List of variants in gene CARD14 reported as not provided

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.1641G>C (p.Arg547Ser)	rs2066964	0.35511
NM_001366385.1(CARD14):c.676-6G>A	rs28674001	0.31201
NM_001366385.1(CARD14):c.185G>A (p.Arg62Gln)	rs115582620	0.00439
NM_001366385.1(CARD14):c.449T>G (p.Leu150Arg)	rs146214639	0.00104
NM_001366385.1(CARD14):c.536G>A (p.Arg179His)	rs199517469	0.00027
NM_001366385.1(CARD14):c.112C>T (p.Arg38Cys)	rs281875217	0.00001
NM_001366385.1(CARD14):c.1778T>A (p.Ile593Asn)	rs281875220	0.00001
NM_001366385.1(CARD14):c.349G>A (p.Gly117Ser)	rs281875215	0.00001
NM_001366385.1(CARD14):c.571G>T (p.Val191Leu)	rs281875218	0.00001
NM_001366385.1(CARD14):c.413A>C (p.Glu138Ala)	rs281875214
NM_001366385.1(CARD14):c.424G>A (p.Glu142Lys)	rs281875212
NM_001366385.1(CARD14):c.425A>G (p.Glu142Gly)	rs281875213
NM_001366385.1(CARD14):c.511C>A (p.His171Asn)	rs281875216
NM_001366385.1(CARD14):c.599G>A (p.Ser200Asn)	rs114688446
NM_001366385.1(CARD14):c.675G>A (p.Glu225=)	rs1598640695
NM_001366385.1(CARD14):c.854A>G (p.Asp285Gly)	rs281875219

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.