ClinVar Miner

List of variants in gene MRE11 reported by Fulgent Genetics,Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_005591.3(MRE11):c.1045C>T (p.Arg349Trp) rs570102851
NM_005591.3(MRE11):c.1145G>C (p.Ser382Thr) rs745769023
NM_005591.3(MRE11):c.1163G>A (p.Arg388Gln) rs587780134
NM_005591.3(MRE11):c.1318G>T (p.Ala440Ser) rs773469981
NM_005591.3(MRE11):c.1334A>G (p.Gln445Arg) rs371730091
NM_005591.3(MRE11):c.1420G>A (p.Val474Met) rs778781414
NM_005591.3(MRE11):c.1478T>G (p.Leu493Arg) rs786203158
NM_005591.3(MRE11):c.1480G>A (p.Glu494Lys) rs104895016
NM_005591.3(MRE11):c.1499A>T (p.Glu500Val) rs786203159
NM_005591.3(MRE11):c.1504C>T (p.Arg502Cys) rs186333183
NM_005591.3(MRE11):c.1667A>G (p.Asn556Ser) rs144896235
NM_005591.3(MRE11):c.1811G>A (p.Arg604His) rs148637964
NM_005591.3(MRE11):c.2099C>G (p.Thr700Ser) rs374685908
NM_005591.3(MRE11):c.274G>A (p.Glu92Lys) rs587780139
NM_005591.3(MRE11):c.529G>A (p.Ala177Thr) rs142996063
NM_005591.3(MRE11):c.640T>C (p.Phe214Leu) rs750929369
NM_005591.3(MRE11):c.818C>G (p.Ser273Cys) rs143400546

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.