu357=) rs587781617
NM_000251.2(MSH2):c.1191A>T (p.Gln397His) rs768694189
NM_000251.2(MSH2):c.1347G>C (p.Lys449Asn) rs587781331
NM_000251.2(MSH2):c.1357A>C (p.Met453Leu) rs1558493602
NM_000251.2(MSH2):c.1429A>C (p.Asn477His) rs587781346
NM_000251.2(MSH2):c.1461C>G (p.Asp487Glu) rs35107951
NM_000251.2(MSH2):c.14C>A (p.Pro5Gln) rs56170584
NM_000251.2(MSH2):c.1600C>T (p.Arg534Cys) rs63750029
NM_000251.2(MSH2):c.1659C>T (p.Asn553=) rs869312796
NM_000251.2(MSH2):c.1796T>C (p.Leu599Ser) rs747504492
NM_000251.2(MSH2):c.1862G>A (p.Arg621Gln) rs759263820
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.2006-1G>T rs267607988
NM_000251.2(MSH2):c.2006G>A (p.Gly669Asp) rs63751640
NM_000251.2(MSH2):c.2017G>A (p.Gly673Arg) rs1558519543
NM_000251.2(MSH2):c.2077T>C (p.Cys693Arg) rs1558519728
NM_000251.2(MSH2):c.2086C>G (p.Pro696Ala) rs546201898
NM_000251.2(MSH2):c.2132G>A (p.Arg711Gln) rs138465383
NM_000251.2(MSH2):c.2285T>C (p.Leu762Ser) rs1558521698
NM_000251.2(MSH2):c.2294C>T (p.Ala765Val) rs1261458082
NM_000251.2(MSH2):c.2360T>G (p.Leu787Arg) rs1558521929
NM_000251.2(MSH2):c.2479G>C (p.Gly827Arg) rs63750478
NM_000251.2(MSH2):c.2516A>G (p.His839Arg) rs63750027
NM_000251.2(MSH2):c.2754G>T (p.Lys918Asn) rs1553370893
NM_000251.2(MSH2):c.432C>T (p.Ser144=) rs1558459072
NM_000251.2(MSH2):c.480G>T (p.Gln160His) rs1558459273
NM_000251.2(MSH2):c.518T>C (p.Leu173Pro) rs63750070
NM_000251.2(MSH2):c.53G>A (p.Gly18Asp) rs1200418561
NM_000251.2(MSH2):c.925G>C (p.Ala309Pro) rs781257094

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