ClinVar Miner

List of variants in gene DOCK8 reported as uncertain significance for not specified

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00276
NM_203447.4(DOCK8):c.452G>A (p.Arg151Gln) rs149918318 0.00136
NM_203447.4(DOCK8):c.5962-9T>C rs1324502895 0.00057
NM_203447.4(DOCK8):c.54-1G>T rs192864327 0.00036
NM_203447.4(DOCK8):c.1623C>G (p.His541Gln) rs200201944 0.00015
NM_203447.4(DOCK8):c.763C>A (p.Pro255Thr) rs754843805 0.00014
NM_203447.4(DOCK8):c.1016C>T (p.Pro339Leu) rs145716710 0.00013
NM_203447.4(DOCK8):c.2740G>A (p.Ala914Thr) rs375665207 0.00008
NM_203447.4(DOCK8):c.2482G>A (p.Ala828Thr) rs138519226 0.00007
NM_203447.4(DOCK8):c.2296G>A (p.Glu766Lys) rs267602235 0.00006
NM_203447.4(DOCK8):c.745G>A (p.Asp249Asn) rs202110964 0.00006
NM_203447.4(DOCK8):c.898T>G (p.Ser300Ala) rs145978391 0.00004
NM_203447.4(DOCK8):c.3454G>A (p.Glu1152Lys) rs1438287343 0.00003
NM_203447.4(DOCK8):c.2381T>C (p.Leu794Pro) rs769117348 0.00002
NM_203447.4(DOCK8):c.405-8C>G rs748853895 0.00002
NM_203447.4(DOCK8):c.4109G>A (p.Arg1370His) rs753480025 0.00002
NM_203447.4(DOCK8):c.1010C>G (p.Thr337Ser) rs747864013 0.00001
NM_203447.4(DOCK8):c.1823C>G (p.Pro608Arg) rs189953367 0.00001
NM_203447.4(DOCK8):c.2675G>A (p.Ser892Asn) rs1340101824 0.00001
NM_203447.4(DOCK8):c.3487C>T (p.Leu1163Phe) rs577097803 0.00001
NM_203447.4(DOCK8):c.4527C>G (p.His1509Gln) rs533492555 0.00001
NM_203447.4(DOCK8):c.5799C>T (p.Ser1933=) rs149602835 0.00001
NM_203447.4(DOCK8):c.6025C>T (p.His2009Tyr) rs534366023 0.00001
GRCh37/hg19 9p24.3(chr9:203861-268590)
GRCh37/hg19 9p24.3(chr9:239666-402280)
GRCh37/hg19 9p24.3(chr9:288826-402280)
NC_000009.11:g.(215030_271626)_(340322_368017)dup
NC_000009.11:g.(340322_368017)_(465260_?)dup
NC_000009.11:g.(407070_414781)_(465260_?)dup
NC_000009.11:g.(?_214864)_(399260_404917)dup
NM_203447.4(DOCK8):c.2017A>T (p.Ile673Phe) rs372858877
NM_203447.4(DOCK8):c.2066C>T (p.Ala689Val)
NM_203447.4(DOCK8):c.2440+13_2440+22del rs769837178
NM_203447.4(DOCK8):c.2T>C (p.Met1Thr) rs760902978
NM_203447.4(DOCK8):c.431_432delinsTT (p.Gly144Val) rs1057518550
NM_203447.4(DOCK8):c.4533C>G (p.Val1511=) rs2056640828
NM_203447.4(DOCK8):c.5207C>G (p.Ala1736Gly) rs139990627
NM_203447.4(DOCK8):c.5275C>T (p.Leu1759=) rs2131809759
NM_203447.4(DOCK8):c.955C>T (p.His319Tyr) rs2050845211

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