List of variants in gene CIDEC reported by Genetic Services Laboratory, University of Chicago

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_001321142.2(CIDEC):c.96G>T (p.Leu32=)	rs456168	0.29400
NM_001321142.2(CIDEC):c.33C>G (p.Leu11=)	rs17851444	0.09372
NM_001321142.2(CIDEC):c.600C>T (p.His200=)	rs17222536	0.07435
NM_001321142.2(CIDEC):c.146C>T (p.Thr49Met)	rs61742367	0.01966
NM_001321142.2(CIDEC):c.181T>C (p.Tyr61His)	rs79419480	0.01577
NM_001321142.2(CIDEC):c.139G>A (p.Val47Ile)	rs150971509	0.00177
NM_001321142.2(CIDEC):c.594A>G (p.Thr198=)	rs147072100	0.00026
NM_001321142.2(CIDEC):c.467T>C (p.Ile156Thr)	rs201709635	0.00016
NM_001321142.2(CIDEC):c.160G>A (p.Val54Met)	rs148744468	0.00009
NM_001321142.2(CIDEC):c.545G>A (p.Arg182His)	rs111713852

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.