ClinVar Miner

List of variants in gene MRE11 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.20+28G>A rs497763 0.43069
NM_005591.4(MRE11):c.1225+19T>C rs641936 0.36920
NM_005591.4(MRE11):c.403-6G>A rs535801 0.28996
NM_005591.4(MRE11):c.1032T>G (p.Leu344=) rs11020793 0.00960
NM_005591.4(MRE11):c.1783+5G>C rs142082313 0.00284
NM_005591.4(MRE11):c.771A>G (p.Glu257=) rs13447632 0.00283
NM_005591.4(MRE11):c.426C>T (p.Asp142=) rs3218740 0.00109
NM_005591.4(MRE11):c.1727G>A (p.Arg576Gln) rs139461096 0.00038
NM_005591.4(MRE11):c.845+11T>C rs140145979 0.00021
NM_005591.4(MRE11):c.1286T>C (p.Val429Ala) rs141293060 0.00020
NM_005591.4(MRE11):c.1667A>G (p.Asn556Ser) rs144896235 0.00018
NM_005591.4(MRE11):c.1726C>G (p.Arg576Gly) rs774277300 0.00016
NM_005591.4(MRE11):c.529G>A (p.Ala177Thr) rs142996063 0.00010
NM_005591.4(MRE11):c.1858A>G (p.Ile620Val) rs144070976 0.00006
NM_005591.4(MRE11):c.2054A>G (p.Asp685Gly) rs554399982 0.00006
NM_005591.4(MRE11):c.81G>A (p.Glu27=) rs190031653 0.00006
NM_005591.4(MRE11):c.940C>T (p.Leu314=) rs368362407 0.00004
NM_005591.4(MRE11):c.1318G>A (p.Ala440Thr) rs773469981 0.00003
NM_005591.4(MRE11):c.1190A>C (p.His397Pro) rs372657126 0.00002
NM_005591.4(MRE11):c.1074A>G (p.Pro358=) rs876659934 0.00001
NM_005591.4(MRE11):c.1350A>G (p.Thr450=) rs876660412 0.00001
NM_005591.4(MRE11):c.1757C>T (p.Ser586Leu) rs753717905 0.00001
NM_005591.4(MRE11):c.1780A>G (p.Arg594Gly) rs576878377 0.00001
NM_005591.4(MRE11):c.267C>G (p.Val89=) rs759547024 0.00001
NM_005591.4(MRE11):c.659+1G>A rs759130031 0.00001
NM_005591.4(MRE11):c.840A>G (p.Val280=) rs786201550 0.00001
NM_005591.4(MRE11):c.1002C>T (p.Ser334=) rs115244417
NM_005591.4(MRE11):c.1098+17T>C rs1805365
NM_005591.4(MRE11):c.1434G>A (p.Leu478=) rs1591672412
NM_005591.4(MRE11):c.1811G>C (p.Arg604Pro) rs148637964
NM_005591.4(MRE11):c.1927-9C>A rs1060504336
NM_005591.4(MRE11):c.2070+5del rs587782048
NM_005591.4(MRE11):c.251T>C (p.Met84Thr) rs1482454029
NM_005591.4(MRE11):c.292T>C (p.Ser98Pro) rs876659583
NM_005591.4(MRE11):c.314+4_314+7del
NM_005591.4(MRE11):c.37T>A (p.Phe13Ile) rs149101834
NM_005591.4(MRE11):c.391G>C (p.Asp131His) rs368403414
NM_005591.4(MRE11):c.924C>A (p.Phe308Leu) rs138595973
NM_005591.4(MRE11):c.924C>T (p.Phe308=) rs138595973

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