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 10 99327762 99327762 + Silent SNP C C T TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr10:99327762C>T c.162C>T c.(160-162)ttC>ttT p.F54F BLCA 10 99327844 99327844 + Missense_Mutation SNP G G A TCGA-GD-A3OQ-01A-32D-A21Z-08 TCGA-GD-A3OQ-10A-01D-A21Z-08 g.chr10:99327844G>A c.244G>A c.(244-246)Gac>Aac p.D82N BLCA 10 99329961 99329961 + Missense_Mutation SNP C C T TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr10:99329961C>T c.365C>T c.(364-366)cCg>cTg p.P122L BRCA 10 99330208 99330208 + Silent SNP C C T TCGA-BH-A0AW-01A-11W-A071-09 TCGA-BH-A0AW-10A-01W-A071-09 g.chr10:99330208C>T c.612C>T c.(610-612)ctC>ctT p.L204L COAD 10 99327783 99327783 + Silent SNP C C T TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr10:99327783C>T c.183C>T c.(181-183)ttC>ttT p.F61F COAD 10 99329931 99329931 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr10:99329931G>A c.335G>A c.(334-336)cGc>cAc p.R112H COAD 10 99329960 99329960 + Missense_Mutation SNP C C T TCGA-AA-A00O-01A-02W-A00E-09 TCGA-AA-A00O-10A-01W-A00E-09 g.chr10:99329960C>T c.364C>T c.(364-366)Ccg>Tcg p.P122S COAD 10 99330059 99330059 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:99330059C>A c.463C>A c.(463-465)Ctg>Atg p.L155M COADREAD 10 99327783 99327783 + Silent SNP C C T TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr10:99327783C>T c.183C>T c.(181-183)ttC>ttT p.F61F COADREAD 10 99329931 99329931 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr10:99329931G>A c.335G>A c.(334-336)cGc>cAc p.R112H COADREAD 10 99329960 99329960 + Missense_Mutation SNP C C T TCGA-AA-A00O-01A-02W-A00E-09 TCGA-AA-A00O-10A-01W-A00E-09 g.chr10:99329960C>T c.364C>T c.(364-366)Ccg>Tcg p.P122S COADREAD 10 99329964 99329964 + Missense_Mutation SNP C C T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr10:99329964C>T c.368C>T c.(367-369)cCg>cTg p.P123L COADREAD 10 99330059 99330059 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:99330059C>A c.463C>A c.(463-465)Ctg>Atg p.L155M ESCA 10 99330073 99330073 + Missense_Mutation SNP G G T TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr10:99330073G>T c.477G>T c.(475-477)aaG>aaT p.K159N GBMLGG 10 99329915 99329915 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:99329915G>A c.319G>A c.(319-321)Gat>Aat p.D107N KICH 10 99329915 99329915 + Missense_Mutation SNP G G A TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr10:99329915G>A c.319G>A c.(319-321)Gat>Aat p.D107N KIPAN 10 99327795 99327795 + Silent SNP G G A TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chr10:99327795G>A c.195G>A c.(193-195)aaG>aaA p.K65K KIPAN 10 99329915 99329915 + Missense_Mutation SNP G G A TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr10:99329915G>A c.319G>A c.(319-321)Gat>Aat p.D107N KIPAN 10 99330070 99330070 + Silent SNP C C A TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr10:99330070C>A c.474C>A c.(472-474)ggC>ggA p.G158G KIRP 10 99327795 99327795 + Silent SNP G G A TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chr10:99327795G>A c.195G>A c.(193-195)aaG>aaA p.K65K KIRP 10 99330070 99330070 + Silent SNP C C A TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr10:99330070C>A c.474C>A c.(472-474)ggC>ggA p.G158G LGG 10 99329915 99329915 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:99329915G>A c.319G>A c.(319-321)Gat>Aat p.D107N LUAD 10 99327766 99327766 + Missense_Mutation SNP G G T TCGA-97-8172-01A-11D-2284-08 TCGA-97-8172-10A-01D-2284-08 g.chr10:99327766G>T c.166G>T c.(166-168)Gac>Tac p.D56Y LUAD 10 99329918 99329918 + Missense_Mutation SNP G G A TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chr10:99329918G>A c.322G>A c.(322-324)Gag>Aag p.E108K LUSC 10 99330049 99330049 + Silent SNP G G A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr10:99330049G>A c.453G>A c.(451-453)ctG>ctA p.L151L PAAD 10 99327681 99327681 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:99327681G>A c.81G>A c.(79-81)gaG>gaA p.E27E PAAD 10 99330200 99330200 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:99330200A>G c.604A>G c.(604-606)Aca>Gca p.T202A READ 10 99329964 99329964 + Missense_Mutation SNP C C T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr10:99329964C>T c.368C>T c.(367-369)cCg>cTg p.P123L

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 10 99330097 99330097 single base substitution G A synonymous_variant L167L 501G>A BLCA-US 10 99327844 99327844 single base substitution G A missense_variant D82N 244G>A BOCA-FR 10 99291516 99291516 single base substitution G A intron_variant BRCA-EU 10 99255444 99255444 single base substitution C G upstream_gene_variant BRCA-EU 10 99256679 99256679 single base substitution A G upstream_gene_variant BRCA-EU 10 99259712 99259712 single base substitution G T intron_variant BRCA-EU 10 99263207 99263207 single base substitution C A intron_variant BRCA-EU 10 99265425 99265425 single base substitution T A intron_variant BRCA-EU 10 99265601 99265601 single base substitution C A intron_variant BRCA-EU 10 99266431 99266431 insertion of <=200bp - C intron_variant BRCA-EU 10 99266837 99266837 single base substitution A C intron_variant BRCA-EU 10 99267012 99267012 single base substitution G T intron_variant BRCA-EU 10 99268102 99268102 single base substitution G C intron_variant BRCA-EU 10 99268791 99268791 single base substitution T C intron_variant BRCA-EU 10 99269407 99269407 deletion of <=200bp T - intron_variant BRCA-EU 10 99271398 99271398 single base substitution G C intron_variant BRCA-EU 10 99271705 99271705 single base substitution G A intron_variant BRCA-EU 10 99271961 99271961 single base substitution G A intron_variant BRCA-EU 10 99272004 99272004 single base substitution G C intron_variant BRCA-EU 10 99272526 99272526 single base substitution G A intron_variant BRCA-EU 10 99273522 99273522 single base substitution T A intron_variant BRCA-EU 10 99273924 99273924 single base substitution G A intron_variant BRCA-EU 10 99274538 99274538 single base substitution C T intron_variant BRCA-EU 10 99274971 99274971 single base substitution C T intron_variant BRCA-EU 10 99278846 99278846 single base substitution C T intron_variant BRCA-EU 10 99279276 99279276 single base substitution C A intron_variant BRCA-EU 10 99279321 99279321 single base substitution G T intron_variant BRCA-EU 10 99280950 99280950 single base substitution C T intron_variant BRCA-EU 10 99281735 99281735 single base substitution T A intron_variant BRCA-EU 10 99281755 99281755 single base substitution A C intron_variant BRCA-EU 10 99285799 99285799 single base substitution G A intron_variant BRCA-EU 10 99287728 99287728 single base substitution C A intron_variant BRCA-EU 10 99289195 99289195 single base substitution G A intron_variant BRCA-EU 10 99290225 99290225 single base substitution G C intron_variant BRCA-EU 10 99290713 99290713 single base substitution C T intron_variant BRCA-EU 10 99291357 99291357 single base substitution G A intron_variant BRCA-EU 10 99291779 99291779 single base substitution G A intron_variant BRCA-EU 10 99291956 99291956 single base substitution C G intron_variant BRCA-EU 10 99292559 99292559 insertion of <=200bp - T intron_variant BRCA-EU 10 99294705 99294705 single base substitution A C intron_variant BRCA-EU 10 99294736 99294736 single base substitution C T intron_variant BRCA-EU 10 99295514 99295514 single base substitution T A intron_variant BRCA-EU 10 99295866 99295866 single base substitution C T intron_variant BRCA-EU 10 99298533 99298533 single base substitution G T intron_variant BRCA-EU 10 99298731 99298731 single base substitution G T intron_variant BRCA-EU 10 99302363 99302363 single base substitution G A intron_variant BRCA-EU 10 99302500 99302500 single base substitution A C intron_variant BRCA-EU 10 99303387 99303387 single base substitution G A intron_variant BRCA-EU 10 99303925 99303925 single base substitution C T intron_variant BRCA-EU 10 99304289 99304289 single base substitution C T intron_variant BRCA-EU 10 99306762 99306762 single base substitution C G intron_variant BRCA-EU 10 99307280 99307280 single base substitution C G intron_variant BRCA-EU 10 99307331 99307331 deletion of <=200bp T - intron_variant BRCA-EU 10 99309909 99309909 single base substitution G C intron_variant BRCA-EU 10 99310331 99310331 single base substitution C T intron_variant BRCA-EU 10 99310443 99310443 single base substitution C T intron_variant BRCA-EU 10 99314908 99314908 single base substitution A G intron_variant BRCA-EU 10 99316452 99316452 single base substitution G C intron_variant BRCA-EU 10 99317529 99317529 single base substitution A T intron_variant BRCA-EU 10 99318556 99318556 single base substitution G A intron_variant BRCA-EU 10 99319745 99319745 deletion of <=200bp T - intron_variant BRCA-EU 10 99320534 99320534 single base substitution T A intron_variant BRCA-EU 10 99322331 99322331 single base substitution C G intron_variant BRCA-EU 10 99323184 99323184 single base substitution T G intron_variant BRCA-EU 10 99323882 99323882 single base substitution A G intron_variant BRCA-EU 10 99325172 99325172 single base substitution G T intron_variant BRCA-EU 10 99325213 99325213 single base substitution C A intron_variant BRCA-EU 10 99325815 99325815 single base substitution T G intron_variant BRCA-EU 10 99326487 99326487 single base substitution A C intron_variant BRCA-EU 10 99327660 99327660 single base substitution G C intron_variant BRCA-EU 10 99328589 99328589 deletion of <=200bp T - intron_variant BRCA-EU 10 99328589 99328589 insertion of <=200bp - T intron_variant BRCA-EU 10 99329823 99329823 deletion of <=200bp G - intron_variant BRCA-EU 10 99330928 99330928 single base substitution C A 3_prime_UTR_variant BRCA-EU 10 99332351 99332351 single base substitution G T downstream_gene_variant BRCA-EU 10 99334344 99334344 single base substitution A C downstream_gene_variant BRCA-EU 10 99334710 99334710 single base substitution C T downstream_gene_variant BRCA-FR 10 99273924 99273924 single base substitution G A intron_variant BRCA-FR 10 99277384 99277384 single base substitution C T intron_variant BRCA-FR 10 99291956 99291956 single base substitution C G intron_variant BRCA-FR 10 99294736 99294736 single base substitution C T intron_variant BRCA-FR 10 99295866 99295866 single base substitution C T intron_variant BRCA-FR 10 99310443 99310443 single base substitution C T intron_variant BRCA-FR 10 99325213 99325213 single base substitution C A intron_variant BRCA-FR 10 99332351 99332351 single base substitution G T downstream_gene_variant BRCA-UK 10 99270713 99270713 single base substitution G C intron_variant BRCA-UK 10 99281735 99281735 single base substitution T A intron_variant BRCA-UK 10 99294530 99294530 single base substitution G A intron_variant BRCA-UK 10 99315252 99315252 single base substitution C T intron_variant BRCA-UK 10 99322331 99322331 single base substitution C G intron_variant BRCA-US 10 99330208 99330208 single base substitution C T synonymous_variant L204L 612C>T BTCA-JP 10 99258325 99258325 single base substitution C G upstream_gene_variant CLLE-ES 10 99262433 99262433 single base substitution G T intron_variant CLLE-ES 10 99262679 99262679 single base substitution T A intron_variant CLLE-ES 10 99305942 99305942 single base substitution C A intron_variant CLLE-ES 10 99311999 99311999 single base substitution T G intron_variant CLLE-ES 10 99324046 99324046 single base substitution G A intron_variant COAD-US 10 99327783 99327783 single base substitution C T synonymous_variant F61F 183C>T COAD-US 10 99329931 99329931 single base substitution G A missense_variant R112H 335G>A COAD-US 10 99330109 99330109 single base substitution G T synonymous_variant V171V 513G>T COCA-CN 10 99258976 99258976 single base substitution G A missense_variant G6R 16G>A COCA-CN 10 99288979 99288979 single base substitution C T intron_variant COCA-CN 10 99292396 99292396 single base substitution A G intron_variant COCA-CN 10 99298786 99298786 single base substitution G C intron_variant COCA-CN 10 99315426 99315426 single base substitution G A intron_variant COCA-CN 10 99328508 99328508 single base substitution C T intron_variant EOPC-DE 10 99292174 99292174 single base substitution A G intron_variant ESAD-UK 10 99256372 99256372 single base substitution C A upstream_gene_variant ESAD-UK 10 99258356 99258356 single base substitution C G upstream_gene_variant ESAD-UK 10 99258456 99258456 single base substitution G A upstream_gene_variant ESAD-UK 10 99261850 99261850 single base substitution A C intron_variant ESAD-UK 10 99261875 99261875 single base substitution A G intron_variant ESAD-UK 10 99262238 99262238 single base substitution G T intron_variant ESAD-UK 10 99262678 99262678 single base substitution T A intron_variant ESAD-UK 10 99262680 99262680 single base substitution T A intron_variant ESAD-UK 10 99263182 99263182 single base substitution C T intron_variant ESAD-UK 10 99264108 99264108 single base substitution T G intron_variant ESAD-UK 10 99266280 99266280 single base substitution G A intron_variant ESAD-UK 10 99272040 99272040 single base substitution C T intron_variant ESAD-UK 10 99276394 99276394 single base substitution C T intron_variant ESAD-UK 10 99277476 99277476 single base substitution G A intron_variant ESAD-UK 10 99282038 99282038 single base substitution C T intron_variant ESAD-UK 10 99285159 99285159 single base substitution G A intron_variant ESAD-UK 10 99285845 99285845 single base substitution G T intron_variant ESAD-UK 10 99291085 99291085 single base substitution A G intron_variant ESAD-UK 10 99292276 99292276 single base substitution C T intron_variant ESAD-UK 10 99293237 99293237 single base substitution G A intron_variant ESAD-UK 10 99301797 99301797 single base substitution C T intron_variant ESAD-UK 10 99301798 99301798 single base substitution T C intron_variant ESAD-UK 10 99306121 99306121 single base substitution G A intron_variant ESAD-UK 10 99307316 99307316 single base substitution T G intron_variant ESAD-UK 10 99307383 99307383 single base substitution G A intron_variant ESAD-UK 10 99307660 99307660 single base substitution A G intron_variant ESAD-UK 10 99308491 99308491 single base substitution G A intron_variant ESAD-UK 10 99308723 99308723 single base substitution G A intron_variant ESAD-UK 10 99309282 99309282 single base substitution T C intron_variant ESAD-UK 10 99311196 99311196 single base substitution G A intron_variant ESAD-UK 10 99315838 99315860 deletion of <=200bp GTGACGAAGTTTTTTATCATTTG - intron_variant ESAD-UK 10 99316423 99316423 single base substitution A C intron_variant ESAD-UK 10 99317748 99317748 single base substitution T C intron_variant ESAD-UK 10 99318616 99318616 single base substitution G A intron_variant ESAD-UK 10 99319485 99319485 single base substitution G A intron_variant ESAD-UK 10 99319714 99319714 single base substitution T C intron_variant ESAD-UK 10 99321340 99321340 single base substitution C T intron_variant ESAD-UK 10 99321656 99321656 single base substitution G T intron_variant ESAD-UK 10 99324113 99324113 single base substitution A G intron_variant ESAD-UK 10 99324196 99324196 single base substitution T A intron_variant ESAD-UK 10 99324825 99324826 deletion of <=200bp AT - intron_variant ESAD-UK 10 99330134 99330134 single base substitution G A missense_variant A180T 538G>A ESAD-UK 10 99332223 99332223 single base substitution C G downstream_gene_variant KIRP-US 10 99327795 99327795 single base substitution G A synonymous_variant K65K 195G>A LAML-KR 10 99269678 99269678 single base substitution G A intron_variant LAML-KR 10 99288834 99288834 single base substitution C T intron_variant LAML-KR 10 99314020 99314020 single base substitution C T intron_variant LAML-KR 10 99318882 99318882 single base substitution G A intron_variant LICA-CN 10 99327881 99327881 single base substitution G T missense_variant S94I 281G>T LICA-FR 10 99258094 99258094 single base substitution T C upstream_gene_variant LICA-FR 10 99280143 99280143 single base substitution G T intron_variant LICA-FR 10 99294335 99294340 deletion of <=200bp CGCACA - intron_variant LICA-FR 10 99297615 99297615 single base substitution C T intron_variant LINC-JP 10 99264074 99264074 single base substitution C T intron_variant LINC-JP 10 99270584 99270584 single base substitution C T intron_variant LINC-JP 10 99286771 99286771 single base substitution T C intron_variant LINC-JP 10 99292124 99292124 single base substitution T C intron_variant LINC-JP 10 99292129 99292129 single base substitution G T intron_variant LINC-JP 10 99330834 99330834 single base substitution T G 3_prime_UTR_variant LIRI-JP 10 99257253 99257253 single base substitution T A upstream_gene_variant LIRI-JP 10 99257495 99257495 single base substitution T G upstream_gene_variant LIRI-JP 10 99260417 99260417 single base substitution A T intron_variant LIRI-JP 10 99261116 99261116 single base substitution G A intron_variant LIRI-JP 10 99261219 99261219 single base substitution C T intron_variant LIRI-JP 10 99264113 99264113 single base substitution G A intron_variant LIRI-JP 10 99264575 99264575 single base substitution C A intron_variant LIRI-JP 10 99265339 99265339 single base substitution T C intron_variant LIRI-JP 10 99268769 99268769 single base substitution A G intron_variant LIRI-JP 10 99274707 99274707 single base substitution A T intron_variant LIRI-JP 10 99275063 99275063 single base substitution A G intron_variant LIRI-JP 10 99275170 99275170 single base substitution G T intron_variant LIRI-JP 10 99275171 99275171 single base substitution T C intron_variant LIRI-JP 10 99278448 99278448 single base substitution T C intron_variant LIRI-JP 10 99279659 99279659 single base substitution C A intron_variant LIRI-JP 10 99280915 99280915 single base substitution G A intron_variant LIRI-JP 10 99291218 99291218 single base substitution G C intron_variant LIRI-JP 10 99291219 99291219 single base substitution G T intron_variant LIRI-JP 10 99293536 99293536 single base substitution T A intron_variant LIRI-JP 10 99294298 99294298 single base substitution C A intron_variant LIRI-JP 10 99302459 99302459 single base substitution C T intron_variant LIRI-JP 10 99303277 99303277 single base substitution A C intron_variant LIRI-JP 10 99310121 99310121 single base substitution C A intron_variant LIRI-JP 10 99313128 99313128 single base substitution T G intron_variant LIRI-JP 10 99314390 99314390 single base substitution C G intron_variant LIRI-JP 10 99318741 99318741 single base substitution C G intron_variant LIRI-JP 10 99322993 99322993 single base substitution G A intron_variant LIRI-JP 10 99324266 99324266 single base substitution G A intron_variant LIRI-JP 10 99329436 99329436 single base substitution G A intron_variant LIRI-JP 10 99335091 99335091 single base substitution T C downstream_gene_variant LIRI-JP 10 99335881 99335881 single base substitution A G downstream_gene_variant LUSC-KR 10 99259040 99259040 single base substitution G T intron_variant LUSC-KR 10 99259435 99259435 single base substitution G T intron_variant LUSC-KR 10 99263456 99263456 single base substitution G T intron_variant LUSC-KR 10 99266923 99266923 single base substitution C T intron_variant LUSC-KR 10 99267730 99267730 single base substitution C G intron_variant LUSC-KR 10 99277807 99277807 single base substitution G T intron_variant LUSC-KR 10 99287775 99287775 single base substitution A G intron_variant LUSC-KR 10 99288035 99288035 single base substitution C T intron_variant LUSC-KR 10 99288068 99288068 single base substitution A C intron_variant LUSC-KR 10 99298148 99298148 single base substitution A G intron_variant LUSC-KR 10 99300963 99300963 single base substitution G T intron_variant LUSC-KR 10 99313818 99313818 single base substitution G A intron_variant LUSC-KR 10 99319376 99319376 single base substitution T G intron_variant LUSC-KR 10 99329886 99329886 single base substitution C G intron_variant LUSC-US 10 99330049 99330049 single base substitution G A synonymous_variant L151L 453G>A MALY-DE 10 99261946 99261946 deletion of <=200bp T - intron_variant MALY-DE 10 99269714 99269714 deletion of <=200bp T - intron_variant MALY-DE 10 99271418 99271418 deletion of <=200bp T - intron_variant MALY-DE 10 99273773 99273773 deletion of <=200bp T - intron_variant MALY-DE 10 99276748 99276748 single base substitution A G intron_variant MALY-DE 10 99287096 99287096 single base substitution G C intron_variant MALY-DE 10 99292108 99292108 single base substitution G A intron_variant MALY-DE 10 99303061 99303061 single base substitution G A intron_variant MALY-DE 10 99304175 99304175 single base substitution G A intron_variant MALY-DE 10 99306277 99306277 single base substitution A T intron_variant MALY-DE 10 99306658 99306659 deletion of <=200bp CT - intron_variant MALY-DE 10 99318450 99318450 single base substitution G A intron_variant MALY-DE 10 99333192 99333192 deletion of <=200bp T - downstream_gene_variant MELA-AU 10 99254343 99254343 single base substitution A G upstream_gene_variant MELA-AU 10 99255846 99255846 single base substitution C T upstream_gene_variant MELA-AU 10 99256726 99256726 single base substitution G A upstream_gene_variant MELA-AU 10 99256763 99256763 single base substitution G A upstream_gene_variant MELA-AU 10 99256939 99256939 single base substitution A T upstream_gene_variant MELA-AU 10 99257855 99257855 single base substitution G A upstream_gene_variant MELA-AU 10 99258229 99258229 single base substitution G A upstream_gene_variant MELA-AU 10 99258931 99258932 multiple base substitution (>=2bp and <=200bp) CG TA 5_prime_UTR_variant MELA-AU 10 99259798 99259798 single base substitution G A intron_variant MELA-AU 10 99260737 99260737 single base substitution T C intron_variant MELA-AU 10 99261439 99261439 single base substitution C T intron_variant MELA-AU 10 99261547 99261548 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99262352 99262352 single base substitution G A intron_variant MELA-AU 10 99262580 99262580 single base substitution G A intron_variant MELA-AU 10 99262654 99262654 single base substitution G A intron_variant MELA-AU 10 99263721 99263721 single base substitution C T intron_variant MELA-AU 10 99263721 99263722 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99263865 99263865 single base substitution C T intron_variant MELA-AU 10 99263934 99263934 single base substitution C T intron_variant MELA-AU 10 99264000 99264000 single base substitution C T intron_variant MELA-AU 10 99264143 99264143 single base substitution C T intron_variant MELA-AU 10 99264930 99264930 single base substitution G A intron_variant MELA-AU 10 99265367 99265367 single base substitution C T intron_variant MELA-AU 10 99266420 99266420 single base substitution C T intron_variant MELA-AU 10 99266727 99266727 single base substitution G A intron_variant MELA-AU 10 99267156 99267156 single base substitution G A intron_variant MELA-AU 10 99270252 99270252 single base substitution C T intron_variant MELA-AU 10 99270914 99270914 single base substitution G C intron_variant MELA-AU 10 99272386 99272386 single base substitution C T intron_variant MELA-AU 10 99272475 99272475 single base substitution G A intron_variant MELA-AU 10 99272641 99272641 single base substitution C T intron_variant MELA-AU 10 99272759 99272759 single base substitution G A intron_variant MELA-AU 10 99273883 99273883 single base substitution C T intron_variant MELA-AU 10 99274974 99274975 multiple base substitution (>=2bp and <=200bp) AA GG intron_variant MELA-AU 10 99274984 99274984 single base substitution G T intron_variant MELA-AU 10 99275657 99275657 single base substitution A C intron_variant MELA-AU 10 99275719 99275719 single base substitution C T intron_variant MELA-AU 10 99276328 99276328 single base substitution C T intron_variant MELA-AU 10 99276496 99276496 single base substitution C T intron_variant MELA-AU 10 99276551 99276551 single base substitution C T intron_variant MELA-AU 10 99277588 99277588 single base substitution C T intron_variant MELA-AU 10 99277825 99277825 single base substitution C T intron_variant MELA-AU 10 99279185 99279185 single base substitution C T intron_variant MELA-AU 10 99279248 99279248 single base substitution G A intron_variant MELA-AU 10 99280013 99280013 single base substitution C T intron_variant MELA-AU 10 99280217 99280217 single base substitution G C intron_variant MELA-AU 10 99280510 99280511 multiple base substitution (>=2bp and <=200bp) GC AA intron_variant MELA-AU 10 99281522 99281523 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99281763 99281763 single base substitution C T intron_variant MELA-AU 10 99281933 99281933 single base substitution C A intron_variant MELA-AU 10 99282702 99282702 single base substitution C T intron_variant MELA-AU 10 99282709 99282709 single base substitution C T intron_variant MELA-AU 10 99283316 99283316 single base substitution C T intron_variant MELA-AU 10 99283614 99283614 single base substitution C T intron_variant MELA-AU 10 99283697 99283697 single base substitution C T intron_variant MELA-AU 10 99284418 99284418 single base substitution T C intron_variant MELA-AU 10 99284474 99284474 single base substitution G A intron_variant MELA-AU 10 99284889 99284889 single base substitution C T intron_variant MELA-AU 10 99284943 99284943 single base substitution C T intron_variant MELA-AU 10 99286588 99286588 single base substitution G A intron_variant MELA-AU 10 99286883 99286883 single base substitution T G intron_variant MELA-AU 10 99288066 99288066 single base substitution C T intron_variant MELA-AU 10 99288122 99288123 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99288848 99288848 single base substitution C G intron_variant MELA-AU 10 99290523 99290523 single base substitution A G intron_variant MELA-AU 10 99290727 99290727 single base substitution C T intron_variant MELA-AU 10 99291520 99291521 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99291740 99291740 single base substitution C T intron_variant MELA-AU 10 99292087 99292087 single base substitution A G intron_variant MELA-AU 10 99292182 99292182 single base substitution C T intron_variant MELA-AU 10 99292184 99292184 single base substitution C T intron_variant MELA-AU 10 99292526 99292526 single base substitution A T intron_variant MELA-AU 10 99292595 99292595 single base substitution G A intron_variant MELA-AU 10 99293354 99293354 single base substitution C T intron_variant MELA-AU 10 99293772 99293772 single base substitution G A intron_variant MELA-AU 10 99293953 99293953 single base substitution C T intron_variant MELA-AU 10 99294485 99294485 single base substitution C T intron_variant MELA-AU 10 99294739 99294739 single base substitution C T intron_variant MELA-AU 10 99295732 99295732 single base substitution A G intron_variant MELA-AU 10 99296566 99296566 single base substitution C T intron_variant MELA-AU 10 99296894 99296894 single base substitution C T intron_variant MELA-AU 10 99297027 99297027 single base substitution C T intron_variant MELA-AU 10 99297488 99297488 single base substitution G A intron_variant MELA-AU 10 99298657 99298657 single base substitution C T intron_variant MELA-AU 10 99298681 99298681 single base substitution C T intron_variant MELA-AU 10 99299281 99299281 single base substitution G T intron_variant MELA-AU 10 99299855 99299855 single base substitution C T intron_variant MELA-AU 10 99299872 99299872 single base substitution C T intron_variant MELA-AU 10 99302702 99302702 single base substitution C T intron_variant MELA-AU 10 99303966 99303966 single base substitution C T intron_variant MELA-AU 10 99304289 99304289 single base substitution C T intron_variant MELA-AU 10 99305396 99305396 single base substitution C T intron_variant MELA-AU 10 99306210 99306210 single base substitution C T intron_variant MELA-AU 10 99306474 99306474 single base substitution G A intron_variant MELA-AU 10 99306919 99306919 single base substitution C T intron_variant MELA-AU 10 99306950 99306950 single base substitution C G intron_variant MELA-AU 10 99307660 99307660 single base substitution A G intron_variant MELA-AU 10 99308516 99308516 single base substitution A G intron_variant MELA-AU 10 99308678 99308678 single base substitution C T intron_variant MELA-AU 10 99308826 99308826 single base substitution C T intron_variant MELA-AU 10 99308997 99308997 single base substitution C T intron_variant MELA-AU 10 99309336 99309336 single base substitution G A intron_variant MELA-AU 10 99309555 99309555 single base substitution C T intron_variant MELA-AU 10 99310595 99310595 single base substitution C T intron_variant MELA-AU 10 99310652 99310652 single base substitution C T intron_variant MELA-AU 10 99310865 99310865 single base substitution C T intron_variant MELA-AU 10 99311267 99311268 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 99312183 99312183 single base substitution C T intron_variant MELA-AU 10 99312368 99312368 single base substitution C T intron_variant MELA-AU 10 99312733 99312733 single base substitution C T intron_variant MELA-AU 10 99313101 99313101 single base substitution C T intron_variant MELA-AU 10 99313907 99313907 single base substitution C T intron_variant MELA-AU 10 99314303 99314303 single base substitution C T intron_variant MELA-AU 10 99315035 99315035 single base substitution C T intron_variant MELA-AU 10 99315121 99315121 single base substitution C T intron_variant MELA-AU 10 99315280 99315280 single base substitution T C intron_variant MELA-AU 10 99315662 99315662 single base substitution C A intron_variant MELA-AU 10 99315827 99315827 single base substitution G A intron_variant MELA-AU 10 99316487 99316487 single base substitution C T intron_variant MELA-AU 10 99316753 99316753 single base substitution C T intron_variant MELA-AU 10 99317035 99317035 single base substitution T G intron_variant MELA-AU 10 99317200 99317200 single base substitution C T intron_variant MELA-AU 10 99317882 99317882 single base substitution C T intron_variant MELA-AU 10 99318551 99318551 single base substitution C T intron_variant MELA-AU 10 99318714 99318714 single base substitution T C intron_variant MELA-AU 10 99318964 99318964 single base substitution T C intron_variant MELA-AU 10 99318981 99318981 single base substitution C T intron_variant MELA-AU 10 99319104 99319104 single base substitution G A intron_variant MELA-AU 10 99319315 99319315 single base substitution T G intron_variant MELA-AU 10 99320475 99320475 single base substitution C T intron_variant MELA-AU 10 99321753 99321753 single base substitution G A intron_variant MELA-AU 10 99321829 99321830 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 99321987 99321987 single base substitution C T intron_variant MELA-AU 10 99322042 99322042 single base substitution C T intron_variant MELA-AU 10 99322724 99322724 single base substitution C T intron_variant MELA-AU 10 99323070 99323070 single base substitution T A intron_variant MELA-AU 10 99323118 99323118 single base substitution T A intron_variant MELA-AU 10 99323369 99323369 single base substitution T G intron_variant MELA-AU 10 99323404 99323405 multiple base substitution (>=2bp and <=200bp) TT GA intron_variant MELA-AU 10 99323963 99323963 single base substitution C T intron_variant MELA-AU 10 99324629 99324629 single base substitution C T intron_variant MELA-AU 10 99324663 99324663 single base substitution C T intron_variant MELA-AU 10 99324766 99324766 single base substitution C T intron_variant MELA-AU 10 99325108 99325108 single base substitution C T intron_variant MELA-AU 10 99325212 99325212 single base substitution C T intron_variant MELA-AU 10 99325576 99325576 single base substitution C T intron_variant MELA-AU 10 99325892 99325892 single base substitution T C intron_variant MELA-AU 10 99326455 99326455 single base substitution C T intron_variant MELA-AU 10 99326829 99326829 single base substitution T C intron_variant MELA-AU 10 99327071 99327071 single base substitution C T intron_variant MELA-AU 10 99327867 99327867 single base substitution C T synonymous_variant I89I 267C>T MELA-AU 10 99329075 99329075 single base substitution C T intron_variant MELA-AU 10 99329836 99329836 single base substitution C G intron_variant MELA-AU 10 99330217 99330217 single base substitution C T synonymous_variant T207T 621C>T MELA-AU 10 99330309 99330309 single base substitution C T 3_prime_UTR_variant MELA-AU 10 99330770 99330770 single base substitution C T 3_prime_UTR_variant MELA-AU 10 99330991 99330991 single base substitution C T downstream_gene_variant MELA-AU 10 99332075 99332075 single base substitution C T downstream_gene_variant MELA-AU 10 99333362 99333362 single base substitution T A downstream_gene_variant MELA-AU 10 99334378 99334379 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 99335166 99335166 single base substitution C T downstream_gene_variant MELA-AU 10 99335306 99335306 single base substitution G A downstream_gene_variant MELA-AU 10 99335354 99335354 single base substitution T G downstream_gene_variant ORCA-IN 10 99255523 99255523 single base substitution C T upstream_gene_variant ORCA-IN 10 99259976 99259976 single base substitution C T intron_variant ORCA-IN 10 99274493 99274493 single base substitution G A intron_variant ORCA-IN 10 99303733 99303733 single base substitution G A intron_variant ORCA-IN 10 99323780 99323780 single base substitution G C intron_variant ORCA-IN 10 99329361 99329361 single base substitution C A intron_variant ORCA-IN 10 99332609 99332609 single base substitution C A downstream_gene_variant OV-AU 10 99256559 99256559 single base substitution C G upstream_gene_variant OV-AU 10 99267321 99267321 single base substitution G A intron_variant OV-AU 10 99268811 99268811 single base substitution C G intron_variant OV-AU 10 99281262 99281262 single base substitution C G intron_variant OV-AU 10 99282665 99282665 single base substitution C G intron_variant OV-AU 10 99283888 99283888 single base substitution G C intron_variant OV-AU 10 99290698 99290698 single base substitution G A intron_variant OV-AU 10 99298871 99298871 single base substitution G A intron_variant OV-AU 10 99300847 99300847 single base substitution C T intron_variant OV-AU 10 99303053 99303053 single base substitution C A intron_variant OV-AU 10 99304244 99304244 single base substitution G C intron_variant OV-AU 10 99306756 99306756 single base substitution C A intron_variant OV-AU 10 99309866 99309866 single base substitution A C intron_variant OV-AU 10 99312666 99312666 single base substitution T C intron_variant OV-AU 10 99313540 99313540 single base substitution C T intron_variant OV-AU 10 99324694 99324694 single base substitution A G intron_variant OV-AU 10 99329006 99329006 single base substitution A G intron_variant OV-AU 10 99330667 99330667 single base substitution C T 3_prime_UTR_variant PACA-AU 10 99253786 99253786 deletion of <=200bp A - upstream_gene_variant PACA-AU 10 99260864 99260864 single base substitution C T intron_variant PACA-AU 10 99270236 99270236 single base substitution A C intron_variant PACA-AU 10 99276079 99276079 single base substitution G A intron_variant PACA-AU 10 99276598 99276598 single base substitution C T intron_variant PACA-AU 10 99276923 99276923 single base substitution C A intron_variant PACA-AU 10 99277318 99277318 single base substitution G A intron_variant PACA-AU 10 99278675 99278675 single base substitution A G intron_variant PACA-AU 10 99288774 99288774 single base substitution A T intron_variant PACA-AU 10 99289477 99289501 deletion of <=200bp GAGAGGGAGACCGTGGAAAGAGAGG - intron_variant PACA-AU 10 99295085 99295085 single base substitution T A intron_variant PACA-AU 10 99296311 99296311 single base substitution C T intron_variant PACA-AU 10 99296710 99296710 single base substitution T A intron_variant PACA-AU 10 99300292 99300292 single base substitution G T intron_variant PACA-AU 10 99300295 99300295 single base substitution C A intron_variant PACA-AU 10 99300688 99300688 single base substitution T C intron_variant PACA-AU 10 99308642 99308642 single base substitution G A intron_variant PACA-AU 10 99311962 99311962 single base substitution A C intron_variant PACA-AU 10 99316396 99316396 single base substitution C T intron_variant PACA-AU 10 99320980 99320980 single base substitution G A intron_variant PACA-AU 10 99321950 99321950 single base substitution C T intron_variant PACA-AU 10 99322024 99322024 single base substitution G A intron_variant PACA-AU 10 99327975 99327975 single base substitution G A intron_variant PACA-CA 10 99261776 99261776 single base substitution C T intron_variant PACA-CA 10 99271588 99271588 single base substitution T G intron_variant PACA-CA 10 99273139 99273139 single base substitution A T intron_variant PACA-CA 10 99273453 99273453 single base substitution C A intron_variant PACA-CA 10 99273786 99273786 single base substitution A T intron_variant PACA-CA 10 99274770 99274770 single base substitution C G intron_variant PACA-CA 10 99275079 99275079 single base substitution G A intron_variant PACA-CA 10 99275429 99275429 single base substitution C G intron_variant PACA-CA 10 99275697 99275697 single base substitution G A intron_variant PACA-CA 10 99280785 99280785 single base substitution G C intron_variant PACA-CA 10 99288696 99288696 single base substitution C T intron_variant PACA-CA 10 99289983 99289983 insertion of <=200bp - AAT intron_variant PACA-CA 10 99289984 99289984 insertion of <=200bp - A intron_variant PACA-CA 10 99290145 99290145 single base substitution C T intron_variant PACA-CA 10 99290794 99290794 single base substitution G A intron_variant PACA-CA 10 99298389 99298389 single base substitution T C intron_variant PACA-CA 10 99304646 99304646 single base substitution G A intron_variant PACA-CA 10 99310708 99310708 single base substitution C A intron_variant PACA-CA 10 99311970 99311970 single base substitution A T intron_variant PACA-CA 10 99314229 99314229 single base substitution C G intron_variant PACA-CA 10 99315476 99315476 single base substitution C T intron_variant PACA-CA 10 99315584 99315584 single base substitution C T intron_variant PACA-CA 10 99319352 99319352 single base substitution G C intron_variant PACA-CA 10 99319534 99319534 single base substitution C T intron_variant PACA-CA 10 99320900 99320900 single base substitution C T intron_variant PACA-CA 10 99322760 99322760 single base substitution G T intron_variant PACA-CA 10 99324808 99324809 deletion of <=200bp TT - intron_variant PACA-CA 10 99325473 99325473 insertion of <=200bp - T intron_variant PACA-CA 10 99327003 99327003 single base substitution A T intron_variant PACA-CA 10 99330088 99330088 single base substitution C T synonymous_variant S164S 492C>T PACA-CA 10 99330950 99330950 single base substitution T C 3_prime_UTR_variant PACA-CA 10 99332163 99332163 single base substitution G T downstream_gene_variant PACA-CA 10 99333319 99333319 single base substitution G A downstream_gene_variant PAEN-AU 10 99254194 99254194 single base substitution G A upstream_gene_variant PAEN-AU 10 99267182 99267182 single base substitution C T intron_variant PAEN-AU 10 99303942 99303942 single base substitution C A intron_variant PAEN-IT 10 99290953 99290953 single base substitution T A intron_variant PAEN-IT 10 99295735 99295735 single base substitution A G intron_variant PBCA-DE 10 99255077 99255077 single base substitution C T upstream_gene_variant PBCA-DE 10 99256963 99256963 single base substitution A T upstream_gene_variant PBCA-DE 10 99257642 99257642 single base substitution G C upstream_gene_variant PBCA-DE 10 99260007 99260007 single base substitution T A intron_variant PBCA-DE 10 99277670 99277670 single base substitution G C intron_variant PBCA-DE 10 99278418 99278418 single base substitution G T intron_variant PBCA-DE 10 99285272 99285272 single base substitution T A intron_variant PBCA-DE 10 99288100 99288100 deletion of <=200bp C - intron_variant PBCA-DE 10 99293772 99293772 single base substitution G A intron_variant PBCA-DE 10 99306615 99306615 single base substitution G A intron_variant PBCA-DE 10 99306658 99306659 deletion of <=200bp CT - intron_variant PBCA-DE 10 99313458 99313458 single base substitution G A intron_variant PBCA-DE 10 99315125 99315125 single base substitution C A intron_variant PBCA-DE 10 99315476 99315476 single base substitution C T intron_variant PBCA-DE 10 99315843 99315843 single base substitution G A intron_variant PBCA-DE 10 99319808 99319808 insertion of <=200bp - T intron_variant PBCA-DE 10 99323667 99323667 single base substitution G A intron_variant PBCA-DE 10 99326836 99326836 deletion of <=200bp T - intron_variant PBCA-DE 10 99330014 99330014 single base substitution G A missense_variant E140K 418G>A PBCA-DE 10 99335466 99335466 insertion of <=200bp - A downstream_gene_variant PBCA-DE 10 99335474 99335474 insertion of <=200bp - A downstream_gene_variant PRAD-CA 10 99275062 99275062 single base substitution T A intron_variant PRAD-CA 10 99306127 99306127 single base substitution C T intron_variant PRAD-CA 10 99306384 99306384 single base substitution C T intron_variant PRAD-UK 10 99274143 99274143 single base substitution T G intron_variant PRAD-UK 10 99274431 99274431 single base substitution G T intron_variant PRAD-UK 10 99290603 99290603 single base substitution T A intron_variant PRAD-UK 10 99297924 99297924 single base substitution T C intron_variant PRAD-UK 10 99301688 99301689 deletion of <=200bp TC - intron_variant PRAD-UK 10 99308285 99308285 single base substitution G C intron_variant PRAD-UK 10 99327225 99327225 single base substitution G T intron_variant PRAD-UK 10 99334660 99334669 multiple base substitution (>=2bp and <=200bp) GACACACAGA GTCC downstream_gene_variant READ-US 10 99329964 99329964 single base substitution C T missense_variant P123L 368C>T RECA-EU 10 99269530 99269530 single base substitution C G intron_variant RECA-EU 10 99270327 99270327 single base substitution C T intron_variant RECA-EU 10 99271994 99271994 single base substitution G A intron_variant RECA-EU 10 99271995 99271995 single base substitution A G intron_variant RECA-EU 10 99283958 99283958 single base substitution C T intron_variant RECA-EU 10 99293295 99293295 single base substitution A T intron_variant RECA-EU 10 99308392 99308392 single base substitution G A intron_variant RECA-EU 10 99326752 99326752 single base substitution T C intron_variant SKCA-BR 10 99260512 99260512 single base substitution T A intron_variant SKCA-BR 10 99263169 99263169 single base substitution T C intron_variant SKCA-BR 10 99264292 99264292 single base substitution C T intron_variant SKCA-BR 10 99264999 99264999 single base substitution A C intron_variant SKCA-BR 10 99267231 99267231 insertion of <=200bp - TA intron_variant SKCA-BR 10 99275380 99275380 single base substitution T G intron_variant SKCA-BR 10 99281793 99281793 single base substitution A G intron_variant SKCA-BR 10 99284041 99284041 insertion of <=200bp - TGGC intron_variant SKCA-BR 10 99287784 99287784 single base substitution G A intron_variant SKCA-BR 10 99287937 99287937 single base substitution T C intron_variant SKCA-BR 10 99288414 99288414 single base substitution G C intron_variant SKCA-BR 10 99288418 99288418 single base substitution G T intron_variant SKCA-BR 10 99291449 99291450 deletion of <=200bp CG - intron_variant SKCA-BR 10 99291451 99291451 single base substitution G T intron_variant SKCA-BR 10 99292271 99292271 single base substitution T G intron_variant SKCA-BR 10 99294334 99294334 insertion of <=200bp - GCACA intron_variant SKCA-BR 10 99295725 99295725 insertion of <=200bp - AATTATTATT intron_variant SKCA-BR 10 99295729 99295729 insertion of <=200bp - ATTATTATTATTATTATTG intron_variant SKCA-BR 10 99295732 99295732 insertion of <=200bp - ATTATTATTATTATTG intron_variant SKCA-BR 10 99295747 99295747 single base substitution A G intron_variant SKCA-BR 10 99296909 99296909 single base substitution C T intron_variant SKCA-BR 10 99299484 99299484 single base substitution G A intron_variant SKCA-BR 10 99304801 99304801 single base substitution C T intron_variant SKCA-BR 10 99305144 99305144 insertion of <=200bp - CGTGTGGGT intron_variant SKCA-BR 10 99309348 99309348 single base substitution G A intron_variant SKCA-BR 10 99309467 99309467 single base substitution C T intron_variant SKCA-BR 10 99314004 99314004 insertion of <=200bp - GT intron_variant SKCA-BR 10 99314229 99314229 single base substitution C T intron_variant SKCA-BR 10 99316320 99316320 single base substitution T G intron_variant SKCA-BR 10 99323411 99323411 single base substitution T G intron_variant SKCA-BR 10 99324540 99324540 single base substitution C T intron_variant SKCA-BR 10 99324817 99324817 single base substitution C T intron_variant SKCA-BR 10 99327195 99327195 single base substitution A G intron_variant SKCA-BR 10 99329378 99329378 single base substitution G T intron_variant SKCA-BR 10 99331442 99331442 single base substitution C T downstream_gene_variant SKCA-BR 10 99331568 99331568 single base substitution C T downstream_gene_variant SKCA-BR 10 99333922 99333922 single base substitution C T downstream_gene_variant SKCA-BR 10 99335289 99335289 single base substitution T A downstream_gene_variant SKCA-BR 10 99335667 99335668 deletion of <=200bp CA - downstream_gene_variant SKCM-US 10 99332524 99332524 single base substitution C T downstream_gene_variant STAD-US 10 99327773 99327773 single base substitution C T missense_variant A58V 173C>T STAD-US 10 99330045 99330045 single base substitution C A missense_variant P150Q 449C>A STAD-US 10 99330046 99330046 single base substitution G T synonymous_variant P150P 450G>T STAD-US 10 99330203 99330203 single base substitution C T missense_variant R203W 607C>T THCA-SA 10 99258223 99258223 single base substitution T G upstream_gene_variant THCA-SA 10 99330411 99330411 single base substitution A G 3_prime_UTR_variant THCA-SA 10 99332488 99332488 single base substitution A C downstream_gene_variant UCEC-US 10 99327804 99327804 single base substitution G A stop_gained W68* 204G>A UCEC-US 10 99329914 99329914 single base substitution C T synonymous_variant Y106Y 318C>T UCEC-US 10 99329931 99329931 single base substitution G A missense_variant R112H 335G>A UCEC-US 10 99330056 99330056 single base substitution C T missense_variant R154C 460C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand STC252 COSM5050442 c.461G>A p.R154H Substitution - Missense 10:97570300-97570300 + ESO-717 COSM1242978 c.492C>T p.S164S Substitution - coding silent 10:97570331-97570331 + TCGA-B5-A11J-01 COSM922036 c.204G>A p.W68* Substitution - Nonsense 10:97568047-97568047 + TCGA-CK-5916-01 COSM3686998 c.513G>T p.V171V Substitution - coding silent 10:97570352-97570352 + TCGA-F1-6177-01 COSM4017079 c.449C>A p.P150Q Substitution - Missense 10:97570288-97570288 + TCGA-AZ-6601-01 COSM5142161 c.509C>T p.T170I Substitution - Missense 10:97570348-97570348 + Pat_65_A COSM1231638 c.191G>A p.R64H Substitution - Missense 10:97568034-97568034 + 10-P1058 COSM4573950 c.608G>A p.R203Q Substitution - Missense 10:97570447-97570447 + TCGA-G7-6793-01 COSM3985840 c.195G>A p.K65K Substitution - coding silent 10:97568038-97568038 + TCGA-GD-A3OQ-01 COSM1297550 c.244G>A p.D82N Substitution - Missense 10:97568087-97568087 + HCC129T COSM5817007 c.281G>T p.S94I Substitution - Missense 10:97568124-97568124 + B109-Tumor COSM1745994 c.501G>A p.L167L Substitution - coding silent 10:97570340-97570340 + ATL004 COSM5703822 c.418G>A p.E140K Substitution - Missense 10:97570257-97570257 + TCGA-BH-A0AW-01 COSM428243 c.612C>T p.L204L Substitution - coding silent 10:97570451-97570451 + TCGA-AA-A00O-01 COSM298943 c.364C>T p.P122S Substitution - Missense 10:97570203-97570203 + MB_Exm516 COSM307161 c.504C>T p.P168P Substitution - coding silent 10:97570343-97570343 + T3152 COSM4738968 c.449C>T p.P150L Substitution - Missense 10:97570288-97570288 + TCGA-D1-A17H-01 COSM922039 c.376C>T p.L126L Substitution - coding silent 10:97570215-97570215 + YUPAER COSM5371451 c.139C>T p.L47L Substitution - coding silent 10:97567982-97567982 + TCGA-DC-5337-01 COSM1561171 c.368C>T p.P123L Substitution - Missense 10:97570207-97570207 + PTC-10C COSM4144997 c.340C>A p.Q114K Substitution - Missense 10:97570179-97570179 + 08-P8005 COSM4573949 c.427C>T p.P143S Substitution - Missense 10:97570266-97570266 + CSCC-18-T COSM4541357 c.298G>A p.G100S Substitution - Missense 10:97568141-97568141 + TCGA-AZ-6601-01 COSM922038 c.335G>A p.R112H Substitution - Missense 10:97570174-97570174 + TCGA-D1-A17A-01 COSM922037 c.318C>T p.Y106Y Substitution - coding silent 10:97570157-97570157 + TCGA-AP-A0LM-01 COSM922040 c.460C>T p.R154C Substitution - Missense 10:97570299-97570299 + PCSI_0083_Pa_P_526 COSM1242978 c.492C>T p.S164S Substitution - coding silent 10:97570331-97570331 + B109 COSM1745994 c.501G>A p.L167L Substitution - coding silent 10:97570340-97570340 + sysucc-880T COSM5461891 c.16G>A p.G6R Substitution - Missense 10:97499219-97499219 + LAU63 COSM233704 c.581C>T p.S194F Substitution - Missense 10:97570420-97570420 + T2979 COSM4738969 c.537C>T p.H179H Substitution - coding silent 10:97570376-97570376 + TCGA-CG-5721-01 COSM4017081 c.607C>T p.R203W Substitution - Missense 10:97570446-97570446 + TCGA-60-2698-01 COSM685897 c.453G>A p.L151L Substitution - coding silent 10:97570292-97570292 + 587248 COSM922040 c.460C>T p.R154C Substitution - Missense 10:97570299-97570299 + PDA_019 COSM4999000 c.334C>T p.R112C Substitution - Missense 10:97570173-97570173 + TCGA-CK-4951-01 COSM428243 c.612C>T p.L204L Substitution - coding silent 10:97570451-97570451 + TCGA-AA-3672-01 COSM267720 c.463C>A p.L155M Substitution - Missense 10:97570302-97570302 + 587262 COSM1231638 c.191G>A p.R64H Substitution - Missense 10:97568034-97568034 + TCGA-BR-4371-01 COSM4017080 c.450G>T p.P150P Substitution - coding silent 10:97570289-97570289 + ESOSCC161T COSM1171735 c.424C>T p.P142S Substitution - Missense 10:97570263-97570263 + C008 COSM5524137 c.627C>T p.I209I Substitution - coding silent 10:97570466-97570466 + TCGA-AA-3675-01 COSM5102943 c.471G>A p.T157T Substitution - coding silent 10:97570310-97570310 + TCGA-AD-6548-01 COSM1350190 c.183C>T p.F61F Substitution - coding silent 10:97568026-97568026 + TCGA-AP-A051-01 COSM922038 c.335G>A p.R112H Substitution - Missense 10:97570174-97570174 + TCGA-BR-6452-01 COSM4017078 c.173C>T p.A58V Substitution - Missense 10:97568016-97568016 + 6481_PT COSM5753571 c.203G>T p.W68L Substitution - Missense 10:97568046-97568046 + PCSI_0083_Pa_X COSM1242978 c.492C>T p.S164S Substitution - coding silent 10:97570331-97570331 + CSCC-31-T COSM1972314 c.250G>A p.E84K Substitution - Missense 10:97568093-97568093 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.500724 10q24.2

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer C A Missense p.P150Q c.449C>A 10 99330045 STAD C T Missense p.P122S c.364C>T 10 99329960 COREAD C T Synonymous p.F193F c.579C>T 10 99330175 CM C T Synonymous p.L204L c.612C>T 10 99330208 BRCA C T Synonymous p.Y106Y c.318C>T 10 99329914 UCEC G A Missense p.D82N c.244G>A 10 99327844 BLCA G A Nonsense p.W68* c.204G>A 10 99327804 UCEC G T Synonymous p.P150P c.450G>T 10 99330046 STAD T A IntronicSNV . c.70+3649T>A 10 99262679 CLL