ClinVar Miner

List of variants in gene DPAGT1 reported as likely benign for DPAGT1-CDG

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
NM_001382.4(DPAGT1):c.1141T>C (p.Leu381=) rs768805817
NM_001382.4(DPAGT1):c.1203C>T (p.Leu401=) rs746759603
NM_001382.4(DPAGT1):c.243C>T (p.Cys81=) rs138519099
NM_001382.4(DPAGT1):c.250A>C (p.Lys84Gln) rs112355069
NM_001382.4(DPAGT1):c.291C>G (p.Ala97=) rs756818317
NM_001382.4(DPAGT1):c.330C>T (p.Phe110=) rs199994118
NM_001382.4(DPAGT1):c.33G>A (p.Leu11=) rs773853061
NM_001382.4(DPAGT1):c.351A>G (p.Val117=) rs146610900
NM_001382.4(DPAGT1):c.644-10G>A rs192269738
NM_001382.4(DPAGT1):c.717C>T (p.Leu239=) rs377263230
NM_001382.4(DPAGT1):c.728+9G>A rs369353136
NM_001382.4(DPAGT1):c.828A>G (p.Leu276=) rs780516960
NM_001382.4(DPAGT1):c.918-4G>A rs201656540
NM_001382.4(DPAGT1):c.918-8C>T rs531346717

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.