ClinVar Miner

List of variants in gene MRE11 reported as uncertain significance by GeneDx

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Total variants: 22
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HGVS dbSNP
NM_005591.3(MRE11):c.1052G>A (p.Arg351His) rs587780133
NM_005591.3(MRE11):c.1090C>G (p.Arg364Gly) rs371077728
NM_005591.3(MRE11):c.1163G>A (p.Arg388Gln) rs587780134
NM_005591.3(MRE11):c.1221A>C (p.Lys407Asn) rs587780135
NM_005591.3(MRE11):c.1462C>T (p.Arg488Cys) rs375261439
NM_005591.3(MRE11):c.1475C>A (p.Ala492Asp) rs61749249
NM_005591.3(MRE11):c.1564G>A (p.Ala522Thr) rs587780136
NM_005591.3(MRE11):c.1727G>A (p.Arg576Gln) rs139461096
NM_005591.3(MRE11):c.1811G>A (p.Arg604His) rs148637964
NM_005591.3(MRE11):c.1811G>C (p.Arg604Pro) rs148637964
NM_005591.3(MRE11):c.1843T>C (p.Ser615Pro) rs587780137
NM_005591.3(MRE11):c.274G>A (p.Glu92Lys) rs587780139
NM_005591.3(MRE11):c.311G>C (p.Ser104Thr) rs587780140
NM_005591.3(MRE11):c.350A>G (p.Asn117Ser) rs137852760
NM_005591.3(MRE11):c.464G>A (p.Arg155His) rs587780141
NM_005591.3(MRE11):c.529G>A (p.Ala177Thr) rs142996063
NM_005591.3(MRE11):c.545-9C>A rs587780142
NM_005591.3(MRE11):c.604A>G (p.Arg202Gly) rs587780143
NM_005591.3(MRE11):c.653A>G (p.Gln218Arg) rs587780144
NM_005591.3(MRE11):c.788T>C (p.Ile263Thr) rs764146299
NM_005591.3(MRE11):c.818C>G (p.Ser273Cys) rs143400546
NM_005591.3(MRE11):c.846-12T>C rs587780145

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