ClinVar Miner

List of variants in gene TRAPPC6B reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001079537.2(TRAPPC6B):c.445+14G>A rs8003807 0.92935
NM_001079537.2(TRAPPC6B):c.268-35A>G rs12147991 0.19285
NM_001079537.2(TRAPPC6B):c.474G>C (p.Leu158=) rs74683746 0.00453
NM_001079537.2(TRAPPC6B):c.327A>G (p.Lys109=) rs192501480 0.00078
NM_001079537.2(TRAPPC6B):c.268-16dup rs142476037
NM_001079537.2(TRAPPC6B):c.352-16dup rs144205574
NM_001079537.2(TRAPPC6B):c.352-17A>G rs142946910
NM_001079537.2(TRAPPC6B):c.446-3del rs150886646
NM_001079537.2(TRAPPC6B):c.446-3dup rs150886646

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.