ClinVar Miner

List of variants in gene MRE11 reported as pathogenic

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Total variants: 40
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HGVS dbSNP
NM_005590.3(MRE11):c.229G>T (p.Glu77Ter) rs779269083
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.1135dupC (p.Leu379Profs) rs786202764
NM_005591.3(MRE11):c.1143delT (p.Phe381Leufs) rs863224508
NM_005591.3(MRE11):c.1222dupA (p.Thr408Asnfs) rs774440500
NM_005591.3(MRE11):c.1252dup (p.Ile418Asnfs) rs1555009931
NM_005591.3(MRE11):c.1336delC (p.Leu446Serfs) rs786203682
NM_005591.3(MRE11):c.140C>T (p.Ala47Val) rs730880378
NM_005591.3(MRE11):c.1414G>T (p.Glu472Ter) rs1376550081
NM_005591.3(MRE11):c.1441delA (p.Thr481Hisfs) rs747832587
NM_005591.3(MRE11):c.1442C>A (p.Thr481Lys) rs137852762
NM_005591.3(MRE11):c.1445_1446delAGinsTTAA (p.Gln482Leufs) rs786203314
NM_005591.3(MRE11):c.1447C>T (p.Arg483Ter) rs780001540
NM_005591.3(MRE11):c.1516G>T (p.Glu506Ter) rs587781384
NM_005591.3(MRE11):c.1633_1640delCTTATGAG (p.Leu545Tyrfs) rs876660186
NM_005591.3(MRE11):c.170T>G (p.Leu57Ter) rs951805101
NM_005591.3(MRE11):c.1714C>T (p.Arg572Ter) rs137852761
NM_005591.3(MRE11):c.1720delA (p.Arg574Glufs) rs767787348
NM_005591.3(MRE11):c.1726C>T (p.Arg576Ter) rs774277300
NM_005591.3(MRE11):c.1771C>T (p.Gln591Ter) rs1215450873
NM_005591.3(MRE11):c.1773_1774delAA (p.Gly593Lysfs) rs1555005270
NM_005591.3(MRE11):c.1826dupA (p.Thr610Aspfs) rs876660269
NM_005591.3(MRE11):c.1869delC (p.Phe624Leufs) rs1264516058
NM_005591.3(MRE11):c.1897C>T (p.Arg633Ter) rs137852759
NM_005591.3(MRE11):c.1897delC (p.Arg633Glufs) rs1555002419
NM_005591.3(MRE11):c.1960_1979dup20 (p.Lys661Thrfs) rs587781442
NM_005591.3(MRE11):c.211delA (p.Thr71Hisfs) rs1555017238
NM_005591.3(MRE11):c.295_298delGTCA (p.Val99Thrfs) rs1555017184
NM_005591.3(MRE11):c.350A>G (p.Asn117Ser) rs137852760
NM_005591.3(MRE11):c.504_511delGCTTCAAA (p.Leu169Argfs) rs786202253
NM_005591.3(MRE11):c.508C>T (p.Gln170Ter) rs587782030
NM_005591.3(MRE11):c.627_628delTT (p.Trp210Valfs) rs730881752
NM_005591.3(MRE11):c.630G>C (p.Trp210Cys) rs137852763
NM_005591.3(MRE11):c.659+1G>A rs759130031
NM_005591.3(MRE11):c.739dupC (p.His247Profs) rs786203931
NM_005591.3(MRE11):c.806C>G (p.Ser269Ter) rs776912688
NM_005591.3(MRE11):c.821_823delTTTinsA (p.Leu274Hisfs) rs786202032
NM_005591.3(MRE11):c.845+2T>A rs587781381
NM_005591.3(MRE11):c.923dupT (p.Met309Hisfs) rs587781828

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