List of variants in gene CTNS reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004937.3(CTNS):c.382C>T (p.Gln128Ter)	rs550254092
NM_004937.3(CTNS):c.423del (p.Phe142fs)	rs1567709909
NM_004937.3(CTNS):c.561+1del	rs786204667
NM_004937.3(CTNS):c.565C>T (p.Gln189Ter)	rs1597654770
NM_004937.3(CTNS):c.61_61+2del	rs2075652654
NM_004937.3(CTNS):c.839A>G (p.Lys280Arg)	rs2150925451
NM_004937.3(CTNS):c.850C>T (p.Gln284Ter)
NM_004937.3(CTNS):c.870C>G (p.Tyr290Ter)	rs776842972

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.