Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 8 11996101 11996101 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr8:11996101G>T c.169C>A c.(169-171)Cct>Act p.P57T BLCA 8 11994748 11994748 + Missense_Mutation SNP G G C TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr8:11994748G>C c.1522C>G c.(1522-1524)Ctg>Gtg p.L508V BLCA 8 11995006 11995006 + Missense_Mutation SNP C C T TCGA-GU-A42P-01A-11D-A23U-08 TCGA-GU-A42P-10A-01D-A23U-08 g.chr8:11995006C>T c.1264G>A c.(1264-1266)Gag>Aag p.E422K BLCA 8 11995859 11995859 + Silent SNP G G A TCGA-GV-A3QH-01A-11D-A21Z-08 TCGA-GV-A3QH-10A-01D-A21Z-08 g.chr8:11995859G>A c.411C>T c.(409-411)caC>caT p.H137H BLCA 8 11995991 11995991 + Silent SNP A A T TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr8:11995991A>T c.279T>A c.(277-279)gcT>gcA p.A93A BLCA 8 11996025 11996025 + Missense_Mutation SNP A A T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr8:11996025A>T c.245T>A c.(244-246)cTc>cAc p.L82H BLCA 8 11996072 11996072 + Silent SNP C C T TCGA-DK-A2HX-01A-12D-A18F-08 TCGA-DK-A2HX-10A-01D-A18F-08 g.chr8:11996072C>T c.198G>A c.(196-198)aaG>aaA p.K66K BRCA 8 11995160 11995160 + Silent SNP G G C TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr8:11995160G>C c.1110C>G c.(1108-1110)ctC>ctG p.L370L BRCA 8 11996086 11996086 + Missense_Mutation SNP G G A TCGA-AC-A3TN-01A-11D-A228-09 TCGA-AC-A3TN-10A-01D-A22A-09 g.chr8:11996086G>A c.184C>T c.(184-186)Ctt>Ttt p.L62F CESC 8 11995421 11995421 + Missense_Mutation SNP G G C TCGA-FU-A40J-01A-11D-A243-09 TCGA-FU-A40J-10A-01D-A243-09 g.chr8:11995421G>C c.849C>G c.(847-849)ttC>ttG p.F283L CESC 8 11995785 11995785 + Missense_Mutation SNP T T A TCGA-C5-A3HE-01A-21D-A22X-09 TCGA-C5-A3HE-10A-01D-A22X-09 g.chr8:11995785T>A c.485A>T c.(484-486)cAt>cTt p.H162L CESC 8 11995849 11995849 + Missense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr8:11995849G>A c.421C>T c.(421-423)Cat>Tat p.H141Y CESC 8 11995989 11995990 + Frame_Shift_Ins INS - - A TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr8:11995989_11995990insA c.280_281insT c.(280-282)tccfs p.S94fs CESC 8 11996239 11996239 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr8:11996239C>G c.31G>C c.(31-33)Gag>Cag p.E11Q COAD 8 11994748 11994748 + Missense_Mutation SNP G G C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr8:11994748G>C c.1522C>G c.(1522-1524)Ctg>Gtg p.L508V COAD 8 11994818 11994818 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr8:11994818G>A c.1452C>T c.(1450-1452)agC>agT p.S484S COAD 8 11994840 11994840 + Missense_Mutation SNP T T C TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr8:11994840T>C c.1430A>G c.(1429-1431)aAc>aGc p.N477S COAD 8 11994864 11994864 + Nonsense_Mutation SNP G G T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr8:11994864G>T c.1406C>A c.(1405-1407)tCg>tAg p.S469* COAD 8 11994886 11994886 + Missense_Mutation SNP T T C TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr8:11994886T>C c.1384A>G c.(1384-1386)Aac>Gac p.N462D COAD 8 11994917 11994917 + Silent SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr8:11994917G>A c.1353C>T c.(1351-1353)aaC>aaT p.N451N COAD 8 11995019 11995019 + Silent SNP T T G TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr8:11995019T>G c.1251A>C c.(1249-1251)gcA>gcC p.A417A COAD 8 11995174 11995174 + Missense_Mutation SNP G G T TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr8:11995174G>T c.1096C>A c.(1096-1098)Cag>Aag p.Q366K COAD 8 11995473 11995473 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:11995473G>A c.797C>T c.(796-798)aCg>aTg p.T266M COAD 8 11995934 11995934 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:11995934C>A c.336G>T c.(334-336)gaG>gaT p.E112D COAD 8 11996002 11996002 + Missense_Mutation SNP A A G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr8:11996002A>G c.268T>C c.(268-270)Tac>Cac p.Y90H COAD 8 11996136 11996136 + Missense_Mutation SNP G G C TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr8:11996136G>C c.134C>G c.(133-135)tCt>tGt p.S45C COADREAD 8 11994748 11994748 + Missense_Mutation SNP G G C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr8:11994748G>C c.1522C>G c.(1522-1524)Ctg>Gtg p.L508V COADREAD 8 11994818 11994818 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr8:11994818G>A c.1452C>T c.(1450-1452)agC>agT p.S484S COADREAD 8 11994840 11994840 + Missense_Mutation SNP T T C TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr8:11994840T>C c.1430A>G c.(1429-1431)aAc>aGc p.N477S COADREAD 8 11994864 11994864 + Nonsense_Mutation SNP G G T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr8:11994864G>T c.1406C>A c.(1405-1407)tCg>tAg p.S469* COADREAD 8 11994886 11994886 + Missense_Mutation SNP T T C TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr8:11994886T>C c.1384A>G c.(1384-1386)Aac>Gac p.N462D COADREAD 8 11994917 11994917 + Silent SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr8:11994917G>A c.1353C>T c.(1351-1353)aaC>aaT p.N451N COADREAD 8 11995019 11995019 + Silent SNP T T G TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr8:11995019T>G c.1251A>C c.(1249-1251)gcA>gcC p.A417A COADREAD 8 11995174 11995174 + Missense_Mutation SNP G G T TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr8:11995174G>T c.1096C>A c.(1096-1098)Cag>Aag p.Q366K COADREAD 8 11995190 11995190 + Silent SNP A A G TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr8:11995190A>G c.1080T>C c.(1078-1080)acT>acC p.T360T COADREAD 8 11995473 11995473 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:11995473G>A c.797C>T c.(796-798)aCg>aTg p.T266M COADREAD 8 11995777 11995777 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:11995777G>T c.493C>A c.(493-495)Ctc>Atc p.L165I COADREAD 8 11995934 11995934 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:11995934C>A c.336G>T c.(334-336)gaG>gaT p.E112D COADREAD 8 11996002 11996002 + Missense_Mutation SNP A A G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr8:11996002A>G c.268T>C c.(268-270)Tac>Cac p.Y90H COADREAD 8 11996136 11996136 + Missense_Mutation SNP G G C TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr8:11996136G>C c.134C>G c.(133-135)tCt>tGt p.S45C DLBC 8 11994795 11994795 + Missense_Mutation SNP G G A TCGA-FF-8041-01A-11D-2210-10 TCGA-FF-8041-10A-01D-2210-10 g.chr8:11994795G>A c.1475C>T c.(1474-1476)aCg>aTg p.T492M DLBC 8 11995004 11995004 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr8:11995004C>T c.1266G>A c.(1264-1266)gaG>gaA p.E422E DLBC 8 11996074 11996074 + Missense_Mutation SNP T T C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr8:11996074T>C c.196A>G c.(196-198)Aag>Gag p.K66E ESCA 8 11994772 11994772 + Missense_Mutation SNP C C T TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr8:11994772C>T c.1498G>A c.(1498-1500)Gtg>Atg p.V500M ESCA 8 11995085 11995085 + Silent SNP G G A TCGA-L5-A8NG-01A-11D-A37C-09 TCGA-L5-A8NG-11A-11D-A37F-09 g.chr8:11995085G>A c.1185C>T c.(1183-1185)ggC>ggT p.G395G ESCA 8 11995298 11995298 + Silent SNP G G C TCGA-L5-A4OR-01A-11D-A27G-09 TCGA-L5-A4OR-11A-11D-A27G-09 g.chr8:11995298G>C c.972C>G c.(970-972)gtC>gtG p.V324V ESCA 8 11995473 11995473 + Missense_Mutation SNP G G T TCGA-VR-A8EO-01A-11D-A36J-09 TCGA-VR-A8EO-10A-01D-A36M-09 g.chr8:11995473G>T c.797C>A c.(796-798)aCg>aAg p.T266K ESCA 8 11996159 11996159 + Silent SNP G G A TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr8:11996159G>A c.111C>T c.(109-111)ctC>ctT p.L37L ESCA 8 11996188 11996188 + Missense_Mutation SNP C C T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr8:11996188C>T c.82G>A c.(82-84)Gct>Act p.A28T GBM 8 11995987 11995987 + Silent SNP G G A TCGA-12-0821-01A-01W-0424-08 TCGA-12-0821-10A-01W-0424-08 g.chr8:11995987G>A c.283C>T c.(283-285)Ctg>Ttg p.L95L GBMLGG 8 11995987 11995987 + Silent SNP G G A TCGA-12-0821-01A-01W-0424-08 TCGA-12-0821-10A-01W-0424-08 g.chr8:11995987G>A c.283C>T c.(283-285)Ctg>Ttg p.L95L HNSC 8 11994694 11994694 + Missense_Mutation SNP G G C TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr8:11994694G>C c.1576C>G c.(1576-1578)Ctg>Gtg p.L526V HNSC 8 11994697 11994697 + Missense_Mutation SNP C C A TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr8:11994697C>A c.1573G>T c.(1573-1575)Gct>Tct p.A525S HNSC 8 11994707 11994707 + Missense_Mutation SNP G G T TCGA-WA-A7GZ-01A-11D-A34J-08 TCGA-WA-A7GZ-10A-01D-A34M-08 g.chr8:11994707G>T c.1563C>A c.(1561-1563)caC>caA p.H521Q HNSC 8 11995148 11995148 + Missense_Mutation SNP C C G TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chr8:11995148C>G c.1122G>C c.(1120-1122)caG>caC p.Q374H HNSC 8 11995295 11995295 + Silent SNP G G A TCGA-BB-8596-01A-11D-2394-08 TCGA-BB-8596-10A-01D-2394-08 g.chr8:11995295G>A c.975C>T c.(973-975)caC>caT p.H325H HNSC 8 11995582 11995582 + Missense_Mutation SNP C C A TCGA-D6-A6EO-01A-11D-A31L-08 TCGA-D6-A6EO-10A-01D-A31J-08 g.chr8:11995582C>A c.688G>T c.(688-690)Gct>Tct p.A230S HNSC 8 11995836 11995836 + Missense_Mutation SNP G G A TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr8:11995836G>A c.434C>T c.(433-435)cCc>cTc p.P145L HNSC 8 11996046 11996046 + Missense_Mutation SNP G G A TCGA-BA-5151-01A-01D-1434-08 TCGA-BA-5151-10A-01D-1434-08 g.chr8:11996046G>A c.224C>T c.(223-225)cCt>cTt p.P75L HNSC 8 11996053 11996053 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr8:11996053T>C c.217A>G c.(217-219)Agg>Ggg p.R73G HNSC 8 11996173 11996173 + Missense_Mutation SNP G G T TCGA-CR-7401-01A-11D-2012-08 TCGA-CR-7401-10A-01D-2013-08 g.chr8:11996173G>T c.97C>A c.(97-99)Cag>Aag p.Q33K KIPAN 8 11995803 11995803 + Missense_Mutation SNP C C T TCGA-BP-4972-01A-01D-1462-08 TCGA-BP-4972-11A-01D-1462-08 g.chr8:11995803C>T c.467G>A c.(466-468)gGc>gAc p.G156D KIPAN 8 11995987 11995987 + Silent SNP G G A TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr8:11995987G>A c.283C>T c.(283-285)Ctg>Ttg p.L95L KIRC 8 11995803 11995803 + Missense_Mutation SNP C C T TCGA-BP-4972-01A-01D-1462-08 TCGA-BP-4972-11A-01D-1462-08 g.chr8:11995803C>T c.467G>A c.(466-468)gGc>gAc p.G156D KIRC 8 11995987 11995987 + Silent SNP G G A TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr8:11995987G>A c.283C>T c.(283-285)Ctg>Ttg p.L95L LUAD 8 11994734 11994734 + Silent SNP G G T TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr8:11994734G>T c.1536C>A c.(1534-1536)acC>acA p.T512T LUAD 8 11994828 11994828 + Missense_Mutation SNP T T A TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr8:11994828T>A c.1442A>T c.(1441-1443)gAa>gTa p.E481V LUAD 8 11994973 11994973 + Missense_Mutation SNP T T G TCGA-55-7815-01A-11D-2167-08 TCGA-55-7815-10A-01D-2167-08 g.chr8:11994973T>G c.1297A>C c.(1297-1299)Acc>Ccc p.T433P LUAD 8 11995031 11995031 + Silent SNP G G T TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr8:11995031G>T c.1239C>A c.(1237-1239)ccC>ccA p.P413P LUAD 8 11995480 11995480 + Missense_Mutation SNP A A T TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr8:11995480A>T c.790T>A c.(790-792)Tcc>Acc p.S264T LUAD 8 11995482 11995482 + Missense_Mutation SNP G G T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr8:11995482G>T c.788C>A c.(787-789)gCc>gAc p.A263D LUAD 8 11995836 11995836 + Missense_Mutation SNP G G T TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr8:11995836G>T c.434C>A c.(433-435)cCc>cAc p.P145H LUAD 8 11995977 11995977 + Missense_Mutation SNP A A T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr8:11995977A>T c.293T>A c.(292-294)cTg>cAg p.L98Q LUSC 8 11995031 11995031 + Silent SNP G G C TCGA-66-2792-01A-01D-0983-08 TCGA-66-2792-11A-01D-0983-08 g.chr8:11995031G>C c.1239C>G c.(1237-1239)ccC>ccG p.P413P LUSC 8 11995293 11995293 + Missense_Mutation SNP G G A TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr8:11995293G>A c.977C>T c.(976-978)gCt>gTt p.A326V LUSC 8 11995788 11995788 + Missense_Mutation SNP G G T TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr8:11995788G>T c.482C>A c.(481-483)gCc>gAc p.A161D PAAD 8 11994753 11994753 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:11994753G>A c.1517C>T c.(1516-1518)gCt>gTt p.A506V PAAD 8 11994754 11994754 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:11994754C>T c.1516G>A c.(1516-1518)Gct>Act p.A506T PAAD 8 11995011 11995011 + Nonsense_Mutation SNP A A T TCGA-YY-A8LH-01A-11D-A36O-08 TCGA-YY-A8LH-10A-01D-A367-08 g.chr8:11995011A>T c.1259T>A c.(1258-1260)tTg>tAg p.L420* PAAD 8 11995139 11995139 + Missense_Mutation SNP T T A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:11995139T>A c.1131A>T c.(1129-1131)gaA>gaT p.E377D PAAD 8 11995503 11995503 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:11995503A>G c.767T>C c.(766-768)cTt>cCt p.L256P PAAD 8 11995994 11995994 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:11995994G>A c.276C>T c.(274-276)aaC>aaT p.N92N PCPG 8 11995945 11995945 + Silent SNP G G A TCGA-WB-A81T-01A-11D-A35I-08 TCGA-WB-A81T-10A-01D-A35G-08 g.chr8:11995945G>A c.325C>T c.(325-327)Ctg>Ttg p.L109L READ 8 11995190 11995190 + Silent SNP A A G TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr8:11995190A>G c.1080T>C c.(1078-1080)acT>acC p.T360T READ 8 11995777 11995777 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:11995777G>T c.493C>A c.(493-495)Ctc>Atc p.L165I SARC 8 11995025 11995025 + Silent SNP G G A TCGA-DX-A6YX-01A-11D-A417-09 TCGA-DX-A6YX-10B-01D-A41A-09 g.chr8:11995025G>A c.1245C>T c.(1243-1245)ctC>ctT p.L415L SARC 8 11995398 11995398 + Missense_Mutation SNP A A G TCGA-DX-A6YQ-01A-12D-A33E-09 TCGA-DX-A6YQ-10A-01D-A33H-09 g.chr8:11995398A>G c.872T>C c.(871-873)cTt>cCt p.L291P SARC 8 11995433 11995433 + Silent SNP G G T TCGA-DX-A6YX-01A-11D-A417-09 TCGA-DX-A6YX-10B-01D-A41A-09 g.chr8:11995433G>T c.837C>A c.(835-837)gtC>gtA p.V279V SARC 8 11995496 11995496 + Silent SNP G G C TCGA-DX-A6YX-01A-11D-A417-09 TCGA-DX-A6YX-10B-01D-A41A-09 g.chr8:11995496G>C c.774C>G c.(772-774)ctC>ctG p.L258L SKCM 8 11994678 11994678 + Splice_Site SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr8:11994678C>T c.1592G>A c.(1591-1593)tGa>tAa p.*531* SKCM 8 11994698 11994698 + Silent SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr8:11994698C>T c.1572G>A c.(1570-1572)agG>agA p.R524R SKCM 8 11994707 11994707 + Missense_Mutation SNP G G C TCGA-EB-A5KH-06A-11D-A27K-08 TCGA-EB-A5KH-10A-01D-A27N-08 g.chr8:11994707G>C c.1563C>G c.(1561-1563)caC>caG p.H521Q SKCM 8 11994741 11994741 + Missense_Mutation SNP C C T TCGA-EE-A3AH-06A-11D-A196-08 TCGA-EE-A3AH-10A-01D-A198-08 g.chr8:11994741C>T c.1529G>A c.(1528-1530)gGg>gAg p.G510E SKCM 8 11994741 11994741 + Missense_Mutation SNP C C T TCGA-FS-A1ZB-06A-12D-A197-08 TCGA-FS-A1ZB-10A-01D-A199-08 g.chr8:11994741C>T c.1529G>A c.(1528-1530)gGg>gAg p.G510E SKCM 8 11994778 11994778 + Missense_Mutation SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr8:11994778C>T c.1492G>A c.(1492-1494)Gag>Aag p.E498K SKCM 8 11994844 11994844 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr8:11994844T>C c.1426A>G c.(1426-1428)Aaa>Gaa p.K476E SKCM 8 11994845 11994845 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr8:11994845C>T c.1425G>A c.(1423-1425)atG>atA p.M475I SKCM 8 11994871 11994871 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr8:11994871G>A c.1399C>T c.(1399-1401)Cat>Tat p.H467Y SKCM 8 11994895 11994895 + Silent SNP G G A TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr8:11994895G>A c.1375C>T c.(1375-1377)Ctg>Ttg p.L459L SKCM 8 11994905 11994905 + Silent SNP G G A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr8:11994905G>A c.1365C>T c.(1363-1365)gtC>gtT p.V455V SKCM 8 11994955 11994955 + Missense_Mutation SNP A A G TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr8:11994955A>G c.1315T>C c.(1315-1317)Ttc>Ctc p.F439L SKCM 8 11994994 11994994 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr8:11994994C>T c.1276G>A c.(1276-1278)Gaa>Aaa p.E426K SKCM 8 11995065 11995065 + Missense_Mutation SNP C C G TCGA-D3-A3CB-06A-11D-A196-08 TCGA-D3-A3CB-10A-01D-A198-08 g.chr8:11995065C>G c.1205G>C c.(1204-1206)cGa>cCa p.R402P SKCM 8 11995072 11995072 + Missense_Mutation SNP C C T TCGA-ER-A199-06A-11D-A197-08 TCGA-ER-A199-10A-01D-A199-08 g.chr8:11995072C>T c.1198G>A c.(1198-1200)Gac>Aac p.D400N SKCM 8 11995102 11995102 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr8:11995102C>T c.1168G>A c.(1168-1170)Gaa>Aaa p.E390K SKCM 8 11995136 11995136 + Nonsense_Mutation SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr8:11995136C>T c.1134G>A c.(1132-1134)tgG>tgA p.W378* SKCM 8 11995223 11995223 + Missense_Mutation SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr8:11995223C>T c.1047G>A c.(1045-1047)atG>atA p.M349I SKCM 8 11995285 11995285 + Missense_Mutation SNP T T A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr8:11995285T>A c.985A>T c.(985-987)Agt>Tgt p.S329C SKCM 8 11995287 11995287 + Nonsense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr8:11995287C>T c.983G>A c.(982-984)tGg>tAg p.W328* SKCM 8 11995291 11995291 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr8:11995291C>T c.979G>A c.(979-981)Ggg>Agg p.G327R SKCM 8 11995377 11995377 + Missense_Mutation SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr8:11995377G>A c.893C>T c.(892-894)cCt>cTt p.P298L SKCM 8 11995636 11995636 + Missense_Mutation SNP C C T TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr8:11995636C>T c.634G>A c.(634-636)Ggg>Agg p.G212R SKCM 8 11995798 11995798 + Nonsense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr8:11995798G>A c.472C>T c.(472-474)Cag>Tag p.Q158* SKCM 8 11996013 11996013 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr8:11996013C>T c.257G>A c.(256-258)gGa>gAa p.G86E SKCM 8 11996035 11996035 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr8:11996035C>T c.235G>A c.(235-237)Ggg>Agg p.G79R SKCM 8 11996046 11996046 + Missense_Mutation SNP G G A TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr8:11996046G>A c.224C>T c.(223-225)cCt>cTt p.P75L SKCM 8 11996079 11996079 + Missense_Mutation SNP G G A TCGA-FS-A1ZD-06A-11D-A197-08 TCGA-FS-A1ZD-10A-01D-A199-08 g.chr8:11996079G>A c.191C>T c.(190-192)cCc>cTc p.P64L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 8 11995166 11995166 single base substitution A G synonymous_variant Y368Y 1104T>C BLCA-CN 8 11995274 11995274 single base substitution G A synonymous_variant D332D 996C>T BLCA-CN 8 11995325 11995325 single base substitution A G synonymous_variant L315L 945T>C BLCA-US 8 11995859 11995859 single base substitution G A synonymous_variant H137H 411C>T BLCA-US 8 11996072 11996072 single base substitution C T synonymous_variant K66K 198G>A BRCA-EU 8 11991657 11991657 single base substitution G A downstream_gene_variant BRCA-EU 8 11991697 11991697 single base substitution A G downstream_gene_variant BRCA-EU 8 11992650 11992650 single base substitution A G downstream_gene_variant BRCA-EU 8 11994064 11994064 single base substitution C G downstream_gene_variant BRCA-EU 8 11994579 11994579 insertion of <=200bp - TG downstream_gene_variant BRCA-EU 8 11994579 11994580 deletion of <=200bp TG - downstream_gene_variant BRCA-EU 8 11998209 11998209 single base substitution C G upstream_gene_variant BRCA-EU 8 11998647 11998647 single base substitution G A upstream_gene_variant BRCA-EU 8 12000271 12000271 deletion of <=200bp T - upstream_gene_variant BRCA-EU 8 12001255 12001255 single base substitution T C upstream_gene_variant BRCA-EU 8 12001280 12001280 single base substitution C G upstream_gene_variant BRCA-FR 8 11998209 11998209 single base substitution C G upstream_gene_variant BRCA-FR 8 12001255 12001255 single base substitution T C upstream_gene_variant BRCA-US 8 11995160 11995160 single base substitution G C synonymous_variant L370L 1110C>G BRCA-US 8 11996086 11996086 single base substitution G A missense_variant L62F 184C>T CESC-US 8 11995421 11995421 single base substitution G C missense_variant F283L 849C>G CESC-US 8 11995785 11995785 single base substitution T A missense_variant H162L 485A>T CESC-US 8 11995849 11995849 single base substitution G A missense_variant H141Y 421C>T CESC-US 8 11995989 11995989 insertion of <=200bp - A frameshift_variant S94S? CESC-US 8 11996239 11996239 single base substitution C G missense_variant E11Q 31G>C CLLE-ES 8 11998405 11998405 single base substitution A G upstream_gene_variant COAD-US 8 11994818 11994818 single base substitution G A synonymous_variant S484S 1452C>T COAD-US 8 11994917 11994917 single base substitution G A synonymous_variant N451N 1353C>T COAD-US 8 11995248 11995248 single base substitution G A missense_variant A341V 1022C>T COAD-US 8 11995276 11995276 single base substitution C T missense_variant D332N 994G>A COCA-CN 8 11991948 11991948 single base substitution G C downstream_gene_variant COCA-CN 8 11992188 11992188 single base substitution C G downstream_gene_variant COCA-CN 8 11996691 11996691 single base substitution G C upstream_gene_variant COCA-CN 8 12000169 12000169 single base substitution G T upstream_gene_variant COCA-CN 8 12000360 12000360 single base substitution G A upstream_gene_variant COCA-CN 8 12000602 12000602 single base substitution G A upstream_gene_variant ESAD-UK 8 11989700 11989700 single base substitution A C downstream_gene_variant ESAD-UK 8 11989703 11989703 single base substitution T G downstream_gene_variant ESAD-UK 8 11990345 11990345 single base substitution T C downstream_gene_variant ESAD-UK 8 11990674 11990674 single base substitution C G downstream_gene_variant ESAD-UK 8 11991381 11991381 single base substitution C T downstream_gene_variant ESAD-UK 8 11994020 11994020 single base substitution G A downstream_gene_variant ESAD-UK 8 11994041 11994041 single base substitution G A downstream_gene_variant ESAD-UK 8 11994360 11994360 single base substitution T A downstream_gene_variant ESAD-UK 8 11994458 11994458 single base substitution T G downstream_gene_variant ESAD-UK 8 11994658 11994658 single base substitution G T downstream_gene_variant ESAD-UK 8 11994672 11994672 single base substitution T G downstream_gene_variant ESAD-UK 8 11994789 11994789 single base substitution C T missense_variant R494Q 1481G>A ESAD-UK 8 11994832 11994832 single base substitution G T missense_variant P480T 1438C>A ESAD-UK 8 11997502 11997502 single base substitution C T upstream_gene_variant ESAD-UK 8 11997902 11997902 single base substitution T A upstream_gene_variant ESAD-UK 8 11998868 11998868 single base substitution T G upstream_gene_variant ESAD-UK 8 11999143 11999143 single base substitution G C upstream_gene_variant ESAD-UK 8 11999881 11999881 single base substitution A C upstream_gene_variant ESAD-UK 8 12000161 12000161 deletion of <=200bp T - upstream_gene_variant ESCA-CN 8 11994435 11994435 single base substitution C T downstream_gene_variant ESCA-CN 8 11994458 11994458 single base substitution T G downstream_gene_variant GBM-US 8 11995987 11995987 single base substitution G A synonymous_variant L95L 283C>T KIRC-US 8 11995803 11995803 single base substitution C T missense_variant G156D 467G>A KIRC-US 8 11995987 11995987 single base substitution G A synonymous_variant L95L 283C>T LAML-KR 8 11991655 11991655 single base substitution G A downstream_gene_variant LAML-KR 8 11991962 11991962 single base substitution G T downstream_gene_variant LAML-KR 8 11995433 11995433 single base substitution G T synonymous_variant V279V 837C>A LAML-KR 8 11995439 11995439 single base substitution G A synonymous_variant I277I 831C>T LAML-KR 8 11996034 11996034 single base substitution C T missense_variant G79E 236G>A LAML-KR 8 11996715 11996715 single base substitution T G upstream_gene_variant LICA-FR 8 11995161 11995161 single base substitution A T missense_variant L370H 1109T>A LICA-FR 8 11995723 11995723 single base substitution C G missense_variant V183L 547G>C LICA-FR 8 11995733 11995733 single base substitution G C synonymous_variant G179G 537C>G LIHC-US 8 11995368 11995368 single base substitution A G missense_variant L301P 902T>C LINC-JP 8 11990315 11990315 single base substitution G T downstream_gene_variant LIRI-JP 8 11998471 11998471 single base substitution G A upstream_gene_variant LIRI-JP 8 11998970 11998970 single base substitution A G upstream_gene_variant LIRI-JP 8 11999597 11999597 single base substitution A G upstream_gene_variant LIRI-JP 8 12001326 12001326 single base substitution A G upstream_gene_variant LIRI-JP 8 12001343 12001343 single base substitution G A upstream_gene_variant LUSC-KR 8 11990047 11990047 single base substitution G A downstream_gene_variant LUSC-KR 8 11990882 11990882 single base substitution C T downstream_gene_variant LUSC-KR 8 11991037 11991037 single base substitution G C downstream_gene_variant LUSC-KR 8 11992510 11992510 single base substitution G A downstream_gene_variant LUSC-KR 8 11994957 11994957 single base substitution T C missense_variant K438R 1313A>G LUSC-KR 8 11995433 11995433 single base substitution G T synonymous_variant V279V 837C>A LUSC-KR 8 11995439 11995439 single base substitution G A synonymous_variant I277I 831C>T LUSC-KR 8 11995475 11995475 single base substitution C G missense_variant K265N 795G>C LUSC-KR 8 11995484 11995484 single base substitution C T synonymous_variant P262P 786G>A LUSC-KR 8 11995791 11995791 single base substitution T C missense_variant D160G 479A>G LUSC-KR 8 11996261 11996261 single base substitution G A synonymous_variant D3D 9C>T LUSC-KR 8 11997174 11997174 single base substitution G A upstream_gene_variant LUSC-KR 8 11997282 11997282 single base substitution A T upstream_gene_variant LUSC-KR 8 11997768 11997768 single base substitution C G upstream_gene_variant LUSC-KR 8 12000067 12000067 single base substitution C A upstream_gene_variant LUSC-US 8 11995031 11995031 single base substitution G C synonymous_variant P413P 1239C>G LUSC-US 8 11995293 11995293 single base substitution G A missense_variant A326V 977C>T LUSC-US 8 11995788 11995788 single base substitution G T missense_variant A161D 482C>A MALY-DE 8 11996690 11996691 deletion of <=200bp TG - upstream_gene_variant MELA-AU 8 11989804 11989804 single base substitution G A downstream_gene_variant MELA-AU 8 11989927 11989927 single base substitution C T downstream_gene_variant MELA-AU 8 11989957 11989957 single base substitution T C downstream_gene_variant MELA-AU 8 11989990 11989990 single base substitution C T downstream_gene_variant MELA-AU 8 11989997 11989997 single base substitution G A downstream_gene_variant MELA-AU 8 11990033 11990033 single base substitution C T downstream_gene_variant MELA-AU 8 11990078 11990078 single base substitution C T downstream_gene_variant MELA-AU 8 11990181 11990181 single base substitution C T downstream_gene_variant MELA-AU 8 11990208 11990208 single base substitution C T downstream_gene_variant MELA-AU 8 11990228 11990228 single base substitution C T downstream_gene_variant MELA-AU 8 11990229 11990229 single base substitution C T downstream_gene_variant MELA-AU 8 11990264 11990264 single base substitution C T downstream_gene_variant MELA-AU 8 11990270 11990270 single base substitution C T downstream_gene_variant MELA-AU 8 11991065 11991065 single base substitution C T downstream_gene_variant MELA-AU 8 11991377 11991378 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 8 11991515 11991515 single base substitution C T downstream_gene_variant MELA-AU 8 11991878 11991878 single base substitution T G downstream_gene_variant MELA-AU 8 11992882 11992882 single base substitution G A downstream_gene_variant MELA-AU 8 11992995 11992995 single base substitution C T downstream_gene_variant MELA-AU 8 11993147 11993147 single base substitution G A downstream_gene_variant MELA-AU 8 11993231 11993231 single base substitution C T downstream_gene_variant MELA-AU 8 11993381 11993381 single base substitution C T downstream_gene_variant MELA-AU 8 11993422 11993422 single base substitution G C downstream_gene_variant MELA-AU 8 11993759 11993759 single base substitution C T downstream_gene_variant MELA-AU 8 11994064 11994064 single base substitution C T downstream_gene_variant MELA-AU 8 11994087 11994087 single base substitution C T downstream_gene_variant MELA-AU 8 11994169 11994169 single base substitution G C downstream_gene_variant MELA-AU 8 11994257 11994257 single base substitution C T downstream_gene_variant MELA-AU 8 11994324 11994324 single base substitution C T downstream_gene_variant MELA-AU 8 11994467 11994467 single base substitution C T downstream_gene_variant MELA-AU 8 11994741 11994741 single base substitution C T missense_variant G510E 1529G>A MELA-AU 8 11994979 11994979 single base substitution C T missense_variant E431K 1291G>A MELA-AU 8 11995417 11995417 single base substitution C T missense_variant D285N 853G>A MELA-AU 8 11996013 11996013 single base substitution C T missense_variant G86E 257G>A MELA-AU 8 11996110 11996110 single base substitution C T missense_variant D54N 160G>A MELA-AU 8 11996422 11996422 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 8 11996717 11996717 single base substitution G T upstream_gene_variant MELA-AU 8 11997053 11997053 single base substitution G A upstream_gene_variant MELA-AU 8 11997054 11997054 single base substitution G A upstream_gene_variant MELA-AU 8 11997245 11997245 single base substitution C T upstream_gene_variant MELA-AU 8 11997279 11997279 single base substitution C T upstream_gene_variant MELA-AU 8 11997635 11997635 single base substitution C T upstream_gene_variant MELA-AU 8 11997726 11997726 single base substitution C A upstream_gene_variant MELA-AU 8 11997831 11997831 single base substitution G A upstream_gene_variant MELA-AU 8 11997914 11997914 single base substitution G A upstream_gene_variant MELA-AU 8 11998021 11998021 single base substitution G A upstream_gene_variant MELA-AU 8 11998109 11998109 single base substitution C T upstream_gene_variant MELA-AU 8 11998188 11998188 single base substitution G A upstream_gene_variant MELA-AU 8 11998503 11998503 single base substitution G T upstream_gene_variant MELA-AU 8 11998564 11998564 single base substitution T C upstream_gene_variant MELA-AU 8 11998587 11998587 single base substitution A G upstream_gene_variant MELA-AU 8 11998738 11998738 single base substitution C T upstream_gene_variant MELA-AU 8 11998797 11998797 single base substitution C T upstream_gene_variant MELA-AU 8 11999283 11999283 deletion of <=200bp T - upstream_gene_variant MELA-AU 8 11999390 11999390 single base substitution G A upstream_gene_variant MELA-AU 8 11999757 11999757 single base substitution C T upstream_gene_variant MELA-AU 8 12000018 12000018 single base substitution C T upstream_gene_variant MELA-AU 8 12000414 12000414 single base substitution C T upstream_gene_variant MELA-AU 8 12001151 12001151 single base substitution C T upstream_gene_variant MELA-AU 8 12001371 12001371 single base substitution T A upstream_gene_variant MELA-AU 8 12001538 12001538 single base substitution C T upstream_gene_variant OV-AU 8 11990838 11990838 single base substitution G T downstream_gene_variant OV-AU 8 11991035 11991035 single base substitution G A downstream_gene_variant OV-AU 8 11991968 11991968 single base substitution G T downstream_gene_variant OV-AU 8 11994599 11994599 single base substitution C T downstream_gene_variant PACA-AU 8 11989853 11989853 single base substitution G A downstream_gene_variant PACA-AU 8 11991172 11991172 single base substitution G A downstream_gene_variant PACA-AU 8 11994075 11994075 single base substitution G A downstream_gene_variant PACA-AU 8 11994355 11994355 single base substitution G A downstream_gene_variant PACA-CA 8 11992764 11992764 single base substitution C T downstream_gene_variant PACA-CA 8 11996683 11996683 insertion of <=200bp - TCTC upstream_gene_variant PACA-CA 8 12000160 12000160 insertion of <=200bp - T upstream_gene_variant PACA-CA 8 12000168 12000169 deletion of <=200bp TG - upstream_gene_variant PAEN-AU 8 11992795 11992795 single base substitution G A downstream_gene_variant PAEN-AU 8 11996713 11996713 single base substitution G T upstream_gene_variant PRAD-CA 8 11990314 11990314 single base substitution G C downstream_gene_variant PRAD-CA 8 11994111 11994111 single base substitution C T downstream_gene_variant PRAD-CA 8 11995041 11995041 single base substitution C A missense_variant R410I 1229G>T PRAD-CA 8 11996715 11996715 single base substitution T G upstream_gene_variant PRAD-CA 8 11997320 11997320 single base substitution A C upstream_gene_variant PRAD-UK 8 11990166 11990166 single base substitution G A downstream_gene_variant PRAD-US 8 11990647 11990647 insertion of <=200bp - GTTTGTT downstream_gene_variant PRAD-US 8 11994626 11994627 deletion of <=200bp GT - downstream_gene_variant READ-US 8 11994798 11994798 single base substitution G A missense_variant S491L 1472C>T RECA-EU 8 11989736 11989736 single base substitution C T downstream_gene_variant RECA-EU 8 11996788 11996788 single base substitution T C upstream_gene_variant RECA-EU 8 12001121 12001121 single base substitution A T upstream_gene_variant SKCA-BR 8 11990181 11990181 single base substitution C T downstream_gene_variant SKCA-BR 8 11990202 11990202 single base substitution G A downstream_gene_variant SKCA-BR 8 11991374 11991374 single base substitution A C downstream_gene_variant SKCA-BR 8 11991461 11991461 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 8 11991934 11991944 deletion of <=200bp CTGTGTGTGTG - downstream_gene_variant SKCA-BR 8 11991968 11991980 deletion of <=200bp GTGTGTGTGTGTT - downstream_gene_variant SKCA-BR 8 11993140 11993140 single base substitution G C downstream_gene_variant SKCA-BR 8 11993196 11993199 deletion of <=200bp GGAT - downstream_gene_variant SKCA-BR 8 11993204 11993204 single base substitution G T downstream_gene_variant SKCA-BR 8 11993348 11993348 single base substitution G A downstream_gene_variant SKCA-BR 8 11993433 11993433 single base substitution G A downstream_gene_variant SKCA-BR 8 11993450 11993450 single base substitution G A downstream_gene_variant SKCA-BR 8 11993463 11993463 single base substitution C T downstream_gene_variant SKCA-BR 8 11993572 11993572 insertion of <=200bp - GTT downstream_gene_variant SKCA-BR 8 11994435 11994435 single base substitution C T downstream_gene_variant SKCA-BR 8 11994669 11994669 single base substitution C T downstream_gene_variant SKCA-BR 8 11994904 11994904 single base substitution C T missense_variant E456K 1366G>A SKCA-BR 8 11995407 11995407 single base substitution C T missense_variant G288D 863G>A SKCA-BR 8 11995433 11995433 single base substitution G T synonymous_variant V279V 837C>A SKCA-BR 8 11995439 11995439 single base substitution G A synonymous_variant I277I 831C>T SKCA-BR 8 11995484 11995484 single base substitution C T synonymous_variant P262P 786G>A SKCA-BR 8 11995601 11995601 single base substitution G A synonymous_variant I223I 669C>T SKCA-BR 8 11995785 11995785 single base substitution T A missense_variant H162L 485A>T SKCA-BR 8 11996683 11996683 insertion of <=200bp - ATC upstream_gene_variant SKCA-BR 8 11997320 11997320 single base substitution A C upstream_gene_variant SKCA-BR 8 11997606 11997606 single base substitution C T upstream_gene_variant SKCA-BR 8 11997679 11997679 single base substitution C T upstream_gene_variant SKCA-BR 8 11997682 11997682 single base substitution C A upstream_gene_variant SKCA-BR 8 11997687 11997687 single base substitution A G upstream_gene_variant SKCA-BR 8 11998013 11998013 single base substitution C G upstream_gene_variant SKCA-BR 8 11998015 11998015 single base substitution A G upstream_gene_variant SKCA-BR 8 11998016 11998016 single base substitution T C upstream_gene_variant SKCA-BR 8 11999921 11999921 single base substitution C T upstream_gene_variant SKCA-BR 8 12000169 12000169 single base substitution G T upstream_gene_variant SKCA-BR 8 12000450 12000450 single base substitution C T upstream_gene_variant SKCA-BR 8 12001076 12001076 single base substitution A C upstream_gene_variant SKCM-US 8 11994678 11994678 single base substitution C T stop_retained_variant *531* 1592G>A SKCM-US 8 11994698 11994698 single base substitution C T synonymous_variant R524R 1572G>A SKCM-US 8 11994738 11994738 single base substitution C T missense_variant R511K 1532G>A SKCM-US 8 11994741 11994741 single base substitution C T missense_variant G510E 1529G>A SKCM-US 8 11994778 11994778 single base substitution C T missense_variant E498K 1492G>A SKCM-US 8 11994844 11994844 single base substitution T C missense_variant K476E 1426A>G SKCM-US 8 11994845 11994845 single base substitution C T missense_variant M475I 1425G>A SKCM-US 8 11994871 11994871 single base substitution G A missense_variant H467Y 1399C>T SKCM-US 8 11994895 11994895 single base substitution G A synonymous_variant L459L 1375C>T SKCM-US 8 11994955 11994955 single base substitution A G missense_variant F439L 1315T>C SKCM-US 8 11994959 11994959 single base substitution C T stop_gained W437* 1311G>A SKCM-US 8 11994994 11994994 single base substitution C T missense_variant E426K 1276G>A SKCM-US 8 11995065 11995065 single base substitution C G missense_variant R402P 1205G>C SKCM-US 8 11995072 11995072 single base substitution C T missense_variant D400N 1198G>A SKCM-US 8 11995102 11995102 single base substitution C T missense_variant E390K 1168G>A SKCM-US 8 11995136 11995136 single base substitution C T stop_gained W378* 1134G>A SKCM-US 8 11995223 11995223 single base substitution C T missense_variant M349I 1047G>A SKCM-US 8 11995285 11995285 single base substitution T A missense_variant S329C 985A>T SKCM-US 8 11995287 11995287 single base substitution C T stop_gained W328* 983G>A SKCM-US 8 11995291 11995291 single base substitution C T missense_variant G327R 979G>A SKCM-US 8 11995377 11995377 single base substitution G A missense_variant P298L 893C>T SKCM-US 8 11995636 11995636 single base substitution C T missense_variant G212R 634G>A SKCM-US 8 11995798 11995798 single base substitution G A stop_gained Q158* 472C>T SKCM-US 8 11996013 11996013 single base substitution C T missense_variant G86E 257G>A SKCM-US 8 11996035 11996035 single base substitution C T missense_variant G79R 235G>A SKCM-US 8 11996046 11996046 single base substitution G A missense_variant P75L 224C>T SKCM-US 8 11996051 11996051 single base substitution C T synonymous_variant R73R 219G>A SKCM-US 8 11996079 11996079 single base substitution G A missense_variant P64L 191C>T STAD-US 8 11994773 11994773 single base substitution G A synonymous_variant S499S 1497C>T STAD-US 8 11994792 11994792 single base substitution G T missense_variant T493N 1478C>A STAD-US 8 11994797 11994797 single base substitution C T synonymous_variant S491S 1473G>A STAD-US 8 11995092 11995092 single base substitution G A missense_variant A393V 1178C>T STAD-US 8 11995172 11995172 single base substitution C A missense_variant Q366H 1098G>T STAD-US 8 11995417 11995417 single base substitution C A missense_variant D285Y 853G>T STAD-US 8 11995964 11995964 single base substitution C T synonymous_variant P102P 306G>A STAD-US 8 11996191 11996191 single base substitution C T missense_variant A27T 79G>A THCA-SA 8 11994957 11994957 single base substitution T C missense_variant K438R 1313A>G THCA-SA 8 11995484 11995484 single base substitution C T synonymous_variant P262P 786G>A THCA-SA 8 11995823 11995823 single base substitution C T synonymous_variant L149L 447G>A UCEC-US 8 11989954 11989954 single base substitution C A downstream_gene_variant UCEC-US 8 11990137 11990137 single base substitution G A downstream_gene_variant UCEC-US 8 11990295 11990295 single base substitution G C downstream_gene_variant UCEC-US 8 11990849 11990849 single base substitution C T downstream_gene_variant UCEC-US 8 11990851 11990851 single base substitution A T downstream_gene_variant UCEC-US 8 11991178 11991178 single base substitution G A downstream_gene_variant UCEC-US 8 11995199 11995199 single base substitution A G synonymous_variant C357C 1071T>C UCEC-US 8 11995979 11995979 single base substitution G T stop_gained C97* 291C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-EE-A181-06 COSM3644600 c.1168G>A p.E390K Substitution - Missense 8:12137593-12137593 - CAL27 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - TCGA-BR-6458-01 COSM3896371 c.1497C>T p.S499S Substitution - coding silent 8:12137264-12137264 - TCGA-ER-A199-06 COSM3644599 c.1198G>A p.D400N Substitution - Missense 8:12137563-12137563 - PTC-77C COSM4162626 c.120G>C p.K40N Substitution - Missense 8:12138641-12138641 - TCGA-ER-A193-06 COSM3644610 c.235G>A p.G79R Substitution - Missense 8:12138526-12138526 - TCGA-C5-A3HE-01 COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - CAL27 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-GF-A6C8-06 COSM3924553 c.1572G>A p.R524R Substitution - coding silent 8:12137189-12137189 - PTC-7C COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - ESO-1488 COSM1270046 c.142C>T p.R48C Substitution - Missense 8:12138619-12138619 - PT27 COSM5905753 c.272A>T p.E91V Substitution - Missense 8:12138489-12138489 - LUAD-CHTN-3090415 COSM357421 c.219G>A p.R73R Substitution - coding silent 8:12138542-12138542 - I2L-P8-Tumor-Organoid COSM3165173 c.653A>T p.D218V Substitution - Missense 8:12138108-12138108 - SNUH_G10_S1 COSM3982369 c.183G>T p.Q61H Substitution - Missense 8:12138578-12138578 - 345973 COSM3726528 c.1388T>C p.V463A Substitution - Missense 8:12137373-12137373 - TCGA-EE-A2MJ-06 COSM3644593 c.1399C>T p.H467Y Substitution - Missense 8:12137362-12137362 - T228 COSM4739660 c.1556A>C p.N519T Substitution - Missense 8:12137205-12137205 - AML_14y_03_DX COSM5956918 c.831C>T p.I277I Substitution - coding silent 8:12137930-12137930 - SNUH_G45_S1 COSM3982368 c.786G>A p.P262P Substitution - coding silent 8:12137975-12137975 - TCGA-AA-3715-01 COSM270525 c.1522C>G p.L508V Substitution - Missense 8:12137239-12137239 - cSCCP7 COSM139748 c.1381C>T p.P461S Substitution - Missense 8:12137380-12137380 - TCGA-EE-A3AH-06 COSM3644591 c.1529G>A p.G510E Substitution - Missense 8:12137232-12137232 - TCGA-GN-A266-06 COSM3644603 c.985A>T p.S329C Substitution - Missense 8:12137776-12137776 - Pat_31_B COSM5873799 c.871C>A p.L291I Substitution - Missense 8:12137890-12137890 - TCGA-AA-3510-01 COSM1454487 c.1452C>T p.S484S Substitution - coding silent 8:12137309-12137309 - TCGA-EE-A20B-06 COSM3644609 c.257G>A p.G86E Substitution - Missense 8:12138504-12138504 - 93VU147T COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - SNUH_G45_S1 COSM3982370 c.9C>T p.D3D Substitution - coding silent 8:12138752-12138752 - CPCG0234-F1 COSM303528 c.1229G>T p.R410I Substitution - Missense 8:12137532-12137532 - UM-SCC-17B COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - TCGA-EB-A431-01 COSM357421 c.219G>A p.R73R Substitution - coding silent 8:12138542-12138542 - PTC-515C COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-FU-A40J-01 COSM4843957 c.849C>G p.F283L Substitution - Missense 8:12137912-12137912 - TCGA-D9-A6EC-06 COSM4402896 c.1426A>G p.K476E Substitution - Missense 8:12137335-12137335 - 93VU147T COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-22-4595-01 COSM748496 c.482C>A p.A161D Substitution - Missense 8:12138279-12138279 - TCGA-RP-A695-06 COSM4896213 c.1592G>A p.*531* Substitution - coding silent 8:12137169-12137169 - Detroit_562 COSM3982368 c.786G>A p.P262P Substitution - coding silent 8:12137975-12137975 - B105-1-Tumor COSM4006825 c.945T>C p.L315L Substitution - coding silent 8:12137816-12137816 - TCGA-B0-4837-01 COSM109807 c.283C>T p.L95L Substitution - coding silent 8:12138478-12138478 - HN_62854 COSM130109 c.1288C>G p.Q430E Substitution - Missense 8:12137473-12137473 - GC7_T COSM150453 c.1208C>T p.A403V Substitution - Missense 8:12137553-12137553 - WSU-HN6 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-EE-A2A2-06 COSM3644602 c.1047G>A p.M349I Substitution - Missense 8:12137714-12137714 - TCGA-EE-A2A2-06 COSM3644608 c.472C>T p.Q158* Substitution - Nonsense 8:12138289-12138289 - TCGA-DA-A1I4-06 COSM3644611 c.224C>T p.P75L Substitution - Missense 8:12138537-12138537 - NOKSI COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - TCGA-EB-A44O-01 COSM3644596 c.1311G>A p.W437* Substitution - Nonsense 8:12137450-12137450 - UM-SCC-47 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - ESO-717 COSM1242986 c.1372A>G p.T458A Substitution - Missense 8:12137389-12137389 - TCGA-JW-A5VL-01 COSM4847932 c.421C>T p.H141Y Substitution - Missense 8:12138340-12138340 - TCGA-A6-3808-01 COSM291365 c.1406C>A p.S469* Substitution - Nonsense 8:12137355-12137355 - TCGA-AM-5821-01 COSM3763014 c.1022C>T p.A341V Substitution - Missense 8:12137739-12137739 - TCGA-AP-A056-01 COSM1095421 c.291C>A p.C97* Substitution - Nonsense 8:12138470-12138470 - SNUH_G73_S1 COSM4415128 c.1313A>G p.K438R Substitution - Missense 8:12137448-12137448 - TCGA-D3-A2JO-06 COSM3644594 c.1375C>T p.L459L Substitution - coding silent 8:12137386-12137386 - TCGA-EE-A2MU-06 COSM3644609 c.257G>A p.G86E Substitution - Missense 8:12138504-12138504 - TCGA-66-2792-01 COSM748498 c.1239C>G p.P413P Substitution - coding silent 8:12137522-12137522 - TCGA-AP-A0LM-01 COSM1095420 c.1071T>C p.C357C Substitution - coding silent 8:12137690-12137690 - CSCC-10-T COSM139748 c.1381C>T p.P461S Substitution - Missense 8:12137380-12137380 - TCGA-AA-A010-01 COSM299609 c.797C>T p.T266M Substitution - Missense 8:12137964-12137964 - LP6007594 COSM5034456 c.1481G>A p.R494Q Substitution - Missense 8:12137280-12137280 - UPCI:SCC090 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-FS-A4F5-06 COSM3644601 c.1134G>A p.W378* Substitution - Nonsense 8:12137627-12137627 - TCGA-GV-A3QH-01 COSM1313667 c.411C>T p.H137H Substitution - coding silent 8:12138350-12138350 - PT35 COSM3644609 c.257G>A p.G86E Substitution - Missense 8:12138504-12138504 - UPCI:SCC090 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - TCGA-E2-A2P6-01 COSM3833932 c.1110C>G p.L370L Substitution - coding silent 8:12137651-12137651 - TCGA-FW-A3R5-06 COSM3924554 c.1425G>A p.M475I Substitution - Missense 8:12137336-12137336 - T263 COSM4739663 c.214A>G p.S72G Substitution - Missense 8:12138547-12138547 - UM-SCC-17B COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - EGC15 COSM5062853 c.325C>T p.L109L Substitution - coding silent 8:12138436-12138436 - PTC-14C COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - AML_14y_03_DX COSM5956917 c.837C>A p.V279V Substitution - coding silent 8:12137924-12137924 - WSU-HN6 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - A673 COSM3165138 c.1575T>A p.A525A Substitution - coding silent 8:12137186-12137186 - UM-SCC-11B COSM4598027 c.249G>C p.Q83H Substitution - Missense 8:12138512-12138512 - Pat_28_B COSM3644599 c.1198G>A p.D400N Substitution - Missense 8:12137563-12137563 - TCGA-AA-A01K-01 COSM299998 c.1251A>C p.A417A Substitution - coding silent 8:12137510-12137510 - LUAD-NYU847 COSM376920 c.892C>G p.P298A Substitution - Missense 8:12137869-12137869 - 10-P4110 COSM4587751 c.338A>T p.H113L Substitution - Missense 8:12138423-12138423 - TCGA-F5-6814-01 COSM3165141 c.1472C>T p.S491L Substitution - Missense 8:12137289-12137289 - T3336 COSM1095421 c.291C>A p.C97* Substitution - Nonsense 8:12138470-12138470 - Patient_1 COSM5044579 c.600C>A p.C200* Substitution - Nonsense 8:12138161-12138161 - PTC-515C COSM4162626 c.120G>C p.K40N Substitution - Missense 8:12138641-12138641 - SNUH_G43_S1 COSM3685305 c.1122G>C p.Q374H Substitution - Missense 8:12137639-12137639 - Pat_06_B COSM5873798 c.1358G>A p.R453K Substitution - Missense 8:12137403-12137403 - TCGA-DM-A1D4-01 COSM115890 c.994G>A p.D332N Substitution - Missense 8:12137767-12137767 - 14_T COSM3951231 c.763G>T p.G255C Substitution - Missense 8:12137998-12137998 - SNUH_G15_S1 COSM3685306 c.30T>G p.G10G Substitution - coding silent 8:12138731-12138731 - MD-088 COSM303528 c.1229G>T p.R410I Substitution - Missense 8:12137532-12137532 - TCGA-BR-4361-01 COSM3165167 c.853G>T p.D285Y Substitution - Missense 8:12137908-12137908 - TCGA-DK-A2HX-01 COSM1313668 c.198G>A p.K66K Substitution - coding silent 8:12138563-12138563 - PDA_004 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - C004 COSM5521963 c.343C>T p.Q115* Substitution - Nonsense 8:12138418-12138418 - PT49 COSM3644597 c.1276G>A p.E426K Substitution - Missense 8:12137485-12137485 - CHEWS012 COSM4587750 c.1520C>A p.S507Y Substitution - Missense 8:12137241-12137241 - SNUH_G73_S1 COSM3982368 c.786G>A p.P262P Substitution - coding silent 8:12137975-12137975 - TCGA-BR-4184-01 COSM3896376 c.79G>A p.A27T Substitution - Missense 8:12138682-12138682 - TCGA-12-0821-01 COSM109807 c.283C>T p.L95L Substitution - coding silent 8:12138478-12138478 - LN18 COSM3165144 c.1399C>A p.H467N Substitution - Missense 8:12137362-12137362 - HCC06T COSM131384 c.670G>A p.A224T Substitution - Missense 8:12138091-12138091 - TCGA-AG-A014-01 COSM290085 c.1080T>C p.T360T Substitution - coding silent 8:12137681-12137681 - TCGA-D7-5578-01 COSM3896372 c.1478C>A p.T493N Substitution - Missense 8:12137283-12137283 - ESO-169 COSM1270047 c.783G>A p.A261A Substitution - coding silent 8:12137978-12137978 - TCGA-AA-3975-01 COSM297492 c.134C>G p.S45C Substitution - Missense 8:12138627-12138627 - UM-SCC-2 COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - 2292383 COSM3763014 c.1022C>T p.A341V Substitution - Missense 8:12137739-12137739 - T2621 COSM4739662 c.226G>A p.A76T Substitution - Missense 8:12138535-12138535 - QC2-26-T2 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-AA-A010-01 COSM286382 c.336G>T p.E112D Substitution - Missense 8:12138425-12138425 - TCGA-BP-4972-01 COSM486004 c.467G>A p.G156D Substitution - Missense 8:12138294-12138294 - TCGA-AC-A3TN-01 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - 24T COSM109807 c.283C>T p.L95L Substitution - coding silent 8:12138478-12138478 - AML_14y_03_DX COSM1664907 c.236G>A p.G79E Substitution - Missense 8:12138525-12138525 - TCGA-D3-A2JF-06 COSM3644597 c.1276G>A p.E426K Substitution - Missense 8:12137485-12137485 - TCGA-EE-A29M-06 COSM3644605 c.979G>A p.G327R Substitution - Missense 8:12137782-12137782 - TCGA-BR-8680-01 COSM3896373 c.1473G>A p.S491S Substitution - coding silent 8:12137288-12137288 - PDA_053 COSM5000819 c.809A>C p.H270P Substitution - Missense 8:12137952-12137952 - Detroit_562 COSM4006824 c.996C>T p.D332D Substitution - coding silent 8:12137765-12137765 - Pat_41_B COSM5873797 c.1454C>T p.S485F Substitution - Missense 8:12137307-12137307 - TCGA-BR-8591-01 COSM3896375 c.1098G>T p.Q366H Substitution - Missense 8:12137663-12137663 - ESO-859 COSM1240617 c.434C>A p.P145H Substitution - Missense 8:12138327-12138327 - LN229 COSM3165162 c.948C>T p.V316V Substitution - coding silent 8:12137813-12137813 - T3724 COSM4739661 c.968T>C p.L323P Substitution - Missense 8:12137793-12137793 - PT41 COSM3644609 c.257G>A p.G86E Substitution - Missense 8:12138504-12138504 - TCGA-FS-A1ZD-06 COSM3644612 c.191C>T p.P64L Substitution - Missense 8:12138570-12138570 - UM-SCC-47 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - TCGA-GN-A266-06 COSM3644604 c.983G>A p.W328* Substitution - Nonsense 8:12137778-12137778 - TCGA-AG-A002-01 COSM289806 c.493C>A p.L165I Substitution - Missense 8:12138268-12138268 - Pat_14_B COSM5873801 c.101G>A p.R34Q Substitution - Missense 8:12138660-12138660 - WSU-HN13 COSM3833933 c.184C>T p.L62F Substitution - Missense 8:12138577-12138577 - TCGA-AA-A02W-01 COSM301009 c.1384A>G p.N462D Substitution - Missense 8:12137377-12137377 - 12T COSM108838 c.475G>A p.E159K Substitution - Missense 8:12138286-12138286 - HN07PT COSM97884 c.112C>T p.P38S Substitution - Missense 8:12138649-12138649 - TCGA-AD-6895-01 COSM1454488 c.1353C>T p.N451N Substitution - coding silent 8:12137408-12137408 - LUAD-S01315 COSM346037 c.1181T>A p.L394H Substitution - Missense 8:12137580-12137580 - TCGA-D3-A1Q6-06 COSM3644606 c.893C>T p.P298L Substitution - Missense 8:12137868-12137868 - B63-Tumor COSM4006823 c.1104T>C p.Y368Y Substitution - coding silent 8:12137657-12137657 - TCGA-EE-A2GI-06 COSM3644592 c.1492G>A p.E498K Substitution - Missense 8:12137269-12137269 - T3724 COSM3165188 c.306G>A p.P102P Substitution - coding silent 8:12138455-12138455 - TCGA-EE-A2MR-06 COSM3644609 c.257G>A p.G86E Substitution - Missense 8:12138504-12138504 - TCGA-D3-A2JF-06 COSM3644595 c.1315T>C p.F439L Substitution - Missense 8:12137446-12137446 - ccRCC-37 COSM1664907 c.236G>A p.G79E Substitution - Missense 8:12138525-12138525 - Pat_46_A COSM5873800 c.464G>A p.R155K Substitution - Missense 8:12138297-12138297 - 2521244 COSM4598027 c.249G>C p.Q83H Substitution - Missense 8:12138512-12138512 - STC232 COSM5062852 c.975C>T p.H325H Substitution - coding silent 8:12137786-12137786 - TCGA-25-2042-01 COSM115890 c.994G>A p.D332N Substitution - Missense 8:12137767-12137767 - SNUH_G73_S1 COSM3982370 c.9C>T p.D3D Substitution - coding silent 8:12138752-12138752 - B80-0-Tumor COSM4006825 c.945T>C p.L315L Substitution - coding silent 8:12137816-12137816 - WSU-HN13 COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - S02274 COSM5682599 c.1245C>G p.L415L Substitution - coding silent 8:12137516-12137516 - S00946 COSM310752 c.1185C>A p.G395G Substitution - coding silent 8:12137576-12137576 - WSU-HN13 COSM4162625 c.485A>T p.H162L Substitution - Missense 8:12138276-12138276 - TCGA-66-2770-01 COSM748497 c.977C>T p.A326V Substitution - Missense 8:12137784-12137784 - TCGA-BR-6852-01 COSM3165188 c.306G>A p.P102P Substitution - coding silent 8:12138455-12138455 - XHDG17 COSM4768667 c.1262A>T p.D421V Substitution - Missense 8:12137499-12137499 - 93VU147T COSM4162624 c.730G>A p.E244K Substitution - Missense 8:12138031-12138031 - B19-Tumor COSM4006824 c.996C>T p.D332D Substitution - coding silent 8:12137765-12137765 - CSCC-32-T COSM4466441 c.1435C>T p.H479Y Substitution - Missense 8:12137326-12137326 - PTC-515C COSM150453 c.1208C>T p.A403V Substitution - Missense 8:12137553-12137553 - TCGA-FS-A4F9-06 COSM3644607 c.634G>A p.G212R Substitution - Missense 8:12138127-12138127 - CSCC-35-T COSM4522864 c.1183G>A p.G395S Substitution - Missense 8:12137578-12137578 - T3724 COSM3165141 c.1472C>T p.S491L Substitution - Missense 8:12137289-12137289 - TCGA-DD-A4NI-01 COSM4926182 c.902T>C p.L301P Substitution - Missense 8:12137859-12137859 - TCGA-JW-A5VL-01 COSM4847566 c.31G>C p.E11Q Substitution - Missense 8:12138730-12138730 - TCGA-D3-A3CB-06 COSM3644598 c.1205G>C p.R402P Substitution - Missense 8:12137556-12137556 - pfg025T COSM1643486 c.6G>A p.E2E Substitution - coding silent 8:12138755-12138755 - TCGA-EB-A44O-01 COSM3644590 c.1532G>A p.R511K Substitution - Missense 8:12137229-12137229 - TCGA-CG-5721-01 COSM3896374 c.1178C>T p.A393V Substitution - Missense 8:12137583-12137583 - CSCC-20-T COSM4462532 c.1250C>T p.A417V Substitution - Missense 8:12137511-12137511 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.531432;Hs.531433;Hs.531437;Hs.531448 8p23.1 610186

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.F439L c.1315T>C 8 11994955 CM A G Synonymous p.T360T c.1080T>C 8 11995190 COREAD A T Missense p.S264T c.790T>A 8 11995480 LUAD C A Missense p.A525S c.1573G>T 8 11994697 HNSC C G Missense p.K293N c.879G>C 8 11995391 LUAD C G Missense p.R402P c.1205G>C 8 11995065 CM C T Missense p.A341T c.1021G>A 8 11995249 PRAD C T Missense p.D400N c.1198G>A 8 11995072 CM C T Missense p.E159K c.475G>A 8 11995795 CM C T Missense p.E390K c.1168G>A 8 11995102 CM C T Missense p.E426K c.1276G>A 8 11994994 CM C T Missense p.E498K c.1492G>A 8 11994778 CM C T Missense p.G156D c.467G>A 8 11995803 RCCC C T Missense p.G327R c.979G>A 8 11995291 CM C T Missense p.G510E c.1529G>A 8 11994741 CM C T Missense p.G79R c.235G>A 8 11996035 CM C T Missense p.G86E c.257G>A 8 11996013 CM C T Missense p.M349I c.1047G>A 8 11995223 CM C T Missense p.M475I c.1425G>A 8 11994845 CM C T Synonymous p.E2E c.6G>A 8 11996264 STAD C T Synonymous p.G81G c.243G>A 8 11996027 THCA C T Synonymous p.K66K c.198G>A 8 11996072 BLCA C T Synonymous p.L280L c.840G>A 8 11995430 CM G A Missense p.A326V c.977C>T 8 11995293 LUSC G A Missense p.H467Y c.1399C>T 8 11994871 CM G A Missense p.P145L c.434C>T 8 11995836 HNSC G A Missense p.P298L c.893C>T 8 11995377 CM G A Missense p.P64L c.191C>T 8 11996079 CM G A Missense p.P75L c.224C>T 8 11996046 CM G A Missense p.P75L c.224C>T 8 11996046 HNSC G A Missense p.R48C c.142C>T 8 11996128 ESCA G A Missense p.S361F c.1082C>T 8 11995188 CM G A Nonsense p.Q158* c.472C>T 8 11995798 CM G A Synonymous p.H137H c.411C>T 8 11995859 BLCA G A Synonymous p.L459L c.1375C>T 8 11994895 CM G A Synonymous p.L489L c.1467C>T 8 11994803 CM G A Synonymous p.L95L c.283C>T 8 11995987 GBM G A Synonymous p.L95L c.283C>T 8 11995987 RCCC G A Synonymous p.S499S c.1497C>T 8 11994773 STAD G C Missense p.Q430E c.1288C>G 8 11994982 HNSC G C Missense p.S45C c.134C>G 8 11996136 COREAD G C Synonymous p.P413P c.1239C>G 8 11995031 LUSC G T Missense p.A161D c.482C>A 8 11995788 LUSC G T Missense p.P145H c.434C>A 8 11995836 LUAD G T Missense p.P413H c.1238C>A 8 11995032 STAD G T Missense p.Q33K c.97C>A 8 11996173 HNSC G T Missense p.T493N c.1478C>A 8 11994792 STAD G T Nonsense p.S469* c.1406C>A 8 11994864 COREAD G T Synonymous p.G395G c.1185C>A 8 11995085 SCLC G T Synonymous p.T512T c.1536C>A 8 11994734 LUAD T C Missense p.K353E c.1057A>G 8 11995213 THCA T C Missense p.N462D c.1384A>G 8 11994886 COREAD T G Synonymous p.A417A c.1251A>C 8 11995019 COREAD