ClinVar Miner

List of variants in gene DOCK8 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 124
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HGVS dbSNP
NC_000009.11:g.(?_214957)_(215049_?)dup
NC_000009.11:g.(?_214957)_(271749_?)dup
NC_000009.11:g.(?_214957)_(289601_?)dup
NC_000009.11:g.(?_214957)_(340341_?)dup
NC_000009.11:g.(?_214957)_(407089_?)dup
NC_000009.11:g.(?_214957)_(422155_?)dup
NC_000009.11:g.(?_214957)_(452137_?)dup
NC_000009.11:g.(?_214957)_(464239_?)dup
NC_000009.11:g.(?_304561)_(464239_?)dup
NC_000009.11:g.(?_325651)_(340341_?)dup
NC_000009.11:g.(?_325651)_(464239_?)dup
NC_000009.11:g.(?_420381)_(464239_?)dup
NM_203447.3(DOCK8):c.1012T>C (p.Tyr338His)
NM_203447.3(DOCK8):c.1016C>T (p.Pro339Leu)
NM_203447.3(DOCK8):c.1090C>T (p.Pro364Ser) rs146777948
NM_203447.3(DOCK8):c.1147C>G (p.Leu383Val)
NM_203447.3(DOCK8):c.1152A>T (p.Lys384Asn)
NM_203447.3(DOCK8):c.1193G>A (p.Arg398Gln) rs147287319
NM_203447.3(DOCK8):c.1238A>T (p.Asn413Ile) rs10970979
NM_203447.3(DOCK8):c.1286-5T>A rs199940668
NM_203447.3(DOCK8):c.1307G>A (p.Arg436Gln)
NM_203447.3(DOCK8):c.1373G>A (p.Gly458Glu)
NM_203447.3(DOCK8):c.1528C>A (p.Leu510Met) rs771479299
NM_203447.3(DOCK8):c.1559A>G (p.Asn520Ser)
NM_203447.3(DOCK8):c.1588G>A (p.Val530Met)
NM_203447.3(DOCK8):c.1619C>T (p.Pro540Leu) rs377334031
NM_203447.3(DOCK8):c.1623C>G (p.His541Gln) rs200201944
NM_203447.3(DOCK8):c.167A>G (p.Tyr56Cys)
NM_203447.3(DOCK8):c.1689C>G (p.Leu563=)
NM_203447.3(DOCK8):c.1765A>T (p.Met589Leu)
NM_203447.3(DOCK8):c.1783A>G (p.Ser595Gly)
NM_203447.3(DOCK8):c.180G>T (p.Glu60Asp)
NM_203447.3(DOCK8):c.1817G>A (p.Ser606Asn)
NM_203447.3(DOCK8):c.1840G>C (p.Val614Leu)
NM_203447.3(DOCK8):c.1868+4A>T
NM_203447.3(DOCK8):c.1868+6T>C
NM_203447.3(DOCK8):c.1876G>T (p.Asp626Tyr)
NM_203447.3(DOCK8):c.2017A>G (p.Ile673Val)
NM_203447.3(DOCK8):c.2017A>T (p.Ile673Phe) rs372858877
NM_203447.3(DOCK8):c.2237G>A (p.Cys746Tyr) rs1563982826
NM_203447.3(DOCK8):c.2275G>A (p.Val759Met) rs148693111
NM_203447.3(DOCK8):c.2296G>A (p.Glu766Lys)
NM_203447.3(DOCK8):c.2372T>C (p.Phe791Ser) rs1389605952
NM_203447.3(DOCK8):c.2383G>C (p.Val795Leu)
NM_203447.3(DOCK8):c.242A>G (p.Gln81Arg)
NM_203447.3(DOCK8):c.2482G>A (p.Ala828Thr)
NM_203447.3(DOCK8):c.2593G>A (p.Val865Met)
NM_203447.3(DOCK8):c.2594T>C (p.Val865Ala)
NM_203447.3(DOCK8):c.2630C>G (p.Pro877Arg)
NM_203447.3(DOCK8):c.2653C>T (p.Arg885Cys) rs562630169
NM_203447.3(DOCK8):c.2707A>G (p.Ser903Gly)
NM_203447.3(DOCK8):c.2740G>A (p.Ala914Thr) rs375665207
NM_203447.3(DOCK8):c.2749G>A (p.Glu917Lys) rs200899164
NM_203447.3(DOCK8):c.2781C>G (p.Ile927Met)
NM_203447.3(DOCK8):c.2791A>C (p.Asn931His)
NM_203447.3(DOCK8):c.280G>C (p.Val94Leu) rs1554655875
NM_203447.3(DOCK8):c.2882A>T (p.His961Leu) rs1554688666
NM_203447.3(DOCK8):c.295G>A (p.Glu99Lys)
NM_203447.3(DOCK8):c.3006C>G (p.Asp1002Glu)
NM_203447.3(DOCK8):c.3010C>T (p.Arg1004Trp)
NM_203447.3(DOCK8):c.3023G>A (p.Arg1008Gln) rs145844320
NM_203447.3(DOCK8):c.3031C>T (p.Arg1011Cys) rs535305490
NM_203447.3(DOCK8):c.3067A>G (p.Ile1023Val) rs140148619
NM_203447.3(DOCK8):c.3158C>T (p.Ala1053Val)
NM_203447.3(DOCK8):c.3194G>T (p.Arg1065Leu)
NM_203447.3(DOCK8):c.3196G>A (p.Gly1066Ser)
NM_203447.3(DOCK8):c.3216C>G (p.Ile1072Met) rs370250940
NM_203447.3(DOCK8):c.3312G>C (p.Glu1104Asp) rs138810908
NM_203447.3(DOCK8):c.3361A>G (p.Thr1121Ala)
NM_203447.3(DOCK8):c.343G>C (p.Asp115His) rs140270895
NM_203447.3(DOCK8):c.3442G>A (p.Asp1148Asn)
NM_203447.3(DOCK8):c.349C>T (p.His117Tyr)
NM_203447.3(DOCK8):c.3509C>T (p.Ala1170Val)
NM_203447.3(DOCK8):c.3573C>G (p.Ser1191Arg) rs13285348
NM_203447.3(DOCK8):c.3612A>T (p.Lys1204Asn)
NM_203447.3(DOCK8):c.3614C>G (p.Pro1205Arg) rs1310119190
NM_203447.3(DOCK8):c.367C>G (p.Gln123Glu)
NM_203447.3(DOCK8):c.3721C>T (p.Arg1241Cys)
NM_203447.3(DOCK8):c.3757G>A (p.Gly1253Ser) rs1395205685
NM_203447.3(DOCK8):c.3769C>G (p.Gln1257Glu)
NM_203447.3(DOCK8):c.3785C>T (p.Ala1262Val)
NM_203447.3(DOCK8):c.3844T>C (p.Tyr1282His)
NM_203447.3(DOCK8):c.4034G>C (p.Ser1345Thr)
NM_203447.3(DOCK8):c.4093G>A (p.Glu1365Lys) rs1554701455
NM_203447.3(DOCK8):c.428G>T (p.Cys143Phe)
NM_203447.3(DOCK8):c.4346C>T (p.Ser1449Leu) rs370123223
NM_203447.3(DOCK8):c.4764G>C (p.Gln1588His)
NM_203447.3(DOCK8):c.476C>T (p.Pro159Leu)
NM_203447.3(DOCK8):c.4774T>C (p.Phe1592Leu)
NM_203447.3(DOCK8):c.4790A>T (p.Glu1597Val)
NM_203447.3(DOCK8):c.4858C>G (p.Pro1620Ala)
NM_203447.3(DOCK8):c.485C>T (p.Thr162Met)
NM_203447.3(DOCK8):c.4886+6C>T
NM_203447.3(DOCK8):c.4904A>G (p.Gln1635Arg)
NM_203447.3(DOCK8):c.4922G>A (p.Arg1641Gln) rs1564065424
NM_203447.3(DOCK8):c.494C>T (p.Ser165Leu) rs146490788
NM_203447.3(DOCK8):c.5044C>T (p.His1682Tyr)
NM_203447.3(DOCK8):c.5059G>T (p.Val1687Leu)
NM_203447.3(DOCK8):c.5222C>T (p.Thr1741Met)
NM_203447.3(DOCK8):c.5223+5G>T
NM_203447.3(DOCK8):c.5266A>T (p.Ile1756Phe)
NM_203447.3(DOCK8):c.528G>C (p.Gln176His) rs1554662110
NM_203447.3(DOCK8):c.5296C>T (p.Arg1766Trp) rs201776049
NM_203447.3(DOCK8):c.539G>A (p.Arg180His)
NM_203447.3(DOCK8):c.5481T>C (p.His1827=) rs1554708887
NM_203447.3(DOCK8):c.550G>A (p.Val184Met) rs143461644
NM_203447.3(DOCK8):c.5581-4T>G
NM_203447.3(DOCK8):c.559G>A (p.Asp187Asn)
NM_203447.3(DOCK8):c.5612A>G (p.Tyr1871Cys) rs140403518
NM_203447.3(DOCK8):c.562G>A (p.Val188Met)
NM_203447.3(DOCK8):c.5828C>T (p.Thr1943Ile) rs148368084
NM_203447.3(DOCK8):c.605G>A (p.Arg202His) rs374288188
NM_203447.3(DOCK8):c.6188G>A (p.Arg2063Gln)
NM_203447.3(DOCK8):c.6238A>G (p.Arg2080Gly)
NM_203447.3(DOCK8):c.623A>G (p.Lys208Arg) rs377430634
NM_203447.3(DOCK8):c.626G>A (p.Arg209Gln) rs151262535
NM_203447.3(DOCK8):c.656C>T (p.Ala219Val) rs144019007
NM_203447.3(DOCK8):c.685G>C (p.Ala229Pro) rs149234127
NM_203447.3(DOCK8):c.742-15T>G
NM_203447.3(DOCK8):c.803T>G (p.Ile268Arg)
NM_203447.3(DOCK8):c.823T>G (p.Leu275Val)
NM_203447.3(DOCK8):c.870C>G (p.Leu290=) rs201244929
NM_203447.3(DOCK8):c.950G>A (p.Arg317Gln)
NM_203447.3(DOCK8):c.971C>A (p.Ala324Asp)

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