ClinVar Miner

List of variants in gene MRE11 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.403-6G>A rs535801 0.28996
NM_005591.4(MRE11):c.2092A>G (p.Met698Val) rs1805362 0.00548
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp) rs61749249 0.00399
NM_005591.4(MRE11):c.822T>C (p.Leu274=) rs137868143 0.00152
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.1286T>C (p.Val429Ala) rs141293060 0.00023
NM_005591.4(MRE11):c.1643T>C (p.Ile548Thr) rs373522639 0.00016
NM_005591.4(MRE11):c.1504C>T (p.Arg502Cys) rs186333183 0.00015
NM_005591.4(MRE11):c.529G>A (p.Ala177Thr) rs142996063 0.00010
NM_005591.4(MRE11):c.534A>G (p.Leu178=) rs374635285 0.00003
NM_005591.4(MRE11):c.1098+10A>G rs1946604458 0.00001
NM_005591.4(MRE11):c.1476C>T (p.Ala492=) rs370397034 0.00001
NM_005591.4(MRE11):c.411A>G (p.Ala137=) rs776033471 0.00001
NM_005591.4(MRE11):c.19C>T (p.Leu7Phe) rs73517551
NM_005591.4(MRE11):c.2007A>G (p.Thr669=) rs1554999945
NM_005591.4(MRE11):c.235T>C (p.Leu79=) rs745332888

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.