ClinVar Miner

List of variants in gene MRE11 studied for cancer

Included ClinVar conditions (475):
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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.1098+614C>T rs140067184 0.01533
NM_005591.4(MRE11):c.1225+572A>T rs397509353 0.00780
NM_005591.4(MRE11):c.1225+577A>C rs397509354 0.00779
NM_005591.4(MRE11):c.1327-461A>C rs185485357 0.00356
NM_005591.4(MRE11):c.545-297G>T rs118024137 0.00272
NM_005591.4(MRE11):c.-105-326A>T rs183829476 0.00268
NM_005591.4(MRE11):c.1098+1177G>A rs369782842 0.00207
NM_005591.4(MRE11):c.-105-387C>T rs397509350 0.00168
NM_005591.4(MRE11):c.314+99A>G rs143677623 0.00092
NM_005591.4(MRE11):c.1098+1408A>G rs200367125 0.00083
NM_005591.4(MRE11):c.1225+605T>C rs397509355 0.00038
NM_005591.4(MRE11):c.1225+40T>C rs192979170 0.00014
NM_005591.4(MRE11):c.818C>G (p.Ser273Cys) rs143400546 0.00009
NM_005591.4(MRE11):c.*570A>C rs397509346 0.00006
NM_005591.4(MRE11):c.1563+281G>A rs397509429 0.00006
NM_005591.4(MRE11):c.863G>A (p.Arg288His) rs190142346 0.00006
NM_005591.4(MRE11):c.1052G>A (p.Arg351His) rs587780133 0.00004
NM_005591.4(MRE11):c.1225+804T>C rs397509356 0.00003
NM_005591.4(MRE11):c.677C>G (p.Thr226Ser) rs201276188 0.00003
NM_005591.4(MRE11):c.1202A>G (p.His401Arg) rs146779325 0.00002
NM_005591.4(MRE11):c.*1359T>C rs397509348 0.00001
NM_005591.4(MRE11):c.1098+1620T>C rs397509352 0.00001
NM_005591.4(MRE11):c.1447C>T (p.Arg483Ter) rs780001540 0.00001
NM_005591.4(MRE11):c.1783+561G>A rs397509357 0.00001
NM_005591.4(MRE11):c.*2731G>A rs397509349
NM_005591.4(MRE11):c.*631C>T rs397509347
NM_005591.4(MRE11):c.1100_1131del (p.Val367fs) rs1946499901
NM_005591.4(MRE11):c.1165G>A (p.Val389Ile) rs876660518
NM_005591.4(MRE11):c.1784-438A>G rs397509358
NM_005591.4(MRE11):c.20+821G>A rs397509351
NM_005591.4(MRE11):c.386A>T (p.His129Leu)
NM_005591.4(MRE11):c.668A>G (p.His223Arg)
NM_005591.4(MRE11):c.901C>G (p.Leu301Val) rs863225441

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