ClinVar Miner

List of variants in gene MSH6 studied for Endometrial carcinoma; Turcot syndrome; Hereditary nonpolyposis colorectal cancer type 5

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Total variants: 36
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HGVS dbSNP
NM_000179.2(MSH6):c.104C>T (p.Ala35Val) rs776547943
NM_000179.2(MSH6):c.1063G>A (p.Gly355Ser) rs587778531
NM_000179.2(MSH6):c.10C>T (p.Gln4Ter) rs786201042
NM_000179.2(MSH6):c.1270G>A (p.Val424Ile) rs768299607
NM_000179.2(MSH6):c.136G>A (p.Gly46Arg) rs863224616
NM_000179.2(MSH6):c.136G>C (p.Gly46Arg) rs863224616
NM_000179.2(MSH6):c.1633A>G (p.Lys545Glu) rs1064793403
NM_000179.2(MSH6):c.1814C>G (p.Thr605Ser) rs587781616
NM_000179.2(MSH6):c.184C>T (p.Arg62Cys) rs876659508
NM_000179.2(MSH6):c.187T>C (p.Ser63Pro) rs763702846
NM_000179.2(MSH6):c.2183A>G (p.Lys728Arg) rs35552856
NM_000179.2(MSH6):c.2300C>G (p.Thr767Ser) rs587781462
NM_000179.2(MSH6):c.2419G>A (p.Glu807Lys) rs587779923
NM_000179.2(MSH6):c.2515G>C (p.Asp839His) rs1553413868
NM_000179.2(MSH6):c.2561A>T (p.Lys854Met) rs34374438
NM_000179.2(MSH6):c.2731C>T (p.Arg911Ter) rs63751017
NM_000179.2(MSH6):c.2959A>G (p.Thr987Ala) rs746631156
NM_000179.2(MSH6):c.3014G>A (p.Arg1005Gln) rs587782324
NM_000179.2(MSH6):c.3103C>T (p.Arg1035Ter) rs63749999
NM_000179.2(MSH6):c.3163G>A (p.Ala1055Thr) rs587779254
NM_000179.2(MSH6):c.3202C>T (p.Arg1068Ter) rs63749843
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3244C>T (p.Pro1082Ser) rs186240214
NM_000179.2(MSH6):c.3259C>T (p.Pro1087Ser) rs63750998
NM_000179.2(MSH6):c.3260C>G (p.Pro1087Arg) rs63750753
NM_000179.2(MSH6):c.3299C>T (p.Thr1100Met) rs63750442
NM_000179.2(MSH6):c.3312T>A (p.Phe1104Leu) rs747441460
NM_000179.2(MSH6):c.3557G>A (p.Gly1186Asp) rs587781690
NM_000179.2(MSH6):c.3605T>C (p.Met1202Thr) rs587779273
NM_000179.2(MSH6):c.3788G>A (p.Arg1263His) rs147852216
NM_000179.2(MSH6):c.3801+1G>T rs876660943
NM_000179.2(MSH6):c.383G>T (p.Arg128Leu) rs63750143
NM_000179.2(MSH6):c.3919A>C (p.Asn1307His) rs730881808
NM_000179.2(MSH6):c.4043A>C (p.Glu1348Ala) rs1449733937
NM_000179.2(MSH6):c.622A>G (p.Met208Val) rs369058374
NM_000179.2(MSH6):c.73G>T (p.Ala25Ser) rs267608026

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