Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 66243098 66243098 + Silent SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr11:66243098C>T c.870C>T c.(868-870)gaC>gaT p.D290D BLCA 11 66236342 66236342 + Missense_Mutation SNP G G C TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr11:66236342G>C c.191G>C c.(190-192)aGa>aCa p.R64T BLCA 11 66241241 66241241 + Silent SNP C C T TCGA-DK-A2HX-01A-12D-A18F-08 TCGA-DK-A2HX-10A-01D-A18F-08 g.chr11:66241241C>T c.685C>T c.(685-687)Ctg>Ttg p.L229L BLCA 11 66241314 66241314 + Missense_Mutation SNP C C T TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr11:66241314C>T c.758C>T c.(757-759)cCg>cTg p.P253L BRCA 11 66236347 66236347 + Nonsense_Mutation SNP G G T TCGA-C8-A1HL-01A-11D-A135-09 TCGA-C8-A1HL-10A-01D-A135-09 g.chr11:66236347G>T c.196G>T c.(196-198)Gaa>Taa p.E66* BRCA 11 66238754 66238754 + Missense_Mutation SNP G G A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr11:66238754G>A c.266G>A c.(265-267)cGa>cAa p.R89Q CESC 11 66238754 66238754 + Missense_Mutation SNP G G A TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr11:66238754G>A c.266G>A c.(265-267)cGa>cAa p.R89Q CESC 11 66240739 66240739 + Missense_Mutation SNP G G A TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr11:66240739G>A c.484G>A c.(484-486)Gac>Aac p.D162N COAD 11 66238792 66238792 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:66238792G>A c.304G>A c.(304-306)Ggg>Agg p.G102R COAD 11 66238807 66238807 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:66238807G>A c.319G>A c.(319-321)Gtc>Atc p.V107I COAD 11 66238834 66238834 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:66238834G>A c.346G>A c.(346-348)Gtc>Atc p.V116I COAD 11 66240860 66240860 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:66240860G>A c.605G>A c.(604-606)cGc>cAc p.R202H COAD 11 66241211 66241211 + Nonsense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:66241211C>T c.655C>T c.(655-657)Cga>Tga p.R219* COAD 11 66241271 66241271 + Missense_Mutation SNP C C A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:66241271C>A c.715C>A c.(715-717)Ctg>Atg p.L239M COAD 11 66243138 66243138 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:66243138C>T c.910C>T c.(910-912)Cgc>Tgc p.R304C COAD 11 66243390 66243390 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:66243390C>T c.1162C>T c.(1162-1164)Cgc>Tgc p.R388C COADREAD 11 66238792 66238792 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:66238792G>A c.304G>A c.(304-306)Ggg>Agg p.G102R COADREAD 11 66238807 66238807 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:66238807G>A c.319G>A c.(319-321)Gtc>Atc p.V107I COADREAD 11 66238834 66238834 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:66238834G>A c.346G>A c.(346-348)Gtc>Atc p.V116I COADREAD 11 66240754 66240754 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:66240754G>T c.499G>T c.(499-501)Gac>Tac p.D167Y COADREAD 11 66240860 66240860 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:66240860G>A c.605G>A c.(604-606)cGc>cAc p.R202H COADREAD 11 66241211 66241211 + Nonsense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:66241211C>T c.655C>T c.(655-657)Cga>Tga p.R219* COADREAD 11 66241271 66241271 + Missense_Mutation SNP C C A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:66241271C>A c.715C>A c.(715-717)Ctg>Atg p.L239M COADREAD 11 66243138 66243138 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:66243138C>T c.910C>T c.(910-912)Cgc>Tgc p.R304C COADREAD 11 66243390 66243390 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:66243390C>T c.1162C>T c.(1162-1164)Cgc>Tgc p.R388C ESCA 11 66235713 66235713 + Silent SNP C C A TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr11:66235713C>A c.114C>A c.(112-114)ggC>ggA p.G38G ESCA 11 66238737 66238737 + Silent SNP G G T TCGA-L5-A8NW-01A-11D-A37C-09 TCGA-L5-A8NW-11A-11D-A37F-09 g.chr11:66238737G>T c.249G>T c.(247-249)ggG>ggT p.G83G ESCA 11 66239874 66239874 + Missense_Mutation SNP A A C TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr11:66239874A>C c.389A>C c.(388-390)tAt>tCt p.Y130S ESCA 11 66239923 66239923 + Silent SNP C C T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr11:66239923C>T c.438C>T c.(436-438)agC>agT p.S146S ESCA 11 66241210 66241210 + Silent SNP G G A TCGA-XP-A8T6-01A-11D-A36J-09 TCGA-XP-A8T6-10A-01D-A36M-09 g.chr11:66241210G>A c.654G>A c.(652-654)gaG>gaA p.E218E ESCA 11 66241227 66241227 + Missense_Mutation SNP G G A TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr11:66241227G>A c.671G>A c.(670-672)cGg>cAg p.R224Q GBMLGG 11 66235654 66235654 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:66235654C>T c.55C>T c.(55-57)Cac>Tac p.H19Y GBMLGG 11 66241285 66241285 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:66241285G>A c.729G>A c.(727-729)ccG>ccA p.P243P GBMLGG 11 66243277 66243277 + Missense_Mutation SNP C C T TCGA-DH-5140-01A-01D-1468-08 TCGA-DH-5140-10A-01D-1468-08 g.chr11:66243277C>T c.1049C>T c.(1048-1050)gCg>gTg p.A350V GBMLGG 11 66243323 66243323 + Silent SNP C C T TCGA-QH-A6X9-01A-12D-A32B-08 TCGA-QH-A6X9-10B-01D-A329-08 g.chr11:66243323C>T c.1095C>T c.(1093-1095)gtC>gtT p.V365V GBMLGG 11 66243444 66243444 + Silent SNP C C T TCGA-S9-A6WQ-01A-12D-A34A-08 TCGA-S9-A6WQ-10A-01D-A34A-08 g.chr11:66243444C>T c.1216C>T c.(1216-1218)Ctg>Ttg p.L406L GBMLGG 11 66243521 66243521 + Silent SNP C C A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr11:66243521C>A c.1293C>A c.(1291-1293)gcC>gcA p.A431A HNSC 11 66238754 66238754 + Missense_Mutation SNP G G A TCGA-CR-7392-01A-11D-2012-08 TCGA-CR-7392-10A-01D-2013-08 g.chr11:66238754G>A c.266G>A c.(265-267)cGa>cAa p.R89Q LGG 11 66235654 66235654 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:66235654C>T c.55C>T c.(55-57)Cac>Tac p.H19Y LGG 11 66241285 66241285 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:66241285G>A c.729G>A c.(727-729)ccG>ccA p.P243P LGG 11 66243277 66243277 + Missense_Mutation SNP C C T TCGA-DH-5140-01A-01D-1468-08 TCGA-DH-5140-10A-01D-1468-08 g.chr11:66243277C>T c.1049C>T c.(1048-1050)gCg>gTg p.A350V LGG 11 66243323 66243323 + Silent SNP C C T TCGA-QH-A6X9-01A-12D-A32B-08 TCGA-QH-A6X9-10B-01D-A329-08 g.chr11:66243323C>T c.1095C>T c.(1093-1095)gtC>gtT p.V365V LGG 11 66243444 66243444 + Silent SNP C C T TCGA-S9-A6WQ-01A-12D-A34A-08 TCGA-S9-A6WQ-10A-01D-A34A-08 g.chr11:66243444C>T c.1216C>T c.(1216-1218)Ctg>Ttg p.L406L LGG 11 66243521 66243521 + Silent SNP C C A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr11:66243521C>A c.1293C>A c.(1291-1293)gcC>gcA p.A431A LIHC 11 66243164 66243164 + Silent SNP T T C TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr11:66243164T>C c.936T>C c.(934-936)gcT>gcC p.A312A LIHC 11 66243202 66243202 + Missense_Mutation SNP C C A TCGA-QA-A7B7-01A-11D-A32G-10 TCGA-QA-A7B7-10A-01D-A32G-10 g.chr11:66243202C>A c.974C>A c.(973-975)gCa>gAa p.A325E LUAD 11 66235598 66235598 + Splice_Site SNP G G A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr11:66235598G>A c.e2-1 LUAD 11 66235688 66235688 + Missense_Mutation SNP C C G TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chr11:66235688C>G c.89C>G c.(88-90)tCt>tGt p.S30C LUAD 11 66238754 66238754 + Missense_Mutation SNP G G A TCGA-55-8505-01A-11D-2393-08 TCGA-55-8505-10A-01D-2393-08 g.chr11:66238754G>A c.266G>A c.(265-267)cGa>cAa p.R89Q LUSC 11 66239871 66239871 + Nonsense_Mutation SNP C C A TCGA-63-5128-01A-01D-1441-08 TCGA-63-5128-10A-01D-1441-08 g.chr11:66239871C>A c.386C>A c.(385-387)tCg>tAg p.S129* LUSC 11 66243384 66243384 + Missense_Mutation SNP C C G TCGA-39-5019-01A-01D-1817-08 TCGA-39-5019-11A-01D-1817-08 g.chr11:66243384C>G c.1156C>G c.(1156-1158)Ctc>Gtc p.L386V OV 11 66240744 66240744 + Silent SNP C C T TCGA-13-1491-01A-01W-0549-09 TCGA-13-1491-10A-01W-0549-09 g.chr11:66240744C>T c.489C>T c.(487-489)ttC>ttT p.F163F PAAD 11 66243552 66243552 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:66243552T>C c.1324T>C c.(1324-1326)Ttc>Ctc p.F442L READ 11 66240754 66240754 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:66240754G>T c.499G>T c.(499-501)Gac>Tac p.D167Y SARC 11 66243176 66243176 + Silent SNP G G A TCGA-DX-A7EU-01A-22D-A36J-09 TCGA-DX-A7EU-10A-01D-A36M-09 g.chr11:66243176G>A c.948G>A c.(946-948)aaG>aaA p.K316K SARC 11 66243493 66243493 + Missense_Mutation SNP G G A TCGA-DX-A7EU-01A-22D-A36J-09 TCGA-DX-A7EU-10A-01D-A36M-09 g.chr11:66243493G>A c.1265G>A c.(1264-1266)tGc>tAc p.C422Y SARC 11 66243577 66243577 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:66243577G>A c.1349G>A c.(1348-1350)gGg>gAg p.G450E SKCM 11 66239884 66239884 + Silent SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr11:66239884C>T c.399C>T c.(397-399)tcC>tcT p.S133S SKCM 11 66239885 66239885 + Missense_Mutation SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr11:66239885C>T c.400C>T c.(400-402)Cgg>Tgg p.R134W SKCM 11 66241232 66241232 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr11:66241232C>T c.676C>T c.(676-678)Cca>Tca p.P226S SKCM 11 66241261 66241261 + Silent SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr11:66241261C>T c.705C>T c.(703-705)acC>acT p.T235T SKCM 11 66243537 66243537 + Missense_Mutation SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr11:66243537C>T c.1309C>T c.(1309-1311)Cac>Tac p.H437Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 11 66236342 66236342 single base substitution G C intron_variant BLCA-US 11 66236342 66236342 single base substitution G C missense_variant R64T 191G>C BLCA-US 11 66236342 66236342 single base substitution G C upstream_gene_variant BLCA-US 11 66241241 66241241 single base substitution C T 3_prime_UTR_variant BLCA-US 11 66241241 66241241 single base substitution C T downstream_gene_variant BLCA-US 11 66241241 66241241 single base substitution C T intron_variant BLCA-US 11 66241241 66241241 single base substitution C T synonymous_variant L122L 364C>T BLCA-US 11 66241241 66241241 single base substitution C T synonymous_variant L16L 46C>T BLCA-US 11 66241241 66241241 single base substitution C T synonymous_variant L205L 613C>T BLCA-US 11 66241241 66241241 single base substitution C T synonymous_variant L229L 685C>T BRCA-EU 11 66232145 66232145 single base substitution A C upstream_gene_variant BRCA-EU 11 66235006 66235006 single base substitution G A 5_prime_UTR_variant BRCA-EU 11 66235006 66235006 single base substitution G A intron_variant BRCA-EU 11 66235298 66235298 single base substitution G A intron_variant BRCA-EU 11 66235378 66235378 single base substitution C A intron_variant BRCA-EU 11 66237922 66237922 single base substitution G C intron_variant BRCA-EU 11 66237922 66237922 single base substitution G C upstream_gene_variant BRCA-EU 11 66238269 66238269 single base substitution G A intron_variant BRCA-EU 11 66238269 66238269 single base substitution G A upstream_gene_variant BRCA-EU 11 66239002 66239002 single base substitution G C downstream_gene_variant BRCA-EU 11 66239002 66239002 single base substitution G C intron_variant BRCA-EU 11 66239002 66239002 single base substitution G C upstream_gene_variant BRCA-EU 11 66239380 66239380 single base substitution G C downstream_gene_variant BRCA-EU 11 66239380 66239380 single base substitution G C intron_variant BRCA-EU 11 66239380 66239380 single base substitution G C upstream_gene_variant BRCA-EU 11 66240431 66240431 single base substitution A G downstream_gene_variant BRCA-EU 11 66240431 66240431 single base substitution A G intron_variant BRCA-EU 11 66240431 66240431 single base substitution A G upstream_gene_variant BRCA-EU 11 66242310 66242310 single base substitution C T downstream_gene_variant BRCA-EU 11 66242310 66242310 single base substitution C T intron_variant BRCA-EU 11 66243575 66243575 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 66243575 66243575 single base substitution C T downstream_gene_variant BRCA-EU 11 66243575 66243575 single base substitution C T synonymous_variant C425C 1275C>T BRCA-EU 11 66243575 66243575 single base substitution C T synonymous_variant C449C 1347C>T BRCA-EU 11 66244725 66244725 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 66244725 66244725 single base substitution G A downstream_gene_variant BRCA-EU 11 66245310 66245310 single base substitution G C downstream_gene_variant BRCA-EU 11 66247540 66247540 single base substitution G A downstream_gene_variant BRCA-EU 11 66248982 66248982 single base substitution G T downstream_gene_variant BRCA-EU 11 66249303 66249303 single base substitution G A downstream_gene_variant BRCA-FR 11 66235298 66235298 single base substitution G A intron_variant BRCA-FR 11 66245310 66245310 single base substitution G C downstream_gene_variant BRCA-UK 11 66237922 66237922 single base substitution G C intron_variant BRCA-UK 11 66237922 66237922 single base substitution G C upstream_gene_variant BRCA-UK 11 66238754 66238754 single base substitution G A 5_prime_UTR_variant BRCA-UK 11 66238754 66238754 single base substitution G A exon_variant BRCA-UK 11 66238754 66238754 single base substitution G A intron_variant BRCA-UK 11 66238754 66238754 single base substitution G A missense_variant R65Q 194G>A BRCA-UK 11 66238754 66238754 single base substitution G A missense_variant R89Q 266G>A BRCA-UK 11 66238754 66238754 single base substitution G A upstream_gene_variant BRCA-UK 11 66239002 66239002 single base substitution G C downstream_gene_variant BRCA-UK 11 66239002 66239002 single base substitution G C intron_variant BRCA-UK 11 66239002 66239002 single base substitution G C upstream_gene_variant BRCA-US 11 66236347 66236347 single base substitution G T intron_variant BRCA-US 11 66236347 66236347 single base substitution G T stop_gained E66* 196G>T BRCA-US 11 66236347 66236347 single base substitution G T upstream_gene_variant BRCA-US 11 66238754 66238754 single base substitution G A 5_prime_UTR_variant BRCA-US 11 66238754 66238754 single base substitution G A exon_variant BRCA-US 11 66238754 66238754 single base substitution G A intron_variant BRCA-US 11 66238754 66238754 single base substitution G A missense_variant R65Q 194G>A BRCA-US 11 66238754 66238754 single base substitution G A missense_variant R89Q 266G>A BRCA-US 11 66238754 66238754 single base substitution G A upstream_gene_variant BTCA-JP 11 66238750 66238750 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BTCA-JP 11 66238750 66238750 single base substitution C T exon_variant BTCA-JP 11 66238750 66238750 single base substitution C T intron_variant BTCA-JP 11 66238750 66238750 single base substitution C T missense_variant R64W 190C>T BTCA-JP 11 66238750 66238750 single base substitution C T missense_variant R88W 262C>T BTCA-JP 11 66238750 66238750 single base substitution C T upstream_gene_variant BTCA-JP 11 66243200 66243200 single base substitution G C 3_prime_UTR_variant BTCA-JP 11 66243200 66243200 single base substitution G C downstream_gene_variant BTCA-JP 11 66243200 66243200 single base substitution G C intron_variant BTCA-JP 11 66243200 66243200 single base substitution G C missense_variant E217D 651G>C BTCA-JP 11 66243200 66243200 single base substitution G C missense_variant E300D 900G>C BTCA-JP 11 66243200 66243200 single base substitution G C missense_variant E324D 972G>C BTCA-JP 11 66243213 66243213 single base substitution C T 3_prime_UTR_variant BTCA-JP 11 66243213 66243213 single base substitution C T downstream_gene_variant BTCA-JP 11 66243213 66243213 single base substitution C T intron_variant BTCA-JP 11 66243213 66243213 single base substitution C T missense_variant R222W 664C>T BTCA-JP 11 66243213 66243213 single base substitution C T missense_variant R305W 913C>T BTCA-JP 11 66243213 66243213 single base substitution C T missense_variant R329W 985C>T BTCA-JP 11 66248122 66248122 single base substitution G T downstream_gene_variant CESC-US 11 66238754 66238754 single base substitution G A 5_prime_UTR_variant CESC-US 11 66238754 66238754 single base substitution G A exon_variant CESC-US 11 66238754 66238754 single base substitution G A intron_variant CESC-US 11 66238754 66238754 single base substitution G A missense_variant R65Q 194G>A CESC-US 11 66238754 66238754 single base substitution G A missense_variant R89Q 266G>A CESC-US 11 66238754 66238754 single base substitution G A upstream_gene_variant CESC-US 11 66240739 66240739 single base substitution G A 3_prime_UTR_variant CESC-US 11 66240739 66240739 single base substitution G A downstream_gene_variant CESC-US 11 66240739 66240739 single base substitution G A intron_variant CESC-US 11 66240739 66240739 single base substitution G A missense_variant D138N 412G>A CESC-US 11 66240739 66240739 single base substitution G A missense_variant D162N 484G>A CESC-US 11 66240739 66240739 single base substitution G A missense_variant D55N 163G>A CESC-US 11 66240739 66240739 single base substitution G A upstream_gene_variant CLLE-ES 11 66247758 66247758 single base substitution C T downstream_gene_variant COAD-US 11 66238792 66238792 single base substitution G A 5_prime_UTR_variant COAD-US 11 66238792 66238792 single base substitution G A exon_variant COAD-US 11 66238792 66238792 single base substitution G A intron_variant COAD-US 11 66238792 66238792 single base substitution G A missense_variant G102R 304G>A COAD-US 11 66238792 66238792 single base substitution G A missense_variant G78R 232G>A COAD-US 11 66238792 66238792 single base substitution G A upstream_gene_variant COAD-US 11 66240860 66240860 single base substitution G A 3_prime_UTR_variant COAD-US 11 66240860 66240860 single base substitution G A downstream_gene_variant COAD-US 11 66240860 66240860 single base substitution G A intron_variant COAD-US 11 66240860 66240860 single base substitution G A missense_variant R178H 533G>A COAD-US 11 66240860 66240860 single base substitution G A missense_variant R202H 605G>A COAD-US 11 66240860 66240860 single base substitution G A missense_variant R95H 284G>A COAD-US 11 66240860 66240860 single base substitution G A upstream_gene_variant COAD-US 11 66241271 66241271 single base substitution C A 3_prime_UTR_variant COAD-US 11 66241271 66241271 single base substitution C A downstream_gene_variant COAD-US 11 66241271 66241271 single base substitution C A intron_variant COAD-US 11 66241271 66241271 single base substitution C A missense_variant L132M 394C>A COAD-US 11 66241271 66241271 single base substitution C A missense_variant L215M 643C>A COAD-US 11 66241271 66241271 single base substitution C A missense_variant L239M 715C>A COAD-US 11 66241271 66241271 single base substitution C A missense_variant L26M 76C>A COAD-US 11 66243138 66243138 single base substitution C T 3_prime_UTR_variant COAD-US 11 66243138 66243138 single base substitution C T downstream_gene_variant COAD-US 11 66243138 66243138 single base substitution C T intron_variant COAD-US 11 66243138 66243138 single base substitution C T missense_variant R197C 589C>T COAD-US 11 66243138 66243138 single base substitution C T missense_variant R280C 838C>T COAD-US 11 66243138 66243138 single base substitution C T missense_variant R304C 910C>T COAD-US 11 66243390 66243390 single base substitution C T 3_prime_UTR_variant COAD-US 11 66243390 66243390 single base substitution C T downstream_gene_variant COAD-US 11 66243390 66243390 single base substitution C T exon_variant COAD-US 11 66243390 66243390 single base substitution C T missense_variant R364C 1090C>T COAD-US 11 66243390 66243390 single base substitution C T missense_variant R388C 1162C>T COAD-US 11 66249769 66249769 single base substitution A G downstream_gene_variant COCA-CN 11 66235581 66235581 single base substitution C A intron_variant COCA-CN 11 66238778 66238778 single base substitution G A 5_prime_UTR_variant COCA-CN 11 66238778 66238778 single base substitution G A exon_variant COCA-CN 11 66238778 66238778 single base substitution G A intron_variant COCA-CN 11 66238778 66238778 single base substitution G A missense_variant R73Q 218G>A COCA-CN 11 66238778 66238778 single base substitution G A missense_variant R97Q 290G>A COCA-CN 11 66238778 66238778 single base substitution G A upstream_gene_variant COCA-CN 11 66238926 66238926 single base substitution C T downstream_gene_variant COCA-CN 11 66238926 66238926 single base substitution C T intron_variant COCA-CN 11 66238926 66238926 single base substitution C T upstream_gene_variant COCA-CN 11 66240781 66240781 single base substitution G A 3_prime_UTR_variant COCA-CN 11 66240781 66240781 single base substitution G A downstream_gene_variant COCA-CN 11 66240781 66240781 single base substitution G A intron_variant COCA-CN 11 66240781 66240781 single base substitution G A missense_variant E152K 454G>A COCA-CN 11 66240781 66240781 single base substitution G A missense_variant E176K 526G>A COCA-CN 11 66240781 66240781 single base substitution G A missense_variant E69K 205G>A COCA-CN 11 66240781 66240781 single base substitution G A upstream_gene_variant COCA-CN 11 66249742 66249742 single base substitution G A downstream_gene_variant EOPC-DE 11 66248985 66248985 single base substitution G T downstream_gene_variant ESAD-UK 11 66232152 66232152 single base substitution T A upstream_gene_variant ESAD-UK 11 66232654 66232654 single base substitution G A upstream_gene_variant ESAD-UK 11 66233730 66233730 single base substitution T G upstream_gene_variant ESAD-UK 11 66233903 66233903 single base substitution G T upstream_gene_variant ESAD-UK 11 66234111 66234111 single base substitution G T upstream_gene_variant ESAD-UK 11 66235424 66235424 single base substitution C T intron_variant ESAD-UK 11 66237694 66237694 single base substitution T G intron_variant ESAD-UK 11 66237694 66237694 single base substitution T G upstream_gene_variant ESAD-UK 11 66240666 66240666 single base substitution T C downstream_gene_variant ESAD-UK 11 66240666 66240666 single base substitution T C intron_variant ESAD-UK 11 66240666 66240666 single base substitution T C upstream_gene_variant ESAD-UK 11 66244484 66244484 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 66244484 66244484 single base substitution C T downstream_gene_variant ESAD-UK 11 66245252 66245252 single base substitution A G downstream_gene_variant ESAD-UK 11 66247672 66247672 single base substitution G C downstream_gene_variant ESAD-UK 11 66249041 66249041 single base substitution C T downstream_gene_variant LGG-US 11 66243277 66243277 single base substitution C T 3_prime_UTR_variant LGG-US 11 66243277 66243277 single base substitution C T downstream_gene_variant LGG-US 11 66243277 66243277 single base substitution C T exon_variant LGG-US 11 66243277 66243277 single base substitution C T missense_variant A243V 728C>T LGG-US 11 66243277 66243277 single base substitution C T missense_variant A326V 977C>T LGG-US 11 66243277 66243277 single base substitution C T missense_variant A350V 1049C>T LGG-US 11 66243521 66243521 single base substitution C A 3_prime_UTR_variant LGG-US 11 66243521 66243521 single base substitution C A downstream_gene_variant LGG-US 11 66243521 66243521 single base substitution C A synonymous_variant A407A 1221C>A LGG-US 11 66243521 66243521 single base substitution C A synonymous_variant A431A 1293C>A LICA-CN 11 66241266 66241266 single base substitution G C 3_prime_UTR_variant LICA-CN 11 66241266 66241266 single base substitution G C downstream_gene_variant LICA-CN 11 66241266 66241266 single base substitution G C intron_variant LICA-CN 11 66241266 66241266 single base substitution G C missense_variant G130A 389G>C LICA-CN 11 66241266 66241266 single base substitution G C missense_variant G213A 638G>C LICA-CN 11 66241266 66241266 single base substitution G C missense_variant G237A 710G>C LICA-CN 11 66241266 66241266 single base substitution G C missense_variant G24A 71G>C LIHC-US 11 66243202 66243202 single base substitution C A 3_prime_UTR_variant LIHC-US 11 66243202 66243202 single base substitution C A downstream_gene_variant LIHC-US 11 66243202 66243202 single base substitution C A intron_variant LIHC-US 11 66243202 66243202 single base substitution C A missense_variant A218E 653C>A LIHC-US 11 66243202 66243202 single base substitution C A missense_variant A301E 902C>A LIHC-US 11 66243202 66243202 single base substitution C A missense_variant A325E 974C>A LINC-JP 11 66238743 66238744 deletion of <=200bp GG - 5_prime_UTR_variant LINC-JP 11 66238743 66238744 deletion of <=200bp GG - exon_variant LINC-JP 11 66238743 66238744 deletion of <=200bp GG - frameshift_variant KG61 LINC-JP 11 66238743 66238744 deletion of <=200bp GG - frameshift_variant KG85 LINC-JP 11 66238743 66238744 deletion of <=200bp GG - intron_variant LINC-JP 11 66238743 66238744 deletion of <=200bp GG - upstream_gene_variant LINC-JP 11 66243384 66243384 single base substitution C A 3_prime_UTR_variant LINC-JP 11 66243384 66243384 single base substitution C A downstream_gene_variant LINC-JP 11 66243384 66243384 single base substitution C A exon_variant LINC-JP 11 66243384 66243384 single base substitution C A missense_variant L362I 1084C>A LINC-JP 11 66243384 66243384 single base substitution C A missense_variant L386I 1156C>A LIRI-JP 11 66230498 66230498 single base substitution A G upstream_gene_variant LIRI-JP 11 66233628 66233628 single base substitution C T upstream_gene_variant LIRI-JP 11 66235649 66235649 single base substitution T C exon_variant LIRI-JP 11 66235649 66235649 single base substitution T C intron_variant LIRI-JP 11 66235649 66235649 single base substitution T C missense_variant L17P 50T>C LIRI-JP 11 66235897 66235897 single base substitution A T intron_variant LIRI-JP 11 66235897 66235897 single base substitution A T upstream_gene_variant LIRI-JP 11 66237296 66237296 single base substitution A T intron_variant LIRI-JP 11 66237296 66237296 single base substitution A T upstream_gene_variant LIRI-JP 11 66240046 66240046 single base substitution C T downstream_gene_variant LIRI-JP 11 66240046 66240046 single base substitution C T intron_variant LIRI-JP 11 66240046 66240046 single base substitution C T upstream_gene_variant LIRI-JP 11 66248002 66248002 single base substitution T C downstream_gene_variant LIRI-JP 11 66249061 66249061 single base substitution G A downstream_gene_variant LUSC-KR 11 66232259 66232259 single base substitution A G upstream_gene_variant LUSC-KR 11 66234993 66234993 single base substitution G A 5_prime_UTR_variant LUSC-KR 11 66234993 66234993 single base substitution G A intron_variant LUSC-KR 11 66235633 66235633 single base substitution C A exon_variant LUSC-KR 11 66235633 66235633 single base substitution C A intron_variant LUSC-KR 11 66235633 66235633 single base substitution C A missense_variant P12T 34C>A LUSC-KR 11 66235830 66235830 single base substitution C T intron_variant LUSC-KR 11 66245635 66245635 single base substitution A G downstream_gene_variant LUSC-US 11 66239871 66239871 single base substitution C A 3_prime_UTR_variant LUSC-US 11 66239871 66239871 single base substitution C A downstream_gene_variant LUSC-US 11 66239871 66239871 single base substitution C A intron_variant LUSC-US 11 66239871 66239871 single base substitution C A stop_gained S105* 314C>A LUSC-US 11 66239871 66239871 single base substitution C A stop_gained S129* 386C>A LUSC-US 11 66239871 66239871 single base substitution C A stop_gained S22* 65C>A LUSC-US 11 66239871 66239871 single base substitution C A upstream_gene_variant LUSC-US 11 66243384 66243384 single base substitution C G 3_prime_UTR_variant LUSC-US 11 66243384 66243384 single base substitution C G downstream_gene_variant LUSC-US 11 66243384 66243384 single base substitution C G exon_variant LUSC-US 11 66243384 66243384 single base substitution C G missense_variant L362V 1084C>G LUSC-US 11 66243384 66243384 single base substitution C G missense_variant L386V 1156C>G MALY-DE 11 66239143 66239143 single base substitution T A downstream_gene_variant MALY-DE 11 66239143 66239143 single base substitution T A intron_variant MALY-DE 11 66239143 66239143 single base substitution T A upstream_gene_variant MALY-DE 11 66239490 66239490 single base substitution C T downstream_gene_variant MALY-DE 11 66239490 66239490 single base substitution C T intron_variant MALY-DE 11 66239490 66239490 single base substitution C T upstream_gene_variant MALY-DE 11 66243606 66243606 single base substitution G A 3_prime_UTR_variant MALY-DE 11 66243606 66243606 single base substitution G A downstream_gene_variant MALY-DE 11 66243606 66243606 single base substitution G A missense_variant V436I 1306G>A MALY-DE 11 66243606 66243606 single base substitution G A missense_variant V460I 1378G>A MALY-DE 11 66247991 66247991 single base substitution A C downstream_gene_variant MELA-AU 11 66229853 66229853 single base substitution C T upstream_gene_variant MELA-AU 11 66229991 66229991 single base substitution C T upstream_gene_variant MELA-AU 11 66230323 66230323 single base substitution G A upstream_gene_variant MELA-AU 11 66230511 66230511 single base substitution G A upstream_gene_variant MELA-AU 11 66231248 66231248 single base substitution C T upstream_gene_variant MELA-AU 11 66231673 66231673 single base substitution G A upstream_gene_variant MELA-AU 11 66231925 66231925 single base substitution G A upstream_gene_variant MELA-AU 11 66231959 66231959 single base substitution G A upstream_gene_variant MELA-AU 11 66231977 66231977 single base substitution G A upstream_gene_variant MELA-AU 11 66232144 66232144 single base substitution A C upstream_gene_variant MELA-AU 11 66232708 66232708 single base substitution G A upstream_gene_variant MELA-AU 11 66232734 66232734 single base substitution G A upstream_gene_variant MELA-AU 11 66232791 66232791 single base substitution G A upstream_gene_variant MELA-AU 11 66233739 66233739 single base substitution C T upstream_gene_variant MELA-AU 11 66234043 66234043 single base substitution G A upstream_gene_variant MELA-AU 11 66234052 66234052 single base substitution G A upstream_gene_variant MELA-AU 11 66234194 66234194 single base substitution G A upstream_gene_variant MELA-AU 11 66234276 66234276 single base substitution G A 5_prime_UTR_variant MELA-AU 11 66234276 66234276 single base substitution G A upstream_gene_variant MELA-AU 11 66234289 66234289 single base substitution C T 5_prime_UTR_variant MELA-AU 11 66234289 66234289 single base substitution C T upstream_gene_variant MELA-AU 11 66234294 66234295 multiple base substitution (>=2bp and <=200bp) GG TA 5_prime_UTR_variant MELA-AU 11 66234294 66234295 multiple base substitution (>=2bp and <=200bp) GG TA upstream_gene_variant MELA-AU 11 66234300 66234301 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 11 66234300 66234301 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 66234301 66234301 single base substitution G A 5_prime_UTR_variant MELA-AU 11 66234301 66234301 single base substitution G A upstream_gene_variant MELA-AU 11 66234319 66234319 single base substitution C T 5_prime_UTR_variant MELA-AU 11 66234319 66234319 single base substitution C T upstream_gene_variant MELA-AU 11 66234944 66234944 single base substitution C T 5_prime_UTR_variant MELA-AU 11 66234944 66234944 single base substitution C T intron_variant MELA-AU 11 66235143 66235143 single base substitution G A intron_variant MELA-AU 11 66235416 66235416 single base substitution C T intron_variant MELA-AU 11 66235932 66235932 single base substitution C T intron_variant MELA-AU 11 66235932 66235932 single base substitution C T upstream_gene_variant MELA-AU 11 66237016 66237016 single base substitution G A intron_variant MELA-AU 11 66237016 66237016 single base substitution G A upstream_gene_variant MELA-AU 11 66239010 66239010 single base substitution C A downstream_gene_variant MELA-AU 11 66239010 66239010 single base substitution C A intron_variant MELA-AU 11 66239010 66239010 single base substitution C A upstream_gene_variant MELA-AU 11 66239833 66239833 single base substitution C T 3_prime_UTR_variant MELA-AU 11 66239833 66239833 single base substitution C T downstream_gene_variant MELA-AU 11 66239833 66239833 single base substitution C T intron_variant MELA-AU 11 66239833 66239833 single base substitution C T splice_region_variant MELA-AU 11 66239833 66239833 single base substitution C T upstream_gene_variant MELA-AU 11 66240133 66240133 single base substitution C T downstream_gene_variant MELA-AU 11 66240133 66240133 single base substitution C T intron_variant MELA-AU 11 66240133 66240133 single base substitution C T upstream_gene_variant MELA-AU 11 66240530 66240530 single base substitution T C downstream_gene_variant MELA-AU 11 66240530 66240530 single base substitution T C intron_variant MELA-AU 11 66240530 66240530 single base substitution T C upstream_gene_variant MELA-AU 11 66241261 66241261 single base substitution C T 3_prime_UTR_variant MELA-AU 11 66241261 66241261 single base substitution C T downstream_gene_variant MELA-AU 11 66241261 66241261 single base substitution C T intron_variant MELA-AU 11 66241261 66241261 single base substitution C T synonymous_variant T128T 384C>T MELA-AU 11 66241261 66241261 single base substitution C T synonymous_variant T211T 633C>T MELA-AU 11 66241261 66241261 single base substitution C T synonymous_variant T22T 66C>T MELA-AU 11 66241261 66241261 single base substitution C T synonymous_variant T235T 705C>T MELA-AU 11 66242459 66242459 single base substitution C T downstream_gene_variant MELA-AU 11 66242459 66242459 single base substitution C T intron_variant MELA-AU 11 66243457 66243457 single base substitution C T 3_prime_UTR_variant MELA-AU 11 66243457 66243457 single base substitution C T downstream_gene_variant MELA-AU 11 66243457 66243457 single base substitution C T exon_variant MELA-AU 11 66243457 66243457 single base substitution C T missense_variant P386L 1157C>T MELA-AU 11 66243457 66243457 single base substitution C T missense_variant P410L 1229C>T MELA-AU 11 66243509 66243509 single base substitution C T 3_prime_UTR_variant MELA-AU 11 66243509 66243509 single base substitution C T downstream_gene_variant MELA-AU 11 66243509 66243509 single base substitution C T synonymous_variant A403A 1209C>T MELA-AU 11 66243509 66243509 single base substitution C T synonymous_variant A427A 1281C>T MELA-AU 11 66244551 66244551 single base substitution G T 3_prime_UTR_variant MELA-AU 11 66244551 66244551 single base substitution G T downstream_gene_variant MELA-AU 11 66244709 66244710 multiple base substitution (>=2bp and <=200bp) CG TC 3_prime_UTR_variant MELA-AU 11 66244709 66244710 multiple base substitution (>=2bp and <=200bp) CG TC downstream_gene_variant MELA-AU 11 66244987 66244987 single base substitution C T downstream_gene_variant MELA-AU 11 66245340 66245340 single base substitution G A downstream_gene_variant MELA-AU 11 66245831 66245831 single base substitution G A downstream_gene_variant MELA-AU 11 66246119 66246119 single base substitution G A downstream_gene_variant MELA-AU 11 66246254 66246254 single base substitution C G downstream_gene_variant MELA-AU 11 66246434 66246434 single base substitution C G downstream_gene_variant MELA-AU 11 66246563 66246563 single base substitution C A downstream_gene_variant MELA-AU 11 66247350 66247350 single base substitution C G downstream_gene_variant MELA-AU 11 66247521 66247521 single base substitution C T downstream_gene_variant MELA-AU 11 66247741 66247741 single base substitution C T downstream_gene_variant MELA-AU 11 66247897 66247897 single base substitution G A downstream_gene_variant MELA-AU 11 66248036 66248036 single base substitution C T downstream_gene_variant MELA-AU 11 66248038 66248038 single base substitution C A downstream_gene_variant MELA-AU 11 66248320 66248320 single base substitution C T downstream_gene_variant MELA-AU 11 66248354 66248354 single base substitution G A downstream_gene_variant MELA-AU 11 66249105 66249105 single base substitution G A downstream_gene_variant MELA-AU 11 66249554 66249554 single base substitution C T downstream_gene_variant MELA-AU 11 66249737 66249737 single base substitution C T downstream_gene_variant ORCA-IN 11 66237187 66237187 single base substitution C A intron_variant ORCA-IN 11 66237187 66237187 single base substitution C A upstream_gene_variant ORCA-IN 11 66239427 66239427 single base substitution T C downstream_gene_variant ORCA-IN 11 66239427 66239427 single base substitution T C intron_variant ORCA-IN 11 66239427 66239427 single base substitution T C upstream_gene_variant OV-AU 11 66229777 66229777 single base substitution A C upstream_gene_variant OV-AU 11 66229778 66229778 single base substitution G C upstream_gene_variant OV-AU 11 66230597 66230597 single base substitution A T upstream_gene_variant OV-AU 11 66233439 66233439 single base substitution C G upstream_gene_variant OV-AU 11 66236770 66236770 single base substitution A G intron_variant OV-AU 11 66236770 66236770 single base substitution A G upstream_gene_variant OV-AU 11 66238585 66238585 single base substitution G T intron_variant OV-AU 11 66238585 66238585 single base substitution G T upstream_gene_variant OV-AU 11 66247615 66247615 single base substitution C T downstream_gene_variant OV-AU 11 66247749 66247749 single base substitution C A downstream_gene_variant OV-AU 11 66249695 66249695 single base substitution G C downstream_gene_variant OV-US 11 66240744 66240744 single base substitution C T 3_prime_UTR_variant OV-US 11 66240744 66240744 single base substitution C T downstream_gene_variant OV-US 11 66240744 66240744 single base substitution C T intron_variant OV-US 11 66240744 66240744 single base substitution C T synonymous_variant F139F 417C>T OV-US 11 66240744 66240744 single base substitution C T synonymous_variant F163F 489C>T OV-US 11 66240744 66240744 single base substitution C T synonymous_variant F56F 168C>T OV-US 11 66240744 66240744 single base substitution C T upstream_gene_variant PACA-AU 11 66230371 66230371 insertion of <=200bp - G upstream_gene_variant PACA-AU 11 66241502 66241502 single base substitution G A downstream_gene_variant PACA-AU 11 66241502 66241502 single base substitution G A intron_variant PACA-AU 11 66241502 66241502 single base substitution G A missense_variant E316K 946G>A PACA-AU 11 66243088 66243088 single base substitution T A 3_prime_UTR_variant PACA-AU 11 66243088 66243088 single base substitution T A downstream_gene_variant PACA-AU 11 66243088 66243088 single base substitution T A intron_variant PACA-AU 11 66243088 66243088 single base substitution T A missense_variant V180E 539T>A PACA-AU 11 66243088 66243088 single base substitution T A missense_variant V263E 788T>A PACA-AU 11 66243088 66243088 single base substitution T A missense_variant V287E 860T>A PACA-AU 11 66247966 66247966 single base substitution C T downstream_gene_variant PACA-AU 11 66249339 66249339 single base substitution G C downstream_gene_variant PACA-CA 11 66235162 66235162 single base substitution C A intron_variant PACA-CA 11 66237878 66237878 single base substitution T C intron_variant PACA-CA 11 66237878 66237878 single base substitution T C upstream_gene_variant PACA-CA 11 66242210 66242210 single base substitution A T downstream_gene_variant PACA-CA 11 66242210 66242210 single base substitution A T intron_variant PACA-CA 11 66243306 66243306 single base substitution G A 3_prime_UTR_variant PACA-CA 11 66243306 66243306 single base substitution G A downstream_gene_variant PACA-CA 11 66243306 66243306 single base substitution G A exon_variant PACA-CA 11 66243306 66243306 single base substitution G A missense_variant V253I 757G>A PACA-CA 11 66243306 66243306 single base substitution G A missense_variant V336I 1006G>A PACA-CA 11 66243306 66243306 single base substitution G A missense_variant V360I 1078G>A PACA-CA 11 66246865 66246865 single base substitution G A downstream_gene_variant PACA-CA 11 66248354 66248354 single base substitution G A downstream_gene_variant PAEN-AU 11 66231223 66231223 single base substitution C A upstream_gene_variant PAEN-IT 11 66239933 66239933 single base substitution A G 3_prime_UTR_variant PAEN-IT 11 66239933 66239933 single base substitution A G downstream_gene_variant PAEN-IT 11 66239933 66239933 single base substitution A G intron_variant PAEN-IT 11 66239933 66239933 single base substitution A G missense_variant M126V 376A>G PAEN-IT 11 66239933 66239933 single base substitution A G missense_variant M150V 448A>G PAEN-IT 11 66239933 66239933 single base substitution A G missense_variant M43V 127A>G PAEN-IT 11 66239933 66239933 single base substitution A G upstream_gene_variant PAEN-IT 11 66245704 66245704 single base substitution G C downstream_gene_variant PBCA-DE 11 66234845 66234845 insertion of <=200bp - T intron_variant PBCA-DE 11 66234845 66234845 insertion of <=200bp - T upstream_gene_variant PBCA-DE 11 66237437 66237437 insertion of <=200bp - ATTTTT intron_variant PBCA-DE 11 66237437 66237437 insertion of <=200bp - ATTTTT upstream_gene_variant PRAD-CA 11 66237275 66237275 single base substitution G T intron_variant PRAD-CA 11 66237275 66237275 single base substitution G T upstream_gene_variant PRAD-UK 11 66231294 66231294 single base substitution G A upstream_gene_variant PRAD-UK 11 66248412 66248412 single base substitution G C downstream_gene_variant READ-US 11 66243238 66243238 single base substitution G T 3_prime_UTR_variant READ-US 11 66243238 66243238 single base substitution G T downstream_gene_variant READ-US 11 66243238 66243238 single base substitution G T intron_variant READ-US 11 66243238 66243238 single base substitution G T missense_variant S230I 689G>T READ-US 11 66243238 66243238 single base substitution G T missense_variant S313I 938G>T READ-US 11 66243238 66243238 single base substitution G T missense_variant S337I 1010G>T READ-US 11 66249709 66249709 single base substitution G A downstream_gene_variant RECA-EU 11 66234776 66234776 single base substitution G T intron_variant RECA-EU 11 66234776 66234776 single base substitution G T upstream_gene_variant SKCA-BR 11 66229276 66229276 single base substitution T G upstream_gene_variant SKCA-BR 11 66229909 66229909 single base substitution G A upstream_gene_variant SKCA-BR 11 66230323 66230323 single base substitution G A upstream_gene_variant SKCA-BR 11 66232776 66232776 single base substitution T C upstream_gene_variant SKCA-BR 11 66234274 66234274 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 66234274 66234274 single base substitution G A upstream_gene_variant SKCA-BR 11 66234276 66234276 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 66234276 66234276 single base substitution G A upstream_gene_variant SKCA-BR 11 66234289 66234289 single base substitution C T 5_prime_UTR_variant SKCA-BR 11 66234289 66234289 single base substitution C T upstream_gene_variant SKCA-BR 11 66234300 66234300 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 66234300 66234300 single base substitution G A upstream_gene_variant SKCA-BR 11 66234307 66234307 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 66234307 66234307 single base substitution G A upstream_gene_variant SKCA-BR 11 66238349 66238349 single base substitution T G intron_variant SKCA-BR 11 66238349 66238349 single base substitution T G upstream_gene_variant SKCA-BR 11 66238384 66238384 single base substitution T C intron_variant SKCA-BR 11 66238384 66238384 single base substitution T C upstream_gene_variant SKCA-BR 11 66241942 66241942 single base substitution C G 3_prime_UTR_variant SKCA-BR 11 66241942 66241942 single base substitution C G downstream_gene_variant SKCA-BR 11 66241942 66241942 single base substitution C G intron_variant SKCA-BR 11 66243355 66243355 single base substitution A G 3_prime_UTR_variant SKCA-BR 11 66243355 66243355 single base substitution A G downstream_gene_variant SKCA-BR 11 66243355 66243355 single base substitution A G exon_variant SKCA-BR 11 66243355 66243355 single base substitution A G missense_variant E352G 1055A>G SKCA-BR 11 66243355 66243355 single base substitution A G missense_variant E376G 1127A>G SKCA-BR 11 66247814 66247814 single base substitution T G downstream_gene_variant SKCA-BR 11 66248431 66248431 single base substitution A C downstream_gene_variant SKCA-BR 11 66249554 66249554 single base substitution C T downstream_gene_variant SKCM-US 11 66241232 66241232 single base substitution C T 3_prime_UTR_variant SKCM-US 11 66241232 66241232 single base substitution C T downstream_gene_variant SKCM-US 11 66241232 66241232 single base substitution C T intron_variant SKCM-US 11 66241232 66241232 single base substitution C T missense_variant P119S 355C>T SKCM-US 11 66241232 66241232 single base substitution C T missense_variant P13S 37C>T SKCM-US 11 66241232 66241232 single base substitution C T missense_variant P202S 604C>T SKCM-US 11 66241232 66241232 single base substitution C T missense_variant P226S 676C>T SKCM-US 11 66241261 66241261 single base substitution C T 3_prime_UTR_variant SKCM-US 11 66241261 66241261 single base substitution C T downstream_gene_variant SKCM-US 11 66241261 66241261 single base substitution C T intron_variant SKCM-US 11 66241261 66241261 single base substitution C T synonymous_variant T128T 384C>T SKCM-US 11 66241261 66241261 single base substitution C T synonymous_variant T211T 633C>T SKCM-US 11 66241261 66241261 single base substitution C T synonymous_variant T22T 66C>T SKCM-US 11 66241261 66241261 single base substitution C T synonymous_variant T235T 705C>T SKCM-US 11 66243537 66243537 single base substitution C T 3_prime_UTR_variant SKCM-US 11 66243537 66243537 single base substitution C T downstream_gene_variant SKCM-US 11 66243537 66243537 single base substitution C T missense_variant H413Y 1237C>T SKCM-US 11 66243537 66243537 single base substitution C T missense_variant H437Y 1309C>T SKCM-US 11 66249785 66249785 single base substitution C T downstream_gene_variant STAD-US 11 66235677 66235677 single base substitution C T exon_variant STAD-US 11 66235677 66235677 single base substitution C T intron_variant STAD-US 11 66235677 66235677 single base substitution C T synonymous_variant C26C 78C>T STAD-US 11 66235678 66235678 single base substitution G A exon_variant STAD-US 11 66235678 66235678 single base substitution G A intron_variant STAD-US 11 66235678 66235678 single base substitution G A missense_variant V27I 79G>A STAD-US 11 66236332 66236332 single base substitution G A intron_variant STAD-US 11 66236332 66236332 single base substitution G A missense_variant E61K 181G>A STAD-US 11 66236332 66236332 single base substitution G A upstream_gene_variant STAD-US 11 66238753 66238753 single base substitution C T 5_prime_UTR_variant STAD-US 11 66238753 66238753 single base substitution C T exon_variant STAD-US 11 66238753 66238753 single base substitution C T intron_variant STAD-US 11 66238753 66238753 single base substitution C T stop_gained R65* 193C>T STAD-US 11 66238753 66238753 single base substitution C T stop_gained R89* 265C>T STAD-US 11 66238753 66238753 single base substitution C T upstream_gene_variant STAD-US 11 66238782 66238782 single base substitution G A 5_prime_UTR_variant STAD-US 11 66238782 66238782 single base substitution G A exon_variant STAD-US 11 66238782 66238782 single base substitution G A intron_variant STAD-US 11 66238782 66238782 single base substitution G A synonymous_variant S74S 222G>A STAD-US 11 66238782 66238782 single base substitution G A synonymous_variant S98S 294G>A STAD-US 11 66238782 66238782 single base substitution G A upstream_gene_variant STAD-US 11 66238785 66238785 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 66238785 66238785 single base substitution C T exon_variant STAD-US 11 66238785 66238785 single base substitution C T intron_variant STAD-US 11 66238785 66238785 single base substitution C T synonymous_variant H75H 225C>T STAD-US 11 66238785 66238785 single base substitution C T synonymous_variant H99H 297C>T STAD-US 11 66238785 66238785 single base substitution C T upstream_gene_variant STAD-US 11 66238826 66238826 single base substitution C T exon_variant STAD-US 11 66238826 66238826 single base substitution C T intron_variant STAD-US 11 66238826 66238826 single base substitution C T missense_variant T113M 338C>T STAD-US 11 66238826 66238826 single base substitution C T missense_variant T6M 17C>T STAD-US 11 66238826 66238826 single base substitution C T missense_variant T89M 266C>T STAD-US 11 66238826 66238826 single base substitution C T upstream_gene_variant STAD-US 11 66240870 66240870 single base substitution C T 3_prime_UTR_variant STAD-US 11 66240870 66240870 single base substitution C T downstream_gene_variant STAD-US 11 66240870 66240870 single base substitution C T intron_variant STAD-US 11 66240870 66240870 single base substitution C T synonymous_variant A181A 543C>T STAD-US 11 66240870 66240870 single base substitution C T synonymous_variant A205A 615C>T STAD-US 11 66240870 66240870 single base substitution C T synonymous_variant A98A 294C>T STAD-US 11 66240870 66240870 single base substitution C T upstream_gene_variant STAD-US 11 66241301 66241301 single base substitution G A 3_prime_UTR_variant STAD-US 11 66241301 66241301 single base substitution G A downstream_gene_variant STAD-US 11 66241301 66241301 single base substitution G A intron_variant STAD-US 11 66241301 66241301 single base substitution G A missense_variant E142K 424G>A STAD-US 11 66241301 66241301 single base substitution G A missense_variant E225K 673G>A STAD-US 11 66241301 66241301 single base substitution G A missense_variant E249K 745G>A STAD-US 11 66241301 66241301 single base substitution G A missense_variant E36K 106G>A STAD-US 11 66241318 66241318 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 11 66241318 66241318 deletion of <=200bp T - downstream_gene_variant STAD-US 11 66241318 66241318 deletion of <=200bp T - frameshift_variant G147 STAD-US 11 66241318 66241318 deletion of <=200bp T - frameshift_variant G230 STAD-US 11 66241318 66241318 deletion of <=200bp T - frameshift_variant G254 STAD-US 11 66241318 66241318 deletion of <=200bp T - frameshift_variant G41 STAD-US 11 66241318 66241318 deletion of <=200bp T - intron_variant STAD-US 11 66243212 66243212 single base substitution G A 3_prime_UTR_variant STAD-US 11 66243212 66243212 single base substitution G A downstream_gene_variant STAD-US 11 66243212 66243212 single base substitution G A intron_variant STAD-US 11 66243212 66243212 single base substitution G A synonymous_variant A221A 663G>A STAD-US 11 66243212 66243212 single base substitution G A synonymous_variant A304A 912G>A STAD-US 11 66243212 66243212 single base substitution G A synonymous_variant A328A 984G>A STAD-US 11 66249741 66249741 single base substitution C T downstream_gene_variant STAD-US 11 66249784 66249784 single base substitution C T downstream_gene_variant THCA-SA 11 66240882 66240882 single base substitution T C 3_prime_UTR_variant THCA-SA 11 66240882 66240882 single base substitution T C downstream_gene_variant THCA-SA 11 66240882 66240882 single base substitution T C intron_variant THCA-SA 11 66240882 66240882 single base substitution T C synonymous_variant D102D 306T>C THCA-SA 11 66240882 66240882 single base substitution T C synonymous_variant D185D 555T>C THCA-SA 11 66240882 66240882 single base substitution T C synonymous_variant D209D 627T>C THCA-SA 11 66240882 66240882 single base substitution T C upstream_gene_variant THCA-SA 11 66241239 66241239 single base substitution G T 3_prime_UTR_variant THCA-SA 11 66241239 66241239 single base substitution G T downstream_gene_variant THCA-SA 11 66241239 66241239 single base substitution G T intron_variant THCA-SA 11 66241239 66241239 single base substitution G T missense_variant G121V 362G>T THCA-SA 11 66241239 66241239 single base substitution G T missense_variant G15V 44G>T THCA-SA 11 66241239 66241239 single base substitution G T missense_variant G204V 611G>T THCA-SA 11 66241239 66241239 single base substitution G T missense_variant G228V 683G>T THCA-SA 11 66243575 66243575 single base substitution C T 3_prime_UTR_variant THCA-SA 11 66243575 66243575 single base substitution C T downstream_gene_variant THCA-SA 11 66243575 66243575 single base substitution C T synonymous_variant C425C 1275C>T THCA-SA 11 66243575 66243575 single base substitution C T synonymous_variant C449C 1347C>T THCA-SA 11 66244702 66244702 single base substitution A G 3_prime_UTR_variant THCA-SA 11 66244702 66244702 single base substitution A G downstream_gene_variant UCEC-US 11 66235658 66235658 single base substitution G A exon_variant UCEC-US 11 66235658 66235658 single base substitution G A intron_variant UCEC-US 11 66235658 66235658 single base substitution G A missense_variant R20Q 59G>A UCEC-US 11 66240719 66240719 single base substitution G A 3_prime_UTR_variant UCEC-US 11 66240719 66240719 single base substitution G A downstream_gene_variant UCEC-US 11 66240719 66240719 single base substitution G A intron_variant UCEC-US 11 66240719 66240719 single base substitution G A missense_variant R131H 392G>A UCEC-US 11 66240719 66240719 single base substitution G A missense_variant R155H 464G>A UCEC-US 11 66240719 66240719 single base substitution G A missense_variant R48H 143G>A UCEC-US 11 66240719 66240719 single base substitution G A upstream_gene_variant UCEC-US 11 66240744 66240744 single base substitution C T 3_prime_UTR_variant UCEC-US 11 66240744 66240744 single base substitution C T downstream_gene_variant UCEC-US 11 66240744 66240744 single base substitution C T intron_variant UCEC-US 11 66240744 66240744 single base substitution C T synonymous_variant F139F 417C>T UCEC-US 11 66240744 66240744 single base substitution C T synonymous_variant F163F 489C>T UCEC-US 11 66240744 66240744 single base substitution C T synonymous_variant F56F 168C>T UCEC-US 11 66240744 66240744 single base substitution C T upstream_gene_variant UCEC-US 11 66241248 66241248 single base substitution A G 3_prime_UTR_variant UCEC-US 11 66241248 66241248 single base substitution A G downstream_gene_variant UCEC-US 11 66241248 66241248 single base substitution A G intron_variant UCEC-US 11 66241248 66241248 single base substitution A G missense_variant D124G 371A>G UCEC-US 11 66241248 66241248 single base substitution A G missense_variant D18G 53A>G UCEC-US 11 66241248 66241248 single base substitution A G missense_variant D207G 620A>G UCEC-US 11 66241248 66241248 single base substitution A G missense_variant D231G 692A>G UCEC-US 11 66241325 66241325 single base substitution C T 3_prime_UTR_variant UCEC-US 11 66241325 66241325 single base substitution C T downstream_gene_variant UCEC-US 11 66241325 66241325 single base substitution C T intron_variant UCEC-US 11 66241325 66241325 single base substitution C T missense_variant R150W 448C>T UCEC-US 11 66241325 66241325 single base substitution C T missense_variant R233W 697C>T UCEC-US 11 66241325 66241325 single base substitution C T missense_variant R257W 769C>T UCEC-US 11 66241325 66241325 single base substitution C T missense_variant R44W 130C>T UCEC-US 11 66249729 66249729 single base substitution C T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-RT-S01477 COSM377420 c.945G>A p.L315L Substitution - coding silent 11:66475702-66475702 + TCGA-C5-A1MH-01 COSM163406 c.266G>A p.R89Q Substitution - Missense 11:66471283-66471283 + TCGA-F5-6814-01 COSM3416145 c.1010G>T p.S337I Substitution - Missense 11:66475767-66475767 + HCC11 COSM1605077 c.1156C>A p.L386I Substitution - Missense 11:66475913-66475913 + TCGA-13-1491-01 COSM81570 c.489C>T p.F163F Substitution - coding silent 11:66473273-66473273 + TCGA-AC-A5XS-01 COSM163406 c.266G>A p.R89Q Substitution - Missense 11:66471283-66471283 + TCGA-A5-A0GB-01 COSM930757 c.464G>A p.R155H Substitution - Missense 11:66473248-66473248 + T3147 COSM4713600 c.1054G>A p.D352N Substitution - Missense 11:66475811-66475811 + S02299 COSM5701421 c.59_60insG p.N22fs*12 Insertion - Frameshift 11:66468187-66468188 + 587288 COSM1220189 c.671G>A p.R224Q Substitution - Missense 11:66473756-66473756 + Z138 COSM1740928 c.431_432delAT p.H144fs*2 Deletion - Frameshift 11:66472445-66472446 + CSCC-41-T COSM4461544 c.1210C>T p.L404F Substitution - Missense 11:66475967-66475967 + TCGA-AX-A0J1-01 COSM930759 c.769C>T p.R257W Substitution - Missense 11:66473854-66473854 + TCGA-C5-A1BL-01 COSM4836915 c.484G>A p.D162N Substitution - Missense 11:66473268-66473268 + ESO-859 COSM1239802 c.272G>A p.R91H Substitution - Missense 11:66471289-66471289 + 587284 COSM1220188 c.806G>A p.R269Q Substitution - Missense 11:66473891-66473891 + S00829 COSM5659888 c.60G>T p.R20R Substitution - coding silent 11:66468188-66468188 + YUMOBER COSM5373325 c.624C>T p.F208F Substitution - coding silent 11:66473408-66473408 + BD57T COSM5510528 c.262C>T p.R88W Substitution - Missense 11:66471279-66471279 + ITNET_0700_T COSM4963772 c.448A>G p.M150V Substitution - Missense 11:66472462-66472462 + TCGA-GV-A3QI-01 COSM1298460 c.191G>C p.R64T Substitution - Missense 11:66468871-66468871 + tumor_4116738 COSM1161009 c.1378G>A p.V460I Substitution - Missense 11:66476135-66476135 + TCGA-63-5128-01 COSM689898 c.386C>A p.S129* Substitution - Nonsense 11:66472400-66472400 + 700T COSM4963772 c.448A>G p.M150V Substitution - Missense 11:66472462-66472462 + ME100L COSM231253 c.209C>T p.P70L Substitution - Missense 11:66468889-66468889 + TCGA-39-5019-01 COSM689897 c.1156C>G p.L386V Substitution - Missense 11:66475913-66475913 + BD57T COSM5510529 c.985C>T p.R329W Substitution - Missense 11:66475742-66475742 + CSCC-56-T COSM4461864 c.1223C>T p.P408L Substitution - Missense 11:66475980-66475980 + HCC063T COSM5812123 c.710G>C p.G237A Substitution - Missense 11:66473795-66473795 + TCGA-EE-A3J5-06 COSM3452085 c.676C>T p.P226S Substitution - Missense 11:66473761-66473761 + TCGA-HT-8564-01 COSM3967760 c.1293C>A p.A431A Substitution - coding silent 11:66476050-66476050 + ESCC_25 COSM5626589 c.74C>G p.S25C Substitution - Missense 11:66468202-66468202 + TCGA-DK-A2HX-01 COSM1298461 c.685C>T p.L229L Substitution - coding silent 11:66473770-66473770 + TCGA-CM-6162-01 COSM1356215 c.910C>T p.R304C Substitution - Missense 11:66475667-66475667 + MedB-1 COSM5621487 c.130T>C p.Y44H Substitution - Missense 11:66468258-66468258 + STC246 COSM1220189 c.671G>A p.R224Q Substitution - Missense 11:66473756-66473756 + Pat_41_B COSM5839314 c.113G>A p.G38D Substitution - Missense 11:66468241-66468241 + 114 COSM5012373 c.916C>G p.P306A Substitution - Missense 11:66475673-66475673 + TCGA-BR-4184-01 COSM4035723 c.78C>T p.C26C Substitution - coding silent 11:66468206-66468206 + LUAD-RT-S01702 COSM378974 c.114C>T p.G38G Substitution - coding silent 11:66468242-66468242 + TCGA-HU-A4H8-01 COSM2040235 c.338C>T p.T113M Substitution - Missense 11:66471355-66471355 + TCGA-AP-A059-01 COSM930756 c.59G>A p.R20Q Substitution - Missense 11:66468187-66468187 + YUPAT COSM1686656 c.153-1G>A p.? Unknown 11:66468832-66468832 + PTC_72 COSM5959682 c.683G>T p.G228V Substitution - Missense 11:66473768-66473768 + TCGA-BR-4368-01 COSM2040230 c.79G>A p.V27I Substitution - Missense 11:66468207-66468207 + SNU-C4 COSM4652035 c.1011C>T p.S337S Substitution - coding silent 11:66475768-66475768 + TCGA-C8-A1HL-01 COSM429656 c.196G>T p.E66* Substitution - Nonsense 11:66468876-66468876 + TCGA-CA-6717-01 COSM1356210 c.304G>A p.G102R Substitution - Missense 11:66471321-66471321 + HCC11T COSM1605077 c.1156C>A p.L386I Substitution - Missense 11:66475913-66475913 + PM-7 COSM5619602 c.805C>T p.R269W Substitution - Missense 11:66473890-66473890 + T3658 COSM4713599 c.920C>T p.A307V Substitution - Missense 11:66475677-66475677 + S02241 COSM5676741 c.832G>T p.G278C Substitution - Missense 11:66473917-66473917 + sysucc-834T COSM5485499 c.290G>A p.R97Q Substitution - Missense 11:66471307-66471307 + TCGA-BR-4201-01 COSM4035729 c.745G>A p.E249K Substitution - Missense 11:66473830-66473830 + PCSI_0083_Pa_P_526 COSM3788030 c.1078G>A p.V360I Substitution - Missense 11:66475835-66475835 + SNU-C4 COSM4652034 c.510T>A p.P170P Substitution - coding silent 11:66473294-66473294 + TCGA-AG-A002-01 COSM262900 c.499G>T p.D167Y Substitution - Missense 11:66473283-66473283 + TCGA-13-0883-01 COSM116033 c.1190G>C p.W397S Substitution - Missense 11:66475947-66475947 + TCGA-QA-A7B7-01 COSM4909916 c.974C>A p.A325E Substitution - Missense 11:66475731-66475731 + TCGA-BR-A452-01 COSM4035724 c.181G>A p.E61K Substitution - Missense 11:66468861-66468861 + TCGA-HU-A4H8-01 COSM4035725 c.265C>T p.R89* Substitution - Nonsense 11:66471282-66471282 + TCGA-D1-A103-01 COSM81570 c.489C>T p.F163F Substitution - coding silent 11:66473273-66473273 + PD4123a COSM163406 c.266G>A p.R89Q Substitution - Missense 11:66471283-66471283 + HCT116 COSM4632011 c.1130G>A p.R377Q Substitution - Missense 11:66475887-66475887 + SW48 COSM2040254 c.1333G>A p.A445T Substitution - Missense 11:66476090-66476090 + Au4 COSM5604476 c.1281C>T p.A427A Substitution - coding silent 11:66476038-66476038 + 61 COSM5739328 c.1312G>T p.G438C Substitution - Missense 11:66476069-66476069 + T407 COSM4713598 c.686T>G p.L229R Substitution - Missense 11:66473771-66473771 + STC252 COSM378974 c.114C>T p.G38G Substitution - coding silent 11:66468242-66468242 + HCT-116 COSM1676208 c.1382G>A p.R461H Substitution - Missense 11:66476139-66476139 + TCGA-CG-5728-01 COSM4035727 c.297C>T p.H99H Substitution - coding silent 11:66471314-66471314 + TCGA-HU-A4GQ-01 COSM2040249 c.984G>A p.A328A Substitution - coding silent 11:66475741-66475741 + 721LT COSM4386218 c.62G>A p.G21E Substitution - Missense 11:66468190-66468190 + RK184_C01 COSM1628178 c.50T>C p.L17P Substitution - Missense 11:66468178-66468178 + CSCC-27-T COSM4507819 c.757C>T p.P253S Substitution - Missense 11:66473842-66473842 + T3225 COSM4713601 c.1164C>T p.R388R Substitution - coding silent 11:66475921-66475921 + 8069168 COSM4406629 c.860T>A p.V287E Substitution - Missense 11:66475617-66475617 + TCGA-EE-A2GJ-06 COSM3452087 c.1309C>T p.H437Y Substitution - Missense 11:66476066-66476066 + TCGA-AZ-6598-01 COSM1356212 c.715C>A p.L239M Substitution - Missense 11:66473800-66473800 + TCGA-DH-5140-01 COSM3967759 c.1049C>T p.A350V Substitution - Missense 11:66475806-66475806 + CSCC-31-T COSM4476704 c.208C>T p.P70S Substitution - Missense 11:66468888-66468888 + SNU-175 COSM4650253 c.1145G>A p.R382H Substitution - Missense 11:66475902-66475902 + TCGA-AD-6895-01 COSM1356216 c.1162C>T p.R388C Substitution - Missense 11:66475919-66475919 + CSCC-27-T COSM4561674 c.894G>A p.G298G Substitution - coding silent 11:66475651-66475651 + TCGA-D1-A168-01 COSM930758 c.692A>G p.D231G Substitution - Missense 11:66473777-66473777 + BD180T COSM5495118 c.972G>C p.E324D Substitution - Missense 11:66475729-66475729 + 389 COSM4427559 c.1120C>T p.R374W Substitution - Missense 11:66475877-66475877 + TCGA-BR-7717-01 COSM4035728 c.615C>T p.A205A Substitution - coding silent 11:66473399-66473399 + WA16 COSM237950 c.1230G>A p.P410P Substitution - coding silent 11:66475987-66475987 + T3090 COSM4713597 c.443C>T p.T148I Substitution - Missense 11:66472457-66472457 + TCGA-AD-6895-01 COSM1356211 c.605G>A p.R202H Substitution - Missense 11:66473389-66473389 + ESCC_108 COSM5638612 c.1163G>A p.R388H Substitution - Missense 11:66475920-66475920 + 587278 COSM1220187 c.1000G>A p.V334M Substitution - Missense 11:66475757-66475757 + Pat_24_A COSM5839315 c.1043G>A p.R348H Substitution - Missense 11:66475800-66475800 + HT115 COSM2040231 c.105G>A p.A35A Substitution - coding silent 11:66468233-66468233 + TCGA-HJ-7597-01 COSM4035726 c.294G>A p.S98S Substitution - coding silent 11:66471311-66471311 + TCGA-EE-A3AA-06 COSM3452086 c.705C>T p.T235T Substitution - coding silent 11:66473790-66473790 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.656871;Hs.656872;Hs.656873;Hs.656875 11q13.2 609827 2418561|CGAP|BC036263|C/T|non-coding||2128|Candidate; 2418561|CGAP|BC061522|C/T|non-coding||1310|Candidate; 2418561|CGAP|BC094882|C/T|non-coding||2295|Candidate; 609799|dbSNP|BC036263|A/G|coding|Ala423Ala|1344|Validated; 609799|dbSNP|BC036263|A/G|coding|Ala465Ala|1470|Validated; 609799|dbSNP|BC036263|A/G|coding|Ala507Ala|1596|Validated; 609799|dbSNP|BC061522|A/G|coding|Ala207Ala|652|Validated; 609799|dbSNP|BC094882|A/G|coding|Ala404Ala|1271|Validated; 609799|dbSNP|BC094882|A/G|coding|Ala526Ala|1637|Validated; 628384|dbSNP|BC036263|C/T|coding|Arg223Cys|742|Validated; 628384|dbSNP|BC061522|C/T|coding|Arg7Cys|50|Validated; 628384|dbSNP|BC094882|C/T|coding|Arg204Cys|669|Validated; 632070|dbSNP|BC036263|C/T|coding|Pro267Pro|876|Candidate; 632070|dbSNP|BC036263|C/T|coding|Pro286Pro|933|Candidate; 632070|dbSNP|BC036263|C/T|coding|Pro305Pro|990|Candidate; 632070|dbSNP|BC036263|C/T|coding|Pro324Pro|1047|Candidate; 632070|dbSNP|BC061522|C/T|coding|Pro108Pro|355|Candidate; 632070|dbSNP|BC061522|C/T|coding|Pro51Pro|184|Candidate; 632070|dbSNP|BC061522|C/T|coding|Pro70Pro|241|Candidate; 632070|dbSNP|BC061522|C/T|coding|Pro89Pro|298|Candidate; 632070|dbSNP|BC094882|C/T|coding|Pro248Pro|803|Candidate; 632070|dbSNP|BC094882|C/T|coding|Pro267Pro|860|Candidate; 632070|dbSNP|BC094882|C/T|coding|Pro286Pro|917|Candidate; 632070|dbSNP|BC094882|C/T|coding|Pro305Pro|974|Candidate; 632070|dbSNP|BC094882|C/T|coding|Pro324Pro|1031|Candidate; 888865|dbSNP|BC036263|A/G|coding|Ala66Ala|273|Validated; 888865|dbSNP|BC094882|A/G|codi

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.D231G c.692A>G 11 66241248 UCEC A T IntronicSNV . c.841-25A>T 11 66243044 CM C A Nonsense p.S129* c.386C>A 11 66239871 LUSC CC TT Missense p.R134W c.399_400delinsTT 11 66239884 CM C G Missense p.L386V c.1156C>G 11 66243384 LUSC C T Missense p.A350V c.1049C>T 11 66243277 LGG C T Missense p.H437Y c.1309C>T 11 66243537 CM C T Missense p.P226S c.676C>T 11 66241232 CM C T Synonymous p.F163F c.489C>T 11 66240744 OV C T Synonymous p.H99H c.297C>T 11 66238785 STAD C T Synonymous p.L229L c.685C>T 11 66241241 BLCA C T Synonymous p.T235T c.705C>T 11 66241261 CM G A Missense p.E249K c.745G>A 11 66241301 STAD G A Missense p.R155H c.464G>A 11 66240719 UCEC G A Missense p.R89Q c.266G>A 11 66238754 BRCA G A Missense p.R89Q c.266G>A 11 66238754 HNSC G A Missense p.V27I c.79G>A 11 66235678 STAD G A Missense p.V460I c.1378G>A 11 66243606 DLBCL G A SpliceAcceptorSNV . c.1-2G>A 11 66235598 LUAD G C Missense p.R64T c.191G>C 11 66236342 BLCA G C Missense p.W397S c.1190G>C 11 66243418 OV G T Nonsense p.E66* c.196G>T 11 66236347 BRCA T - Frameshift p.V255Sfs*61 c.762delT 11 66241318 STAD