ClinVar Miner

List of variants in gene DOCK7 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001367561.1(DOCK7):c.2605G>A (p.Gly869Ser) rs201823761 0.00069
NM_001367561.1(DOCK7):c.1265T>C (p.Val422Ala) rs199708701 0.00029
NM_001367561.1(DOCK7):c.2578C>A (p.Pro860Thr) rs150032045 0.00016
NM_001367561.1(DOCK7):c.692G>A (p.Arg231His) rs757667036 0.00006
NM_001367561.1(DOCK7):c.2630C>G (p.Ala877Gly) rs139050582 0.00004
NM_001367561.1(DOCK7):c.3152C>T (p.Thr1051Met) rs757960377 0.00003
NM_001367561.1(DOCK7):c.3211A>G (p.Asn1071Asp) rs371894094 0.00003
NM_001367561.1(DOCK7):c.1884T>G (p.Phe628Leu) rs1188863501 0.00001
NM_001367561.1(DOCK7):c.3761C>T (p.Pro1254Leu) rs1427395524 0.00001
NM_001367561.1(DOCK7):c.5359A>G (p.Met1787Val) rs775189099 0.00001
NM_001367561.1(DOCK7):c.5810A>G (p.Asn1937Ser) rs764578433 0.00001
NM_001367561.1(DOCK7):c.1900G>C (p.Val634Leu) rs774732062
NM_001367561.1(DOCK7):c.1985C>T (p.Pro662Leu) rs1417203749
NM_001367561.1(DOCK7):c.3852_3854del (p.Met1284del) rs751833296
NM_001367561.1(DOCK7):c.5731A>G (p.Ile1911Val) rs1645957860

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.