NM_000251.3(MSH2):c.2785C>T (p.Arg929Ter)
|
rs551060742
|
0.00011
|
NM_000249.4(MLH1):c.453G>A (p.Thr151=)
|
rs369521379
|
0.00006
|
NM_000251.3(MSH2):c.1963G>A (p.Val655Ile)
|
rs549467183
|
0.00003
|
NM_000251.3(MSH2):c.991A>G (p.Asn331Asp)
|
rs267607938
|
0.00003
|
NM_000249.4(MLH1):c.306+4A>G
|
rs267607733
|
0.00001
|
NM_000249.4(MLH1):c.306G>A (p.Glu102=)
|
rs63751665
|
0.00001
|
NM_000251.3(MSH2):c.2437A>G (p.Met813Val)
|
rs63749841
|
0.00001
|
NM_000179.3(MSH6):c.3338T>G (p.Ile1113Ser)
|
rs41295272
|
|
NM_000179.3(MSH6):c.4064_4065insGTCA (p.Leu1356fs)
|
rs267608141
|
|
NM_000249.4(MLH1):c.116G>A (p.Cys39Tyr)
|
rs63751701
|
|
NM_000249.4(MLH1):c.116G>T (p.Cys39Phe)
|
rs63751701
|
|
NM_000249.4(MLH1):c.1612T>G (p.Trp538Gly)
|
rs1559575214
|
|
NM_000249.4(MLH1):c.1676T>G (p.Leu559Arg)
|
rs63750059
|
|
NM_000249.4(MLH1):c.1731+6T>G
|
rs587778940
|
|
NM_000249.4(MLH1):c.1823C>A (p.Ala608Asp)
|
rs267607864
|
|
NM_000249.4(MLH1):c.1988A>C (p.Glu663Ala)
|
rs63751682
|
|
NM_000249.4(MLH1):c.2103G>A (p.Gln701=)
|
rs63750603
|
|
NM_000249.4(MLH1):c.2250C>A (p.Tyr750Ter)
|
rs267607893
|
|
NM_000249.4(MLH1):c.2250C>G (p.Tyr750Ter)
|
rs267607893
|
|
NM_000249.4(MLH1):c.2252_2253dup (p.Val752fs)
|
rs267607901
|
|
NM_000249.4(MLH1):c.2262del (p.Arg755fs)
|
rs267607904
|
|
NM_000249.4(MLH1):c.2265G>C (p.Arg755Ser)
|
rs267607895
|
|
NM_000249.4(MLH1):c.2269T>A (p.Ter757Lys)
|
rs587778995
|
|
NM_000249.4(MLH1):c.306G>T (p.Glu102Asp)
|
rs63751665
|
|
NM_000249.4(MLH1):c.884G>C (p.Ser295Thr)
|
rs63750144
|
|
NM_000251.3(MSH2):c.1277-14C>G
|
rs267607951
|
|
NM_000251.3(MSH2):c.1510G>C (p.Gly504Arg)
|
rs63751600
|
|
NM_000251.3(MSH2):c.1662-18T>C
|
rs376235435
|
|
NM_000251.3(MSH2):c.1807G>A (p.Asp603Asn)
|
rs63750657
|
|
NM_000251.3(MSH2):c.1A>C (p.Met1Leu)
|
rs267607911
|
|
NM_000251.3(MSH2):c.1A>G (p.Met1Val)
|
rs267607911
|
|
NM_000251.3(MSH2):c.1A>T (p.Met1Leu)
|
rs267607911
|
|
NM_000251.3(MSH2):c.2005G>C (p.Gly669Arg)
|
rs63751668
|
|
NM_000251.3(MSH2):c.2634G>C (p.Glu878Asp)
|
rs63751624
|
|
NM_000251.3(MSH2):c.2740G>T (p.Glu914Ter)
|
rs267608024
|
|
NM_000251.3(MSH2):c.2797dup (p.Thr933fs)
|
rs587779156
|
|
NM_000251.3(MSH2):c.792G>C (p.Gln264His)
|
rs587779183
|
|
NM_000535.7(PMS2):c.2186_2187del (p.Leu729fs)
|
rs587779335
|
|