List of variants in gene CARD11 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.1695C>T (p.Ala565=)	rs41454944	0.02103
NM_032415.7(CARD11):c.220+16C>T	rs41400946	0.01297
NM_032415.7(CARD11):c.3019+6C>T	rs199705831	0.00408
NM_032415.7(CARD11):c.180G>T (p.Val60=)	rs117016854	0.00091
NM_032415.7(CARD11):c.2060C>T (p.Ala687Val)	rs41493047	0.00088
NM_032415.7(CARD11):c.3145-3C>T	rs200456391	0.00077
NM_032415.7(CARD11):c.2670G>A (p.Ser890=)	rs146545469	0.00061
NM_032415.7(CARD11):c.3145-14C>T	rs201827805	0.00037
NM_032415.7(CARD11):c.2499C>T (p.Pro833=)	rs150171618	0.00019
NM_032415.7(CARD11):c.3303C>T (p.Arg1101=)	rs764369378	0.00005
NM_032415.7(CARD11):c.1341+15G>A
NM_032415.7(CARD11):c.224G>A (p.Arg75Gln)	rs1064795280

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.