Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 1 156013835 156013835 + Silent SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr1:156013835C>T c.1080G>A c.(1078-1080)ccG>ccA p.P360P BLCA 1 156020243 156020243 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr1:156020243C>G c.580G>C c.(580-582)Gag>Cag p.E194Q BLCA 1 156020285 156020285 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr1:156020285C>G c.538G>C c.(538-540)Gag>Cag p.E180Q BLCA 1 156020908 156020908 + Silent SNP G G A TCGA-FD-A5C0-01A-11D-A289-08 TCGA-FD-A5C0-10A-01D-A289-08 g.chr1:156020908G>A c.471C>T c.(469-471)tcC>tcT p.S157S BRCA 1 156011319 156011319 + Missense_Mutation SNP A A G TCGA-BH-A0C0-01A-21W-A071-09 TCGA-BH-A0C0-11A-21W-A100-09 g.chr1:156011319A>G c.1610T>C c.(1609-1611)aTg>aCg p.M537T BRCA 1 156012608 156012608 + Missense_Mutation SNP C C G TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr1:156012608C>G c.1223G>C c.(1222-1224)aGc>aCc p.S408T BRCA 1 156012655 156012655 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:156012655C>A c.1176G>T c.(1174-1176)gaG>gaT p.E392D BRCA 1 156018375 156018375 + Missense_Mutation SNP C C G TCGA-C8-A1HJ-01A-11D-A13L-09 TCGA-C8-A1HJ-10A-01D-A13O-09 g.chr1:156018375C>G c.817G>C c.(817-819)Gag>Cag p.E273Q BRCA 1 156021546 156021546 + Missense_Mutation SNP C C T TCGA-AN-A0XN-01A-21D-A10G-09 TCGA-AN-A0XN-10A-01D-A10G-09 g.chr1:156021546C>T c.211G>A c.(211-213)Gga>Aga p.G71R CESC 1 156020186 156020186 + Missense_Mutation SNP C C T TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr1:156020186C>T c.637G>A c.(637-639)Gat>Aat p.D213N COAD 1 156006913 156006913 + Silent SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:156006913C>T c.1662G>A c.(1660-1662)acG>acA p.T554T COAD 1 156011727 156011727 + Missense_Mutation SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:156011727C>T c.1402G>A c.(1402-1404)Gca>Aca p.A468T COAD 1 156018326 156018326 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:156018326A>G c.866T>C c.(865-867)aTc>aCc p.I289T COAD 1 156021084 156021084 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr1:156021084G>T c.295C>A c.(295-297)Ccc>Acc p.P99T COADREAD 1 156006913 156006913 + Silent SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:156006913C>T c.1662G>A c.(1660-1662)acG>acA p.T554T COADREAD 1 156011727 156011727 + Missense_Mutation SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:156011727C>T c.1402G>A c.(1402-1404)Gca>Aca p.A468T COADREAD 1 156018300 156018300 + Missense_Mutation SNP G G A TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr1:156018300G>A c.892C>T c.(892-894)Cgg>Tgg p.R298W COADREAD 1 156018326 156018326 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:156018326A>G c.866T>C c.(865-867)aTc>aCc p.I289T COADREAD 1 156021084 156021084 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr1:156021084G>T c.295C>A c.(295-297)Ccc>Acc p.P99T ESCA 1 156018300 156018300 + Silent SNP G G T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr1:156018300G>T c.892C>A c.(892-894)Cgg>Agg p.R298R ESCA 1 156018405 156018405 + Missense_Mutation SNP G G A TCGA-L5-A8NR-01A-11D-A37C-09 TCGA-L5-A8NR-11A-11D-A37F-09 g.chr1:156018405G>A c.787C>T c.(787-789)Cgg>Tgg p.R263W ESCA 1 156020165 156020165 + Missense_Mutation SNP T T A TCGA-IG-A97H-01A-11D-A387-09 TCGA-IG-A97H-10A-01D-A38A-09 g.chr1:156020165T>A c.658A>T c.(658-660)Atg>Ttg p.M220L GBM 1 156011962 156011962 + Silent SNP G G C TCGA-19-2619-01A-01D-1495-08 TCGA-19-2619-10A-01D-1495-08 g.chr1:156011962G>C c.1332C>G c.(1330-1332)ctC>ctG p.L444L GBM 1 156021545 156021545 + Missense_Mutation SNP C C G TCGA-19-2619-01A-01D-1495-08 TCGA-19-2619-10A-01D-1495-08 g.chr1:156021545C>G c.212G>C c.(211-213)gGa>gCa p.G71A GBMLGG 1 156011962 156011962 + Silent SNP G G C TCGA-19-2619-01A-01D-1495-08 TCGA-19-2619-10A-01D-1495-08 g.chr1:156011962G>C c.1332C>G c.(1330-1332)ctC>ctG p.L444L GBMLGG 1 156021545 156021545 + Missense_Mutation SNP C C G TCGA-19-2619-01A-01D-1495-08 TCGA-19-2619-10A-01D-1495-08 g.chr1:156021545C>G c.212G>C c.(211-213)gGa>gCa p.G71A HNSC 1 156020169 156020169 + Missense_Mutation SNP C C T TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chr1:156020169C>T c.654G>A c.(652-654)atG>atA p.M218I HNSC 1 156020253 156020253 + Missense_Mutation SNP C C T TCGA-UF-A7JH-01A-21D-A34J-08 TCGA-UF-A7JH-10A-01D-A34M-08 g.chr1:156020253C>T c.570G>A c.(568-570)atG>atA p.M190I HNSC 1 156021499 156021499 + Silent SNP C C T TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr1:156021499C>T c.258G>A c.(256-258)caG>caA p.Q86Q HNSC 1 156021624 156021624 + Missense_Mutation SNP A A C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr1:156021624A>C c.133T>G c.(133-135)Ttt>Gtt p.F45V KIPAN 1 156011344 156011344 + Frame_Shift_Del DEL C C - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:156011344delC c.1585delG c.(1585-1587)gctfs p.A529fs KIRC 1 156011344 156011344 + Frame_Shift_Del DEL C C - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:156011344delC c.1585delG c.(1585-1587)gctfs p.A529fs LIHC 1 156011369 156011371 + In_Frame_Del DEL CGT CGT - TCGA-BC-A10W-01A-11D-A12Z-10 TCGA-BC-A10W-11A-11D-A12Z-10 g.chr1:156011369_156011371delCGT c.1558_1560delACG c.(1558-1560)acgdel p.T520del LIHC 1 156021615 156021615 + Nonsense_Mutation SNP G G A TCGA-2V-A95S-01A-11D-A36X-10 TCGA-2V-A95S-10D-01D-A370-10 g.chr1:156021615G>A c.142C>T c.(142-144)Cag>Tag p.Q48* LUAD 1 156011313 156011313 + Missense_Mutation SNP T T A TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr1:156011313T>A c.1616A>T c.(1615-1617)cAg>cTg p.Q539L LUAD 1 156012595 156012595 + Silent SNP C C A TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr1:156012595C>A c.1236G>T c.(1234-1236)acG>acT p.T412T LUAD 1 156013886 156013886 + Silent SNP G G A TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr1:156013886G>A c.1029C>T c.(1027-1029)ccC>ccT p.P343P LUAD 1 156020169 156020169 + Missense_Mutation SNP C C T TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr1:156020169C>T c.654G>A c.(652-654)atG>atA p.M218I LUAD 1 156020194 156020194 + Missense_Mutation SNP G G A TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chr1:156020194G>A c.629C>T c.(628-630)tCt>tTt p.S210F LUAD 1 156020953 156020953 + Silent SNP C C A TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr1:156020953C>A c.426G>T c.(424-426)ggG>ggT p.G142G LUAD 1 156021524 156021524 + Missense_Mutation SNP A A T TCGA-55-8096-01A-11D-2238-08 TCGA-55-8096-10A-01D-2238-08 g.chr1:156021524A>T c.233T>A c.(232-234)gTc>gAc p.V78D LUAD 1 156021556 156021556 + Silent SNP C C T TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr1:156021556C>T c.201G>A c.(199-201)ctG>ctA p.L67L LUSC 1 156011382 156011382 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr1:156011382G>A c.1547C>T c.(1546-1548)tCc>tTc p.S516F LUSC 1 156020106 156020106 + Silent SNP G G C TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr1:156020106G>C c.717C>G c.(715-717)ctC>ctG p.L239L LUSC 1 156020177 156020177 + Missense_Mutation SNP G G A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr1:156020177G>A c.646C>T c.(646-648)Cgt>Tgt p.R216C PAAD 1 156012004 156012004 + Silent SNP G G A TCGA-3A-A9J0-01A-11D-A40W-08 TCGA-3A-A9J0-10A-01D-A40W-08 g.chr1:156012004G>A c.1290C>T c.(1288-1290)ttC>ttT p.F430F PRAD 1 156011291 156011292 + Frame_Shift_Ins INS - - A TCGA-KC-A4BV-01A-31D-A26M-08 TCGA-KC-A4BV-10A-01D-A26K-08 g.chr1:156011291_156011292insA c.1637_1638insT c.(1636-1638)ggafs p.G546fs PRAD 1 156013896 156013896 + Missense_Mutation SNP G G A TCGA-ZG-A9KY-01A-11D-A41K-08 TCGA-ZG-A9KY-10A-01D-A41N-08 g.chr1:156013896G>A c.1019C>T c.(1018-1020)tCc>tTc p.S340F READ 1 156018300 156018300 + Missense_Mutation SNP G G A TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr1:156018300G>A c.892C>T c.(892-894)Cgg>Tgg p.R298W SKCM 1 156006855 156006855 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:156006855G>A c.1720C>T c.(1720-1722)Cgt>Tgt p.R574C SKCM 1 156011382 156011382 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:156011382G>A c.1547C>T c.(1546-1548)tCc>tTc p.S516F SKCM 1 156013850 156013850 + Silent SNP G G A TCGA-EE-A3AH-06A-11D-A196-08 TCGA-EE-A3AH-10A-01D-A198-08 g.chr1:156013850G>A c.1065C>T c.(1063-1065)acC>acT p.T355T SKCM 1 156013888 156013888 + Missense_Mutation SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr1:156013888G>A c.1027C>T c.(1027-1029)Ccc>Tcc p.P343S SKCM 1 156013896 156013896 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr1:156013896G>A c.1019C>T c.(1018-1020)tCc>tTc p.S340F SKCM 1 156018388 156018388 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:156018388G>A c.804C>T c.(802-804)gcC>gcT p.A268A SKCM 1 156020207 156020207 + Nonsense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr1:156020207G>A c.616C>T c.(616-618)Cag>Tag p.Q206* SKCM 1 156020298 156020298 + Silent SNP A A C TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr1:156020298A>C c.525T>G c.(523-525)tcT>tcG p.S175S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 1 156020988 156020988 single base substitution C A exon_variant BLCA-CN 1 156020988 156020988 single base substitution C A missense_variant A131S 391G>T BRCA-EU 1 156000719 156000719 single base substitution G A downstream_gene_variant BRCA-EU 1 156000993 156000993 insertion of <=200bp - A downstream_gene_variant BRCA-EU 1 156001525 156001525 single base substitution A G downstream_gene_variant BRCA-EU 1 156002085 156002085 single base substitution G A downstream_gene_variant BRCA-EU 1 156002755 156002755 deletion of <=200bp G - downstream_gene_variant BRCA-EU 1 156003791 156003791 single base substitution T C downstream_gene_variant BRCA-EU 1 156005946 156005946 single base substitution C G 3_prime_UTR_variant BRCA-EU 1 156006822 156006822 single base substitution C A downstream_gene_variant BRCA-EU 1 156006822 156006822 single base substitution C A stop_gained G585* 1753G>T BRCA-EU 1 156007687 156007687 single base substitution G C downstream_gene_variant BRCA-EU 1 156007687 156007687 single base substitution G C intron_variant BRCA-EU 1 156008408 156008408 single base substitution A G downstream_gene_variant BRCA-EU 1 156008408 156008408 single base substitution A G intron_variant BRCA-EU 1 156009489 156009489 single base substitution G A downstream_gene_variant BRCA-EU 1 156009489 156009489 single base substitution G A intron_variant BRCA-EU 1 156009684 156009684 single base substitution G C downstream_gene_variant BRCA-EU 1 156009684 156009684 single base substitution G C intron_variant BRCA-EU 1 156009785 156009785 single base substitution C T downstream_gene_variant BRCA-EU 1 156009785 156009785 single base substitution C T intron_variant BRCA-EU 1 156010895 156010895 single base substitution A T downstream_gene_variant BRCA-EU 1 156010895 156010895 single base substitution A T intron_variant BRCA-EU 1 156011066 156011066 single base substitution G A downstream_gene_variant BRCA-EU 1 156011066 156011066 single base substitution G A intron_variant BRCA-EU 1 156011257 156011257 single base substitution C G downstream_gene_variant BRCA-EU 1 156011257 156011257 single base substitution C G intron_variant BRCA-EU 1 156011542 156011542 single base substitution T A downstream_gene_variant BRCA-EU 1 156011542 156011542 single base substitution T A intron_variant BRCA-EU 1 156012274 156012274 single base substitution T C exon_variant BRCA-EU 1 156012274 156012274 single base substitution T C intron_variant BRCA-EU 1 156012466 156012466 single base substitution C A intron_variant BRCA-EU 1 156012466 156012466 single base substitution C A upstream_gene_variant BRCA-EU 1 156012877 156012877 single base substitution A C intron_variant BRCA-EU 1 156012877 156012877 single base substitution A C upstream_gene_variant BRCA-EU 1 156013183 156013183 single base substitution G T intron_variant BRCA-EU 1 156013183 156013183 single base substitution G T upstream_gene_variant BRCA-EU 1 156013660 156013660 single base substitution G A downstream_gene_variant BRCA-EU 1 156013660 156013660 single base substitution G A intron_variant BRCA-EU 1 156013660 156013660 single base substitution G A upstream_gene_variant BRCA-EU 1 156013826 156013826 single base substitution C T downstream_gene_variant BRCA-EU 1 156013826 156013826 single base substitution C T synonymous_variant S363S 1089G>A BRCA-EU 1 156013826 156013826 single base substitution C T upstream_gene_variant BRCA-EU 1 156013945 156013945 single base substitution C T downstream_gene_variant BRCA-EU 1 156013945 156013945 single base substitution C T missense_variant E324K 970G>A BRCA-EU 1 156013945 156013945 single base substitution C T upstream_gene_variant BRCA-EU 1 156014048 156014048 single base substitution G A downstream_gene_variant BRCA-EU 1 156014048 156014048 single base substitution G A intron_variant BRCA-EU 1 156014048 156014048 single base substitution G A upstream_gene_variant BRCA-EU 1 156014744 156014744 single base substitution G A downstream_gene_variant BRCA-EU 1 156014744 156014744 single base substitution G A intron_variant BRCA-EU 1 156014744 156014744 single base substitution G A upstream_gene_variant BRCA-EU 1 156014804 156014804 single base substitution C G downstream_gene_variant BRCA-EU 1 156014804 156014804 single base substitution C G intron_variant BRCA-EU 1 156014804 156014804 single base substitution C G upstream_gene_variant BRCA-EU 1 156015368 156015368 single base substitution C G downstream_gene_variant BRCA-EU 1 156015368 156015368 single base substitution C G intron_variant BRCA-EU 1 156015368 156015368 single base substitution C G upstream_gene_variant BRCA-EU 1 156016001 156016001 single base substitution G A downstream_gene_variant BRCA-EU 1 156016001 156016001 single base substitution G A intron_variant BRCA-EU 1 156016001 156016001 single base substitution G A upstream_gene_variant BRCA-EU 1 156017243 156017243 single base substitution C G downstream_gene_variant BRCA-EU 1 156017243 156017243 single base substitution C G intron_variant BRCA-EU 1 156017243 156017243 single base substitution C G upstream_gene_variant BRCA-EU 1 156017750 156017750 single base substitution T C downstream_gene_variant BRCA-EU 1 156017750 156017750 single base substitution T C intron_variant BRCA-EU 1 156018310 156018310 single base substitution G A exon_variant BRCA-EU 1 156018310 156018310 single base substitution G A synonymous_variant F294F 882C>T BRCA-EU 1 156019414 156019414 single base substitution G A intron_variant BRCA-EU 1 156022174 156022174 single base substitution G C intron_variant BRCA-EU 1 156022819 156022819 single base substitution G T intron_variant BRCA-EU 1 156022975 156022975 single base substitution C A intron_variant BRCA-EU 1 156025409 156025409 single base substitution G A upstream_gene_variant BRCA-EU 1 156025727 156025727 single base substitution A G upstream_gene_variant BRCA-EU 1 156025941 156025941 single base substitution T A upstream_gene_variant BRCA-EU 1 156027031 156027031 single base substitution C T upstream_gene_variant BRCA-EU 1 156027647 156027647 deletion of <=200bp C - upstream_gene_variant BRCA-EU 1 156027650 156027650 single base substitution G A upstream_gene_variant BRCA-EU 1 156028262 156028262 single base substitution T A upstream_gene_variant BRCA-EU 1 156028309 156028309 single base substitution T A upstream_gene_variant BRCA-FR 1 156008408 156008408 single base substitution A G downstream_gene_variant BRCA-FR 1 156008408 156008408 single base substitution A G intron_variant BRCA-FR 1 156009555 156009555 single base substitution C T downstream_gene_variant BRCA-FR 1 156009555 156009555 single base substitution C T intron_variant BRCA-FR 1 156009684 156009684 single base substitution G C downstream_gene_variant BRCA-FR 1 156009684 156009684 single base substitution G C intron_variant BRCA-FR 1 156013945 156013945 single base substitution C T downstream_gene_variant BRCA-FR 1 156013945 156013945 single base substitution C T missense_variant E324K 970G>A BRCA-FR 1 156013945 156013945 single base substitution C T upstream_gene_variant BRCA-FR 1 156014048 156014048 single base substitution G A downstream_gene_variant BRCA-FR 1 156014048 156014048 single base substitution G A intron_variant BRCA-FR 1 156014048 156014048 single base substitution G A upstream_gene_variant BRCA-FR 1 156015368 156015368 single base substitution C G downstream_gene_variant BRCA-FR 1 156015368 156015368 single base substitution C G intron_variant BRCA-FR 1 156015368 156015368 single base substitution C G upstream_gene_variant BRCA-FR 1 156024360 156024360 single base substitution C G upstream_gene_variant BRCA-UK 1 156027684 156027684 single base substitution C G upstream_gene_variant BRCA-UK 1 156027702 156027702 single base substitution C G upstream_gene_variant BRCA-UK 1 156027752 156027752 single base substitution C T upstream_gene_variant BRCA-US 1 156011319 156011319 single base substitution A G downstream_gene_variant BRCA-US 1 156011319 156011319 single base substitution A G missense_variant M537T 1610T>C BRCA-US 1 156012608 156012608 single base substitution C G missense_variant S408T 1223G>C BRCA-US 1 156012608 156012608 single base substitution C G upstream_gene_variant BRCA-US 1 156012655 156012655 single base substitution C A missense_variant E392D 1176G>T BRCA-US 1 156012655 156012655 single base substitution C A upstream_gene_variant BRCA-US 1 156018375 156018375 single base substitution C G exon_variant BRCA-US 1 156018375 156018375 single base substitution C G missense_variant E273Q 817G>C BRCA-US 1 156021546 156021546 single base substitution C T exon_variant BRCA-US 1 156021546 156021546 single base substitution C T missense_variant G71R 211G>A BRCA-US 1 156024726 156024726 single base substitution A G upstream_gene_variant BRCA-US 1 156025001 156025001 single base substitution A T upstream_gene_variant BRCA-US 1 156025183 156025183 insertion of <=200bp - G upstream_gene_variant BTCA-JP 1 156025199 156025199 single base substitution A G upstream_gene_variant CESC-US 1 156020186 156020186 single base substitution C T intron_variant CESC-US 1 156020186 156020186 single base substitution C T missense_variant D213N 637G>A CESC-US 1 156024646 156024646 single base substitution C T upstream_gene_variant CESC-US 1 156028174 156028174 single base substitution G T upstream_gene_variant CLLE-ES 1 156001945 156001945 single base substitution C A downstream_gene_variant CLLE-ES 1 156023996 156023996 single base substitution G C upstream_gene_variant CLLE-ES 1 156026661 156026661 single base substitution A C upstream_gene_variant COAD-US 1 156011727 156011727 single base substitution C T exon_variant COAD-US 1 156011727 156011727 single base substitution C T missense_variant A468T 1402G>A COAD-US 1 156018326 156018326 single base substitution A G exon_variant COAD-US 1 156018326 156018326 single base substitution A G missense_variant I289T 866T>C COAD-US 1 156021084 156021084 single base substitution G T exon_variant COAD-US 1 156021084 156021084 single base substitution G T missense_variant P99T 295C>A COAD-US 1 156027790 156027790 single base substitution C T upstream_gene_variant COCA-CN 1 156006855 156006855 single base substitution G A downstream_gene_variant COCA-CN 1 156006855 156006855 single base substitution G A missense_variant R574C 1720C>T COCA-CN 1 156012041 156012041 single base substitution G T exon_variant COCA-CN 1 156012041 156012041 single base substitution G T intron_variant COCA-CN 1 156012726 156012726 single base substitution G T intron_variant COCA-CN 1 156012726 156012726 single base substitution G T upstream_gene_variant COCA-CN 1 156013676 156013676 single base substitution C T downstream_gene_variant COCA-CN 1 156013676 156013676 single base substitution C T intron_variant COCA-CN 1 156013676 156013676 single base substitution C T upstream_gene_variant COCA-CN 1 156014113 156014113 single base substitution G T downstream_gene_variant COCA-CN 1 156014113 156014113 single base substitution G T intron_variant COCA-CN 1 156014113 156014113 single base substitution G T upstream_gene_variant COCA-CN 1 156028214 156028214 single base substitution C T upstream_gene_variant ESAD-UK 1 156001897 156001897 single base substitution G A downstream_gene_variant ESAD-UK 1 156002368 156002368 single base substitution G A downstream_gene_variant ESAD-UK 1 156002442 156002442 single base substitution C T downstream_gene_variant ESAD-UK 1 156003647 156003647 single base substitution C A downstream_gene_variant ESAD-UK 1 156004810 156004810 single base substitution C A downstream_gene_variant ESAD-UK 1 156009495 156009495 single base substitution G C downstream_gene_variant ESAD-UK 1 156009495 156009495 single base substitution G C intron_variant ESAD-UK 1 156011336 156011336 single base substitution G A downstream_gene_variant ESAD-UK 1 156011336 156011336 single base substitution G A synonymous_variant S531S 1593C>T ESAD-UK 1 156013317 156013317 single base substitution C T downstream_gene_variant ESAD-UK 1 156013317 156013317 single base substitution C T intron_variant ESAD-UK 1 156013317 156013317 single base substitution C T upstream_gene_variant ESAD-UK 1 156015382 156015382 single base substitution G A downstream_gene_variant ESAD-UK 1 156015382 156015382 single base substitution G A intron_variant ESAD-UK 1 156015382 156015382 single base substitution G A upstream_gene_variant ESAD-UK 1 156018166 156018166 single base substitution C G downstream_gene_variant ESAD-UK 1 156018166 156018166 single base substitution C G intron_variant ESAD-UK 1 156018621 156018621 single base substitution C A intron_variant ESAD-UK 1 156019677 156019677 single base substitution C T intron_variant ESAD-UK 1 156020734 156020734 single base substitution G C intron_variant ESAD-UK 1 156020743 156020743 single base substitution C A intron_variant ESAD-UK 1 156025244 156025244 insertion of <=200bp - TG upstream_gene_variant ESAD-UK 1 156026121 156026121 single base substitution G C upstream_gene_variant ESAD-UK 1 156027637 156027637 single base substitution C T upstream_gene_variant ESAD-UK 1 156027776 156027776 single base substitution G A upstream_gene_variant ESAD-UK 1 156027997 156027997 single base substitution A T upstream_gene_variant ESCA-CN 1 156021033 156021033 single base substitution C T exon_variant ESCA-CN 1 156021033 156021033 single base substitution C T missense_variant A116T 346G>A GBM-US 1 156011962 156011962 single base substitution G C exon_variant GBM-US 1 156011962 156011962 single base substitution G C synonymous_variant L444L 1332C>G GBM-US 1 156021545 156021545 single base substitution C G exon_variant GBM-US 1 156021545 156021545 single base substitution C G missense_variant G71A 212G>C GBM-US 1 156025122 156025122 single base substitution C T upstream_gene_variant KIRC-US 1 156025137 156025137 single base substitution A C upstream_gene_variant KIRP-US 1 156027791 156027791 deletion of <=200bp G - upstream_gene_variant LAML-KR 1 156027796 156027796 single base substitution G T upstream_gene_variant LICA-CN 1 156012586 156012586 single base substitution C T synonymous_variant Q415Q 1245G>A LICA-CN 1 156012586 156012586 single base substitution C T upstream_gene_variant LICA-FR 1 156001613 156001613 single base substitution T C downstream_gene_variant LICA-FR 1 156004088 156004088 insertion of <=200bp - T downstream_gene_variant LICA-FR 1 156013856 156013856 single base substitution C T downstream_gene_variant LICA-FR 1 156013856 156013856 single base substitution C T synonymous_variant S353S 1059G>A LICA-FR 1 156013856 156013856 single base substitution C T upstream_gene_variant LICA-FR 1 156020960 156020960 single base substitution C T exon_variant LICA-FR 1 156020960 156020960 single base substitution C T missense_variant G140D 419G>A LINC-JP 1 156000162 156000162 single base substitution G A downstream_gene_variant LINC-JP 1 156006791 156006791 single base substitution A T downstream_gene_variant LINC-JP 1 156006791 156006791 single base substitution A T missense_variant L595Q 1784T>A LINC-JP 1 156006802 156006802 single base substitution A C downstream_gene_variant LINC-JP 1 156006802 156006802 single base substitution A C synonymous_variant A591A 1773T>G LINC-JP 1 156011431 156011431 single base substitution C T downstream_gene_variant LINC-JP 1 156011431 156011431 single base substitution C T missense_variant A500T 1498G>A LINC-JP 1 156011792 156011792 single base substitution A G intron_variant LINC-JP 1 156011967 156011967 single base substitution G A exon_variant LINC-JP 1 156011967 156011967 single base substitution G A stop_gained Q443* 1327C>T LINC-JP 1 156012600 156012600 single base substitution G T missense_variant Q411K 1231C>A LINC-JP 1 156012600 156012600 single base substitution G T upstream_gene_variant LINC-JP 1 156014575 156014575 single base substitution A G downstream_gene_variant LINC-JP 1 156014575 156014575 single base substitution A G intron_variant LINC-JP 1 156014575 156014575 single base substitution A G upstream_gene_variant LINC-JP 1 156020027 156020027 single base substitution G A intron_variant LINC-JP 1 156020028 156020028 single base substitution C T intron_variant LINC-JP 1 156025114 156025114 single base substitution G T upstream_gene_variant LIRI-JP 1 156003715 156003715 single base substitution C A downstream_gene_variant LIRI-JP 1 156006609 156006609 single base substitution A G 3_prime_UTR_variant LIRI-JP 1 156007440 156007440 single base substitution C G downstream_gene_variant LIRI-JP 1 156007440 156007440 single base substitution C G intron_variant LIRI-JP 1 156008271 156008271 single base substitution C T downstream_gene_variant LIRI-JP 1 156008271 156008271 single base substitution C T intron_variant LIRI-JP 1 156008503 156008503 single base substitution G C downstream_gene_variant LIRI-JP 1 156008503 156008503 single base substitution G C intron_variant LIRI-JP 1 156012159 156012159 single base substitution T C exon_variant LIRI-JP 1 156012159 156012159 single base substitution T C intron_variant LIRI-JP 1 156014340 156014340 single base substitution G A downstream_gene_variant LIRI-JP 1 156014340 156014340 single base substitution G A intron_variant LIRI-JP 1 156014340 156014340 single base substitution G A upstream_gene_variant LIRI-JP 1 156019193 156019193 single base substitution G A intron_variant LIRI-JP 1 156019938 156019938 single base substitution C T intron_variant LIRI-JP 1 156021737 156021737 single base substitution T C intron_variant LIRI-JP 1 156022340 156022340 single base substitution C T intron_variant LIRI-JP 1 156022654 156022654 single base substitution T C intron_variant LIRI-JP 1 156025717 156025717 single base substitution A T upstream_gene_variant LIRI-JP 1 156026762 156026762 single base substitution T G upstream_gene_variant LIRI-JP 1 156027903 156027903 single base substitution T C upstream_gene_variant LIRI-JP 1 156027909 156027909 single base substitution T G upstream_gene_variant LUSC-KR 1 156008473 156008473 single base substitution T C downstream_gene_variant LUSC-KR 1 156008473 156008473 single base substitution T C intron_variant LUSC-KR 1 156010602 156010602 single base substitution C T downstream_gene_variant LUSC-KR 1 156010602 156010602 single base substitution C T intron_variant LUSC-KR 1 156021749 156021749 single base substitution C A intron_variant LUSC-KR 1 156022174 156022174 single base substitution G A intron_variant LUSC-KR 1 156027020 156027020 single base substitution A T upstream_gene_variant LUSC-US 1 156011382 156011382 single base substitution G A downstream_gene_variant LUSC-US 1 156011382 156011382 single base substitution G A missense_variant S516F 1547C>T LUSC-US 1 156020106 156020106 single base substitution G C exon_variant LUSC-US 1 156020106 156020106 single base substitution G C synonymous_variant L239L 717C>G LUSC-US 1 156020177 156020177 single base substitution G A intron_variant LUSC-US 1 156020177 156020177 single base substitution G A missense_variant R216C 646C>T LUSC-US 1 156027821 156027821 single base substitution C A upstream_gene_variant MALY-DE 1 156001859 156001859 insertion of <=200bp - T downstream_gene_variant MALY-DE 1 156009465 156009465 single base substitution A T downstream_gene_variant MALY-DE 1 156009465 156009465 single base substitution A T intron_variant MALY-DE 1 156017031 156017031 single base substitution G T downstream_gene_variant MALY-DE 1 156017031 156017031 single base substitution G T intron_variant MALY-DE 1 156017031 156017031 single base substitution G T upstream_gene_variant MALY-DE 1 156018863 156018863 single base substitution G A intron_variant MALY-DE 1 156023710 156023710 single base substitution G A upstream_gene_variant MALY-DE 1 156023806 156023806 single base substitution G A upstream_gene_variant MELA-AU 1 156000757 156000757 single base substitution G A downstream_gene_variant MELA-AU 1 156000953 156000953 single base substitution G A downstream_gene_variant MELA-AU 1 156000996 156000996 single base substitution A C downstream_gene_variant MELA-AU 1 156001359 156001359 single base substitution G A downstream_gene_variant MELA-AU 1 156001479 156001479 single base substitution C T downstream_gene_variant MELA-AU 1 156002492 156002492 single base substitution C T downstream_gene_variant MELA-AU 1 156002644 156002644 single base substitution G A downstream_gene_variant MELA-AU 1 156002713 156002713 single base substitution G A downstream_gene_variant MELA-AU 1 156002750 156002750 single base substitution A T downstream_gene_variant MELA-AU 1 156002753 156002753 single base substitution G A downstream_gene_variant MELA-AU 1 156002814 156002814 single base substitution G A downstream_gene_variant MELA-AU 1 156002952 156002952 single base substitution G A downstream_gene_variant MELA-AU 1 156003061 156003061 single base substitution G A downstream_gene_variant MELA-AU 1 156003462 156003462 single base substitution C T downstream_gene_variant MELA-AU 1 156003545 156003545 single base substitution G A downstream_gene_variant MELA-AU 1 156003647 156003647 single base substitution C A downstream_gene_variant MELA-AU 1 156003956 156003956 single base substitution A G downstream_gene_variant MELA-AU 1 156004299 156004299 single base substitution G A downstream_gene_variant MELA-AU 1 156004882 156004882 single base substitution T A downstream_gene_variant MELA-AU 1 156004967 156004967 single base substitution T A downstream_gene_variant MELA-AU 1 156005031 156005031 single base substitution G A downstream_gene_variant MELA-AU 1 156006257 156006257 single base substitution G A 3_prime_UTR_variant MELA-AU 1 156006680 156006680 single base substitution G A 3_prime_UTR_variant MELA-AU 1 156006680 156006680 single base substitution G A downstream_gene_variant MELA-AU 1 156008345 156008345 single base substitution G A downstream_gene_variant MELA-AU 1 156008345 156008345 single base substitution G A intron_variant MELA-AU 1 156008551 156008551 single base substitution G A downstream_gene_variant MELA-AU 1 156008551 156008551 single base substitution G A intron_variant MELA-AU 1 156008568 156008568 single base substitution G A downstream_gene_variant MELA-AU 1 156008568 156008568 single base substitution G A intron_variant MELA-AU 1 156008677 156008677 single base substitution G A downstream_gene_variant MELA-AU 1 156008677 156008677 single base substitution G A intron_variant MELA-AU 1 156008821 156008821 single base substitution G A downstream_gene_variant MELA-AU 1 156008821 156008821 single base substitution G A intron_variant MELA-AU 1 156008984 156008984 single base substitution T C downstream_gene_variant MELA-AU 1 156008984 156008984 single base substitution T C intron_variant MELA-AU 1 156009105 156009105 single base substitution G A downstream_gene_variant MELA-AU 1 156009105 156009105 single base substitution G A intron_variant MELA-AU 1 156009437 156009437 single base substitution C T downstream_gene_variant MELA-AU 1 156009437 156009437 single base substitution C T intron_variant MELA-AU 1 156009933 156009933 single base substitution C T downstream_gene_variant MELA-AU 1 156009933 156009933 single base substitution C T intron_variant MELA-AU 1 156010718 156010718 single base substitution C T downstream_gene_variant MELA-AU 1 156010718 156010718 single base substitution C T intron_variant MELA-AU 1 156011461 156011461 single base substitution G A downstream_gene_variant MELA-AU 1 156011461 156011461 single base substitution G A missense_variant L490F 1468C>T MELA-AU 1 156011562 156011562 single base substitution G A downstream_gene_variant MELA-AU 1 156011562 156011562 single base substitution G A intron_variant MELA-AU 1 156011896 156011896 single base substitution G A intron_variant MELA-AU 1 156011897 156011897 single base substitution G A intron_variant MELA-AU 1 156012280 156012280 single base substitution G A exon_variant MELA-AU 1 156012280 156012280 single base substitution G A intron_variant MELA-AU 1 156012514 156012514 single base substitution A G intron_variant MELA-AU 1 156012514 156012514 single base substitution A G upstream_gene_variant MELA-AU 1 156013120 156013120 single base substitution G A intron_variant MELA-AU 1 156013120 156013120 single base substitution G A upstream_gene_variant MELA-AU 1 156013555 156013555 single base substitution G A downstream_gene_variant MELA-AU 1 156013555 156013555 single base substitution G A intron_variant MELA-AU 1 156013555 156013555 single base substitution G A upstream_gene_variant MELA-AU 1 156013850 156013850 single base substitution G A downstream_gene_variant MELA-AU 1 156013850 156013850 single base substitution G A synonymous_variant T355T 1065C>T MELA-AU 1 156013850 156013850 single base substitution G A upstream_gene_variant MELA-AU 1 156014456 156014456 single base substitution G A downstream_gene_variant MELA-AU 1 156014456 156014456 single base substitution G A intron_variant MELA-AU 1 156014456 156014456 single base substitution G A upstream_gene_variant MELA-AU 1 156014680 156014680 single base substitution C T downstream_gene_variant MELA-AU 1 156014680 156014680 single base substitution C T intron_variant MELA-AU 1 156014680 156014680 single base substitution C T upstream_gene_variant MELA-AU 1 156016519 156016519 single base substitution G A downstream_gene_variant MELA-AU 1 156016519 156016519 single base substitution G A intron_variant MELA-AU 1 156016519 156016519 single base substitution G A upstream_gene_variant MELA-AU 1 156016658 156016658 single base substitution A G downstream_gene_variant MELA-AU 1 156016658 156016658 single base substitution A G intron_variant MELA-AU 1 156016658 156016658 single base substitution A G upstream_gene_variant MELA-AU 1 156017546 156017546 single base substitution C T downstream_gene_variant MELA-AU 1 156017546 156017546 single base substitution C T intron_variant MELA-AU 1 156017581 156017581 single base substitution G A downstream_gene_variant MELA-AU 1 156017581 156017581 single base substitution G A intron_variant MELA-AU 1 156017615 156017615 single base substitution G A downstream_gene_variant MELA-AU 1 156017615 156017615 single base substitution G A intron_variant MELA-AU 1 156017691 156017691 single base substitution A C downstream_gene_variant MELA-AU 1 156017691 156017691 single base substitution A C intron_variant MELA-AU 1 156018317 156018317 single base substitution G A exon_variant MELA-AU 1 156018317 156018317 single base substitution G A missense_variant P292L 875C>T MELA-AU 1 156018791 156018791 single base substitution G A intron_variant MELA-AU 1 156020207 156020207 single base substitution G A intron_variant MELA-AU 1 156020207 156020207 single base substitution G A stop_gained Q206* 616C>T MELA-AU 1 156020553 156020553 single base substitution G A intron_variant MELA-AU 1 156020852 156020852 single base substitution C T intron_variant MELA-AU 1 156021142 156021142 single base substitution C T intron_variant MELA-AU 1 156021589 156021589 single base substitution G A exon_variant MELA-AU 1 156021589 156021589 single base substitution G A synonymous_variant F56F 168C>T MELA-AU 1 156021703 156021703 single base substitution G A intron_variant MELA-AU 1 156022384 156022384 single base substitution G A intron_variant MELA-AU 1 156022634 156022634 single base substitution G C intron_variant MELA-AU 1 156023233 156023233 single base substitution C T intron_variant MELA-AU 1 156024407 156024407 single base substitution C T upstream_gene_variant MELA-AU 1 156024447 156024447 single base substitution G A upstream_gene_variant MELA-AU 1 156024491 156024491 single base substitution G A upstream_gene_variant MELA-AU 1 156024535 156024535 single base substitution C T upstream_gene_variant MELA-AU 1 156024806 156024806 single base substitution C T upstream_gene_variant MELA-AU 1 156026657 156026657 single base substitution C T upstream_gene_variant MELA-AU 1 156027967 156027967 single base substitution C T upstream_gene_variant MELA-AU 1 156028408 156028408 single base substitution C T upstream_gene_variant ORCA-IN 1 156000182 156000182 single base substitution G C downstream_gene_variant ORCA-IN 1 156024087 156024087 single base substitution C G upstream_gene_variant ORCA-IN 1 156024805 156024805 single base substitution C T upstream_gene_variant OV-AU 1 156012041 156012041 single base substitution G T exon_variant OV-AU 1 156012041 156012041 single base substitution G T intron_variant OV-AU 1 156016532 156016532 single base substitution C G downstream_gene_variant OV-AU 1 156016532 156016532 single base substitution C G intron_variant OV-AU 1 156016532 156016532 single base substitution C G upstream_gene_variant OV-AU 1 156027041 156027041 single base substitution T G upstream_gene_variant PACA-AU 1 156005763 156005763 deletion of <=200bp G - 3_prime_UTR_variant PACA-AU 1 156006067 156006067 single base substitution C T 3_prime_UTR_variant PACA-AU 1 156008484 156008484 single base substitution A T downstream_gene_variant PACA-AU 1 156008484 156008484 single base substitution A T intron_variant PACA-AU 1 156009850 156009850 single base substitution C T downstream_gene_variant PACA-AU 1 156009850 156009850 single base substitution C T intron_variant PACA-AU 1 156011305 156011305 single base substitution G A downstream_gene_variant PACA-AU 1 156011305 156011305 single base substitution G A stop_gained Q542* 1624C>T PACA-AU 1 156016017 156016017 single base substitution G A downstream_gene_variant PACA-AU 1 156016017 156016017 single base substitution G A intron_variant PACA-AU 1 156016017 156016017 single base substitution G A upstream_gene_variant PACA-AU 1 156018319 156018319 single base substitution C A exon_variant PACA-AU 1 156018319 156018319 single base substitution C A missense_variant E291D 873G>T PACA-AU 1 156020499 156020499 deletion of <=200bp A - intron_variant PACA-AU 1 156021075 156021075 single base substitution G C exon_variant PACA-AU 1 156021075 156021075 single base substitution G C missense_variant P102A 304C>G PACA-AU 1 156021534 156021534 single base substitution C T exon_variant PACA-AU 1 156021534 156021534 single base substitution C T missense_variant G75R 223G>A PACA-AU 1 156022211 156022211 single base substitution G A intron_variant PACA-AU 1 156025826 156025826 single base substitution C T upstream_gene_variant PACA-CA 1 156000768 156000768 single base substitution A G downstream_gene_variant PACA-CA 1 156010822 156010822 single base substitution C A downstream_gene_variant PACA-CA 1 156010822 156010822 single base substitution C A intron_variant PACA-CA 1 156011444 156011444 single base substitution T C downstream_gene_variant PACA-CA 1 156011444 156011444 single base substitution T C missense_variant I495M 1485A>G PACA-CA 1 156021874 156021874 single base substitution C A intron_variant PACA-CA 1 156022598 156022598 single base substitution T C intron_variant PAEN-AU 1 156021781 156021781 single base substitution G A intron_variant PBCA-DE 1 156001711 156001711 insertion of <=200bp - AT downstream_gene_variant PBCA-DE 1 156001859 156001859 insertion of <=200bp - T downstream_gene_variant PBCA-DE 1 156004440 156004440 single base substitution G C downstream_gene_variant PBCA-DE 1 156009799 156009799 single base substitution T C downstream_gene_variant PBCA-DE 1 156009799 156009799 single base substitution T C intron_variant PRAD-CA 1 156000162 156000162 single base substitution G A downstream_gene_variant PRAD-CA 1 156002651 156002651 single base substitution C T downstream_gene_variant PRAD-CA 1 156006809 156006809 single base substitution T C downstream_gene_variant PRAD-CA 1 156006809 156006809 single base substitution T C missense_variant N589S 1766A>G PRAD-CA 1 156007886 156007886 single base substitution G C downstream_gene_variant PRAD-CA 1 156007886 156007886 single base substitution G C intron_variant PRAD-CA 1 156019674 156019674 single base substitution T G intron_variant PRAD-UK 1 156017816 156017816 single base substitution C T downstream_gene_variant PRAD-UK 1 156017816 156017816 single base substitution C T intron_variant PRAD-US 1 156025148 156025148 single base substitution G A upstream_gene_variant READ-US 1 156018300 156018300 single base substitution G A exon_variant READ-US 1 156018300 156018300 single base substitution G A missense_variant R298W 892C>T RECA-EU 1 156008690 156008690 single base substitution C A downstream_gene_variant RECA-EU 1 156008690 156008690 single base substitution C A intron_variant RECA-EU 1 156010965 156010965 single base substitution G A downstream_gene_variant RECA-EU 1 156010965 156010965 single base substitution G A intron_variant SKCA-BR 1 156001368 156001370 deletion of <=200bp CTT - downstream_gene_variant SKCA-BR 1 156002304 156002305 deletion of <=200bp GA - downstream_gene_variant SKCA-BR 1 156003408 156003408 single base substitution C A downstream_gene_variant SKCA-BR 1 156007177 156007177 single base substitution A G downstream_gene_variant SKCA-BR 1 156007177 156007177 single base substitution A G intron_variant SKCA-BR 1 156007443 156007443 single base substitution A G downstream_gene_variant SKCA-BR 1 156007443 156007443 single base substitution A G intron_variant SKCA-BR 1 156007461 156007461 single base substitution C T downstream_gene_variant SKCA-BR 1 156007461 156007461 single base substitution C T intron_variant SKCA-BR 1 156009036 156009037 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 1 156009036 156009037 deletion of <=200bp CT - intron_variant SKCA-BR 1 156009092 156009092 single base substitution A G downstream_gene_variant SKCA-BR 1 156009092 156009092 single base substitution A G intron_variant SKCA-BR 1 156009695 156009695 single base substitution T C downstream_gene_variant SKCA-BR 1 156009695 156009695 single base substitution T C intron_variant SKCA-BR 1 156010474 156010474 single base substitution A C downstream_gene_variant SKCA-BR 1 156010474 156010474 single base substitution A C intron_variant SKCA-BR 1 156011533 156011533 single base substitution G A downstream_gene_variant SKCA-BR 1 156011533 156011533 single base substitution G A intron_variant SKCA-BR 1 156012975 156012975 single base substitution T C intron_variant SKCA-BR 1 156012975 156012975 single base substitution T C upstream_gene_variant SKCA-BR 1 156017580 156017580 single base substitution G A downstream_gene_variant SKCA-BR 1 156017580 156017580 single base substitution G A intron_variant SKCA-BR 1 156018129 156018129 single base substitution G A downstream_gene_variant SKCA-BR 1 156018129 156018129 single base substitution G A intron_variant SKCA-BR 1 156019606 156019606 single base substitution T C intron_variant SKCA-BR 1 156019838 156019838 single base substitution C A intron_variant SKCA-BR 1 156023782 156023782 single base substitution C G upstream_gene_variant SKCA-BR 1 156023786 156023786 single base substitution T C upstream_gene_variant SKCA-BR 1 156023801 156023801 single base substitution A G upstream_gene_variant SKCA-BR 1 156024546 156024546 single base substitution T A upstream_gene_variant SKCA-BR 1 156025867 156025867 single base substitution C T upstream_gene_variant SKCM-US 1 156006855 156006855 single base substitution G A downstream_gene_variant SKCM-US 1 156006855 156006855 single base substitution G A missense_variant R574C 1720C>T SKCM-US 1 156011382 156011382 single base substitution G A downstream_gene_variant SKCM-US 1 156011382 156011382 single base substitution G A missense_variant S516F 1547C>T SKCM-US 1 156011741 156011741 single base substitution G A exon_variant SKCM-US 1 156011741 156011741 single base substitution G A missense_variant P463L 1388C>T SKCM-US 1 156013850 156013850 single base substitution G A downstream_gene_variant SKCM-US 1 156013850 156013850 single base substitution G A synonymous_variant T355T 1065C>T SKCM-US 1 156013850 156013850 single base substitution G A upstream_gene_variant SKCM-US 1 156013888 156013888 single base substitution G A downstream_gene_variant SKCM-US 1 156013888 156013888 single base substitution G A missense_variant P343S 1027C>T SKCM-US 1 156013888 156013888 single base substitution G A upstream_gene_variant SKCM-US 1 156013896 156013896 single base substitution G A downstream_gene_variant SKCM-US 1 156013896 156013896 single base substitution G A missense_variant S340F 1019C>T SKCM-US 1 156013896 156013896 single base substitution G A upstream_gene_variant SKCM-US 1 156018388 156018388 single base substitution G A exon_variant SKCM-US 1 156018388 156018388 single base substitution G A synonymous_variant A268A 804C>T SKCM-US 1 156020207 156020207 single base substitution G A intron_variant SKCM-US 1 156020207 156020207 single base substitution G A stop_gained Q206* 616C>T SKCM-US 1 156020298 156020298 single base substitution A C intron_variant SKCM-US 1 156020298 156020298 single base substitution A C synonymous_variant S175S 525T>G SKCM-US 1 156028139 156028139 single base substitution C T upstream_gene_variant STAD-US 1 156012626 156012626 single base substitution G A missense_variant S402L 1205C>T STAD-US 1 156012626 156012626 single base substitution G A upstream_gene_variant STAD-US 1 156013976 156013976 single base substitution G A downstream_gene_variant STAD-US 1 156013976 156013976 single base substitution G A synonymous_variant S313S 939C>T STAD-US 1 156013976 156013976 single base substitution G A upstream_gene_variant STAD-US 1 156018332 156018332 single base substitution G A exon_variant STAD-US 1 156018332 156018332 single base substitution G A missense_variant T287M 860C>T STAD-US 1 156020124 156020124 single base substitution A G exon_variant STAD-US 1 156020124 156020124 single base substitution A G synonymous_variant P233P 699T>C STAD-US 1 156020296 156020296 single base substitution G A intron_variant STAD-US 1 156020296 156020296 single base substitution G A missense_variant A176V 527C>T STAD-US 1 156024741 156024741 single base substitution A C upstream_gene_variant UCEC-US 1 156011374 156011374 single base substitution C T downstream_gene_variant UCEC-US 1 156011374 156011374 single base substitution C T missense_variant A519T 1555G>A UCEC-US 1 156011743 156011743 single base substitution A G exon_variant UCEC-US 1 156011743 156011743 single base substitution A G synonymous_variant N462N 1386T>C UCEC-US 1 156012661 156012661 single base substitution G T synonymous_variant I390I 1170C>A UCEC-US 1 156012661 156012661 single base substitution G T upstream_gene_variant UCEC-US 1 156018388 156018388 single base substitution G T exon_variant UCEC-US 1 156018388 156018388 single base substitution G T synonymous_variant A268A 804C>A UCEC-US 1 156020177 156020177 single base substitution G A intron_variant UCEC-US 1 156020177 156020177 single base substitution G A missense_variant R216C 646C>T UCEC-US 1 156020912 156020912 single base substitution G A exon_variant UCEC-US 1 156020912 156020912 single base substitution G A missense_variant A156V 467C>T UCEC-US 1 156020972 156020972 single base substitution C T exon_variant UCEC-US 1 156020972 156020972 single base substitution C T missense_variant R136Q 407G>A UCEC-US 1 156021546 156021546 single base substitution C T exon_variant UCEC-US 1 156021546 156021546 single base substitution C T missense_variant G71R 211G>A UCEC-US 1 156028077 156028077 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-19-2619-01 COSM2156139 c.212G>C p.G71A Substitution - Missense 1:156051754-156051754 - TCGA-A5-A0VP-01 COSM897102 c.407G>A p.R136Q Substitution - Missense 1:156051181-156051181 - TCGA-B5-A11E-01 COSM897101 c.467C>T p.A156V Substitution - Missense 1:156051121-156051121 - HCC149T COSM5817272 c.1245G>A p.Q415Q Substitution - coding silent 1:156042795-156042795 - YUPRO COSM1688746 c.871G>A p.E291K Substitution - Missense 1:156048530-156048530 - TCGA-EB-A431-01 COSM3475134 c.1388C>T p.P463L Substitution - Missense 1:156041950-156041950 - SMS-CTR COSM4989644 c.1661C>T p.T554M Substitution - Missense 1:156037123-156037123 - HCC74 COSM3705067 c.1773T>G p.A591A Substitution - coding silent 1:156037011-156037011 - DLD1 COSM1982946 c.663C>T p.A221A Substitution - coding silent 1:156050369-156050369 - PCSI_0058_Pa_X COSM5420315 c.1485A>G p.I495M Substitution - Missense 1:156041653-156041653 - 8031867 COSM3385253 c.223G>A p.G75R Substitution - Missense 1:156051743-156051743 - 2492703 COSM5600812 c.1287C>T p.L429L Substitution - coding silent 1:156042216-156042216 - ESCC_103 COSM5638088 c.1519G>T p.A507S Substitution - Missense 1:156041619-156041619 - 2_PRE-TREATMENT COSM1722902 c.1489C>T p.R497W Substitution - Missense 1:156041649-156041649 - LUAD-B02077 COSM335094 c.1266+1G>A p.? Unknown 1:156042773-156042773 - HCC62 COSM1600948 c.1231C>A p.Q411K Substitution - Missense 1:156042809-156042809 - CSCC-35-T COSM4566653 c.433_434CC>TT p.P145L Substitution - Missense 1:156051154-156051155 - CSCC-7-T COSM4477626 c.216C>G p.I72M Substitution - Missense 1:156051750-156051750 - HCT15 COSM1982924 c.1185G>T p.Q395H Substitution - Missense 1:156042855-156042855 - TCGA-CG-5733-01 COSM4023158 c.527C>T p.A176V Substitution - Missense 1:156050505-156050505 - TCGA-F4-6703-01 COSM5172611 c.1322G>A p.R441H Substitution - Missense 1:156042181-156042181 - TCGA-AA-3663-01 COSM1334755 c.866T>C p.I289T Substitution - Missense 1:156048535-156048535 - CT-TC COSM4989644 c.1661C>T p.T554M Substitution - Missense 1:156037123-156037123 - PT08_2 COSM5892672 c.577C>T p.P193S Substitution - Missense 1:156050455-156050455 - TCGA-AA-3715-01 COSM270494 c.1662G>A p.T554T Substitution - coding silent 1:156037122-156037122 - 2492700 COSM5600812 c.1287C>T p.L429L Substitution - coding silent 1:156042216-156042216 - TCGA-D1-A103-01 COSM675681 c.646C>T p.R216C Substitution - Missense 1:156050386-156050386 - TCGA-HU-A4H3-01 COSM4023155 c.939C>T p.S313S Substitution - coding silent 1:156044185-156044185 - TCGA-AP-A0LM-01 COSM424107 c.211G>A p.G71R Substitution - Missense 1:156051755-156051755 - 51T COSM106883 c.1642G>T p.G548* Substitution - Nonsense 1:156041496-156041496 - Pat_26_B COSM5843942 c.67A>G p.K23E Substitution - Missense 1:156053635-156053635 - TCGA-EI-6506-01 COSM1559932 c.892C>T p.R298W Substitution - Missense 1:156048509-156048509 - CHC429T COSM3667020 c.419G>A p.G140D Substitution - Missense 1:156051169-156051169 - TCGA-GN-A266-06 COSM3475133 c.1720C>T p.R574C Substitution - Missense 1:156037064-156037064 - S0029 COSM5881533 c.1789G>A p.G597S Substitution - Missense 1:156036995-156036995 - PT08_1 COSM5892672 c.577C>T p.P193S Substitution - Missense 1:156050455-156050455 - HCC74T COSM3705067 c.1773T>G p.A591A Substitution - coding silent 1:156037011-156037011 - STC252 COSM5052636 c.1705A>G p.M569V Substitution - Missense 1:156037079-156037079 - T3724 COSM424107 c.211G>A p.G71R Substitution - Missense 1:156051755-156051755 - TCGA-18-3409-01 COSM675684 c.1547C>T p.S516F Substitution - Missense 1:156041591-156041591 - T3225 COSM897101 c.467C>T p.A156V Substitution - Missense 1:156051121-156051121 - 8014777 COSM3385252 c.873G>T p.E291D Substitution - Missense 1:156048528-156048528 - TCGA-19-2619 COSM2156145 c.1332C>G p.L444L Substitution - coding silent 1:156042171-156042171 - TCGA-A6-2675-01 COSM5082029 c.848G>A p.R283H Substitution - Missense 1:156048553-156048553 - PT16_1 COSM5898123 c.1532C>T p.P511L Substitution - Missense 1:156041606-156041606 - 01-P8014 COSM4576361 c.1279G>A p.V427M Substitution - Missense 1:156042224-156042224 - TCGA-39-5030-01 COSM675681 c.646C>T p.R216C Substitution - Missense 1:156050386-156050386 - 388 COSM3724068 c.1723G>T p.E575* Substitution - Nonsense 1:156037061-156037061 - TCGA-EE-A2GD-06 COSM3475139 c.525T>G p.S175S Substitution - coding silent 1:156050507-156050507 - TCGA-DR-A0ZM-01 COSM458546 c.637G>A p.D213N Substitution - Missense 1:156050395-156050395 - C086 COSM5541292 c.295C>T p.P99S Substitution - Missense 1:156051293-156051293 - 587316 COSM1231601 c.1036G>A p.G346S Substitution - Missense 1:156044088-156044088 - Au2 COSM5600812 c.1287C>T p.L429L Substitution - coding silent 1:156042216-156042216 - TCGA-EE-A2MD-06 COSM1982948 c.616C>T p.Q206* Substitution - Nonsense 1:156050416-156050416 - PT36 COSM5914812 c.1301C>T p.P434L Substitution - Missense 1:156042202-156042202 - Pa38X COSM83932 c.396C>T p.G132G Substitution - coding silent 1:156051192-156051192 - 2_RESISTANT COSM1722902 c.1489C>T p.R497W Substitution - Missense 1:156041649-156041649 - TCGA-CK-4951-01 COSM5146849 c.603G>A p.E201E Substitution - coding silent 1:156050429-156050429 - HCC174T COSM3705068 c.1498G>A p.A500T Substitution - Missense 1:156041640-156041640 - CHC1700T COSM4800469 c.1059G>A p.S353S Substitution - coding silent 1:156044065-156044065 - TCGA-A5-A0VP-01 COSM897097 c.1555G>A p.A519T Substitution - Missense 1:156041583-156041583 - HX36T COSM1600947 c.1327C>T p.Q443* Substitution - Nonsense 1:156042176-156042176 - SNU-175 COSM675681 c.646C>T p.R216C Substitution - Missense 1:156050386-156050386 - TCGA-EE-A29S-06 COSM3475136 c.1027C>T p.P343S Substitution - Missense 1:156044097-156044097 - DLD1 COSM1982924 c.1185G>T p.Q395H Substitution - Missense 1:156042855-156042855 - CHC429T COSM3667020 c.419G>A p.G140D Substitution - Missense 1:156051169-156051169 - HCC29 COSM1600947 c.1327C>T p.Q443* Substitution - Nonsense 1:156042176-156042176 - TCGA-BP-5185-01 COSM463137 c.1695G>T p.Q565H Substitution - Missense 1:156037089-156037089 - N742T COSM236604 c.1319T>G p.L440R Substitution - Missense 1:156042184-156042184 - TCGA-D1-A103-01 COSM897098 c.1386T>C p.N462N Substitution - coding silent 1:156041952-156041952 - TCGA-BR-8487-01 COSM4023156 c.860C>T p.T287M Substitution - Missense 1:156048541-156048541 - ME020T COSM225443 c.976C>T p.R326* Substitution - Nonsense 1:156044148-156044148 - TCGA-EE-A2MS-06 COSM3475137 c.1019C>T p.S340F Substitution - Missense 1:156044105-156044105 - TCGA-A6-3809-01 COSM5086548 c.1088C>T p.S363L Substitution - Missense 1:156044036-156044036 - CPCG0259-F1 COSM4880007 c.1766A>G p.N589S Substitution - Missense 1:156037018-156037018 - TCGA-GN-A266-06 COSM675684 c.1547C>T p.S516F Substitution - Missense 1:156041591-156041591 - cSCCP2 COSM137322 c.1373C>T p.S458F Substitution - Missense 1:156041965-156041965 - CSCC-20-T COSM4560902 c.861G>A p.T287T Substitution - coding silent 1:156048540-156048540 - S01453 COSM5701192 c.36_37insC p.I13fs*34 Insertion - Frameshift 1:156053665-156053666 - TCGA-19-2619-01 COSM2156145 c.1332C>G p.L444L Substitution - coding silent 1:156042171-156042171 - 8015299 COSM3771475 c.304C>G p.P102A Substitution - Missense 1:156051284-156051284 - TCGA-AN-A046-01 COSM3802182 c.1176G>T p.E392D Substitution - Missense 1:156042864-156042864 - ESCC-116T COSM3934133 c.346G>A p.A116T Substitution - Missense 1:156051242-156051242 - HCC74T COSM3705066 c.1784T>A p.L595Q Substitution - Missense 1:156037000-156037000 - CHC1700T COSM4800469 c.1059G>A p.S353S Substitution - coding silent 1:156044065-156044065 - LC_S27 COSM1185616 c.500G>A p.G167E Substitution - Missense 1:156050532-156050532 - TCGA-D1-A103-01 COSM897099 c.1170C>A p.I390I Substitution - coding silent 1:156042870-156042870 - 2492702 COSM5600812 c.1287C>T p.L429L Substitution - coding silent 1:156042216-156042216 - TCGA-19-2619 COSM2156139 c.212G>C p.G71A Substitution - Missense 1:156051754-156051754 - TCGA-A7-A0DA-01 COSM424106 c.1223G>C p.S408T Substitution - Missense 1:156042817-156042817 - HCC74 COSM3705066 c.1784T>A p.L595Q Substitution - Missense 1:156037000-156037000 - ccRCC-43 COSM1664862 c.712A>G p.M238V Substitution - Missense 1:156050320-156050320 - YUKAT COSM5377861 c.725C>T p.P242L Substitution - Missense 1:156050307-156050307 - CLL108 COSM1289996 c.1272G>A p.M424I Substitution - Missense 1:156042231-156042231 - B86-Tumor COSM3930430 c.391G>T p.A131S Substitution - Missense 1:156051197-156051197 - TCGA-HU-8602-01 COSM4023157 c.699T>C p.P233P Substitution - coding silent 1:156050333-156050333 - 49M COSM5593823 c.1776C>T p.I592I Substitution - coding silent 1:156037008-156037008 - 587224 COSM1180698 c.426delG p.S144fs*28 Deletion - Frameshift 1:156051162-156051162 - 587374 COSM1231602 c.893G>A p.R298Q Substitution - Missense 1:156048508-156048508 - SNUH_G16_S1 COSM1982957 c.169G>T p.A57S Substitution - Missense 1:156051797-156051797 - CSCC-7-T COSM4457185 c.1035C>T p.S345S Substitution - coding silent 1:156044089-156044089 - NPC1F COSM4995287 c.177G>T p.K59N Substitution - Missense 1:156051789-156051789 - 6948_PT COSM5754221 c.1036G>T p.G346C Substitution - Missense 1:156044088-156044088 - CSCC-41-T COSM3475137 c.1019C>T p.S340F Substitution - Missense 1:156044105-156044105 - TCGA-BH-A0C0-01 COSM424104 c.1610T>C p.M537T Substitution - Missense 1:156041528-156041528 - CSCC-16-T COSM1982933 c.987C>T p.L329L Substitution - coding silent 1:156044137-156044137 - TCGA-EE-A3AH-06 COSM3475135 c.1065C>T p.T355T Substitution - coding silent 1:156044059-156044059 - CCK81 COSM1982932 c.1007C>A p.S336* Substitution - Nonsense 1:156044117-156044117 - TCGA-CK-4951-01 COSM5146848 c.621T>A p.D207E Substitution - Missense 1:156050411-156050411 - MO_1176 COSM5569780 c.1016C>A p.T339N Substitution - Missense 1:156044108-156044108 - UM-SCC-4 COSM4599771 c.634C>T p.P212S Substitution - Missense 1:156050398-156050398 - Pat_41_B COSM5843941 c.1211C>T p.P404L Substitution - Missense 1:156042829-156042829 - SC_9008 COSM5563763 c.1431G>A p.Q477Q Substitution - coding silent 1:156041907-156041907 - CSCC-49-T COSM137322 c.1373C>T p.S458F Substitution - Missense 1:156041965-156041965 - TCGA-HF-7136-01 COSM4023154 c.1205C>T p.S402L Substitution - Missense 1:156042835-156042835 - CSCC-60-T COSM1982915 c.1678C>T p.Q560* Substitution - Nonsense 1:156037106-156037106 - 8057711 COSM3385251 c.1624C>T p.Q542* Substitution - Nonsense 1:156041514-156041514 - TCGA-AP-A051-01 COSM897100 c.804C>A p.A268A Substitution - coding silent 1:156048597-156048597 - CSB1 COSM5025375 c.972G>C p.E324D Substitution - Missense 1:156044152-156044152 - TCGA-CM-4746-01 COSM1334754 c.1402G>A p.A468T Substitution - Missense 1:156041936-156041936 - TCGA-AN-A0XN-01 COSM424107 c.211G>A p.G71R Substitution - Missense 1:156051755-156051755 - Au10 COSM5598919 c.123C>T p.I41I Substitution - coding silent 1:156051843-156051843 - TCGA-66-2791-01 COSM675682 c.717C>G p.L239L Substitution - coding silent 1:156050315-156050315 - TCGA-FW-A3R5-06 COSM3862956 c.804C>T p.A268A Substitution - coding silent 1:156048597-156048597 - HCC174 COSM3705068 c.1498G>A p.A500T Substitution - Missense 1:156041640-156041640 - HCT15 COSM1982946 c.663C>T p.A221A Substitution - coding silent 1:156050369-156050369 - HCC62T COSM1600948 c.1231C>A p.Q411K Substitution - Missense 1:156042809-156042809 - pfg068T COSM1982922 c.1321C>T p.R441C Substitution - Missense 1:156042182-156042182 - S0029 COSM5881532 c.1790G>A p.G597D Substitution - Missense 1:156036994-156036994 - TCGA-G4-6588-01 COSM1334756 c.295C>A p.P99T Substitution - Missense 1:156051293-156051293 - 6948_CLM COSM5754221 c.1036G>T p.G346C Substitution - Missense 1:156044088-156044088 - SH-0034 COSM5018711 c.104delA p.K35fs*20 Deletion - Frameshift 1:156053598-156053598 - Pat_26_A COSM5843942 c.67A>G p.K23E Substitution - Missense 1:156053635-156053635 - 2492701 COSM5600812 c.1287C>T p.L429L Substitution - coding silent 1:156042216-156042216 - 2_PRE-TREATMENT COSM1722901 c.1534G>A p.E512K Substitution - Missense 1:156041604-156041604 - TCGA-12-0691 COSM2154117 c.1248C>A p.N416K Substitution - Missense 1:156042792-156042792 - CSCC-29-T COSM4458701 c.1095C>T p.P365P Substitution - coding silent 1:156044029-156044029 - LUAD-F00282 COSM366975 c.781A>G p.M261V Substitution - Missense 1:156048620-156048620 - TCGA-C8-A1HJ-01 COSM1472741 c.817G>C p.E273Q Substitution - Missense 1:156048584-156048584 - HCC29T COSM1600947 c.1327C>T p.Q443* Substitution - Nonsense 1:156042176-156042176 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.283739 1q21 605440

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Synonymous p.S175S c.525T>G 1 156020298 CM - A Frameshift p.G546Vfs*30 c.1636_1637insT 1 156011292 PRAD A G Missense p.M537T c.1610T>C 1 156011319 BRCA C A IntronicSNV . c.1267-115G>T 1 156012142 CM C A Synonymous p.G142G c.426G>T 1 156020953 LUAD C G Missense p.E273Q c.817G>C 1 156018375 BRCA C G Missense p.E324D c.972G>C 1 156013943 BRCA C G Missense p.G71A c.212G>C 1 156021545 GBM C G Missense p.S408T c.1223G>C 1 156012608 BRCA C T Missense p.A519T c.1555G>A 1 156011374 UCEC C T Missense p.G508R c.1522G>A 1 156011407 CM C T Missense p.G71R c.211G>A 1 156021546 BRCA C T Missense p.M218I c.654G>A 1 156020169 HNSC C T Missense p.M218I c.654G>A 1 156020169 LUAD C T Missense p.M257I c.771G>A 1 156018421 CM C T Missense p.M424I c.1272G>A 1 156012022 CLL C T Missense p.R136Q c.407G>A 1 156020972 UCEC C T Synonymous p.G132G c.396C>T 1 156020983 PAAD G A 3-UTRSNV . c.1803+6C>T 1 156006766 CM G A IntronicSNV . c.1127-22C>T 1 156012726 STAD G A Missense p.A176V c.527C>T 1 156020296 STAD G A Missense p.P343S c.1027C>T 1 156013888 CM G A Missense p.P463S c.1387C>T 1 156011742 CM G A Missense p.R216C c.646C>T 1 156020177 LUSC G A Missense p.S340F c.1019C>T 1 156013896 CM G A Nonsense p.Q206* c.616C>T 1 156020207 CM G A Synonymous p.P12P c.36C>T 1 156023457 CM G A Synonymous p.T355T c.1065C>T 1 156013850 CM G C Synonymous p.L239L c.717C>G 1 156020106 LUSC G C Synonymous p.L444L c.1332C>G 1 156011962 GBM T A Missense p.Q539L c.1616A>T 1 156011313 LUAD T G Synonymous p.S517S c.1551A>C 1 156011378 BRCA