ClinVar Miner

List of variants in gene NEXN reported as benign by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_144573.3(NEXN):c.1422G>A (p.Arg474=) rs775204901
NM_144573.3(NEXN):c.732C>T (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.4(NEXN):c.1065T>C (p.Asp355=) rs369897647
NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln) rs35366555
NM_144573.4(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.4(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys) rs146245480
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.