ClinVar Miner

List of variants in gene DOCK8 reported as benign by Invitae

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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_001193536.1(DOCK8):c.3815A>G (p.Tyr1272Cys) rs116920018
NM_203447.3(DOCK8):c.1017G>A (p.Pro339=) rs35746964
NM_203447.3(DOCK8):c.1356G>A (p.Leu452=) rs113175936
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.1881T>C (p.Phe627=) rs140134223
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.2739C>T (p.Ser913=) rs116523732
NM_203447.3(DOCK8):c.2862A>T (p.Pro954=) rs117610764
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.3058A>G (p.Ile1020Val) rs151094543
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.3441C>T (p.Phe1147=) rs34621129
NM_203447.3(DOCK8):c.3460C>T (p.Arg1154Cys) rs34390308
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.3606T>C (p.Cys1202=) rs143919622
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.404+16delT rs727505303
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.5154C>T (p.Cys1718=) rs140431229
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.528+7C>A rs114833839
NM_203447.3(DOCK8):c.6201A>G (p.Glu2067=) rs145573166
NM_203447.3(DOCK8):c.663C>A (p.Asp221Glu) rs139391329
NM_203447.3(DOCK8):c.709G>A (p.Glu237Lys) rs11789099
NM_203447.3(DOCK8):c.952G>A (p.Ala318Thr) rs35482838

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