ClinVar Miner

List of variants in gene DOCK8 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00276
NM_203447.4(DOCK8):c.4724G>A (p.Arg1575Lys) rs141252560 0.00121
NM_203447.4(DOCK8):c.550G>A (p.Val184Met) rs143461644 0.00105
NM_203447.4(DOCK8):c.3988C>G (p.Leu1330Val) rs148081681 0.00076
NM_203447.4(DOCK8):c.3263C>T (p.Thr1088Met) rs149065013 0.00067
NM_203447.4(DOCK8):c.3023G>A (p.Arg1008Gln) rs145844320 0.00064
NM_203447.4(DOCK8):c.494C>T (p.Ser165Leu) rs146490788 0.00061
NM_203447.4(DOCK8):c.685G>C (p.Ala229Pro) rs149234127 0.00060
NM_203447.4(DOCK8):c.5155G>A (p.Ala1719Thr) rs144279637 0.00055
NM_203447.4(DOCK8):c.986C>T (p.Ala329Val) rs75352090 0.00055
NM_203447.4(DOCK8):c.3312G>C (p.Glu1104Asp) rs138810908 0.00054
NM_203447.4(DOCK8):c.5612A>G (p.Tyr1871Cys) rs140403518 0.00048
NM_203447.4(DOCK8):c.3067A>G (p.Ile1023Val) rs140148619 0.00041
NM_203447.4(DOCK8):c.1193G>A (p.Arg398Gln) rs147287319 0.00040
NM_203447.4(DOCK8):c.2749G>A (p.Glu917Lys) rs200899164 0.00030
NM_203447.4(DOCK8):c.5828C>T (p.Thr1943Ile) rs148368084 0.00025
NM_203447.4(DOCK8):c.1979C>A (p.Ala660Asp) rs550289472 0.00021
NM_203447.4(DOCK8):c.2275G>A (p.Val759Met) rs148693111 0.00021
NM_203447.4(DOCK8):c.3220C>A (p.His1074Asn) rs150298985 0.00019
NM_203447.4(DOCK8):c.5223+4A>G rs117109271 0.00017
NM_203447.4(DOCK8):c.626G>A (p.Arg209Gln) rs151262535 0.00017
NM_203447.4(DOCK8):c.1623C>G (p.His541Gln) rs200201944 0.00015
NM_203447.4(DOCK8):c.950G>A (p.Arg317Gln) rs191413750 0.00015
NM_203447.4(DOCK8):c.4774T>C (p.Phe1592Leu) rs200152962 0.00012
NM_203447.4(DOCK8):c.3712C>T (p.Arg1238Cys) rs764380170 0.00010
NM_203447.4(DOCK8):c.3603C>G (p.Arg1201=) rs149908718 0.00009
NM_203447.4(DOCK8):c.1325C>T (p.Ser442Phe) rs745498345 0.00006
NM_203447.4(DOCK8):c.2296G>A (p.Glu766Lys) rs267602235 0.00006
NM_203447.4(DOCK8):c.2779A>G (p.Ile927Val) rs759239515 0.00006
NM_203447.4(DOCK8):c.4003G>T (p.Val1335Leu) rs141863163 0.00006
NM_203447.4(DOCK8):c.3323A>G (p.Asn1108Ser) rs151210108 0.00005
NM_203447.4(DOCK8):c.3414C>A (p.Phe1138Leu) rs781435688 0.00004
NM_203447.4(DOCK8):c.5595C>G (p.Ile1865Met) rs151208894 0.00004
NM_203447.4(DOCK8):c.559G>A (p.Asp187Asn) rs111842279 0.00004
NM_203447.4(DOCK8):c.689G>A (p.Arg230Gln) rs771753565 0.00004
NM_203447.4(DOCK8):c.1475A>G (p.Lys492Arg) rs747740764 0.00003
NM_203447.4(DOCK8):c.1528C>A (p.Leu510Met) rs771479299 0.00003
NM_203447.4(DOCK8):c.4154-5C>G rs760043749 0.00002
NM_203447.4(DOCK8):c.5250G>T (p.Glu1750Asp) rs1329426200 0.00002
NM_203447.4(DOCK8):c.1004C>T (p.Ser335Leu) rs778329456 0.00001
NM_203447.4(DOCK8):c.1433G>A (p.Arg478His) rs757667271 0.00001
NM_203447.4(DOCK8):c.148C>T (p.Leu50Phe) rs1045835531 0.00001
NM_203447.4(DOCK8):c.3044G>A (p.Arg1015His) rs200494857 0.00001
NM_203447.4(DOCK8):c.3508G>A (p.Ala1170Thr) rs749729496 0.00001
NM_203447.4(DOCK8):c.3614C>G (p.Pro1205Arg) rs1310119190 0.00001
NM_203447.4(DOCK8):c.3844T>C (p.Tyr1282His) rs945093849 0.00001
NM_203447.4(DOCK8):c.4252G>A (p.Glu1418Lys) rs764918764 0.00001
NM_203447.4(DOCK8):c.472C>G (p.Leu158Val) rs542942121 0.00001
NM_203447.4(DOCK8):c.4895A>G (p.Lys1632Arg) rs760713559 0.00001
NM_203447.4(DOCK8):c.4999C>T (p.His1667Tyr) rs373762198 0.00001
NM_203447.4(DOCK8):c.5491-4C>T rs780798376 0.00001
NM_203447.4(DOCK8):c.5548C>T (p.Pro1850Ser) rs369327204 0.00001
NM_203447.4(DOCK8):c.5580+3A>G rs759762552 0.00001
NM_203447.4(DOCK8):c.5731G>C (p.Glu1911Gln) rs759086407 0.00001
NM_203447.4(DOCK8):c.919C>G (p.Leu307Val) rs560133135 0.00001
NM_203447.4(DOCK8):c.930C>G (p.Asp310Glu) rs770327895 0.00001
GRCh37/hg19 9p24.3(chr9:203861-228301)x1
GRCh37/hg19 9p24.3(chr9:203861-238536)x1
GRCh37/hg19 9p24.3(chr9:203861-258459)x1
GRCh37/hg19 9p24.3(chr9:203861-259575)x3
GRCh37/hg19 9p24.3(chr9:203861-265340)x1
GRCh37/hg19 9p24.3(chr9:203861-268590)x1
GRCh37/hg19 9p24.3(chr9:203861-273057)x3
GRCh37/hg19 9p24.3(chr9:203861-273071)x3
GRCh37/hg19 9p24.3(chr9:203861-273233)x3
GRCh37/hg19 9p24.3(chr9:203861-289697)x3
GRCh37/hg19 9p24.3(chr9:203861-302936)x3
GRCh37/hg19 9p24.3(chr9:203861-305975)x3
GRCh37/hg19 9p24.3(chr9:203861-309108)x1
GRCh37/hg19 9p24.3(chr9:203861-340662)x3
GRCh37/hg19 9p24.3(chr9:203861-341078)x3
GRCh37/hg19 9p24.3(chr9:203861-352855)x3
GRCh37/hg19 9p24.3(chr9:203861-355137)x3
GRCh37/hg19 9p24.3(chr9:203861-355137)x4
GRCh37/hg19 9p24.3(chr9:203861-360381)x4
GRCh37/hg19 9p24.3(chr9:203861-388367)x1
GRCh37/hg19 9p24.3(chr9:203861-398309)x3
GRCh37/hg19 9p24.3(chr9:203861-399039)x1
GRCh37/hg19 9p24.3(chr9:203861-399039)x3
GRCh37/hg19 9p24.3(chr9:203861-402280)x3
GRCh37/hg19 9p24.3(chr9:203861-417448)x1
GRCh37/hg19 9p24.3(chr9:203861-429474)x3
GRCh37/hg19 9p24.3(chr9:203861-450060)x3
GRCh37/hg19 9p24.3(chr9:203862-258973)x1
GRCh37/hg19 9p24.3(chr9:204193-349093)x3
GRCh37/hg19 9p24.3(chr9:209753-236828)x1
GRCh37/hg19 9p24.3(chr9:209753-246900)x1
GRCh37/hg19 9p24.3(chr9:211086-416351)x3
GRCh37/hg19 9p24.3(chr9:221948-277621)x3
GRCh37/hg19 9p24.3(chr9:222579-355137)x3
GRCh37/hg19 9p24.3(chr9:230227-309108)x1
GRCh37/hg19 9p24.3(chr9:236176-402280)x3
GRCh37/hg19 9p24.3(chr9:242583-353602)x1
GRCh37/hg19 9p24.3(chr9:249919-410357)x4
GRCh37/hg19 9p24.3(chr9:250117-410357)x3
GRCh37/hg19 9p24.3(chr9:265307-454023)x3
GRCh37/hg19 9p24.3(chr9:265308-328178)x1
GRCh37/hg19 9p24.3(chr9:268079-309108)x1
GRCh37/hg19 9p24.3(chr9:304136-399039)x3
GRCh37/hg19 9p24.3(chr9:328022-464219)x3
GRCh37/hg19 9p24.3(chr9:335731-425611)x1
GRCh37/hg19 9p24.3(chr9:388405-430789)x1
GRCh37/hg19 9p24.3(chr9:409135-436983)x1
NM_203447.4(DOCK8):c.1090C>A (p.Pro364Thr)
NM_203447.4(DOCK8):c.1090C>T (p.Pro364Ser) rs146777948
NM_203447.4(DOCK8):c.1422G>A (p.Gln474=) rs1563936093
NM_203447.4(DOCK8):c.1516G>A (p.Gly506Ser)
NM_203447.4(DOCK8):c.1637A>G (p.Glu546Gly) rs2051518779
NM_203447.4(DOCK8):c.1798-4A>G rs774596616
NM_203447.4(DOCK8):c.2017A>T (p.Ile673Phe) rs372858877
NM_203447.4(DOCK8):c.2071G>A (p.Glu691Lys) rs1586828062
NM_203447.4(DOCK8):c.2441-3C>A rs1184305319
NM_203447.4(DOCK8):c.2485A>C (p.Asn829His)
NM_203447.4(DOCK8):c.2590G>A (p.Asp864Asn) rs746815514
NM_203447.4(DOCK8):c.2816G>C (p.Cys939Ser) rs2131324863
NM_203447.4(DOCK8):c.2992G>T (p.Val998Leu) rs751201571
NM_203447.4(DOCK8):c.3275T>C (p.Met1092Thr)
NM_203447.4(DOCK8):c.3423G>C (p.Gln1141His) rs775919190
NM_203447.4(DOCK8):c.3556G>A (p.Val1186Ile)
NM_203447.4(DOCK8):c.3573C>G (p.Ser1191Arg) rs13285348
NM_203447.4(DOCK8):c.3612A>T (p.Lys1204Asn) rs758993681
NM_203447.4(DOCK8):c.4283A>G (p.Asn1428Ser) rs150057289
NM_203447.4(DOCK8):c.4283A>T (p.Asn1428Ile) rs150057289
NM_203447.4(DOCK8):c.4339-3C>G rs954072908
NM_203447.4(DOCK8):c.4387_4395del (p.Arg1463_Leu1465del) rs1554704402
NM_203447.4(DOCK8):c.4504G>C (p.Glu1502Gln)
NM_203447.4(DOCK8):c.5128C>G (p.Leu1710Val)
NM_203447.4(DOCK8):c.5337C>A (p.Phe1779Leu) rs149082704
NM_203447.4(DOCK8):c.5653G>A (p.Glu1885Lys) rs1564078658
NM_203447.4(DOCK8):c.569G>A (p.Gly190Glu)
NM_203447.4(DOCK8):c.5711G>A (p.Arg1904Gln) rs140539006
NM_203447.4(DOCK8):c.5858AGA[2] (p.Lys1955del) rs1587092842
NM_203447.4(DOCK8):c.5864A>C (p.Lys1955Thr) rs2131866624
NM_203447.4(DOCK8):c.6187C>T (p.Arg2063Trp) rs754936136
NM_203447.4(DOCK8):c.6254G>A (p.Arg2085Lys) rs1322916600

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.