ClinVar Miner

List of variants in gene DOCK2 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004946.3(DOCK2):c.3945T>C (p.Tyr1315=) rs34133853 0.00985
NM_004946.3(DOCK2):c.631A>G (p.Met211Val) rs151191554 0.00305
NM_004946.3(DOCK2):c.90G>C (p.Gln30His) rs141894939 0.00226
NM_004946.3(DOCK2):c.1360G>A (p.Ala454Thr) rs114888195 0.00210
NM_004946.3(DOCK2):c.4201G>T (p.Ala1401Ser) rs143100569 0.00161
NM_004946.3(DOCK2):c.753G>A (p.Thr251=) rs146746458 0.00113
NM_004946.3(DOCK2):c.5425A>G (p.Thr1809Ala) rs146886839 0.00110
NM_004946.3(DOCK2):c.2587A>G (p.Lys863Glu) rs141501849 0.00100
NM_004946.3(DOCK2):c.5484G>A (p.Thr1828=) rs140198889 0.00095
NM_004946.3(DOCK2):c.1316A>G (p.Asn439Ser) rs113673055 0.00094
NM_004946.3(DOCK2):c.5445G>A (p.Ser1815=) rs200128185 0.00090
NM_004946.3(DOCK2):c.3836C>T (p.Thr1279Met) rs145873210 0.00066
NM_004946.3(DOCK2):c.3756+9A>T rs570358398 0.00021
NM_004946.3(DOCK2):c.2858C>T (p.Ser953Phe) rs35395501 0.00011
NM_004946.3(DOCK2):c.2704-3C>T rs144101028 0.00006
NM_004946.3(DOCK2):c.1437T>C (p.Val479=) rs147336443 0.00001
NM_004946.3(DOCK2):c.360G>A (p.Met120Ile) rs752809346 0.00001
NM_004946.3(DOCK2):c.1716A>T (p.Arg572=)
NM_004946.3(DOCK2):c.1767T>G (p.Val589=) rs34864600
NM_004946.3(DOCK2):c.4449G>A (p.Glu1483=)
NM_004946.3(DOCK2):c.660C>A (p.Thr220=)

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.