ClinVar Miner

List of variants in gene MSH6 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 54
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HGVS dbSNP
NM_000179.2(MSH6):c.-8C>T rs565211544
NM_000179.2(MSH6):c.1061G>T (p.Gly354Val) rs730881788
NM_000179.2(MSH6):c.1186C>G (p.Leu396Val) rs2020908
NM_000179.2(MSH6):c.1241G>A (p.Trp414Ter) rs587779914
NM_000179.2(MSH6):c.1345C>T (p.Leu449=) rs3136333
NM_000179.2(MSH6):c.1508C>G (p.Ser503Cys) rs63750897
NM_000179.2(MSH6):c.1524G>A (p.Val508=) rs878853705
NM_000179.2(MSH6):c.1665A>G (p.Ala555=) rs146785465
NM_000179.2(MSH6):c.1795G>C (p.Gly599Arg) rs756043669
NM_000179.2(MSH6):c.1795G>T (p.Gly599Ter) rs756043669
NM_000179.2(MSH6):c.2161A>C (p.Arg721=) rs537604099
NM_000179.2(MSH6):c.2253T>C (p.Asn751=) rs2020913
NM_000179.2(MSH6):c.2281A>G (p.Arg761Gly) rs199876321
NM_000179.2(MSH6):c.2314C>A (p.Arg772=) rs63750138
NM_000179.2(MSH6):c.260+10T>G rs193922342
NM_000179.2(MSH6):c.260+22C>G rs55927047
NM_000179.2(MSH6):c.261-36A>G rs1800931
NM_000179.2(MSH6):c.2633T>C (p.Val878Ala) rs2020912
NM_000179.2(MSH6):c.2653A>G (p.Lys885Glu) rs587782593
NM_000179.2(MSH6):c.2731C>T (p.Arg911Ter) rs63751017
NM_000179.2(MSH6):c.2832_2833del (p.Ile944fs) rs730881827
NM_000179.2(MSH6):c.3084A>T (p.Ser1028=) rs786201843
NM_000179.2(MSH6):c.3306T>A (p.Thr1102=) rs2020910
NM_000179.2(MSH6):c.3339T>G (p.Ile1113Met) rs786202044
NM_000179.2(MSH6):c.3478G>T (p.Val1160Phe) rs376799914
NM_000179.2(MSH6):c.3725G>A (p.Arg1242His) rs63750119
NM_000179.2(MSH6):c.3729A>G (p.Thr1243=) rs773807182
NM_000179.2(MSH6):c.3801+17T>C rs3136365
NM_000179.2(MSH6):c.457+13A>G rs1800933
NM_000179.2(MSH6):c.457+52T>A rs3136282
NM_000179.2(MSH6):c.628-2A>G rs1114167725
NM_000179.2(MSH6):c.628-56C>T rs1800936
NM_000179.2(MSH6):c.81C>G (p.Ala27=) rs781496151
NM_000179.2(MSH6):c.984C>T (p.Ser328=) rs138143769
NM_000179.3(MSH6):c.1164C>T (p.His388=) rs55708305
NM_000179.3(MSH6):c.116G>A (p.Gly39Glu) rs1042821
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala) rs63751005
NM_000179.3(MSH6):c.186C>A (p.Arg62=) rs1042820
NM_000179.3(MSH6):c.2272C>T (p.Leu758=) rs56371757
NM_000179.3(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.3(MSH6):c.2429del (p.Glu810fs) rs1572727176
NM_000179.3(MSH6):c.276A>G (p.Pro92=) rs1800932
NM_000179.3(MSH6):c.3202C>T rs63749843
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=) rs3136351
NM_000179.3(MSH6):c.3261del rs267608078
NM_000179.3(MSH6):c.3270G>C (p.Glu1090Asp) rs876660165
NM_000179.3(MSH6):c.3438+14A>T rs2020911
NM_000179.3(MSH6):c.3439-2A>G rs267608098
NM_000179.3(MSH6):c.354A>G (p.Thr118=) rs558590898
NM_000179.3(MSH6):c.3586G>T (p.Glu1196Ter) rs75095286
NM_000179.3(MSH6):c.540T>C (p.Asp180=) rs1800935
NM_000179.3(MSH6):c.642C>T (p.Tyr214=) rs1800937
NM_000179.3(MSH6):c.663A>C (p.Glu221Asp) rs41557217
NM_001281492.1(MSH6):c.1887_1888AG[2] (p.Arg631fs) rs1114167721

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