ClinVar Miner

List of variants in gene DOCK8 reported as likely benign for Hyper-IgE syndrome

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Total variants: 25
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HGVS dbSNP
NM_203447.3(DOCK8):c.*112T>C rs10974618
NM_203447.3(DOCK8):c.*757T>G rs116697485
NM_203447.3(DOCK8):c.*867C>T rs12067
NM_203447.3(DOCK8):c.-69T>C rs62533313
NM_203447.3(DOCK8):c.1790C>T (p.Ala597Val) rs17673268
NM_203447.3(DOCK8):c.187G>A (p.Asp63Asn) rs3209441
NM_203447.3(DOCK8):c.2295C>T (p.Ser765=) rs12348944
NM_203447.3(DOCK8):c.2739C>T (p.Ser913=) rs116523732
NM_203447.3(DOCK8):c.2971-14A>G rs140114637
NM_203447.3(DOCK8):c.3021T>C (p.Phe1007=) rs7034926
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+15delC rs375864618
NM_203447.3(DOCK8):c.3441C>T (p.Phe1147=) rs34621129
NM_203447.3(DOCK8):c.3565A>G (p.Ile1189Val) rs77399114
NM_203447.3(DOCK8):c.3840+3A>G rs16938572
NM_203447.3(DOCK8):c.404+16delT rs727505303
NM_203447.3(DOCK8):c.5001C>T (p.His1667=) rs35662752
NM_203447.3(DOCK8):c.5187A>G (p.Val1729=) rs111535933
NM_203447.3(DOCK8):c.528+13A>G rs116483820
NM_203447.3(DOCK8):c.5818-14C>T rs10124592
NM_203447.3(DOCK8):c.5832G>A (p.Pro1944=) rs10491684
NM_203447.3(DOCK8):c.5908G>C (p.Ala1970Pro) rs34908836
NM_203447.3(DOCK8):c.709G>A (p.Glu237Lys) rs11789099
NM_203447.3(DOCK8):c.952G>A (p.Ala318Thr) rs35482838

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