List of variants in gene MRE11 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1480G>A (p.Glu494Lys)	rs104895016	0.00032
NM_005591.4(MRE11):c.1667A>G (p.Asn556Ser)	rs144896235	0.00018
NM_005591.4(MRE11):c.1504C>T (p.Arg502Cys)	rs186333183	0.00015
NM_005591.4(MRE11):c.1334A>G (p.Gln445Arg)	rs371730091	0.00014
NM_005591.4(MRE11):c.529G>A (p.Ala177Thr)	rs142996063	0.00010
NM_005591.4(MRE11):c.818C>G (p.Ser273Cys)	rs143400546	0.00009
NM_005591.4(MRE11):c.913C>T (p.Arg305Trp)	rs372000848	0.00008
NM_005591.4(MRE11):c.1858A>G (p.Ile620Val)	rs144070976	0.00006
NM_005591.4(MRE11):c.274G>A (p.Glu92Lys)	rs587780139	0.00006
NM_005591.4(MRE11):c.1852A>G (p.Met618Val)	rs375630981	0.00005
NM_005591.4(MRE11):c.1507C>T (p.Arg503Cys)	rs761458720	0.00003
NM_005591.4(MRE11):c.640T>C (p.Phe214Leu)	rs750929369	0.00003
NM_005591.4(MRE11):c.1145G>C (p.Ser382Thr)	rs745769023	0.00002
NM_005591.4(MRE11):c.1163G>A (p.Arg388Gln)	rs587780134	0.00002
NM_005591.4(MRE11):c.2042C>T (p.Ser681Leu)	rs587782166	0.00002
NM_005591.4(MRE11):c.2099C>G (p.Thr700Ser)	rs374685908	0.00002
NM_005591.4(MRE11):c.1045C>T (p.Arg349Trp)	rs570102851	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.1318G>T (p.Ala440Ser)	rs773469981
NM_005591.4(MRE11):c.1326G>A (p.Lys442=)	rs1591674710
NM_005591.4(MRE11):c.1420G>A (p.Val474Met)	rs778781414
NM_005591.4(MRE11):c.1811G>A (p.Arg604His)	rs148637964
NM_005591.4(MRE11):c.729G>C (p.Trp243Cys)	rs587782105

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.