ClinVar Miner

List of variants in gene MRE11 reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.1714C>T (p.Arg572Ter) rs137852761 0.00007
NM_005591.4(MRE11):c.1015A>T (p.Lys339Ter) rs984874083 0.00004
NM_005591.4(MRE11):c.1516G>T (p.Glu506Ter) rs587781384 0.00004
NM_005591.4(MRE11):c.659+1G>A rs759130031 0.00002
NM_005591.4(MRE11):c.1096C>T (p.Arg366Ter) rs372411821 0.00001
NM_005591.4(MRE11):c.1414G>T (p.Glu472Ter) rs1376550081 0.00001
NM_005591.4(MRE11):c.1447C>T (p.Arg483Ter) rs780001540 0.00001
NM_005591.4(MRE11):c.1603G>T (p.Glu535Ter) rs1440482403 0.00001
NM_005591.4(MRE11):c.170T>G (p.Leu57Ter) rs951805101 0.00001
NM_005591.4(MRE11):c.1771C>T (p.Gln591Ter) rs1215450873 0.00001
NM_005591.4(MRE11):c.1897C>T (p.Arg633Ter) rs137852759 0.00001
NM_005591.4(MRE11):c.1090C>T (p.Arg364Ter) rs371077728
NM_005591.4(MRE11):c.1112_1127del (p.Gly371fs) rs1169667763
NM_005591.4(MRE11):c.1124del (p.Pro375fs)
NM_005591.4(MRE11):c.1135dup (p.Leu379fs) rs786202764
NM_005591.4(MRE11):c.1143del (p.Phe381fs) rs863224508
NM_005591.4(MRE11):c.1196del (p.Phe399fs)
NM_005591.4(MRE11):c.1210C>T (p.Gln404Ter) rs1180352898
NM_005591.4(MRE11):c.1222dup (p.Thr408fs) rs774440500
NM_005591.4(MRE11):c.1252dup (p.Ile418fs) rs1555009931
NM_005591.4(MRE11):c.1336del (p.Leu446fs) rs786203682
NM_005591.4(MRE11):c.1378G>T (p.Glu460Ter)
NM_005591.4(MRE11):c.1441del (p.Thr481fs) rs747832587
NM_005591.4(MRE11):c.1441dup (p.Thr481fs)
NM_005591.4(MRE11):c.1444_1445del (p.Gln482fs) rs1245161888
NM_005591.4(MRE11):c.1445_1446delinsTTAA (p.Gln482fs) rs786203314
NM_005591.4(MRE11):c.1485del (p.Asp495fs) rs1591672201
NM_005591.4(MRE11):c.1531_1532del (p.Asn511fs) rs757691558
NM_005591.4(MRE11):c.1532del (p.Asn511fs)
NM_005591.4(MRE11):c.1532dup (p.Asn511fs)
NM_005591.4(MRE11):c.1552G>T (p.Glu518Ter)
NM_005591.4(MRE11):c.157del (p.Asp53fs)
NM_005591.4(MRE11):c.1633_1640del (p.Leu545fs) rs876660186
NM_005591.4(MRE11):c.1720del (p.Arg574fs) rs767787348
NM_005591.4(MRE11):c.1726C>T (p.Arg576Ter) rs774277300
NM_005591.4(MRE11):c.1773_1774del (p.Gly593fs) rs1555005270
NM_005591.4(MRE11):c.1806_1809del (p.Thr603fs) rs1591652976
NM_005591.4(MRE11):c.1826dup (p.Thr610fs) rs876660269
NM_005591.4(MRE11):c.1869del (p.Phe624fs) rs1264516058
NM_005591.4(MRE11):c.1882A>T (p.Arg628Ter) rs1411087205
NM_005591.4(MRE11):c.1885C>T (p.Gln629Ter) rs1157436927
NM_005591.4(MRE11):c.1897del (p.Arg633fs) rs1555002419
NM_005591.4(MRE11):c.1957G>T (p.Glu653Ter)
NM_005591.4(MRE11):c.1997G>A (p.Trp666Ter)
NM_005591.4(MRE11):c.211del (p.Thr71fs) rs1555017238
NM_005591.4(MRE11):c.215_219dup (p.Thr74fs) rs1591719208
NM_005591.4(MRE11):c.229G>T (p.Glu77Ter) rs779269083
NM_005591.4(MRE11):c.295_298del (p.Val99fs) rs1555017184
NM_005591.4(MRE11):c.504_511del (p.Leu169fs) rs786202253
NM_005591.4(MRE11):c.508C>T (p.Gln170Ter) rs587782030
NM_005591.4(MRE11):c.571C>T (p.Arg191Ter) rs1157413766
NM_005591.4(MRE11):c.592del (p.Lys197_Val198insTer) rs1359551200
NM_005591.4(MRE11):c.627_628del (p.Trp210fs) rs730881752
NM_005591.4(MRE11):c.628del (p.Trp210fs)
NM_005591.4(MRE11):c.652C>T (p.Gln218Ter) rs1591703044
NM_005591.4(MRE11):c.739dup (p.His247fs) rs786203931
NM_005591.4(MRE11):c.775C>T (p.Gln259Ter) rs1060501788
NM_005591.4(MRE11):c.784del (p.Tyr262fs)
NM_005591.4(MRE11):c.806C>G (p.Ser269Ter) rs776912688
NM_005591.4(MRE11):c.820_821del (p.Leu274fs) rs1565228898
NM_005591.4(MRE11):c.821_823delinsA (p.Leu274fs) rs786202032
NM_005591.4(MRE11):c.832G>T (p.Glu278Ter)
NM_005591.4(MRE11):c.842del (p.Lys281fs)
NM_005591.4(MRE11):c.895del (p.Ile299fs) rs1591692886
NM_005591.4(MRE11):c.916C>T (p.Gln306Ter)
NM_005591.4(MRE11):c.923dup (p.Met309fs) rs587781828
NM_005591.4(MRE11):c.939del (p.Val313_Leu314insTer)
NM_005591.4(MRE11):c.988C>T (p.Gln330Ter)

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