ClinVar Miner

List of variants in gene DOCK8 reported as pathogenic 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
NM_203447.3(DOCK8):c.2606-1G>A rs886041535
NM_203447.3(DOCK8):c.2805_2811del (p.Met935fs) rs1554687151
NM_203447.3(DOCK8):c.2971-1G>A rs777066716
NM_203447.3(DOCK8):c.4162C>T (p.Arg1388Ter) rs1476130680
NM_203447.3(DOCK8):c.5132C>A (p.Ser1711Ter) rs1554707993
NM_203447.3(DOCK8):c.5261del (p.Leu1754fs) rs886041815
NM_203447.3(DOCK8):c.54-1G>T rs192864327
NM_203447.3(DOCK8):c.918_919insTTGAACT (p.Asp310fs) rs1064793335
NM_203447.3(DOCK8):c.949C>T (p.Arg317Ter) rs113432057

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.