ClinVar Miner

List of variants in gene MSH2 reported as likely benign for not provided

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Gene type:
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Total variants: 175
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HGVS dbSNP
NM_000251.2(MSH2):c.-179C>T rs17224094
NM_000251.2(MSH2):c.-185C>A rs188036046
NM_000251.2(MSH2):c.-68-34T>C rs17217709
NM_000251.2(MSH2):c.1017A>G (p.Gln339=) rs876659238
NM_000251.2(MSH2):c.1077-15G>T rs753277524
NM_000251.2(MSH2):c.108T>G (p.Leu36=) rs876659034
NM_000251.2(MSH2):c.1155A>G (p.Pro385=) rs1553356617
NM_000251.2(MSH2):c.1158T>C (p.Asp386=) rs1060504421
NM_000251.2(MSH2):c.1176G>A (p.Lys392=) rs1573484863
NM_000251.2(MSH2):c.1185A>G (p.Gln395=) rs1032873228
NM_000251.2(MSH2):c.1191A>G (p.Gln397=) rs768694189
NM_000251.2(MSH2):c.1209T>C (p.Asp403=) rs1060504420
NM_000251.2(MSH2):c.1217G>A (p.Arg406Gln) rs146567853
NM_000251.2(MSH2):c.123C>T (p.Asp41=) rs761960690
NM_000251.2(MSH2):c.1251T>C (p.Val417=) rs1553356731
NM_000251.2(MSH2):c.1275A>G (p.Glu425=) rs63751650
NM_000251.2(MSH2):c.1277-16T>C rs368653974
NM_000251.2(MSH2):c.1277-4T>C rs1057521428
NM_000251.2(MSH2):c.132G>A (p.Thr44=) rs766856128
NM_000251.2(MSH2):c.1353G>A (p.Gln451=) rs1060504415
NM_000251.2(MSH2):c.1356A>G (p.Glu452=) rs63751212
NM_000251.2(MSH2):c.135G>A (p.Ala45=) rs890172773
NM_000251.2(MSH2):c.1386+104C>T rs17224444
NM_000251.2(MSH2):c.1387-4G>C rs376796243
NM_000251.2(MSH2):c.1387-8G>T rs187525243
NM_000251.2(MSH2):c.1389G>T (p.Val463=) rs1553365702
NM_000251.2(MSH2):c.1440A>G (p.Glu480=) rs138049198
NM_000251.2(MSH2):c.1488A>G (p.Leu496=) rs267607960
NM_000251.2(MSH2):c.1510+189C>G rs17218202
NM_000251.2(MSH2):c.1513T>C (p.Leu505=) rs1553366502
NM_000251.2(MSH2):c.1545C>T (p.Ser515=) rs1553366537
NM_000251.2(MSH2):c.156G>A (p.Leu52=) rs750241099
NM_000251.2(MSH2):c.156G>C (p.Leu52=) rs750241099
NM_000251.2(MSH2):c.159C>T (p.Ala53=) rs780178752
NM_000251.2(MSH2):c.15G>A (p.Pro5=) rs758054171
NM_000251.2(MSH2):c.1605C>T (p.Asn535=) rs587779098
NM_000251.2(MSH2):c.162C>T (p.Ala54=) rs1045377929
NM_000251.2(MSH2):c.1638G>A (p.Lys546=) rs372350768
NM_000251.2(MSH2):c.1647T>C (p.Val549=) rs763525239
NM_000251.2(MSH2):c.1656C>T (p.Thr552=) rs876660600
NM_000251.2(MSH2):c.165G>A (p.Arg55=) rs772201676
NM_000251.2(MSH2):c.1661+6dup rs863224832
NM_000251.2(MSH2):c.1666T>C (p.Leu556=) rs61756466
NM_000251.2(MSH2):c.1680T>C (p.Asn560=) rs200056411
NM_000251.2(MSH2):c.1719C>G (p.Ala573=) rs1553367674
NM_000251.2(MSH2):c.1737A>G (p.Lys579=) rs61756467
NM_000251.2(MSH2):c.1746C>A (p.Val582=) rs786201486
NM_000251.2(MSH2):c.1760-10T>A rs767536391
NM_000251.2(MSH2):c.1760-3C>T rs786202843
NM_000251.2(MSH2):c.1760-4A>G rs1060504409
NM_000251.2(MSH2):c.1764T>C (p.Tyr588=) rs63750844
NM_000251.2(MSH2):c.1863A>T (p.Arg621=) rs786203119
NM_000251.2(MSH2):c.186G>A (p.Gly62=) rs750058876
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.2005+10C>T rs1558518671
NM_000251.2(MSH2):c.2006-15T>C rs1057524452
NM_000251.2(MSH2):c.2006-4G>A rs369853630
NM_000251.2(MSH2):c.2043A>G (p.Gln681=) rs730881763
NM_000251.2(MSH2):c.2061C>G (p.Leu687=) rs63750032
NM_000251.2(MSH2):c.207G>A (p.Pro69=) rs1295445617
NM_000251.2(MSH2):c.2094G>A (p.Glu698=) rs773555449
NM_000251.2(MSH2):c.2106G>A (p.Val702=) rs786201108
NM_000251.2(MSH2):c.211+8C>T rs267607916
NM_000251.2(MSH2):c.2112T>C (p.Ile704=) rs1553369124
NM_000251.2(MSH2):c.212-3A>T rs879255341
NM_000251.2(MSH2):c.213A>G (p.Gly71=) rs878853808
NM_000251.2(MSH2):c.2154A>G (p.Gln718=) rs63750810
NM_000251.2(MSH2):c.2166C>A (p.Val722=) rs1057520969
NM_000251.2(MSH2):c.2210+7G>T rs374675118
NM_000251.2(MSH2):c.2210+9A>G rs878853810
NM_000251.2(MSH2):c.2211-6C>T rs267608003
NM_000251.2(MSH2):c.2211-7G>A rs764972956
NM_000251.2(MSH2):c.2241A>T (p.Ile747=) rs1060504411
NM_000251.2(MSH2):c.2248T>C (p.Leu750=) rs527725593
NM_000251.2(MSH2):c.2289A>G (p.Ala763=) rs1553369710
NM_000251.2(MSH2):c.2310T>C (p.Ile770=) rs1195669050
NM_000251.2(MSH2):c.2403T>C (p.His801=) rs1060504410
NM_000251.2(MSH2):c.2415C>T (p.Leu805=) rs139317211
NM_000251.2(MSH2):c.2418C>T (p.Thr806=) rs876660451
NM_000251.2(MSH2):c.2459-5T>C rs1060504417
NM_000251.2(MSH2):c.2500G>A (p.Ala834Thr) rs63750757
NM_000251.2(MSH2):c.2508C>T (p.Phe836=) rs965790911
NM_000251.2(MSH2):c.2520A>G (p.Val840=) rs1057522090
NM_000251.2(MSH2):c.2545C>T (p.Leu849=) rs587778527
NM_000251.2(MSH2):c.2574A>G (p.Gly858=) rs1553370416
NM_000251.2(MSH2):c.2580G>T (p.Ser860=) rs752428475
NM_000251.2(MSH2):c.2583A>G (p.Gln861=) rs63751093
NM_000251.2(MSH2):c.2595C>T (p.Ile865=) rs547695133
NM_000251.2(MSH2):c.2616G>A (p.Lys872=) rs1573579171
NM_000251.2(MSH2):c.279_281delTCT rs267607919
NM_000251.2(MSH2):c.2802G>A (p.Thr934=) rs150259097
NM_000251.2(MSH2):c.2804G>A (p.Ter935=) rs876658335
NM_000251.2(MSH2):c.285T>C (p.Val95=) rs1369335343
NM_000251.2(MSH2):c.317G>A (p.Arg106Lys) rs41295286
NM_000251.2(MSH2):c.333A>G (p.Ala111=) rs1060504408
NM_000251.2(MSH2):c.336C>A (p.Ser112=) rs34312619
NM_000251.2(MSH2):c.366+4A>C rs876659880
NM_000251.2(MSH2):c.366+88G>A rs864622763
NM_000251.2(MSH2):c.384C>A (p.Leu128=) rs766694099
NM_000251.2(MSH2):c.447T>C (p.Gly149=) rs786203142
NM_000251.2(MSH2):c.4G>A (p.Ala2Thr) rs63750466
NM_000251.2(MSH2):c.501T>C (p.Asp167=) rs757733033
NM_000251.2(MSH2):c.531A>G (p.Glu177=) rs1060504416
NM_000251.2(MSH2):c.552C>T (p.Phe184=) rs786202238
NM_000251.2(MSH2):c.606C>G (p.Pro202=) rs63750600
NM_000251.2(MSH2):c.606C>T (p.Pro202=) rs63750600
NM_000251.2(MSH2):c.663A>G (p.Gly221=) rs1553351570
NM_000251.2(MSH2):c.699C>A (p.Ser233=) rs1403583908
NM_000251.2(MSH2):c.6G>C (p.Ala2=) rs368270856
NM_000251.2(MSH2):c.762T>C (p.Asn254=) rs587779180
NM_000251.2(MSH2):c.792+205C>T rs138284283
NM_000251.2(MSH2):c.798A>T (p.Ala266=) rs878853825
NM_000251.2(MSH2):c.810G>T (p.Leu270=) rs876660293
NM_000251.2(MSH2):c.816G>T (p.Ala272=) rs368912987
NM_000251.2(MSH2):c.819A>G (p.Val273=) rs146577635
NM_000251.2(MSH2):c.843A>G (p.Ser281=) rs150197753
NM_000251.2(MSH2):c.858T>C (p.Phe286=) rs1553352479
NM_000251.2(MSH2):c.933C>T (p.Asn311=) rs1060504424
NM_000251.2(MSH2):c.939T>C (p.Phe313=) rs970103452
NM_000251.2(MSH2):c.942+20_942+29del rs11309117
NM_000251.2(MSH2):c.966C>T (p.Gly322=) rs878853829
NM_000251.2(MSH2):c.972G>A (p.Gln324=) rs63750505
NM_000251.2(MSH2):c.978G>A (p.Leu326=) rs1060504418
NM_000251.2(MSH2):c.978G>C (p.Leu326=) rs1060504418
NM_000251.2(MSH2):c.984C>G (p.Ala328=) rs4987189
NM_000251.2(MSH2):c.984C>T (p.Ala328=) rs4987189
NM_000251.3(MSH2):c.1095T>C (p.Ala365=) rs746989189
NM_000251.3(MSH2):c.1152C>T (p.Phe384=) rs1553356612
NM_000251.3(MSH2):c.1212T>C (p.Cys404=) rs1316998014
NM_000251.3(MSH2):c.1269A>G (p.Lys423=) rs1573485542
NM_000251.3(MSH2):c.1387-14_1387-11del rs370436680
NM_000251.3(MSH2):c.1387-7T>C rs1246482962
NM_000251.3(MSH2):c.1441T>C (p.Leu481=) rs1573547857
NM_000251.3(MSH2):c.1461C>T (p.Asp487=) rs35107951
NM_000251.3(MSH2):c.1511-10G>A rs587779096
NM_000251.3(MSH2):c.1511-10G>C rs587779096
NM_000251.3(MSH2):c.1511-10_1511-7del rs864622529
NM_000251.3(MSH2):c.1524C>G (p.Gly508=) rs1573553127
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=) rs63750330
NM_000251.3(MSH2):c.1661+8A>G rs1573553877
NM_000251.3(MSH2):c.1671T>A (p.Thr557=) rs1573560272
NM_000251.3(MSH2):c.171G>A (p.Val57=) rs1321481324
NM_000251.3(MSH2):c.1730T>C (p.Ile577Thr) rs63749910
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser) rs41295288
NM_000251.3(MSH2):c.1794G>A (p.Val598=) rs1573566431
NM_000251.3(MSH2):c.1797A>G (p.Leu599=) rs1573566472
NM_000251.3(MSH2):c.1890A>G (p.Gly630=) rs778523544
NM_000251.3(MSH2):c.189G>C (p.Val63=) rs1283798201
NM_000251.3(MSH2):c.2005+7A>T rs1573567708
NM_000251.3(MSH2):c.2037T>C (p.Ile679=) rs1573569810
NM_000251.3(MSH2):c.2049G>A (p.Gly683=) rs1573569899
NM_000251.3(MSH2):c.2211-11_2211-9del rs1338860818
NM_000251.3(MSH2):c.223C>T (p.Leu75=) rs1573436246
NM_000251.3(MSH2):c.2250G>A (p.Leu750=) rs1573573760
NM_000251.3(MSH2):c.2307C>T (p.Tyr769=) rs1573574086
NM_000251.3(MSH2):c.2568T>C (p.Tyr856=) rs768137500
NM_000251.3(MSH2):c.258A>G (p.Glu86=) rs1573436461
NM_000251.3(MSH2):c.2635-8T>A rs1573582329
NM_000251.3(MSH2):c.2790A>C (p.Ile930=) rs587779155
NM_000251.3(MSH2):c.282G>C (p.Leu94=) rs752387348
NM_000251.3(MSH2):c.339G>A (p.Lys113=) rs35898375
NM_000251.3(MSH2):c.366+4_366+7dup rs1233795904
NM_000251.3(MSH2):c.366+9C>A rs1553350269
NM_000251.3(MSH2):c.367-4T>C rs876660764
NM_000251.3(MSH2):c.39C>T (p.Ser13=) rs1060502015
NM_000251.3(MSH2):c.435T>C (p.Ile145=) rs63750124
NM_000251.3(MSH2):c.477A>G (p.Arg159=) rs1573440947
NM_000251.3(MSH2):c.51C>T (p.Val17=) rs397515879
NM_000251.3(MSH2):c.55T>C (p.Phe19Leu) rs141711342
NM_000251.3(MSH2):c.579G>A (p.Gln193=) rs1453901558
NM_000251.3(MSH2):c.646-5A>T rs1400699567
NM_000251.3(MSH2):c.696T>C (p.Phe232=) rs1286296966
NM_000251.3(MSH2):c.720C>T (p.Asp240=) rs1259574366
NM_000251.3(MSH2):c.815C>T (p.Ala272Val) rs34136999
NM_000251.3(MSH2):c.943-10T>G rs1573456010

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