ClinVar Miner

List of variants in gene DOCK8 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.5433G>A (p.Glu1811=) rs1887957 0.75495
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.895-16T>C rs2296828 0.66765
NM_203447.4(DOCK8):c.4107C>G (p.Leu1369=) rs2297079 0.44487
NM_203447.4(DOCK8):c.65C>T (p.Ala22Val) rs506121 0.32449
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.1790C>T (p.Ala597Val) rs17673268 0.07826
NM_203447.4(DOCK8):c.5154C>T (p.Cys1718=) rs140431229 0.00514
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00276
NM_203447.4(DOCK8):c.1582C>A (p.Leu528Met) rs146250176 0.00213
NM_203447.4(DOCK8):c.380G>A (p.Arg127His) rs150742426 0.00196
NM_203447.4(DOCK8):c.663C>A (p.Asp221Glu) rs139391329 0.00173
NM_203447.4(DOCK8):c.3460C>T (p.Arg1154Cys) rs34390308 0.00170
NM_203447.4(DOCK8):c.452G>A (p.Arg151Gln) rs149918318 0.00136
NM_203447.4(DOCK8):c.5781C>T (p.Tyr1927=) rs138225192 0.00122
NM_203447.4(DOCK8):c.3826G>T (p.Val1276Leu) rs148796842 0.00120
NM_203447.4(DOCK8):c.4588C>G (p.Leu1530Val) rs536373496 0.00084
NM_203447.4(DOCK8):c.3988C>G (p.Leu1330Val) rs148081681 0.00076
NM_203447.4(DOCK8):c.679G>A (p.Glu227Lys) rs76276364 0.00068
NM_203447.4(DOCK8):c.2971-4G>A rs186097329 0.00057
NM_203447.4(DOCK8):c.4887-16C>T rs200781199 0.00056
NM_203447.4(DOCK8):c.3058A>G (p.Ile1020Val) rs151094543 0.00046
NM_203447.4(DOCK8):c.54-1G>T rs192864327 0.00036
NM_203447.4(DOCK8):c.828-7A>G rs200243583 0.00030
NM_203447.4(DOCK8):c.1839A>G (p.Glu613=) rs377593459 0.00027
NM_203447.4(DOCK8):c.3867C>T (p.Asn1289=) rs146984705 0.00020
NM_203447.4(DOCK8):c.657C>T (p.Ala219=) rs368709669 0.00019
NM_203447.4(DOCK8):c.5058C>T (p.Pro1686=) rs190854825 0.00014
NM_203447.4(DOCK8):c.3756C>T (p.Ala1252=) rs150935084 0.00011
NM_203447.4(DOCK8):c.4704G>A (p.Glu1568=) rs201433235 0.00011
NM_203447.4(DOCK8):c.6138C>G (p.Leu2046=) rs139515839 0.00011
NM_203447.4(DOCK8):c.1868+6T>C rs777072262 0.00006
NM_203447.4(DOCK8):c.4346C>T (p.Ser1449Leu) rs370123223 0.00006
NM_203447.4(DOCK8):c.2646G>A (p.Thr882=) rs373515697 0.00005
NM_203447.4(DOCK8):c.1098G>A (p.Thr366=) rs139297216 0.00004
NM_203447.4(DOCK8):c.5868C>T (p.Thr1956=) rs757384331 0.00004
NM_203447.4(DOCK8):c.6068+6A>C rs760845840 0.00004
NM_203447.4(DOCK8):c.1656A>G (p.Val552=) rs150595667 0.00003
NM_203447.4(DOCK8):c.3180C>G (p.Leu1060=) rs371145573 0.00003
NM_203447.4(DOCK8):c.3270T>C (p.Ile1090=) rs377297446 0.00002
NM_203447.4(DOCK8):c.3870G>A (p.Ala1290=) rs750379098 0.00001
NM_203447.4(DOCK8):c.3905G>C (p.Trp1302Ser) rs149116813 0.00001
NM_203447.4(DOCK8):c.470C>T (p.Thr157Met) rs575314722 0.00001
NM_203447.4(DOCK8):c.5310C>G (p.Leu1770=) rs1347537082 0.00001
NM_203447.4(DOCK8):c.895-9C>T rs1057523638 0.00001
NM_203447.4(DOCK8):c.1071_1072del (p.Glu357fs)
NM_203447.4(DOCK8):c.1404T>C (p.Val468=)
NM_203447.4(DOCK8):c.1423-8C>G
NM_203447.4(DOCK8):c.1455C>T (p.Phe485=)
NM_203447.4(DOCK8):c.1797+71G>A
NM_203447.4(DOCK8):c.1868+9A>G rs370471790
NM_203447.4(DOCK8):c.2017A>T (p.Ile673Phe) rs372858877
NM_203447.4(DOCK8):c.2691G>C (p.Gln897His)
NM_203447.4(DOCK8):c.2916C>T (p.Thr972=) rs2297075
NM_203447.4(DOCK8):c.2971-3C>T
NM_203447.4(DOCK8):c.3625G>C (p.Val1209Leu)
NM_203447.4(DOCK8):c.388C>G (p.Leu130Val)
NM_203447.4(DOCK8):c.404+16del rs727505303
NM_203447.4(DOCK8):c.4117G>A (p.Gly1373Arg)
NM_203447.4(DOCK8):c.4217G>A (p.Arg1406Gln) rs1564048056
NM_203447.4(DOCK8):c.4401T>C (p.Asn1467=)
NM_203447.4(DOCK8):c.5481T>C (p.His1827=) rs1554708887
NM_203447.4(DOCK8):c.5490+3A>T
NM_203447.4(DOCK8):c.5581-18G>C rs10814952
NM_203447.4(DOCK8):c.5845A>G (p.Ile1949Val) rs1324228204
NM_203447.4(DOCK8):c.5962-13_5962-9del
NM_203447.4(DOCK8):c.6108G>A (p.Thr2036=)
NM_203447.4(DOCK8):c.699T>C (p.Asn233=) rs2039045

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