List of variants in gene CST9L studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_080610.3(CST9L):c.170C>T (p.Thr57Ile)	rs200065971	0.00007
NM_080610.3(CST9L):c.110G>A (p.Cys37Tyr)	rs1331496453	0.00003
NM_080610.3(CST9L):c.127A>G (p.Met43Val)	rs2515301573
NM_080610.3(CST9L):c.136T>A (p.Tyr46Asn)	rs769999853
NM_080610.3(CST9L):c.142C>T (p.Pro48Ser)	rs758015425
NM_080610.3(CST9L):c.143C>T (p.Pro48Leu)
NM_080610.3(CST9L):c.158T>C (p.Phe53Ser)	rs2515301481
NM_080610.3(CST9L):c.219C>G (p.Ile73Met)
NM_080610.3(CST9L):c.227C>A (p.Ser76Tyr)	rs2515301310
NM_080610.3(CST9L):c.74T>C (p.Leu25Pro)

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.