ClinVar Miner

Variants in gene DOK7 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 15
Download table as spreadsheet
HGVS dbSNP
NM_173660.5(DOK7):c.-30G>T rs146168804
NM_173660.5(DOK7):c.-6C>G rs191800156
NM_173660.5(DOK7):c.1091G>A (p.Arg364Gln) rs201304841
NM_173660.5(DOK7):c.1143C>T (p.Pro381=) rs56769879
NM_173660.5(DOK7):c.1317C>T (p.Ser439=) rs16844467
NM_173660.5(DOK7):c.134C>T (p.Ser45Leu) rs62272670
NM_173660.5(DOK7):c.1351C>T (p.Arg451Trp) rs16844470
NM_173660.5(DOK7):c.189C>T (p.Cys63=) rs372989037
NM_173660.5(DOK7):c.332-4G>A rs199578351
NM_173660.5(DOK7):c.589G>A (p.Asp197Asn) rs16844422
NM_173660.5(DOK7):c.652+50G>A rs2006802
NM_173660.5(DOK7):c.782G>A (p.Arg261His) rs16844460
NM_173660.5(DOK7):c.918C>T (p.Ala306=) rs141947707
NM_173660.5(DOK7):c.921C>T (p.Ala307=) rs138148221
NM_173660.5(DOK7):c.967C>T (p.Arg323Cys) rs150728781

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.