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 9 36170340 36170340 + Missense_Mutation SNP G G A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr9:36170340G>A c.841G>A c.(841-843)Gtg>Atg p.V281M ACC 9 36170452 36170452 + Missense_Mutation SNP C C A TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr9:36170452C>A c.953C>A c.(952-954)gCa>gAa p.A318E ACC 9 36170696 36170696 + Silent SNP G G C TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr9:36170696G>C c.1197G>C c.(1195-1197)cgG>cgC p.R399R ACC 9 36170829 36170829 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr9:36170829G>T c.1330G>T c.(1330-1332)Gta>Tta p.V444L BLCA 9 36170156 36170156 + Missense_Mutation SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr9:36170156C>G c.657C>G c.(655-657)ttC>ttG p.F219L BLCA 9 36170177 36170177 + Missense_Mutation SNP T T A TCGA-KQ-A41N-01A-11D-A339-08 TCGA-KQ-A41N-10D-01D-A339-08 g.chr9:36170177T>A c.678T>A c.(676-678)aaT>aaA p.N226K BLCA 9 36170285 36170285 + Silent SNP G G A TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr9:36170285G>A c.786G>A c.(784-786)caG>caA p.Q262Q BLCA 9 36170617 36170617 + Missense_Mutation SNP G G C TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr9:36170617G>C c.1118G>C c.(1117-1119)tGt>tCt p.C373S BLCA 9 36170642 36170642 + Silent SNP C C T TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chr9:36170642C>T c.1143C>T c.(1141-1143)ggC>ggT p.G381G BLCA 9 36170889 36170889 + Missense_Mutation SNP G G C TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr9:36170889G>C c.1390G>C c.(1390-1392)Gag>Cag p.E464Q BRCA 9 36169514 36169514 + Missense_Mutation SNP C C A TCGA-E2-A10F-01A-11D-A10M-09 TCGA-E2-A10F-10A-01D-A10M-09 g.chr9:36169514C>A c.15C>A c.(13-15)ttC>ttA p.F5L BRCA 9 36169591 36169591 + Missense_Mutation SNP C C T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr9:36169591C>T c.92C>T c.(91-93)gCc>gTc p.A31V BRCA 9 36169863 36169863 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr9:36169863G>A c.364G>A c.(364-366)Gac>Aac p.D122N BRCA 9 36170027 36170027 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr9:36170027A>C c.528A>C c.(526-528)ccA>ccC p.P176P BRCA 9 36170435 36170435 + Missense_Mutation SNP C C A TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr9:36170435C>A c.936C>A c.(934-936)gaC>gaA p.D312E BRCA 9 36170527 36170527 + Missense_Mutation SNP A A G TCGA-A8-A09I-01A-22W-A050-09 TCGA-A8-A09I-10A-01W-A055-09 g.chr9:36170527A>G c.1028A>G c.(1027-1029)aAg>aGg p.K343R BRCA 9 36170592 36170592 + Missense_Mutation SNP C C T TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr9:36170592C>T c.1093C>T c.(1093-1095)Ctt>Ttt p.L365F CESC 9 36170051 36170051 + Silent SNP C C G TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr9:36170051C>G c.552C>G c.(550-552)ctC>ctG p.L184L COAD 9 36169589 36169589 + Missense_Mutation SNP G G A TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr9:36169589G>A c.90G>A c.(88-90)atG>atA p.M30I COAD 9 36169849 36169849 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:36169849G>A c.350G>A c.(349-351)cGa>cAa p.R117Q COAD 9 36169902 36169902 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:36169902C>T c.403C>T c.(403-405)Cgc>Tgc p.R135C COAD 9 36169968 36169968 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:36169968C>T c.469C>T c.(469-471)Cgg>Tgg p.R157W COAD 9 36170096 36170096 + Silent SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr9:36170096C>T c.597C>T c.(595-597)agC>agT p.S199S COAD 9 36170133 36170133 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr9:36170133C>T c.634C>T c.(634-636)Cgg>Tgg p.R212W COAD 9 36170694 36170694 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:36170694C>T c.1195C>T c.(1195-1197)Cgg>Tgg p.R399W COAD 9 36171259 36171259 + Missense_Mutation SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:36171259G>T c.1760G>T c.(1759-1761)aGg>aTg p.R587M COADREAD 9 36169589 36169589 + Missense_Mutation SNP G G A TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr9:36169589G>A c.90G>A c.(88-90)atG>atA p.M30I COADREAD 9 36169700 36169700 + Missense_Mutation SNP G G T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:36169700G>T c.201G>T c.(199-201)gaG>gaT p.E67D COADREAD 9 36169849 36169849 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:36169849G>A c.350G>A c.(349-351)cGa>cAa p.R117Q COADREAD 9 36169902 36169902 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:36169902C>T c.403C>T c.(403-405)Cgc>Tgc p.R135C COADREAD 9 36169968 36169968 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:36169968C>T c.469C>T c.(469-471)Cgg>Tgg p.R157W COADREAD 9 36170096 36170096 + Silent SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr9:36170096C>T c.597C>T c.(595-597)agC>agT p.S199S COADREAD 9 36170133 36170133 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr9:36170133C>T c.634C>T c.(634-636)Cgg>Tgg p.R212W COADREAD 9 36170694 36170694 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:36170694C>T c.1195C>T c.(1195-1197)Cgg>Tgg p.R399W COADREAD 9 36171259 36171259 + Missense_Mutation SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:36171259G>T c.1760G>T c.(1759-1761)aGg>aTg p.R587M ESCA 9 36169562 36169562 + Missense_Mutation SNP G G T TCGA-L5-A8NQ-01A-11D-A36J-09 TCGA-L5-A8NQ-11A-11D-A36M-09 g.chr9:36169562G>T c.63G>T c.(61-63)caG>caT p.Q21H ESCA 9 36169685 36169685 + Missense_Mutation SNP G G T TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr9:36169685G>T c.186G>T c.(184-186)atG>atT p.M62I ESCA 9 36170618 36170619 + Frame_Shift_Ins INS - - G TCGA-L5-A4ON-01A-11D-A27G-09 TCGA-L5-A4ON-11A-21D-A27G-09 g.chr9:36170618_36170619insG c.1119_1120insG c.(1120-1122)gggfs p.G374fs ESCA 9 36170954 36170954 + Silent SNP G G A TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr9:36170954G>A c.1455G>A c.(1453-1455)cgG>cgA p.R485R GBM 9 36169599 36169599 + Missense_Mutation SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:36169599G>A c.100G>A c.(100-102)Gtg>Atg p.V34M GBM 9 36170861 36170861 + Silent SNP C C T TCGA-12-5301-01A-01D-1486-08 TCGA-12-5301-10A-01D-1486-08 g.chr9:36170861C>T c.1362C>T c.(1360-1362)gaC>gaT p.D454D GBMLGG 9 36169599 36169599 + Missense_Mutation SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:36169599G>A c.100G>A c.(100-102)Gtg>Atg p.V34M GBMLGG 9 36170045 36170045 + Silent SNP C C A TCGA-DB-A4XF-01A-11D-A27K-08 TCGA-DB-A4XF-10A-01D-A27N-08 g.chr9:36170045C>A c.546C>A c.(544-546)cgC>cgA p.R182R GBMLGG 9 36170121 36170121 + Missense_Mutation SNP C C T TCGA-FG-8186-01A-11D-2253-08 TCGA-FG-8186-10A-01D-2253-08 g.chr9:36170121C>T c.622C>T c.(622-624)Cgg>Tgg p.R208W GBMLGG 9 36170642 36170642 + Silent SNP C C T TCGA-QH-A6X5-01A-12D-A32B-08 TCGA-QH-A6X5-10B-01D-A329-08 g.chr9:36170642C>T c.1143C>T c.(1141-1143)ggC>ggT p.G381G GBMLGG 9 36170732 36170732 + Frame_Shift_Del DEL C C - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr9:36170732delC c.1233delC c.(1231-1233)atcfs p.I411fs GBMLGG 9 36170748 36170748 + Missense_Mutation SNP G G A TCGA-DU-6408-01A-11D-1705-08 TCGA-DU-6408-10A-01D-1705-08 g.chr9:36170748G>A c.1249G>A c.(1249-1251)Gcc>Acc p.A417T GBMLGG 9 36170861 36170861 + Silent SNP C C T TCGA-12-5301-01A-01D-1486-08 TCGA-12-5301-10A-01D-1486-08 g.chr9:36170861C>T c.1362C>T c.(1360-1362)gaC>gaT p.D454D HNSC 9 36169709 36169709 + Silent SNP C C T TCGA-CV-7406-01A-11D-2078-08 TCGA-CV-7406-10A-01D-2078-08 g.chr9:36169709C>T c.210C>T c.(208-210)atC>atT p.I70I HNSC 9 36169867 36169867 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr9:36169867T>C c.368T>C c.(367-369)tTc>tCc p.F123S HNSC 9 36170445 36170445 + Missense_Mutation SNP C C T TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr9:36170445C>T c.946C>T c.(946-948)Cgg>Tgg p.R316W HNSC 9 36170588 36170588 + Silent SNP C C T TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr9:36170588C>T c.1089C>T c.(1087-1089)atC>atT p.I363I HNSC 9 36170744 36170744 + Silent SNP C C T TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr9:36170744C>T c.1245C>T c.(1243-1245)ggC>ggT p.G415G KIPAN 9 36169599 36169599 + Missense_Mutation SNP G G A TCGA-B9-5155-01A-01D-1589-08 TCGA-B9-5155-10A-01D-1589-08 g.chr9:36169599G>A c.100G>A c.(100-102)Gtg>Atg p.V34M KIPAN 9 36170395 36170395 + Missense_Mutation SNP C C T TCGA-A4-7915-01A-11D-2201-08 TCGA-A4-7915-10A-01D-2201-08 g.chr9:36170395C>T c.896C>T c.(895-897)gCt>gTt p.A299V KIRP 9 36169599 36169599 + Missense_Mutation SNP G G A TCGA-B9-5155-01A-01D-1589-08 TCGA-B9-5155-10A-01D-1589-08 g.chr9:36169599G>A c.100G>A c.(100-102)Gtg>Atg p.V34M KIRP 9 36170395 36170395 + Missense_Mutation SNP C C T TCGA-A4-7915-01A-11D-2201-08 TCGA-A4-7915-10A-01D-2201-08 g.chr9:36170395C>T c.896C>T c.(895-897)gCt>gTt p.A299V LGG 9 36170045 36170045 + Silent SNP C C A TCGA-DB-A4XF-01A-11D-A27K-08 TCGA-DB-A4XF-10A-01D-A27N-08 g.chr9:36170045C>A c.546C>A c.(544-546)cgC>cgA p.R182R LGG 9 36170121 36170121 + Missense_Mutation SNP C C T TCGA-FG-8186-01A-11D-2253-08 TCGA-FG-8186-10A-01D-2253-08 g.chr9:36170121C>T c.622C>T c.(622-624)Cgg>Tgg p.R208W LGG 9 36170642 36170642 + Silent SNP C C T TCGA-QH-A6X5-01A-12D-A32B-08 TCGA-QH-A6X5-10B-01D-A329-08 g.chr9:36170642C>T c.1143C>T c.(1141-1143)ggC>ggT p.G381G LGG 9 36170732 36170732 + Frame_Shift_Del DEL C C - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr9:36170732delC c.1233delC c.(1231-1233)atcfs p.I411fs LGG 9 36170748 36170748 + Missense_Mutation SNP G G A TCGA-DU-6408-01A-11D-1705-08 TCGA-DU-6408-10A-01D-1705-08 g.chr9:36170748G>A c.1249G>A c.(1249-1251)Gcc>Acc p.A417T LIHC 9 36169649 36169649 + Silent SNP C C A TCGA-DD-AADR-01A-11D-A40R-10 TCGA-DD-AADR-10A-01D-A40U-10 g.chr9:36169649C>A c.150C>A c.(148-150)tcC>tcA p.S50S LIHC 9 36169807 36169807 + Missense_Mutation SNP A A T TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr9:36169807A>T c.308A>T c.(307-309)gAg>gTg p.E103V LIHC 9 36170372 36170372 + Silent SNP C C T TCGA-DD-AACO-01A-11D-A40R-10 TCGA-DD-AACO-10A-01D-A40U-10 g.chr9:36170372C>T c.873C>T c.(871-873)ggC>ggT p.G291G LIHC 9 36170794 36170794 + Missense_Mutation SNP G G T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr9:36170794G>T c.1295G>T c.(1294-1296)cGg>cTg p.R432L LUAD 9 36169749 36169749 + Missense_Mutation SNP C C A TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr9:36169749C>A c.250C>A c.(250-252)Cag>Aag p.Q84K LUAD 9 36169749 36169749 + Nonsense_Mutation SNP C C T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr9:36169749C>T c.250C>T c.(250-252)Cag>Tag p.Q84* LUAD 9 36170205 36170205 + Missense_Mutation SNP G G T TCGA-05-4430-01A-02D-1265-08 TCGA-05-4430-10A-01D-1265-08 g.chr9:36170205G>T c.706G>T c.(706-708)Gcc>Tcc p.A236S LUAD 9 36170263 36170263 + Missense_Mutation SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr9:36170263G>T c.764G>T c.(763-765)aGt>aTt p.S255I LUAD 9 36170277 36170277 + Missense_Mutation SNP C C T TCGA-44-A47G-01A-21D-A24D-08 TCGA-44-A47G-10A-01D-A24F-08 g.chr9:36170277C>T c.778C>T c.(778-780)Cgc>Tgc p.R260C LUAD 9 36170349 36170349 + Missense_Mutation SNP C C T TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chr9:36170349C>T c.850C>T c.(850-852)Ctc>Ttc p.L284F LUAD 9 36170358 36170358 + Missense_Mutation SNP C C A TCGA-55-8514-01A-11D-2393-08 TCGA-55-8514-10A-01D-2393-08 g.chr9:36170358C>A c.859C>A c.(859-861)Cag>Aag p.Q287K LUAD 9 36170550 36170550 + Missense_Mutation SNP G G T TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr9:36170550G>T c.1051G>T c.(1051-1053)Gat>Tat p.D351Y LUAD 9 36170694 36170694 + Missense_Mutation SNP C C G TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr9:36170694C>G c.1195C>G c.(1195-1197)Cgg>Ggg p.R399G LUAD 9 36170865 36170865 + Missense_Mutation SNP G G T TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr9:36170865G>T c.1366G>T c.(1366-1368)Gtc>Ttc p.V456F LUAD 9 36171016 36171016 + Missense_Mutation SNP T T C TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr9:36171016T>C c.1517T>C c.(1516-1518)gTc>gCc p.V506A LUAD 9 36171041 36171042 + Frame_Shift_Del DEL TG TG - TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr9:36171041_36171042delTG c.1542_1543delTG c.(1540-1545)gatgtgfs p.V515fs LUSC 9 36169849 36169849 + Missense_Mutation SNP G G T TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr9:36169849G>T c.350G>T c.(349-351)cGa>cTa p.R117L LUSC 9 36170237 36170237 + Silent SNP C C A TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr9:36170237C>A c.738C>A c.(736-738)acC>acA p.T246T OV 9 36169916 36169916 + Missense_Mutation SNP G G T TCGA-24-1847-01A-01W-0633-09 TCGA-24-1847-10A-01W-0634-09 g.chr9:36169916G>T c.417G>T c.(415-417)ttG>ttT p.L139F OV 9 36170089 36170089 + Missense_Mutation SNP C C T TCGA-29-1778-01A-01W-0639-09 TCGA-29-1778-10A-01W-0639-09 g.chr9:36170089C>T c.590C>T c.(589-591)gCg>gTg p.A197V OV 9 36170503 36170503 + Missense_Mutation SNP C C A TCGA-59-2354-01A-01W-0799-08 TCGA-59-2354-11A-01W-0800-08 g.chr9:36170503C>A c.1004C>A c.(1003-1005)aCc>aAc p.T335N PAAD 9 36169849 36169849 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:36169849G>A c.350G>A c.(349-351)cGa>cAa p.R117Q PAAD 9 36169888 36169888 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:36169888G>A c.389G>A c.(388-390)cGt>cAt p.R130H PAAD 9 36170825 36170825 + Silent SNP C C T TCGA-FB-AAPU-01A-31D-A40W-08 TCGA-FB-AAPU-11A-12D-A40W-08 g.chr9:36170825C>T c.1326C>T c.(1324-1326)gtC>gtT p.V442V READ 9 36169700 36169700 + Missense_Mutation SNP G G T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:36169700G>T c.201G>T c.(199-201)gaG>gaT p.E67D SKCM 9 36169514 36169514 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:36169514C>T c.15C>T c.(13-15)ttC>ttT p.F5F SKCM 9 36169518 36169518 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:36169518G>A c.19G>A c.(19-21)Gag>Aag p.E7K SKCM 9 36170051 36170051 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr9:36170051C>T c.552C>T c.(550-552)ctC>ctT p.L184L SKCM 9 36170052 36170052 + Missense_Mutation SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr9:36170052C>T c.553C>T c.(553-555)Cgt>Tgt p.R185C SKCM 9 36170243 36170243 + Silent SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr9:36170243C>T c.744C>T c.(742-744)tcC>tcT p.S248S SKCM 9 36170244 36170244 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr9:36170244C>T c.745C>T c.(745-747)Cat>Tat p.H249Y SKCM 9 36170360 36170360 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:36170360G>A c.861G>A c.(859-861)caG>caA p.Q287Q SKCM 9 36170445 36170445 + Missense_Mutation SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr9:36170445C>T c.946C>T c.(946-948)Cgg>Tgg p.R316W SKCM 9 36170567 36170567 + Silent SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr9:36170567C>T c.1068C>T c.(1066-1068)acC>acT p.T356T SKCM 9 36170609 36170609 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:36170609G>A c.1110G>A c.(1108-1110)atG>atA p.M370I SKCM 9 36170723 36170723 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:36170723G>A c.1224G>A c.(1222-1224)aaG>aaA p.K408K SKCM 9 36171103 36171103 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr9:36171103C>T c.1604C>T c.(1603-1605)aCt>aTt p.T535I SKCM 9 36171241 36171241 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr9:36171241C>T c.1742C>T c.(1741-1743)cCt>cTt p.P581L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BOCA-FR 9 36164486 36164486 single base substitution C T upstream_gene_variant BOCA-FR 9 36172640 36172640 single base substitution G A downstream_gene_variant BRCA-EU 9 36164491 36164505 deletion of <=200bp GGTAGGAAGCTGACG - upstream_gene_variant BRCA-EU 9 36164562 36164562 single base substitution C T upstream_gene_variant BRCA-EU 9 36164593 36164593 deletion of <=200bp C - upstream_gene_variant BRCA-EU 9 36164866 36164866 single base substitution G A upstream_gene_variant BRCA-EU 9 36165388 36165388 single base substitution G A upstream_gene_variant BRCA-EU 9 36165972 36165972 single base substitution C G upstream_gene_variant BRCA-EU 9 36166020 36166020 single base substitution C T upstream_gene_variant BRCA-EU 9 36166098 36166098 single base substitution G A upstream_gene_variant BRCA-EU 9 36166110 36166110 single base substitution G A upstream_gene_variant BRCA-EU 9 36168340 36168340 single base substitution C A upstream_gene_variant BRCA-EU 9 36169369 36169369 single base substitution C T upstream_gene_variant BRCA-EU 9 36169680 36169680 single base substitution G A missense_variant D61N 181G>A BRCA-EU 9 36170862 36170862 single base substitution G A missense_variant V455M 1363G>A BRCA-EU 9 36170956 36170957 deletion of <=200bp AG - frameshift_variant Q486 BRCA-EU 9 36171001 36171001 single base substitution C A missense_variant T501N 1502C>A BRCA-EU 9 36172031 36172031 single base substitution G C downstream_gene_variant BRCA-EU 9 36172296 36172296 single base substitution G T downstream_gene_variant BRCA-EU 9 36172943 36172943 single base substitution C G downstream_gene_variant BRCA-EU 9 36175910 36175910 single base substitution C T downstream_gene_variant BRCA-EU 9 36176130 36176130 deletion of <=200bp T - downstream_gene_variant BRCA-FR 9 36164562 36164562 single base substitution C T upstream_gene_variant BRCA-FR 9 36166098 36166098 single base substitution G A upstream_gene_variant BRCA-FR 9 36169680 36169680 single base substitution G A missense_variant D61N 181G>A BRCA-FR 9 36170862 36170862 single base substitution G A missense_variant V455M 1363G>A BRCA-FR 9 36175195 36175195 single base substitution G A downstream_gene_variant BRCA-UK 9 36169569 36169569 single base substitution C T missense_variant R24C 70C>T BRCA-UK 9 36171192 36171192 single base substitution C G missense_variant P565A 1693C>G BRCA-UK 9 36172943 36172943 single base substitution C G downstream_gene_variant BRCA-US 9 36169514 36169514 single base substitution C A missense_variant F5L 15C>A BRCA-US 9 36169591 36169591 single base substitution C T missense_variant A31V 92C>T BRCA-US 9 36169863 36169863 single base substitution G A missense_variant D122N 364G>A BRCA-US 9 36170027 36170027 single base substitution A C synonymous_variant P176P 528A>C BRCA-US 9 36170527 36170527 single base substitution A G missense_variant K343R 1028A>G BRCA-US 9 36170592 36170592 single base substitution C T missense_variant L365F 1093C>T BTCA-JP 9 36169816 36169816 single base substitution G A missense_variant R106H 317G>A BTCA-JP 9 36169862 36169862 single base substitution C T synonymous_variant N121N 363C>T BTCA-JP 9 36170352 36170352 single base substitution G T missense_variant G285C 853G>T CESC-US 9 36170051 36170051 single base substitution C G synonymous_variant L184L 552C>G COAD-US 9 36169589 36169589 single base substitution G A missense_variant M30I 90G>A COAD-US 9 36169723 36169723 single base substitution G A missense_variant S75N 224G>A COAD-US 9 36169902 36169902 single base substitution C T missense_variant R135C 403C>T COAD-US 9 36169968 36169968 single base substitution C T missense_variant R157W 469C>T COAD-US 9 36170290 36170290 single base substitution G A missense_variant R264Q 791G>A COCA-CN 9 36169602 36169602 single base substitution G T missense_variant D35Y 103G>T COCA-CN 9 36169974 36169974 single base substitution A T missense_variant N159Y 475A>T COCA-CN 9 36170164 36170164 single base substitution A G missense_variant Y222C 665A>G COCA-CN 9 36170411 36170411 single base substitution G T missense_variant E304D 912G>T COCA-CN 9 36170682 36170682 single base substitution C T missense_variant R395C 1183C>T COCA-CN 9 36170745 36170745 single base substitution A T missense_variant T416S 1246A>T COCA-CN 9 36171307 36171307 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 36164593 36164593 deletion of <=200bp C - upstream_gene_variant ESAD-UK 9 36164593 36164593 insertion of <=200bp - C upstream_gene_variant ESAD-UK 9 36165763 36165763 single base substitution C T upstream_gene_variant ESAD-UK 9 36166828 36166828 single base substitution C A upstream_gene_variant ESAD-UK 9 36168566 36168566 single base substitution A G upstream_gene_variant ESAD-UK 9 36168955 36168955 single base substitution C A upstream_gene_variant ESAD-UK 9 36172486 36172486 single base substitution G T downstream_gene_variant ESAD-UK 9 36174284 36174284 single base substitution T G downstream_gene_variant ESAD-UK 9 36176328 36176328 single base substitution A T downstream_gene_variant ESCA-CN 9 36170939 36170939 single base substitution C T synonymous_variant C480C 1440C>T GBM-US 9 36169599 36169599 single base substitution G A missense_variant V34M 100G>A GBM-US 9 36170861 36170861 single base substitution C T synonymous_variant D454D 1362C>T KIRC-US 9 36170277 36170277 single base substitution C T missense_variant R260C 778C>T KIRP-US 9 36169599 36169599 single base substitution G A missense_variant V34M 100G>A KIRP-US 9 36170075 36170075 single base substitution C T synonymous_variant L192L 576C>T KIRP-US 9 36170395 36170395 single base substitution C T missense_variant A299V 896C>T LGG-US 9 36170045 36170045 single base substitution C A synonymous_variant R182R 546C>A LGG-US 9 36170121 36170121 single base substitution C T missense_variant R208W 622C>T LGG-US 9 36170732 36170732 deletion of <=200bp C - frameshift_variant I411 LGG-US 9 36170748 36170748 single base substitution G A missense_variant A417T 1249G>A LICA-FR 9 36169747 36169747 single base substitution A G missense_variant D83G 248A>G LIHC-US 9 36169807 36169807 single base substitution A T missense_variant E103V 308A>T LIHC-US 9 36170794 36170794 single base substitution G T missense_variant R432L 1295G>T LINC-JP 9 36165255 36165255 single base substitution A T upstream_gene_variant LINC-JP 9 36165295 36165295 single base substitution A G upstream_gene_variant LINC-JP 9 36170305 36170305 single base substitution T C missense_variant L269P 806T>C LINC-JP 9 36170555 36170555 single base substitution C A missense_variant D352E 1056C>A LINC-JP 9 36173151 36173151 single base substitution A G downstream_gene_variant LIRI-JP 9 36164698 36164698 single base substitution T C upstream_gene_variant LIRI-JP 9 36165839 36165839 single base substitution G A upstream_gene_variant LIRI-JP 9 36168173 36168173 single base substitution A G upstream_gene_variant LIRI-JP 9 36168960 36168960 single base substitution T C upstream_gene_variant LIRI-JP 9 36170968 36170968 single base substitution T C missense_variant I490T 1469T>C LIRI-JP 9 36175593 36175593 single base substitution C T downstream_gene_variant LIRI-JP 9 36176116 36176116 single base substitution C A downstream_gene_variant LUSC-KR 9 36166646 36166646 single base substitution G T upstream_gene_variant LUSC-KR 9 36168242 36168242 single base substitution T A upstream_gene_variant LUSC-KR 9 36168601 36168601 single base substitution A C upstream_gene_variant LUSC-KR 9 36176164 36176164 single base substitution C A downstream_gene_variant LUSC-US 9 36169849 36169849 single base substitution G T missense_variant R117L 350G>T LUSC-US 9 36170237 36170237 single base substitution C A synonymous_variant T246T 738C>A MELA-AU 9 36165511 36165511 single base substitution C T upstream_gene_variant MELA-AU 9 36166158 36166158 single base substitution C T upstream_gene_variant MELA-AU 9 36166688 36166688 single base substitution C T upstream_gene_variant MELA-AU 9 36167329 36167329 single base substitution G A upstream_gene_variant MELA-AU 9 36167613 36167613 single base substitution G A upstream_gene_variant MELA-AU 9 36167615 36167615 single base substitution G A upstream_gene_variant MELA-AU 9 36169106 36169106 single base substitution C T upstream_gene_variant MELA-AU 9 36169146 36169146 single base substitution G A upstream_gene_variant MELA-AU 9 36169387 36169387 single base substitution C T upstream_gene_variant MELA-AU 9 36169790 36169790 single base substitution C T synonymous_variant S97S 291C>T MELA-AU 9 36169968 36169968 single base substitution C T missense_variant R157W 469C>T MELA-AU 9 36170028 36170028 single base substitution C T missense_variant P177S 529C>T MELA-AU 9 36170133 36170133 single base substitution C T missense_variant R212W 634C>T MELA-AU 9 36170623 36170623 single base substitution G A missense_variant G375E 1124G>A MELA-AU 9 36170699 36170699 single base substitution G A synonymous_variant K400K 1200G>A MELA-AU 9 36171021 36171021 single base substitution C A missense_variant P508T 1522C>A MELA-AU 9 36171039 36171039 single base substitution G A missense_variant D514N 1540G>A MELA-AU 9 36171195 36171196 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P566L 1696CC>TT MELA-AU 9 36171308 36171308 single base substitution G A 3_prime_UTR_variant MELA-AU 9 36171518 36171518 single base substitution G A downstream_gene_variant MELA-AU 9 36172261 36172261 single base substitution G A downstream_gene_variant MELA-AU 9 36172540 36172540 single base substitution C T downstream_gene_variant MELA-AU 9 36173280 36173280 single base substitution G A downstream_gene_variant MELA-AU 9 36173311 36173311 single base substitution G A downstream_gene_variant MELA-AU 9 36173832 36173832 single base substitution A C downstream_gene_variant MELA-AU 9 36173961 36173961 single base substitution G A downstream_gene_variant MELA-AU 9 36174332 36174332 single base substitution C A downstream_gene_variant MELA-AU 9 36175312 36175312 single base substitution G A downstream_gene_variant MELA-AU 9 36175332 36175332 single base substitution C T downstream_gene_variant MELA-AU 9 36175594 36175594 single base substitution G A downstream_gene_variant MELA-AU 9 36175646 36175646 single base substitution C T downstream_gene_variant MELA-AU 9 36175722 36175722 single base substitution C T downstream_gene_variant MELA-AU 9 36176190 36176190 single base substitution C T downstream_gene_variant ORCA-IN 9 36164608 36164608 single base substitution T C upstream_gene_variant ORCA-IN 9 36170122 36170122 single base substitution G A missense_variant R208Q 623G>A OV-AU 9 36170723 36170723 single base substitution G A synonymous_variant K408K 1224G>A PACA-AU 9 36167328 36167328 single base substitution C T upstream_gene_variant PACA-AU 9 36170339 36170339 single base substitution C T synonymous_variant S280S 840C>T PACA-AU 9 36171279 36171279 single base substitution G T 3_prime_UTR_variant PACA-AU 9 36172885 36172885 single base substitution T G downstream_gene_variant PACA-CA 9 36165545 36165545 single base substitution G A upstream_gene_variant PACA-CA 9 36166417 36166417 single base substitution C T upstream_gene_variant PACA-CA 9 36170566 36170566 single base substitution C T missense_variant T356I 1067C>T PACA-CA 9 36170619 36170619 single base substitution G T missense_variant G374W 1120G>T PACA-CA 9 36172945 36172945 single base substitution G C downstream_gene_variant PACA-CA 9 36173399 36173399 single base substitution C A downstream_gene_variant PACA-CA 9 36175647 36175647 single base substitution A G downstream_gene_variant PACA-CA 9 36175979 36175979 single base substitution G A downstream_gene_variant PAEN-IT 9 36166409 36166409 single base substitution C A upstream_gene_variant PBCA-DE 9 36167117 36167117 single base substitution T G upstream_gene_variant PBCA-DE 9 36175781 36175781 single base substitution G A downstream_gene_variant READ-US 9 36169700 36169700 single base substitution G T missense_variant E67D 201G>T READ-US 9 36169902 36169902 single base substitution C T missense_variant R135C 403C>T READ-US 9 36170793 36170793 single base substitution C A synonymous_variant R432R 1294C>A SKCA-BR 9 36164411 36164411 single base substitution A C upstream_gene_variant SKCA-BR 9 36164608 36164608 insertion of <=200bp - TAC upstream_gene_variant SKCA-BR 9 36166688 36166688 single base substitution C T upstream_gene_variant SKCA-BR 9 36167793 36167793 single base substitution G A upstream_gene_variant SKCA-BR 9 36167797 36167797 single base substitution C T upstream_gene_variant SKCA-BR 9 36169335 36169335 single base substitution C T upstream_gene_variant SKCA-BR 9 36170589 36170589 single base substitution G A missense_variant G364R 1090G>A SKCA-BR 9 36171630 36171630 single base substitution C T downstream_gene_variant SKCA-BR 9 36172274 36172274 single base substitution G A downstream_gene_variant SKCA-BR 9 36172628 36172628 single base substitution T C downstream_gene_variant SKCA-BR 9 36173255 36173255 single base substitution C T downstream_gene_variant SKCA-BR 9 36174175 36174175 single base substitution G A downstream_gene_variant SKCA-BR 9 36174423 36174423 single base substitution A C downstream_gene_variant SKCA-BR 9 36176161 36176161 single base substitution C A downstream_gene_variant SKCM-US 9 36169514 36169514 single base substitution C T synonymous_variant F5F 15C>T SKCM-US 9 36169518 36169518 single base substitution G A missense_variant E7K 19G>A SKCM-US 9 36170051 36170051 single base substitution C T synonymous_variant L184L 552C>T SKCM-US 9 36170052 36170052 single base substitution C T missense_variant R185C 553C>T SKCM-US 9 36170243 36170243 single base substitution C T synonymous_variant S248S 744C>T SKCM-US 9 36170244 36170244 single base substitution C T missense_variant H249Y 745C>T SKCM-US 9 36170360 36170360 single base substitution G A synonymous_variant Q287Q 861G>A SKCM-US 9 36170445 36170445 single base substitution C T missense_variant R316W 946C>T SKCM-US 9 36170567 36170567 single base substitution C T synonymous_variant T356T 1068C>T SKCM-US 9 36170609 36170609 single base substitution G A missense_variant M370I 1110G>A SKCM-US 9 36170723 36170723 single base substitution G A synonymous_variant K408K 1224G>A SKCM-US 9 36171103 36171103 single base substitution C T missense_variant T535I 1604C>T SKCM-US 9 36171241 36171241 single base substitution C T missense_variant P581L 1742C>T STAD-US 9 36169823 36169823 single base substitution T G synonymous_variant A108A 324T>G STAD-US 9 36170020 36170020 single base substitution G A missense_variant R174H 521G>A STAD-US 9 36170043 36170043 single base substitution C T missense_variant R182C 544C>T STAD-US 9 36170316 36170316 single base substitution C T missense_variant R273W 817C>T STAD-US 9 36170715 36170715 single base substitution G A missense_variant A406T 1216G>A STAD-US 9 36171031 36171031 single base substitution G A missense_variant C511Y 1532G>A UCEC-US 9 36169538 36169538 single base substitution C T synonymous_variant F13F 39C>T UCEC-US 9 36170073 36170073 single base substitution C T missense_variant L192F 574C>T UCEC-US 9 36170079 36170079 single base substitution G T stop_gained E194* 580G>T UCEC-US 9 36170084 36170084 single base substitution C A missense_variant D195E 585C>A UCEC-US 9 36170194 36170194 single base substitution C T missense_variant T232M 695C>T UCEC-US 9 36170340 36170340 single base substitution G A missense_variant V281M 841G>A UCEC-US 9 36170537 36170537 single base substitution G A stop_gained W346* 1038G>A UCEC-US 9 36170569 36170569 single base substitution A C missense_variant K357T 1070A>C UCEC-US 9 36171159 36171159 single base substitution G T missense_variant D554Y 1660G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESCC-148T COSM3943024 c.1440C>T p.C480C Substitution - coding silent 9:36170942-36170942 + TCGA-FS-A1Z3-06 COSM3657334 c.1604C>T p.T535I Substitution - Missense 9:36171106-36171106 + D-14 COSM2775266 c.1441G>A p.V481M Substitution - Missense 9:36170943-36170943 + LUAD-RT-S01774 COSM381677 c.1360G>T p.D454Y Substitution - Missense 9:36170862-36170862 + T3064 COSM2775264 c.1249G>A p.A417T Substitution - Missense 9:36170751-36170751 + ACINAR29 COSM1734369 c.1541A>T p.D514V Substitution - Missense 9:36171043-36171043 + LS174T COSM2775249 c.933A>G p.S311S Substitution - coding silent 9:36170435-36170435 + CSCC-40-T COSM4549999 c.488G>A p.W163* Substitution - Nonsense 9:36169990-36169990 + CSCC-10-T COSM4554797 c.631G>A p.D211N Substitution - Missense 9:36170133-36170133 + cSCCP6 COSM136713 c.628G>A p.E210K Substitution - Missense 9:36170130-36170130 + TCGA-A5-A0GA-01 COSM1108888 c.585C>A p.D195E Substitution - Missense 9:36170087-36170087 + BD165T COSM2775236 c.317G>A p.R106H Substitution - Missense 9:36169819-36169819 + C086 COSM5528306 c.164G>A p.S55N Substitution - Missense 9:36169666-36169666 + CHC205T COSM3763924 c.791G>A p.R264Q Substitution - Missense 9:36170293-36170293 + TCGA-BS-A0UV-01 COSM1108891 c.1038G>A p.W346* Substitution - Nonsense 9:36170540-36170540 + DLD1 COSM159818 c.70C>T p.R24C Substitution - Missense 9:36169572-36169572 + 587238 COSM1200115 c.520C>T p.R174C Substitution - Missense 9:36170022-36170022 + C086 COSM5528307 c.3G>A p.M1I Substitution - Missense 9:36169505-36169505 + 8014396 COSM3395812 c.840C>T p.S280S Substitution - coding silent 9:36170342-36170342 + TCGA-19-1786 COSM159819 c.1693C>G p.P565A Substitution - Missense 9:36171195-36171195 + OSCC-GB_00810111 COSM2775244 c.623G>A p.R208Q Substitution - Missense 9:36170125-36170125 + YUKAE COSM5411070 c.1349C>T p.T450I Substitution - Missense 9:36170851-36170851 + TCGA-BR-7707-01 COSM3907314 c.817C>T p.R273W Substitution - Missense 9:36170319-36170319 + T1154 COSM1108890 c.841G>A p.V281M Substitution - Missense 9:36170343-36170343 + CSCC-45-T COSM4519464 c.1011G>A p.E337E Substitution - coding silent 9:36170513-36170513 + TCGA-AA-3672-01 COSM266197 c.1760G>T p.R587M Substitution - Missense 9:36171262-36171262 + pfg122T COSM4752768 c.392C>T p.A131V Substitution - Missense 9:36169894-36169894 + PCSI_0311_Pa_P_526 COSM3782256 c.1120G>T p.G374W Substitution - Missense 9:36170622-36170622 + S00944 COSM309926 c.1434C>A p.I478I Substitution - coding silent 9:36170936-36170936 + TCGA-EE-A3J5-06 COSM3657335 c.1742C>T p.P581L Substitution - Missense 9:36171244-36171244 + TCGA-B7-5816-01 COSM3907311 c.324T>G p.A108A Substitution - coding silent 9:36169826-36169826 + S02294 COSM5688946 c.720G>A p.L240L Substitution - coding silent 9:36170222-36170222 + T407 COSM4670148 c.1198A>G p.K400E Substitution - Missense 9:36170700-36170700 + TCGA-BC-A3KF-01 COSM4927791 c.308A>T p.E103V Substitution - Missense 9:36169810-36169810 + TCGA-DU-6408-01 COSM2775264 c.1249G>A p.A417T Substitution - Missense 9:36170751-36170751 + 222 COSM4425352 c.238G>A p.V80I Substitution - Missense 9:36169740-36169740 + TCGA-EE-A29V-06 COSM3657332 c.946C>T p.R316W Substitution - Missense 9:36170448-36170448 + cSCCP6 COSM136712 c.247G>A p.D83N Substitution - Missense 9:36169749-36169749 + 1_PRE-TREATMENT COSM1718353 c.1320C>T p.S440S Substitution - coding silent 9:36170822-36170822 + LUAD_E01166 COSM390892 c.510G>A p.M170I Substitution - Missense 9:36170012-36170012 + TCGA-EE-A2MJ-06 COSM3657326 c.19G>A p.E7K Substitution - Missense 9:36169521-36169521 + PD13163a COSM5770293 c.1363G>A p.V455M Substitution - Missense 9:36170865-36170865 + 43T COSM107672 c.779G>A p.R260H Substitution - Missense 9:36170281-36170281 + TCGA-AM-5821-01 COSM3763923 c.224G>A p.S75N Substitution - Missense 9:36169726-36169726 + PT49 COSM5935465 c.1017T>G p.I339M Substitution - Missense 9:36170519-36170519 + CSCC-44-T COSM4523668 c.1227G>C p.M409I Substitution - Missense 9:36170729-36170729 + CHC320T COSM217452 c.248A>G p.D83G Substitution - Missense 9:36169750-36169750 + TCGA-A4-7915-01 COSM3996552 c.896C>T p.A299V Substitution - Missense 9:36170398-36170398 + TCGA-EP-A2KB-01 COSM4921558 c.1295G>T p.R432L Substitution - Missense 9:36170797-36170797 + TCGA-18-3421-01 COSM753453 c.350G>T p.R117L Substitution - Missense 9:36169852-36169852 + TCGA-LP-A5U2-01 COSM4833687 c.552C>G p.L184L Substitution - coding silent 9:36170054-36170054 + 2318491 COSM4776860 c.1227G>A p.M409I Substitution - Missense 9:36170729-36170729 + CSCC-29-T COSM4555125 c.642G>A p.K214K Substitution - coding silent 9:36170144-36170144 + TCGA-AZ-4315-01 COSM1462348 c.403C>T p.R135C Substitution - Missense 9:36169905-36169905 + TCGA-EE-A29D-06 COSM3657331 c.745C>T p.H249Y Substitution - Missense 9:36170247-36170247 + 2521243 COSM5886613 c.1124G>A p.G375E Substitution - Missense 9:36170626-36170626 + LUAD_E00623 COSM354685 c.124C>A p.H42N Substitution - Missense 9:36169626-36169626 + 587220 COSM1200116 c.128G>A p.R43H Substitution - Missense 9:36169630-36169630 + TCGA-AP-A059-01 COSM1108889 c.695C>T p.T232M Substitution - Missense 9:36170197-36170197 + RK178_C01 COSM3745998 c.1469T>C p.I490T Substitution - Missense 9:36170971-36170971 + CSCC-55-T COSM1462349 c.469C>T p.R157W Substitution - Missense 9:36169971-36169971 + TCGA-EE-A181-06 COSM3657328 c.552C>T p.L184L Substitution - coding silent 9:36170054-36170054 + TCGA-BR-7851-01 COSM3907312 c.521G>A p.R174H Substitution - Missense 9:36170023-36170023 + TCGA-AM-5820-01 COSM3763924 c.791G>A p.R264Q Substitution - Missense 9:36170293-36170293 + HCC60T COSM1624984 c.806T>C p.L269P Substitution - Missense 9:36170308-36170308 + HCC2998 COSM2775260 c.1179C>A p.I393I Substitution - coding silent 9:36170681-36170681 + AOCS-139-19-0 COSM3926796 c.1224G>A p.K408K Substitution - coding silent 9:36170726-36170726 + S02351 COSM5695244 c.1538T>C p.L513S Substitution - Missense 9:36171040-36171040 + 2293776 COSM4608057 c.1559G>T p.C520F Substitution - Missense 9:36171061-36171061 + PD24212a COSM5781118 c.1502C>A p.T501N Substitution - Missense 9:36171004-36171004 + 2293782 COSM4609458 c.414C>A p.F138L Substitution - Missense 9:36169916-36169916 + PT48 COSM5932371 c.32A>G p.N11S Substitution - Missense 9:36169534-36169534 + HCC111T COSM1624985 c.1056C>A p.D352E Substitution - Missense 9:36170558-36170558 + LS180 COSM2775249 c.933A>G p.S311S Substitution - coding silent 9:36170435-36170435 + TCGA-A8-A0A6-01 COSM3848532 c.528A>C p.P176P Substitution - coding silent 9:36170030-36170030 + TCGA-BR-4292-01 COSM3907316 c.1532G>A p.C511Y Substitution - Missense 9:36171034-36171034 + TCGA-06-5858-01 COSM3413649 c.100G>A p.V34M Substitution - Missense 9:36169602-36169602 + CHC320T COSM217452 c.248A>G p.D83G Substitution - Missense 9:36169750-36169750 + 1_RESISTANT COSM1718353 c.1320C>T p.S440S Substitution - coding silent 9:36170822-36170822 + BD6T COSM5499032 c.363C>T p.N121N Substitution - coding silent 9:36169865-36169865 + TCGA-A8-A09Z-01 COSM3848530 c.92C>T p.A31V Substitution - Missense 9:36169594-36169594 + 8 COSM4166931 c.127C>T p.R43C Substitution - Missense 9:36169629-36169629 + LUAD-F00162 COSM366720 c.870C>A p.H290Q Substitution - Missense 9:36170372-36170372 + HCT15 COSM159818 c.70C>T p.R24C Substitution - Missense 9:36169572-36169572 + PD4125a COSM159819 c.1693C>G p.P565A Substitution - Missense 9:36171195-36171195 + TCGA-BS-A0UF-01 COSM1108893 c.1660G>T p.D554Y Substitution - Missense 9:36171162-36171162 + PD4111a COSM159818 c.70C>T p.R24C Substitution - Missense 9:36169572-36169572 + TCGA-FW-A3R5-06 COSM3926794 c.15C>T p.F5F Substitution - coding silent 9:36169517-36169517 + TCGA-BS-A0UF-01 COSM1108885 c.39C>T p.F13F Substitution - coding silent 9:36169541-36169541 + TCGA-24-1847-01 COSM1331552 c.417G>T p.L139F Substitution - Missense 9:36169919-36169919 + TCGA-59-2354-01 COSM70054 c.1004C>A p.T335N Substitution - Missense 9:36170506-36170506 + DN120F1 COSM5770293 c.1363G>A p.V455M Substitution - Missense 9:36170865-36170865 + TCGA-E2-A10F-01 COSM455939 c.15C>A p.F5L Substitution - Missense 9:36169517-36169517 + TCGA-29-1778-01 COSM1331551 c.590C>T p.A197V Substitution - Missense 9:36170092-36170092 + HCC111 COSM1624985 c.1056C>A p.D352E Substitution - Missense 9:36170558-36170558 + 587376 COSM1200118 c.979C>T p.R327C Substitution - Missense 9:36170481-36170481 + BN50T COSM1624984 c.806T>C p.L269P Substitution - Missense 9:36170308-36170308 + PD11385a COSM5801374 c.1457_1458delAG p.S487fs*>102 Deletion - Frameshift 9:36170959-36170960 + S00944 COSM309926 c.1434C>A p.I478I Substitution - coding silent 9:36170936-36170936 + TCGA-HU-A4GX-01 COSM3907315 c.1216G>A p.A406T Substitution - Missense 9:36170718-36170718 + TCGA-FG-8186-01 COSM2775243 c.622C>T p.R208W Substitution - Missense 9:36170124-36170124 + CHC320T COSM217452 c.248A>G p.D83G Substitution - Missense 9:36169750-36169750 + 3844_T COSM3952706 c.1746C>T p.C582C Substitution - coding silent 9:36171248-36171248 + TCGA-B9-5155-01 COSM3413649 c.100G>A p.V34M Substitution - Missense 9:36169602-36169602 + TCGA-HU-A4H8-01 COSM3907313 c.544C>T p.R182C Substitution - Missense 9:36170046-36170046 + TCGA-D3-A3MR-06 COSM3657330 c.744C>T p.S248S Substitution - coding silent 9:36170246-36170246 + ESCC_124 COSM5641051 c.1092G>A p.G364G Substitution - coding silent 9:36170594-36170594 + TCGA-EE-A3AC-06 COSM3657333 c.1068C>T p.T356T Substitution - coding silent 9:36170570-36170570 + BN50 COSM1624984 c.806T>C p.L269P Substitution - Missense 9:36170308-36170308 + TCGA-EI-6882-01 COSM3433134 c.1294C>A p.R432R Substitution - coding silent 9:36170796-36170796 + HT115 COSM2775265 c.1279T>C p.Y427H Substitution - Missense 9:36170781-36170781 + sysucc-1150T COSM5452648 c.103G>T p.D35Y Substitution - Missense 9:36169605-36169605 + HCT8 COSM159818 c.70C>T p.R24C Substitution - Missense 9:36169572-36169572 + sysucc-311T COSM5467705 c.665A>G p.Y222C Substitution - Missense 9:36170167-36170167 + TCGA-EI-6507-01 COSM1569272 c.201G>T p.E67D Substitution - Missense 9:36169703-36169703 + TCGA-FW-A3R5-06 COSM3926795 c.861G>A p.Q287Q Substitution - coding silent 9:36170363-36170363 + TCGA-D9-A4Z6-01 COSM3657327 c.149C>T p.S50F Substitution - Missense 9:36169651-36169651 + TCGA-AX-A05Z-01 COSM1108887 c.580G>T p.E194* Substitution - Nonsense 9:36170082-36170082 + TCGA-D8-A1XQ-01 COSM3848533 c.1093C>T p.L365F Substitution - Missense 9:36170595-36170595 + HT115 COSM4638436 c.570C>T p.H190H Substitution - coding silent 9:36170072-36170072 + TCGA-AC-A23H-01 COSM3848531 c.364G>A p.D122N Substitution - Missense 9:36169866-36169866 + 1_RESISTANT COSM1718352 c.109C>T p.H37Y Substitution - Missense 9:36169611-36169611 + TCGA-D3-A3C7-06 COSM3657329 c.553C>T p.R185C Substitution - Missense 9:36170055-36170055 + CSCC-6-T COSM4464067 c.1317C>T p.I439I Substitution - coding silent 9:36170819-36170819 + LUAD-S01357 COSM387974 c.231G>T p.L77L Substitution - coding silent 9:36169733-36169733 + TCGA-B5-A11E-01 COSM1108892 c.1070A>C p.K357T Substitution - Missense 9:36170572-36170572 + C086 COSM5528304 c.854G>A p.G285D Substitution - Missense 9:36170356-36170356 + YUSCA COSM5411069 c.580G>A p.E194K Substitution - Missense 9:36170082-36170082 + cSCCP4 COSM138712 c.559G>A p.E187K Substitution - Missense 9:36170061-36170061 + HCC60 COSM1624984 c.806T>C p.L269P Substitution - Missense 9:36170308-36170308 + CSCC-49-T COSM4558638 c.775G>A p.D259N Substitution - Missense 9:36170277-36170277 + CCK81 COSM2775243 c.622C>T p.R208W Substitution - Missense 9:36170124-36170124 + TCGA-B5-A0K2-01 COSM1108890 c.841G>A p.V281M Substitution - Missense 9:36170343-36170343 + 3N48-VS-3T48 COSM4982825 c.1271G>T p.R424M Substitution - Missense 9:36170773-36170773 + PCSI_0468_Pa_P_526 COSM4809307 c.1067C>T p.T356I Substitution - Missense 9:36170569-36170569 + TCGA-66-2787-01 COSM753452 c.738C>A p.T246T Substitution - coding silent 9:36170240-36170240 + TCGA-FW-A3R5-06 COSM3926796 c.1224G>A p.K408K Substitution - coding silent 9:36170726-36170726 + TCGA-12-5301-01 COSM3413650 c.1362C>T p.D454D Substitution - coding silent 9:36170864-36170864 + TCGA-CA-6717-01 COSM1462349 c.469C>T p.R157W Substitution - Missense 9:36169971-36169971 + YUNEKI COSM5411071 c.1449C>T p.S483S Substitution - coding silent 9:36170951-36170951 + 587342 COSM1200117 c.529C>T p.P177S Substitution - Missense 9:36170031-36170031 + CSCC-17-T COSM4512562 c.907C>A p.Q303K Substitution - Missense 9:36170409-36170409 + TCGA-BP-4763-01 COSM3367716 c.778C>T p.R260C Substitution - Missense 9:36170280-36170280 + SC_9047 COSM5551254 c.1558T>G p.C520G Substitution - Missense 9:36171060-36171060 + CSCC-20-T COSM4550489 c.501G>A p.E167E Substitution - coding silent 9:36170003-36170003 + TCGA-D9-A6EC-06 COSM4403760 c.1110G>A p.M370I Substitution - Missense 9:36170612-36170612 + 1_PRE-TREATMENT COSM1718352 c.109C>T p.H37Y Substitution - Missense 9:36169611-36169611 + TCGA-EV-5903-01 COSM3996551 c.576C>T p.L192L Substitution - coding silent 9:36170078-36170078 + TCGA-DB-A4XF-01 COSM3930060 c.546C>A p.R182R Substitution - coding silent 9:36170048-36170048 + TCGA-A8-A09I-01 COSM455940 c.1028A>G p.K343R Substitution - Missense 9:36170530-36170530 + TCGA-BS-A0UV-01 COSM1108886 c.574C>T p.L192F Substitution - Missense 9:36170076-36170076 + C086 COSM5528305 c.1163G>A p.R388Q Substitution - Missense 9:36170665-36170665 + TCGA-EI-6917-01 COSM1462348 c.403C>T p.R135C Substitution - Missense 9:36169905-36169905 + PTC-10C COSM4163839 c.606C>A p.I202I Substitution - coding silent 9:36170108-36170108 + TCGA-CM-6677-01 COSM1462347 c.90G>A p.M30I Substitution - Missense 9:36169592-36169592 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.115440;Hs.115460 9p13.3 603960

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.D83G c.248A>G 9 36169747 HC A G Missense p.K343R c.1028A>G 9 36170527 BRCA A G Missense p.N9S c.26A>G 9 36169525 CM C A Missense p.D195E c.585C>A 9 36170084 UCEC C A Missense p.F5L c.15C>A 9 36169514 BRCA C A Missense p.T335N c.1004C>A 9 36170503 OV C A Synonymous p.I478I c.1434C>A 9 36170933 SCLC C A Synonymous p.T246T c.738C>A 9 36170237 LUSC C G Missense p.P565A c.1693C>G 9 36171192 BRCA C T 5-UTRSNV . c.1-49C>T 9 36169451 CM C T Missense p.P581L c.1742C>T 9 36171241 CM C T Missense p.R185C c.553C>T 9 36170052 CM C T Missense p.R208W c.622C>T 9 36170121 LGG C T Missense p.R24C c.70C>T 9 36169569 BRCA C T Missense p.R316W c.946C>T 9 36170445 CM C T Missense p.T535I c.1604C>T 9 36171103 CM C T Synonymous p.A345A c.1035C>T 9 36170534 BRCA C T Synonymous p.D454D c.1362C>T 9 36170861 GBM C T Synonymous p.G415G c.1245C>T 9 36170744 HNSC C T Synonymous p.I70I c.210C>T 9 36169709 HNSC C T Synonymous p.L184L c.552C>T 9 36170051 CM C T Synonymous p.S248S c.744C>T 9 36170243 CM C T Synonymous p.T356T c.1068C>T 9 36170567 CM G A Missense p.A417T c.1249G>A 9 36170748 LGG G A Missense p.C511Y c.1532G>A 9 36171031 STAD G A Missense p.D349N c.1045G>A 9 36170544 HNSC G A Missense p.E7K c.19G>A 9 36169518 CM G A Missense p.R185H c.554G>A 9 36170053 HNSC G A Missense p.V191M c.571G>A 9 36170070 HNSC G A Missense p.V281M c.841G>A 9 36170340 UCEC G C Missense p.G375R c.1123G>C 9 36170622 CM G T Missense p.A236S c.706G>T 9 36170205 LUAD G T Missense p.R117L c.350G>T 9 36169849 LUSC G T Synonymous p.G453G c.1359G>T 9 36170858 COREAD T C Missense p.V506A c.1517T>C 9 36171016 LUAD TG - Frameshift p.S516Pfs*103 c.1545_1546delGT 9 36171041 LUAD T G Synonymous p.A108A c.324T>G 9 36169823 STAD