ClinVar Miner

List of variants in gene MRE11 reported as uncertain significance for not specified

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.1726C>G (p.Arg576Gly) rs774277300 0.00016
NM_005591.4(MRE11):c.913C>T (p.Arg305Trp) rs372000848 0.00008
NM_005591.4(MRE11):c.482A>G (p.Lys161Arg) rs587782294 0.00007
NM_005591.4(MRE11):c.358A>G (p.Ile120Val) rs372131911 0.00006
NM_005591.4(MRE11):c.391G>A (p.Asp131Asn) rs368403414 0.00006
NM_005591.4(MRE11):c.1852A>G (p.Met618Val) rs375630981 0.00005
NM_005591.4(MRE11):c.1052G>A (p.Arg351His) rs587780133 0.00004
NM_005591.4(MRE11):c.1972A>G (p.Thr658Ala) rs587782756 0.00004
NM_005591.4(MRE11):c.476T>C (p.Val159Ala) rs140130291 0.00003
NM_005591.4(MRE11):c.1139G>A (p.Arg380His) rs587781646 0.00002
NM_005591.4(MRE11):c.1501-4C>G rs377584386 0.00002
NM_005591.4(MRE11):c.77T>C (p.Met26Thr) rs372068015 0.00002
NM_005591.4(MRE11):c.1046G>A (p.Arg349Gln) rs864622683 0.00001
NM_005591.4(MRE11):c.1936G>A (p.Val646Ile) rs531090481 0.00001
NM_005591.4(MRE11):c.463C>T (p.Arg155Cys) rs587782512 0.00001
NM_005591.4(MRE11):c.661A>C (p.Ser221Arg) rs587781272 0.00001
NM_005591.4(MRE11):c.931G>T (p.Asp311Tyr) rs150138701 0.00001
NM_005591.4(MRE11):c.1151A>T (p.Lys384Ile) rs1193534253
NM_005591.4(MRE11):c.1462C>G (p.Arg488Gly) rs375261439
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.2021T>A (p.Ile674Asn) rs1591633964
NM_005591.4(MRE11):c.314+6T>C rs864622413
NM_005591.4(MRE11):c.402+7_402+9del
NM_005591.4(MRE11):c.52_54del (p.Ala18del) rs876658216
NM_005591.4(MRE11):c.562A>G (p.Arg188Gly) rs1946857150
NM_005591.4(MRE11):c.660-7G>T rs761857022
NM_005591.4(MRE11):c.986C>G (p.Thr329Ser) rs370645480

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