ClinVar Miner

List of variants in gene MSH6 reported by University of Washington Department of Laboratory Medicine,University of Washington

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Total variants: 98
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HGVS dbSNP
NM_000179.2(MSH6):c.1021T>G (p.Ser341Ala) rs1558660119
NM_000179.2(MSH6):c.1046A>G (p.Gln349Arg) rs869312797
NM_000179.2(MSH6):c.1081C>T (p.Arg361Cys) rs587782651
NM_000179.2(MSH6):c.1082G>A (p.Arg361His) rs63750440
NM_000179.2(MSH6):c.1093T>C (p.Trp365Arg) rs752628520
NM_000179.2(MSH6):c.10C>T (p.Gln4Ter) rs786201042
NM_000179.2(MSH6):c.1106C>T (p.Thr369Ile) rs375974046
NM_000179.2(MSH6):c.1109T>C (p.Leu370Ser) rs587779204
NM_000179.2(MSH6):c.1130_1134AGAGA[1] (p.Arg378_Arg379insTer) rs267608077
NM_000179.2(MSH6):c.1168G>A (p.Asp390Asn) rs147737737
NM_000179.2(MSH6):c.1184C>T (p.Thr395Ile) rs767658494
NM_000179.2(MSH6):c.1207C>A (p.Leu403Ile) rs876659223
NM_000179.2(MSH6):c.1290G>A (p.Gly430=) rs1558661242
NM_000179.2(MSH6):c.133G>T (p.Gly45Cys) rs978968846
NM_000179.2(MSH6):c.1352del (p.Phe451fs) rs869312769
NM_000179.2(MSH6):c.1364A>C (p.Asn455Thr) rs200938360
NM_000179.2(MSH6):c.1400G>A (p.Gly467Asp) rs1558661547
NM_000179.2(MSH6):c.1401C>T (p.Gly467=) rs1558661556
NM_000179.2(MSH6):c.1402C>T (p.Arg468Cys) rs369456858
NM_000179.2(MSH6):c.1483C>T (p.Arg495Ter) rs587779212
NM_000179.2(MSH6):c.1599G>C (p.Glu533Asp) rs373726731
NM_000179.2(MSH6):c.1615_1617CTT[1] (p.Leu540del) rs1064793600
NM_000179.2(MSH6):c.1675T>C (p.Cys559Arg) rs1558662565
NM_000179.2(MSH6):c.1754T>C (p.Leu585Pro) rs587779220
NM_000179.2(MSH6):c.1809G>A (p.Lys603=) rs876660790
NM_000179.2(MSH6):c.1822A>G (p.Ile608Val) rs201613780
NM_000179.2(MSH6):c.1847C>G (p.Ser616Cys) rs772363120
NM_000179.2(MSH6):c.1904G>A (p.Arg635Lys) rs1558663439
NM_000179.2(MSH6):c.1915G>A (p.Glu639Lys) rs143517321
NM_000179.2(MSH6):c.2079dup (p.Cys694fs) rs267608083
NM_000179.2(MSH6):c.2150_2153del (p.Val717fs) rs267608058
NM_000179.2(MSH6):c.2161A>C (p.Arg721=) rs537604099
NM_000179.2(MSH6):c.2195G>A (p.Arg732Gln) rs749746725
NM_000179.2(MSH6):c.2210C>T (p.Ala737Val) rs869312798
NM_000179.2(MSH6):c.2287G>A (p.Asp763Asn) rs1558664969
NM_000179.2(MSH6):c.2315G>A (p.Arg772Gln) rs63750725
NM_000179.2(MSH6):c.2342C>T (p.Pro781Leu) rs1553413710
NM_000179.2(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.2(MSH6):c.260+265G>A rs3136231
NM_000179.2(MSH6):c.260+279C>T rs869312601
NM_000179.2(MSH6):c.260+84T>G rs869312603
NM_000179.2(MSH6):c.261-14C>T rs369366445
NM_000179.2(MSH6):c.261-3611A>G rs528466684
NM_000179.2(MSH6):c.261-565C>T rs553631780
NM_000179.2(MSH6):c.2636C>A (p.Ala879Asp) rs1558666061
NM_000179.2(MSH6):c.2660T>C (p.Leu887Pro) rs1558666142
NM_000179.2(MSH6):c.2701C>A (p.Arg901Ser) rs772514245
NM_000179.2(MSH6):c.2743G>A (p.Ala915Thr) rs1558666565
NM_000179.2(MSH6):c.2743G>T (p.Ala915Ser) rs1558666565
NM_000179.2(MSH6):c.2846_2847AG[1] (p.Ser950fs) rs869312770
NM_000179.2(MSH6):c.2876G>A (p.Arg959His) rs757653982
NM_000179.2(MSH6):c.3010A>G (p.Lys1004Glu) rs1558667702
NM_000179.2(MSH6):c.3029C>T (p.Thr1010Ile) rs768925694
NM_000179.2(MSH6):c.3067G>T (p.Glu1023Ter) rs267608059
NM_000179.2(MSH6):c.3126A>C (p.Lys1042Asn) rs1558668218
NM_000179.2(MSH6):c.3139T>C (p.Trp1047Arg) rs1114167753
NM_000179.2(MSH6):c.3172+875A>C rs187192537
NM_000179.2(MSH6):c.3173-18T>A rs189672273
NM_000179.2(MSH6):c.3185G>A (p.Cys1062Tyr) rs1558386797
NM_000179.2(MSH6):c.3203G>A (p.Arg1068Gln) rs398123230
NM_000179.2(MSH6):c.3214G>A (p.Gly1072Ser) rs1558386938
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3227G>A (p.Arg1076His) rs779617676
NM_000179.2(MSH6):c.3261dup (p.Phe1088fs) rs267608078
NM_000179.2(MSH6):c.3283C>T (p.Arg1095Cys) rs376243329
NM_000179.2(MSH6):c.3300G>A (p.Thr1100=) rs540252208
NM_000179.2(MSH6):c.3426G>A (p.Thr1142=) rs747771350
NM_000179.2(MSH6):c.3431T>G (p.Met1144Arg) rs864622607
NM_000179.2(MSH6):c.3438+2T>C rs1033749344
NM_000179.2(MSH6):c.3442G>A (p.Gly1148Ser) rs63750257
NM_000179.2(MSH6):c.3470G>A (p.Gly1157Asp) rs752212361
NM_000179.2(MSH6):c.3508A>C (p.Ile1170Leu) rs1558389423
NM_000179.2(MSH6):c.3557-40T>A rs189436849
NM_000179.2(MSH6):c.3610G>A (p.Ala1204Thr) rs869312799
NM_000179.2(MSH6):c.3722G>A (p.Cys1241Tyr) rs1021631442
NM_000179.2(MSH6):c.3801+2T>C rs1558392617
NM_000179.2(MSH6):c.3801+5G>A rs201080919
NM_000179.2(MSH6):c.3939_3957dup (p.Ala1320delinsSerLysGlyThrTer) rs63750767
NM_000179.2(MSH6):c.3963A>G (p.Arg1321=) rs267608125
NM_000179.2(MSH6):c.3964G>A (p.Glu1322Lys) rs1553333707
NM_000179.2(MSH6):c.4018A>G (p.Ser1340Gly) rs1558395603
NM_000179.2(MSH6):c.44C>T (p.Pro15Leu) rs869312800
NM_000179.2(MSH6):c.457G>T (p.Gly153Cys) rs1060502885
NM_000179.2(MSH6):c.458-1174T>C rs869312602
NM_000179.2(MSH6):c.458-509G>A rs556222101
NM_000179.2(MSH6):c.458-518G>T rs869312600
NM_000179.2(MSH6):c.475G>A (p.Ala159Thr) rs1553411396
NM_000179.2(MSH6):c.511G>C (p.Glu171Gln) rs1558656518
NM_000179.2(MSH6):c.542A>C (p.Glu181Ala) rs1558656620
NM_000179.2(MSH6):c.556G>T (p.Asp186Tyr) rs1212607928
NM_000179.2(MSH6):c.627+267G>A rs772499816
NM_000179.2(MSH6):c.627+566T>G rs869312604
NM_000179.2(MSH6):c.73G>T (p.Ala25Ser) rs267608026
NM_000179.2(MSH6):c.884A>G (p.Lys295Arg) rs267608051
NM_000179.2(MSH6):c.884A>T (p.Lys295Ile) rs267608051
NM_000179.2(MSH6):c.893G>A (p.Arg298Gln) rs765237563
NM_000179.2(MSH6):c.911T>C (p.Val304Ala) rs1481054050
NM_000179.2(MSH6):c.971A>G (p.Lys324Arg) rs1558659961

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