ClinVar Miner

List of variants in gene DOK7 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_173660.5(DOK7):c.332-39T>C rs114948213 0.05163
NM_173660.5(DOK7):c.332-69A>G rs2857985 0.03470
NM_173660.5(DOK7):c.100+174C>A rs149895148 0.02135
NM_173660.5(DOK7):c.332-24C>A rs112637134 0.01918
NM_173660.5(DOK7):c.332-38G>A rs115931214 0.01540
NM_173660.5(DOK7):c.332-112G>A rs34427903 0.01425
NM_173660.5(DOK7):c.773-51G>A rs73195197 0.01184
NM_173660.5(DOK7):c.*67C>T rs73195198 0.01088
NM_001301071.2(DOK7):c.1620C>T (p.Pro540=) rs143778632 0.00976
NM_173660.5(DOK7):c.773-234G>A rs115385122 0.00955
NM_173660.5(DOK7):c.653-271G>A rs79739689 0.00907
NM_001301071.2(DOK7):c.*113G>A rs115864629 0.00883
NM_173660.5(DOK7):c.332-4G>A rs199578351 0.00790
NM_001301071.2(DOK7):c.1541-196del rs200094046 0.00629
NM_173660.5(DOK7):c.532+61T>C rs141667136 0.00593
NM_173660.5(DOK7):c.332-66C>T rs115797134 0.00523
NM_173660.5(DOK7):c.772+256T>G rs562196705 0.00523
NM_173660.5(DOK7):c.1204C>T (p.Arg402Trp) rs149905649 0.00516
NM_173660.5(DOK7):c.134C>T (p.Ser45Leu) rs62272670 0.00470
NM_001301071.2(DOK7):c.1599G>A (p.Ser533=) rs115742102 0.00363
NM_173660.5(DOK7):c.773-300C>G rs75837017 0.00363
NM_173660.5(DOK7):c.*155G>A rs186419797 0.00271
NM_173660.5(DOK7):c.773-320G>A rs116709196 0.00266
NM_173660.5(DOK7):c.1295G>A (p.Arg432Lys) rs145419117 0.00243
NM_173660.5(DOK7):c.904G>C (p.Ala302Pro) rs79063654 0.00237
NM_173660.5(DOK7):c.178G>A (p.Glu60Lys) rs199980106 0.00227
NM_173660.5(DOK7):c.919G>A (p.Ala307Thr) rs150415034 0.00210
NM_173660.5(DOK7):c.812G>C (p.Ser271Thr) rs144592743 0.00202
NM_173660.5(DOK7):c.921C>T (p.Ala307=) rs138148221 0.00170
NM_173660.5(DOK7):c.1480G>A (p.Val494Ile) rs202073484 0.00135
NM_173660.5(DOK7):c.1008G>A (p.Ser336=) rs185050737 0.00131
NM_173660.5(DOK7):c.1507C>A (p.Pro503Thr) rs184556570 0.00117
NM_173660.5(DOK7):c.831C>T (p.Ala277=) rs150549589 0.00113
NM_173660.5(DOK7):c.332-43_332-18del rs781466203 0.00108
NM_173660.5(DOK7):c.972G>A (p.Pro324=) rs373041663 0.00036
NM_173660.5(DOK7):c.282C>T (p.His94=) rs377025553 0.00022
NM_173660.5(DOK7):c.846C>T (p.Thr282=) rs141147662 0.00022
NM_173660.5(DOK7):c.*10A>C rs770677473 0.00021
NM_173660.5(DOK7):c.665C>T (p.Pro222Leu) rs141141719 0.00021
NM_173660.5(DOK7):c.1091G>A (p.Arg364Gln) rs201304841 0.00019
NM_173660.5(DOK7):c.1346C>T (p.Thr449Met) rs373864257 0.00013
NM_173660.5(DOK7):c.189C>T (p.Cys63=) rs372989037 0.00011
NM_173660.5(DOK7):c.1144G>A (p.Glu382Lys) rs560463670 0.00009
NM_173660.5(DOK7):c.652+5G>A rs772918388 0.00001
NC_000004.12:g.3463202G>A rs535749814
NM_001301071.2(DOK7):c.1540+105T>G rs879039610
NM_173660.4(DOK7):c.332-121_332-18del104ins234
NM_173660.4(DOK7):c.332-69_332-18del52ins182
NM_173660.5(DOK7):c.*147G>A rs73793944
NM_173660.5(DOK7):c.101-349G>C rs73793916
NM_173660.5(DOK7):c.1305C>A (p.Gly435=) rs201894731
NM_173660.5(DOK7):c.1323G>A (p.Gly441=) rs755615582
NM_173660.5(DOK7):c.1470G>C (p.Ser490=) rs543344505
NM_173660.5(DOK7):c.332-49C>T rs114112298
NM_173660.5(DOK7):c.332-50T>C rs137909368
NM_173660.5(DOK7):c.332-56G>T rs2699424
NM_173660.5(DOK7):c.332-70_332-69insGCCCCGCCCACCCTCGATGCCCTCTCGCCCCACCCGCCCATGATGCCCTCTC rs1560212351
NM_173660.5(DOK7):c.54+29G>T rs767030857
NM_173660.5(DOK7):c.652+65G>A rs144007944
NM_173660.5(DOK7):c.653-4A>G rs1577171863
NM_173660.5(DOK7):c.772+156C>T rs74720042
NM_173660.5(DOK7):c.772+270C>T rs79661487
NM_173660.5(DOK7):c.772+292_772+293del rs144492714
NM_173660.5(DOK7):c.773-184A>G rs112482136
NM_173660.5(DOK7):c.773-326G>T rs73793943
NM_173660.5(DOK7):c.918C>T (p.Ala306=) rs141947707

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