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 DLBC 16 11348767 11348767 + Missense_Mutation SNP T T C TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348767T>C c.569A>G c.(568-570)aAc>aGc p.N190S DLBC 16 11348807 11348807 + Silent SNP G G A TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348807G>A c.529C>T c.(529-531)Ctg>Ttg p.L177L DLBC 16 11348808 11348808 + Silent SNP C C T TCGA-FF-8041-01A-11D-2210-10 TCGA-FF-8041-10A-01D-2210-10 g.chr16:11348808C>T c.528G>A c.(526-528)gaG>gaA p.E176E DLBC 16 11348810 11348810 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr16:11348810C>T c.526G>A c.(526-528)Gag>Aag p.E176K DLBC 16 11348889 11348889 + Missense_Mutation SNP C C G TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348889C>G c.447G>C c.(445-447)gaG>gaC p.E149D DLBC 16 11348920 11348920 + Missense_Mutation SNP C C T TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348920C>T c.416G>A c.(415-417)gGc>gAc p.G139D DLBC 16 11348972 11348972 + Nonsense_Mutation SNP C C A TCGA-FA-A7Q1-01A-11D-A382-10 TCGA-FA-A7Q1-10A-01D-A385-10 g.chr16:11348972C>A c.364G>T c.(364-366)Gga>Tga p.G122* DLBC 16 11348978 11348978 + Missense_Mutation SNP C C T TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348978C>T c.358G>A c.(358-360)Gcc>Acc p.A120T DLBC 16 11348988 11348988 + Silent SNP G G A TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11348988G>A c.348C>T c.(346-348)agC>agT p.S116S DLBC 16 11349096 11349096 + Silent SNP G G A TCGA-FA-A7Q1-01A-11D-A382-10 TCGA-FA-A7Q1-10A-01D-A385-10 g.chr16:11349096G>A c.240C>T c.(238-240)taC>taT p.Y80Y DLBC 16 11349102 11349103 + Frame_Shift_Del DEL TC TC - TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr16:11349102_11349103delTC c.233_234delGA c.(232-234)ggafs p.G78fs DLBC 16 11349190 11349190 + Missense_Mutation SNP G G A TCGA-VB-A8QN-01A-11D-A382-10 TCGA-VB-A8QN-10A-01D-A385-10 g.chr16:11349190G>A c.146C>T c.(145-147)gCc>gTc p.A49V DLBC 16 11349329 11349329 + Missense_Mutation SNP C C T TCGA-FF-8041-01A-11D-2210-10 TCGA-FF-8041-10A-01D-2210-10 g.chr16:11349329C>T c.7G>A c.(7-9)Gca>Aca p.A3T GBM 16 11348719 11348719 + Missense_Mutation SNP G G T TCGA-32-4213-01A-01D-1353-08 TCGA-32-4213-10A-01D-1353-08 g.chr16:11348719G>T c.617C>A c.(616-618)tCc>tAc p.S206Y GBMLGG 16 11348719 11348719 + Missense_Mutation SNP G G T TCGA-32-4213-01A-01D-1353-08 TCGA-32-4213-10A-01D-1353-08 g.chr16:11348719G>T c.617C>A c.(616-618)tCc>tAc p.S206Y GBMLGG 16 11349039 11349039 + Silent SNP G G T TCGA-FG-8185-01A-11D-2253-08 TCGA-FG-8185-10A-01D-2253-08 g.chr16:11349039G>T c.297C>A c.(295-297)ggC>ggA p.G99G HNSC 16 11349065 11349065 + Missense_Mutation SNP C C T TCGA-IQ-A61H-01A-11D-A30E-08 TCGA-IQ-A61H-10A-01D-A30H-08 g.chr16:11349065C>T c.271G>A c.(271-273)Gag>Aag p.E91K KIPAN 16 11348785 11348785 + Missense_Mutation SNP G G A TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chr16:11348785G>A c.551C>T c.(550-552)gCc>gTc p.A184V KIRP 16 11348785 11348785 + Missense_Mutation SNP G G A TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chr16:11348785G>A c.551C>T c.(550-552)gCc>gTc p.A184V LGG 16 11349039 11349039 + Silent SNP G G T TCGA-FG-8185-01A-11D-2253-08 TCGA-FG-8185-10A-01D-2253-08 g.chr16:11349039G>T c.297C>A c.(295-297)ggC>ggA p.G99G SKCM 16 11348858 11348858 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr16:11348858G>A c.478C>T c.(478-480)Cgc>Tgc p.R160C SKCM 16 11348859 11348859 + Silent SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr16:11348859G>A c.477C>T c.(475-477)cgC>cgT p.R159R

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 16 11348978 11348978 single base substitution C T missense_variant A120T 358G>A BRCA-EU 16 11343559 11343559 single base substitution C T downstream_gene_variant BRCA-EU 16 11343843 11343843 single base substitution G A downstream_gene_variant BRCA-EU 16 11344246 11344246 single base substitution C G downstream_gene_variant BRCA-EU 16 11345928 11345928 single base substitution G A downstream_gene_variant BRCA-EU 16 11346733 11346733 single base substitution G A downstream_gene_variant BRCA-EU 16 11349721 11349721 single base substitution G A intron_variant BRCA-EU 16 11350111 11350111 single base substitution G T upstream_gene_variant BRCA-EU 16 11351410 11351410 single base substitution C A upstream_gene_variant BRCA-EU 16 11352102 11352102 single base substitution A T upstream_gene_variant BRCA-EU 16 11352186 11352186 single base substitution G T upstream_gene_variant BRCA-EU 16 11354440 11354440 single base substitution G T upstream_gene_variant BRCA-FR 16 11344246 11344246 single base substitution C G downstream_gene_variant BRCA-FR 16 11352102 11352102 single base substitution A T upstream_gene_variant CLLE-ES 16 11345255 11345255 single base substitution C T downstream_gene_variant CLLE-ES 16 11349030 11349030 single base substitution C T synonymous_variant L102L 306G>A CLLE-ES 16 11349528 11349528 single base substitution C G intron_variant COCA-CN 16 11349310 11349310 single base substitution G A missense_variant A9V 26C>T ESAD-UK 16 11343446 11343446 single base substitution C T downstream_gene_variant ESAD-UK 16 11343464 11343464 single base substitution G A downstream_gene_variant ESAD-UK 16 11348203 11348203 single base substitution C G downstream_gene_variant ESAD-UK 16 11348273 11348273 single base substitution T A 3_prime_UTR_variant ESAD-UK 16 11353295 11353295 single base substitution C A upstream_gene_variant ESAD-UK 16 11354709 11354709 single base substitution C T upstream_gene_variant GBM-US 16 11348719 11348719 single base substitution G T missense_variant S206Y 617C>A LGG-US 16 11349039 11349039 single base substitution G T synonymous_variant G99G 297C>A LIRI-JP 16 11346109 11346116 deletion of <=200bp CGCACACA - downstream_gene_variant LIRI-JP 16 11352617 11352617 single base substitution G T upstream_gene_variant LIRI-JP 16 11353314 11353314 single base substitution C G upstream_gene_variant LIRI-JP 16 11354393 11354393 single base substitution G A upstream_gene_variant LUSC-KR 16 11348395 11348395 single base substitution G C 3_prime_UTR_variant LUSC-KR 16 11351445 11351445 single base substitution G A upstream_gene_variant LUSC-KR 16 11354426 11354426 single base substitution A G upstream_gene_variant MALY-DE 16 11346056 11346057 deletion of <=200bp GA - downstream_gene_variant MALY-DE 16 11347154 11347154 single base substitution C T downstream_gene_variant MALY-DE 16 11347647 11347647 single base substitution T G downstream_gene_variant MALY-DE 16 11347660 11347660 single base substitution G C downstream_gene_variant MALY-DE 16 11347728 11347728 single base substitution G A downstream_gene_variant MALY-DE 16 11347731 11347731 single base substitution G A downstream_gene_variant MALY-DE 16 11347746 11347746 single base substitution G T downstream_gene_variant MALY-DE 16 11347800 11347800 single base substitution G C downstream_gene_variant MALY-DE 16 11347801 11347801 single base substitution C G downstream_gene_variant MALY-DE 16 11347990 11347990 single base substitution G C downstream_gene_variant MALY-DE 16 11347999 11347999 single base substitution A T downstream_gene_variant MALY-DE 16 11348006 11348006 single base substitution A C downstream_gene_variant MALY-DE 16 11348047 11348047 single base substitution C T downstream_gene_variant MALY-DE 16 11348059 11348059 single base substitution C T downstream_gene_variant MALY-DE 16 11348115 11348115 single base substitution G A downstream_gene_variant MALY-DE 16 11348121 11348121 single base substitution G T downstream_gene_variant MALY-DE 16 11348157 11348157 single base substitution C A downstream_gene_variant MALY-DE 16 11348222 11348222 single base substitution C T downstream_gene_variant MALY-DE 16 11348245 11348245 single base substitution C T downstream_gene_variant MALY-DE 16 11348249 11348249 single base substitution C T downstream_gene_variant MALY-DE 16 11348261 11348261 single base substitution C G downstream_gene_variant MALY-DE 16 11348263 11348263 single base substitution T C 3_prime_UTR_variant MALY-DE 16 11348302 11348302 single base substitution T A 3_prime_UTR_variant MALY-DE 16 11348306 11348306 single base substitution C G 3_prime_UTR_variant MALY-DE 16 11348311 11348311 single base substitution C G 3_prime_UTR_variant MALY-DE 16 11348333 11348333 single base substitution A T 3_prime_UTR_variant MALY-DE 16 11348395 11348395 single base substitution G C 3_prime_UTR_variant MALY-DE 16 11348398 11348398 single base substitution A C 3_prime_UTR_variant MALY-DE 16 11348402 11348402 single base substitution G A 3_prime_UTR_variant MALY-DE 16 11348406 11348406 single base substitution T C 3_prime_UTR_variant MALY-DE 16 11348422 11348422 single base substitution G C 3_prime_UTR_variant MALY-DE 16 11348445 11348445 single base substitution C G 3_prime_UTR_variant MALY-DE 16 11348456 11348456 single base substitution T C 3_prime_UTR_variant MALY-DE 16 11348458 11348458 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348463 11348463 single base substitution A C 3_prime_UTR_variant MALY-DE 16 11348527 11348527 single base substitution G A 3_prime_UTR_variant MALY-DE 16 11348531 11348531 single base substitution G A 3_prime_UTR_variant MALY-DE 16 11348555 11348555 single base substitution A G 3_prime_UTR_variant MALY-DE 16 11348557 11348557 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348586 11348586 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348591 11348591 single base substitution C G 3_prime_UTR_variant MALY-DE 16 11348605 11348605 single base substitution C G 3_prime_UTR_variant MALY-DE 16 11348622 11348622 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348623 11348623 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348630 11348630 single base substitution G T 3_prime_UTR_variant MALY-DE 16 11348637 11348637 single base substitution G A 3_prime_UTR_variant MALY-DE 16 11348660 11348660 single base substitution G T 3_prime_UTR_variant MALY-DE 16 11348664 11348664 single base substitution C T 3_prime_UTR_variant MALY-DE 16 11348668 11348668 single base substitution G C 3_prime_UTR_variant MALY-DE 16 11348707 11348708 deletion of <=200bp TG - frameshift_variant Q210 MALY-DE 16 11348714 11348714 single base substitution G A missense_variant P208S 622C>T MALY-DE 16 11348714 11348729 deletion of <=200bp GGAAGGAGCTCAGGTA - frameshift_variant YLSSFP203 MALY-DE 16 11348720 11348720 single base substitution A G missense_variant S206P 616T>C MALY-DE 16 11348722 11348722 single base substitution C T missense_variant S205N 614G>A MALY-DE 16 11348738 11348738 single base substitution G A missense_variant L200F 598C>T MALY-DE 16 11348744 11348744 single base substitution G A missense_variant P198S 592C>T MALY-DE 16 11348744 11348744 single base substitution G C missense_variant P198A 592C>G MALY-DE 16 11348783 11348796 deletion of <=200bp TGGCCACGATGCGC - frameshift_variant QRIVAT180 MALY-DE 16 11348805 11348805 single base substitution C T synonymous_variant L177L 531G>A MALY-DE 16 11348807 11348807 single base substitution G T missense_variant L177M 529C>A MALY-DE 16 11348808 11348808 single base substitution C G missense_variant E176D 528G>C MALY-DE 16 11348810 11348810 single base substitution C T missense_variant E176K 526G>A MALY-DE 16 11348811 11348811 single base substitution C A missense_variant Q175H 525G>T MALY-DE 16 11348841 11348841 single base substitution C T synonymous_variant P165P 495G>A MALY-DE 16 11348851 11348851 single base substitution A C missense_variant L162R 485T>G MALY-DE 16 11348857 11348857 single base substitution C T missense_variant R160H 479G>A MALY-DE 16 11348888 11348888 single base substitution G C missense_variant L150V 448C>G MALY-DE 16 11348907 11348907 single base substitution G A synonymous_variant S143S 429C>T MALY-DE 16 11348908 11348908 single base substitution C T missense_variant S143N 428G>A MALY-DE 16 11348920 11348920 single base substitution C G missense_variant G139A 416G>C MALY-DE 16 11348932 11348932 single base substitution A C missense_variant F135C 404T>G MALY-DE 16 11348962 11348962 single base substitution C G missense_variant S125T 374G>C MALY-DE 16 11348976 11348976 single base substitution G A synonymous_variant A120A 360C>T MALY-DE 16 11348989 11348989 single base substitution C T missense_variant S116N 347G>A MALY-DE 16 11349001 11349001 single base substitution A T missense_variant F112Y 335T>A MALY-DE 16 11349010 11349010 single base substitution C T missense_variant R109Q 326G>A MALY-DE 16 11349018 11349018 single base substitution G C missense_variant S106R 318C>G MALY-DE 16 11349037 11349037 single base substitution G A missense_variant T100I 299C>T MALY-DE 16 11349055 11349064 deletion of <=200bp CGCAGCCGCT - frameshift_variant ERLR91 MALY-DE 16 11349060 11349060 single base substitution C G synonymous_variant R92R 276G>C MALY-DE 16 11349082 11349082 single base substitution C T missense_variant S85N 254G>A MALY-DE 16 11349137 11349137 single base substitution T A missense_variant I67F 199A>T MALY-DE 16 11349138 11349138 single base substitution G A synonymous_variant R66R 198C>T MALY-DE 16 11349139 11349139 single base substitution C G missense_variant R66P 197G>C MALY-DE 16 11349139 11349139 single base substitution C T missense_variant R66H 197G>A MALY-DE 16 11349141 11349141 single base substitution C T synonymous_variant R65R 195G>A MALY-DE 16 11349145 11349145 single base substitution T G missense_variant Y64S 191A>C MALY-DE 16 11349146 11349146 single base substitution A T missense_variant Y64N 190T>A MALY-DE 16 11349152 11349152 single base substitution C A missense_variant A62S 184G>T MALY-DE 16 11349162 11349162 single base substitution G A synonymous_variant F58F 174C>T MALY-DE 16 11349249 11349249 single base substitution G A synonymous_variant S29S 87C>T MALY-DE 16 11349287 11349287 single base substitution C T missense_variant A17T 49G>A MALY-DE 16 11349290 11349290 single base substitution C A missense_variant A16S 46G>T MALY-DE 16 11349290 11349290 single base substitution C G missense_variant A16P 46G>C MALY-DE 16 11349290 11349290 single base substitution C T missense_variant A16T 46G>A MALY-DE 16 11349292 11349292 single base substitution G C missense_variant T15R 44C>G MALY-DE 16 11349314 11349314 single base substitution C T missense_variant A8T 22G>A MALY-DE 16 11349317 11349317 single base substitution C G missense_variant V7L 19G>C MALY-DE 16 11349318 11349318 single base substitution C G missense_variant Q6H 18G>C MALY-DE 16 11349328 11349328 single base substitution G A missense_variant A3V 8C>T MALY-DE 16 11349329 11349329 single base substitution C T missense_variant A3T 7G>A MALY-DE 16 11349331 11349331 single base substitution A T missense_variant V2E 5T>A MALY-DE 16 11349332 11349332 single base substitution C T missense_variant V2I 4G>A MALY-DE 16 11349337 11349337 single base substitution C G 5_prime_UTR_variant MALY-DE 16 11349338 11349338 single base substitution T G 5_prime_UTR_variant MALY-DE 16 11349409 11349409 single base substitution G A intron_variant MALY-DE 16 11349409 11349409 single base substitution G C intron_variant MALY-DE 16 11349410 11349410 single base substitution C T intron_variant MALY-DE 16 11349434 11349434 single base substitution G A intron_variant MALY-DE 16 11349440 11349440 insertion of <=200bp - GCCG intron_variant MALY-DE 16 11349470 11349470 single base substitution C T intron_variant MALY-DE 16 11349489 11349489 single base substitution G T intron_variant MALY-DE 16 11349497 11349497 single base substitution G A intron_variant MALY-DE 16 11349497 11349497 single base substitution G T intron_variant MALY-DE 16 11349498 11349498 single base substitution C G intron_variant MALY-DE 16 11349500 11349500 single base substitution C T intron_variant MALY-DE 16 11349528 11349528 single base substitution C T intron_variant MALY-DE 16 11349545 11349545 single base substitution G A intron_variant MALY-DE 16 11349545 11349545 single base substitution G C intron_variant MALY-DE 16 11349557 11349557 single base substitution G C intron_variant MALY-DE 16 11349562 11349562 single base substitution G A intron_variant MALY-DE 16 11349565 11349565 single base substitution C G intron_variant MALY-DE 16 11349574 11349574 single base substitution G C intron_variant MALY-DE 16 11349575 11349575 single base substitution C G intron_variant MALY-DE 16 11349581 11349581 single base substitution C T intron_variant MALY-DE 16 11349587 11349587 single base substitution G A intron_variant MALY-DE 16 11349594 11349594 single base substitution G A intron_variant MALY-DE 16 11349626 11349626 single base substitution G A intron_variant MALY-DE 16 11349629 11349629 single base substitution C G intron_variant MALY-DE 16 11349629 11349629 single base substitution C T intron_variant MALY-DE 16 11349650 11349650 single base substitution C A intron_variant MALY-DE 16 11349656 11349656 single base substitution G C intron_variant MALY-DE 16 11349708 11349708 single base substitution C G intron_variant MALY-DE 16 11349716 11349716 single base substitution G A intron_variant MALY-DE 16 11349720 11349720 single base substitution G A intron_variant MALY-DE 16 11349735 11349735 single base substitution C T intron_variant MALY-DE 16 11349748 11349748 single base substitution G A intron_variant MALY-DE 16 11349771 11349771 single base substitution C T intron_variant MALY-DE 16 11349777 11349777 single base substitution G C intron_variant MALY-DE 16 11349826 11349826 single base substitution G C intron_variant MALY-DE 16 11349878 11349878 single base substitution G A intron_variant MALY-DE 16 11350027 11350027 single base substitution C T 5_prime_UTR_variant MALY-DE 16 11350369 11350369 single base substitution C G upstream_gene_variant MALY-DE 16 11350421 11350421 single base substitution C T upstream_gene_variant MALY-DE 16 11350422 11350422 single base substitution C T upstream_gene_variant MALY-DE 16 11350435 11350435 single base substitution G A upstream_gene_variant MALY-DE 16 11350463 11350463 single base substitution C T upstream_gene_variant MALY-DE 16 11350623 11350623 single base substitution C A upstream_gene_variant MALY-DE 16 11351155 11351155 single base substitution T G upstream_gene_variant MALY-DE 16 11351875 11351875 single base substitution G T upstream_gene_variant MELA-AU 16 11343353 11343353 single base substitution G A downstream_gene_variant MELA-AU 16 11343400 11343400 single base substitution G A downstream_gene_variant MELA-AU 16 11343554 11343554 single base substitution G A downstream_gene_variant MELA-AU 16 11343595 11343595 single base substitution G A downstream_gene_variant MELA-AU 16 11343628 11343628 single base substitution G A downstream_gene_variant MELA-AU 16 11343666 11343666 single base substitution C T downstream_gene_variant MELA-AU 16 11343680 11343680 single base substitution C T downstream_gene_variant MELA-AU 16 11343732 11343732 single base substitution C T downstream_gene_variant MELA-AU 16 11343903 11343903 single base substitution G A downstream_gene_variant MELA-AU 16 11344082 11344082 single base substitution G A downstream_gene_variant MELA-AU 16 11344282 11344282 single base substitution C T downstream_gene_variant MELA-AU 16 11344344 11344344 single base substitution C T downstream_gene_variant MELA-AU 16 11344518 11344518 single base substitution C T downstream_gene_variant MELA-AU 16 11344717 11344717 single base substitution C T downstream_gene_variant MELA-AU 16 11344923 11344923 single base substitution G A downstream_gene_variant MELA-AU 16 11345434 11345434 single base substitution A G downstream_gene_variant MELA-AU 16 11345719 11345719 single base substitution C T downstream_gene_variant MELA-AU 16 11346084 11346084 single base substitution G A downstream_gene_variant MELA-AU 16 11346288 11346289 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 11346458 11346458 single base substitution C T downstream_gene_variant MELA-AU 16 11347318 11347318 single base substitution A C downstream_gene_variant MELA-AU 16 11347827 11347827 single base substitution T A downstream_gene_variant MELA-AU 16 11347947 11347947 single base substitution G A downstream_gene_variant MELA-AU 16 11348043 11348043 single base substitution A T downstream_gene_variant MELA-AU 16 11348136 11348136 single base substitution G A downstream_gene_variant MELA-AU 16 11348273 11348273 single base substitution T A 3_prime_UTR_variant MELA-AU 16 11348454 11348454 single base substitution G C 3_prime_UTR_variant MELA-AU 16 11348857 11348857 single base substitution C T missense_variant R160H 479G>A MELA-AU 16 11349379 11349379 single base substitution G A 5_prime_UTR_variant MELA-AU 16 11349501 11349501 single base substitution G A intron_variant MELA-AU 16 11349757 11349757 single base substitution G A intron_variant MELA-AU 16 11350098 11350098 single base substitution G A upstream_gene_variant MELA-AU 16 11350120 11350120 single base substitution G A upstream_gene_variant MELA-AU 16 11350361 11350361 single base substitution C T upstream_gene_variant MELA-AU 16 11350456 11350456 single base substitution G A upstream_gene_variant MELA-AU 16 11350864 11350864 single base substitution G A upstream_gene_variant MELA-AU 16 11351695 11351695 single base substitution C T upstream_gene_variant MELA-AU 16 11351949 11351949 single base substitution C T upstream_gene_variant MELA-AU 16 11352505 11352505 single base substitution G A upstream_gene_variant MELA-AU 16 11352871 11352871 single base substitution G A upstream_gene_variant MELA-AU 16 11353703 11353703 single base substitution G A upstream_gene_variant MELA-AU 16 11353867 11353867 single base substitution G A upstream_gene_variant MELA-AU 16 11353905 11353905 single base substitution G A upstream_gene_variant MELA-AU 16 11354247 11354247 single base substitution C T upstream_gene_variant MELA-AU 16 11354575 11354575 single base substitution G A upstream_gene_variant MELA-AU 16 11354753 11354753 single base substitution G A upstream_gene_variant ORCA-IN 16 11344287 11344287 single base substitution C G downstream_gene_variant ORCA-IN 16 11351042 11351042 single base substitution C G upstream_gene_variant OV-AU 16 11346079 11346079 single base substitution A C downstream_gene_variant OV-AU 16 11349841 11349841 single base substitution C T intron_variant OV-AU 16 11350324 11350324 single base substitution C G upstream_gene_variant OV-AU 16 11350569 11350569 single base substitution A C upstream_gene_variant OV-AU 16 11353814 11353814 single base substitution A G upstream_gene_variant PACA-AU 16 11343294 11343294 single base substitution T C downstream_gene_variant PACA-AU 16 11343499 11343499 single base substitution G T downstream_gene_variant PACA-AU 16 11346492 11346492 single base substitution C T downstream_gene_variant PACA-AU 16 11347898 11347898 single base substitution A T downstream_gene_variant PACA-AU 16 11349076 11349076 single base substitution T C missense_variant H87R 260A>G PACA-AU 16 11352456 11352456 single base substitution T A upstream_gene_variant PACA-AU 16 11354762 11354762 single base substitution C T upstream_gene_variant PACA-CA 16 11344560 11344560 single base substitution T C downstream_gene_variant PACA-CA 16 11346452 11346452 single base substitution A G downstream_gene_variant PACA-CA 16 11346700 11346700 single base substitution T C downstream_gene_variant PACA-CA 16 11346775 11346775 deletion of <=200bp C - downstream_gene_variant PACA-CA 16 11350037 11350037 single base substitution G A upstream_gene_variant PAEN-AU 16 11344181 11344181 single base substitution A C downstream_gene_variant PAEN-AU 16 11344182 11344182 single base substitution T C downstream_gene_variant PAEN-AU 16 11347499 11347499 single base substitution A C downstream_gene_variant PBCA-DE 16 11343496 11343496 single base substitution G A downstream_gene_variant PRAD-CA 16 11348453 11348453 single base substitution A T 3_prime_UTR_variant PRAD-CA 16 11348593 11348593 single base substitution G A 3_prime_UTR_variant PRAD-CA 16 11351874 11351874 single base substitution A C upstream_gene_variant RECA-EU 16 11345073 11345073 single base substitution G A downstream_gene_variant RECA-EU 16 11353494 11353494 single base substitution T A upstream_gene_variant SKCA-BR 16 11343588 11343588 single base substitution G A downstream_gene_variant SKCA-BR 16 11346387 11346387 single base substitution G A downstream_gene_variant SKCA-BR 16 11346739 11346739 single base substitution C T downstream_gene_variant SKCA-BR 16 11346956 11346965 deletion of <=200bp AAAAGAAAAG - downstream_gene_variant SKCA-BR 16 11346965 11346965 single base substitution G A downstream_gene_variant SKCA-BR 16 11348546 11348546 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 11349991 11349991 single base substitution C T 5_prime_UTR_variant SKCA-BR 16 11349992 11349992 single base substitution C T 5_prime_UTR_variant STAD-US 16 11348957 11348957 single base substitution G A missense_variant R127C 379C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 988834 COSM19362 c.186_323del138 p.D63_Q108del Deletion - In frame 16:11255156-11255293 - OCI-LY-1 COSM36158 c.195G>A p.R65R Substitution - coding silent 16:11255284-11255284 - MT-439-T2 COSM5656352 c.195_201delGCGCATC p.I67fs*16 Deletion - Frameshift 16:11255278-11255284 - PM-5 COSM5620116 c.49G>T p.A17S Substitution - Missense 16:11255430-11255430 - 099-T1 COSM5576347 c.3_3delG p.? Unknown 16:11255476-11255476 - 37 COSM36138 c.630G>C p.Q210H Substitution - Missense 16:11254849-11254849 - TCGA-FG-8185-01 COSM3969372 c.297C>A p.G99G Substitution - coding silent 16:11255182-11255182 - 49_tFL COSM4170734 c.227C>T p.A76V Substitution - Missense 16:11255252-11255252 - 467-02-1TD COSM5419422 c.306G>A p.L102L Substitution - coding silent 16:11255173-11255173 - tumor_4159421 COSM5946732 c.416G>C p.G139A Substitution - Missense 16:11255063-11255063 - NCI-H209 COSM25362 c.99C>T p.P33P Substitution - coding silent 16:11255380-11255380 - 731-T1 COSM36133 c.190T>A p.Y64N Substitution - Missense 16:11255289-11255289 - TCGA-AB-2815-03 COSM1317726 c.342C>T p.A114A Substitution - coding silent 16:11255137-11255137 - CTV1 COSM327257 c.203C>T p.T68M Substitution - Missense 16:11255276-11255276 - OCI-LY-19 COSM36162 c.? p.? Unknown 16:11254783-11254784 - 988841 COSM19367 c.150_166del17 p.G51fs*60 Deletion - Frameshift 16:11255313-11255329 - 1295381 COSM36181 c.528G>A p.E176E Substitution - coding silent 16:11254951-11254951 - 2492720 COSM5722399 c.623C>T p.P208L Substitution - Missense 16:11254856-11254856 - 49_tFL COSM4170736 c.184G>C p.A62P Substitution - Missense 16:11255295-11255295 - 1295381 COSM36132 c.614G>A p.S205N Substitution - Missense 16:11254865-11254865 - GHE0605 COSM5713978 c.368C>G p.P123R Substitution - Missense 16:11255111-11255111 - 11_tFL COSM4170733 c.314A>C p.D105A Substitution - Missense 16:11255165-11255165 - 988836 COSM19361 c.236_237ins39 p.F79_Y80ins13 Insertion - In frame 16:11255242-11255243 - 368-T1 COSM36144 c.347G>A p.S116N Substitution - Missense 16:11255132-11255132 - NCI-H209 COSM25361 c.83C>T p.S28F Substitution - Missense 16:11255396-11255396 - tumor_4159421 COSM4170735 c.197G>C p.R66P Substitution - Missense 16:11255282-11255282 - 2492729 COSM5729494 c.107C>T p.P36L Substitution - Missense 16:11255372-11255372 - SU-DHL-18 COSM36148 c.? p.? Unknown KM12 COSM2142171 c.356T>C p.M119T Substitution - Missense 16:11255123-11255123 - 988711 COSM19357 c.343_349delCTTAGCG p.L115fs*1 Deletion - Frameshift 16:11255130-11255136 - tumor_4115001 COSM5947646 c.254G>A p.S85N Substitution - Missense 16:11255225-11255225 - 423-T1 COSM5576342 c.8C>T p.A3V Substitution - Missense 16:11255471-11255471 - 988706 COSM19355 c.388_402del15 p.F130_R134del Deletion - In frame 16:11255077-11255091 - PM-2 COSM5619705 c.502C>T p.Q168* Substitution - Nonsense 16:11254977-11254977 - Farage COSM36183 c.621C>T p.F207F Substitution - coding silent 16:11254858-11254858 - MedB-1 COSM19174 c.526_533delGAGCTGTG p.E176fs*35 Deletion - Frameshift 16:11254946-11254953 - GHE0645 COSM5713482 c.216_217delGC p.L73fs*43 Deletion - Frameshift 16:11255262-11255263 - 416-T1 COSM5576341 c.380G>A p.R127H Substitution - Missense 16:11255099-11255099 - 2492723 COSM5722399 c.623C>T p.P208L Substitution - Missense 16:11254856-11254856 - DLBCL899 COSM1581769 c.14A>G p.N5S Substitution - Missense 16:11255465-11255465 - 1295386 COSM36140 c.190_200del11 p.Y64fs*49 Deletion - Frameshift 16:11255279-11255289 - 1295382 COSM36135 c.240C>G p.Y80* Substitution - Nonsense 16:11255239-11255239 - 988839 COSM19366 c.108_171del64 p.A37fs*27 Deletion - Frameshift 16:11255308-11255371 - Farage COSM36153 c.49G>A p.A17T Substitution - Missense 16:11255430-11255430 - 293-T1 COSM5576350 c.3_4GG>TT p.M1_V2>IL Complex - compound substitution 16:11255475-11255476 - 22-T1 COSM5576346 c.191A>C p.Y64S Substitution - Missense 16:11255288-11255288 - tumor_4159421 COSM5946713 c.607_622del16 p.Y203fs*>4 Deletion - Frameshift 16:11254857-11254872 - DLBCL789 COSM1581767 c.602G>A p.R201H Substitution - Missense 16:11254877-11254877 - Au3 COSM5602346 c.618C>T p.S206S Substitution - coding silent 16:11254861-11254861 - AML53 COSM19319 c.592C>T p.P198S Substitution - Missense 16:11254887-11254887 - 587222 COSM1227089 c.265G>A p.A89T Substitution - Missense 16:11255214-11255214 - 2521262 COSM5892302 c.52G>A p.E18K Substitution - Missense 16:11255427-11255427 - HDLM-2 COSM19164 c.431_512del82 p.F144fs*34 Deletion - Frameshift 16:11254967-11255048 - 1140493 COSM28504 c.145_149delGCCCC p.A49fs*66 Deletion - Frameshift 16:11255330-11255334 - GHE0536 COSM5713438 c.187_212del26 p.D63fs*45 Deletion - Frameshift 16:11255267-11255292 - 1295436 COSM36147 c.80C>T p.S27F Substitution - Missense 16:11255399-11255399 - I2L-P7-Tumor-Organoid COSM2142173 c.225C>T p.D75D Substitution - coding silent 16:11255254-11255254 - 224 COSM4425609 c.603C>T p.R201R Substitution - coding silent 16:11254876-11254876 - 988710 COSM19167 c.349_359del11 p.V117fs*93 Deletion - Frameshift 16:11255120-11255130 - PM-7 COSM5619618 c.330C>G p.N110K Substitution - Missense 16:11255149-11255149 - 2492721 COSM5722399 c.623C>T p.P208L Substitution - Missense 16:11254856-11254856 - B23-Tumor COSM1749401 c.358G>A p.A120T Substitution - Missense 16:11255121-11255121 - L428 COSM19168 c.393_407del15 p.Q131_H136>H Deletion - In frame 16:11255072-11255086 - 988709 COSM19356 c.454_464del11 p.E152fs*58 Deletion - Frameshift 16:11255015-11255025 - sysucc-1370T COSM5470428 c.26C>T p.A9V Substitution - Missense 16:11255453-11255453 - PM-2 COSM5619706 c.338T>G p.F113C Substitution - Missense 16:11255141-11255141 - 1295382 COSM36133 c.190T>A p.Y64N Substitution - Missense 16:11255289-11255289 - DLBCL690 COSM1581768 c.348C>A p.S116R Substitution - Missense 16:11255131-11255131 - 988840 COSM19366 c.108_171del64 p.A37fs*27 Deletion - Frameshift 16:11255308-11255371 - 2492722 COSM5722399 c.623C>T p.P208L Substitution - Missense 16:11254856-11254856 - tumor_4133263 COSM5714368 c.448C>G p.L150V Substitution - Missense 16:11255031-11255031 - PM-5 COSM5620115 c.530T>A p.L177Q Substitution - Missense 16:11254949-11254949 - SC_9008 COSM5547499 c.108delC p.A37fs*48 Deletion - Frameshift 16:11255371-11255371 - QC2-35-T2 COSM36144 c.347G>A p.S116N Substitution - Missense 16:11255132-11255132 - 1295408 COSM36143 c.127C>T p.P43S Substitution - Missense 16:11255352-11255352 - 293-T1 COSM36144 c.347G>A p.S116N Substitution - Missense 16:11255132-11255132 - tumor_4120193 COSM36158 c.195G>A p.R65R Substitution - coding silent 16:11255284-11255284 - GHE0645 COSM5714600 c.416G>T p.G139V Substitution - Missense 16:11255063-11255063 - QC2-39-T2 COSM5656358 c.215_216ins49 p.H90fs*43 Insertion - Frameshift 16:11255263-11255264 - L1236 COSM19166 c.435_448>GG p.D145_L150>EV Complex - deletion inframe 16:11255031-11255044 - GHE0605 COSM5655781 c.192C>G p.Y64* Substitution - Nonsense 16:11255287-11255287 - Farage COSM36182 c.616T>C p.S206P Substitution - Missense 16:11254863-11254863 - PM-5 COSM5620114 c.532T>A p.C178S Substitution - Missense 16:11254947-11254947 - 1295410 COSM36138 c.630G>C p.Q210H Substitution - Missense 16:11254849-11254849 - 293-T1 COSM4170733 c.314A>C p.D105A Substitution - Missense 16:11255165-11255165 - GHE0624 COSM5714368 c.448C>G p.L150V Substitution - Missense 16:11255031-11255031 - T3262 COSM4170731 c.541C>T p.R181C Substitution - Missense 16:11254938-11254938 - tumor_4138885 COSM5946965 c.628_629delCA p.Q210fs*>2 Deletion - Frameshift 16:11254850-11254851 - QC2-39-T2 COSM5576340 c.332G>A p.C111Y Substitution - Missense 16:11255147-11255147 - Farage COSM36154 c.511_537del27 p.V171_R179del Deletion - In frame 16:11254942-11254968 - 988835 COSM19363 c.318_377del60 p.R107_I126del Deletion - In frame 16:11255102-11255161 - tumor_4120193 COSM3927532 c.318C>G p.S106R Substitution - Missense 16:11255161-11255161 - OCI-LY-19 COSM36149 c.379_636del258 p.R127_*212del Deletion - In frame 16:11254843-11255100 - L428 COSM19167 c.349_359del11 p.V117fs*93 Deletion - Frameshift 16:11255120-11255130 - 988842 COSM19368 c.483_489delGCTGGGG p.L162fs*41 Deletion - Frameshift 16:11254990-11254996 - L1236 COSM19165 c.191_218del28 p.Y64fs*12 Deletion - Frameshift 16:11255261-11255288 - 988836 COSM19360 c.471_482del12 p.P158_M161del Deletion - In frame 16:11254997-11255008 - QC2-39-T2 COSM5656340 c.7G>C p.A3P Substitution - Missense 16:11255472-11255472 - 1295451 COSM36148 c.? p.? Unknown tumor_4163639 COSM36152 c.46G>A p.A16T Substitution - Missense 16:11255433-11255433 - 265-T1 COSM5576348 c.15_15delC p.Q6fs*79 Deletion - Frameshift 16:11255464-11255464 - PM-1 COSM5620112 c.50C>A p.A17E Substitution - Missense 16:11255429-11255429 - GHE0605 COSM5713980 c.235T>A p.F79I Substitution - Missense 16:11255244-11255244 - NCI-H209 COSM25362 c.99C>T p.P33P Substitution - coding silent 16:11255380-11255380 - S09-2518-TP COSM4990826 c.564C>T p.R188R Substitution - coding silent 16:11254915-11254915 - 988712 COSM19358 c.208_257del50 p.S71fs*29 Deletion - Frameshift 16:11255222-11255271 - QC2-39-T2 COSM5655781 c.192C>G p.Y64* Substitution - Nonsense 16:11255287-11255287 - GHE0605 COSM5713979 c.299C>A p.T100N Substitution - Missense 16:11255180-11255180 - PM-7 COSM5619745 c.383T>A p.V128E Substitution - Missense 16:11255096-11255096 - tumor_4163639 COSM1161153 c.360C>T p.A120A Substitution - coding silent 16:11255119-11255119 - 1295384 COSM36138 c.630G>C p.Q210H Substitution - Missense 16:11254849-11254849 - 27_tFL COSM4170731 c.541C>T p.R181C Substitution - Missense 16:11254938-11254938 - 731-T1 COSM5576343 c.174C>G p.F58L Substitution - Missense 16:11255305-11255305 - 1295407 COSM36142 c.353_367del15 p.K118_P123>T Complex - deletion inframe 16:11255112-11255126 - 27_tFL COSM4170732 c.534C>G p.C178W Substitution - Missense 16:11254945-11254945 - tumor_4138885 COSM36133 c.190T>A p.Y64N Substitution - Missense 16:11255289-11255289 - QC2-39-T2 COSM5656341 c.4G>T p.V2L Substitution - Missense 16:11255475-11255475 - tumor_4163639 COSM1161151 c.479G>A p.R160H Substitution - Missense 16:11255000-11255000 - 988837 COSM19364 c.192_541del350 p.Y64fs*1 Deletion - Frameshift 16:11254938-11255287 - 1295381 COSM36152 c.46G>A p.A16T Substitution - Missense 16:11255433-11255433 - 731-T1 COSM5576344 c.200T>C p.I67T Substitution - Missense 16:11255279-11255279 - MT-260-T2 COSM5656348 c.166_204del39 p.T57_R69del13 Deletion - In frame 16:11255275-11255313 - PM-5 COSM2142169 c.485T>G p.L162R Substitution - Missense 16:11254994-11254994 - tumor_4163639 COSM1161152 c.404T>G p.F135C Substitution - Missense 16:11255075-11255075 - S08-41239-TP COSM4990827 c.409C>T p.L137L Substitution - coding silent 16:11255070-11255070 - MT-439-T2 COSM5656351 c.202A>C p.T68P Substitution - Missense 16:11255277-11255277 - 988838 COSM19365 c.216_225del10 p.L73fs*9 Deletion - Frameshift 16:11255254-11255263 - QC2-39-T2 COSM5655780 c.305T>A p.L102Q Substitution - Missense 16:11255174-11255174 - QC2-39-T2 COSM5656338 c.49G>C p.A17P Substitution - Missense 16:11255430-11255430 - CSCC-4-T COSM4589681 c.491_492insG p.L166fs*>47 Insertion - Frameshift 16:11254987-11254988 - tumor_4120193 COSM36153 c.49G>A p.A17T Substitution - Missense 16:11255430-11255430 - 731-T1 COSM5576345 c.296G>A p.G99D Substitution - Missense 16:11255183-11255183 - 1295381 COSM36148 c.? p.? Unknown MT-260-T2 COSM5655781 c.192C>G p.Y64* Substitution - Nonsense 16:11255287-11255287 - GHE0605 COSM5713452 c.195_199delGCGCA p.R66fs*49 Deletion - Frameshift 16:11255280-11255284 - 1295422 COSM36146 c.391C>A p.Q131K Substitution - Missense 16:11255088-11255088 - tumor_4159421 COSM5946746 c.598C>T p.L200F Substitution - Missense 16:11254881-11254881 - 988708 COSM19356 c.454_464del11 p.E152fs*58 Deletion - Frameshift 16:11255015-11255025 - tumor_4163639 COSM1161155 c.4G>A p.V2I Substitution - Missense 16:11255475-11255475 - GHE1438 COSM5713535 c.305_319del15 p.L102_S106delLVRDS Deletion - In frame 16:11255160-11255174 - 988713 COSM19359 c.193_203del11 p.R65fs*48 Deletion - Frameshift 16:11255276-11255286 - JURKAT COSM327258 c.384G>A p.V128V Substitution - coding silent 16:11255095-11255095 - TCGA-32-4213-01 COSM3402064 c.617C>A p.S206Y Substitution - Missense 16:11254862-11254862 - PM-5 COSM1161154 c.18G>C p.Q6H Substitution - Missense 16:11255461-11255461 - tumor_4163639 COSM1161154 c.18G>C p.Q6H Substitution - Missense 16:11255461-11255461 - tumor_4133263 COSM5947826 c.374G>C p.S125T Substitution - Missense 16:11255105-11255105 - 49_tFL COSM4170735 c.197G>C p.R66P Substitution - Missense 16:11255282-11255282 - SU-DHL-8 COSM36157 c.177_195del19 p.S60fs*19 Deletion - Frameshift 16:11255284-11255302 - 1295382 COSM36136 c.241T>A p.W81R Substitution - Missense 16:11255238-11255238 - GHE0536 COSM5713844 c.316A>T p.S106C Substitution - Missense 16:11255163-11255163 - TCGA-CG-5721-01 COSM4058200 c.379C>T p.R127C Substitution - Missense 16:11255100-11255100 - GHE0645 COSM5713980 c.235T>A p.F79I Substitution - Missense 16:11255244-11255244 - tumor_4120193 COSM3927533 c.46G>C p.A16P Substitution - Missense 16:11255433-11255433 - 988707 COSM19174 c.526_533delGAGCTGTG p.E176fs*35 Deletion - Frameshift 16:11254946-11254953 - 988833 COSM19175 c.552_575del24 p.A184_L191del Deletion - In frame 16:11254904-11254927 - MedB-1 COSM19175 c.552_575del24 p.A184_L191del Deletion - In frame 16:11254904-11254927 - tumor_4133263 COSM5947817 c.276G>C p.R92R Substitution - coding silent 16:11255203-11255203 - 24_tFL COSM4170737 c.16C>T p.Q6* Substitution - Nonsense 16:11255463-11255463 - PM-2 COSM5619707 c.35C>A p.A12E Substitution - Missense 16:11255444-11255444 - 1350382 COSM43358 c.636+24A>G p.? Unknown 16:11254819-11254819 - GHE0609 COSM5713465 c.449_462del14 p.L150fs*>58 Deletion - Frameshift 16:11255017-11255030 - QC2-39-T2 COSM5656339 c.46G>T p.A16S Substitution - Missense 16:11255433-11255433 - 1295385 COSM36139 c.7G>A p.A3T Substitution - Missense 16:11255472-11255472 - Jurkat COSM19320 c.490delG p.A164fs*41 Deletion - Frameshift 16:11254989-11254989 - GHE0645 COSM5714601 c.301T>G p.F101V Substitution - Missense 16:11255178-11255178 - GHE0605 COSM36135 c.240C>G p.Y80* Substitution - Nonsense 16:11255239-11255239 - 1295382 COSM36134 c.236T>G p.F79C Substitution - Missense 16:11255243-11255243 - 2538137 COSM36143 c.127C>T p.P43S Substitution - Missense 16:11255352-11255352 - QC2-39-T2 COSM5656357 c.240_241ins49 p.H90fs*43 Insertion - Frameshift 16:11255238-11255239 - 1295387 COSM36141 c.? p.? Unknown 16:11255480-11255480 - tumor_4163639 COSM36158 c.195G>A p.R65R Substitution - coding silent 16:11255284-11255284 - B23 COSM1749401 c.358G>A p.A120T Substitution - Missense 16:11255121-11255121 - DM26 COSM5610667 c.585C>T p.P195P Substitution - coding silent 16:11254894-11254894 - LIM2551 COSM4058200 c.379C>T p.R127C Substitution - Missense 16:11255100-11255100 - 265-T1 COSM5576349 c.113_210del98 p.R38fs*46 Deletion - Frameshift 16:11255269-11255366 - AML36 COSM19319 c.592C>T p.P198S Substitution - Missense 16:11254887-11254887 - 099-T1 COSM5576340 c.332G>A p.C111Y Substitution - Missense 16:11255147-11255147 - Farage COSM36152 c.46G>A p.A16T Substitution - Missense 16:11255433-11255433 - PM-4 COSM36144 c.347G>A p.S116N Substitution - Missense 16:11255132-11255132 - 1295409 COSM36144 c.347G>A p.S116N Substitution - Missense 16:11255132-11255132 - tumor_4163639 COSM36139 c.7G>A p.A3T Substitution - Missense 16:11255472-11255472 - PM-3 COSM5620113 c.401G>A p.R134H Substitution - Missense 16:11255078-11255078 - 416-T1 COSM36135 c.240C>G p.Y80* Substitution - Nonsense 16:11255239-11255239 - 8067216 COSM3772128 c.260A>G p.H87R Substitution - Missense 16:11255219-11255219 - Farage COSM36148 c.? p.? Unknown tumor_4163639 COSM1161150 c.622C>T p.P208S Substitution - Missense 16:11254857-11254857 - 1295381 COSM36180 c.345T>G p.L115L Substitution - coding silent 16:11255134-11255134 - 1295383 COSM36137 c.495_502delGCTGCGCC p.L166fs*45 Deletion - Frameshift 16:11254977-11254984 - tumor_4159421 COSM5946594 c.199A>T p.I67F Substitution - Missense 16:11255280-11255280 - 988833 COSM19174 c.526_533delGAGCTGTG p.E176fs*35 Deletion - Frameshift 16:11254946-11254953 - GHE0605 COSM5713977 c.610C>G p.L204V Substitution - Missense 16:11254869-11254869 - KM12 COSM4638932 c.372G>A p.T124T Substitution - coding silent 16:11255107-11255107 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.50563;Hs.50571;Hs.50607;Hs.50640 16p13.13 603597

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.633+240T>G 16 11348463 DLBCL A C Missense p.F135C c.404T>G 16 11348932 DLBCL C G 3-UTRSNV . c.633+112G>C 16 11348591 DLBCL C G 3-UTRSNV . c.633+98G>C 16 11348605 DLBCL C G Missense p.Q6H c.18G>C 16 11349318 DLBCL C T 3-UTRSNV . c.633+117G>A 16 11348586 DLBCL C T 3-UTRSNV . c.633+39G>A 16 11348664 DLBCL C T Missense p.A16T c.46G>A 16 11349290 DLBCL C T Missense p.A3T c.7G>A 16 11349329 DLBCL C T Missense p.R160H c.479G>A 16 11348857 DLBCL C T Missense p.V2I c.4G>A 16 11349332 DLBCL C T Synonymous p.L102L c.306G>A 16 11349030 CLL C T Synonymous p.R65R c.195G>A 16 11349141 DLBCL G A 3-UTRSNV . c.633+176C>T 16 11348527 DLBCL G A Missense p.P208S c.622C>T 16 11348714 DLBCL G A Synonymous p.A120A c.360C>T 16 11348976 DLBCL G C 3-UTRSNV . c.633+281C>G 16 11348422 DLBCL G T Missense p.S206Y c.617C>A 16 11348719 GBM