ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by Mayo Clinic Genetic Testing Laboratories,Mayo Clinic

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Total variants: 33
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HGVS dbSNP
NM_000179.2(MSH6):c.-8C>T rs565211544
NM_000179.2(MSH6):c.1109T>C (p.Leu370Ser) rs587779204
NM_000179.2(MSH6):c.1295T>C (p.Phe432Ser) rs750528093
NM_000179.2(MSH6):c.1526T>C (p.Val509Ala) rs63751005
NM_000179.2(MSH6):c.2057G>A (p.Gly686Asp) rs587779227
NM_000179.2(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.2(MSH6):c.2555_2557AGA[2] (p.Lys854del) rs587782858
NM_000179.2(MSH6):c.2830A>G (p.Ile944Val) rs878853723
NM_000179.2(MSH6):c.2872C>G (p.Gln958Glu) rs1553414236
NM_000179.2(MSH6):c.3097A>G (p.Met1033Val) rs1553414508
NM_000179.2(MSH6):c.3172G>C (p.Asp1058His) rs863225404
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.3246G>A (p.Pro1082=) rs3136351
NM_000179.2(MSH6):c.3260C>A (p.Pro1087His) rs63750753
NM_000179.2(MSH6):c.3469G>A (p.Gly1157Ser) rs587779264
NM_000179.2(MSH6):c.3478G>A (p.Val1160Ile) rs376799914
NM_000179.2(MSH6):c.3488A>T (p.Glu1163Val) rs63750252
NM_000179.2(MSH6):c.3647-15A>C rs371171254
NM_000179.2(MSH6):c.3647-15A>G rs371171254
NM_000179.2(MSH6):c.369A>T (p.Lys123Asn) rs587782106
NM_000179.2(MSH6):c.3744_3773del (p.His1248_Ser1257del) rs863225412
NM_000179.2(MSH6):c.3911G>A (p.Arg1304Lys) rs34625968
NM_000179.2(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278
NM_000179.2(MSH6):c.4001G>A (p.Arg1334Gln) rs267608122
NM_000179.2(MSH6):c.4075G>A (p.Glu1359Lys) rs267608081
NM_000179.2(MSH6):c.59C>T (p.Ala20Val) rs63750664
NM_000179.2(MSH6):c.643G>A (p.Val215Ile) rs145959653
NM_000179.2(MSH6):c.660A>C (p.Glu220Asp) rs1800938
NM_000179.2(MSH6):c.661_672del (p.Glu221_Glu224del) rs1553412079
NM_000179.2(MSH6):c.663A>C (p.Glu221Asp) rs41557217
NM_000179.2(MSH6):c.749T>C (p.Val250Ala) rs587781275
NM_000179.2(MSH6):c.818G>T (p.Gly273Val) rs769610487

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