NM_203447.4(DOCK8):c.986C>T (p.Ala329Val)
|
rs75352090
|
0.00055
|
NM_203447.4(DOCK8):c.3067A>G (p.Ile1023Val)
|
rs140148619
|
0.00041
|
NM_203447.4(DOCK8):c.4736C>G (p.Ala1579Gly)
|
rs145202369
|
0.00031
|
NM_203447.4(DOCK8):c.5207C>T (p.Ala1736Val)
|
rs139990627
|
0.00026
|
NM_203447.4(DOCK8):c.6221G>C (p.Arg2074Thr)
|
rs375011475
|
0.00024
|
NM_203447.4(DOCK8):c.2272C>T (p.Arg758Cys)
|
rs749523267
|
0.00011
|
NM_203447.4(DOCK8):c.3052G>A (p.Asp1018Asn)
|
rs142910397
|
0.00011
|
NM_203447.4(DOCK8):c.3721C>T (p.Arg1241Cys)
|
rs556936872
|
0.00011
|
NM_203447.4(DOCK8):c.2393A>G (p.Lys798Arg)
|
rs140546511
|
0.00010
|
NM_203447.4(DOCK8):c.5266A>C (p.Ile1756Leu)
|
rs373154957
|
0.00009
|
NM_203447.4(DOCK8):c.605G>A (p.Arg202His)
|
rs374288188
|
0.00008
|
NM_203447.4(DOCK8):c.3713G>A (p.Arg1238His)
|
rs767874435
|
0.00006
|
NM_203447.4(DOCK8):c.4003G>T (p.Val1335Leu)
|
rs141863163
|
0.00006
|
NM_203447.4(DOCK8):c.5645C>A (p.Thr1882Lys)
|
rs376529318
|
0.00006
|
NM_203447.4(DOCK8):c.6107C>T (p.Thr2036Met)
|
rs767198480
|
0.00006
|
NM_203447.4(DOCK8):c.5671C>T (p.Arg1891Trp)
|
rs144951842
|
0.00005
|
NM_203447.4(DOCK8):c.2033G>A (p.Arg678His)
|
rs146223665
|
0.00004
|
NM_203447.4(DOCK8):c.2731A>G (p.Thr911Ala)
|
rs754915792
|
0.00004
|
NM_203447.4(DOCK8):c.3869C>T (p.Ala1290Val)
|
rs138180879
|
0.00004
|
NM_203447.4(DOCK8):c.559G>A (p.Asp187Asn)
|
rs111842279
|
0.00004
|
NM_203447.4(DOCK8):c.3123A>C (p.Glu1041Asp)
|
rs377274335
|
0.00003
|
NM_203447.4(DOCK8):c.3209A>G (p.Asn1070Ser)
|
rs368569393
|
0.00003
|
NM_203447.4(DOCK8):c.893A>G (p.Lys298Arg)
|
rs759089561
|
0.00003
|
NM_203447.4(DOCK8):c.3758G>T (p.Gly1253Val)
|
rs774890293
|
0.00002
|
NM_203447.4(DOCK8):c.3881G>A (p.Arg1294His)
|
rs759725406
|
0.00002
|
NM_203447.4(DOCK8):c.3910A>G (p.Met1304Val)
|
rs376247401
|
0.00002
|
NM_203447.4(DOCK8):c.4004T>C (p.Val1335Ala)
|
rs763029509
|
0.00002
|
NM_203447.4(DOCK8):c.5408A>C (p.Lys1803Thr)
|
rs534744136
|
0.00002
|
NM_203447.4(DOCK8):c.5620G>A (p.Glu1874Lys)
|
rs779199376
|
0.00002
|
NM_203447.4(DOCK8):c.1823C>G (p.Pro608Arg)
|
rs189953367
|
0.00001
|
NM_203447.4(DOCK8):c.2093C>T (p.Ser698Phe)
|
rs763006372
|
0.00001
|
NM_203447.4(DOCK8):c.3511C>G (p.Leu1171Val)
|
rs367567088
|
0.00001
|
NM_203447.4(DOCK8):c.4958C>A (p.Thr1653Asn)
|
rs1401659010
|
0.00001
|
NM_203447.4(DOCK8):c.4999C>T (p.His1667Tyr)
|
rs373762198
|
0.00001
|
NM_203447.4(DOCK8):c.5629A>G (p.Met1877Val)
|
rs369626419
|
0.00001
|
NM_203447.4(DOCK8):c.914G>A (p.Cys305Tyr)
|
rs778114411
|
0.00001
|
NM_203447.4(DOCK8):c.1027A>G (p.Ile343Val)
|
|
|
NM_203447.4(DOCK8):c.1369G>T (p.Val457Phe)
|
|
|
NM_203447.4(DOCK8):c.1406G>C (p.Ser469Thr)
|
|
|
NM_203447.4(DOCK8):c.1448A>T (p.Asp483Val)
|
|
|
NM_203447.4(DOCK8):c.1450T>G (p.Leu484Val)
|
|
|
NM_203447.4(DOCK8):c.1618C>G (p.Pro540Ala)
|
|
|
NM_203447.4(DOCK8):c.1726C>G (p.Leu576Val)
|
|
|
NM_203447.4(DOCK8):c.2198A>G (p.His733Arg)
|
|
|
NM_203447.4(DOCK8):c.2410G>T (p.Val804Leu)
|
|
|
NM_203447.4(DOCK8):c.2585A>C (p.Gln862Pro)
|
|
|
NM_203447.4(DOCK8):c.2687T>G (p.Leu896Arg)
|
|
|
NM_203447.4(DOCK8):c.2736C>G (p.His912Gln)
|
rs747112580
|
|
NM_203447.4(DOCK8):c.2953T>C (p.Phe985Leu)
|
|
|
NM_203447.4(DOCK8):c.2971G>C (p.Val991Leu)
|
|
|
NM_203447.4(DOCK8):c.3217A>G (p.Arg1073Gly)
|
|
|
NM_203447.4(DOCK8):c.3342G>T (p.Met1114Ile)
|
|
|
NM_203447.4(DOCK8):c.358G>T (p.Asp120Tyr)
|
|
|
NM_203447.4(DOCK8):c.3612A>T (p.Lys1204Asn)
|
rs758993681
|
|
NM_203447.4(DOCK8):c.3629A>G (p.Lys1210Arg)
|
|
|
NM_203447.4(DOCK8):c.3877A>G (p.Thr1293Ala)
|
|
|
NM_203447.4(DOCK8):c.3922G>A (p.Asp1308Asn)
|
|
|
NM_203447.4(DOCK8):c.398A>G (p.Asn133Ser)
|
|
|
NM_203447.4(DOCK8):c.412G>C (p.Gly138Arg)
|
|
|
NM_203447.4(DOCK8):c.4423A>G (p.Thr1475Ala)
|
|
|
NM_203447.4(DOCK8):c.4472A>G (p.Lys1491Arg)
|
|
|
NM_203447.4(DOCK8):c.4511G>A (p.Cys1504Tyr)
|
|
|
NM_203447.4(DOCK8):c.4588C>T (p.Leu1530Phe)
|
|
|
NM_203447.4(DOCK8):c.5245A>G (p.Asn1749Asp)
|
|
|
NM_203447.4(DOCK8):c.5356G>A (p.Asp1786Asn)
|
|
|
NM_203447.4(DOCK8):c.5396T>A (p.Phe1799Tyr)
|
rs2131813614
|
|
NM_203447.4(DOCK8):c.5408A>G (p.Lys1803Arg)
|
|
|
NM_203447.4(DOCK8):c.5602G>C (p.Val1868Leu)
|
|
|
NM_203447.4(DOCK8):c.5617G>C (p.Asp1873His)
|
|
|
NM_203447.4(DOCK8):c.5744G>C (p.Arg1915Thr)
|
|
|
NM_203447.4(DOCK8):c.636C>G (p.Asn212Lys)
|
rs1223609550
|
|
NM_203447.4(DOCK8):c.759A>G (p.Ile253Met)
|
|
|
NM_203447.4(DOCK8):c.84T>G (p.Phe28Leu)
|
rs2048168645
|
|
NM_203447.4(DOCK8):c.857C>T (p.Ala286Val)
|
|
|
NM_203447.4(DOCK8):c.859A>C (p.Ser287Arg)
|
|
|
NM_203447.4(DOCK8):c.941G>T (p.Gly314Val)
|
|
|