ClinVar Miner

List of variants in gene DOCK8 reported by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 132
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HGVS dbSNP
NC_000009.12:g.(?_214957)_(215049_?)del
NC_000009.12:g.(?_214957)_(215049_?)dup
NC_000009.12:g.(?_214957)_(271749_?)dup
NC_000009.12:g.(?_214957)_(289601_?)dup
NC_000009.12:g.(?_214957)_(340341_?)dup
NC_000009.12:g.(?_214957)_(464239_?)dup
NC_000009.12:g.(?_271607)_(328191_?)dup
NC_000009.12:g.(?_271627)_(382685_?)dup
NC_000009.12:g.(?_271627)_(399259_?)dup
NC_000009.12:g.(?_286441)_(289601_?)del
NC_000009.12:g.(?_286441)_(464239_?)del
NC_000009.12:g.(?_304561)_(464239_?)del
NC_000009.12:g.(?_325651)_(340341_?)dup
NM_001193536.1(DOCK8):c.3815A>G (p.Tyr1272Cys) rs116920018
NM_203447.3(DOCK8):c.1012T>C (p.Tyr338His)
NM_203447.3(DOCK8):c.1017G>A (p.Pro339=) rs35746964
NM_203447.3(DOCK8):c.1090C>T (p.Pro364Ser) rs146777948
NM_203447.3(DOCK8):c.1152A>T (p.Lys384Asn)
NM_203447.3(DOCK8):c.1238A>T (p.Asn413Ile) rs10970979
NM_203447.3(DOCK8):c.1286-5T>A rs199940668
NM_203447.3(DOCK8):c.1356G>A (p.Leu452=) rs113175936
NM_203447.3(DOCK8):c.1371T>C (p.Val457=) rs145968092
NM_203447.3(DOCK8):c.1528C>A (p.Leu510Met) rs771479299
NM_203447.3(DOCK8):c.1559A>G (p.Asn520Ser)
NM_203447.3(DOCK8):c.1582C>A (p.Leu528Met) rs146250176
NM_203447.3(DOCK8):c.1587C>G (p.Pro529=) rs146289269
NM_203447.3(DOCK8):c.1619C>T (p.Pro540Leu) rs377334031
NM_203447.3(DOCK8):c.1680-2A>G
NM_203447.3(DOCK8):c.1765A>T (p.Met589Leu)
NM_203447.3(DOCK8):c.1783A>G (p.Ser595Gly)
NM_203447.3(DOCK8):c.1788T>C (p.Asn596=) rs1486199563
NM_203447.3(DOCK8):c.1840G>C (p.Val614Leu)
NM_203447.3(DOCK8):c.1868+6T>C
NM_203447.3(DOCK8):c.1881T>C (p.Phe627=) rs140134223
NM_203447.3(DOCK8):c.2237G>A (p.Cys746Tyr)
NM_203447.3(DOCK8):c.2275G>A (p.Val759Met) rs148693111
NM_203447.3(DOCK8):c.2295C>T (p.Ser765=) rs12348944
NM_203447.3(DOCK8):c.2310G>A (p.Glu770=) rs116175117
NM_203447.3(DOCK8):c.2372T>C (p.Phe791Ser)
NM_203447.3(DOCK8):c.2383G>C (p.Val795Leu)
NM_203447.3(DOCK8):c.2511G>A (p.Leu837=) rs140248537
NM_203447.3(DOCK8):c.2553C>T (p.Tyr851=) rs372565541
NM_203447.3(DOCK8):c.2562C>T (p.Tyr854=) rs376592918
NM_203447.3(DOCK8):c.2653C>T (p.Arg885Cys) rs562630169
NM_203447.3(DOCK8):c.2739C>T (p.Ser913=) rs116523732
NM_203447.3(DOCK8):c.2749G>A (p.Glu917Lys) rs200899164
NM_203447.3(DOCK8):c.2779-2A>C rs776399238
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.2862A>T (p.Pro954=) rs117610764
NM_203447.3(DOCK8):c.2882A>T (p.His961Leu) rs1554688666
NM_203447.3(DOCK8):c.2971-4G>A rs186097329
NM_203447.3(DOCK8):c.2971-6C>T rs773500215
NM_203447.3(DOCK8):c.3010C>T (p.Arg1004Trp)
NM_203447.3(DOCK8):c.3021T>C (p.Phe1007=) rs7034926
NM_203447.3(DOCK8):c.3022C>T (p.Arg1008Trp) rs16937932
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.3058A>G (p.Ile1020Val) rs151094543
NM_203447.3(DOCK8):c.3067A>G (p.Ile1023Val) rs140148619
NM_203447.3(DOCK8):c.3208A>G (p.Asn1070Asp) rs73382631
NM_203447.3(DOCK8):c.3230G>A (p.Ser1077Asn) rs34627722
NM_203447.3(DOCK8):c.3234+2T>C
NM_203447.3(DOCK8):c.3234+8delT rs112565335
NM_203447.3(DOCK8):c.3312G>C (p.Glu1104Asp) rs138810908
NM_203447.3(DOCK8):c.343G>C (p.Asp115His) rs140270895
NM_203447.3(DOCK8):c.3441C>T (p.Phe1147=) rs34621129
NM_203447.3(DOCK8):c.3460C>T (p.Arg1154Cys) rs34390308
NM_203447.3(DOCK8):c.3530+1G>A
NM_203447.3(DOCK8):c.3565A>G (p.Ile1189Val) rs77399114
NM_203447.3(DOCK8):c.3573C>G (p.Ser1191Arg) rs13285348
NM_203447.3(DOCK8):c.3573C>T (p.Ser1191=) rs13285348
NM_203447.3(DOCK8):c.3606T>C (p.Cys1202=) rs143919622
NM_203447.3(DOCK8):c.3614C>G (p.Pro1205Arg) rs1310119190
NM_203447.3(DOCK8):c.3756C>T (p.Ala1252=) rs150935084
NM_203447.3(DOCK8):c.3757G>A (p.Gly1253Ser)
NM_203447.3(DOCK8):c.380G>A (p.Arg127His) rs150742426
NM_203447.3(DOCK8):c.3813A>G (p.Lys1271=) rs75411647
NM_203447.3(DOCK8):c.3840+3A>G rs16938572
NM_203447.3(DOCK8):c.3844T>C (p.Tyr1282His)
NM_203447.3(DOCK8):c.393C>T (p.Ile131=) rs139097471
NM_203447.3(DOCK8):c.4034G>C (p.Ser1345Thr)
NM_203447.3(DOCK8):c.404+16delT rs727505303
NM_203447.3(DOCK8):c.405-8C>G rs748853895
NM_203447.3(DOCK8):c.4093G>A (p.Glu1365Lys) rs1554701455
NM_203447.3(DOCK8):c.4346C>T (p.Ser1449Leu) rs370123223
NM_203447.3(DOCK8):c.4473+9G>A rs368932755
NM_203447.3(DOCK8):c.4491C>T (p.Phe1497=) rs7854035
NM_203447.3(DOCK8):c.452G>A (p.Arg151Gln) rs149918318
NM_203447.3(DOCK8):c.4774T>C (p.Phe1592Leu)
NM_203447.3(DOCK8):c.4790A>T (p.Glu1597Val)
NM_203447.3(DOCK8):c.4922G>A (p.Arg1641Gln)
NM_203447.3(DOCK8):c.5001C>T (p.His1667=) rs35662752
NM_203447.3(DOCK8):c.5010G>A (p.Ala1670=) rs142208336
NM_203447.3(DOCK8):c.5058C>T (p.Pro1686=) rs190854825
NM_203447.3(DOCK8):c.5079+7dupT rs762095035
NM_203447.3(DOCK8):c.5154C>T (p.Cys1718=) rs140431229
NM_203447.3(DOCK8):c.5155G>A (p.Ala1719Thr) rs144279637
NM_203447.3(DOCK8):c.5184G>C (p.Leu1728=) rs371723484
NM_203447.3(DOCK8):c.5187A>G (p.Val1729=) rs111535933
NM_203447.3(DOCK8):c.5211G>A (p.Glu1737=) rs34098809
NM_203447.3(DOCK8):c.5266A>T (p.Ile1756Phe)
NM_203447.3(DOCK8):c.528+7C>A rs114833839
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.52A>G (p.Arg18Gly) rs200689054
NM_203447.3(DOCK8):c.5386C>T (p.Arg1796Ter)
NM_203447.3(DOCK8):c.539G>A (p.Arg180His)
NM_203447.3(DOCK8):c.54-1G>T rs192864327
NM_203447.3(DOCK8):c.550G>A (p.Val184Met) rs143461644
NM_203447.3(DOCK8):c.5581-4T>G
NM_203447.3(DOCK8):c.5612A>G (p.Tyr1871Cys) rs140403518
NM_203447.3(DOCK8):c.562G>A (p.Val188Met)
NM_203447.3(DOCK8):c.580G>A (p.Val194Ile) rs141210649
NM_203447.3(DOCK8):c.5962-16_5962-8delTTTTTTTTC rs767478064
NM_203447.3(DOCK8):c.605G>A (p.Arg202His) rs374288188
NM_203447.3(DOCK8):c.6068+9G>A rs1554711795
NM_203447.3(DOCK8):c.6188G>A (p.Arg2063Gln)
NM_203447.3(DOCK8):c.6201A>G (p.Glu2067=) rs145573166
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.663C>A (p.Asp221Glu) rs139391329
NM_203447.3(DOCK8):c.708C>T (p.Ala236=) rs370735655
NM_203447.3(DOCK8):c.709G>A (p.Glu237Lys) rs11789099
NM_203447.3(DOCK8):c.742-15T>G
NM_203447.3(DOCK8):c.803T>G (p.Ile268Arg)
NM_203447.3(DOCK8):c.870C>G (p.Leu290=) rs201244929
NM_203447.3(DOCK8):c.952G>A (p.Ala318Thr) rs35482838
NM_203447.3(DOCK8):c.986C>T (p.Ala329Val) rs75352090

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