ClinVar Miner

List of variants in gene DOCK8 reported as uncertain significance for Hyper-IgE syndrome

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Gene type:
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Total variants: 75
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HGVS dbSNP
NM_203447.3(DOCK8):c.*1031G>A rs149002313
NM_203447.3(DOCK8):c.*150A>T rs886063981
NM_203447.3(DOCK8):c.*258T>C rs145094924
NM_203447.3(DOCK8):c.*366C>T rs886063982
NM_203447.3(DOCK8):c.*407C>T rs886063983
NM_203447.3(DOCK8):c.*603T>C rs886063984
NM_203447.3(DOCK8):c.*845T>C rs10157
NM_203447.3(DOCK8):c.*847A>G rs924532099
NM_203447.3(DOCK8):c.*990T>C rs1057515587
NM_203447.3(DOCK8):c.*99G>A rs554634853
NM_203447.3(DOCK8):c.-100T>A rs886063778
NM_203447.3(DOCK8):c.-105G>T rs886063777
NM_203447.3(DOCK8):c.-58C>T rs144097790
NM_203447.3(DOCK8):c.1044+13G>T rs754374567
NM_203447.3(DOCK8):c.1193G>A (p.Arg398Gln) rs147287319
NM_203447.3(DOCK8):c.1391C>A (p.Ser464Tyr) rs531279290
NM_203447.3(DOCK8):c.1391C>T (p.Ser464Phe) rs531279290
NM_203447.3(DOCK8):c.1441G>A (p.Asp481Asn) rs374938180
NM_203447.3(DOCK8):c.1623C>G (p.His541Gln) rs200201944
NM_203447.3(DOCK8):c.1649G>A (p.Arg550Gln) rs886063879
NM_203447.3(DOCK8):c.1797+13A>C rs776147775
NM_203447.3(DOCK8):c.218A>G (p.Asn73Ser) rs886063849
NM_203447.3(DOCK8):c.2275G>A (p.Val759Met) rs148693111
NM_203447.3(DOCK8):c.2428G>A (p.Ala810Thr) rs752978895
NM_203447.3(DOCK8):c.2438C>T (p.Thr813Ile) rs762799448
NM_203447.3(DOCK8):c.2527G>A (p.Gly843Arg) rs886063934
NM_203447.3(DOCK8):c.2605+14G>C rs886063935
NM_203447.3(DOCK8):c.2740G>A (p.Ala914Thr) rs375665207
NM_203447.3(DOCK8):c.277G>T (p.Val93Leu) rs375686155
NM_203447.3(DOCK8):c.2862A>T (p.Pro954=) rs117610764
NM_203447.3(DOCK8):c.2937C>G (p.Val979=) rs751748445
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.3067A>G (p.Ile1023Val) rs140148619
NM_203447.3(DOCK8):c.3134C>T (p.Ala1045Val) rs755658263
NM_203447.3(DOCK8):c.3193C>T (p.Arg1065Trp) rs146891937
NM_203447.3(DOCK8):c.3195G>A (p.Arg1065=) rs781062154
NM_203447.3(DOCK8):c.3220C>A (p.His1074Asn) rs150298985
NM_203447.3(DOCK8):c.3234+15dupC rs375864618
NM_203447.3(DOCK8):c.3254A>G (p.Asn1085Ser) rs527474230
NM_203447.3(DOCK8):c.3270T>C (p.Ile1090=) rs377297446
NM_203447.3(DOCK8):c.3312G>C (p.Glu1104Asp) rs138810908
NM_203447.3(DOCK8):c.34T>G (p.Phe12Val) rs886063779
NM_203447.3(DOCK8):c.3519C>T (p.Ala1173=) rs144299704
NM_203447.3(DOCK8):c.3543A>G (p.Val1181=) rs753242273
NM_203447.3(DOCK8):c.3606T>C (p.Cys1202=) rs143919622
NM_203447.3(DOCK8):c.36C>A (p.Phe12Leu) rs566738926
NM_203447.3(DOCK8):c.3790G>T (p.Ala1264Ser) rs886063955
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.4024-4C>T rs111306749
NM_203447.3(DOCK8):c.4148C>G (p.Ala1383Gly) rs745583957
NM_203447.3(DOCK8):c.447A>G (p.Gly149=) rs763034264
NM_203447.3(DOCK8):c.4497G>A (p.Glu1499=) rs886063957
NM_203447.3(DOCK8):c.452G>A (p.Arg151Gln) rs149918318
NM_203447.3(DOCK8):c.494C>T (p.Ser165Leu) rs146490788
NM_203447.3(DOCK8):c.5139C>T (p.Asp1713=) rs568641163
NM_203447.3(DOCK8):c.5211G>A (p.Glu1737=) rs34098809
NM_203447.3(DOCK8):c.5223+4A>G rs117109271
NM_203447.3(DOCK8):c.5266A>C (p.Ile1756Leu) rs373154957
NM_203447.3(DOCK8):c.5296C>T (p.Arg1766Trp) rs201776049
NM_203447.3(DOCK8):c.53+11C>T rs764626266
NM_203447.3(DOCK8):c.536C>T (p.Pro179Leu) rs772181121
NM_203447.3(DOCK8):c.5467C>T (p.Pro1823Ser) rs766493394
NM_203447.3(DOCK8):c.5491-7T>A rs184867151
NM_203447.3(DOCK8):c.550G>A (p.Val184Met) rs143461644
NM_203447.3(DOCK8):c.5585A>G (p.Tyr1862Cys) rs752479766
NM_203447.3(DOCK8):c.5828C>T (p.Thr1943Ile) rs148368084
NM_203447.3(DOCK8):c.6068+11A>C rs886063964
NM_203447.3(DOCK8):c.6201A>G (p.Glu2067=) rs145573166
NM_203447.3(DOCK8):c.626G>A (p.Arg209Gln) rs151262535
NM_203447.3(DOCK8):c.663C>A (p.Asp221Glu) rs139391329
NM_203447.3(DOCK8):c.686C>A (p.Ala229Asp) rs745614955
NM_203447.3(DOCK8):c.72A>G (p.Ile24Met) rs531628086
NM_203447.3(DOCK8):c.828-7A>G rs200243583

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