ClinVar Miner

List of variants in gene MRE11 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.315-281G>A rs13447608 0.02098
NM_005591.4(MRE11):c.659+79A>C rs13447622 0.01363
NM_005591.4(MRE11):c.153+254A>G rs72980413 0.01351
NM_005591.4(MRE11):c.1994+10G>A rs1805366 0.01130
NM_005591.4(MRE11):c.1926+195A>G rs13447715 0.01086
NM_005591.4(MRE11):c.845+110C>A rs12277561 0.00807
NM_005591.4(MRE11):c.1563+233A>G rs13447688 0.00712
NM_005591.4(MRE11):c.1225+333T>C rs534789007 0.00669
NM_005591.4(MRE11):c.314+62A>G rs148085738 0.00663
NM_005591.4(MRE11):c.659+203A>T rs116830173 0.00645
NM_005591.4(MRE11):c.1926+102A>G rs115453745 0.00641
NM_005591.4(MRE11):c.659+30C>G rs11020795 0.00639
NM_005591.4(MRE11):c.1867+241T>C rs150080172 0.00635
NM_005591.4(MRE11):c.1326+93G>T rs115203193 0.00633
NM_005591.4(MRE11):c.1099-105C>G rs114538678 0.00632
NM_005591.4(MRE11):c.1225+224G>A rs183192375 0.00632
NM_005591.4(MRE11):c.1501-219G>A rs116250383 0.00631
NM_005591.4(MRE11):c.1225+27A>G rs116366202 0.00628
NM_005591.4(MRE11):c.2071-53G>T rs13447742 0.00597
NM_005591.4(MRE11):c.403-146A>G rs77142496 0.00504
NM_005591.4(MRE11):c.314+55del rs572848562 0.00429
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp) rs61749249 0.00399
NM_005591.4(MRE11):c.2070+231del rs368453957 0.00390
NM_005591.4(MRE11):c.1225+124_1225+137dup rs368479556 0.00336
NM_005591.4(MRE11):c.315-30G>A rs115810281 0.00335
NM_005591.4(MRE11):c.315-246A>G rs114406328 0.00333
NM_005591.4(MRE11):c.402+145T>C rs114468375 0.00333
NM_005591.4(MRE11):c.1098+215G>T rs557705036 0.00315
NM_005591.4(MRE11):c.544+290T>G rs115630811 0.00315
NM_005591.4(MRE11):c.121G>A (p.Asp41Asn) rs116679717 0.00293
NM_005591.4(MRE11):c.1783+5G>C rs142082313 0.00284
NM_005591.4(MRE11):c.315-228G>C rs13447609 0.00251
NM_005591.4(MRE11):c.822T>C (p.Leu274=) rs137868143 0.00152
NM_005591.4(MRE11):c.426C>T (p.Asp142=) rs3218740 0.00109
NM_005591.4(MRE11):c.1798G>C (p.Glu600Gln) rs145415033 0.00103
NM_005591.4(MRE11):c.120C>T (p.Leu40=) rs1805364 0.00066
NM_005591.4(MRE11):c.1727G>A (p.Arg576Gln) rs139461096 0.00038
NM_005591.4(MRE11):c.1480G>A (p.Glu494Lys) rs104895016 0.00032
NM_005591.4(MRE11):c.1667A>G (p.Asn556Ser) rs144896235 0.00018
NM_005591.4(MRE11):c.529G>A (p.Ala177Thr) rs142996063 0.00010
NM_005591.4(MRE11):c.469A>G (p.Met157Val) rs147771140 0.00006
NM_005591.4(MRE11):c.753A>C (p.Ile251=) rs544844010 0.00005
NM_005591.4(MRE11):c.2049G>A (p.Gly683=) rs758931835 0.00004
NM_005591.4(MRE11):c.534A>G (p.Leu178=) rs374635285 0.00003
NM_005591.4(MRE11):c.1191T>C (p.His397=) rs759856523 0.00002
NM_005591.4(MRE11):c.1086T>C (p.Leu362=) rs786201488 0.00001
NM_005591.4(MRE11):c.1259A>C (p.Lys420Thr) rs201153937 0.00001
NM_005591.4(MRE11):c.1476C>T (p.Ala492=) rs370397034 0.00001
NM_005591.4(MRE11):c.2043G>A (p.Ser681=) rs876659873 0.00001
NM_005591.4(MRE11):c.690A>G (p.Pro230=) rs786203787 0.00001
NM_005591.4(MRE11):c.-105-152dup rs529272099
NM_005591.4(MRE11):c.-105-282G>A rs138069250
NM_005591.4(MRE11):c.1093C>T (p.Leu365=) rs1591688088
NM_005591.4(MRE11):c.1099-118_1099-115del rs200364698
NM_005591.4(MRE11):c.1210C>A (p.Gln404Lys) rs1180352898
NM_005591.4(MRE11):c.1216G>A (p.Glu406Lys) rs1205023888
NM_005591.4(MRE11):c.1226-53A>G rs115997947
NM_005591.4(MRE11):c.154-84_154-82dup rs199539992
NM_005591.4(MRE11):c.1564-251_1564-249dup rs56850566
NM_005591.4(MRE11):c.1811G>A (p.Arg604His) rs148637964
NM_005591.4(MRE11):c.1811G>C (p.Arg604Pro) rs148637964
NM_005591.4(MRE11):c.228C>T (p.Leu76=) rs748605250
NM_005591.4(MRE11):c.235T>C (p.Leu79=) rs745332888
NM_005591.4(MRE11):c.303T>C (p.Phe101=) rs786201176
NM_005591.4(MRE11):c.315-14dup rs35062043
NM_005591.4(MRE11):c.315-34G>T rs115461304
NM_005591.4(MRE11):c.403-212C>A rs12281066
NM_005591.4(MRE11):c.545-319dup rs201610051
NM_005591.4(MRE11):c.564G>A (p.Arg188=) rs200213865
NM_005591.4(MRE11):c.807A>C (p.Ser269=) rs1306806501
NM_005591.4(MRE11):c.845+267G>T rs12291000

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