ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance for not specified

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Gene type:
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Total variants: 153
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HGVS dbSNP
NM_000251.2(MSH2):c.-8G>T rs1064795641
NM_000251.2(MSH2):c.1012G>A (p.Gly338Arg) rs63751004
NM_000251.2(MSH2):c.1077-3C>A rs758182607
NM_000251.2(MSH2):c.1079T>G (p.Leu360Trp) rs1558478097
NM_000251.2(MSH2):c.1083T>C (p.Asn361=) rs864622544
NM_000251.2(MSH2):c.1083_1100delinsATCTTCTAC (p.Asn361_Val367delinsLysSerSerThr) rs1553356523
NM_000251.2(MSH2):c.1139T>C (p.Leu380Ser) rs730881755
NM_000251.2(MSH2):c.114C>G (p.Asp38Glu) rs587779074
NM_000251.2(MSH2):c.116G>C (p.Arg39Pro) rs587782759
NM_000251.2(MSH2):c.1171G>A (p.Ala391Thr) rs878853798
NM_000251.2(MSH2):c.118G>A (p.Gly40Ser) rs63751260
NM_000251.2(MSH2):c.1194A>G (p.Ala398=) rs1060504412
NM_000251.2(MSH2):c.1217G>A (p.Arg406Gln) rs146567853
NM_000251.2(MSH2):c.1243C>T (p.Pro415Ser) rs35717997
NM_000251.2(MSH2):c.1275A>G (p.Glu425=) rs63751650
NM_000251.2(MSH2):c.1276+7A>G rs748554540
NM_000251.2(MSH2):c.1277-12A>T rs1181142850
NM_000251.2(MSH2):c.1277-13T>A rs1553361114
NM_000251.2(MSH2):c.1277-8T>C rs145400590
NM_000251.2(MSH2):c.128A>G (p.Tyr43Cys) rs17217723
NM_000251.2(MSH2):c.1294T>C (p.Leu432=) rs937218360
NM_000251.2(MSH2):c.1311G>T (p.Val437=) rs730881781
NM_000251.2(MSH2):c.1314T>C (p.Thr438=) rs761558457
NM_000251.2(MSH2):c.1316C>T (p.Pro439Leu) rs771789692
NM_000251.2(MSH2):c.132G>T (p.Thr44=) rs766856128
NM_000251.2(MSH2):c.1331G>A (p.Arg444His) rs557339938
NM_000251.2(MSH2):c.1347G>C (p.Lys449Asn) rs587781331
NM_000251.2(MSH2):c.1387-4G>C rs376796243
NM_000251.2(MSH2):c.138C>G (p.His46Gln) rs33946261
NM_000251.2(MSH2):c.1462T>G (p.Leu488Val) rs587781314
NM_000251.2(MSH2):c.14C>A (p.Pro5Gln) rs56170584
NM_000251.2(MSH2):c.1511-41G>C rs202215396
NM_000251.2(MSH2):c.1570C>T (p.Arg524Cys) rs755818010
NM_000251.2(MSH2):c.1601G>A (p.Arg534His) rs587778523
NM_000251.2(MSH2):c.1607A>T (p.Asn536Ile) rs201722703
NM_000251.2(MSH2):c.160G>T (p.Ala54Ser) rs749212640
NM_000251.2(MSH2):c.1640A>G (p.Asn547Ser) rs267607967
NM_000251.2(MSH2):c.1662-9G>A rs17218356
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.1714_1715delinsAT (p.Glu572Ile) rs1558514635
NM_000251.2(MSH2):c.1730T>C (p.Ile577Thr) rs63749910
NM_000251.2(MSH2):c.1748A>G (p.Asn583Ser) rs201118107
NM_000251.2(MSH2):c.174C>A (p.Phe58Leu) rs372189599
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.1786_1790delinsGG (p.Asn596_Asp597delinsGly) rs1558517764
NM_000251.2(MSH2):c.1787A>G (p.Asn596Ser) rs41295288
NM_000251.2(MSH2):c.1790A>C (p.Asp597Ala) rs548407418
NM_000251.2(MSH2):c.1819A>G (p.Ser607Gly) rs772991620
NM_000251.2(MSH2):c.1825G>C (p.Ala609Pro) rs150980616
NM_000251.2(MSH2):c.1828C>T (p.His610Tyr) rs267607980
NM_000251.2(MSH2):c.1862G>T (p.Arg621Leu) rs759263820
NM_000251.2(MSH2):c.1865C>A (p.Pro622Gln) rs28929483
NM_000251.2(MSH2):c.1865C>G (p.Pro622Arg) rs28929483
NM_000251.2(MSH2):c.1937A>G (p.Asp646Gly) rs41295290
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.1A>C (p.Met1Leu) rs267607911
NM_000251.2(MSH2):c.2005+3_2005+14del rs587779125
NM_000251.2(MSH2):c.2005G>T (p.Gly669Cys) rs63751668
NM_000251.2(MSH2):c.2006-4G>A rs369853630
NM_000251.2(MSH2):c.2006G>T (p.Gly669Val) rs63751640
NM_000251.2(MSH2):c.2014A>G (p.Met672Val) rs763690339
NM_000251.2(MSH2):c.2027C>T (p.Ser676Leu) rs1057520735
NM_000251.2(MSH2):c.2043A>G (p.Gln681=) rs730881763
NM_000251.2(MSH2):c.2047G>A (p.Gly683Arg) rs267607995
NM_000251.2(MSH2):c.2048G>T (p.Gly683Val) rs755920849
NM_000251.2(MSH2):c.2053A>G (p.Ile685Val) rs1060499876
NM_000251.2(MSH2):c.206C>T (p.Pro69Leu) rs983555044
NM_000251.2(MSH2):c.2078G>A (p.Cys693Tyr) rs1057524909
NM_000251.2(MSH2):c.2087C>T (p.Pro696Leu) rs267607994
NM_000251.2(MSH2):c.211+8C>T rs267607916
NM_000251.2(MSH2):c.212-4T>G rs1558456954
NM_000251.2(MSH2):c.2152C>G (p.Gln718Glu) rs587779139
NM_000251.2(MSH2):c.2178G>C (p.Met726Ile) rs587782396
NM_000251.2(MSH2):c.2197G>A (p.Ala733Thr) rs772662439
NM_000251.2(MSH2):c.2211-6C>A rs267608003
NM_000251.2(MSH2):c.2228C>T (p.Ser743Leu) rs63751155
NM_000251.2(MSH2):c.2260A>T (p.Thr754Ser) rs757268664
NM_000251.2(MSH2):c.2266_2267insAGA (p.Thr756_Tyr757insLys) rs1553369686
NM_000251.2(MSH2):c.2267C>G (p.Thr756Ser) rs372383829
NM_000251.2(MSH2):c.228G>T (p.Gln76His) rs587782857
NM_000251.2(MSH2):c.2296A>G (p.Ile766Val) rs374399939
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.2400A>G (p.Leu800=) rs201298777
NM_000251.2(MSH2):c.2437A>G (p.Met813Val) rs63749841
NM_000251.2(MSH2):c.2458+8C>G rs189025757
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.2545C>T (p.Leu849=) rs587778527
NM_000251.2(MSH2):c.2556G>C (p.Glu852Asp) rs587781453
NM_000251.2(MSH2):c.2558A>C (p.Glu853Ala) rs63750797
NM_000251.2(MSH2):c.2571T>G (p.Ile857Met) rs1400051085
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.2621A>G (p.Tyr874Cys) rs775390721
NM_000251.2(MSH2):c.2634+7C>G rs905179122
NM_000251.2(MSH2):c.2680dup (p.Met894fs) rs876658211
NM_000251.2(MSH2):c.2714C>T (p.Thr905Ile) rs267608022
NM_000251.2(MSH2):c.2732T>G (p.Leu911Arg) rs41295182
NM_000251.2(MSH2):c.2777T>A (p.Ile926Asn) rs199747712
NM_000251.2(MSH2):c.2782T>G (p.Ser928Ala) rs587781852
NM_000251.2(MSH2):c.2785C>T (p.Arg929Ter) rs551060742
NM_000251.2(MSH2):c.2801C>A (p.Thr934Lys) rs587779969
NM_000251.2(MSH2):c.304G>A (p.Val102Ile) rs193922373
NM_000251.2(MSH2):c.317G>A (p.Arg106Lys) rs41295286
NM_000251.2(MSH2):c.367-19A>T rs730881783
NM_000251.2(MSH2):c.367-3T>C rs1558458845
NM_000251.2(MSH2):c.374C>T (p.Pro125Leu) rs876659113
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.403C>G (p.Leu135Val) rs193096019
NM_000251.2(MSH2):c.409G>C (p.Gly137Arg) rs587781795
NM_000251.2(MSH2):c.416A>G (p.Asn139Ser) rs1553350676
NM_000251.2(MSH2):c.433A>G (p.Ile145Val) rs876659264
NM_000251.2(MSH2):c.435T>G (p.Ile145Met) rs63750124
NM_000251.2(MSH2):c.43G>A (p.Ala15Thr) rs1183892581
NM_000251.2(MSH2):c.464T>G (p.Val155Gly) rs876658188
NM_000251.2(MSH2):c.470G>C (p.Gly157Ala) rs765489269
NM_000251.2(MSH2):c.476G>T (p.Arg159Ile) rs786202921
NM_000251.2(MSH2):c.490G>T (p.Gly164Trp) rs63750582
NM_000251.2(MSH2):c.4G>A (p.Ala2Thr) rs63750466
NM_000251.2(MSH2):c.557A>G (p.Asn186Ser) rs151129360
NM_000251.2(MSH2):c.55T>C (p.Phe19Leu) rs141711342
NM_000251.2(MSH2):c.571C>T (p.Leu191Phe) rs1553350898
NM_000251.2(MSH2):c.588A>C (p.Pro196=) rs1553350915
NM_000251.2(MSH2):c.589A>C (p.Lys197Gln) rs778573140
NM_000251.2(MSH2):c.5C>T (p.Ala2Val) rs587778521
NM_000251.2(MSH2):c.633G>A (p.Gly211=) rs1558459840
NM_000251.2(MSH2):c.645+3A>G rs587779168
NM_000251.2(MSH2):c.646-11T>C rs879254124
NM_000251.2(MSH2):c.654A>G (p.Gln218=) rs1045119422
NM_000251.2(MSH2):c.667C>G (p.Leu223Val) rs1558461660
NM_000251.2(MSH2):c.716A>G (p.Gln239Arg) rs199676483
NM_000251.2(MSH2):c.728G>A (p.Arg243Gln) rs63751455
NM_000251.2(MSH2):c.731T>C (p.Leu244Ser) rs1553351657
NM_000251.2(MSH2):c.764G>A (p.Ser255Asn) rs763184168
NM_000251.2(MSH2):c.775C>T (p.Pro259Ser) rs587781294
NM_000251.2(MSH2):c.812C>G (p.Ser271Cys) rs139891783
NM_000251.2(MSH2):c.814G>A (p.Ala272Thr) rs1558463956
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.835C>G (p.Leu279Val) rs375351205
NM_000251.2(MSH2):c.843A>T (p.Ser281=) rs150197753
NM_000251.2(MSH2):c.855C>G (p.Asn285Lys) rs759242666
NM_000251.2(MSH2):c.905T>C (p.Leu302Ser) rs63749914
NM_000251.2(MSH2):c.913G>A (p.Ala305Thr) rs63751454
NM_000251.2(MSH2):c.95C>G (p.Thr32Ser) rs552361923
NM_000251.2(MSH2):c.97A>C (p.Thr33Pro) rs63751107
NM_000251.2(MSH2):c.991A>G (p.Asn331Asp) rs267607938
NM_001258281.1(MSH2):c.-87G>A rs552303079

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