ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance for Hereditary nonpolyposis colorectal cancer type 5

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Total variants: 188
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HGVS dbSNP
NM_000179.2(MSH6):c.*1A>G rs587781604
NM_000179.2(MSH6):c.*24_*28del rs587779200
NM_000179.2(MSH6):c.-6G>C rs730881822
NM_000179.2(MSH6):c.-8C>T rs565211544
NM_000179.2(MSH6):c.102_104CGC[1] (p.Ala37del) rs1553408197
NM_000179.2(MSH6):c.1037C>T (p.Ser346Phe) rs567785169
NM_000179.2(MSH6):c.1061G>T (p.Gly354Val) rs730881788
NM_000179.2(MSH6):c.1063G>A (p.Gly355Ser) rs587778531
NM_000179.2(MSH6):c.107C>T (p.Ala36Val) rs61756469
NM_000179.2(MSH6):c.1082G>A (p.Arg361His) rs63750440
NM_000179.2(MSH6):c.1106C>T (p.Thr369Ile) rs375974046
NM_000179.2(MSH6):c.1144C>T (p.His382Tyr) rs587779207
NM_000179.2(MSH6):c.115G>C (p.Gly39Arg) rs751838296
NM_000179.2(MSH6):c.118G>A (p.Ala40Thr) rs754231971
NM_000179.2(MSH6):c.1190A>G (p.Tyr397Cys) rs63750065
NM_000179.2(MSH6):c.124C>T (p.Pro42Ser) rs34014629
NM_000179.2(MSH6):c.1364A>C (p.Asn455Thr) rs200938360
NM_000179.2(MSH6):c.136G>A (p.Gly46Arg) rs863224616
NM_000179.2(MSH6):c.150G>T (p.Trp50Cys) rs876659674
NM_000179.2(MSH6):c.1526T>C (p.Val509Ala) rs63751005
NM_000179.2(MSH6):c.1528_1530AGG[1] (p.Arg511del) rs993163672
NM_000179.2(MSH6):c.1565A>G (p.Gln522Arg) rs63751009
NM_000179.2(MSH6):c.1599G>C (p.Glu533Asp) rs373726731
NM_000179.2(MSH6):c.1633A>G (p.Lys545Glu) rs1064793403
NM_000179.2(MSH6):c.1652G>A (p.Gly551Asp) rs587779917
NM_000179.2(MSH6):c.1696G>A (p.Gly566Arg) rs63749973
NM_000179.2(MSH6):c.1729C>T (p.Arg577Cys) rs542838372
NM_000179.2(MSH6):c.1730G>A (p.Arg577His) rs376220212
NM_000179.2(MSH6):c.1732C>T (p.His578Tyr) rs768854566
NM_000179.2(MSH6):c.1746T>G (p.Phe582Leu) rs201518545
NM_000179.2(MSH6):c.175C>A (p.Pro59Thr) rs761033647
NM_000179.2(MSH6):c.1763A>G (p.His588Arg) rs786202725
NM_000179.2(MSH6):c.1786T>A (p.Phe596Ile) rs587779918
NM_000179.2(MSH6):c.1793A>G (p.Lys598Arg) rs587779919
NM_000179.2(MSH6):c.1820C>G (p.Thr607Arg) rs786201676
NM_000179.2(MSH6):c.1844G>C (p.Cys615Ser) rs730881793
NM_000179.2(MSH6):c.1847C>G (p.Ser616Cys) rs772363120
NM_000179.2(MSH6):c.1858G>A (p.Gly620Ser) rs876661043
NM_000179.2(MSH6):c.1867C>G (p.Pro623Ala) rs3136334
NM_000179.2(MSH6):c.1870G>A (p.Gly624Ser) rs868760377
NM_000179.2(MSH6):c.187T>C (p.Ser63Pro) rs763702846
NM_000179.2(MSH6):c.188C>A (p.Ser63Tyr) rs587779920
NM_000179.2(MSH6):c.1894A>G (p.Lys632Glu) rs755847154
NM_000179.2(MSH6):c.1932G>C (p.Arg644Ser) rs34938432
NM_000179.2(MSH6):c.1995G>C (p.Glu665Asp) rs587778532
NM_000179.2(MSH6):c.1999G>C (p.Asp667His) rs151086192
NM_000179.2(MSH6):c.2025G>C (p.Glu675Asp) rs587779223
NM_000179.2(MSH6):c.2027A>G (p.Lys676Arg) rs143643688
NM_000179.2(MSH6):c.2092C>G (p.Gln698Glu) rs63750832
NM_000179.2(MSH6):c.2107A>G (p.Met703Val) rs751867550
NM_000179.2(MSH6):c.2147C>T (p.Thr716Ile) rs587782805
NM_000179.2(MSH6):c.2175C>G (p.Ile725Met) rs63750304
NM_000179.2(MSH6):c.2177T>A (p.Phe726Tyr) rs574358605
NM_000179.2(MSH6):c.2203C>A (p.Leu735Ile) rs786204071
NM_000179.2(MSH6):c.2235T>G (p.Ile745Met) rs556339046
NM_000179.2(MSH6):c.2249C>A (p.Thr750Lys) rs730881817
NM_000179.2(MSH6):c.2281A>G (p.Arg761Gly) rs199876321
NM_000179.2(MSH6):c.2282G>A (p.Arg761Lys) rs587779233
NM_000179.2(MSH6):c.2291C>A (p.Thr764Asn) rs561198849
NM_000179.2(MSH6):c.2300C>G (p.Thr767Ser) rs587781462
NM_000179.2(MSH6):c.2300C>T (p.Thr767Ile) rs587781462
NM_000179.2(MSH6):c.2320C>G (p.Leu774Val) rs864622324
NM_000179.2(MSH6):c.2341C>A (p.Pro781Thr) rs587779235
NM_000179.2(MSH6):c.2384T>C (p.Ile795Thr) rs202127474
NM_000179.2(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.2(MSH6):c.2408A>G (p.Asp803Gly) rs63751450
NM_000179.2(MSH6):c.2417C>G (p.Ser806Cys) rs372990379
NM_000179.2(MSH6):c.2419G>A (p.Glu807Lys) rs587779923
NM_000179.2(MSH6):c.242C>T (p.Ala81Val) rs587779924
NM_000179.2(MSH6):c.2511C>G (p.His837Gln) rs587779925
NM_000179.2(MSH6):c.2518A>C (p.Ser840Arg) rs863224624
NM_000179.2(MSH6):c.254_256CCA[1] (p.Thr86del) rs1553408448
NM_000179.2(MSH6):c.2597A>C (p.Lys866Thr) rs190075874
NM_000179.2(MSH6):c.2624T>C (p.Met875Thr) rs774774596
NM_000179.2(MSH6):c.2633T>C (p.Val878Ala) rs2020912
NM_000179.2(MSH6):c.2641delinsAAAA (p.Gly881delinsLysSer) rs63751408
NM_000179.2(MSH6):c.2667G>T (p.Gln889His) rs149945495
NM_000179.2(MSH6):c.267C>G (p.Asp89Glu) rs762818044
NM_000179.2(MSH6):c.2827G>T (p.Asp943Tyr) rs143520357
NM_000179.2(MSH6):c.2876G>A (p.Arg959His) rs757653982
NM_000179.2(MSH6):c.2906A>T (p.Tyr969Phe) rs63749919
NM_000179.2(MSH6):c.2950A>C (p.Asn984His) rs146359682
NM_000179.2(MSH6):c.2951A>C (p.Asn984Thr) rs587779927
NM_000179.2(MSH6):c.2959A>G (p.Thr987Ala) rs746631156
NM_000179.2(MSH6):c.2960C>T (p.Thr987Ile) rs587779928
NM_000179.2(MSH6):c.2992T>A (p.Ser998Thr) rs730881800
NM_000179.2(MSH6):c.3037_3039AAG[1] (p.Lys1014del) rs267608073
NM_000179.2(MSH6):c.3071G>A (p.Arg1024Gln) rs372705506
NM_000179.2(MSH6):c.3100C>T (p.Arg1034Trp) rs587779930
NM_000179.2(MSH6):c.3111C>A (p.Phe1037Leu) rs587781673
NM_000179.2(MSH6):c.3113A>G (p.Tyr1038Cys) rs773357672
NM_000179.2(MSH6):c.3151G>A (p.Val1051Ile) rs576269342
NM_000179.2(MSH6):c.3163G>A (p.Ala1055Thr) rs587779254
NM_000179.2(MSH6):c.3181C>G (p.Leu1061Val) rs1553331250
NM_000179.2(MSH6):c.3200G>C (p.Ser1067Thr) rs730881803
NM_000179.2(MSH6):c.3205G>C (p.Gly1069Arg) rs764113705
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3220A>T (p.Met1074Leu) rs730881804
NM_000179.2(MSH6):c.3232G>C (p.Val1078Leu) rs587779932
NM_000179.2(MSH6):c.3233T>C (p.Val1078Ala) rs376452612
NM_000179.2(MSH6):c.3244C>T (p.Pro1082Ser) rs186240214
NM_000179.2(MSH6):c.3256C>G (p.Pro1086Ala) rs756108143
NM_000179.2(MSH6):c.3259C>G (p.Pro1087Ala) rs63750998
NM_000179.2(MSH6):c.3283C>T (p.Arg1095Cys) rs376243329
NM_000179.2(MSH6):c.3284G>A (p.Arg1095His) rs63750253
NM_000179.2(MSH6):c.3299C>T (p.Thr1100Met) rs63750442
NM_000179.2(MSH6):c.3334G>A (p.Asp1112Asn) rs773955368
NM_000179.2(MSH6):c.3364C>G (p.Gln1122Glu) rs1060502892
NM_000179.2(MSH6):c.3438+17G>C rs759737239
NM_000179.2(MSH6):c.3439-10T>A rs730881819
NM_000179.2(MSH6):c.3452C>G (p.Ala1151Gly) rs587782625
NM_000179.2(MSH6):c.3467T>C (p.Met1156Thr) rs876659549
NM_000179.2(MSH6):c.3478G>A (p.Val1160Ile) rs376799914
NM_000179.2(MSH6):c.3478G>T (p.Val1160Phe) rs376799914
NM_000179.2(MSH6):c.3529C>G (p.Leu1177Val) rs748398941
NM_000179.2(MSH6):c.3543C>G (p.Asp1181Glu) rs267608100
NM_000179.2(MSH6):c.3600A>G (p.Ile1200Met) rs587781482
NM_000179.2(MSH6):c.3604A>G (p.Met1202Val) rs369778514
NM_000179.2(MSH6):c.3605T>C (p.Met1202Thr) rs587779273
NM_000179.2(MSH6):c.3610G>A (p.Ala1204Thr) rs869312799
NM_000179.2(MSH6):c.361C>T (p.Arg121Cys) rs763593669
NM_000179.2(MSH6):c.3634G>A (p.Val1212Met) rs864622748
NM_000179.2(MSH6):c.364G>A (p.Glu122Lys) rs143036974
NM_000179.2(MSH6):c.3674C>T (p.Thr1225Met) rs63750370
NM_000179.2(MSH6):c.3679A>T (p.Ile1227Leu) rs587779282
NM_000179.2(MSH6):c.3686A>G (p.Asn1229Ser) rs730881807
NM_000179.2(MSH6):c.3706G>C (p.Ala1236Pro) rs1553333039
NM_000179.2(MSH6):c.3727A>T (p.Thr1243Ser) rs147453999
NM_000179.2(MSH6):c.3740C>G (p.Thr1247Ser) rs786204182
NM_000179.2(MSH6):c.3758T>C (p.Val1253Ala) rs202066386
NM_000179.2(MSH6):c.3762A>T (p.Glu1254Asp) rs375459388
NM_000179.2(MSH6):c.3787C>T (p.Arg1263Cys) rs367912290
NM_000179.2(MSH6):c.3788G>A (p.Arg1263His) rs147852216
NM_000179.2(MSH6):c.3800T>C (p.Met1267Thr) rs148445930
NM_000179.2(MSH6):c.3801+5G>A rs201080919
NM_000179.2(MSH6):c.3803C>T (p.Ala1268Val) rs587779293
NM_000179.2(MSH6):c.3824G>A (p.Cys1275Tyr) rs150990541
NM_000179.2(MSH6):c.3833C>G (p.Pro1278Arg) rs201191389
NM_000179.2(MSH6):c.3836G>A (p.Ser1279Asn) rs864622400
NM_000179.2(MSH6):c.3851C>T (p.Thr1284Met) rs63750836
NM_000179.2(MSH6):c.38A>C (p.Lys13Thr) rs41294988
NM_000179.2(MSH6):c.3939_3959dup (p.Gln1314_Ala1320dup) rs1553333670
NM_000179.2(MSH6):c.3949C>G (p.His1317Asp) rs759092293
NM_000179.2(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278
NM_000179.2(MSH6):c.3971_3973AGA[1] (p.Lys1325del) rs587779300
NM_000179.2(MSH6):c.3972G>C (p.Glu1324Asp) rs587779938
NM_000179.2(MSH6):c.4000C>T (p.Arg1334Trp) rs773763465
NM_000179.2(MSH6):c.4000_4001+17dup rs1064794929
NM_000179.2(MSH6):c.4002-14T>C rs587781041
NM_000179.2(MSH6):c.4002-4T>C rs370428032
NM_000179.2(MSH6):c.4004A>C (p.Glu1335Ala) rs564434147
NM_000179.2(MSH6):c.4005A>C (p.Glu1335Asp) rs786204130
NM_000179.2(MSH6):c.4039G>C (p.Ala1347Pro) rs730881809
NM_000179.2(MSH6):c.4068G>C (p.Leu1356Phe) rs192740549
NM_000179.2(MSH6):c.4077_4080dup (p.Ter1361IleextTer?) rs575068534
NM_000179.2(MSH6):c.4083_*3GACT[3] (p.Ter1361=) rs765313977
NM_000179.2(MSH6):c.41C>T (p.Ser14Phe) rs863224628
NM_000179.2(MSH6):c.431G>T (p.Ser144Ile) rs3211299
NM_000179.2(MSH6):c.457+52_457+53dup rs397839804
NM_000179.2(MSH6):c.458-13C>G rs1057522695
NM_000179.2(MSH6):c.491A>C (p.His164Pro) rs146469162
NM_000179.2(MSH6):c.503C>G (p.Ala168Gly) rs774162322
NM_000179.2(MSH6):c.521G>A (p.Arg174Lys) rs863224629
NM_000179.2(MSH6):c.533G>A (p.Arg178His) rs786204186
NM_000179.2(MSH6):c.535G>T (p.Ala179Ser) rs587781817
NM_000179.2(MSH6):c.59C>T (p.Ala20Val) rs63750664
NM_000179.2(MSH6):c.628-7C>A rs373129248
NM_000179.2(MSH6):c.637A>C (p.Thr213Pro) rs876659071
NM_000179.2(MSH6):c.643G>A (p.Val215Ile) rs145959653
NM_000179.2(MSH6):c.650A>G (p.Asp217Gly) rs554012110
NM_000179.2(MSH6):c.663A>C (p.Glu221Asp) rs41557217
NM_000179.2(MSH6):c.677A>G (p.Glu226Gly) rs587781777
NM_000179.2(MSH6):c.682G>A (p.Glu228Lys) rs587779947
NM_000179.2(MSH6):c.698C>G (p.Pro233Arg) rs142949377
NM_000179.2(MSH6):c.713C>A (p.Ser238Tyr) rs587782510
NM_000179.2(MSH6):c.719G>A (p.Arg240Gln) rs542848931
NM_000179.2(MSH6):c.727C>T (p.Arg243Cys) rs377216828
NM_000179.2(MSH6):c.73G>T (p.Ala25Ser) rs267608026
NM_000179.2(MSH6):c.749T>C (p.Val250Ala) rs587781275
NM_000179.2(MSH6):c.751A>G (p.Ile251Val) rs554884560
NM_000179.2(MSH6):c.831A>C (p.Glu277Asp) rs374486449
NM_000179.2(MSH6):c.866_867delinsAA (p.Gly289Glu) rs267608079
NM_000179.2(MSH6):c.884A>G (p.Lys295Arg) rs267608051
NM_000179.2(MSH6):c.905G>C (p.Arg302Thr) rs587781510
NM_000179.2(MSH6):c.910G>A (p.Val304Met) rs876661207
NM_000179.2(MSH6):c.941G>A (p.Ser314Asn) rs760100983
NM_000179.2(MSH6):c.94G>T (p.Gly32Cys) rs776859837
NM_000179.2(MSH6):c.972A>C (p.Lys324Asn) rs876658610

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