ClinVar Miner

List of variants in gene MRE11 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.1334A>G (p.Gln445Arg) rs371730091 0.00014
NM_005591.4(MRE11):c.311G>C (p.Ser104Thr) rs587780140 0.00011
NM_005591.4(MRE11):c.818C>G (p.Ser273Cys) rs143400546 0.00009
NM_005591.4(MRE11):c.482A>G (p.Lys161Arg) rs587782294 0.00007
NM_005591.4(MRE11):c.274G>A (p.Glu92Lys) rs587780139 0.00006
NM_005591.4(MRE11):c.391G>A (p.Asp131Asn) rs368403414 0.00006
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.1163G>A (p.Arg388Gln) rs587780134 0.00002
NM_005591.4(MRE11):c.259C>T (p.Arg87Trp) rs758112386 0.00002
NM_005591.4(MRE11):c.1154T>C (p.Phe385Ser) rs786201817 0.00001
NM_005591.4(MRE11):c.1238A>G (p.Asn413Ser) rs587782457 0.00001
NM_005591.4(MRE11):c.1478T>G (p.Leu493Arg) rs786203158 0.00001
NM_005591.4(MRE11):c.1499A>T (p.Glu500Val) rs786203159 0.00001
NM_005591.4(MRE11):c.1699A>G (p.Asn567Asp) rs778585671 0.00001
NM_005591.4(MRE11):c.1718G>A (p.Gly573Glu) rs587781461 0.00001
NM_005591.4(MRE11):c.1875A>C (p.Lys625Asn) rs907660509 0.00001
NM_005591.4(MRE11):c.250A>G (p.Met84Val) rs786203222 0.00001
NM_005591.4(MRE11):c.826C>T (p.Pro276Ser) rs587782742 0.00001
NM_005591.4(MRE11):c.83A>C (p.Lys28Thr) rs876658611 0.00001
NM_005591.4(MRE11):c.1007G>A (p.Cys336Tyr) rs1228681022
NM_005591.4(MRE11):c.1185T>C (p.Ile395=) rs1001831519
NM_005591.4(MRE11):c.1269A>C (p.Glu423Asp)
NM_005591.4(MRE11):c.1270G>A (p.Gly424Arg) rs2135000168
NM_005591.4(MRE11):c.1462C>G (p.Arg488Gly) rs375261439
NM_005591.4(MRE11):c.1526A>C (p.Gln509Pro) rs1591667851
NM_005591.4(MRE11):c.1559G>C (p.Arg520Pro) rs753148077
NM_005591.4(MRE11):c.1669G>A (p.Asp557Asn) rs1591655152
NM_005591.4(MRE11):c.1724G>T (p.Gly575Val) rs376555330
NM_005591.4(MRE11):c.1811G>A (p.Arg604His) rs148637964
NM_005591.4(MRE11):c.1904T>G (p.Val635Gly) rs780850078
NM_005591.4(MRE11):c.2071GAT[6] (p.Asp695dup) rs779409748
NM_005591.4(MRE11):c.391G>T (p.Asp131Tyr) rs368403414

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.