ClinVar Miner

List of variants in gene NEXN reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP
NM_001172309.1(NEXN):c.28-356T>C rs749182975
NM_144573.3(NEXN):c.1083T>C (p.Tyr361=) rs1060504549
NM_144573.3(NEXN):c.1089A>C (p.Thr363=) rs878855209
NM_144573.3(NEXN):c.1137A>G (p.Glu379=) rs1553240026
NM_144573.3(NEXN):c.1252-6T>C rs1571156994
NM_144573.3(NEXN):c.1401A>T (p.Ile467=) rs1571157558
NM_144573.3(NEXN):c.1413A>G (p.Arg471=) rs780858511
NM_144573.3(NEXN):c.1422G>A (p.Arg474=) rs775204901
NM_144573.3(NEXN):c.1450C>A (p.Arg484=) rs767792289
NM_144573.3(NEXN):c.1474-10T>C rs374541562
NM_144573.3(NEXN):c.1488T>C (p.Asp496=) rs754485056
NM_144573.3(NEXN):c.1533G>T (p.Val511=) rs765353395
NM_144573.3(NEXN):c.1582G>C (p.Glu528Gln) rs200071700
NM_144573.3(NEXN):c.1605A>G (p.Gln535=) rs778477679
NM_144573.3(NEXN):c.1743T>G (p.Ala581=) rs772313224
NM_144573.3(NEXN):c.1806G>A (p.Thr602=) rs373102543
NM_144573.3(NEXN):c.1809T>G (p.Val603=) rs1571175311
NM_144573.3(NEXN):c.1938A>C (p.Pro646=) rs1571176052
NM_144573.3(NEXN):c.222T>C (p.Ile74=) rs767610015
NM_144573.3(NEXN):c.292T>C (p.Leu98=) rs539220077
NM_144573.3(NEXN):c.299-10A>G rs1452768769
NM_144573.3(NEXN):c.321T>A (p.Ala107=) rs1553236762
NM_144573.3(NEXN):c.456C>T (p.Asp152=) rs760312569
NM_144573.3(NEXN):c.468G>A (p.Thr156=) rs199988442
NM_144573.3(NEXN):c.492A>G (p.Glu164=) rs1571134764
NM_144573.3(NEXN):c.507A>G (p.Leu169=) rs776106290
NM_144573.3(NEXN):c.579A>G (p.Glu193=) rs1476054611
NM_144573.3(NEXN):c.732C>T (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.739T>C (p.Leu247=) rs781118443
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.865-9T>C rs182083204
NM_144573.3(NEXN):c.987A>C (p.Ala329=) rs1270187994
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.4(NEXN):c.1257G>A (p.Glu419=)
NM_144573.4(NEXN):c.1266T>C (p.Asn422=)
NM_144573.4(NEXN):c.133A>C (p.Arg45=)
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845
NM_144573.4(NEXN):c.1368A>G (p.Gly456=)
NM_144573.4(NEXN):c.1372T>C (p.Leu458=)
NM_144573.4(NEXN):c.1377T>A (p.Ser459=)
NM_144573.4(NEXN):c.1419A>G (p.Arg473=)
NM_144573.4(NEXN):c.1651C>T (p.Leu551=)
NM_144573.4(NEXN):c.1662A>G (p.Lys554=)
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.1704C>T (p.Gly568=) rs397517850
NM_144573.4(NEXN):c.1950A>G (p.Gly650=)
NM_144573.4(NEXN):c.1995T>C (p.Ser665=)
NM_144573.4(NEXN):c.207G>A (p.Arg69=)
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.4(NEXN):c.270A>G (p.Val90=)
NM_144573.4(NEXN):c.448-10C>T
NM_144573.4(NEXN):c.591A>G (p.Glu197=)
NM_144573.4(NEXN):c.669G>A (p.Lys223=)
NM_144573.4(NEXN):c.688-10G>A rs370574269
NM_144573.4(NEXN):c.711A>C (p.Ala237=)
NM_144573.4(NEXN):c.855G>A (p.Arg285=)
NM_144573.4(NEXN):c.865-5G>A rs727505353
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.4(NEXN):c.949A>C (p.Met317Leu) rs559464457

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.