ClinVar Miner

List of variants in gene DOCK8 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP
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.15G>A (p.Pro5=) rs148276394
NM_203447.3(DOCK8):c.1881T>C (p.Phe627=) rs140134223
NM_203447.3(DOCK8):c.2310G>A (p.Glu770=) rs116175117
NM_203447.3(DOCK8):c.2646G>A (p.Thr882=) rs373515697
NM_203447.3(DOCK8):c.2739C>T (p.Ser913=) rs116523732
NM_203447.3(DOCK8):c.3058A>G (p.Ile1020Val) rs151094543
NM_203447.3(DOCK8):c.3234+8T>C rs112290938
NM_203447.3(DOCK8):c.3234+8del rs112565335
NM_203447.3(DOCK8):c.332+9T>G rs113744378
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.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.3988C>G (p.Leu1330Val) rs148081681
NM_203447.3(DOCK8):c.404+16del rs727505303
NM_203447.3(DOCK8):c.4158C>T (p.Asn1386=) rs77803650
NM_203447.3(DOCK8):c.4588C>G (p.Leu1530Val) rs536373496
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.5355+6C>T rs188141951
NM_203447.3(DOCK8):c.5781C>T (p.Tyr1927=) rs138225192
NM_203447.3(DOCK8):c.6201A>G (p.Glu2067=) rs145573166
NM_203447.3(DOCK8):c.640C>T (p.Leu214=) rs150446322
NM_203447.3(DOCK8):c.663C>A (p.Asp221Glu) rs139391329
NM_203447.3(DOCK8):c.679G>A (p.Glu227Lys) rs76276364
NM_203447.3(DOCK8):c.828-7A>G rs200243583
NM_203447.3(DOCK8):c.952G>A (p.Ala318Thr) rs35482838
NM_203447.4(DOCK8):c.2295C>T (p.Ser765=) rs12348944
NM_203447.4(DOCK8):c.2862A>T (p.Pro954=) rs117610764
NM_203447.4(DOCK8):c.3021T>C (p.Phe1007=) rs7034926
NM_203447.4(DOCK8):c.3022C>T (p.Arg1008Trp) rs16937932
NM_203447.4(DOCK8):c.3208A>G (p.Asn1070Asp) rs73382631
NM_203447.4(DOCK8):c.3230G>A (p.Ser1077Asn) rs34627722
NM_203447.4(DOCK8):c.3460C>T rs34390308
NM_203447.4(DOCK8):c.3573C>T (p.Ser1191=) rs13285348
NM_203447.4(DOCK8):c.3840+3A>G rs16938572
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018
NM_203447.4(DOCK8):c.4024-4C>T rs111306749
NM_203447.4(DOCK8):c.5001C>T (p.His1667=) rs35662752
NM_203447.4(DOCK8):c.709G>A (p.Glu237Lys) rs11789099

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.