ClinVar Miner

List of variants in gene MRE11 reported as pathogenic

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Total variants: 62
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HGVS dbSNP
NC_000011.10:g.(?_94470461)_(94492811_?)del
NM_005590.4(MRE11):c.1047_1048del (p.Glu350fs) rs1591688367
NM_005590.4(MRE11):c.1135dup (p.Leu379fs) rs786202764
NM_005590.4(MRE11):c.1222dup (p.Thr408fs) rs774440500
NM_005590.4(MRE11):c.1252dup (p.Ile418fs) rs1555009931
NM_005590.4(MRE11):c.1336del (p.Leu446fs) rs786203682
NM_005590.4(MRE11):c.1441del (p.Thr481fs) rs747832587
NM_005590.4(MRE11):c.1445_1446delinsTTAA (p.Gln482fs) rs786203314
NM_005590.4(MRE11):c.1516G>T (p.Glu506Ter) rs587781384
NM_005590.4(MRE11):c.1633_1640del (p.Leu545fs) rs876660186
NM_005590.4(MRE11):c.1720del (p.Arg574fs) rs767787348
NM_005590.4(MRE11):c.1726C>T (p.Arg576Ter) rs774277300
NM_005590.4(MRE11):c.1773_1774del (p.Gly593fs) rs1555005270
NM_005590.4(MRE11):c.1783+1366dup rs876660269
NM_005590.4(MRE11):c.1785del (p.Phe596fs) rs1264516058
NM_005590.4(MRE11):c.1813del (p.Arg605fs) rs1555002419
NM_005590.4(MRE11):c.1876_1895dup (p.Lys633fs) rs587781442
NM_005590.4(MRE11):c.211del (p.Thr71fs) rs1555017238
NM_005590.4(MRE11):c.229G>T (p.Glu77Ter) rs779269083
NM_005590.4(MRE11):c.291_294GTCA[1] (p.Val99fs) rs1555017184
NM_005590.4(MRE11):c.627_628del (p.Trp210fs) rs730881752
NM_005590.4(MRE11):c.739dup (p.His247fs) rs786203931
NM_005590.4(MRE11):c.821_823delinsA (p.Leu274fs) rs786202032
NM_005590.4(MRE11):c.923dup (p.Met309fs) rs587781828
NM_005591.3(MRE11):c.1015A>T (p.Lys339Ter) rs984874083
NM_005591.3(MRE11):c.1090C>T (p.Arg364Ter) rs371077728
NM_005591.3(MRE11):c.1143del (p.Phe381fs) rs863224508
NM_005591.3(MRE11):c.1414G>T (p.Glu472Ter) rs1376550081
NM_005591.3(MRE11):c.1447C>T (p.Arg483Ter) rs780001540
NM_005591.3(MRE11):c.170T>G (p.Leu57Ter) rs951805101
NM_005591.3(MRE11):c.1771C>T (p.Gln591Ter) rs1215450873
NM_005591.3(MRE11):c.504_511del (p.Leu169fs) rs786202253
NM_005591.3(MRE11):c.508C>T (p.Gln170Ter) rs587782030
NM_005591.3(MRE11):c.659+1G>A rs759130031
NM_005591.3(MRE11):c.664A>T (p.Lys222Ter) rs371455048
NM_005591.3(MRE11):c.806C>G (p.Ser269Ter) rs776912688
NM_005591.3(MRE11):c.845+2T>A rs587781381
NM_005591.4(MRE11):c.1112_1127del (p.Gly371fs) rs1169667763
NM_005591.4(MRE11):c.1112dup (p.Gly372fs) rs1591681273
NM_005591.4(MRE11):c.1210C>T (p.Gln404Ter) rs1180352898
NM_005591.4(MRE11):c.1326+1del
NM_005591.4(MRE11):c.140C>T (p.Ala47Val) rs730880378
NM_005591.4(MRE11):c.1442C>A (p.Thr481Lys) rs137852762
NM_005591.4(MRE11):c.1442_1443CA[1] (p.Gln482fs) rs1245161888
NM_005591.4(MRE11):c.1485del (p.Asp495fs) rs1591672201
NM_005591.4(MRE11):c.1531_1532del (p.Asn511fs) rs757691558
NM_005591.4(MRE11):c.1603G>T (p.Glu535Ter)
NM_005591.4(MRE11):c.1714C>T (p.Arg572Ter) rs137852761
NM_005591.4(MRE11):c.1806_1809del (p.Thr603fs) rs1591652976
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.1897C>T (p.Arg633Ter) rs137852759
NM_005591.4(MRE11):c.1960_1979dup (p.Lys661fs) rs587781442
NM_005591.4(MRE11):c.215_219dup (p.Thr74fs) rs1591719208
NM_005591.4(MRE11):c.350A>G (p.Asn117Ser) rs137852760
NM_005591.4(MRE11):c.552del (p.Pro185fs)
NM_005591.4(MRE11):c.571C>T (p.Arg191Ter) rs1157413766
NM_005591.4(MRE11):c.630G>C (p.Trp210Cys) rs137852763
NM_005591.4(MRE11):c.652C>T (p.Gln218Ter) rs1591703044
NM_005591.4(MRE11):c.775C>T (p.Gln259Ter) rs1060501788
NM_005591.4(MRE11):c.818_819CT[1] (p.Leu274fs) rs1565228898
NM_005591.4(MRE11):c.895del (p.Ile299fs) rs1591692886

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