ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Total variants: 131
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HGVS dbSNP
NM_000251.2(MSH2):c.-3G>C rs587779960
NM_000251.2(MSH2):c.-9G>A rs547444746
NM_000251.2(MSH2):c.1043A>G (p.Gln348Arg) rs773177076
NM_000251.2(MSH2):c.1045C>G (p.Pro349Ala) rs267607939
NM_000251.2(MSH2):c.1077-7A>G rs370807334
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.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.1223A>G (p.Tyr408Cys) rs63750379
NM_000251.2(MSH2):c.1225C>A (p.Gln409Lys) rs151244108
NM_000251.2(MSH2):c.123C>G (p.Asp41Glu) rs761960690
NM_000251.2(MSH2):c.1243C>T (p.Pro415Ser) rs35717997
NM_000251.2(MSH2):c.1276+16G>A rs368120695
NM_000251.2(MSH2):c.1276+7A>G rs748554540
NM_000251.2(MSH2):c.128A>G (p.Tyr43Cys) rs17217723
NM_000251.2(MSH2):c.1301C>T (p.Ala434Val) rs768070717
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>T (p.Arg444Leu) rs557339938
NM_000251.2(MSH2):c.1347G>C (p.Lys449Asn) rs587781331
NM_000251.2(MSH2):c.1360A>G (p.Ile454Val) rs587781627
NM_000251.2(MSH2):c.1361T>G (p.Ile454Arg) rs1060502025
NM_000251.2(MSH2):c.1387-4G>C rs376796243
NM_000251.2(MSH2):c.138C>G (p.His46Gln) rs33946261
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.1560A>G (p.Gly520=) rs63750820
NM_000251.2(MSH2):c.1593A>C (p.Lys531Asn) rs1553366599
NM_000251.2(MSH2):c.159C>T (p.Ala53=) rs780178752
NM_000251.2(MSH2):c.1600C>T (p.Arg534Cys) rs63750029
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.1662-10C>T rs752606387
NM_000251.2(MSH2):c.1706A>G (p.Glu569Gly) rs786201077
NM_000251.2(MSH2):c.1714_1715delinsAT (p.Glu572Ile) rs1558514635
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.1792G>A (p.Val598Met) rs778152746
NM_000251.2(MSH2):c.1819A>G (p.Ser607Gly) rs772991620
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.1927G>A (p.Glu643Lys) rs374840361
NM_000251.2(MSH2):c.1938T>C (p.Asp646=) rs775484022
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.2005G>T (p.Gly669Cys) rs63751668
NM_000251.2(MSH2):c.2010C>T (p.Pro670=) rs766618212
NM_000251.2(MSH2):c.2038C>G (p.Arg680Gly) rs63749932
NM_000251.2(MSH2):c.2048G>T (p.Gly683Val) rs755920849
NM_000251.2(MSH2):c.2060T>C (p.Leu687Pro) rs587779133
NM_000251.2(MSH2):c.2082T>C (p.Phe694=) rs748210094
NM_000251.2(MSH2):c.211+8C>T rs267607916
NM_000251.2(MSH2):c.2110A>G (p.Ile704Val) rs730881764
NM_000251.2(MSH2):c.212-4T>G rs1558456954
NM_000251.2(MSH2):c.2203A>G (p.Ile735Val) rs2229061
NM_000251.2(MSH2):c.220A>C (p.Asn74His) rs150548839
NM_000251.2(MSH2):c.2211-5T>G rs368596736
NM_000251.2(MSH2):c.2211-6C>A rs267608003
NM_000251.2(MSH2):c.2260A>G (p.Thr754Ala) rs757268664
NM_000251.2(MSH2):c.2260A>T (p.Thr754Ser) rs757268664
NM_000251.2(MSH2):c.2267C>G (p.Thr756Ser) rs372383829
NM_000251.2(MSH2):c.2308A>G (p.Ile770Val) rs63750684
NM_000251.2(MSH2):c.2354A>C (p.His785Pro) rs200252727
NM_000251.2(MSH2):c.2354A>G (p.His785Arg) rs200252727
NM_000251.2(MSH2):c.2362A>C (p.Thr788Pro) rs774440277
NM_000251.2(MSH2):c.2400A>G (p.Leu800=) rs201298777
NM_000251.2(MSH2):c.2407A>G (p.Thr803Ala) rs63751168
NM_000251.2(MSH2):c.2437A>G (p.Met813Val) rs63749841
NM_000251.2(MSH2):c.2458+8C>G rs189025757
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.2571T>G (p.Ile857Met) rs1400051085
NM_000251.2(MSH2):c.2580G>T (p.Ser860=) rs752428475
NM_000251.2(MSH2):c.2621A>G (p.Tyr874Cys) rs775390721
NM_000251.2(MSH2):c.2634+7C>G rs905179122
NM_000251.2(MSH2):c.2714C>T (p.Thr905Ile) rs267608022
NM_000251.2(MSH2):c.2729A>G (p.Gln910Arg) rs1553370878
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.2785C>T (p.Arg929Ter) rs551060742
NM_000251.2(MSH2):c.2798C>T (p.Thr933Ile) rs587779968
NM_000251.2(MSH2):c.2801C>A (p.Thr934Lys) rs587779969
NM_000251.2(MSH2):c.2802G>A (p.Thr934=) rs150259097
NM_000251.2(MSH2):c.336C>A (p.Ser112=) rs34312619
NM_000251.2(MSH2):c.367-19A>T rs730881783
NM_000251.2(MSH2):c.367-3T>C rs1558458845
NM_000251.2(MSH2):c.383T>G (p.Leu128Arg) rs730881768
NM_000251.2(MSH2):c.386C>G (p.Ser129Cys) rs587779972
NM_000251.2(MSH2):c.421A>G (p.Met141Val) rs193922374
NM_000251.2(MSH2):c.433A>G (p.Ile145Val) rs876659264
NM_000251.2(MSH2):c.440T>G (p.Val147Gly) rs760851623
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.478C>A (p.Gln160Lys) rs63751426
NM_000251.2(MSH2):c.4_21dup (p.Ala2_Glu7dup) rs281864943
NM_000251.2(MSH2):c.547C>A (p.Gln183Lys) rs63750037
NM_000251.2(MSH2):c.557A>G (p.Asn186Ser) rs151129360
NM_000251.2(MSH2):c.566C>G (p.Ala189Gly) rs141021599
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.633G>A (p.Gly211=) rs1558459840
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.6G>C (p.Ala2=) rs368270856
NM_000251.2(MSH2):c.728G>A (p.Arg243Gln) rs63751455
NM_000251.2(MSH2):c.786G>T (p.Glu262Asp) rs754820584
NM_000251.2(MSH2):c.792+5A>G rs267607935
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.820A>G (p.Ile274Val) rs371944271
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.849T>C (p.Asp283=) rs876659344
NM_000251.2(MSH2):c.860G>C (p.Gly287Ala) rs587782567
NM_000251.2(MSH2):c.885C>G (p.Asp295Glu) rs201334592
NM_000251.2(MSH2):c.894G>C (p.Gln298His) rs587781397
NM_000251.2(MSH2):c.917C>T (p.Ala306Val) rs1553352536
NM_000251.2(MSH2):c.964G>A (p.Gly322Ser) rs773301485
NM_000251.2(MSH2):c.968C>T (p.Ser323Phe) rs63750732
NM_000251.2(MSH2):c.991A>G (p.Asn331Asp) rs267607938
NM_000251.2(MSH2):c.996G>A (p.Lys332=) rs863224343

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