ClinVar Miner

List of variants in gene NEXN reported as uncertain significance for Dilated cardiomyopathy 1CC; Familial hypertrophic cardiomyopathy 20

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP
NM_144573.3(NEXN):c.1046G>C (p.Arg349Thr)
NM_144573.3(NEXN):c.1053+1G>A rs397517843
NM_144573.3(NEXN):c.1055T>C (p.Val352Ala)
NM_144573.3(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.3(NEXN):c.1174C>T (p.Arg392Ter) rs750076188
NM_144573.3(NEXN):c.1244T>C (p.Met415Thr) rs1172366391
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.3(NEXN):c.1348dup (p.Ser450fs) rs1553240600
NM_144573.3(NEXN):c.134G>T (p.Arg45Ile)
NM_144573.3(NEXN):c.1401_1403AGA[2] (p.Glu470del) rs397517846
NM_144573.3(NEXN):c.1415C>G (p.Ala472Gly) rs539665448
NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del) rs794729091
NM_144573.3(NEXN):c.1422G>A (p.Arg474=) rs775204901
NM_144573.3(NEXN):c.1429A>G (p.Ile477Val) rs1553240667
NM_144573.3(NEXN):c.1430T>C (p.Ile477Thr)
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1457C>G (p.Ala486Gly) rs397517847
NM_144573.3(NEXN):c.1471G>C (p.Glu491Gln) rs373057251
NM_144573.3(NEXN):c.1573_1575GAA[3] (p.Glu528del) rs764505909
NM_144573.3(NEXN):c.1640T>C (p.Ile547Thr) rs753636624
NM_144573.3(NEXN):c.1664_1666del (p.Arg555_Glu556delinsLys) rs1221963637
NM_144573.3(NEXN):c.1671_1673GGA[3] (p.Glu562del) rs397517848
NM_144573.3(NEXN):c.1687G>T (p.Gly563Cys) rs1060499571
NM_144573.3(NEXN):c.1697T>C (p.Met566Thr)
NM_144573.3(NEXN):c.1739G>A (p.Gly580Glu)
NM_144573.3(NEXN):c.1753_1755AAG[1] (p.Lys586del) rs397517851
NM_144573.3(NEXN):c.1788T>G (p.Ser596Arg) rs199738750
NM_144573.3(NEXN):c.1852G>A (p.Glu618Lys) rs1060502321
NM_144573.3(NEXN):c.1877A>G (p.Glu626Gly)
NM_144573.3(NEXN):c.1901_1904delinsTCT (p.Gly634fs) rs1553242300
NM_144573.3(NEXN):c.1918_1922del (p.Tyr640fs) rs1222794437
NM_144573.3(NEXN):c.1946_1948GAG[1] (p.Gly650del) rs397517853
NM_144573.3(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197
NM_144573.3(NEXN):c.1994G>T (p.Ser665Ile) rs777703689
NM_144573.3(NEXN):c.1997C>A (p.Thr666Asn) rs749271412
NM_144573.3(NEXN):c.2008A>T (p.Thr670Ser)
NM_144573.3(NEXN):c.242A>T (p.Asp81Val) rs367871780
NM_144573.3(NEXN):c.250G>A (p.Glu84Lys)
NM_144573.3(NEXN):c.277G>C (p.Ala93Pro) rs1256690084
NM_144573.3(NEXN):c.379C>T (p.Arg127Cys) rs771113424
NM_144573.3(NEXN):c.392A>C (p.Gln131Pro) rs397517858
NM_144573.3(NEXN):c.431C>T (p.Ala144Val)
NM_144573.3(NEXN):c.491A>G (p.Glu164Gly) rs1553238441
NM_144573.3(NEXN):c.542C>T (p.Thr181Ile)
NM_144573.3(NEXN):c.586C>T (p.Arg196Cys) rs369486891
NM_144573.3(NEXN):c.613G>A (p.Glu205Lys) rs201447781
NM_144573.3(NEXN):c.643C>G (p.Gln215Glu) rs1557981819
NM_144573.3(NEXN):c.671G>A (p.Cys224Tyr) rs886046534
NM_144573.3(NEXN):c.687+4A>T rs754061340
NM_144573.3(NEXN):c.752T>G (p.Phe251Cys)
NM_144573.3(NEXN):c.767G>A (p.Arg256Gln) rs748921688
NM_144573.3(NEXN):c.818G>A (p.Arg273His) rs765385072
NM_144573.3(NEXN):c.857G>A (p.Arg286Gln)
NM_144573.3(NEXN):c.86G>T (p.Gly29Val) rs876657931
NM_144573.3(NEXN):c.871G>A (p.Glu291Lys) rs770120245
NM_144573.3(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.3(NEXN):c.902T>A (p.Ile301Asn) rs373878384

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.