ClinVar Miner

List of variants in gene DOCK8 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 102
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.4491T>C (p.Phe1497=) rs7854035 0.99726
NM_203447.4(DOCK8):c.2606-141A>G rs913702 0.99479
NM_203447.4(DOCK8):c.2605+30T>C rs10758420 0.93542
NM_203447.4(DOCK8):c.5433G>A (p.Glu1811=) rs1887957 0.75495
NM_203447.4(DOCK8):c.5356-48C>T rs10974467 0.71940
NM_203447.4(DOCK8):c.4785+6C>G rs7036567 0.70190
NM_203447.4(DOCK8):c.4886+3A>G rs2360712 0.69369
NM_203447.4(DOCK8):c.4627-85T>C rs1329377 0.68824
NM_203447.4(DOCK8):c.894+74_894+75insC rs3831138 0.67848
NM_203447.4(DOCK8):c.895-16T>C rs2296828 0.66765
NM_203447.4(DOCK8):c.895-84G>C rs2296825 0.63039
NM_203447.4(DOCK8):c.4241+22T>C rs10217719 0.57971
NM_203447.4(DOCK8):c.5223+65G>C rs10758598 0.57714
NM_203447.4(DOCK8):c.53+28T>C rs481905 0.56560
NM_203447.4(DOCK8):c.827+67G>A rs10813355 0.55088
NM_203447.4(DOCK8):c.2206-48A>G rs7020921 0.53910
NM_203447.4(DOCK8):c.742-45C>T rs2296824 0.48186
NM_203447.4(DOCK8):c.4107C>G (p.Leu1369=) rs2297079 0.44487
NM_203447.4(DOCK8):c.4154-68T>A rs2297081 0.43281
NM_203447.4(DOCK8):c.3120+116A>T rs3818619 0.41390
NM_203447.4(DOCK8):c.333-29_333-28insAT rs34722895 0.38956
NM_203447.4(DOCK8):c.2606-123T>C rs748429 0.38499
NM_203447.4(DOCK8):c.3701-78T>C rs7027996 0.37853
NM_203447.4(DOCK8):c.895-65T>G rs2296826 0.36072
NM_203447.4(DOCK8):c.3701-150A>G rs7024113 0.35110
NM_203447.4(DOCK8):c.3840+65T>C rs7031432 0.33889
NM_203447.4(DOCK8):c.65C>T (p.Ala22Val) rs506121 0.32449
NM_203447.4(DOCK8):c.2441-130A>G rs10814493 0.31427
NM_203447.4(DOCK8):c.2441-128C>T rs10814494 0.31418
NM_203447.4(DOCK8):c.2605+100G>T rs11790531 0.25146
NM_203447.4(DOCK8):c.1238A>G (p.Asn413Ser) rs10970979 0.24995
NM_203447.4(DOCK8):c.2340G>C (p.Leu780=) rs10814431 0.24804
NM_203447.4(DOCK8):c.1812A>G (p.Lys604=) rs913703 0.23408
NM_203447.4(DOCK8):c.3701-65T>C rs10814836 0.21379
NM_203447.4(DOCK8):c.2971-36T>G rs2297077 0.21185
NM_203447.4(DOCK8):c.2971-35C>A rs2297078 0.21170
NM_203447.4(DOCK8):c.2971-73T>A rs2297076 0.21044
NM_203447.4(DOCK8):c.2110-88C>T rs10973003 0.20984
NM_203447.4(DOCK8):c.2778+125C>G rs3739598 0.20533
NM_203447.4(DOCK8):c.2970+70A>G rs10814649 0.18015
NM_203447.4(DOCK8):c.3700+93A>C rs55709009 0.17006
NM_203447.4(DOCK8):c.2110-31T>A rs35724655 0.16616
NM_203447.4(DOCK8):c.528+65G>A rs13292474 0.14289
NM_203447.4(DOCK8):c.1692T>C (p.Tyr564=) rs10972587 0.13521
NM_203447.4(DOCK8):c.3840+69T>G rs12352911 0.13267
NM_203447.4(DOCK8):c.895-26T>C rs2296827 0.12249
NM_203447.4(DOCK8):c.1798-31A>G rs12156499 0.10528
NM_203447.4(DOCK8):c.5832G>A (p.Pro1944=) rs10491684 0.09400
NM_203447.4(DOCK8):c.1790C>T (p.Ala597Val) rs17673268 0.07826
NM_203447.4(DOCK8):c.5908G>C (p.Ala1970Pro) rs34908836 0.07052
NM_203447.4(DOCK8):c.3234+8del rs112565335 0.07045
NM_203447.4(DOCK8):c.3230G>A (p.Ser1077Asn) rs34627722 0.05757
NM_203447.4(DOCK8):c.741+28A>T rs12344468 0.05350
NM_203447.4(DOCK8):c.3208A>G (p.Asn1070Asp) rs73382631 0.03284
NM_203447.4(DOCK8):c.2295C>T (p.Ser765=) rs12348944 0.03237
NM_203447.4(DOCK8):c.5818-14C>T rs10124592 0.02927
NM_203447.4(DOCK8):c.3021T>C (p.Phe1007=) rs7034926 0.02921
NM_203447.4(DOCK8):c.952G>A (p.Ala318Thr) rs35482838 0.02279
NM_203447.4(DOCK8):c.709G>A (p.Glu237Lys) rs11789099 0.02275
NM_203447.4(DOCK8):c.3565A>G (p.Ile1189Val) rs77399114 0.02082
NM_203447.4(DOCK8):c.528+13A>G rs116483820 0.01176
NM_203447.4(DOCK8):c.3234+16A>C rs77395345 0.01120
NM_203447.4(DOCK8):c.5001C>T (p.His1667=) rs35662752 0.01091
NM_203447.4(DOCK8):c.5211G>A (p.Glu1737=) rs34098809 0.00985
NM_203447.4(DOCK8):c.3840+3A>G rs16938572 0.00865
NM_203447.4(DOCK8):c.2971-14A>G rs140114637 0.00841
NM_203447.4(DOCK8):c.2862A>T (p.Pro954=) rs117610764 0.00615
NM_203447.4(DOCK8):c.5154C>T (p.Cys1718=) rs140431229 0.00514
NM_203447.4(DOCK8):c.5187A>G (p.Val1729=) rs111535933 0.00493
NM_203447.4(DOCK8):c.3573C>T (p.Ser1191=) rs13285348 0.00471
NM_203447.4(DOCK8):c.3701-17C>T rs376111035 0.00409
NM_203447.4(DOCK8):c.1017G>A (p.Pro339=) rs35746964 0.00395
NM_203447.4(DOCK8):c.3022C>T (p.Arg1008Trp) rs16937932 0.00387
NM_203447.4(DOCK8):c.1356G>A (p.Leu452=) rs113175936 0.00301
NM_203447.4(DOCK8):c.1582C>A (p.Leu528Met) rs146250176 0.00213
NM_203447.4(DOCK8):c.528+7C>A rs114833839 0.00207
NM_203447.4(DOCK8):c.4024-4C>T rs111306749 0.00196
NM_203447.4(DOCK8):c.3234+8T>C rs112290938 0.00132
NM_203447.4(DOCK8):c.5010G>A (p.Ala1670=) rs142208336 0.00128
NM_203447.4(DOCK8):c.679G>A (p.Glu227Lys) rs76276364 0.00068
NM_203447.4(DOCK8):c.5962-8C>T rs749575443 0.00061
NM_203447.4(DOCK8):c.3058A>G (p.Ile1020Val) rs151094543 0.00046
NM_203447.4(DOCK8):c.5491-7T>A rs184867151 0.00010
NM_203447.4(DOCK8):c.2778+20G>A rs587780923 0.00005
NM_203447.4(DOCK8):c.3079G>A (p.Val1027Ile) rs199782622 0.00001
NM_203447.4(DOCK8):c.157-5432A>G
NM_203447.4(DOCK8):c.1868+70G>C rs11515377
NM_203447.4(DOCK8):c.2440+159del rs57180068
NM_203447.4(DOCK8):c.2916C>T (p.Thr972=) rs2297075
NM_203447.4(DOCK8):c.3234+15C>A rs79462548
NM_203447.4(DOCK8):c.3234+21dup rs3831174
NM_203447.4(DOCK8):c.3530+94dup rs60568745
NM_203447.4(DOCK8):c.404+16del rs727505303
NM_203447.4(DOCK8):c.4627-13_4627-12del rs34439675
NM_203447.4(DOCK8):c.5080-143G>C rs10733508
NM_203447.4(DOCK8):c.5223+79A>C rs10217568
NM_203447.4(DOCK8):c.5490+21C>T rs1887958
NM_203447.4(DOCK8):c.5581-18G>C rs10814952
NM_203447.4(DOCK8):c.5818-84G>T rs2031946
NM_203447.4(DOCK8):c.699T>C (p.Asn233=) rs2039045
NM_203447.4(DOCK8):c.741+2043G>A
NM_203447.4(DOCK8):c.894+80T>C rs2360277

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