ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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Total variants: 26
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HGVS dbSNP
NM_000179.2(MSH6):c.-2G>T rs374748889
NM_000179.2(MSH6):c.1474A>G (p.Met492Val) rs61754783
NM_000179.2(MSH6):c.1553C>A (p.Thr518Asn) rs1553412945
NM_000179.2(MSH6):c.1669G>A (p.Gly557Ser) rs1553413048
NM_000179.2(MSH6):c.1750A>C (p.Thr584Pro) rs1553413123
NM_000179.2(MSH6):c.2061T>G (p.Cys687Trp) rs267608068
NM_000179.2(MSH6):c.2300C>T (p.Thr767Ile) rs587781462
NM_000179.2(MSH6):c.2342C>T (p.Pro781Leu) rs1553413710
NM_000179.2(MSH6):c.2561A>T (p.Lys854Met) rs34374438
NM_000179.2(MSH6):c.2855T>C (p.Leu952Pro) rs587781743
NM_000179.2(MSH6):c.2905T>C (p.Tyr969His) rs1348956744
NM_000179.2(MSH6):c.2936T>C (p.Leu979Pro) rs1218426245
NM_000179.2(MSH6):c.2949G>C (p.Glu983Asp) rs780485157
NM_000179.2(MSH6):c.2989A>G (p.Lys997Glu) rs1064794943
NM_000179.2(MSH6):c.3079G>C (p.Val1027Leu) rs876658397
NM_000179.2(MSH6):c.3172G>C (p.Asp1058His) rs863225404
NM_000179.2(MSH6):c.3173-3C>G rs1060502944
NM_000179.2(MSH6):c.3226C>G (p.Arg1076Gly) rs63750617
NM_000179.2(MSH6):c.3401G>C (p.Gly1134Ala) rs1376398586
NM_000179.2(MSH6):c.3438+11_3438+14del rs377746844
NM_000179.2(MSH6):c.3727A>T (p.Thr1243Ser) rs147453999
NM_000179.2(MSH6):c.3946G>A (p.Gly1316Arg) rs773675555
NM_000179.2(MSH6):c.866_867delinsAA (p.Gly289Glu) rs267608079
NM_000179.2(MSH6):c.926C>G (p.Ser309Cys) rs544222338
NM_000179.2(MSH6):c.979A>G (p.Thr327Ala) rs730881814
NM_001281492.1(MSH6):c.3611+4_3611+8dup rs587782853

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