NM_005391.5(PDK3):c.562G>A (p.Asp188Asn)
|
rs1165981822
|
0.00009
|
NM_005391.5(PDK3):c.422C>T (p.Pro141Leu)
|
rs898354567
|
0.00006
|
NM_005391.5(PDK3):c.820G>A (p.Val274Ile)
|
rs773597771
|
0.00004
|
NM_005391.5(PDK3):c.1126G>A (p.Ala376Thr)
|
rs781166988
|
0.00002
|
NM_005391.5(PDK3):c.1211C>T (p.Ala404Val)
|
rs375862167
|
0.00002
|
NM_005391.5(PDK3):c.1148C>T (p.Thr383Met)
|
rs1442646183
|
0.00001
|
NM_005391.5(PDK3):c.1205A>G (p.Tyr402Cys)
|
rs762702094
|
0.00001
|
NM_005391.5(PDK3):c.149G>A (p.Arg50Gln)
|
rs757407648
|
0.00001
|
NM_005391.5(PDK3):c.160C>T (p.Pro54Ser)
|
rs1569221445
|
0.00001
|
NM_005391.5(PDK3):c.203C>T (p.Pro68Leu)
|
rs373610926
|
0.00001
|
NM_005391.5(PDK3):c.320+6T>C
|
rs748960946
|
0.00001
|
NM_005391.5(PDK3):c.338T>C (p.Ile113Thr)
|
rs1569223291
|
0.00001
|
NM_005391.5(PDK3):c.427A>G (p.Ile143Val)
|
rs1057438680
|
0.00001
|
NM_005391.5(PDK3):c.474C>T (p.Arg158=)
|
rs756879455
|
0.00001
|
NM_005391.5(PDK3):c.577G>A (p.Val193Met)
|
rs764909872
|
0.00001
|
NM_005391.5(PDK3):c.595+3A>G
|
rs1227104182
|
0.00001
|
NM_005391.5(PDK3):c.692C>G (p.Pro231Arg)
|
rs1051776582
|
0.00001
|
NM_005391.5(PDK3):c.811A>G (p.Lys271Glu)
|
rs1569227273
|
0.00001
|
NM_005391.5(PDK3):c.883C>A (p.Arg295=)
|
rs868382375
|
0.00001
|
NC_000023.10:g.(?_24483553)_(24557301_?)dup
|
|
|
NC_000023.10:g.(?_24483563)_(24557291_?)dup
|
|
|
NC_000023.10:g.(?_24483573)_(24483698_?)del
|
|
|
NC_000023.10:g.(?_24483573)_(24557281_?)del
|
|
|
NC_000023.10:g.(?_24512849)_(24537137_?)dup
|
|
|
NC_000023.10:g.(?_24544295)_(24557281_?)dup
|
|
|
NC_000023.10:g.(?_24549754)_(24549907_?)del
|
|
|
NC_000023.11:g.(?_24465436)_(24465581_?)del
|
|
|
NC_000023.11:g.(?_24494722)_(24539184_?)del
|
|
|
NM_001142386.3(PDK3):c.1218A>G (p.Gln406=)
|
|
|
NM_001142386.3(PDK3):c.1226T>C (p.Ile409Thr)
|
|
|
NM_005391.5(PDK3):c.1028A>C (p.Lys343Thr)
|
rs2148203320
|
|
NM_005391.5(PDK3):c.1077+2T>G
|
|
|
NM_005391.5(PDK3):c.1079C>T (p.Ala360Val)
|
rs1569228203
|
|
NM_005391.5(PDK3):c.1087dup (p.Ser363fs)
|
rs1569228214
|
|
NM_005391.5(PDK3):c.1097T>G (p.Phe366Cys)
|
rs1922715042
|
|
NM_005391.5(PDK3):c.1106T>C (p.Leu369Pro)
|
rs1922715462
|
|
NM_005391.5(PDK3):c.1159G>A (p.Asp387Asn)
|
|
|
NM_005391.5(PDK3):c.1193A>G (p.Asp398Gly)
|
|
|
NM_005391.5(PDK3):c.1202A>G (p.Lys401Arg)
|
rs371788046
|
|
NM_005391.5(PDK3):c.1213A>G (p.Lys405Glu)
|
|
|
NM_005391.5(PDK3):c.1217del (p.Gln406fs)
|
|
|
NM_005391.5(PDK3):c.1218dup (p.Ter407ValextTer?)
|
rs2148204361
|
|
NM_005391.5(PDK3):c.132_134del (p.Ser45del)
|
|
|
NM_005391.5(PDK3):c.137A>G (p.Tyr46Cys)
|
rs2148188298
|
|
NM_005391.5(PDK3):c.13C>T (p.Arg5Trp)
|
rs1940054079
|
|
NM_005391.5(PDK3):c.149_158dup (p.Pro54fs)
|
|
|
NM_005391.5(PDK3):c.18G>C (p.Trp6Cys)
|
rs2148176546
|
|
NM_005391.5(PDK3):c.217_226del (p.Asn73fs)
|
|
|
NM_005391.5(PDK3):c.220C>T (p.Arg74Cys)
|
|
|
NM_005391.5(PDK3):c.221G>A (p.Arg74His)
|
|
|
NM_005391.5(PDK3):c.223C>A (p.Pro75Thr)
|
rs2148188335
|
|
NM_005391.5(PDK3):c.23T>C (p.Leu8Pro)
|
|
|
NM_005391.5(PDK3):c.248+3A>G
|
|
|
NM_005391.5(PDK3):c.293G>A (p.Ser98Asn)
|
|
|
NM_005391.5(PDK3):c.302A>G (p.Asp101Gly)
|
|
|
NM_005391.5(PDK3):c.308A>G (p.Gln103Arg)
|
rs2148190126
|
|
NM_005391.5(PDK3):c.316G>A (p.Asp106Asn)
|
|
|
NM_005391.5(PDK3):c.321-3C>T
|
|
|
NM_005391.5(PDK3):c.335T>C (p.Leu112Pro)
|
rs2148191720
|
|
NM_005391.5(PDK3):c.340A>G (p.Lys114Glu)
|
|
|
NM_005391.5(PDK3):c.355C>T (p.His119Tyr)
|
|
|
NM_005391.5(PDK3):c.382C>A (p.Gln128Lys)
|
|
|
NM_005391.5(PDK3):c.382C>G (p.Gln128Glu)
|
|
|
NM_005391.5(PDK3):c.392T>C (p.Ile131Thr)
|
|
|
NM_005391.5(PDK3):c.434C>G (p.Thr145Ser)
|
|
|
NM_005391.5(PDK3):c.472C>G (p.Arg158Gly)
|
|
|
NM_005391.5(PDK3):c.485G>A (p.Arg162His)
|
rs867468579
|
|
NM_005391.5(PDK3):c.49G>C (p.Glu17Gln)
|
rs2148176569
|
|
NM_005391.5(PDK3):c.505+3A>T
|
rs1921912997
|
|
NM_005391.5(PDK3):c.577G>C (p.Val193Leu)
|
rs764909872
|
|
NM_005391.5(PDK3):c.596A>G (p.Asp199Gly)
|
|
|
NM_005391.5(PDK3):c.597del (p.Asp199fs)
|
rs1569225940
|
|
NM_005391.5(PDK3):c.608C>G (p.Thr203Arg)
|
rs1555949588
|
|
NM_005391.5(PDK3):c.674-5T>G
|
rs2148201118
|
|
NM_005391.5(PDK3):c.707A>G (p.Tyr236Cys)
|
rs2148201163
|
|
NM_005391.5(PDK3):c.86T>A (p.Ile29Asn)
|
|
|
NM_005391.5(PDK3):c.895C>T (p.Arg299Cys)
|
|
|
NM_005391.5(PDK3):c.896G>A (p.Arg299His)
|
|
|
NM_005391.5(PDK3):c.940G>T (p.Glu314Ter)
|
rs1922567942
|
|
NM_005391.5(PDK3):c.974G>T (p.Gly325Val)
|
|
|