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 BLCA 1 20140951 20140951 + Missense_Mutation SNP C C T TCGA-UY-A9PD-01A-11D-A38G-08 TCGA-UY-A9PD-10A-01D-A38J-08 g.chr1:20140951C>T c.644G>A c.(643-645)tGc>tAc p.C215Y BLCA 1 20141360 20141360 + Missense_Mutation SNP A A T TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr1:20141360A>T c.235T>A c.(235-237)Tcc>Acc p.S79T BLCA 1 20141394 20141394 + Silent SNP C C T TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr1:20141394C>T c.201G>A c.(199-201)ctG>ctA p.L67L BRCA 1 20141048 20141048 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr1:20141048T>G c.547A>C c.(547-549)Acc>Ccc p.T183P BRCA 1 20141288 20141288 + Missense_Mutation SNP C C T TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr1:20141288C>T c.307G>A c.(307-309)Gag>Aag p.E103K COAD 1 20141577 20141577 + Silent SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:20141577G>T c.18C>A c.(16-18)acC>acA p.T6T COADREAD 1 20141577 20141577 + Silent SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:20141577G>T c.18C>A c.(16-18)acC>acA p.T6T ESCA 1 20141125 20141125 + Missense_Mutation SNP G G A TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr1:20141125G>A c.470C>T c.(469-471)gCg>gTg p.A157V GBMLGG 1 20141126 20141126 + Missense_Mutation SNP C C T TCGA-DB-A4XE-01A-11D-A27K-08 TCGA-DB-A4XE-10A-01D-A27N-08 g.chr1:20141126C>T c.469G>A c.(469-471)Gcg>Acg p.A157T KIPAN 1 20141319 20141319 + Silent SNP G G C TCGA-B0-5085-01A-01D-1462-08 TCGA-B0-5085-11A-01D-1462-08 g.chr1:20141319G>C c.276C>G c.(274-276)ccC>ccG p.P92P KIRC 1 20141319 20141319 + Silent SNP G G C TCGA-B0-5085-01A-01D-1462-08 TCGA-B0-5085-11A-01D-1462-08 g.chr1:20141319G>C c.276C>G c.(274-276)ccC>ccG p.P92P LGG 1 20141126 20141126 + Missense_Mutation SNP C C T TCGA-DB-A4XE-01A-11D-A27K-08 TCGA-DB-A4XE-10A-01D-A27N-08 g.chr1:20141126C>T c.469G>A c.(469-471)Gcg>Acg p.A157T LUAD 1 20141127 20141127 + Silent SNP G G C TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr1:20141127G>C c.468C>G c.(466-468)gcC>gcG p.A156A LUAD 1 20141245 20141245 + Missense_Mutation SNP G G A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr1:20141245G>A c.350C>T c.(349-351)tCg>tTg p.S117L LUSC 1 20141183 20141183 + Nonsense_Mutation SNP C C A TCGA-39-5016-01A-01D-1441-08 TCGA-39-5016-11A-01D-1441-08 g.chr1:20141183C>A c.412G>T c.(412-414)Gga>Tga p.G138* LUSC 1 20141334 20141334 + Missense_Mutation SNP C C G TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr1:20141334C>G c.261G>C c.(259-261)aaG>aaC p.K87N LUSC 1 20141492 20141492 + Nonsense_Mutation SNP C C A TCGA-21-5782-01A-01D-1632-08 TCGA-21-5782-10A-01D-1632-08 g.chr1:20141492C>A c.103G>T c.(103-105)Gaa>Taa p.E35* PRAD 1 20141158 20141158 + Missense_Mutation SNP C C T TCGA-YL-A9WH-01A-11D-A377-08 TCGA-YL-A9WH-10A-01D-A37A-08 g.chr1:20141158C>T c.437G>A c.(436-438)aGt>aAt p.S146N PRAD 1 20141239 20141239 + Missense_Mutation SNP C C A TCGA-XK-AAK1-01A-11D-A41K-08 TCGA-XK-AAK1-10A-01D-A41N-08 g.chr1:20141239C>A c.356G>T c.(355-357)tGt>tTt p.C119F PRAD 1 20141347 20141347 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:20141347G>A c.248C>T c.(247-249)cCg>cTg p.P83L SKCM 1 20140998 20140998 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:20140998G>A c.597C>T c.(595-597)ctC>ctT p.L199L SKCM 1 20141037 20141037 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:20141037G>A c.558C>T c.(556-558)atC>atT p.I186I SKCM 1 20141139 20141139 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:20141139G>A c.456C>T c.(454-456)gcC>gcT p.A152A SKCM 1 20141231 20141231 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr1:20141231C>T c.364G>A c.(364-366)Ggg>Agg p.G122R SKCM 1 20141286 20141286 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:20141286C>T c.309G>A c.(307-309)gaG>gaA p.E103E SKCM 1 20141519 20141519 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:20141519G>A c.76C>T c.(76-78)Cct>Tct p.P26S

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 1 20141319 20141319 single base substitution G A synonymous_variant P92P 276C>T BLCA-US 1 20141360 20141360 single base substitution A T missense_variant S79T 235T>A BRCA-EU 1 20138175 20138175 single base substitution C G downstream_gene_variant BRCA-EU 1 20139589 20139589 single base substitution G T downstream_gene_variant BRCA-EU 1 20139777 20139777 single base substitution C G downstream_gene_variant BRCA-EU 1 20139889 20139889 single base substitution C T downstream_gene_variant BRCA-EU 1 20142248 20142248 single base substitution A T upstream_gene_variant BRCA-EU 1 20143002 20143002 single base substitution T C upstream_gene_variant BRCA-EU 1 20143310 20143310 single base substitution C T upstream_gene_variant BRCA-EU 1 20143600 20143600 single base substitution C T upstream_gene_variant BRCA-EU 1 20144874 20144874 single base substitution C A upstream_gene_variant BRCA-EU 1 20146226 20146226 single base substitution C G upstream_gene_variant BRCA-EU 1 20146278 20146278 single base substitution C T upstream_gene_variant BRCA-EU 1 20146344 20146344 single base substitution G T upstream_gene_variant BRCA-FR 1 20136903 20136903 single base substitution G A downstream_gene_variant BRCA-FR 1 20145842 20145842 single base substitution G A upstream_gene_variant BRCA-FR 1 20146226 20146226 single base substitution C G upstream_gene_variant BRCA-UK 1 20142064 20142064 single base substitution C T upstream_gene_variant BRCA-UK 1 20146344 20146344 single base substitution G T upstream_gene_variant BRCA-US 1 20141048 20141048 single base substitution T G missense_variant T183P 547A>C BRCA-US 1 20141288 20141288 single base substitution C T missense_variant E103K 307G>A BTCA-JP 1 20140996 20140996 single base substitution G A missense_variant P200L 599C>T BTCA-JP 1 20141663 20141663 single base substitution G A 5_prime_UTR_variant CLLE-ES 1 20145941 20145941 single base substitution G T upstream_gene_variant COAD-US 1 20141512 20141512 single base substitution C A missense_variant G28V 83G>T COAD-US 1 20141528 20141528 single base substitution C T missense_variant A23T 67G>A COAD-US 1 20141577 20141577 single base substitution G T synonymous_variant T6T 18C>A COCA-CN 1 20141263 20141263 single base substitution T C missense_variant Q111R 332A>G COCA-CN 1 20141309 20141309 single base substitution T A missense_variant I96F 286A>T COCA-CN 1 20141348 20141348 single base substitution G A missense_variant P83S 247C>T ESAD-UK 1 20135854 20135854 single base substitution G T downstream_gene_variant ESAD-UK 1 20140643 20140643 single base substitution C T 3_prime_UTR_variant ESAD-UK 1 20141781 20141781 single base substitution C G upstream_gene_variant ESAD-UK 1 20142394 20142394 single base substitution G T upstream_gene_variant ESAD-UK 1 20145584 20145584 single base substitution A G upstream_gene_variant ESCA-CN 1 20141010 20141010 single base substitution G A synonymous_variant L195L 585C>T KIRC-US 1 20141319 20141319 single base substitution G C synonymous_variant P92P 276C>G LAML-KR 1 20141528 20141528 single base substitution C T missense_variant A23T 67G>A LGG-US 1 20141126 20141126 single base substitution C T missense_variant A157T 469G>A LINC-JP 1 20136433 20136433 single base substitution G C downstream_gene_variant LINC-JP 1 20140121 20140121 single base substitution T C downstream_gene_variant LINC-JP 1 20141260 20141260 single base substitution G C missense_variant P112R 335C>G LINC-JP 1 20146043 20146043 single base substitution C T upstream_gene_variant LIRI-JP 1 20136219 20136219 single base substitution A C downstream_gene_variant LIRI-JP 1 20139907 20139907 single base substitution C T downstream_gene_variant LIRI-JP 1 20141929 20141929 single base substitution T C upstream_gene_variant LIRI-JP 1 20143274 20143274 single base substitution G T upstream_gene_variant LIRI-JP 1 20143380 20143380 single base substitution A G upstream_gene_variant LIRI-JP 1 20144769 20144769 single base substitution A G upstream_gene_variant LIRI-JP 1 20144919 20144919 single base substitution A T upstream_gene_variant LIRI-JP 1 20145343 20145343 single base substitution G T upstream_gene_variant LIRI-JP 1 20146062 20146062 single base substitution A G upstream_gene_variant LUSC-KR 1 20140224 20140224 single base substitution C A downstream_gene_variant LUSC-KR 1 20140901 20140901 single base substitution C T 3_prime_UTR_variant LUSC-KR 1 20144149 20144149 single base substitution C A upstream_gene_variant LUSC-US 1 20141183 20141183 single base substitution C A stop_gained G138* 412G>T LUSC-US 1 20141334 20141334 single base substitution C G missense_variant K87N 261G>C LUSC-US 1 20141492 20141492 single base substitution C A stop_gained E35* 103G>T MELA-AU 1 20135813 20135813 single base substitution G A downstream_gene_variant MELA-AU 1 20135889 20135889 single base substitution G A downstream_gene_variant MELA-AU 1 20136405 20136405 single base substitution C T downstream_gene_variant MELA-AU 1 20136469 20136469 single base substitution C T downstream_gene_variant MELA-AU 1 20136500 20136500 single base substitution C T downstream_gene_variant MELA-AU 1 20136508 20136508 single base substitution C T downstream_gene_variant MELA-AU 1 20136743 20136743 single base substitution C T downstream_gene_variant MELA-AU 1 20137311 20137311 single base substitution C T downstream_gene_variant MELA-AU 1 20137621 20137621 single base substitution C T downstream_gene_variant MELA-AU 1 20138113 20138113 single base substitution C T downstream_gene_variant MELA-AU 1 20138117 20138117 single base substitution C T downstream_gene_variant MELA-AU 1 20138207 20138207 single base substitution C T downstream_gene_variant MELA-AU 1 20138219 20138219 single base substitution C T downstream_gene_variant MELA-AU 1 20138325 20138325 single base substitution G A downstream_gene_variant MELA-AU 1 20138412 20138412 single base substitution G A downstream_gene_variant MELA-AU 1 20138891 20138891 single base substitution C T downstream_gene_variant MELA-AU 1 20139154 20139154 single base substitution G T downstream_gene_variant MELA-AU 1 20139161 20139161 single base substitution G A downstream_gene_variant MELA-AU 1 20139207 20139207 single base substitution G A downstream_gene_variant MELA-AU 1 20139258 20139258 single base substitution G T downstream_gene_variant MELA-AU 1 20139435 20139435 single base substitution C T downstream_gene_variant MELA-AU 1 20139702 20139702 single base substitution G A downstream_gene_variant MELA-AU 1 20139853 20139853 single base substitution C T downstream_gene_variant MELA-AU 1 20139908 20139908 single base substitution G A downstream_gene_variant MELA-AU 1 20140408 20140408 single base substitution C T downstream_gene_variant MELA-AU 1 20140495 20140495 single base substitution G A downstream_gene_variant MELA-AU 1 20141388 20141388 single base substitution G A synonymous_variant L69L 207C>T MELA-AU 1 20141811 20141811 single base substitution C T upstream_gene_variant MELA-AU 1 20141975 20141975 single base substitution C T upstream_gene_variant MELA-AU 1 20142443 20142443 single base substitution C T upstream_gene_variant MELA-AU 1 20142732 20142732 single base substitution C T upstream_gene_variant MELA-AU 1 20143007 20143007 single base substitution C T upstream_gene_variant MELA-AU 1 20143104 20143104 single base substitution C A upstream_gene_variant MELA-AU 1 20143131 20143131 single base substitution T A upstream_gene_variant MELA-AU 1 20143579 20143579 single base substitution G A upstream_gene_variant MELA-AU 1 20143653 20143653 single base substitution C G upstream_gene_variant MELA-AU 1 20144016 20144016 single base substitution G A upstream_gene_variant MELA-AU 1 20144764 20144764 single base substitution G A upstream_gene_variant MELA-AU 1 20144932 20144932 single base substitution G A upstream_gene_variant MELA-AU 1 20144988 20144989 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 20145006 20145006 single base substitution G A upstream_gene_variant MELA-AU 1 20145647 20145647 single base substitution C T upstream_gene_variant ORCA-IN 1 20138857 20138857 single base substitution C T downstream_gene_variant ORCA-IN 1 20139868 20139868 single base substitution T A downstream_gene_variant ORCA-IN 1 20141293 20141293 single base substitution T C missense_variant D101G 302A>G ORCA-IN 1 20145941 20145941 single base substitution G A upstream_gene_variant OV-AU 1 20136033 20136033 single base substitution A G downstream_gene_variant OV-AU 1 20136815 20136815 single base substitution T C downstream_gene_variant OV-AU 1 20146550 20146550 single base substitution A C upstream_gene_variant PACA-AU 1 20146620 20146620 single base substitution G T upstream_gene_variant PACA-CA 1 20140482 20140482 insertion of <=200bp - A downstream_gene_variant PACA-CA 1 20142134 20142134 single base substitution G T upstream_gene_variant PACA-CA 1 20142405 20142406 deletion of <=200bp CA - upstream_gene_variant PACA-CA 1 20144711 20144711 single base substitution G A upstream_gene_variant PBCA-DE 1 20137110 20137110 single base substitution C A downstream_gene_variant PBCA-DE 1 20137126 20137126 single base substitution C A downstream_gene_variant RECA-EU 1 20137169 20137169 single base substitution T A downstream_gene_variant RECA-EU 1 20141088 20141088 single base substitution G A synonymous_variant I169I 507C>T RECA-EU 1 20144058 20144058 single base substitution C A upstream_gene_variant RECA-EU 1 20144989 20144989 single base substitution C T upstream_gene_variant SKCA-BR 1 20138447 20138447 single base substitution C T downstream_gene_variant SKCA-BR 1 20140932 20140932 single base substitution G A synonymous_variant S221S 663C>T SKCA-BR 1 20141291 20141291 single base substitution G A missense_variant H102Y 304C>T SKCA-BR 1 20142447 20142447 single base substitution A G upstream_gene_variant SKCM-US 1 20140998 20140998 single base substitution G A synonymous_variant L199L 597C>T SKCM-US 1 20141037 20141037 single base substitution G A synonymous_variant I186I 558C>T SKCM-US 1 20141139 20141139 single base substitution G A synonymous_variant A152A 456C>T SKCM-US 1 20141231 20141231 single base substitution C T missense_variant G122R 364G>A SKCM-US 1 20141286 20141286 single base substitution C T synonymous_variant E103E 309G>A SKCM-US 1 20141519 20141519 single base substitution G A missense_variant P26S 76C>T STAD-US 1 20141050 20141050 single base substitution A T missense_variant L182H 545T>A THCA-SA 1 20141283 20141283 single base substitution C T synonymous_variant A104A 312G>A THCA-SA 1 20141443 20141443 single base substitution C T missense_variant R51Q 152G>A THCA-US 1 20141106 20141106 single base substitution G A synonymous_variant A163A 489C>T UCEC-US 1 20141040 20141040 single base substitution G A synonymous_variant I185I 555C>T UCEC-US 1 20141107 20141107 single base substitution G A missense_variant A163V 488C>T UCEC-US 1 20141384 20141384 single base substitution G A synonymous_variant L71L 211C>T UCEC-US 1 20141514 20141514 single base substitution A G synonymous_variant A27A 81T>C UCEC-US 1 20141521 20141521 single base substitution G A missense_variant A25V 74C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-D7-A4YY-01 COSM4026941 c.545T>A p.L182H Substitution - Missense 1:19814557-19814557 - TCGA-21-5782-01 COSM678176 c.103G>T p.E35* Substitution - Nonsense 1:19814999-19814999 - TCGA-EE-A2MR-06 COSM3481566 c.558C>T p.I186I Substitution - coding silent 1:19814544-19814544 - TCGA-FW-A3R5-06 COSM3864099 c.456C>T p.A152A Substitution - coding silent 1:19814646-19814646 - TCGA-BS-A0UV-01 COSM902199 c.74C>T p.A25V Substitution - Missense 1:19815028-19815028 - TCGA-EE-A2MS-06 COSM3481567 c.364G>A p.G122R Substitution - Missense 1:19814738-19814738 - TCGA-66-2759-01 COSM678177 c.261G>C p.K87N Substitution - Missense 1:19814841-19814841 - 12-P2194 COSM4576752 c.476T>C p.L159P Substitution - Missense 1:19814626-19814626 - BD225T COSM5508662 c.599C>T p.P200L Substitution - Missense 1:19814503-19814503 - TCGA-39-5016-01 COSM678178 c.412G>T p.G138* Substitution - Nonsense 1:19814690-19814690 - LIM2551 COSM4643630 c.163C>A p.L55M Substitution - Missense 1:19814939-19814939 - 308_T COSM3976844 c.404G>T p.S135I Substitution - Missense 1:19814698-19814698 - YUWAND COSM1687122 c.350C>T p.S117L Substitution - Missense 1:19814752-19814752 - TCGA-BS-A0UF-01 COSM902198 c.81T>C p.A27A Substitution - coding silent 1:19815021-19815021 - TCGA-DK-A1A3-01 COSM414710 c.235T>A p.S79T Substitution - Missense 1:19814867-19814867 - ESCC_BICR_042T COSM5443618 c.585C>T p.L195L Substitution - coding silent 1:19814517-19814517 - Pat_45_A COSM5845095 c.130C>T p.R44W Substitution - Missense 1:19814972-19814972 - TCGA-FW-A3R5-06 COSM3864101 c.76C>T p.P26S Substitution - Missense 1:19815026-19815026 - CN-AML-CR-14-Dx COSM3750763 c.67G>A p.A23T Substitution - Missense 1:19815035-19815035 - TCGA-FW-A3R5-06 COSM3864098 c.597C>T p.L199L Substitution - coding silent 1:19814505-19814505 - C0004T COSM2212433 c.507C>T p.I169I Substitution - coding silent 1:19814595-19814595 - TCGA-C8-A3M7-01 COSM3803449 c.307G>A p.E103K Substitution - Missense 1:19814795-19814795 - TCGA-AX-A0J1-01 COSM902197 c.211C>T p.L71L Substitution - coding silent 1:19814891-19814891 - HCC47T COSM1601518 c.335C>G p.P112R Substitution - Missense 1:19814767-19814767 - S02296 COSM5689320 c.458G>T p.R153L Substitution - Missense 1:19814644-19814644 - TCGA-B5-A11N-01 COSM902196 c.488C>T p.A163V Substitution - Missense 1:19814614-19814614 - SNUH_G26_S1 COSM3997142 c.312G>A p.A104A Substitution - coding silent 1:19814790-19814790 - TCGA-DB-A4XE-01 COSM3966177 c.469G>A p.A157T Substitution - Missense 1:19814633-19814633 - B111-Tumor COSM1748077 c.276C>T p.P92P Substitution - coding silent 1:19814826-19814826 - PAPNNX COSM5005100 c.471G>A p.A157A Substitution - coding silent 1:19814631-19814631 - TCGA-A8-A0A6-01 COSM3803448 c.547A>C p.T183P Substitution - Missense 1:19814555-19814555 - TCGA-AM-5821-01 COSM3750763 c.67G>A p.A23T Substitution - Missense 1:19815035-19815035 - S01861 COSM5670910 c.513C>T p.P171P Substitution - coding silent 1:19814589-19814589 - sysucc-880T COSM5462113 c.332A>G p.Q111R Substitution - Missense 1:19814770-19814770 - TCGA-AA-3492-01 COSM1337866 c.18C>A p.T6T Substitution - coding silent 1:19815084-19815084 - B111 COSM1748077 c.276C>T p.P92P Substitution - coding silent 1:19814826-19814826 - TCGA-G4-6302-01 COSM3689267 c.83G>T p.G28V Substitution - Missense 1:19815019-19815019 - CSCC-29-T COSM4483932 c.274C>T p.P92S Substitution - Missense 1:19814828-19814828 - sysucc-834T COSM5485532 c.286A>T p.I96F Substitution - Missense 1:19814816-19814816 - SC_9037 COSM5558668 c.477A>G p.L159L Substitution - coding silent 1:19814625-19814625 - TCGA-FY-A3R6-01 COSM3369503 c.489C>T p.A163A Substitution - coding silent 1:19814613-19814613 - TCGA-B5-A11R-01 COSM902195 c.555C>T p.I185I Substitution - coding silent 1:19814547-19814547 - CSCC-7-T COSM3864101 c.76C>T p.P26S Substitution - Missense 1:19815026-19815026 - TCGA-FW-A3R5-06 COSM3864100 c.309G>A p.E103E Substitution - coding silent 1:19814793-19814793 - TCGA-B0-5085-01 COSM463751 c.276C>G p.P92P Substitution - coding silent 1:19814826-19814826 - OSCC-GB_01210111 COSM5955030 c.302A>G p.D101G Substitution - Missense 1:19814800-19814800 - 529 COSM5612283 c.103G>A p.E35K Substitution - Missense 1:19814999-19814999 - CHC205T COSM3746724 c.440C>A p.A147E Substitution - Missense 1:19814662-19814662 - HCC47 COSM1601518 c.335C>G p.P112R Substitution - Missense 1:19814767-19814767 - 61 COSM5735309 c.667A>G p.I223V Substitution - Missense 1:19814435-19814435 - HCC2998 COSM2212434 c.470C>T p.A157V Substitution - Missense 1:19814632-19814632 - STC252 COSM5052970 c.393A>G p.A131A Substitution - coding silent 1:19814709-19814709 - J10_T COSM3976845 c.152G>T p.R51L Substitution - Missense 1:19814950-19814950 - SNUH_G76_S1 COSM3997142 c.312G>A p.A104A Substitution - coding silent 1:19814790-19814790 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.124835 1p36.13

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T Missense p.S79T c.235T>A 1 20141360 BLCA C A Nonsense p.E35* c.103G>T 1 20141492 LUSC C A Nonsense p.G138* c.412G>T 1 20141183 LUSC C G Missense p.K87N c.261G>C 1 20141334 LUSC C T Missense p.G122R c.364G>A 1 20141231 CM G A Nonsense p.R179* c.535C>T 1 20141060 LUAD G A Synonymous p.A163A c.489C>T 1 20141106 THCA G A Synonymous p.I185I c.555C>T 1 20141040 UCEC G A Synonymous p.L160L c.480C>T 1 20141115 CM G C Synonymous p.P92P c.276C>G 1 20141319 RCCC G T Missense p.L55M c.163C>A 1 20141432 CM