ClinVar Miner

List of variants in gene MRE11 reported as likely benign for DNA repair disease

Included ClinVar conditions (97):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_005591.3(MRE11):c.*1743dup rs200848216
NM_005591.3(MRE11):c.*1766G>C rs13447752
NM_005591.3(MRE11):c.*183G>A rs13447745
NM_005591.3(MRE11):c.*2699A>T rs13447760
NM_005591.3(MRE11):c.*442A>G rs1061956
NM_005591.3(MRE11):c.*511G>A rs13447749
NM_005591.3(MRE11):c.-106+5G>A rs1805363
NM_005591.3(MRE11):c.-178G>A rs1805360
NM_005591.3(MRE11):c.1002C>G (p.Ser334Arg) rs115244417
NM_005591.3(MRE11):c.1074A>G (p.Pro358=) rs876659934
NM_005591.3(MRE11):c.1096C>A (p.Arg366=) rs372411821
NM_005591.3(MRE11):c.1098+8C>A rs749039246
NM_005591.3(MRE11):c.120C>T (p.Leu40=) rs1805364
NM_005591.3(MRE11):c.121G>A (p.Asp41Asn) rs116679717
NM_005591.3(MRE11):c.1225+8A>T rs748847974
NM_005591.3(MRE11):c.1226-5T>C rs1555009952
NM_005591.3(MRE11):c.1404T>C (p.Asp468=) rs368144567
NM_005591.3(MRE11):c.1443A>C (p.Thr481=) rs375077574
NM_005591.3(MRE11):c.1443A>G (p.Thr481=) rs375077574
NM_005591.3(MRE11):c.1475C>A (p.Ala492Asp) rs61749249
NM_005591.3(MRE11):c.1476C>T (p.Ala492=) rs370397034
NM_005591.3(MRE11):c.1491C>T (p.Ile497=) rs199634245
NM_005591.3(MRE11):c.1783+5G>C rs142082313
NM_005591.3(MRE11):c.1783+7A>G rs774520952
NM_005591.3(MRE11):c.1784-6T>C rs978608099
NM_005591.3(MRE11):c.1798G>C (p.Glu600Gln) rs145415033
NM_005591.3(MRE11):c.1868-4C>A rs768257868
NM_005591.3(MRE11):c.1868-7A>G rs761270600
NM_005591.3(MRE11):c.1868-9del rs770953646
NM_005591.3(MRE11):c.1927-9C>A rs1060504336
NM_005591.3(MRE11):c.1994+10G>A rs1805366
NM_005591.3(MRE11):c.20+8C>A rs766581183
NM_005591.3(MRE11):c.2049G>A (p.Gly683=) rs758931835
NM_005591.3(MRE11):c.2070+14A>C rs369127675
NM_005591.3(MRE11):c.291G>A (p.Gln97=) rs776642337
NM_005591.3(MRE11):c.315-4del rs35062043
NM_005591.3(MRE11):c.37T>A (p.Phe13Ile) rs149101834
NM_005591.3(MRE11):c.403-6_403-5delinsAT rs1555015255
NM_005591.3(MRE11):c.426C>T (p.Asp142=) rs3218740
NM_005591.3(MRE11):c.498G>A (p.Pro166=) rs753061100
NM_005591.3(MRE11):c.597A>G (p.Thr199=) rs1555014527
NM_005591.3(MRE11):c.618T>C (p.Asp206=) rs786201438
NM_005591.3(MRE11):c.690A>G (p.Pro230=) rs786203787
NM_005591.3(MRE11):c.777G>A (p.Gln259=) rs774144789
NM_005591.3(MRE11):c.822T>C (p.Leu274=) rs137868143
NM_005591.3(MRE11):c.845+11T>C rs140145979
NM_005591.3(MRE11):c.942A>G (p.Leu314=) rs1555012700
NM_005591.3(MRE11):c.969A>G (p.Pro323=) rs13447633
NM_005591.3(MRE11):c.999A>G (p.Gln333=) rs747898039

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