IKBKG
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA23153770605153770605+IntronDELGG-TCGA-4Z-AA87-01A-11D-A391-08TCGA-4Z-AA87-10A-01D-A394-08g.chrX:153770605delG
BLCA23153780345153780345+Missense_MutationSNPCCTTCGA-SY-A9G5-01A-11D-A38G-08TCGA-SY-A9G5-10A-01D-A38J-08g.chrX:153780345C>Tc.128C>Tc.(127-129)tCa>tTap.S43L
BLCA23153780359153780359+Missense_MutationSNPCCGTCGA-FD-A6TC-01A-21D-A339-08TCGA-FD-A6TC-10A-21D-A339-08g.chrX:153780359C>Gc.142C>Gc.(142-144)Cct>Gctp.P48A
COAD23153792576153792577+Frame_Shift_InsINS--CTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chrX:153792576_153792577insCc.1160_1161insCc.(1159-1164)agccccfsp.SP387fs
COAD23153792577153792577+Frame_Shift_DelDELCC-TCGA-CK-6746-01A-11D-1835-10TCGA-CK-6746-10A-01D-1835-10g.chrX:153792577delCc.1161delCc.(1159-1161)agcfsp.S387fs
COADREAD23153792576153792577+Frame_Shift_InsINS--CTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chrX:153792576_153792577insCc.1160_1161insCc.(1159-1164)agccccfsp.SP387fs
COADREAD23153792577153792577+Frame_Shift_DelDELCC-TCGA-CK-6746-01A-11D-1835-10TCGA-CK-6746-10A-01D-1835-10g.chrX:153792577delCc.1161delCc.(1159-1161)agcfsp.S387fs
GBMLGG23153780226153780226+SilentSNPGGATCGA-P5-A77X-01A-11D-A32B-08TCGA-P5-A77X-10A-01D-A329-08g.chrX:153780226G>Ac.9G>Ac.(7-9)agG>agAp.R3R
KICH23153770612153770612+IntronSNPGGCTCGA-KL-8341-01A-11D-2310-10TCGA-KL-8341-11A-01D-2310-10g.chrX:153770612G>C
KIPAN23153770607153770607+IntronSNPGGTTCGA-A3-3311-01A-01D-0966-08TCGA-A3-3311-11A-01D-0966-08g.chrX:153770607G>T
KIPAN23153770612153770612+IntronSNPGGCTCGA-KL-8341-01A-11D-2310-10TCGA-KL-8341-11A-01D-2310-10g.chrX:153770612G>C
KIPAN23153770658153770658+IntronSNPGGTTCGA-MH-A854-01A-11D-A34Z-10TCGA-MH-A854-10A-01D-A34Z-10g.chrX:153770658G>T
KIRC23153770607153770607+IntronSNPGGTTCGA-A3-3311-01A-01D-0966-08TCGA-A3-3311-11A-01D-0966-08g.chrX:153770607G>T
KIRP23153770658153770658+IntronSNPGGTTCGA-MH-A854-01A-11D-A34Z-10TCGA-MH-A854-10A-01D-A34Z-10g.chrX:153770658G>T
LGG23153780226153780226+SilentSNPGGATCGA-P5-A77X-01A-11D-A32B-08TCGA-P5-A77X-10A-01D-A329-08g.chrX:153780226G>Ac.9G>Ac.(7-9)agG>agAp.R3R
LIHC23153770550153770550+5'UTRSNPTTCTCGA-ES-A2HT-01A-12D-A183-10TCGA-ES-A2HT-11A-11D-A183-10g.chrX:153770550T>C
LUAD23153770605153770608+IntronDELGGGGGGGG-TCGA-86-8669-01A-11D-2393-08TCGA-86-8669-10A-01D-2393-08g.chrX:153770605_153770608delGGGG
LUAD23153780267153780267+Missense_MutationSNPGGCTCGA-95-A4VN-01A-11D-A25L-08TCGA-95-A4VN-10A-01D-A25L-08g.chrX:153780267G>Cc.50G>Cc.(49-51)aGt>aCtp.S17T
LUAD23153780355153780355+SilentSNPCCATCGA-05-4390-01A-02D-1753-08TCGA-05-4390-10A-01D-1753-08g.chrX:153780355C>Ac.138C>Ac.(136-138)ggC>ggAp.G46G
OV23153770592153770592+5'UTRSNPGGATCGA-23-1122-01A-01W-0486-08TCGA-23-1122-10A-01W-0486-08g.chrX:153770592G>A
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.43396;Hs.43463;Hs.43505Xq28300248
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
CASynonymousp.G114Gc.342C>AX153780355LUAD
CGMissensep.I37Mc.111C>GX153770589BRCA
CTSynonymousp.G96Gc.288C>TX153780301UCEC
GTMissensep.E128Dc.384G>TX153780397STAD