ClinVar Miner

List of variants in gene DOCK8, LOC126860552 studied for immune system disorder

Included ClinVar conditions (908):
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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.289C>A (p.Pro97Thr) rs529208 0.47790
NM_203447.4(DOCK8):c.187G>A (p.Asp63Asn) rs3209441 0.11431
NM_203447.4(DOCK8):c.332+9T>G rs113744378 0.00145
NM_203447.4(DOCK8):c.223C>G (p.Leu75Val) rs368133450 0.00023
NM_203447.4(DOCK8):c.180G>T (p.Glu60Asp) rs370107163 0.00021
NM_203447.4(DOCK8):c.314C>G (p.Pro105Arg) rs201472678 0.00012
NM_203447.4(DOCK8):c.276C>T (p.Asp92=) rs769215982 0.00010
NM_203447.4(DOCK8):c.157-4C>G rs748270658 0.00009
NM_203447.4(DOCK8):c.249C>T (p.Leu83=) rs370609644 0.00006
NM_203447.4(DOCK8):c.277G>T (p.Val93Leu) rs375686155 0.00003
NM_203447.4(DOCK8):c.165T>C (p.Phe55=) rs371059454 0.00002
NM_203447.4(DOCK8):c.250G>A (p.Gly84Arg) rs1318020471 0.00002
NM_203447.4(DOCK8):c.277G>A (p.Val93Met) rs375686155 0.00002
NM_203447.4(DOCK8):c.313C>G (p.Pro105Ala) rs756344239 0.00002
NM_203447.4(DOCK8):c.167A>G (p.Tyr56Cys) rs373301364 0.00001
NM_203447.4(DOCK8):c.204G>A (p.Leu68=) rs138521760 0.00001
NM_203447.4(DOCK8):c.236T>C (p.Leu79Pro) rs754852811 0.00001
NM_203447.4(DOCK8):c.317C>G (p.Ser106Cys) rs896673386 0.00001
NM_203447.4(DOCK8):c.319T>C (p.Leu107=) rs199565980 0.00001
NM_203447.4(DOCK8):c.332+18A>C rs1481542055 0.00001
NC_000009.12:g.(?_286441)_(289601_?)del
NC_000009.12:g.(?_286441)_(464239_?)del
NM_203447.4(DOCK8):c.157-12C>G
NM_203447.4(DOCK8):c.157-13C>G rs1196879732
NM_203447.4(DOCK8):c.157-13C>T
NM_203447.4(DOCK8):c.157-19C>T
NM_203447.4(DOCK8):c.157-20C>A rs2048826477
NM_203447.4(DOCK8):c.157-4C>T
NM_203447.4(DOCK8):c.157-6C>A
NM_203447.4(DOCK8):c.157-6C>T rs2048827233
NM_203447.4(DOCK8):c.157-8C>A
NM_203447.4(DOCK8):c.158C>G (p.Pro53Arg) rs777781052
NM_203447.4(DOCK8):c.179A>T (p.Glu60Val)
NM_203447.4(DOCK8):c.185T>G (p.Val62Gly)
NM_203447.4(DOCK8):c.189C>T (p.Asp63=) rs2048828820
NM_203447.4(DOCK8):c.196G>A (p.Gly66Arg)
NM_203447.4(DOCK8):c.198A>G (p.Gly66=)
NM_203447.4(DOCK8):c.202C>A (p.Leu68Met)
NM_203447.4(DOCK8):c.218A>G (p.Asn73Ser) rs886063849
NM_203447.4(DOCK8):c.221G>T (p.Ser74Ile)
NM_203447.4(DOCK8):c.240C>G (p.Ala80=) rs1424086240
NM_203447.4(DOCK8):c.242A>G (p.Gln81Arg) rs1586600892
NM_203447.4(DOCK8):c.247C>T (p.Leu83Phe)
NM_203447.4(DOCK8):c.260C>T (p.Thr87Ile)
NM_203447.4(DOCK8):c.261T>C (p.Thr87=)
NM_203447.4(DOCK8):c.261T>G (p.Thr87=)
NM_203447.4(DOCK8):c.265G>A (p.Asp89Asn) rs2048832030
NM_203447.4(DOCK8):c.265GAC[1] (p.Asp90del) rs776468911
NM_203447.4(DOCK8):c.268G>A (p.Asp90Asn) rs113165814
NM_203447.4(DOCK8):c.278T>C (p.Val93Ala)
NM_203447.4(DOCK8):c.280G>C (p.Val94Leu) rs1554655875
NM_203447.4(DOCK8):c.287C>T (p.Thr96Met) rs1442708191
NM_203447.4(DOCK8):c.289C>G (p.Pro97Ala)
NM_203447.4(DOCK8):c.290C>T (p.Pro97Leu) rs760271664
NM_203447.4(DOCK8):c.295G>A (p.Glu99Lys) rs547012088
NM_203447.4(DOCK8):c.296A>G (p.Glu99Gly)
NM_203447.4(DOCK8):c.298T>C (p.Cys100Arg)
NM_203447.4(DOCK8):c.300T>C (p.Cys100=)
NM_203447.4(DOCK8):c.303G>A (p.Arg101=)
NM_203447.4(DOCK8):c.305C>G (p.Thr102Ser) rs375895643
NM_203447.4(DOCK8):c.310C>T (p.Gln104Ter)
NM_203447.4(DOCK8):c.314C>A (p.Pro105His)
NM_203447.4(DOCK8):c.323C>T (p.Pro108Leu)
NM_203447.4(DOCK8):c.324G>A (p.Pro108=)
NM_203447.4(DOCK8):c.332+13C>A
NM_203447.4(DOCK8):c.332+4_332+7del rs759319822

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