ClinVar Miner

List of variants in gene DOCK8 reported by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00274
NM_203447.4(DOCK8):c.5612A>G (p.Tyr1871Cys) rs140403518 0.00048
NM_203447.4(DOCK8):c.1193G>A (p.Arg398Gln) rs147287319 0.00040
NM_203447.4(DOCK8):c.54-1G>T rs192864327 0.00036
NM_203447.4(DOCK8):c.2749G>A (p.Glu917Lys) rs200899164 0.00030
NM_203447.4(DOCK8):c.5828C>T (p.Thr1943Ile) rs148368084 0.00022
NM_203447.4(DOCK8):c.1623C>G (p.His541Gln) rs200201944 0.00017
NM_203447.4(DOCK8):c.950G>A (p.Arg317Gln) rs191413750 0.00015
NM_203447.4(DOCK8):c.5671C>T (p.Arg1891Trp) rs144951842 0.00005
NM_203447.4(DOCK8):c.1610G>A (p.Arg537Gln) rs564090348 0.00004
NM_203447.4(DOCK8):c.3414C>A (p.Phe1138Leu) rs781435688 0.00004
NM_203447.4(DOCK8):c.623A>G (p.Lys208Arg) rs377430634 0.00003
NM_203447.4(DOCK8):c.3889A>G (p.Met1297Val) rs765205695 0.00001
NM_203447.4(DOCK8):c.5128C>G (p.Leu1710Val) rs759116308 0.00001
NM_203447.4(DOCK8):c.1090C>A (p.Pro364Thr) rs146777948
NM_203447.4(DOCK8):c.1090C>T (p.Pro364Ser) rs146777948
NM_203447.4(DOCK8):c.1984G>A (p.Val662Met) rs1241904702
NM_203447.4(DOCK8):c.2816G>C (p.Cys939Ser) rs2131324863
NM_203447.4(DOCK8):c.3612A>T (p.Lys1204Asn) rs758993681

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