ClinVar Miner

List of variants in gene DOCK8 reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_203447.3(DOCK8):c.1238A>G (p.Asn413Ser) rs10970979
NM_203447.3(DOCK8):c.1692T>C (p.Tyr564=) rs10972587
NM_203447.3(DOCK8):c.1790C>T (p.Ala597Val) rs17673268
NM_203447.3(DOCK8):c.1812A>G (p.Lys604=) rs913703
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.2340G>C (p.Leu780=) rs10814431
NM_203447.3(DOCK8):c.2862A>T (p.Pro954=) rs117610764
NM_203447.3(DOCK8):c.289C>A (p.Pro97Thr) rs529208
NM_203447.3(DOCK8):c.2916C>T (p.Thr972=) rs2297075
NM_203447.3(DOCK8):c.2971-14A>G rs140114637
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.3208A>G (p.Asn1070Asp) rs73382631
NM_203447.3(DOCK8):c.3230G>A (p.Ser1077Asn) rs34627722
NM_203447.3(DOCK8):c.3234+8delT rs112565335
NM_203447.3(DOCK8):c.3565A>G (p.Ile1189Val) rs77399114
NM_203447.3(DOCK8):c.3573C>T (p.Ser1191=) rs13285348
NM_203447.3(DOCK8):c.3840+3A>G rs16938572
NM_203447.3(DOCK8):c.4024-4C>T rs111306749
NM_203447.3(DOCK8):c.404+16del rs727505303
NM_203447.3(DOCK8):c.4107C>G (p.Leu1369=) rs2297079
NM_203447.3(DOCK8):c.4491= (p.Phe1497=) rs7854035
NM_203447.3(DOCK8):c.4785+6C>G rs7036567
NM_203447.3(DOCK8):c.4886+3A>G rs2360712
NM_203447.3(DOCK8):c.5001C>T (p.His1667=) rs35662752
NM_203447.3(DOCK8):c.5211G>A (p.Glu1737=) rs34098809
NM_203447.3(DOCK8):c.528+13A>G rs116483820
NM_203447.3(DOCK8):c.5433G>A (p.Glu1811=) rs1887957
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.65C>T (p.Ala22Val) rs506121
NM_203447.3(DOCK8):c.699T>C (p.Asn233=) rs2039045
NM_203447.3(DOCK8):c.709G>A (p.Glu237Lys) rs11789099
NM_203447.3(DOCK8):c.895-16T>C rs2296828
NM_203447.3(DOCK8):c.952G>A (p.Ala318Thr) rs35482838

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