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 140115250 140115251 + Missense_Mutation DNP CG CG TA TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr9:140115250_140115251CG>TA c.414_415CG>TA c.(412-417)ggCGag>ggTAag p.E139K BLCA 9 140115097 140115097 + Missense_Mutation SNP G G A TCGA-XF-AAN7-01A-11D-A42E-08 TCGA-XF-AAN7-10A-01D-A42H-08 g.chr9:140115097G>A c.568C>T c.(568-570)Cgc>Tgc p.R190C BLCA 9 140115104 140115104 + Silent SNP G G C TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr9:140115104G>C c.561C>G c.(559-561)ccC>ccG p.P187P BLCA 9 140115581 140115581 + Silent SNP G G T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr9:140115581G>T c.84C>A c.(82-84)ctC>ctA p.L28L BRCA 9 140114992 140114992 + Missense_Mutation SNP C C T TCGA-AR-A24H-01A-11D-A167-09 TCGA-AR-A24H-10A-01D-A167-09 g.chr9:140114992C>T c.673G>A c.(673-675)Ggt>Agt p.G225S BRCA 9 140115554 140115554 + Missense_Mutation SNP G G C TCGA-E9-A244-01A-11D-A167-09 TCGA-E9-A244-10A-01D-A167-09 g.chr9:140115554G>C c.111C>G c.(109-111)caC>caG p.H37Q CESC 9 140114971 140114971 + Missense_Mutation SNP C C T TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr9:140114971C>T c.694G>A c.(694-696)Gag>Aag p.E232K CHOL 9 140114946 140114946 + Missense_Mutation SNP C C A TCGA-W5-AA2I-01A-32D-A417-09 TCGA-W5-AA2I-10A-01D-A41A-09 g.chr9:140114946C>A c.719G>T c.(718-720)cGg>cTg p.R240L COAD 9 140115424 140115424 + Frame_Shift_Del DEL C C - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr9:140115424delC c.241delG c.(241-243)gacfs p.D81fs COADREAD 9 140115424 140115424 + Frame_Shift_Del DEL C C - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr9:140115424delC c.241delG c.(241-243)gacfs p.D81fs ESCA 9 140115495 140115495 + Missense_Mutation SNP G G T TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr9:140115495G>T c.170C>A c.(169-171)aCc>aAc p.T57N GBMLGG 9 140114928 140114928 + Missense_Mutation SNP G G A TCGA-HT-7854-01A-11D-2253-08 TCGA-HT-7854-10A-01D-2253-08 g.chr9:140114928G>A c.737C>T c.(736-738)gCg>gTg p.A246V HNSC 9 140114909 140114909 + Silent SNP C C T TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr9:140114909C>T c.756G>A c.(754-756)cgG>cgA p.R252R HNSC 9 140115191 140115191 + Silent SNP G G A TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr9:140115191G>A c.474C>T c.(472-474)cgC>cgT p.R158R HNSC 9 140115259 140115259 + Missense_Mutation SNP C C T TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr9:140115259C>T c.406G>A c.(406-408)Gcg>Acg p.A136T KICH 9 140115390 140115390 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:140115390G>A c.275C>T c.(274-276)cCg>cTg p.P92L KIPAN 9 140115231 140115231 + Missense_Mutation SNP G G A TCGA-Y8-A896-01A-11D-A35Z-10 TCGA-Y8-A896-10A-01D-A35Z-10 g.chr9:140115231G>A c.434C>T c.(433-435)aCc>aTc p.T145I KIPAN 9 140115390 140115390 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:140115390G>A c.275C>T c.(274-276)cCg>cTg p.P92L KIRP 9 140115231 140115231 + Missense_Mutation SNP G G A TCGA-Y8-A896-01A-11D-A35Z-10 TCGA-Y8-A896-10A-01D-A35Z-10 g.chr9:140115231G>A c.434C>T c.(433-435)aCc>aTc p.T145I LGG 9 140114928 140114928 + Missense_Mutation SNP G G A TCGA-HT-7854-01A-11D-2253-08 TCGA-HT-7854-10A-01D-2253-08 g.chr9:140114928G>A c.737C>T c.(736-738)gCg>gTg p.A246V LIHC 9 140115059 140115059 + Silent SNP G G A TCGA-CC-A8HS-01A-11D-A35Z-10 TCGA-CC-A8HS-10A-01D-A35Z-10 g.chr9:140115059G>A c.606C>T c.(604-606)gcC>gcT p.A202A LIHC 9 140115610 140115610 + Missense_Mutation SNP A A G TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr9:140115610A>G c.55T>C c.(55-57)Tcc>Ccc p.S19P LUAD 9 140115059 140115059 + Silent SNP G G A TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr9:140115059G>A c.606C>T c.(604-606)gcC>gcT p.A202A LUSC 9 140115307 140115307 + Missense_Mutation SNP G G C TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr9:140115307G>C c.358C>G c.(358-360)Cag>Gag p.Q120E PAAD 9 140115570 140115570 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:140115570G>A c.95C>T c.(94-96)gCc>gTc p.A32V PRAD 9 140115423 140115424 + Frame_Shift_Ins INS - - C TCGA-HC-7818-01A-11D-2114-08 TCGA-HC-7818-10A-01D-2115-08 g.chr9:140115423_140115424insC c.241_242insG c.(241-243)gacfs p.D81fs SKCM 9 140114995 140114995 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr9:140114995C>G c.670G>C c.(670-672)Ggg>Cgg p.G224R SKCM 9 140115071 140115071 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr9:140115071G>A c.594C>T c.(592-594)gaC>gaT p.D198D SKCM 9 140115218 140115218 + Silent SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr9:140115218G>A c.447C>T c.(445-447)tcC>tcT p.S149S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 9 140115141 140115141 single base substitution T C missense_variant Y175C 524A>G BLCA-US 9 140115104 140115104 single base substitution G C synonymous_variant P187P 561C>G BLCA-US 9 140115581 140115581 single base substitution G T synonymous_variant L28L 84C>A BRCA-EU 9 140113274 140113274 single base substitution C A downstream_gene_variant BRCA-EU 9 140113337 140113337 single base substitution G T downstream_gene_variant BRCA-EU 9 140114068 140114068 single base substitution T A downstream_gene_variant BRCA-EU 9 140114874 140114874 single base substitution C A 3_prime_UTR_variant BRCA-EU 9 140116431 140116431 single base substitution C G upstream_gene_variant BRCA-EU 9 140117029 140117029 single base substitution T C upstream_gene_variant BRCA-EU 9 140117811 140117811 single base substitution C T upstream_gene_variant BRCA-EU 9 140118573 140118573 single base substitution C T upstream_gene_variant BRCA-EU 9 140119120 140119120 single base substitution G A upstream_gene_variant BRCA-EU 9 140119206 140119206 single base substitution T A upstream_gene_variant BRCA-EU 9 140119670 140119670 single base substitution C A upstream_gene_variant BRCA-EU 9 140120592 140120592 single base substitution T A upstream_gene_variant BRCA-FR 9 140113337 140113337 single base substitution G T downstream_gene_variant BRCA-US 9 140114992 140114992 single base substitution C T missense_variant G225S 673G>A BRCA-US 9 140115554 140115554 single base substitution G C missense_variant H37Q 111C>G BTCA-JP 9 140110001 140110001 single base substitution G T downstream_gene_variant BTCA-JP 9 140120170 140120170 single base substitution G A upstream_gene_variant CESC-US 9 140114971 140114971 single base substitution C T missense_variant E232K 694G>A COAD-US 9 140110182 140110182 single base substitution A G downstream_gene_variant COAD-US 9 140120128 140120128 single base substitution C T upstream_gene_variant COAD-US 9 140120396 140120396 single base substitution C T upstream_gene_variant COAD-US 9 140120447 140120447 single base substitution A C upstream_gene_variant COCA-CN 9 140109969 140109969 single base substitution G C downstream_gene_variant COCA-CN 9 140110727 140110727 single base substitution C T downstream_gene_variant COCA-CN 9 140115434 140115434 single base substitution G T synonymous_variant A77A 231C>A ESAD-UK 9 140110356 140110356 single base substitution T G downstream_gene_variant ESAD-UK 9 140110754 140110754 single base substitution G A downstream_gene_variant ESAD-UK 9 140114038 140114038 deletion of <=200bp T - downstream_gene_variant ESAD-UK 9 140114100 140114100 single base substitution C G downstream_gene_variant ESAD-UK 9 140114245 140114245 single base substitution C A downstream_gene_variant ESAD-UK 9 140120460 140120460 deletion of <=200bp C - upstream_gene_variant ESCA-CN 9 140109962 140109962 single base substitution A G downstream_gene_variant ESCA-CN 9 140110130 140110130 single base substitution C G downstream_gene_variant KIRP-US 9 140110791 140110791 single base substitution C G downstream_gene_variant KIRP-US 9 140115401 140115401 single base substitution T G synonymous_variant A88A 264A>C LGG-US 9 140110623 140110623 single base substitution A G downstream_gene_variant LGG-US 9 140114928 140114928 single base substitution G A missense_variant A246V 737C>T LICA-CN 9 140119617 140119617 single base substitution G T upstream_gene_variant LICA-FR 9 140110617 140110617 single base substitution G C downstream_gene_variant LICA-FR 9 140115373 140115373 single base substitution G A missense_variant P98S 292C>T LICA-FR 9 140120147 140120147 single base substitution A G upstream_gene_variant LICA-FR 9 140120351 140120351 single base substitution G A upstream_gene_variant LINC-JP 9 140119098 140119098 single base substitution G C upstream_gene_variant LINC-JP 9 140120090 140120090 single base substitution T A upstream_gene_variant LIRI-JP 9 140120650 140120650 single base substitution G A upstream_gene_variant LIRI-JP 9 140120849 140120849 single base substitution C T upstream_gene_variant LUSC-KR 9 140111242 140111242 single base substitution C T downstream_gene_variant LUSC-KR 9 140111957 140111957 single base substitution G A downstream_gene_variant LUSC-KR 9 140112554 140112554 single base substitution C T downstream_gene_variant LUSC-KR 9 140118353 140118353 single base substitution C G upstream_gene_variant LUSC-KR 9 140119572 140119572 single base substitution C T upstream_gene_variant LUSC-KR 9 140120294 140120294 single base substitution G T upstream_gene_variant LUSC-KR 9 140120827 140120827 single base substitution C G upstream_gene_variant LUSC-US 9 140110455 140110455 single base substitution T C downstream_gene_variant LUSC-US 9 140115307 140115307 single base substitution G C missense_variant Q120E 358C>G MALY-DE 9 140117166 140117166 single base substitution G C upstream_gene_variant MELA-AU 9 140109922 140109922 single base substitution C T downstream_gene_variant MELA-AU 9 140110118 140110118 single base substitution C T downstream_gene_variant MELA-AU 9 140110307 140110307 single base substitution G A downstream_gene_variant MELA-AU 9 140110578 140110578 single base substitution G A downstream_gene_variant MELA-AU 9 140111591 140111591 single base substitution C T downstream_gene_variant MELA-AU 9 140111846 140111846 single base substitution G A downstream_gene_variant MELA-AU 9 140112199 140112199 single base substitution C G downstream_gene_variant MELA-AU 9 140112383 140112383 single base substitution G A downstream_gene_variant MELA-AU 9 140112609 140112609 single base substitution G C downstream_gene_variant MELA-AU 9 140113113 140113113 single base substitution C T downstream_gene_variant MELA-AU 9 140114118 140114118 single base substitution T A downstream_gene_variant MELA-AU 9 140114223 140114223 single base substitution G A downstream_gene_variant MELA-AU 9 140114643 140114643 single base substitution G T downstream_gene_variant MELA-AU 9 140114681 140114681 single base substitution G A downstream_gene_variant MELA-AU 9 140115371 140115372 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P98L 293CC>TT MELA-AU 9 140115796 140115796 single base substitution G A intron_variant MELA-AU 9 140115796 140115796 single base substitution G A upstream_gene_variant MELA-AU 9 140116156 140116156 single base substitution G A upstream_gene_variant MELA-AU 9 140116587 140116587 single base substitution G A upstream_gene_variant MELA-AU 9 140117577 140117577 single base substitution G A upstream_gene_variant MELA-AU 9 140117901 140117901 single base substitution G A upstream_gene_variant MELA-AU 9 140118073 140118073 single base substitution C T upstream_gene_variant MELA-AU 9 140118123 140118123 single base substitution G A upstream_gene_variant MELA-AU 9 140118139 140118139 single base substitution C T upstream_gene_variant MELA-AU 9 140118140 140118140 single base substitution C T upstream_gene_variant MELA-AU 9 140118161 140118161 single base substitution C T upstream_gene_variant MELA-AU 9 140118965 140118965 single base substitution T C upstream_gene_variant MELA-AU 9 140119297 140119297 single base substitution G A upstream_gene_variant MELA-AU 9 140119572 140119572 single base substitution C T upstream_gene_variant MELA-AU 9 140119585 140119585 single base substitution C T upstream_gene_variant MELA-AU 9 140119719 140119719 single base substitution C T upstream_gene_variant MELA-AU 9 140119742 140119742 single base substitution C T upstream_gene_variant MELA-AU 9 140119827 140119827 single base substitution G A upstream_gene_variant MELA-AU 9 140120387 140120387 single base substitution C T upstream_gene_variant MELA-AU 9 140120433 140120433 single base substitution C T upstream_gene_variant MELA-AU 9 140120702 140120703 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 140120798 140120798 single base substitution G A upstream_gene_variant ORCA-IN 9 140109882 140109882 single base substitution C T downstream_gene_variant ORCA-IN 9 140110119 140110119 single base substitution C A downstream_gene_variant ORCA-IN 9 140110280 140110280 single base substitution C A downstream_gene_variant ORCA-IN 9 140115044 140115044 single base substitution G T missense_variant N207K 621C>A OV-AU 9 140111335 140111335 single base substitution G A downstream_gene_variant OV-AU 9 140112973 140112973 single base substitution G C downstream_gene_variant OV-AU 9 140114807 140114807 single base substitution G A 3_prime_UTR_variant PACA-AU 9 140110484 140110484 single base substitution G A downstream_gene_variant PACA-AU 9 140115302 140115302 single base substitution G A synonymous_variant Y121Y 363C>T PACA-AU 9 140120105 140120105 single base substitution C A upstream_gene_variant PACA-AU 9 140120276 140120276 single base substitution G T upstream_gene_variant PACA-CA 9 140110617 140110617 single base substitution G T downstream_gene_variant PACA-CA 9 140110654 140110654 single base substitution C T downstream_gene_variant PACA-CA 9 140112397 140112397 deletion of <=200bp C - downstream_gene_variant PACA-CA 9 140115506 140115506 single base substitution A C synonymous_variant A53A 159T>G PACA-CA 9 140118475 140118475 single base substitution A C upstream_gene_variant PAEN-AU 9 140116776 140116776 single base substitution T G upstream_gene_variant PBCA-DE 9 140117934 140117934 insertion of <=200bp - C upstream_gene_variant PBCA-DE 9 140120095 140120095 single base substitution G A upstream_gene_variant PRAD-CA 9 140111580 140111580 single base substitution G A downstream_gene_variant PRAD-CA 9 140111832 140111832 single base substitution G C downstream_gene_variant PRAD-CA 9 140113407 140113407 single base substitution G A downstream_gene_variant PRAD-CA 9 140118214 140118214 single base substitution A G upstream_gene_variant PRAD-US 9 140115423 140115423 insertion of <=200bp - C frameshift_variant D81E? RECA-EU 9 140118057 140118057 single base substitution A G upstream_gene_variant RECA-EU 9 140119852 140119852 single base substitution C G upstream_gene_variant SKCA-BR 9 140110417 140110417 single base substitution A G downstream_gene_variant SKCA-BR 9 140112571 140112571 single base substitution G A downstream_gene_variant SKCA-BR 9 140113865 140113866 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 9 140115407 140115407 single base substitution T C synonymous_variant E86E 258A>G SKCA-BR 9 140115431 140115431 single base substitution A C missense_variant C78W 234T>G SKCA-BR 9 140115825 140115825 single base substitution G C intron_variant SKCA-BR 9 140115825 140115825 single base substitution G C upstream_gene_variant SKCA-BR 9 140116342 140116342 single base substitution T C upstream_gene_variant SKCA-BR 9 140116809 140116809 single base substitution T C upstream_gene_variant SKCA-BR 9 140117354 140117354 single base substitution C T upstream_gene_variant SKCA-BR 9 140118073 140118073 single base substitution C T upstream_gene_variant SKCA-BR 9 140118121 140118121 single base substitution G A upstream_gene_variant SKCA-BR 9 140119551 140119551 single base substitution A C upstream_gene_variant SKCM-US 9 140109922 140109922 single base substitution C T downstream_gene_variant SKCM-US 9 140110460 140110460 single base substitution C T downstream_gene_variant SKCM-US 9 140110573 140110573 single base substitution C T downstream_gene_variant SKCM-US 9 140114995 140114995 single base substitution C G missense_variant G224R 670G>C SKCM-US 9 140115071 140115071 single base substitution G A synonymous_variant D198D 594C>T SKCM-US 9 140115218 140115218 single base substitution G A synonymous_variant S149S 447C>T STAD-US 9 140110800 140110800 single base substitution C T downstream_gene_variant STAD-US 9 140110805 140110805 single base substitution C T downstream_gene_variant STAD-US 9 140110812 140110812 single base substitution G A downstream_gene_variant STAD-US 9 140115251 140115251 single base substitution G A synonymous_variant G138G 414C>T STAD-US 9 140115423 140115423 insertion of <=200bp - C frameshift_variant D81E? STAD-US 9 140115502 140115502 deletion of <=200bp G - frameshift_variant R55 THCA-SA 9 140112631 140112631 single base substitution G A downstream_gene_variant UCEC-US 9 140110210 140110210 single base substitution C T downstream_gene_variant UCEC-US 9 140110586 140110586 single base substitution G A downstream_gene_variant UCEC-US 9 140110730 140110730 single base substitution C T downstream_gene_variant UCEC-US 9 140110748 140110748 single base substitution C T downstream_gene_variant UCEC-US 9 140114925 140114925 single base substitution C T missense_variant C247Y 740G>A UCEC-US 9 140115175 140115175 single base substitution G A missense_variant H164Y 490C>T UCEC-US 9 140120100 140120100 single base substitution G T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CHC121T COSM4407048 c.292C>T p.P98S Substitution - Missense 9:137220921-137220921 - UD-SCC-2 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - PASLZM COSM5006448 c.524A>G p.Y175C Substitution - Missense 9:137220689-137220689 - TCGA-B5-A11E-01 COSM1107077 c.740G>A p.C247Y Substitution - Missense 9:137220473-137220473 - TCGA-A4-A4ZT-01 COSM3996468 c.264A>C p.A88A Substitution - coding silent 9:137220949-137220949 - 8016470 COSM3395694 c.363C>T p.Y121Y Substitution - coding silent 9:137220850-137220850 - ESCC_87 COSM5636757 c.393G>A p.A131A Substitution - coding silent 9:137220820-137220820 - SW480 COSM4656041 c.771C>A p.A257A Substitution - coding silent 9:137220442-137220442 - OSCC-GB_00220111 COSM3716261 c.621C>A p.N207K Substitution - Missense 9:137220592-137220592 - NPC15F COSM4997042 c.275C>A p.P92Q Substitution - Missense 9:137220938-137220938 - 11M COSM5577007 c.401C>T p.S134L Substitution - Missense 9:137220812-137220812 - ESCC_55 COSM5632131 c.383C>T p.S128L Substitution - Missense 9:137220830-137220830 - TCGA-AR-A24H-01 COSM1489839 c.673G>A p.G225S Substitution - Missense 9:137220540-137220540 - TCGA-BT-A3PH-01 COSM1314664 c.84C>A p.L28L Substitution - coding silent 9:137221129-137221129 - UM-SCC-4 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - TCGA-DA-A1HV-06 COSM3655986 c.447C>T p.S149S Substitution - coding silent 9:137220766-137220766 - SW48 COSM1461354 c.241delG p.D81fs*38 Deletion - Frameshift 9:137220972-137220972 - TCGA-FU-A5XV-01 COSM4844205 c.694G>A p.E232K Substitution - Missense 9:137220519-137220519 - T3064 COSM3088944 c.685delG p.A229fs*>33 Deletion - Frameshift 9:137220528-137220528 - WSU-HN6 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - UM-SCC-11B COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - ORL-48 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - SCC-9 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - SNU-175 COSM3088956 c.140C>T p.A47V Substitution - Missense 9:137221073-137221073 - PCSI_0047_Pa_P_526 COSM3788219 c.159T>G p.A53A Substitution - coding silent 9:137221054-137221054 - BHY COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - LUAD-D01603 COSM338102 c.729T>C p.C243C Substitution - coding silent 9:137220484-137220484 - TCGA-FP-A4BE-01 COSM3906016 c.414C>T p.G138G Substitution - coding silent 9:137220799-137220799 - sysucc-880T COSM5463781 c.231C>A p.A77A Substitution - coding silent 9:137220982-137220982 - 313 COSM1742087 c.203C>G p.S68* Substitution - Nonsense 9:137221010-137221010 - CSCC-16-T COSM4566587 c.419_420CC>TT p.P140L Substitution - Missense 9:137220793-137220794 - 22T COSM3716261 c.621C>A p.N207K Substitution - Missense 9:137220592-137220592 - 2293772 COSM4607273 c.322C>T p.P108S Substitution - Missense 9:137220891-137220891 - Pat_44_A COSM5875943 c.43G>A p.G15S Substitution - Missense 9:137221170-137221170 - CSCC-11-T COSM4459553 c.112C>T p.P38S Substitution - Missense 9:137221101-137221101 - CSCC-37-T COSM4564750 c.141_142CC>TT p.P48S Substitution - Missense 9:137221071-137221072 - PTC-54C COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - TCGA-BT-A3PH-01 COSM1314663 c.561C>G p.P187P Substitution - coding silent 9:137220652-137220652 - 587376 COSM1223961 c.398C>A p.S133Y Substitution - Missense 9:137220815-137220815 - UPCI:SCC090 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - SCC-15 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - CCK81 COSM3088948 c.506A>G p.Q169R Substitution - Missense 9:137220707-137220707 - Detroit_562 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - CHC121T COSM4407048 c.292C>T p.P98S Substitution - Missense 9:137220921-137220921 - WSU-HN12 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - 325 COSM3723393 c.695A>G p.E232G Substitution - Missense 9:137220518-137220518 - PTC-50C COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - ESO-007 COSM1264373 c.614C>G p.A205G Substitution - Missense 9:137220599-137220599 - UM-SCC-17B COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - TCGA-E9-A244-01 COSM3848113 c.111C>G p.H37Q Substitution - Missense 9:137221102-137221102 - CSCC-35-T COSM4508231 c.768C>T p.S256S Substitution - coding silent 9:137220445-137220445 - CSCC-55-T COSM4517651 c.390_391GG>AA p.A131T Substitution - Missense 9:137220822-137220823 - TCGA-66-2785-01 COSM753053 c.358C>G p.Q120E Substitution - Missense 9:137220855-137220855 - TCGA-D1-A15X-01 COSM1107078 c.490C>T p.H164Y Substitution - Missense 9:137220723-137220723 - 367 COSM3723392 c.149T>C p.F50S Substitution - Missense 9:137221064-137221064 - WSU-HN13 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - CSCC-35-T COSM4487859 c.323C>T p.P108L Substitution - Missense 9:137220890-137220890 - WSU-HN30 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - ESO-2143 COSM1264374 c.574G>A p.E192K Substitution - Missense 9:137220639-137220639 - Pat_11_A COSM5577007 c.401C>T p.S134L Substitution - Missense 9:137220812-137220812 - UM-SCC-47 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - TCGA-HT-7854-01 COSM3929963 c.737C>T p.A246V Substitution - Missense 9:137220476-137220476 - WSU-HN8 COSM3088954 c.271A>C p.T91P Substitution - Missense 9:137220942-137220942 - TCGA-ER-A19P-06 COSM3655984 c.670G>C p.G224R Substitution - Missense 9:137220543-137220543 - T2950 COSM4722082 c.153G>A p.P51P Substitution - coding silent 9:137221060-137221060 - TCGA-EE-A29D-06 COSM3655985 c.594C>T p.D198D Substitution - coding silent 9:137220619-137220619 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.512765;Hs.512767 9q34.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - C Frameshift p.D81Gfs*20 c.241dupG 9 140115424 PRAD C G Missense p.G224R c.670G>C 9 140114995 CM C T Missense p.A136T c.406G>A 9 140115259 HNSC C T Missense p.E192K c.574G>A 9 140115091 ESCA C T Missense p.G225S c.673G>A 9 140114992 BRCA C T Synonymous p.R252R c.756G>A 9 140114909 HNSC G A Missense p.A246V c.737C>T 9 140114928 LGG G A Missense p.P157S c.469C>T 9 140115196 CM G A Missense p.R99C c.295C>T 9 140115370 STAD G A Synonymous p.L211L c.631C>T 9 140115034 CM G A Synonymous p.S149S c.447C>T 9 140115218 CM G C Missense p.A205G c.614C>G 9 140115051 ESCA G C Synonymous p.P187P c.561C>G 9 140115104 BLCA G T Synonymous p.L28L c.84C>A 9 140115581 BLCA