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 155149435 155149435 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr1:155149435G>A c.697G>A c.(697-699)Gag>Aag p.E233K BLCA 1 155149754 155149754 + Silent SNP G G A TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr1:155149754G>A c.897G>A c.(895-897)gtG>gtA p.V299V BLCA 1 155150509 155150509 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr1:155150509C>T c.941C>T c.(940-942)tCg>tTg p.S314L BLCA 1 155152224 155152224 + Missense_Mutation SNP C C A TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr1:155152224C>A c.1402C>A c.(1402-1404)Cgc>Agc p.R468S BLCA 1 155152267 155152267 + Missense_Mutation SNP G G A TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr1:155152267G>A c.1445G>A c.(1444-1446)cGg>cAg p.R482Q BLCA 1 155154441 155154441 + Missense_Mutation SNP G G A TCGA-DK-A6B1-01A-12D-A30E-08 TCGA-DK-A6B1-10A-01D-A30H-08 g.chr1:155154441G>A c.1702G>A c.(1702-1704)Gac>Aac p.D568N BLCA 1 155154488 155154488 + Silent SNP C C T TCGA-GU-A42R-01A-11D-A23M-08 TCGA-GU-A42R-10A-01D-A23K-08 g.chr1:155154488C>T c.1749C>T c.(1747-1749)ggC>ggT p.G583G BLCA 1 155154564 155154564 + Missense_Mutation SNP G G A TCGA-BT-A2LD-01A-12D-A20D-08 TCGA-BT-A2LD-10A-01D-A20D-08 g.chr1:155154564G>A c.1825G>A c.(1825-1827)Gtc>Atc p.V609I BRCA 1 155148580 155148580 + Missense_Mutation SNP A A G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:155148580A>G c.542A>G c.(541-543)gAg>gGg p.E181G BRCA 1 155150624 155150625 + Missense_Mutation DNP GC GC AT TCGA-A8-A09A-01A-11W-A019-09 TCGA-A8-A09A-10A-01W-A062-09 g.chr1:155150624_155150625GC>AT c.1056_1057GC>AT c.(1054-1059)gaGCac>gaATac p.H353Y BRCA 1 155150660 155150660 + Silent SNP C C G TCGA-E2-A159-01A-11D-A10Y-09 TCGA-E2-A159-10A-01D-A110-09 g.chr1:155150660C>G c.1092C>G c.(1090-1092)ggC>ggG p.G364G BRCA 1 155150988 155150988 + Frame_Shift_Del DEL C C - TCGA-A8-A08F-01A-11W-A019-09 TCGA-A8-A08F-10A-01W-A021-09 g.chr1:155150988delC c.1184delC c.(1183-1185)gccfs p.A395fs BRCA 1 155152140 155152140 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr1:155152140A>C c.1318A>C c.(1318-1320)Acc>Ccc p.T440P BRCA 1 155152321 155152321 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:155152321C>T c.1499C>T c.(1498-1500)tCt>tTt p.S500F BRCA 1 155152365 155152365 + Missense_Mutation SNP G G T TCGA-A7-A0CE-01A-11W-A019-09 TCGA-A7-A0CE-10A-01W-A021-09 g.chr1:155152365G>T c.1543G>T c.(1543-1545)Ggc>Tgc p.G515C BRCA 1 155154369 155154369 + Missense_Mutation SNP G G C TCGA-E2-A1LE-01A-12D-A19Y-09 TCGA-E2-A1LE-11A-23D-A19Y-09 g.chr1:155154369G>C c.1630G>C c.(1630-1632)Gag>Cag p.E544Q BRCA 1 155156289 155156289 + Missense_Mutation SNP G G A TCGA-A8-A07C-01A-11D-A045-09 TCGA-A8-A07C-10A-01W-A055-09 g.chr1:155156289G>A c.1903G>A c.(1903-1905)Ggg>Agg p.G635R BRCA 1 155156289 155156289 + Missense_Mutation SNP G G T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr1:155156289G>T c.1903G>T c.(1903-1905)Ggg>Tgg p.G635W CESC 1 155148617 155148617 + Silent SNP C C T TCGA-EA-A3HT-01A-61D-A21Q-09 TCGA-EA-A3HT-10A-01D-A21Q-09 g.chr1:155148617C>T c.579C>T c.(577-579)ttC>ttT p.F193F CESC 1 155154367 155154367 + Missense_Mutation SNP G G A TCGA-C5-A1M7-01A-11D-A13W-08 TCGA-C5-A1M7-10A-01D-A13W-08 g.chr1:155154367G>A c.1628G>A c.(1627-1629)cGa>cAa p.R543Q COAD 1 155147968 155147968 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:155147968C>T c.170C>T c.(169-171)gCc>gTc p.A57V COAD 1 155149444 155149444 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:155149444C>A c.706C>A c.(706-708)Cac>Aac p.H236N COAD 1 155149496 155149496 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr1:155149496G>A c.758G>A c.(757-759)cGc>cAc p.R253H COAD 1 155149718 155149718 + Silent SNP G G A TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr1:155149718G>A c.861G>A c.(859-861)acG>acA p.T287T COAD 1 155150502 155150502 + Nonsense_Mutation SNP G G T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:155150502G>T c.934G>T c.(934-936)Gag>Tag p.E312* COAD 1 155151086 155151086 + Nonsense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr1:155151086C>T c.1282C>T c.(1282-1284)Cga>Tga p.R428* COAD 1 155152178 155152179 + Frame_Shift_Ins INS - - C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr1:155152178_155152179insC c.1356_1357insC c.(1357-1359)cccfs p.P453fs COAD 1 155152179 155152179 + Frame_Shift_Del DEL C C - TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:155152179delC c.1357delC c.(1357-1359)cccfs p.P454fs COAD 1 155152336 155152336 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:155152336G>A c.1514G>A c.(1513-1515)cGt>cAt p.R505H COAD 1 155154359 155154359 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:155154359C>T c.1620C>T c.(1618-1620)ggC>ggT p.G540G COAD 1 155154431 155154431 + Silent SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr1:155154431G>A c.1692G>A c.(1690-1692)ctG>ctA p.L564L COAD 1 155154504 155154504 + Missense_Mutation SNP C C A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:155154504C>A c.1765C>A c.(1765-1767)Cag>Aag p.Q589K COAD 1 155154505 155154505 + Missense_Mutation SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr1:155154505A>G c.1766A>G c.(1765-1767)cAg>cGg p.Q589R COAD 1 155154564 155154564 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr1:155154564G>A c.1825G>A c.(1825-1827)Gtc>Atc p.V609I COAD 1 155154615 155154615 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr1:155154615A>C c.1876A>C c.(1876-1878)Atc>Ctc p.I626L COAD 1 155156329 155156329 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:155156329C>T c.1943C>T c.(1942-1944)tCg>tTg p.S648L COAD 1 155156455 155156455 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr1:155156455G>A c.2069G>A c.(2068-2070)cGc>cAc p.R690H COAD 1 155156533 155156534 + Frame_Shift_Ins INS - - C TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr1:155156533_155156534insC c.2147_2148insC c.(2146-2151)tgccccfs p.CP716fs COAD 1 155156643 155156643 + Missense_Mutation SNP G G A TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr1:155156643G>A c.2257G>A c.(2257-2259)Ggg>Agg p.G753R COADREAD 1 155147968 155147968 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:155147968C>T c.170C>T c.(169-171)gCc>gTc p.A57V COADREAD 1 155149444 155149444 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr1:155149444C>A c.706C>A c.(706-708)Cac>Aac p.H236N COADREAD 1 155149496 155149496 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr1:155149496G>A c.758G>A c.(757-759)cGc>cAc p.R253H COADREAD 1 155149718 155149718 + Silent SNP G G A TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr1:155149718G>A c.861G>A c.(859-861)acG>acA p.T287T COADREAD 1 155150502 155150502 + Nonsense_Mutation SNP G G T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr1:155150502G>T c.934G>T c.(934-936)Gag>Tag p.E312* COADREAD 1 155151086 155151086 + Nonsense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr1:155151086C>T c.1282C>T c.(1282-1284)Cga>Tga p.R428* COADREAD 1 155152178 155152179 + Frame_Shift_Ins INS - - C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr1:155152178_155152179insC c.1356_1357insC c.(1357-1359)cccfs p.P453fs COADREAD 1 155152179 155152179 + Frame_Shift_Del DEL C C - TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr1:155152179delC c.1357delC c.(1357-1359)cccfs p.P454fs COADREAD 1 155152336 155152336 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr1:155152336G>A c.1514G>A c.(1513-1515)cGt>cAt p.R505H COADREAD 1 155154359 155154359 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:155154359C>T c.1620C>T c.(1618-1620)ggC>ggT p.G540G COADREAD 1 155154431 155154431 + Silent SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr1:155154431G>A c.1692G>A c.(1690-1692)ctG>ctA p.L564L COADREAD 1 155154504 155154504 + Missense_Mutation SNP C C A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr1:155154504C>A c.1765C>A c.(1765-1767)Cag>Aag p.Q589K COADREAD 1 155154505 155154505 + Missense_Mutation SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr1:155154505A>G c.1766A>G c.(1765-1767)cAg>cGg p.Q589R COADREAD 1 155154564 155154564 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr1:155154564G>A c.1825G>A c.(1825-1827)Gtc>Atc p.V609I COADREAD 1 155154615 155154615 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr1:155154615A>C c.1876A>C c.(1876-1878)Atc>Ctc p.I626L COADREAD 1 155156329 155156329 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:155156329C>T c.1943C>T c.(1942-1944)tCg>tTg p.S648L COADREAD 1 155156455 155156455 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr1:155156455G>A c.2069G>A c.(2068-2070)cGc>cAc p.R690H COADREAD 1 155156533 155156534 + Frame_Shift_Ins INS - - C TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr1:155156533_155156534insC c.2147_2148insC c.(2146-2151)tgccccfs p.CP716fs COADREAD 1 155156643 155156643 + Missense_Mutation SNP G G A TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr1:155156643G>A c.2257G>A c.(2257-2259)Ggg>Agg p.G753R ESCA 1 155150650 155150650 + Missense_Mutation SNP G G T TCGA-L5-A4OS-01A-11D-A28B-09 TCGA-L5-A4OS-11A-11D-A28E-09 g.chr1:155150650G>T c.1082G>T c.(1081-1083)gGt>gTt p.G361V ESCA 1 155150676 155150676 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr1:155150676C>T c.1108C>T c.(1108-1110)Ctt>Ttt p.L370F ESCA 1 155156330 155156330 + Silent SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr1:155156330G>A c.1944G>A c.(1942-1944)tcG>tcA p.S648S ESCA 1 155156434 155156434 + Missense_Mutation SNP G G A TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr1:155156434G>A c.2048G>A c.(2047-2049)tGc>tAc p.C683Y GBM 1 155150608 155150608 + Missense_Mutation SNP G G A TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr1:155150608G>A c.1040G>A c.(1039-1041)aGc>aAc p.S347N GBMLGG 1 155150608 155150608 + Missense_Mutation SNP G G A TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr1:155150608G>A c.1040G>A c.(1039-1041)aGc>aAc p.S347N GBMLGG 1 155152225 155152225 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:155152225G>A c.1403G>A c.(1402-1404)cGc>cAc p.R468H HNSC 1 155148051 155148051 + Missense_Mutation SNP T T C TCGA-CR-6477-01A-11D-1870-08 TCGA-CR-6477-10A-01D-1870-08 g.chr1:155148051T>C c.253T>C c.(253-255)Tcc>Ccc p.S85P HNSC 1 155152365 155152365 + Missense_Mutation SNP G G A TCGA-CQ-6223-01A-11D-1912-08 TCGA-CQ-6223-10A-01D-1912-08 g.chr1:155152365G>A c.1543G>A c.(1543-1545)Ggc>Agc p.G515S HNSC 1 155152367 155152367 + Silent SNP C C T TCGA-CR-6482-01A-11D-1870-08 TCGA-CR-6482-10A-01D-1870-08 g.chr1:155152367C>T c.1545C>T c.(1543-1545)ggC>ggT p.G515G HNSC 1 155152405 155152405 + Missense_Mutation SNP C C A TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chr1:155152405C>A c.1583C>A c.(1582-1584)gCa>gAa p.A528E HNSC 1 155156625 155156625 + Missense_Mutation SNP G G A TCGA-CV-6441-01A-11D-1683-08 TCGA-CV-6441-11A-01D-1683-08 g.chr1:155156625G>A c.2239G>A c.(2239-2241)Gag>Aag p.E747K KIPAN 1 155148034 155148034 + Missense_Mutation SNP C C G TCGA-G7-6790-01A-11D-1961-08 TCGA-G7-6790-10A-01D-1962-08 g.chr1:155148034C>G c.236C>G c.(235-237)tCt>tGt p.S79C KIPAN 1 155150596 155150597 + Frame_Shift_Ins INS - - G TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr1:155150596_155150597insG c.1028_1029insG c.(1027-1032)ctggccfs p.A344fs KIRC 1 155150596 155150597 + Frame_Shift_Ins INS - - G TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr1:155150596_155150597insG c.1028_1029insG c.(1027-1032)ctggccfs p.A344fs KIRP 1 155148034 155148034 + Missense_Mutation SNP C C G TCGA-G7-6790-01A-11D-1961-08 TCGA-G7-6790-10A-01D-1962-08 g.chr1:155148034C>G c.236C>G c.(235-237)tCt>tGt p.S79C LGG 1 155152225 155152225 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:155152225G>A c.1403G>A c.(1402-1404)cGc>cAc p.R468H LIHC 1 155147913 155147913 + Missense_Mutation SNP A A C TCGA-DD-AACX-01A-11D-A40R-10 TCGA-DD-AACX-10A-01D-A40U-10 g.chr1:155147913A>C c.115A>C c.(115-117)Atg>Ctg p.M39L LIHC 1 155148089 155148089 + Silent SNP C C A TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr1:155148089C>A c.291C>A c.(289-291)ccC>ccA p.P97P LIHC 1 155148663 155148663 + Missense_Mutation SNP G G T TCGA-BW-A5NQ-01A-11D-A27I-10 TCGA-BW-A5NQ-10A-01D-A27I-10 g.chr1:155148663G>T c.625G>T c.(625-627)Gcc>Tcc p.A209S LIHC 1 155151089 155151089 + Splice_Site SNP G G T TCGA-DD-A1EA-01A-11D-A12Z-10 TCGA-DD-A1EA-10A-01D-A12Z-10 g.chr1:155151089G>T c.1285G>T c.(1285-1287)Gtg>Ttg p.V429L LIHC 1 155156381 155156381 + Frame_Shift_Del DEL G G - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr1:155156381delG c.1995delG c.(1993-1995)tcgfs p.S665fs LUAD 1 155147917 155147917 + Missense_Mutation SNP A A T TCGA-44-A47G-01A-21D-A24D-08 TCGA-44-A47G-10A-01D-A24F-08 g.chr1:155147917A>T c.119A>T c.(118-120)tAc>tTc p.Y40F LUAD 1 155148068 155148068 + Silent SNP C C T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr1:155148068C>T c.270C>T c.(268-270)cgC>cgT p.R90R LUAD 1 155148465 155148465 + Missense_Mutation SNP G G T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr1:155148465G>T c.427G>T c.(427-429)Ggt>Tgt p.G143C LUAD 1 155149759 155149759 + Missense_Mutation SNP A A T TCGA-67-4679-01B-01D-1753-08 TCGA-67-4679-10A-01D-1753-08 g.chr1:155149759A>T c.902A>T c.(901-903)cAc>cTc p.H301L LUAD 1 155150586 155150586 + Missense_Mutation SNP C C A TCGA-55-7815-01A-11D-2167-08 TCGA-55-7815-10A-01D-2167-08 g.chr1:155150586C>A c.1018C>A c.(1018-1020)Cag>Aag p.Q340K LUAD 1 155154467 155154467 + Silent SNP G G A TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr1:155154467G>A c.1728G>A c.(1726-1728)ctG>ctA p.L576L LUSC 1 155148067 155148067 + Missense_Mutation SNP G G A TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chr1:155148067G>A c.269G>A c.(268-270)cGc>cAc p.R90H LUSC 1 155148375 155148375 + Missense_Mutation SNP T T C TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chr1:155148375T>C c.337T>C c.(337-339)Tac>Cac p.Y113H LUSC 1 155148600 155148600 + Missense_Mutation SNP G G A TCGA-56-6545-01A-11D-1817-08 TCGA-56-6545-10A-01D-1817-08 g.chr1:155148600G>A c.562G>A c.(562-564)Gag>Aag p.E188K LUSC 1 155156413 155156413 + Missense_Mutation SNP G G T TCGA-39-5029-01A-01D-1441-08 TCGA-39-5029-11A-01D-1441-08 g.chr1:155156413G>T c.2027G>T c.(2026-2028)aGg>aTg p.R676M OV 1 155148389 155148389 + Missense_Mutation SNP G G T TCGA-29-2434-01A-01D-1526-09 TCGA-29-2434-10A-01D-1526-09 g.chr1:155148389G>T c.351G>T c.(349-351)aaG>aaT p.K117N OV 1 155154504 155154504 + Missense_Mutation SNP C C G TCGA-13-0755-01A-01W-0372-09 TCGA-13-0755-10A-01W-0372-09 g.chr1:155154504C>G c.1765C>G c.(1765-1767)Cag>Gag p.Q589E PAAD 1 155148076 155148076 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:155148076G>A c.278G>A c.(277-279)cGc>cAc p.R93H PAAD 1 155149492 155149492 + Missense_Mutation SNP C C T TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chr1:155149492C>T c.754C>T c.(754-756)Cgg>Tgg p.R252W PAAD 1 155154489 155154489 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:155154489G>A c.1750G>A c.(1750-1752)Gac>Aac p.D584N PRAD 1 155147951 155147951 + Silent SNP C C T TCGA-QU-A6IL-01A-11D-A31L-08 TCGA-QU-A6IL-10A-01D-A31J-08 g.chr1:155147951C>T c.153C>T c.(151-153)aaC>aaT p.N51N PRAD 1 155156326 155156326 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:155156326C>T c.1940C>T c.(1939-1941)gCg>gTg p.A647V PRAD 1 155156356 155156356 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:155156356G>A c.1970G>A c.(1969-1971)gGc>gAc p.G657D SARC 1 155150521 155150521 + Frame_Shift_Del DEL G G - TCGA-DX-AB2O-01A-12D-A38Z-09 TCGA-DX-AB2O-10A-01D-A38Z-09 g.chr1:155150521delG c.953delG c.(952-954)cggfs p.R318fs SARC 1 155154488 155154488 + Silent SNP C C T TCGA-DX-A8BM-01A-11D-A417-09 TCGA-DX-A8BM-10B-01D-A41A-09 g.chr1:155154488C>T c.1749C>T c.(1747-1749)ggC>ggT p.G583G SKCM 1 155147898 155147898 + Missense_Mutation SNP C C T TCGA-FS-A4F0-06A-11D-A24R-08 TCGA-FS-A4F0-10A-01D-A24R-08 g.chr1:155147898C>T c.100C>T c.(100-102)Cca>Tca p.P34S SKCM 1 155148391 155148391 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:155148391G>A c.353G>A c.(352-354)cGa>cAa p.R118Q SKCM 1 155148665 155148665 + Silent SNP C C T TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr1:155148665C>T c.627C>T c.(625-627)gcC>gcT p.A209A SKCM 1 155149752 155149752 + Missense_Mutation SNP G G T TCGA-D3-A1Q5-06A-11D-A196-08 TCGA-D3-A1Q5-10A-01D-A198-08 g.chr1:155149752G>T c.895G>T c.(895-897)Gtg>Ttg p.V299L SKCM 1 155149757 155149757 + Silent SNP G G A TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr1:155149757G>A c.900G>A c.(898-900)agG>agA p.R300R SKCM 1 155150523 155150523 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:155150523G>A c.955G>A c.(955-957)Ggg>Agg p.G319R SKCM 1 155150656 155150656 + Missense_Mutation SNP T T A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr1:155150656T>A c.1088T>A c.(1087-1089)gTg>gAg p.V363E SKCM 1 155150687 155150687 + Silent SNP A A T TCGA-FS-A1ZF-06A-12D-A197-08 TCGA-FS-A1ZF-10A-01D-A199-08 g.chr1:155150687A>T c.1119A>T c.(1117-1119)acA>acT p.T373T SKCM 1 155152210 155152210 + Missense_Mutation SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr1:155152210C>T c.1388C>T c.(1387-1389)aCc>aTc p.T463I SKCM 1 155154622 155154622 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr1:155154622C>T c.1883C>T c.(1882-1884)cCc>cTc p.P628L SKCM 1 155154623 155154623 + Silent SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr1:155154623C>T c.1884C>T c.(1882-1884)ccC>ccT p.P628P SKCM 1 155156339 155156339 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:155156339C>T c.1953C>T c.(1951-1953)ttC>ttT p.F651F SKCM 1 155156498 155156498 + Silent SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr1:155156498C>T c.2112C>T c.(2110-2112)ttC>ttT p.F704F SKCM 1 155156512 155156512 + Missense_Mutation SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr1:155156512C>T c.2126C>T c.(2125-2127)tCc>tTc p.S709F SKCM 1 155156563 155156563 + Missense_Mutation SNP C C T TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr1:155156563C>T c.2177C>T c.(2176-2178)cCt>cTt p.P726L SKCM 1 155156586 155156586 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr1:155156586G>A c.2200G>A c.(2200-2202)Ggc>Agc p.G734S

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 1 155145044 155145044 single base substitution C T upstream_gene_variant BLCA-US 1 155145217 155145217 single base substitution G A upstream_gene_variant BLCA-US 1 155149435 155149435 single base substitution G A exon_variant BLCA-US 1 155149435 155149435 single base substitution G A missense_variant E107K 319G>A BLCA-US 1 155149435 155149435 single base substitution G A missense_variant E210K 628G>A BLCA-US 1 155149435 155149435 single base substitution G A missense_variant E233K 697G>A BLCA-US 1 155149435 155149435 single base substitution G A missense_variant E240K 718G>A BLCA-US 1 155152267 155152267 single base substitution G A downstream_gene_variant BLCA-US 1 155152267 155152267 single base substitution G A exon_variant BLCA-US 1 155152267 155152267 single base substitution G A missense_variant G495S 1483G>A BLCA-US 1 155152267 155152267 single base substitution G A missense_variant G502S 1504G>A BLCA-US 1 155152267 155152267 single base substitution G A missense_variant R356Q 1067G>A BLCA-US 1 155152267 155152267 single base substitution G A missense_variant R459Q 1376G>A BLCA-US 1 155152267 155152267 single base substitution G A missense_variant R482Q 1445G>A BLCA-US 1 155154488 155154488 single base substitution C T 3_prime_UTR_variant BLCA-US 1 155154488 155154488 single base substitution C T downstream_gene_variant BLCA-US 1 155154488 155154488 single base substitution C T exon_variant BLCA-US 1 155154488 155154488 single base substitution C T synonymous_variant G457G 1371C>T BLCA-US 1 155154488 155154488 single base substitution C T synonymous_variant G560G 1680C>T BLCA-US 1 155154488 155154488 single base substitution C T synonymous_variant G583G 1749C>T BLCA-US 1 155154564 155154564 single base substitution G A 3_prime_UTR_variant BLCA-US 1 155154564 155154564 single base substitution G A downstream_gene_variant BLCA-US 1 155154564 155154564 single base substitution G A exon_variant BLCA-US 1 155154564 155154564 single base substitution G A missense_variant V483I 1447G>A BLCA-US 1 155154564 155154564 single base substitution G A missense_variant V586I 1756G>A BLCA-US 1 155154564 155154564 single base substitution G A missense_variant V609I 1825G>A BLCA-US 1 155161799 155161799 single base substitution T G downstream_gene_variant BLCA-US 1 155161824 155161824 single base substitution G A downstream_gene_variant BOCA-FR 1 155142349 155142349 single base substitution G T upstream_gene_variant BOCA-FR 1 155149956 155149956 single base substitution G T intron_variant BRCA-EU 1 155140897 155140897 single base substitution C A upstream_gene_variant BRCA-EU 1 155142597 155142597 single base substitution G T upstream_gene_variant BRCA-EU 1 155142730 155142730 single base substitution C A upstream_gene_variant BRCA-EU 1 155144283 155144283 single base substitution C T upstream_gene_variant BRCA-EU 1 155145889 155145889 single base substitution G T missense_variant G5V 14G>T BRCA-EU 1 155145889 155145889 single base substitution G T upstream_gene_variant BRCA-EU 1 155146078 155146078 single base substitution C G intron_variant BRCA-EU 1 155146078 155146078 single base substitution C G upstream_gene_variant BRCA-EU 1 155146184 155146184 single base substitution G A intron_variant BRCA-EU 1 155146184 155146184 single base substitution G A upstream_gene_variant BRCA-EU 1 155147856 155147856 single base substitution C A intron_variant BRCA-EU 1 155147856 155147856 single base substitution C A splice_region_variant BRCA-EU 1 155148022 155148022 single base substitution C G exon_variant BRCA-EU 1 155148022 155148022 single base substitution C G intron_variant BRCA-EU 1 155148022 155148022 single base substitution C G missense_variant S52C 155C>G BRCA-EU 1 155148022 155148022 single base substitution C G missense_variant S75C 224C>G BRCA-EU 1 155148022 155148022 single base substitution C G missense_variant S82C 245C>G BRCA-EU 1 155149101 155149101 single base substitution G C intron_variant BRCA-EU 1 155149751 155149751 single base substitution C G exon_variant BRCA-EU 1 155149751 155149751 single base substitution C G synonymous_variant A172A 516C>G BRCA-EU 1 155149751 155149751 single base substitution C G synonymous_variant A275A 825C>G BRCA-EU 1 155149751 155149751 single base substitution C G synonymous_variant A298A 894C>G BRCA-EU 1 155149751 155149751 single base substitution C G synonymous_variant A305A 915C>G BRCA-EU 1 155152343 155152343 single base substitution C T 3_prime_UTR_variant BRCA-EU 1 155152343 155152343 single base substitution C T downstream_gene_variant BRCA-EU 1 155152343 155152343 single base substitution C T exon_variant BRCA-EU 1 155152343 155152343 single base substitution C T synonymous_variant R381R 1143C>T BRCA-EU 1 155152343 155152343 single base substitution C T synonymous_variant R484R 1452C>T BRCA-EU 1 155152343 155152343 single base substitution C T synonymous_variant R507R 1521C>T BRCA-EU 1 155153259 155153259 single base substitution G A downstream_gene_variant BRCA-EU 1 155153259 155153259 single base substitution G A intron_variant BRCA-EU 1 155154711 155154711 single base substitution G C 3_prime_UTR_variant BRCA-EU 1 155154711 155154711 single base substitution G C downstream_gene_variant BRCA-EU 1 155154711 155154711 single base substitution G C exon_variant BRCA-EU 1 155154711 155154711 single base substitution G C intron_variant BRCA-EU 1 155155115 155155115 single base substitution G A 3_prime_UTR_variant BRCA-EU 1 155155115 155155115 single base substitution G A downstream_gene_variant BRCA-EU 1 155155115 155155115 single base substitution G A exon_variant BRCA-EU 1 155155115 155155115 single base substitution G A intron_variant BRCA-EU 1 155156845 155156845 deletion of <=200bp C - 3_prime_UTR_variant BRCA-EU 1 155156845 155156845 deletion of <=200bp C - downstream_gene_variant BRCA-EU 1 155156845 155156845 deletion of <=200bp C - exon_variant BRCA-EU 1 155156854 155156854 single base substitution C G 3_prime_UTR_variant BRCA-EU 1 155156854 155156854 single base substitution C G downstream_gene_variant BRCA-EU 1 155156854 155156854 single base substitution C G exon_variant BRCA-EU 1 155156915 155156915 single base substitution C G 3_prime_UTR_variant BRCA-EU 1 155156915 155156915 single base substitution C G downstream_gene_variant BRCA-EU 1 155156915 155156915 single base substitution C G exon_variant BRCA-EU 1 155158594 155158594 single base substitution C A downstream_gene_variant BRCA-EU 1 155159334 155159334 single base substitution C T downstream_gene_variant BRCA-EU 1 155161505 155161505 single base substitution G T downstream_gene_variant BRCA-EU 1 155161508 155161508 single base substitution G C downstream_gene_variant BRCA-EU 1 155161534 155161534 single base substitution G C downstream_gene_variant BRCA-EU 1 155161536 155161536 single base substitution G C downstream_gene_variant BRCA-EU 1 155161672 155161672 single base substitution T G downstream_gene_variant BRCA-FR 1 155141839 155141839 single base substitution G A upstream_gene_variant BRCA-FR 1 155146184 155146184 single base substitution G A intron_variant BRCA-FR 1 155146184 155146184 single base substitution G A upstream_gene_variant BRCA-FR 1 155147856 155147856 single base substitution C A intron_variant BRCA-FR 1 155147856 155147856 single base substitution C A splice_region_variant BRCA-FR 1 155148022 155148022 single base substitution C G exon_variant BRCA-FR 1 155148022 155148022 single base substitution C G intron_variant BRCA-FR 1 155148022 155148022 single base substitution C G missense_variant S52C 155C>G BRCA-FR 1 155148022 155148022 single base substitution C G missense_variant S75C 224C>G BRCA-FR 1 155148022 155148022 single base substitution C G missense_variant S82C 245C>G BRCA-FR 1 155148333 155148333 single base substitution C T intron_variant BRCA-KR 1 155145849 155145849 single base substitution G T upstream_gene_variant BRCA-KR 1 155148485 155148485 single base substitution G T exon_variant BRCA-KR 1 155148485 155148485 single base substitution G T synonymous_variant R126R 378G>T BRCA-KR 1 155148485 155148485 single base substitution G T synonymous_variant R149R 447G>T BRCA-KR 1 155148485 155148485 single base substitution G T synonymous_variant R156R 468G>T BRCA-KR 1 155148485 155148485 single base substitution G T synonymous_variant R23R 69G>T BRCA-KR 1 155150570 155150570 single base substitution C T exon_variant BRCA-KR 1 155150570 155150570 single base substitution C T synonymous_variant A208A 624C>T BRCA-KR 1 155150570 155150570 single base substitution C T synonymous_variant A311A 933C>T BRCA-KR 1 155150570 155150570 single base substitution C T synonymous_variant A334A 1002C>T BRCA-KR 1 155150570 155150570 single base substitution C T synonymous_variant A341A 1023C>T BRCA-KR 1 155152151 155152151 single base substitution T G downstream_gene_variant BRCA-KR 1 155152151 155152151 single base substitution T G exon_variant BRCA-KR 1 155152151 155152151 single base substitution T G missense_variant M456R 1367T>G BRCA-KR 1 155152151 155152151 single base substitution T G missense_variant M463R 1388T>G BRCA-KR 1 155152151 155152151 single base substitution T G stop_gained Y317* 951T>G BRCA-KR 1 155152151 155152151 single base substitution T G stop_gained Y420* 1260T>G BRCA-KR 1 155152151 155152151 single base substitution T G stop_gained Y443* 1329T>G BRCA-UK 1 155149762 155149762 single base substitution C G exon_variant BRCA-UK 1 155149762 155149762 single base substitution C G missense_variant T176S 527C>G BRCA-UK 1 155149762 155149762 single base substitution C G missense_variant T279S 836C>G BRCA-UK 1 155149762 155149762 single base substitution C G missense_variant T302S 905C>G BRCA-UK 1 155149762 155149762 single base substitution C G missense_variant T309S 926C>G BRCA-US 1 155144934 155144934 single base substitution T G upstream_gene_variant BRCA-US 1 155145235 155145235 single base substitution A G upstream_gene_variant BRCA-US 1 155145340 155145340 single base substitution G C upstream_gene_variant BRCA-US 1 155148580 155148580 single base substitution A G exon_variant BRCA-US 1 155148580 155148580 single base substitution A G missense_variant E158G 473A>G BRCA-US 1 155148580 155148580 single base substitution A G missense_variant E181G 542A>G BRCA-US 1 155148580 155148580 single base substitution A G missense_variant E188G 563A>G BRCA-US 1 155148580 155148580 single base substitution A G missense_variant E55G 164A>G BRCA-US 1 155150624 155150624 single base substitution G A exon_variant BRCA-US 1 155150624 155150624 single base substitution G A synonymous_variant E226E 678G>A BRCA-US 1 155150624 155150624 single base substitution G A synonymous_variant E329E 987G>A BRCA-US 1 155150624 155150624 single base substitution G A synonymous_variant E352E 1056G>A BRCA-US 1 155150624 155150624 single base substitution G A synonymous_variant E359E 1077G>A BRCA-US 1 155150625 155150625 single base substitution C T exon_variant BRCA-US 1 155150625 155150625 single base substitution C T missense_variant H227Y 679C>T BRCA-US 1 155150625 155150625 single base substitution C T missense_variant H330Y 988C>T BRCA-US 1 155150625 155150625 single base substitution C T missense_variant H353Y 1057C>T BRCA-US 1 155150625 155150625 single base substitution C T missense_variant H360Y 1078C>T BRCA-US 1 155150660 155150660 single base substitution C G downstream_gene_variant BRCA-US 1 155150660 155150660 single base substitution C G exon_variant BRCA-US 1 155150660 155150660 single base substitution C G synonymous_variant G238G 714C>G BRCA-US 1 155150660 155150660 single base substitution C G synonymous_variant G341G 1023C>G BRCA-US 1 155150660 155150660 single base substitution C G synonymous_variant G364G 1092C>G BRCA-US 1 155150660 155150660 single base substitution C G synonymous_variant G371G 1113C>G BRCA-US 1 155150988 155150988 deletion of <=200bp C - downstream_gene_variant BRCA-US 1 155150988 155150988 deletion of <=200bp C - exon_variant BRCA-US 1 155150988 155150988 deletion of <=200bp C - frameshift_variant A269 BRCA-US 1 155150988 155150988 deletion of <=200bp C - frameshift_variant A372 BRCA-US 1 155150988 155150988 deletion of <=200bp C - frameshift_variant A395 BRCA-US 1 155150988 155150988 deletion of <=200bp C - frameshift_variant A402 BRCA-US 1 155152140 155152140 single base substitution A C downstream_gene_variant BRCA-US 1 155152140 155152140 single base substitution A C exon_variant BRCA-US 1 155152140 155152140 single base substitution A C missense_variant T314P 940A>C BRCA-US 1 155152140 155152140 single base substitution A C missense_variant T417P 1249A>C BRCA-US 1 155152140 155152140 single base substitution A C missense_variant T440P 1318A>C BRCA-US 1 155152140 155152140 single base substitution A C synonymous_variant A452A 1356A>C BRCA-US 1 155152140 155152140 single base substitution A C synonymous_variant A459A 1377A>C BRCA-US 1 155152321 155152321 single base substitution C T 3_prime_UTR_variant BRCA-US 1 155152321 155152321 single base substitution C T downstream_gene_variant BRCA-US 1 155152321 155152321 single base substitution C T exon_variant BRCA-US 1 155152321 155152321 single base substitution C T missense_variant S374F 1121C>T BRCA-US 1 155152321 155152321 single base substitution C T missense_variant S477F 1430C>T BRCA-US 1 155152321 155152321 single base substitution C T missense_variant S500F 1499C>T BRCA-US 1 155152365 155152365 single base substitution G T 3_prime_UTR_variant BRCA-US 1 155152365 155152365 single base substitution G T downstream_gene_variant BRCA-US 1 155152365 155152365 single base substitution G T exon_variant BRCA-US 1 155152365 155152365 single base substitution G T missense_variant G389C 1165G>T BRCA-US 1 155152365 155152365 single base substitution G T missense_variant G492C 1474G>T BRCA-US 1 155152365 155152365 single base substitution G T missense_variant G515C 1543G>T BRCA-US 1 155154369 155154369 single base substitution G C 3_prime_UTR_variant BRCA-US 1 155154369 155154369 single base substitution G C downstream_gene_variant BRCA-US 1 155154369 155154369 single base substitution G C exon_variant BRCA-US 1 155154369 155154369 single base substitution G C missense_variant E418Q 1252G>C BRCA-US 1 155154369 155154369 single base substitution G C missense_variant E521Q 1561G>C BRCA-US 1 155154369 155154369 single base substitution G C missense_variant E544Q 1630G>C BRCA-US 1 155156289 155156289 single base substitution G A 3_prime_UTR_variant BRCA-US 1 155156289 155156289 single base substitution G A downstream_gene_variant BRCA-US 1 155156289 155156289 single base substitution G A exon_variant BRCA-US 1 155156289 155156289 single base substitution G A missense_variant G509R 1525G>A BRCA-US 1 155156289 155156289 single base substitution G A missense_variant G612R 1834G>A BRCA-US 1 155156289 155156289 single base substitution G A missense_variant G635R 1903G>A BRCA-US 1 155156289 155156289 single base substitution G T 3_prime_UTR_variant BRCA-US 1 155156289 155156289 single base substitution G T downstream_gene_variant BRCA-US 1 155156289 155156289 single base substitution G T exon_variant BRCA-US 1 155156289 155156289 single base substitution G T missense_variant G509W 1525G>T BRCA-US 1 155156289 155156289 single base substitution G T missense_variant G612W 1834G>T BRCA-US 1 155156289 155156289 single base substitution G T missense_variant G635W 1903G>T BRCA-US 1 155159223 155159223 single base substitution C T downstream_gene_variant BRCA-US 1 155160204 155160204 single base substitution C A downstream_gene_variant BRCA-US 1 155160715 155160715 single base substitution T C downstream_gene_variant BTCA-JP 1 155146642 155146642 single base substitution G A intron_variant BTCA-JP 1 155146642 155146642 single base substitution G A upstream_gene_variant BTCA-JP 1 155147043 155147043 deletion of <=200bp C - intron_variant BTCA-JP 1 155147043 155147043 deletion of <=200bp C - upstream_gene_variant BTCA-JP 1 155148452 155148452 single base substitution G A exon_variant BTCA-JP 1 155148452 155148452 single base substitution G A synonymous_variant E115E 345G>A BTCA-JP 1 155148452 155148452 single base substitution G A synonymous_variant E12E 36G>A BTCA-JP 1 155148452 155148452 single base substitution G A synonymous_variant E138E 414G>A BTCA-JP 1 155148452 155148452 single base substitution G A synonymous_variant E145E 435G>A BTCA-JP 1 155148679 155148679 single base substitution C T exon_variant BTCA-JP 1 155148679 155148679 single base substitution C T missense_variant T191I 572C>T BTCA-JP 1 155148679 155148679 single base substitution C T missense_variant T214I 641C>T BTCA-JP 1 155148679 155148679 single base substitution C T missense_variant T221I 662C>T BTCA-JP 1 155148679 155148679 single base substitution C T missense_variant T88I 263C>T BTCA-JP 1 155159220 155159222 deletion of <=200bp CTT - downstream_gene_variant BTCA-JP 1 155160178 155160178 single base substitution A T downstream_gene_variant BTCA-JP 1 155160466 155160466 single base substitution C T downstream_gene_variant BTCA-JP 1 155160861 155160862 deletion of <=200bp AG - downstream_gene_variant BTCA-JP 1 155161733 155161733 single base substitution G C downstream_gene_variant BTCA-JP 1 155161737 155161737 single base substitution G C downstream_gene_variant CESC-US 1 155142356 155142356 single base substitution G A upstream_gene_variant CESC-US 1 155147102 155147102 single base substitution G A exon_variant CESC-US 1 155147102 155147102 single base substitution G A intron_variant CESC-US 1 155147102 155147102 single base substitution G A upstream_gene_variant CESC-US 1 155148617 155148617 single base substitution C T exon_variant CESC-US 1 155148617 155148617 single base substitution C T synonymous_variant F170F 510C>T CESC-US 1 155148617 155148617 single base substitution C T synonymous_variant F193F 579C>T CESC-US 1 155148617 155148617 single base substitution C T synonymous_variant F200F 600C>T CESC-US 1 155148617 155148617 single base substitution C T synonymous_variant F67F 201C>T CESC-US 1 155154367 155154367 single base substitution G A 3_prime_UTR_variant CESC-US 1 155154367 155154367 single base substitution G A downstream_gene_variant CESC-US 1 155154367 155154367 single base substitution G A exon_variant CESC-US 1 155154367 155154367 single base substitution G A missense_variant R417Q 1250G>A CESC-US 1 155154367 155154367 single base substitution G A missense_variant R520Q 1559G>A CESC-US 1 155154367 155154367 single base substitution G A missense_variant R543Q 1628G>A CESC-US 1 155156672 155156672 single base substitution C T 3_prime_UTR_variant CESC-US 1 155156672 155156672 single base substitution C T downstream_gene_variant CESC-US 1 155156672 155156672 single base substitution C T exon_variant CESC-US 1 155161913 155161913 single base substitution G C downstream_gene_variant CLLE-ES 1 155150672 155150672 single base substitution A T downstream_gene_variant CLLE-ES 1 155150672 155150672 single base substitution A T exon_variant CLLE-ES 1 155150672 155150672 single base substitution A T missense_variant E242D 726A>T CLLE-ES 1 155150672 155150672 single base substitution A T missense_variant E345D 1035A>T CLLE-ES 1 155150672 155150672 single base substitution A T missense_variant E368D 1104A>T CLLE-ES 1 155150672 155150672 single base substitution A T missense_variant E375D 1125A>T CLLE-ES 1 155155323 155155323 single base substitution A C 3_prime_UTR_variant CLLE-ES 1 155155323 155155323 single base substitution A C downstream_gene_variant CLLE-ES 1 155155323 155155323 single base substitution A C exon_variant CLLE-ES 1 155155323 155155323 single base substitution A C intron_variant COAD-US 1 155141942 155141942 single base substitution T C upstream_gene_variant COAD-US 1 155142286 155142286 single base substitution G A upstream_gene_variant COAD-US 1 155149718 155149718 single base substitution G A exon_variant COAD-US 1 155149718 155149718 single base substitution G A synonymous_variant T161T 483G>A COAD-US 1 155149718 155149718 single base substitution G A synonymous_variant T264T 792G>A COAD-US 1 155149718 155149718 single base substitution G A synonymous_variant T287T 861G>A COAD-US 1 155149718 155149718 single base substitution G A synonymous_variant T294T 882G>A COAD-US 1 155150502 155150502 single base substitution G T exon_variant COAD-US 1 155150502 155150502 single base substitution G T stop_gained E186* 556G>T COAD-US 1 155150502 155150502 single base substitution G T stop_gained E289* 865G>T COAD-US 1 155150502 155150502 single base substitution G T stop_gained E312* 934G>T COAD-US 1 155150502 155150502 single base substitution G T stop_gained E319* 955G>T COAD-US 1 155151086 155151086 single base substitution C T downstream_gene_variant COAD-US 1 155151086 155151086 single base substitution C T exon_variant COAD-US 1 155151086 155151086 single base substitution C T stop_gained R302* 904C>T COAD-US 1 155151086 155151086 single base substitution C T stop_gained R405* 1213C>T COAD-US 1 155151086 155151086 single base substitution C T stop_gained R428* 1282C>T COAD-US 1 155151086 155151086 single base substitution C T stop_gained R435* 1303C>T COAD-US 1 155152178 155152178 insertion of <=200bp - C downstream_gene_variant COAD-US 1 155152178 155152178 insertion of <=200bp - C exon_variant COAD-US 1 155152178 155152178 insertion of <=200bp - C frameshift_variant C465S? COAD-US 1 155152178 155152178 insertion of <=200bp - C frameshift_variant C472S? COAD-US 1 155152178 155152178 insertion of <=200bp - C frameshift_variant L326L? COAD-US 1 155152178 155152178 insertion of <=200bp - C frameshift_variant L429L? COAD-US 1 155152178 155152178 insertion of <=200bp - C frameshift_variant L452L? COAD-US 1 155154359 155154359 single base substitution C T 3_prime_UTR_variant COAD-US 1 155154359 155154359 single base substitution C T downstream_gene_variant COAD-US 1 155154359 155154359 single base substitution C T exon_variant COAD-US 1 155154359 155154359 single base substitution C T synonymous_variant G414G 1242C>T COAD-US 1 155154359 155154359 single base substitution C T synonymous_variant G517G 1551C>T COAD-US 1 155154359 155154359 single base substitution C T synonymous_variant G540G 1620C>T COAD-US 1 155154431 155154431 single base substitution G A 3_prime_UTR_variant COAD-US 1 155154431 155154431 single base substitution G A downstream_gene_variant COAD-US 1 155154431 155154431 single base substitution G A exon_variant COAD-US 1 155154431 155154431 single base substitution G A synonymous_variant L438L 1314G>A COAD-US 1 155154431 155154431 single base substitution G A synonymous_variant L541L 1623G>A COAD-US 1 155154431 155154431 single base substitution G A synonymous_variant L564L 1692G>A COAD-US 1 155154564 155154564 single base substitution G A 3_prime_UTR_variant COAD-US 1 155154564 155154564 single base substitution G A downstream_gene_variant COAD-US 1 155154564 155154564 single base substitution G A exon_variant COAD-US 1 155154564 155154564 single base substitution G A missense_variant V483I 1447G>A COAD-US 1 155154564 155154564 single base substitution G A missense_variant V586I 1756G>A COAD-US 1 155154564 155154564 single base substitution G A missense_variant V609I 1825G>A COAD-US 1 155161794 155161794 single base substitution C T downstream_gene_variant COAD-US 1 155162059 155162059 single base substitution C T downstream_gene_variant COAD-US 1 155162067 155162067 single base substitution C T downstream_gene_variant COAD-US 1 155162068 155162068 single base substitution G C downstream_gene_variant COCA-CN 1 155141969 155141969 single base substitution C T upstream_gene_variant COCA-CN 1 155146367 155146367 single base substitution G T 5_prime_UTR_variant COCA-CN 1 155146367 155146367 single base substitution G T intron_variant COCA-CN 1 155146367 155146367 single base substitution G T upstream_gene_variant COCA-CN 1 155147971 155147971 single base substitution G A exon_variant COCA-CN 1 155147971 155147971 single base substitution G A intron_variant COCA-CN 1 155147971 155147971 single base substitution G A missense_variant R35Q 104G>A COCA-CN 1 155147971 155147971 single base substitution G A missense_variant R58Q 173G>A COCA-CN 1 155147971 155147971 single base substitution G A missense_variant R65Q 194G>A COCA-CN 1 155148502 155148502 single base substitution G A exon_variant COCA-CN 1 155148502 155148502 single base substitution G A missense_variant R132H 395G>A COCA-CN 1 155148502 155148502 single base substitution G A missense_variant R155H 464G>A COCA-CN 1 155148502 155148502 single base substitution G A missense_variant R162H 485G>A COCA-CN 1 155148502 155148502 single base substitution G A missense_variant R29H 86G>A COCA-CN 1 155148641 155148641 single base substitution C T exon_variant COCA-CN 1 155148641 155148641 single base substitution C T synonymous_variant F178F 534C>T COCA-CN 1 155148641 155148641 single base substitution C T synonymous_variant F201F 603C>T COCA-CN 1 155148641 155148641 single base substitution C T synonymous_variant F208F 624C>T COCA-CN 1 155148641 155148641 single base substitution C T synonymous_variant F75F 225C>T COCA-CN 1 155149301 155149301 single base substitution C T intron_variant COCA-CN 1 155150855 155150855 single base substitution T A downstream_gene_variant COCA-CN 1 155150855 155150855 single base substitution T A intron_variant COCA-CN 1 155151493 155151493 single base substitution C T downstream_gene_variant COCA-CN 1 155151493 155151493 single base substitution C T intron_variant COCA-CN 1 155152091 155152091 single base substitution G A downstream_gene_variant COCA-CN 1 155152091 155152091 single base substitution G A intron_variant COCA-CN 1 155154391 155154391 single base substitution A G 3_prime_UTR_variant COCA-CN 1 155154391 155154391 single base substitution A G downstream_gene_variant COCA-CN 1 155154391 155154391 single base substitution A G exon_variant COCA-CN 1 155154391 155154391 single base substitution A G missense_variant D425G 1274A>G COCA-CN 1 155154391 155154391 single base substitution A G missense_variant D528G 1583A>G COCA-CN 1 155154391 155154391 single base substitution A G missense_variant D551G 1652A>G COCA-CN 1 155159212 155159212 single base substitution T C downstream_gene_variant ESAD-UK 1 155146392 155146392 single base substitution G A 5_prime_UTR_variant ESAD-UK 1 155146392 155146392 single base substitution G A exon_variant ESAD-UK 1 155146392 155146392 single base substitution G A intron_variant ESAD-UK 1 155146392 155146392 single base substitution G A upstream_gene_variant ESAD-UK 1 155150055 155150055 single base substitution C T intron_variant ESAD-UK 1 155150158 155150158 single base substitution T C intron_variant ESAD-UK 1 155151736 155151736 single base substitution C G downstream_gene_variant ESAD-UK 1 155151736 155151736 single base substitution C G intron_variant ESAD-UK 1 155152007 155152007 insertion of <=200bp - C downstream_gene_variant ESAD-UK 1 155152007 155152007 insertion of <=200bp - C intron_variant ESAD-UK 1 155152121 155152121 single base substitution C T downstream_gene_variant ESAD-UK 1 155152121 155152121 single base substitution C T exon_variant ESAD-UK 1 155152121 155152121 single base substitution C T missense_variant P446L 1337C>T ESAD-UK 1 155152121 155152121 single base substitution C T missense_variant P453L 1358C>T ESAD-UK 1 155152121 155152121 single base substitution C T synonymous_variant P307P 921C>T ESAD-UK 1 155152121 155152121 single base substitution C T synonymous_variant P410P 1230C>T ESAD-UK 1 155152121 155152121 single base substitution C T synonymous_variant P433P 1299C>T ESAD-UK 1 155152258 155152258 single base substitution G T downstream_gene_variant ESAD-UK 1 155152258 155152258 single base substitution G T exon_variant ESAD-UK 1 155152258 155152258 single base substitution G T missense_variant A492S 1474G>T ESAD-UK 1 155152258 155152258 single base substitution G T missense_variant A499S 1495G>T ESAD-UK 1 155152258 155152258 single base substitution G T missense_variant R353L 1058G>T ESAD-UK 1 155152258 155152258 single base substitution G T missense_variant R456L 1367G>T ESAD-UK 1 155152258 155152258 single base substitution G T missense_variant R479L 1436G>T ESAD-UK 1 155153589 155153589 single base substitution G A downstream_gene_variant ESAD-UK 1 155153589 155153589 single base substitution G A intron_variant ESAD-UK 1 155153770 155153770 single base substitution G T downstream_gene_variant ESAD-UK 1 155153770 155153770 single base substitution G T intron_variant ESAD-UK 1 155154223 155154223 single base substitution T C downstream_gene_variant ESAD-UK 1 155154223 155154223 single base substitution T C intron_variant ESAD-UK 1 155154599 155154599 single base substitution G C 3_prime_UTR_variant ESAD-UK 1 155154599 155154599 single base substitution G C downstream_gene_variant ESAD-UK 1 155154599 155154599 single base substitution G C exon_variant ESAD-UK 1 155154599 155154599 single base substitution G C missense_variant Q494H 1482G>C ESAD-UK 1 155154599 155154599 single base substitution G C missense_variant Q597H 1791G>C ESAD-UK 1 155154599 155154599 single base substitution G C missense_variant Q620H 1860G>C ESAD-UK 1 155154870 155154870 single base substitution G A 3_prime_UTR_variant ESAD-UK 1 155154870 155154870 single base substitution G A downstream_gene_variant ESAD-UK 1 155154870 155154870 single base substitution G A exon_variant ESAD-UK 1 155154870 155154870 single base substitution G A intron_variant ESAD-UK 1 155158643 155158643 single base substitution G T downstream_gene_variant ESAD-UK 1 155159660 155159660 single base substitution C T downstream_gene_variant ESCA-CN 1 155159706 155159706 single base substitution C T downstream_gene_variant GBM-US 1 155150608 155150608 single base substitution G A exon_variant GBM-US 1 155150608 155150608 single base substitution G A missense_variant S221N 662G>A GBM-US 1 155150608 155150608 single base substitution G A missense_variant S324N 971G>A GBM-US 1 155150608 155150608 single base substitution G A missense_variant S347N 1040G>A GBM-US 1 155150608 155150608 single base substitution G A missense_variant S354N 1061G>A GBM-US 1 155161953 155161953 single base substitution T C downstream_gene_variant KIRC-US 1 155145769 155145771 deletion of <=200bp CTA - upstream_gene_variant KIRC-US 1 155150596 155150596 insertion of <=200bp - G exon_variant KIRC-US 1 155150596 155150596 insertion of <=200bp - G frameshift_variant L217R? KIRC-US 1 155150596 155150596 insertion of <=200bp - G frameshift_variant L320R? KIRC-US 1 155150596 155150596 insertion of <=200bp - G frameshift_variant L343R? KIRC-US 1 155150596 155150596 insertion of <=200bp - G frameshift_variant L350R? KIRC-US 1 155160211 155160211 single base substitution G T downstream_gene_variant KIRP-US 1 155148034 155148034 single base substitution C G exon_variant KIRP-US 1 155148034 155148034 single base substitution C G intron_variant KIRP-US 1 155148034 155148034 single base substitution C G missense_variant S56C 167C>G KIRP-US 1 155148034 155148034 single base substitution C G missense_variant S79C 236C>G KIRP-US 1 155148034 155148034 single base substitution C G missense_variant S86C 257C>G LAML-KR 1 155150666 155150666 single base substitution C A downstream_gene_variant LAML-KR 1 155150666 155150666 single base substitution C A exon_variant LAML-KR 1 155150666 155150666 single base substitution C A synonymous_variant A240A 720C>A LAML-KR 1 155150666 155150666 single base substitution C A synonymous_variant A343A 1029C>A LAML-KR 1 155150666 155150666 single base substitution C A synonymous_variant A366A 1098C>A LAML-KR 1 155150666 155150666 single base substitution C A synonymous_variant A373A 1119C>A LAML-KR 1 155155364 155155364 single base substitution A C downstream_gene_variant LAML-KR 1 155155364 155155364 single base substitution A C intron_variant LGG-US 1 155160204 155160204 single base substitution C T downstream_gene_variant LGG-US 1 155161799 155161799 single base substitution T G downstream_gene_variant LICA-CN 1 155145251 155145251 single base substitution C G upstream_gene_variant LICA-CN 1 155145734 155145734 single base substitution G C upstream_gene_variant LICA-CN 1 155148108 155148108 single base substitution C T exon_variant LICA-CN 1 155148108 155148108 single base substitution C T intron_variant LICA-CN 1 155148108 155148108 single base substitution C T missense_variant R104W 310C>T LICA-CN 1 155148108 155148108 single base substitution C T missense_variant R111W 331C>T LICA-CN 1 155148108 155148108 single base substitution C T missense_variant R81W 241C>T LICA-CN 1 155148641 155148641 single base substitution C A exon_variant LICA-CN 1 155148641 155148641 single base substitution C A missense_variant F178L 534C>A LICA-CN 1 155148641 155148641 single base substitution C A missense_variant F201L 603C>A LICA-CN 1 155148641 155148641 single base substitution C A missense_variant F208L 624C>A LICA-CN 1 155148641 155148641 single base substitution C A missense_variant F75L 225C>A LICA-CN 1 155156591 155156591 single base substitution A T 3_prime_UTR_variant LICA-CN 1 155156591 155156591 single base substitution A T downstream_gene_variant LICA-CN 1 155156591 155156591 single base substitution A T exon_variant LICA-CN 1 155156591 155156591 single base substitution A T synonymous_variant A609A 1827A>T LICA-CN 1 155156591 155156591 single base substitution A T synonymous_variant A712A 2136A>T LICA-CN 1 155156591 155156591 single base substitution A T synonymous_variant A735A 2205A>T LICA-FR 1 155141956 155141956 insertion of <=200bp - CCGAAGCACAGGCTCTGGAATTAGACTGCTGGGATGCAAACCCTGGCTCACTGTT upstream_gene_variant LIHC-US 1 155145067 155145067 single base substitution C A upstream_gene_variant LIHC-US 1 155148663 155148663 single base substitution G T exon_variant LIHC-US 1 155148663 155148663 single base substitution G T missense_variant A186S 556G>T LIHC-US 1 155148663 155148663 single base substitution G T missense_variant A209S 625G>T LIHC-US 1 155148663 155148663 single base substitution G T missense_variant A216S 646G>T LIHC-US 1 155148663 155148663 single base substitution G T missense_variant A83S 247G>T LIHC-US 1 155151089 155151089 single base substitution G T downstream_gene_variant LIHC-US 1 155151089 155151089 single base substitution G T missense_variant G429C 1285G>T LIHC-US 1 155151089 155151089 single base substitution G T missense_variant G436C 1306G>T LIHC-US 1 155151089 155151089 single base substitution G T missense_variant V303L 907G>T LIHC-US 1 155151089 155151089 single base substitution G T missense_variant V406L 1216G>T LIHC-US 1 155151089 155151089 single base substitution G T missense_variant V429L 1285G>T LIHC-US 1 155151089 155151089 single base substitution G T splice_region_variant LIHC-US 1 155154372 155154372 single base substitution C T 3_prime_UTR_variant LIHC-US 1 155154372 155154372 single base substitution C T downstream_gene_variant LIHC-US 1 155154372 155154372 single base substitution C T exon_variant LIHC-US 1 155154372 155154372 single base substitution C T missense_variant R419W 1255C>T LIHC-US 1 155154372 155154372 single base substitution C T missense_variant R522W 1564C>T LIHC-US 1 155154372 155154372 single base substitution C T missense_variant R545W 1633C>T LIHC-US 1 155160803 155160803 single base substitution C T downstream_gene_variant LINC-JP 1 155142064 155142064 single base substitution G A upstream_gene_variant LINC-JP 1 155143387 155143387 single base substitution C T upstream_gene_variant LINC-JP 1 155145176 155145176 single base substitution C A upstream_gene_variant LINC-JP 1 155150637 155150637 single base substitution C T downstream_gene_variant LINC-JP 1 155150637 155150637 single base substitution C T exon_variant LINC-JP 1 155150637 155150637 single base substitution C T synonymous_variant L231L 691C>T LINC-JP 1 155150637 155150637 single base substitution C T synonymous_variant L334L 1000C>T LINC-JP 1 155150637 155150637 single base substitution C T synonymous_variant L357L 1069C>T LINC-JP 1 155150637 155150637 single base substitution C T synonymous_variant L364L 1090C>T LINC-JP 1 155152401 155152401 single base substitution C T 3_prime_UTR_variant LINC-JP 1 155152401 155152401 single base substitution C T downstream_gene_variant LINC-JP 1 155152401 155152401 single base substitution C T exon_variant LINC-JP 1 155152401 155152401 single base substitution C T missense_variant P401S 1201C>T LINC-JP 1 155152401 155152401 single base substitution C T missense_variant P504S 1510C>T LINC-JP 1 155152401 155152401 single base substitution C T missense_variant P527S 1579C>T LINC-JP 1 155154264 155154264 single base substitution G A downstream_gene_variant LINC-JP 1 155154264 155154264 single base substitution G A intron_variant LINC-JP 1 155154455 155154455 single base substitution C T 3_prime_UTR_variant LINC-JP 1 155154455 155154455 single base substitution C T downstream_gene_variant LINC-JP 1 155154455 155154455 single base substitution C T exon_variant LINC-JP 1 155154455 155154455 single base substitution C T synonymous_variant T446T 1338C>T LINC-JP 1 155154455 155154455 single base substitution C T synonymous_variant T549T 1647C>T LINC-JP 1 155154455 155154455 single base substitution C T synonymous_variant T572T 1716C>T LINC-JP 1 155154511 155154511 single base substitution G A 3_prime_UTR_variant LINC-JP 1 155154511 155154511 single base substitution G A downstream_gene_variant LINC-JP 1 155154511 155154511 single base substitution G A exon_variant LINC-JP 1 155154511 155154511 single base substitution G A missense_variant R465H 1394G>A LINC-JP 1 155154511 155154511 single base substitution G A missense_variant R568H 1703G>A LINC-JP 1 155154511 155154511 single base substitution G A missense_variant R591H 1772G>A LINC-JP 1 155158969 155158969 single base substitution T G downstream_gene_variant LINC-JP 1 155158972 155158972 single base substitution G T downstream_gene_variant LINC-JP 1 155159717 155159717 single base substitution C T downstream_gene_variant LINC-JP 1 155159802 155159802 single base substitution G A downstream_gene_variant LINC-JP 1 155159989 155159989 single base substitution G A downstream_gene_variant LINC-JP 1 155160669 155160671 deletion of <=200bp GTA - downstream_gene_variant LINC-JP 1 155160809 155160809 deletion of <=200bp T - downstream_gene_variant LINC-JP 1 155161671 155161671 single base substitution T C downstream_gene_variant LINC-JP 1 155161733 155161733 single base substitution G C downstream_gene_variant LINC-JP 1 155161737 155161737 single base substitution G C downstream_gene_variant LIRI-JP 1 155145088 155145088 single base substitution T A upstream_gene_variant LIRI-JP 1 155145532 155145532 single base substitution G T upstream_gene_variant LIRI-JP 1 155149257 155149283 deletion of <=200bp ATGTACCACCAGGTGGCACTGTGGAGC - intron_variant LIRI-JP 1 155149925 155149925 single base substitution C T intron_variant LIRI-JP 1 155154960 155154960 single base substitution A T 3_prime_UTR_variant LIRI-JP 1 155154960 155154960 single base substitution A T downstream_gene_variant LIRI-JP 1 155154960 155154960 single base substitution A T exon_variant LIRI-JP 1 155154960 155154960 single base substitution A T intron_variant LIRI-JP 1 155156358 155156358 single base substitution A G 3_prime_UTR_variant LIRI-JP 1 155156358 155156358 single base substitution A G downstream_gene_variant LIRI-JP 1 155156358 155156358 single base substitution A G exon_variant LIRI-JP 1 155156358 155156358 single base substitution A G missense_variant M532V 1594A>G LIRI-JP 1 155156358 155156358 single base substitution A G missense_variant M635V 1903A>G LIRI-JP 1 155156358 155156358 single base substitution A G missense_variant M658V 1972A>G LIRI-JP 1 155157049 155157049 single base substitution C A 3_prime_UTR_variant LIRI-JP 1 155157049 155157049 single base substitution C A downstream_gene_variant LIRI-JP 1 155157049 155157049 single base substitution C A exon_variant LIRI-JP 1 155157648 155157648 single base substitution G A downstream_gene_variant LUSC-CN 1 155149587 155149587 single base substitution C G intron_variant LUSC-KR 1 155144606 155144606 single base substitution T A upstream_gene_variant LUSC-KR 1 155144607 155144607 single base substitution A T upstream_gene_variant LUSC-KR 1 155145217 155145217 single base substitution G A upstream_gene_variant LUSC-KR 1 155148944 155148944 single base substitution G C intron_variant LUSC-KR 1 155151310 155151310 single base substitution C T downstream_gene_variant LUSC-KR 1 155151310 155151310 single base substitution C T exon_variant LUSC-KR 1 155151310 155151310 single base substitution C T intron_variant LUSC-KR 1 155151310 155151310 single base substitution C T synonymous_variant S437S 1311C>T LUSC-KR 1 155151310 155151310 single base substitution C T synonymous_variant S444S 1332C>T LUSC-KR 1 155151349 155151349 single base substitution C T downstream_gene_variant LUSC-KR 1 155151349 155151349 single base substitution C T intron_variant LUSC-KR 1 155151803 155151803 single base substitution G C downstream_gene_variant LUSC-KR 1 155151803 155151803 single base substitution G C intron_variant LUSC-KR 1 155157155 155157155 single base substitution C T 3_prime_UTR_variant LUSC-KR 1 155157155 155157155 single base substitution C T downstream_gene_variant LUSC-KR 1 155157155 155157155 single base substitution C T exon_variant LUSC-US 1 155148067 155148067 single base substitution G A exon_variant LUSC-US 1 155148067 155148067 single base substitution G A intron_variant LUSC-US 1 155148067 155148067 single base substitution G A missense_variant R67H 200G>A LUSC-US 1 155148067 155148067 single base substitution G A missense_variant R90H 269G>A LUSC-US 1 155148067 155148067 single base substitution G A missense_variant R97H 290G>A LUSC-US 1 155148375 155148375 single base substitution T C 5_prime_UTR_variant LUSC-US 1 155148375 155148375 single base substitution T C exon_variant LUSC-US 1 155148375 155148375 single base substitution T C missense_variant Y113H 337T>C LUSC-US 1 155148375 155148375 single base substitution T C missense_variant Y120H 358T>C LUSC-US 1 155148375 155148375 single base substitution T C missense_variant Y90H 268T>C LUSC-US 1 155148600 155148600 single base substitution G A exon_variant LUSC-US 1 155148600 155148600 single base substitution G A missense_variant E165K 493G>A LUSC-US 1 155148600 155148600 single base substitution G A missense_variant E188K 562G>A LUSC-US 1 155148600 155148600 single base substitution G A missense_variant E195K 583G>A LUSC-US 1 155148600 155148600 single base substitution G A missense_variant E62K 184G>A LUSC-US 1 155156413 155156413 single base substitution G T 3_prime_UTR_variant LUSC-US 1 155156413 155156413 single base substitution G T downstream_gene_variant LUSC-US 1 155156413 155156413 single base substitution G T exon_variant LUSC-US 1 155156413 155156413 single base substitution G T missense_variant R550M 1649G>T LUSC-US 1 155156413 155156413 single base substitution G T missense_variant R653M 1958G>T LUSC-US 1 155156413 155156413 single base substitution G T missense_variant R676M 2027G>T LUSC-US 1 155162052 155162052 single base substitution T A downstream_gene_variant MALY-DE 1 155141323 155141323 single base substitution A G upstream_gene_variant MALY-DE 1 155142751 155142751 single base substitution A C upstream_gene_variant MALY-DE 1 155149039 155149039 single base substitution T C intron_variant MELA-AU 1 155140889 155140889 single base substitution C A upstream_gene_variant MELA-AU 1 155141179 155141179 single base substitution T A upstream_gene_variant MELA-AU 1 155141551 155141551 single base substitution G A upstream_gene_variant MELA-AU 1 155142397 155142397 single base substitution G A upstream_gene_variant MELA-AU 1 155142545 155142546 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 155142943 155142943 single base substitution G A upstream_gene_variant MELA-AU 1 155143107 155143107 single base substitution G A upstream_gene_variant MELA-AU 1 155143670 155143670 single base substitution G A upstream_gene_variant MELA-AU 1 155143821 155143821 single base substitution G A upstream_gene_variant MELA-AU 1 155144739 155144740 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 1 155145869 155145869 single base substitution G A upstream_gene_variant MELA-AU 1 155146248 155146248 single base substitution C G intron_variant MELA-AU 1 155146248 155146248 single base substitution C G upstream_gene_variant MELA-AU 1 155147048 155147048 single base substitution C T intron_variant MELA-AU 1 155147048 155147048 single base substitution C T upstream_gene_variant MELA-AU 1 155147174 155147174 single base substitution G A intron_variant MELA-AU 1 155147174 155147174 single base substitution G A upstream_gene_variant MELA-AU 1 155147175 155147175 single base substitution G T intron_variant MELA-AU 1 155147175 155147175 single base substitution G T upstream_gene_variant MELA-AU 1 155147185 155147185 single base substitution C T intron_variant MELA-AU 1 155147185 155147185 single base substitution C T upstream_gene_variant MELA-AU 1 155147501 155147501 single base substitution C A intron_variant MELA-AU 1 155148036 155148036 single base substitution C T exon_variant MELA-AU 1 155148036 155148036 single base substitution C T intron_variant MELA-AU 1 155148036 155148036 single base substitution C T missense_variant P57S 169C>T MELA-AU 1 155148036 155148036 single base substitution C T missense_variant P80S 238C>T MELA-AU 1 155148036 155148036 single base substitution C T missense_variant P87S 259C>T MELA-AU 1 155148108 155148108 single base substitution C T exon_variant MELA-AU 1 155148108 155148108 single base substitution C T intron_variant MELA-AU 1 155148108 155148108 single base substitution C T missense_variant R104W 310C>T MELA-AU 1 155148108 155148108 single base substitution C T missense_variant R111W 331C>T MELA-AU 1 155148108 155148108 single base substitution C T missense_variant R81W 241C>T MELA-AU 1 155148316 155148316 single base substitution C T intron_variant MELA-AU 1 155148385 155148385 single base substitution G A 5_prime_UTR_variant MELA-AU 1 155148385 155148385 single base substitution G A exon_variant MELA-AU 1 155148385 155148385 single base substitution G A missense_variant R116K 347G>A MELA-AU 1 155148385 155148385 single base substitution G A missense_variant R123K 368G>A MELA-AU 1 155148385 155148385 single base substitution G A missense_variant R93K 278G>A MELA-AU 1 155149272 155149272 single base substitution G A intron_variant MELA-AU 1 155149704 155149704 single base substitution G A exon_variant MELA-AU 1 155149704 155149704 single base substitution G A missense_variant G157R 469G>A MELA-AU 1 155149704 155149704 single base substitution G A missense_variant G260R 778G>A MELA-AU 1 155149704 155149704 single base substitution G A missense_variant G283R 847G>A MELA-AU 1 155149704 155149704 single base substitution G A missense_variant G290R 868G>A MELA-AU 1 155150137 155150137 single base substitution G A intron_variant MELA-AU 1 155150265 155150265 single base substitution C T intron_variant MELA-AU 1 155150301 155150301 single base substitution C T intron_variant MELA-AU 1 155150370 155150370 single base substitution C T intron_variant MELA-AU 1 155151095 155151095 single base substitution G A downstream_gene_variant MELA-AU 1 155151095 155151095 single base substitution G A splice_region_variant MELA-AU 1 155151140 155151140 single base substitution C T downstream_gene_variant MELA-AU 1 155151140 155151140 single base substitution C T intron_variant MELA-AU 1 155151213 155151213 single base substitution C T downstream_gene_variant MELA-AU 1 155151213 155151213 single base substitution C T intron_variant MELA-AU 1 155151402 155151402 single base substitution C T downstream_gene_variant MELA-AU 1 155151402 155151402 single base substitution C T intron_variant MELA-AU 1 155151559 155151560 multiple base substitution (>=2bp and <=200bp) AC TT downstream_gene_variant MELA-AU 1 155151559 155151560 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 1 155151563 155151563 single base substitution C T downstream_gene_variant MELA-AU 1 155151563 155151563 single base substitution C T intron_variant MELA-AU 1 155151579 155151579 single base substitution C T downstream_gene_variant MELA-AU 1 155151579 155151579 single base substitution C T intron_variant MELA-AU 1 155151606 155151606 single base substitution C T downstream_gene_variant MELA-AU 1 155151606 155151606 single base substitution C T intron_variant MELA-AU 1 155151907 155151907 single base substitution C T downstream_gene_variant MELA-AU 1 155151907 155151907 single base substitution C T intron_variant MELA-AU 1 155151930 155151930 single base substitution C T downstream_gene_variant MELA-AU 1 155151930 155151930 single base substitution C T intron_variant MELA-AU 1 155151939 155151939 single base substitution C A downstream_gene_variant MELA-AU 1 155151939 155151939 single base substitution C A intron_variant MELA-AU 1 155151945 155151945 single base substitution C T downstream_gene_variant MELA-AU 1 155151945 155151945 single base substitution C T intron_variant MELA-AU 1 155152251 155152251 single base substitution C T downstream_gene_variant MELA-AU 1 155152251 155152251 single base substitution C T exon_variant MELA-AU 1 155152251 155152251 single base substitution C T missense_variant P351S 1051C>T MELA-AU 1 155152251 155152251 single base substitution C T missense_variant P454S 1360C>T MELA-AU 1 155152251 155152251 single base substitution C T missense_variant P477S 1429C>T MELA-AU 1 155152251 155152251 single base substitution C T synonymous_variant A489A 1467C>T MELA-AU 1 155152251 155152251 single base substitution C T synonymous_variant A496A 1488C>T MELA-AU 1 155152319 155152319 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155152319 155152319 single base substitution C T downstream_gene_variant MELA-AU 1 155152319 155152319 single base substitution C T exon_variant MELA-AU 1 155152319 155152319 single base substitution C T synonymous_variant G373G 1119C>T MELA-AU 1 155152319 155152319 single base substitution C T synonymous_variant G476G 1428C>T MELA-AU 1 155152319 155152319 single base substitution C T synonymous_variant G499G 1497C>T MELA-AU 1 155152434 155152434 single base substitution C T downstream_gene_variant MELA-AU 1 155152434 155152434 single base substitution C T intron_variant MELA-AU 1 155152715 155152715 single base substitution G A downstream_gene_variant MELA-AU 1 155152715 155152715 single base substitution G A intron_variant MELA-AU 1 155153025 155153025 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155153025 155153025 single base substitution C T downstream_gene_variant MELA-AU 1 155153025 155153025 single base substitution C T intron_variant MELA-AU 1 155153074 155153074 single base substitution G C 3_prime_UTR_variant MELA-AU 1 155153074 155153074 single base substitution G C downstream_gene_variant MELA-AU 1 155153074 155153074 single base substitution G C intron_variant MELA-AU 1 155153303 155153303 single base substitution T C downstream_gene_variant MELA-AU 1 155153303 155153303 single base substitution T C intron_variant MELA-AU 1 155153333 155153333 single base substitution C T downstream_gene_variant MELA-AU 1 155153333 155153333 single base substitution C T intron_variant MELA-AU 1 155154057 155154057 single base substitution C T downstream_gene_variant MELA-AU 1 155154057 155154057 single base substitution C T intron_variant MELA-AU 1 155154105 155154105 single base substitution C T downstream_gene_variant MELA-AU 1 155154105 155154105 single base substitution C T intron_variant MELA-AU 1 155154124 155154124 single base substitution C T downstream_gene_variant MELA-AU 1 155154124 155154124 single base substitution C T intron_variant MELA-AU 1 155154181 155154181 single base substitution C T downstream_gene_variant MELA-AU 1 155154181 155154181 single base substitution C T intron_variant MELA-AU 1 155154251 155154251 single base substitution C T downstream_gene_variant MELA-AU 1 155154251 155154251 single base substitution C T intron_variant MELA-AU 1 155154316 155154316 single base substitution C T downstream_gene_variant MELA-AU 1 155154316 155154316 single base substitution C T intron_variant MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA stop_gained WA468*T MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA stop_gained WA571*T MELA-AU 1 155154521 155154522 multiple base substitution (>=2bp and <=200bp) GG AA stop_gained WA594*T MELA-AU 1 155154529 155154529 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155154529 155154529 single base substitution C T downstream_gene_variant MELA-AU 1 155154529 155154529 single base substitution C T exon_variant MELA-AU 1 155154529 155154529 single base substitution C T missense_variant A471V 1412C>T MELA-AU 1 155154529 155154529 single base substitution C T missense_variant A574V 1721C>T MELA-AU 1 155154529 155154529 single base substitution C T missense_variant A597V 1790C>T MELA-AU 1 155154637 155154637 single base substitution C T downstream_gene_variant MELA-AU 1 155154637 155154637 single base substitution C T exon_variant MELA-AU 1 155154637 155154637 single base substitution C T intron_variant MELA-AU 1 155154637 155154637 single base substitution C T missense_variant S633F 1898C>T MELA-AU 1 155154643 155154644 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 155154643 155154644 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 1 155154643 155154644 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 155154643 155154644 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant R635K 1904GG>AA MELA-AU 1 155154851 155154851 single base substitution G A 3_prime_UTR_variant MELA-AU 1 155154851 155154851 single base substitution G A downstream_gene_variant MELA-AU 1 155154851 155154851 single base substitution G A exon_variant MELA-AU 1 155154851 155154851 single base substitution G A intron_variant MELA-AU 1 155155229 155155229 single base substitution G A 3_prime_UTR_variant MELA-AU 1 155155229 155155229 single base substitution G A downstream_gene_variant MELA-AU 1 155155229 155155229 single base substitution G A exon_variant MELA-AU 1 155155229 155155229 single base substitution G A intron_variant MELA-AU 1 155155602 155155602 single base substitution G A downstream_gene_variant MELA-AU 1 155155602 155155602 single base substitution G A intron_variant MELA-AU 1 155156049 155156049 single base substitution C T downstream_gene_variant MELA-AU 1 155156049 155156049 single base substitution C T intron_variant MELA-AU 1 155156209 155156209 single base substitution C T downstream_gene_variant MELA-AU 1 155156209 155156209 single base substitution C T intron_variant MELA-AU 1 155156249 155156249 single base substitution C T downstream_gene_variant MELA-AU 1 155156249 155156249 single base substitution C T intron_variant MELA-AU 1 155156345 155156345 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155156345 155156345 single base substitution C T downstream_gene_variant MELA-AU 1 155156345 155156345 single base substitution C T exon_variant MELA-AU 1 155156345 155156345 single base substitution C T synonymous_variant F527F 1581C>T MELA-AU 1 155156345 155156345 single base substitution C T synonymous_variant F630F 1890C>T MELA-AU 1 155156345 155156345 single base substitution C T synonymous_variant F653F 1959C>T MELA-AU 1 155156453 155156453 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155156453 155156453 single base substitution C T downstream_gene_variant MELA-AU 1 155156453 155156453 single base substitution C T exon_variant MELA-AU 1 155156453 155156453 single base substitution C T synonymous_variant P563P 1689C>T MELA-AU 1 155156453 155156453 single base substitution C T synonymous_variant P666P 1998C>T MELA-AU 1 155156453 155156453 single base substitution C T synonymous_variant P689P 2067C>T MELA-AU 1 155156559 155156559 single base substitution T C 3_prime_UTR_variant MELA-AU 1 155156559 155156559 single base substitution T C downstream_gene_variant MELA-AU 1 155156559 155156559 single base substitution T C exon_variant MELA-AU 1 155156559 155156559 single base substitution T C missense_variant C599R 1795T>C MELA-AU 1 155156559 155156559 single base substitution T C missense_variant C702R 2104T>C MELA-AU 1 155156559 155156559 single base substitution T C missense_variant C725R 2173T>C MELA-AU 1 155156961 155156961 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155156961 155156961 single base substitution C T downstream_gene_variant MELA-AU 1 155156961 155156961 single base substitution C T exon_variant MELA-AU 1 155157038 155157038 single base substitution C G 3_prime_UTR_variant MELA-AU 1 155157038 155157038 single base substitution C G downstream_gene_variant MELA-AU 1 155157038 155157038 single base substitution C G exon_variant MELA-AU 1 155157077 155157077 single base substitution G A 3_prime_UTR_variant MELA-AU 1 155157077 155157077 single base substitution G A downstream_gene_variant MELA-AU 1 155157077 155157077 single base substitution G A exon_variant MELA-AU 1 155157284 155157284 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155157284 155157284 single base substitution C T downstream_gene_variant MELA-AU 1 155157284 155157284 single base substitution C T exon_variant MELA-AU 1 155157300 155157300 single base substitution C T 3_prime_UTR_variant MELA-AU 1 155157300 155157300 single base substitution C T downstream_gene_variant MELA-AU 1 155157300 155157300 single base substitution C T exon_variant MELA-AU 1 155157744 155157744 single base substitution G A downstream_gene_variant MELA-AU 1 155157775 155157775 single base substitution C T downstream_gene_variant MELA-AU 1 155157825 155157825 single base substitution C T downstream_gene_variant MELA-AU 1 155157850 155157850 single base substitution G A downstream_gene_variant MELA-AU 1 155158353 155158353 single base substitution C T downstream_gene_variant MELA-AU 1 155158355 155158355 single base substitution C T downstream_gene_variant MELA-AU 1 155158545 155158546 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 1 155158704 155158704 single base substitution G A downstream_gene_variant MELA-AU 1 155158981 155158981 single base substitution G A downstream_gene_variant MELA-AU 1 155159038 155159038 single base substitution G A downstream_gene_variant MELA-AU 1 155159765 155159765 single base substitution G A downstream_gene_variant MELA-AU 1 155159833 155159833 single base substitution G A downstream_gene_variant MELA-AU 1 155159881 155159881 single base substitution G A downstream_gene_variant MELA-AU 1 155160345 155160346 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 155160515 155160515 single base substitution C T downstream_gene_variant MELA-AU 1 155160577 155160577 single base substitution G C downstream_gene_variant MELA-AU 1 155161857 155161857 single base substitution G A downstream_gene_variant MELA-AU 1 155161936 155161937 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 155162142 155162142 single base substitution G A downstream_gene_variant ORCA-IN 1 155145708 155145708 single base substitution C T upstream_gene_variant ORCA-IN 1 155147912 155147912 single base substitution G T exon_variant ORCA-IN 1 155147912 155147912 single base substitution G T intron_variant ORCA-IN 1 155147912 155147912 single base substitution G T missense_variant E15D 45G>T ORCA-IN 1 155147912 155147912 single base substitution G T missense_variant E38D 114G>T ORCA-IN 1 155147912 155147912 single base substitution G T missense_variant E45D 135G>T ORCA-IN 1 155149730 155149730 single base substitution G T exon_variant ORCA-IN 1 155149730 155149730 single base substitution G T missense_variant Q165H 495G>T ORCA-IN 1 155149730 155149730 single base substitution G T missense_variant Q268H 804G>T ORCA-IN 1 155149730 155149730 single base substitution G T missense_variant Q291H 873G>T ORCA-IN 1 155149730 155149730 single base substitution G T missense_variant Q298H 894G>T ORCA-IN 1 155150106 155150106 single base substitution C T intron_variant ORCA-IN 1 155151132 155151132 single base substitution C T downstream_gene_variant ORCA-IN 1 155151132 155151132 single base substitution C T intron_variant ORCA-IN 1 155161834 155161834 single base substitution G A downstream_gene_variant OV-AU 1 155143173 155143173 single base substitution A G upstream_gene_variant OV-AU 1 155157552 155157552 single base substitution G C downstream_gene_variant OV-AU 1 155160351 155160351 single base substitution G C downstream_gene_variant OV-US 1 155154504 155154504 single base substitution C G 3_prime_UTR_variant OV-US 1 155154504 155154504 single base substitution C G downstream_gene_variant OV-US 1 155154504 155154504 single base substitution C G exon_variant OV-US 1 155154504 155154504 single base substitution C G missense_variant Q463E 1387C>G OV-US 1 155154504 155154504 single base substitution C G missense_variant Q566E 1696C>G OV-US 1 155154504 155154504 single base substitution C G missense_variant Q589E 1765C>G PACA-AU 1 155142186 155142186 single base substitution A G upstream_gene_variant PACA-AU 1 155146830 155146830 single base substitution C G intron_variant PACA-AU 1 155146830 155146830 single base substitution C G upstream_gene_variant PACA-AU 1 155149104 155149104 single base substitution G A intron_variant PACA-AU 1 155149701 155149701 single base substitution C G exon_variant PACA-AU 1 155149701 155149701 single base substitution C G missense_variant L156V 466C>G PACA-AU 1 155149701 155149701 single base substitution C G missense_variant L259V 775C>G PACA-AU 1 155149701 155149701 single base substitution C G missense_variant L282V 844C>G PACA-AU 1 155149701 155149701 single base substitution C G missense_variant L289V 865C>G PACA-AU 1 155150629 155150629 single base substitution G T exon_variant PACA-AU 1 155150629 155150629 single base substitution G T missense_variant R228L 683G>T PACA-AU 1 155150629 155150629 single base substitution G T missense_variant R331L 992G>T PACA-AU 1 155150629 155150629 single base substitution G T missense_variant R354L 1061G>T PACA-AU 1 155150629 155150629 single base substitution G T missense_variant R361L 1082G>T PACA-AU 1 155150651 155150651 single base substitution T C downstream_gene_variant PACA-AU 1 155150651 155150651 single base substitution T C exon_variant PACA-AU 1 155150651 155150651 single base substitution T C synonymous_variant G235G 705T>C PACA-AU 1 155150651 155150651 single base substitution T C synonymous_variant G338G 1014T>C PACA-AU 1 155150651 155150651 single base substitution T C synonymous_variant G361G 1083T>C PACA-AU 1 155150651 155150651 single base substitution T C synonymous_variant G368G 1104T>C PACA-AU 1 155150947 155150947 single base substitution C T downstream_gene_variant PACA-AU 1 155150947 155150947 single base substitution C T intron_variant PACA-AU 1 155155511 155155511 single base substitution C T downstream_gene_variant PACA-AU 1 155155511 155155511 single base substitution C T intron_variant PACA-AU 1 155158305 155158305 single base substitution G C downstream_gene_variant PACA-AU 1 155159182 155159182 insertion of <=200bp - A downstream_gene_variant PACA-AU 1 155161733 155161733 single base substitution G C downstream_gene_variant PACA-AU 1 155161737 155161737 single base substitution G C downstream_gene_variant PACA-CA 1 155143196 155143219 deletion of <=200bp AGGGCCCCACCTGCCCAGGTGGAG - upstream_gene_variant PACA-CA 1 155144645 155144645 single base substitution T A upstream_gene_variant PACA-CA 1 155147410 155147410 single base substitution G T exon_variant PACA-CA 1 155147410 155147410 single base substitution G T intron_variant PACA-CA 1 155148732 155148732 single base substitution G T intron_variant PACA-CA 1 155152341 155152341 single base substitution C T 3_prime_UTR_variant PACA-CA 1 155152341 155152341 single base substitution C T downstream_gene_variant PACA-CA 1 155152341 155152341 single base substitution C T exon_variant PACA-CA 1 155152341 155152341 single base substitution C T missense_variant R381C 1141C>T PACA-CA 1 155152341 155152341 single base substitution C T missense_variant R484C 1450C>T PACA-CA 1 155152341 155152341 single base substitution C T missense_variant R507C 1519C>T PACA-CA 1 155152368 155152368 single base substitution G A 3_prime_UTR_variant PACA-CA 1 155152368 155152368 single base substitution G A downstream_gene_variant PACA-CA 1 155152368 155152368 single base substitution G A exon_variant PACA-CA 1 155152368 155152368 single base substitution G A missense_variant E390K 1168G>A PACA-CA 1 155152368 155152368 single base substitution G A missense_variant E493K 1477G>A PACA-CA 1 155152368 155152368 single base substitution G A missense_variant E516K 1546G>A PACA-CA 1 155153570 155153570 single base substitution G A downstream_gene_variant PACA-CA 1 155153570 155153570 single base substitution G A intron_variant PACA-CA 1 155154201 155154201 deletion of <=200bp C - downstream_gene_variant PACA-CA 1 155154201 155154201 deletion of <=200bp C - intron_variant PACA-CA 1 155154482 155154482 single base substitution C G 3_prime_UTR_variant PACA-CA 1 155154482 155154482 single base substitution C G downstream_gene_variant PACA-CA 1 155154482 155154482 single base substitution C G exon_variant PACA-CA 1 155154482 155154482 single base substitution C G synonymous_variant V455V 1365C>G PACA-CA 1 155154482 155154482 single base substitution C G synonymous_variant V558V 1674C>G PACA-CA 1 155154482 155154482 single base substitution C G synonymous_variant V581V 1743C>G PACA-CA 1 155155076 155155076 single base substitution G T 3_prime_UTR_variant PACA-CA 1 155155076 155155076 single base substitution G T downstream_gene_variant PACA-CA 1 155155076 155155076 single base substitution G T exon_variant PACA-CA 1 155155076 155155076 single base substitution G T intron_variant PACA-CA 1 155155489 155155489 single base substitution C A downstream_gene_variant PACA-CA 1 155155489 155155489 single base substitution C A intron_variant PACA-CA 1 155156867 155156867 single base substitution G A 3_prime_UTR_variant PACA-CA 1 155156867 155156867 single base substitution G A downstream_gene_variant PACA-CA 1 155156867 155156867 single base substitution G A exon_variant PACA-CA 1 155156981 155156981 single base substitution G A 3_prime_UTR_variant PACA-CA 1 155156981 155156981 single base substitution G A downstream_gene_variant PACA-CA 1 155156981 155156981 single base substitution G A exon_variant PACA-CA 1 155161005 155161005 single base substitution T A downstream_gene_variant PAEN-IT 1 155149132 155149132 single base substitution A G intron_variant PBCA-DE 1 155143226 155143226 single base substitution G A upstream_gene_variant PBCA-DE 1 155151598 155151598 single base substitution T C downstream_gene_variant PBCA-DE 1 155151598 155151598 single base substitution T C intron_variant PBCA-DE 1 155156330 155156330 single base substitution G A 3_prime_UTR_variant PBCA-DE 1 155156330 155156330 single base substitution G A downstream_gene_variant PBCA-DE 1 155156330 155156330 single base substitution G A exon_variant PBCA-DE 1 155156330 155156330 single base substitution G A synonymous_variant S522S 1566G>A PBCA-DE 1 155156330 155156330 single base substitution G A synonymous_variant S625S 1875G>A PBCA-DE 1 155156330 155156330 single base substitution G A synonymous_variant S648S 1944G>A PBCA-DE 1 155160783 155160783 single base substitution G T downstream_gene_variant PRAD-CA 1 155144592 155144592 single base substitution G T upstream_gene_variant PRAD-UK 1 155144714 155144714 single base substitution C T upstream_gene_variant PRAD-US 1 155147951 155147951 single base substitution C T exon_variant PRAD-US 1 155147951 155147951 single base substitution C T intron_variant PRAD-US 1 155147951 155147951 single base substitution C T synonymous_variant N28N 84C>T PRAD-US 1 155147951 155147951 single base substitution C T synonymous_variant N51N 153C>T PRAD-US 1 155147951 155147951 single base substitution C T synonymous_variant N58N 174C>T PRAD-US 1 155161799 155161799 single base substitution T G downstream_gene_variant READ-US 1 155159827 155159827 single base substitution C A downstream_gene_variant RECA-EU 1 155148449 155148449 single base substitution G A exon_variant RECA-EU 1 155148449 155148449 single base substitution G A synonymous_variant V114V 342G>A RECA-EU 1 155148449 155148449 single base substitution G A synonymous_variant V11V 33G>A RECA-EU 1 155148449 155148449 single base substitution G A synonymous_variant V137V 411G>A RECA-EU 1 155148449 155148449 single base substitution G A synonymous_variant V144V 432G>A RECA-EU 1 155150988 155150988 single base substitution C A downstream_gene_variant RECA-EU 1 155150988 155150988 single base substitution C A exon_variant RECA-EU 1 155150988 155150988 single base substitution C A missense_variant A269D 806C>A RECA-EU 1 155150988 155150988 single base substitution C A missense_variant A372D 1115C>A RECA-EU 1 155150988 155150988 single base substitution C A missense_variant A395D 1184C>A RECA-EU 1 155150988 155150988 single base substitution C A missense_variant A402D 1205C>A RECA-EU 1 155151831 155151831 single base substitution G C downstream_gene_variant RECA-EU 1 155151831 155151831 single base substitution G C intron_variant SKCA-BR 1 155141882 155141882 single base substitution G A upstream_gene_variant SKCA-BR 1 155142926 155142926 single base substitution G A upstream_gene_variant SKCA-BR 1 155143666 155143666 single base substitution G A upstream_gene_variant SKCA-BR 1 155144697 155144697 single base substitution C T upstream_gene_variant SKCA-BR 1 155146431 155146431 single base substitution C T 5_prime_UTR_variant SKCA-BR 1 155146431 155146431 single base substitution C T exon_variant SKCA-BR 1 155146431 155146431 single base substitution C T intron_variant SKCA-BR 1 155146431 155146431 single base substitution C T upstream_gene_variant SKCA-BR 1 155149910 155149910 single base substitution G A intron_variant SKCA-BR 1 155149911 155149911 single base substitution G A intron_variant SKCA-BR 1 155150189 155150189 single base substitution C T intron_variant SKCA-BR 1 155150952 155150952 single base substitution C T downstream_gene_variant SKCA-BR 1 155150952 155150952 single base substitution C T intron_variant SKCA-BR 1 155153918 155153918 single base substitution G A downstream_gene_variant SKCA-BR 1 155153918 155153918 single base substitution G A intron_variant SKCA-BR 1 155154317 155154317 single base substitution C T downstream_gene_variant SKCA-BR 1 155154317 155154317 single base substitution C T intron_variant SKCA-BR 1 155155114 155155114 single base substitution C T 3_prime_UTR_variant SKCA-BR 1 155155114 155155114 single base substitution C T downstream_gene_variant SKCA-BR 1 155155114 155155114 single base substitution C T exon_variant SKCA-BR 1 155155114 155155114 single base substitution C T intron_variant SKCA-BR 1 155155389 155155389 insertion of <=200bp - GTT downstream_gene_variant SKCA-BR 1 155155389 155155389 insertion of <=200bp - GTT intron_variant SKCA-BR 1 155156039 155156039 single base substitution C T downstream_gene_variant SKCA-BR 1 155156039 155156039 single base substitution C T intron_variant SKCA-BR 1 155157139 155157139 single base substitution G A 3_prime_UTR_variant SKCA-BR 1 155157139 155157139 single base substitution G A downstream_gene_variant SKCA-BR 1 155157139 155157139 single base substitution G A exon_variant SKCA-BR 1 155158697 155158697 single base substitution G A downstream_gene_variant SKCM-US 1 155145290 155145290 insertion of <=200bp - G upstream_gene_variant SKCM-US 1 155147898 155147898 single base substitution C T exon_variant SKCM-US 1 155147898 155147898 single base substitution C T intron_variant SKCM-US 1 155147898 155147898 single base substitution C T missense_variant P11S 31C>T SKCM-US 1 155147898 155147898 single base substitution C T missense_variant P34S 100C>T SKCM-US 1 155147898 155147898 single base substitution C T missense_variant P41S 121C>T SKCM-US 1 155148391 155148391 single base substitution G A 5_prime_UTR_variant SKCM-US 1 155148391 155148391 single base substitution G A exon_variant SKCM-US 1 155148391 155148391 single base substitution G A missense_variant R118Q 353G>A SKCM-US 1 155148391 155148391 single base substitution G A missense_variant R125Q 374G>A SKCM-US 1 155148391 155148391 single base substitution G A missense_variant R95Q 284G>A SKCM-US 1 155148412 155148412 single base substitution T G 5_prime_UTR_variant SKCM-US 1 155148412 155148412 single base substitution T G exon_variant SKCM-US 1 155148412 155148412 single base substitution T G missense_variant V102G 305T>G SKCM-US 1 155148412 155148412 single base substitution T G missense_variant V125G 374T>G SKCM-US 1 155148412 155148412 single base substitution T G missense_variant V132G 395T>G SKCM-US 1 155148665 155148665 single base substitution C T exon_variant SKCM-US 1 155148665 155148665 single base substitution C T synonymous_variant A186A 558C>T SKCM-US 1 155148665 155148665 single base substitution C T synonymous_variant A209A 627C>T SKCM-US 1 155148665 155148665 single base substitution C T synonymous_variant A216A 648C>T SKCM-US 1 155148665 155148665 single base substitution C T synonymous_variant A83A 249C>T SKCM-US 1 155149752 155149752 single base substitution G T exon_variant SKCM-US 1 155149752 155149752 single base substitution G T missense_variant V173L 517G>T SKCM-US 1 155149752 155149752 single base substitution G T missense_variant V276L 826G>T SKCM-US 1 155149752 155149752 single base substitution G T missense_variant V299L 895G>T SKCM-US 1 155149752 155149752 single base substitution G T missense_variant V306L 916G>T SKCM-US 1 155149757 155149757 single base substitution G A exon_variant SKCM-US 1 155149757 155149757 single base substitution G A synonymous_variant R174R 522G>A SKCM-US 1 155149757 155149757 single base substitution G A synonymous_variant R277R 831G>A SKCM-US 1 155149757 155149757 single base substitution G A synonymous_variant R300R 900G>A SKCM-US 1 155149757 155149757 single base substitution G A synonymous_variant R307R 921G>A SKCM-US 1 155150499 155150499 single base substitution G A exon_variant SKCM-US 1 155150499 155150499 single base substitution G A missense_variant E185K 553G>A SKCM-US 1 155150499 155150499 single base substitution G A missense_variant E288K 862G>A SKCM-US 1 155150499 155150499 single base substitution G A missense_variant E311K 931G>A SKCM-US 1 155150499 155150499 single base substitution G A missense_variant E318K 952G>A SKCM-US 1 155150523 155150523 single base substitution G A exon_variant SKCM-US 1 155150523 155150523 single base substitution G A missense_variant G193R 577G>A SKCM-US 1 155150523 155150523 single base substitution G A missense_variant G296R 886G>A SKCM-US 1 155150523 155150523 single base substitution G A missense_variant G319R 955G>A SKCM-US 1 155150523 155150523 single base substitution G A missense_variant G326R 976G>A SKCM-US 1 155150656 155150656 single base substitution T A downstream_gene_variant SKCM-US 1 155150656 155150656 single base substitution T A exon_variant SKCM-US 1 155150656 155150656 single base substitution T A missense_variant V237E 710T>A SKCM-US 1 155150656 155150656 single base substitution T A missense_variant V340E 1019T>A SKCM-US 1 155150656 155150656 single base substitution T A missense_variant V363E 1088T>A SKCM-US 1 155150656 155150656 single base substitution T A missense_variant V370E 1109T>A SKCM-US 1 155150687 155150687 single base substitution A T downstream_gene_variant SKCM-US 1 155150687 155150687 single base substitution A T exon_variant SKCM-US 1 155150687 155150687 single base substitution A T synonymous_variant T247T 741A>T SKCM-US 1 155150687 155150687 single base substitution A T synonymous_variant T350T 1050A>T SKCM-US 1 155150687 155150687 single base substitution A T synonymous_variant T373T 1119A>T SKCM-US 1 155150687 155150687 single base substitution A T synonymous_variant T380T 1140A>T SKCM-US 1 155152210 155152210 single base substitution C T downstream_gene_variant SKCM-US 1 155152210 155152210 single base substitution C T exon_variant SKCM-US 1 155152210 155152210 single base substitution C T missense_variant P476S 1426C>T SKCM-US 1 155152210 155152210 single base substitution C T missense_variant P483S 1447C>T SKCM-US 1 155152210 155152210 single base substitution C T missense_variant T337I 1010C>T SKCM-US 1 155152210 155152210 single base substitution C T missense_variant T440I 1319C>T SKCM-US 1 155152210 155152210 single base substitution C T missense_variant T463I 1388C>T SKCM-US 1 155156314 155156314 single base substitution C T 3_prime_UTR_variant SKCM-US 1 155156314 155156314 single base substitution C T downstream_gene_variant SKCM-US 1 155156314 155156314 single base substitution C T exon_variant SKCM-US 1 155156314 155156314 single base substitution C T missense_variant A517V 1550C>T SKCM-US 1 155156314 155156314 single base substitution C T missense_variant A620V 1859C>T SKCM-US 1 155156314 155156314 single base substitution C T missense_variant A643V 1928C>T SKCM-US 1 155156339 155156339 single base substitution C T 3_prime_UTR_variant SKCM-US 1 155156339 155156339 single base substitution C T downstream_gene_variant SKCM-US 1 155156339 155156339 single base substitution C T exon_variant SKCM-US 1 155156339 155156339 single base substitution C T synonymous_variant F525F 1575C>T SKCM-US 1 155156339 155156339 single base substitution C T synonymous_variant F628F 1884C>T SKCM-US 1 155156339 155156339 single base substitution C T synonymous_variant F651F 1953C>T SKCM-US 1 155156498 155156498 single base substitution C T 3_prime_UTR_variant SKCM-US 1 155156498 155156498 single base substitution C T downstream_gene_variant SKCM-US 1 155156498 155156498 single base substitution C T exon_variant SKCM-US 1 155156498 155156498 single base substitution C T synonymous_variant F578F 1734C>T SKCM-US 1 155156498 155156498 single base substitution C T synonymous_variant F681F 2043C>T SKCM-US 1 155156498 155156498 single base substitution C T synonymous_variant F704F 2112C>T SKCM-US 1 155156512 155156512 single base substitution C T 3_prime_UTR_variant SKCM-US 1 155156512 155156512 single base substitution C T downstream_gene_variant SKCM-US 1 155156512 155156512 single base substitution C T exon_variant SKCM-US 1 155156512 155156512 single base substitution C T missense_variant S583F 1748C>T SKCM-US 1 155156512 155156512 single base substitution C T missense_variant S686F 2057C>T SKCM-US 1 155156512 155156512 single base substitution C T missense_variant S709F 2126C>T SKCM-US 1 155156563 155156563 single base substitution C T 3_prime_UTR_variant SKCM-US 1 155156563 155156563 single base substitution C T downstream_gene_variant SKCM-US 1 155156563 155156563 single base substitution C T exon_variant SKCM-US 1 155156563 155156563 single base substitution C T missense_variant P600L 1799C>T SKCM-US 1 155156563 155156563 single base substitution C T missense_variant P703L 2108C>T SKCM-US 1 155156563 155156563 single base substitution C T missense_variant P726L 2177C>T SKCM-US 1 155156586 155156586 single base substitution G A 3_prime_UTR_variant SKCM-US 1 155156586 155156586 single base substitution G A downstream_gene_variant SKCM-US 1 155156586 155156586 single base substitution G A exon_variant SKCM-US 1 155156586 155156586 single base substitution G A missense_variant G608S 1822G>A SKCM-US 1 155156586 155156586 single base substitution G A missense_variant G711S 2131G>A SKCM-US 1 155156586 155156586 single base substitution G A missense_variant G734S 2200G>A SKCM-US 1 155159934 155159934 single base substitution G A downstream_gene_variant SKCM-US 1 155160214 155160214 single base substitution C T downstream_gene_variant SKCM-US 1 155160286 155160286 single base substitution G T downstream_gene_variant SKCM-US 1 155161850 155161850 single base substitution C T downstream_gene_variant SKCM-US 1 155162036 155162036 single base substitution C T downstream_gene_variant STAD-US 1 155147963 155147963 single base substitution C A exon_variant STAD-US 1 155147963 155147963 single base substitution C A intron_variant STAD-US 1 155147963 155147963 single base substitution C A synonymous_variant A32A 96C>A STAD-US 1 155147963 155147963 single base substitution C A synonymous_variant A55A 165C>A STAD-US 1 155147963 155147963 single base substitution C A synonymous_variant A62A 186C>A STAD-US 1 155148062 155148062 deletion of <=200bp C - exon_variant STAD-US 1 155148062 155148062 deletion of <=200bp C - frameshift_variant S65 STAD-US 1 155148062 155148062 deletion of <=200bp C - frameshift_variant S88 STAD-US 1 155148062 155148062 deletion of <=200bp C - frameshift_variant S95 STAD-US 1 155148062 155148062 deletion of <=200bp C - intron_variant STAD-US 1 155148109 155148109 single base substitution G A exon_variant STAD-US 1 155148109 155148109 single base substitution G A intron_variant STAD-US 1 155148109 155148109 single base substitution G A missense_variant R104Q 311G>A STAD-US 1 155148109 155148109 single base substitution G A missense_variant R111Q 332G>A STAD-US 1 155148109 155148109 single base substitution G A missense_variant R81Q 242G>A STAD-US 1 155149471 155149471 single base substitution G T exon_variant STAD-US 1 155149471 155149471 single base substitution G T missense_variant V119L 355G>T STAD-US 1 155149471 155149471 single base substitution G T missense_variant V222L 664G>T STAD-US 1 155149471 155149471 single base substitution G T missense_variant V245L 733G>T STAD-US 1 155149471 155149471 single base substitution G T missense_variant V252L 754G>T STAD-US 1 155150501 155150501 deletion of <=200bp G - exon_variant STAD-US 1 155150501 155150501 deletion of <=200bp G - frameshift_variant E185 STAD-US 1 155150501 155150501 deletion of <=200bp G - frameshift_variant E288 STAD-US 1 155150501 155150501 deletion of <=200bp G - frameshift_variant E311 STAD-US 1 155150501 155150501 deletion of <=200bp G - frameshift_variant E318 STAD-US 1 155150709 155150709 single base substitution G A downstream_gene_variant STAD-US 1 155150709 155150709 single base substitution G A exon_variant STAD-US 1 155150709 155150709 single base substitution G A missense_variant A255T 763G>A STAD-US 1 155150709 155150709 single base substitution G A missense_variant A358T 1072G>A STAD-US 1 155150709 155150709 single base substitution G A missense_variant A381T 1141G>A STAD-US 1 155150709 155150709 single base substitution G A missense_variant A388T 1162G>A STAD-US 1 155152112 155152112 single base substitution T C downstream_gene_variant STAD-US 1 155152112 155152112 single base substitution T C exon_variant STAD-US 1 155152112 155152112 single base substitution T C missense_variant L443P 1328T>C STAD-US 1 155152112 155152112 single base substitution T C missense_variant L450P 1349T>C STAD-US 1 155152112 155152112 single base substitution T C synonymous_variant P304P 912T>C STAD-US 1 155152112 155152112 single base substitution T C synonymous_variant P407P 1221T>C STAD-US 1 155152112 155152112 single base substitution T C synonymous_variant P430P 1290T>C STAD-US 1 155152138 155152138 single base substitution G A downstream_gene_variant STAD-US 1 155152138 155152138 single base substitution G A exon_variant STAD-US 1 155152138 155152138 single base substitution G A missense_variant A452T 1354G>A STAD-US 1 155152138 155152138 single base substitution G A missense_variant A459T 1375G>A STAD-US 1 155152138 155152138 single base substitution G A missense_variant R313H 938G>A STAD-US 1 155152138 155152138 single base substitution G A missense_variant R416H 1247G>A STAD-US 1 155152138 155152138 single base substitution G A missense_variant R439H 1316G>A STAD-US 1 155152179 155152179 deletion of <=200bp C - downstream_gene_variant STAD-US 1 155152179 155152179 deletion of <=200bp C - exon_variant STAD-US 1 155152179 155152179 deletion of <=200bp C - frameshift_variant C465 STAD-US 1 155152179 155152179 deletion of <=200bp C - frameshift_variant C472 STAD-US 1 155152179 155152179 deletion of <=200bp C - frameshift_variant P327 STAD-US 1 155152179 155152179 deletion of <=200bp C - frameshift_variant P430 STAD-US 1 155152179 155152179 deletion of <=200bp C - frameshift_variant P453 STAD-US 1 155152179 155152179 insertion of <=200bp - C downstream_gene_variant STAD-US 1 155152179 155152179 insertion of <=200bp - C exon_variant STAD-US 1 155152179 155152179 insertion of <=200bp - C frameshift_variant C465C? STAD-US 1 155152179 155152179 insertion of <=200bp - C frameshift_variant C472C? STAD-US 1 155152179 155152179 insertion of <=200bp - C frameshift_variant P327P? STAD-US 1 155152179 155152179 insertion of <=200bp - C frameshift_variant P430P? STAD-US 1 155152179 155152179 insertion of <=200bp - C frameshift_variant P453P? STAD-US 1 155154445 155154445 single base substitution G A 3_prime_UTR_variant STAD-US 1 155154445 155154445 single base substitution G A downstream_gene_variant STAD-US 1 155154445 155154445 single base substitution G A exon_variant STAD-US 1 155154445 155154445 single base substitution G A missense_variant R443Q 1328G>A STAD-US 1 155154445 155154445 single base substitution G A missense_variant R546Q 1637G>A STAD-US 1 155154445 155154445 single base substitution G A missense_variant R569Q 1706G>A STAD-US 1 155154492 155154492 single base substitution G A 3_prime_UTR_variant STAD-US 1 155154492 155154492 single base substitution G A downstream_gene_variant STAD-US 1 155154492 155154492 single base substitution G A exon_variant STAD-US 1 155154492 155154492 single base substitution G A missense_variant V459M 1375G>A STAD-US 1 155154492 155154492 single base substitution G A missense_variant V562M 1684G>A STAD-US 1 155154492 155154492 single base substitution G A missense_variant V585M 1753G>A STAD-US 1 155154563 155154563 single base substitution C T 3_prime_UTR_variant STAD-US 1 155154563 155154563 single base substitution C T downstream_gene_variant STAD-US 1 155154563 155154563 single base substitution C T exon_variant STAD-US 1 155154563 155154563 single base substitution C T synonymous_variant G482G 1446C>T STAD-US 1 155154563 155154563 single base substitution C T synonymous_variant G585G 1755C>T STAD-US 1 155154563 155154563 single base substitution C T synonymous_variant G608G 1824C>T STAD-US 1 155154567 155154567 single base substitution G A 3_prime_UTR_variant STAD-US 1 155154567 155154567 single base substitution G A downstream_gene_variant STAD-US 1 155154567 155154567 single base substitution G A exon_variant STAD-US 1 155154567 155154567 single base substitution G A missense_variant G484R 1450G>A STAD-US 1 155154567 155154567 single base substitution G A missense_variant G587R 1759G>A STAD-US 1 155154567 155154567 single base substitution G A missense_variant G610R 1828G>A STAD-US 1 155156381 155156381 single base substitution G A 3_prime_UTR_variant STAD-US 1 155156381 155156381 single base substitution G A downstream_gene_variant STAD-US 1 155156381 155156381 single base substitution G A exon_variant STAD-US 1 155156381 155156381 single base substitution G A synonymous_variant S539S 1617G>A STAD-US 1 155156381 155156381 single base substitution G A synonymous_variant S642S 1926G>A STAD-US 1 155156381 155156381 single base substitution G A synonymous_variant S665S 1995G>A STAD-US 1 155160514 155160514 single base substitution C T downstream_gene_variant STAD-US 1 155160774 155160774 single base substitution G T downstream_gene_variant STAD-US 1 155161799 155161799 single base substitution T G downstream_gene_variant STAD-US 1 155161828 155161828 single base substitution G A downstream_gene_variant THCA-SA 1 155161711 155161711 single base substitution G T downstream_gene_variant THCA-US 1 155147749 155147749 single base substitution G A intron_variant THCA-US 1 155147749 155147749 single base substitution G A splice_donor_variant THCA-US 1 155149705 155149705 single base substitution G A exon_variant THCA-US 1 155149705 155149705 single base substitution G A missense_variant G157E 470G>A THCA-US 1 155149705 155149705 single base substitution G A missense_variant G260E 779G>A THCA-US 1 155149705 155149705 single base substitution G A missense_variant G283E 848G>A THCA-US 1 155149705 155149705 single base substitution G A missense_variant G290E 869G>A THCA-US 1 155156425 155156425 single base substitution C T 3_prime_UTR_variant THCA-US 1 155156425 155156425 single base substitution C T downstream_gene_variant THCA-US 1 155156425 155156425 single base substitution C T exon_variant THCA-US 1 155156425 155156425 single base substitution C T missense_variant T554I 1661C>T THCA-US 1 155156425 155156425 single base substitution C T missense_variant T657I 1970C>T THCA-US 1 155156425 155156425 single base substitution C T missense_variant T680I 2039C>T UCEC-US 1 155141923 155141923 single base substitution C T upstream_gene_variant UCEC-US 1 155145054 155145054 single base substitution C A upstream_gene_variant UCEC-US 1 155145087 155145087 single base substitution C A upstream_gene_variant UCEC-US 1 155145239 155145239 single base substitution G A upstream_gene_variant UCEC-US 1 155148067 155148067 single base substitution G T exon_variant UCEC-US 1 155148067 155148067 single base substitution G T intron_variant UCEC-US 1 155148067 155148067 single base substitution G T missense_variant R67L 200G>T UCEC-US 1 155148067 155148067 single base substitution G T missense_variant R90L 269G>T UCEC-US 1 155148067 155148067 single base substitution G T missense_variant R97L 290G>T UCEC-US 1 155148678 155148678 single base substitution A G exon_variant UCEC-US 1 155148678 155148678 single base substitution A G missense_variant T191A 571A>G UCEC-US 1 155148678 155148678 single base substitution A G missense_variant T214A 640A>G UCEC-US 1 155148678 155148678 single base substitution A G missense_variant T221A 661A>G UCEC-US 1 155148678 155148678 single base substitution A G missense_variant T88A 262A>G UCEC-US 1 155150601 155150601 single base substitution C T exon_variant UCEC-US 1 155150601 155150601 single base substitution C T missense_variant R219C 655C>T UCEC-US 1 155150601 155150601 single base substitution C T missense_variant R322C 964C>T UCEC-US 1 155150601 155150601 single base substitution C T missense_variant R345C 1033C>T UCEC-US 1 155150601 155150601 single base substitution C T missense_variant R352C 1054C>T UCEC-US 1 155150626 155150626 single base substitution A G exon_variant UCEC-US 1 155150626 155150626 single base substitution A G missense_variant H227R 680A>G UCEC-US 1 155150626 155150626 single base substitution A G missense_variant H330R 989A>G UCEC-US 1 155150626 155150626 single base substitution A G missense_variant H353R 1058A>G UCEC-US 1 155150626 155150626 single base substitution A G missense_variant H360R 1079A>G UCEC-US 1 155150701 155150701 single base substitution T G downstream_gene_variant UCEC-US 1 155150701 155150701 single base substitution T G exon_variant UCEC-US 1 155150701 155150701 single base substitution T G missense_variant F252C 755T>G UCEC-US 1 155150701 155150701 single base substitution T G missense_variant F355C 1064T>G UCEC-US 1 155150701 155150701 single base substitution T G missense_variant F378C 1133T>G UCEC-US 1 155150701 155150701 single base substitution T G missense_variant F385C 1154T>G UCEC-US 1 155151011 155151011 single base substitution G A downstream_gene_variant UCEC-US 1 155151011 155151011 single base substitution G A exon_variant UCEC-US 1 155151011 155151011 single base substitution G A missense_variant A277T 829G>A UCEC-US 1 155151011 155151011 single base substitution G A missense_variant A380T 1138G>A UCEC-US 1 155151011 155151011 single base substitution G A missense_variant A403T 1207G>A UCEC-US 1 155151011 155151011 single base substitution G A missense_variant A410T 1228G>A UCEC-US 1 155152380 155152380 single base substitution G C 3_prime_UTR_variant UCEC-US 1 155152380 155152380 single base substitution G C downstream_gene_variant UCEC-US 1 155152380 155152380 single base substitution G C exon_variant UCEC-US 1 155152380 155152380 single base substitution G C missense_variant D394H 1180G>C UCEC-US 1 155152380 155152380 single base substitution G C missense_variant D497H 1489G>C UCEC-US 1 155152380 155152380 single base substitution G C missense_variant D520H 1558G>C UCEC-US 1 155156430 155156430 single base substitution G A 3_prime_UTR_variant UCEC-US 1 155156430 155156430 single base substitution G A downstream_gene_variant UCEC-US 1 155156430 155156430 single base substitution G A exon_variant UCEC-US 1 155156430 155156430 single base substitution G A missense_variant G556S 1666G>A UCEC-US 1 155156430 155156430 single base substitution G A missense_variant G659S 1975G>A UCEC-US 1 155156430 155156430 single base substitution G A missense_variant G682S 2044G>A UCEC-US 1 155156517 155156517 single base substitution C A 3_prime_UTR_variant UCEC-US 1 155156517 155156517 single base substitution C A downstream_gene_variant UCEC-US 1 155156517 155156517 single base substitution C A exon_variant UCEC-US 1 155156517 155156517 single base substitution C A missense_variant R585S 1753C>A UCEC-US 1 155156517 155156517 single base substitution C A missense_variant R688S 2062C>A UCEC-US 1 155156517 155156517 single base substitution C A missense_variant R711S 2131C>A UCEC-US 1 155156524 155156524 single base substitution T G 3_prime_UTR_variant UCEC-US 1 155156524 155156524 single base substitution T G downstream_gene_variant UCEC-US 1 155156524 155156524 single base substitution T G exon_variant UCEC-US 1 155156524 155156524 single base substitution T G missense_variant L587R 1760T>G UCEC-US 1 155156524 155156524 single base substitution T G missense_variant L690R 2069T>G UCEC-US 1 155156524 155156524 single base substitution T G missense_variant L713R 2138T>G UCEC-US 1 155158646 155158646 single base substitution T G downstream_gene_variant UCEC-US 1 155160214 155160214 single base substitution C T downstream_gene_variant UCEC-US 1 155161969 155161969 single base substitution C T downstream_gene_variant UCEC-US 1 155162101 155162101 single base substitution G T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PACA73 COSM1158346 c.1083T>C p.G361G Substitution - coding silent 1:155178175-155178175 + YUOMEGA COSM5377819 c.1435C>T p.R479C Substitution - Missense 1:155179781-155179781 + TCGA-FW-A3R5-06 COSM3862905 c.353G>A p.R118Q Substitution - Missense 1:155175915-155175915 + TCGA-EE-A2GR-06 COSM3474868 c.1388C>T p.T463I Substitution - Missense 1:155179734-155179734 + UM-SCC-17B COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + RK228_C01 COSM4780321 c.1972A>G p.M658V Substitution - Missense 1:155183882-155183882 + LOVO COSM1334566 c.1357delC p.H455fs*32 Deletion - Frameshift 1:155179703-155179703 + sysucc-274T COSM5475529 c.464G>A p.R155H Substitution - Missense 1:155176026-155176026 + S02351 COSM5694923 c.1396T>C p.F466L Substitution - Missense 1:155179742-155179742 + HCC47 COSM1600907 c.1579C>T p.P527S Substitution - Missense 1:155179925-155179925 + TCGA-BW-A5NQ-01 COSM4911880 c.625G>T p.A209S Substitution - Missense 1:155176187-155176187 + TCGA-AY-6197-01 COSM1334564 c.1282C>T p.R428* Substitution - Nonsense 1:155178610-155178610 + WA37 COSM238347 c.1692G>C p.L564L Substitution - coding silent 1:155181955-155181955 + TCGA-EA-A3HT-01 COSM4843340 c.579C>T p.F193F Substitution - coding silent 1:155176141-155176141 + CSCC-27-T COSM4475364 c.1983C>T p.I661I Substitution - coding silent 1:155183893-155183893 + TCGA-AA-3715-01 COSM270395 c.706C>A p.H236N Substitution - Missense 1:155176968-155176968 + HCC118T COSM5813666 c.2205A>T p.A735A Substitution - coding silent 1:155184115-155184115 + WSU-HN13 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + HCC47T COSM1600907 c.1579C>T p.P527S Substitution - Missense 1:155179925-155179925 + HCC143T COSM1600906 c.1069C>T p.L357L Substitution - coding silent 1:155178161-155178161 + TCGA-BH-A18G-01 COSM3802093 c.1903G>T p.G635W Substitution - Missense 1:155183813-155183813 + T55 COSM4736119 c.1915G>A p.G639S Substitution - Missense 1:155183825-155183825 + TCGA-56-6545-01 COSM675800 c.562G>A p.E188K Substitution - Missense 1:155176124-155176124 + 2492722 COSM5719367 c.1225C>T p.H409Y Substitution - Missense 1:155178553-155178553 + TCGA-EM-A1YB-01 COSM3369315 c.848G>A p.G283E Substitution - Missense 1:155177229-155177229 + TCGA-EM-A22N-01 COSM3369316 c.2039C>T p.T680I Substitution - Missense 1:155183949-155183949 + CACO2 COSM2209964 c.402A>C p.Q134H Substitution - Missense 1:155175964-155175964 + 2492720 COSM5719367 c.1225C>T p.H409Y Substitution - Missense 1:155178553-155178553 + TCGA-AP-A051-01 COSM896781 c.269G>T p.R90L Substitution - Missense 1:155175591-155175591 + TCGA-DK-A3X1-01 COSM3788772 c.697G>A p.E233K Substitution - Missense 1:155176959-155176959 + HCT15 COSM2209963 c.394G>T p.A132S Substitution - Missense 1:155175956-155175956 + TCGA-13-0755-01 COSM76822 c.1765C>G p.Q589E Substitution - Missense 1:155182028-155182028 + TCGA-E2-A159-01 COSM424031 c.1092C>G p.G364G Substitution - coding silent 1:155178184-155178184 + T2932 COSM4736118 c.1292A>G p.E431G Substitution - Missense 1:155179638-155179638 + TCGA-CM-5861-01 COSM1230343 c.1825G>A p.V609I Substitution - Missense 1:155182088-155182088 + pfg212T COSM4762976 c.754C>T p.R252W Substitution - Missense 1:155177016-155177016 + TCGA-ER-A19D-06 COSM3474864 c.900G>A p.R300R Substitution - coding silent 1:155177281-155177281 + TCGA-AD-6964-01 COSM1334563 c.934G>T p.E312* Substitution - Nonsense 1:155178026-155178026 + BN01T COSM1600905 c.259C>T p.R87C Substitution - Missense 1:155175581-155175581 + TCGA-CD-A4MG-01 COSM4022948 c.1995G>A p.S665S Substitution - coding silent 1:155183905-155183905 + OSCC-GB_00610111 COSM4886889 c.114G>T p.E38D Substitution - Missense 1:155175436-155175436 + TCGA-FS-A1ZQ-06 COSM3474872 c.2126C>T p.S709F Substitution - Missense 1:155184036-155184036 + YUMER COSM1688704 c.1217C>T p.S406F Substitution - Missense 1:155178545-155178545 + TCGA-FW-A3TU-06 COSM3474862 c.627C>T p.A209A Substitution - coding silent 1:155176189-155176189 + TCGA-AP-A059-01 COSM896787 c.1207G>A p.A403T Substitution - Missense 1:155178535-155178535 + TCGA-CD-A4MG-01 COSM4022940 c.733G>T p.V245L Substitution - Missense 1:155176995-155176995 + T2940 COSM4736116 c.256A>G p.T86A Substitution - Missense 1:155175578-155175578 + HT115 COSM4638118 c.2193C>T p.I731I Substitution - coding silent 1:155184103-155184103 + TCGA-AO-A128-01 COSM3802087 c.542A>G p.E181G Substitution - Missense 1:155176104-155176104 + KPOPBR-39-T COSM5964528 c.1002C>T p.A334A Substitution - coding silent 1:155178094-155178094 + PD13418a COSM2209990 c.1521C>T p.R507R Substitution - coding silent 1:155179867-155179867 + 8013014 COSM3385228 c.844C>G p.L282V Substitution - Missense 1:155177225-155177225 + TCGA-EB-A5SE-01 COSM3474869 c.1928C>T p.A643V Substitution - Missense 1:155183838-155183838 + YUWAND COSM1688703 c.994C>T p.L332F Substitution - Missense 1:155178086-155178086 + 2290929 COSM4439797 c.310C>T p.R104W Substitution - Missense 1:155175632-155175632 + CSCC-7-T COSM4527848 c.1494G>A p.T498T Substitution - coding silent 1:155179840-155179840 + TCGA-AP-A05N-01 COSM896789 c.1627C>T p.R543* Substitution - Nonsense 1:155181890-155181890 + 2492723 COSM5719367 c.1225C>T p.H409Y Substitution - Missense 1:155178553-155178553 + CSCC-27-T COSM4559433 c.804G>A p.Q268Q Substitution - coding silent 1:155177066-155177066 + XHDG27 COSM4769131 c.445C>T p.R149W Substitution - Missense 1:155176007-155176007 + TCGA-AA-3715-01 COSM270394 c.170C>T p.A57V Substitution - Missense 1:155175492-155175492 + LP6005334-DNA_A04 COSM4412294 c.1299C>T p.P433P Substitution - coding silent 1:155179645-155179645 + HN_62854 COSM129899 c.2116G>C p.D706H Substitution - Missense 1:155184026-155184026 + TCGA-06-0749 COSM2151874 c.1451A>G p.E484G Substitution - Missense 1:155179797-155179797 + TCGA-B5-A11N-01 COSM896791 c.2131C>A p.R711S Substitution - Missense 1:155184041-155184041 + CSCC-11-T COSM4470410 c.165C>T p.A55A Substitution - coding silent 1:155175487-155175487 + BICR_22 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + PD4602a COSM165136 c.905C>G p.T302S Substitution - Missense 1:155177286-155177286 + TCGA-A7-A0CE-01 COSM424033 c.1543G>T p.G515C Substitution - Missense 1:155179889-155179889 + DLD1 COSM4622140 c.2226G>A p.V742V Substitution - coding silent 1:155184136-155184136 + TCGA-GU-A42R-01 COSM3788773 c.1749C>T p.G583G Substitution - coding silent 1:155182012-155182012 + TCGA-FS-A1ZF-06 COSM3474867 c.1119A>T p.T373T Substitution - coding silent 1:155178211-155178211 + TCGA-AJ-A23M-01 COSM896788 c.1558G>C p.D520H Substitution - Missense 1:155179904-155179904 + TCGA-BR-4362-01 COSM4022943 c.1316G>A p.R439H Substitution - Missense 1:155179662-155179662 + TCGA-EE-A2MR-06 COSM3474870 c.1953C>T p.F651F Substitution - coding silent 1:155183863-155183863 + Pat_63_B COSM5843858 c.2056C>T p.P686S Substitution - Missense 1:155183966-155183966 + Au3 COSM5602472 c.384C>T p.F128F Substitution - coding silent 1:155175946-155175946 + TCGA-B5-A0JY-01 COSM896786 c.1133T>G p.F378C Substitution - Missense 1:155178225-155178225 + WSU-HN30 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + 2492721 COSM5719367 c.1225C>T p.H409Y Substitution - Missense 1:155178553-155178553 + TCGA-EB-A41B-01 COSM3474861 c.374T>G p.V125G Substitution - Missense 1:155175936-155175936 + TCGA-DK-A1A5-01 COSM414011 c.1445G>A p.R482Q Substitution - Missense 1:155179791-155179791 + TCGA-A8-A09A-01 COSM3802088 c.1056G>A p.E352E Substitution - coding silent 1:155178148-155178148 + 71M COSM5596096 c.1884C>T p.P628P Substitution - coding silent 1:155182147-155182147 + TCGA-BR-6452-01 COSM4022944 c.1706G>A p.R569Q Substitution - Missense 1:155181969-155181969 + CSCC-15-T COSM4471831 c.1743C>T p.V581V Substitution - coding silent 1:155182006-155182006 + 1604875 COSM140962 c.230C>T p.P77L Substitution - Missense 1:155175552-155175552 + ACINAR01 COSM1733429 c.1522G>A p.G508S Substitution - Missense 1:155179868-155179868 + SCC-25 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + BD49T COSM5497577 c.641C>T p.T214I Substitution - Missense 1:155176203-155176203 + TCGA-CA-6717-01 COSM1334567 c.1620C>T p.G540G Substitution - coding silent 1:155181883-155181883 + 8033414 COSM3385229 c.1061G>T p.R354L Substitution - Missense 1:155178153-155178153 + 2492703 COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + 39T COSM3711158 c.873G>T p.Q291H Substitution - Missense 1:155177254-155177254 + TCGA-18-3416-01 COSM675801 c.337T>C p.Y113H Substitution - Missense 1:155175899-155175899 + CSCC-44-T COSM4549267 c.468G>A p.V156V Substitution - coding silent 1:155176030-155176030 + LS180 COSM2209992 c.1576delC p.P527fs*45 Deletion - Frameshift 1:155179922-155179922 + KM12 COSM2209997 c.1875G>A p.V625V Substitution - coding silent 1:155182138-155182138 + TCGA-EB-A3Y7-01 COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + CSCC-31-T COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + WSU-HN8 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + CN-AML-CR-4-Dx COSM5426997 c.1098C>A p.A366A Substitution - coding silent 1:155178190-155178190 + TCGA-FW-A3R5-06 COSM2209977 c.955G>A p.G319R Substitution - Missense 1:155178047-155178047 + TCGA-AA-3845-01 COSM295361 c.2147_2148insC p.L718fs*28 Insertion - Frameshift 1:155184057-155184058 + BD114T COSM5502329 c.414G>A p.E138E Substitution - coding silent 1:155175976-155175976 + 2521243 COSM5886113 c.1164-5C>T p.? Unknown 1:155178487-155178487 + RMS2032 COSM5880573 c.277C>T p.R93C Substitution - Missense 1:155175599-155175599 + TCGA-G7-6790-01 COSM3984289 c.236C>G p.S79C Substitution - Missense 1:155175558-155175558 + CSCC-31-T COSM4518336 c.607_608CC>TT p.P203F Substitution - Missense 1:155176169-155176170 + TCGA-CG-5723-01 COSM4022942 c.1290T>C p.P430P Substitution - coding silent 1:155179636-155179636 + TCGA-AC-A23H-01 COSM3802091 c.1499C>T p.S500F Substitution - Missense 1:155179845-155179845 + TCGA-EE-A181-06 COSM3474874 c.2200G>A p.G734S Substitution - Missense 1:155184110-155184110 + CH-60-T2 COSM5651210 c.1240G>A p.V414M Substitution - Missense 1:155178568-155178568 + 585205 COSM323985 c.82G>T p.E28* Substitution - Nonsense 1:155175404-155175404 + PTC-7C COSM675803 c.269G>A p.R90H Substitution - Missense 1:155175591-155175591 + TCGA-29-2434-01 COSM1319916 c.351G>T p.K117N Substitution - Missense 1:155175913-155175913 + WSU-HN12 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + RW2982 COSM4649467 c.1994C>T p.S665L Substitution - Missense 1:155183904-155183904 + HCC25 COSM1600909 c.1772G>A p.R591H Substitution - Missense 1:155182035-155182035 + 029T COSM1728184 c.949G>T p.V317L Substitution - Missense 1:155178041-155178041 + 2492700 COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + NOKSI COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + TCGA-D3-A51R-06 COSM3474866 c.1088T>A p.V363E Substitution - Missense 1:155178180-155178180 + 2492702 COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + TCGA-39-5029-01 COSM675799 c.2027G>T p.R676M Substitution - Missense 1:155183937-155183937 + 587224 COSM1230344 c.1336A>G p.I446V Substitution - Missense 1:155179682-155179682 + IGROV-1 COSM1668023 c.1919C>T p.A640V Substitution - Missense 1:155183829-155183829 + sysucc-1370T COSM5469637 c.173G>A p.R58Q Substitution - Missense 1:155175495-155175495 + HCC143 COSM1600906 c.1069C>T p.L357L Substitution - coding silent 1:155178161-155178161 + HCC25T COSM1600909 c.1772G>A p.R591H Substitution - Missense 1:155182035-155182035 + CSCC-31-T COSM4478153 c.2214C>T p.L738L Substitution - coding silent 1:155184124-155184124 + WSU-HN30 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + 61 COSM414011 c.1445G>A p.R482Q Substitution - Missense 1:155179791-155179791 + 3N46-VS-3T46 COSM4982444 c.412G>A p.E138K Substitution - Missense 1:155175974-155175974 + CSCC-19-T COSM4472658 c.1799C>T p.P600L Substitution - Missense 1:155182062-155182062 + 264-01-7TD COSM146042 c.1104A>T p.E368D Substitution - Missense 1:155178196-155178196 + HN_62854 COSM129900 c.2239G>C p.E747Q Substitution - Missense 1:155184149-155184149 + TCGA-BR-8487-01 COSM4022941 c.1141G>A p.A381T Substitution - Missense 1:155178233-155178233 + TCGA-FS-A4F0-06 COSM3474860 c.100C>T p.P34S Substitution - Missense 1:155175422-155175422 + HCC078T COSM5806232 c.603C>A p.F201L Substitution - Missense 1:155176165-155176165 + TCGA-B5-A11Y-01 COSM896790 c.2044G>A p.G682S Substitution - Missense 1:155183954-155183954 + TCGA-AM-5821-01 COSM1334562 c.861G>A p.T287T Substitution - coding silent 1:155177242-155177242 + C0077T COSM4140861 c.1184C>A p.A395D Substitution - Missense 1:155178512-155178512 + LUAD-NYU408 COSM373925 c.1963A>C p.T655P Substitution - Missense 1:155183873-155183873 + YUOMEGA COSM5377817 c.1434C>T p.T478T Substitution - coding silent 1:155179780-155179780 + TCGA-06-2569-01 COSM3399794 c.1040G>A p.S347N Substitution - Missense 1:155178132-155178132 + TCGA-FS-A4F5-06 COSM3474871 c.2112C>T p.F704F Substitution - coding silent 1:155184022-155184022 + 90142 COSM330273 c.612G>C p.W204C Substitution - Missense 1:155176174-155176174 + CSCC-17-T COSM108085 c.385C>T p.P129S Substitution - Missense 1:155175947-155175947 + TCGA-BR-6452-01 COSM4022938 c.165C>A p.A55A Substitution - coding silent 1:155175487-155175487 + SCC-15 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + WSU-HN8 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + Pat_31_B COSM5843855 c.253T>A p.S85T Substitution - Missense 1:155175575-155175575 + TCGA-A8-A0A6-01 COSM3802090 c.1318A>C p.T440P Substitution - Missense 1:155179664-155179664 + 2_RESISTANT COSM1723325 c.436delG p.L147fs*5 Deletion - Frameshift 1:155175998-155175998 + LIM2405 COSM1334566 c.1357delC p.H455fs*32 Deletion - Frameshift 1:155179703-155179703 + sysucc-274T COSM5475531 c.603C>T p.F201F Substitution - coding silent 1:155176165-155176165 + TCGA-A8-A07C-01 COSM424034 c.1903G>A p.G635R Substitution - Missense 1:155183813-155183813 + TCGA-EE-A2MC-06 COSM3474873 c.2177C>T p.P726L Substitution - Missense 1:155184087-155184087 + Pat_31_B COSM2209991 c.1546G>A p.E516K Substitution - Missense 1:155179892-155179892 + 93VU147T COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + TCGA-BT-A2LD-01 COSM1230343 c.1825G>A p.V609I Substitution - Missense 1:155182088-155182088 + TCGA-ES-A2HS-01 COSM4910319 c.1633C>T p.R545W Substitution - Missense 1:155181896-155181896 + LU-1991 COSM5613767 c.909G>A p.E303E Substitution - coding silent 1:155177290-155177290 + PT36 COSM5914804 c.1164G>A p.R388R Substitution - coding silent 1:155178492-155178492 + 2492701 COSM3474865 c.931G>A p.E311K Substitution - Missense 1:155178023-155178023 + HCT116 COSM2209984 c.1224C>A p.R408R Substitution - coding silent 1:155178552-155178552 + SC_9034 COSM5565732 c.1060C>A p.R354R Substitution - coding silent 1:155178152-155178152 + WSU-HN13 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + TCGA-CG-4442-01 COSM4022946 c.1824C>T p.G608G Substitution - coding silent 1:155182087-155182087 + TCGA-AY-6196-01 COSM1334568 c.1692G>A p.L564L Substitution - coding silent 1:155181955-155181955 + ESO-135 COSM1268544 c.2194G>T p.G732W Substitution - Missense 1:155184104-155184104 + 264 COSM146042 c.1104A>T p.E368D Substitution - Missense 1:155178196-155178196 + 587238 COSM1230343 c.1825G>A p.V609I Substitution - Missense 1:155182088-155182088 + TCGA-AD-6889-01 COSM1334565 c.1356_1357insC p.H455fs*11 Insertion - Frameshift 1:155179702-155179703 + SCC-25 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + TCGA-D1-A0ZN-01 COSM896784 c.1033C>T p.R345C Substitution - Missense 1:155178125-155178125 + LUAD-NYU704 COSM376155 c.1980G>C p.K660N Substitution - Missense 1:155183890-155183890 + WSU-HN12 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + C0089T COSM4140860 c.411G>A p.V137V Substitution - coding silent 1:155175973-155175973 + TCGA-66-2786-01 COSM675803 c.269G>A p.R90H Substitution - Missense 1:155175591-155175591 + 8057574 COSM3385228 c.844C>G p.L282V Substitution - Missense 1:155177225-155177225 + SS6003314 COSM4127577 c.1436G>T p.R479L Substitution - Missense 1:155179782-155179782 + TCGA-BR-7851-01 COSM4022945 c.1753G>A p.V585M Substitution - Missense 1:155182016-155182016 + CAL27 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + SNUH_G22_S1 COSM3996965 c.1622C>A p.A541E Substitution - Missense 1:155181885-155181885 + TCGA-CG-4300-01 COSM4022947 c.1828G>A p.G610R Substitution - Missense 1:155182091-155182091 + CSCC-29-T COSM4476303 c.2058C>T p.P686P Substitution - coding silent 1:155183968-155183968 + YUHAMA COSM5377821 c.1750G>A p.D584N Substitution - Missense 1:155182013-155182013 + OSCC-GB_00390111 COSM3711158 c.873G>T p.Q291H Substitution - Missense 1:155177254-155177254 + ACINAR01 COSM1733428 c.938T>C p.V313A Substitution - Missense 1:155178030-155178030 + KPOPBR-03-T COSM5965728 c.447G>T p.R149R Substitution - coding silent 1:155176009-155176009 + PT28 COSM5906268 c.2057C>T p.P686L Substitution - Missense 1:155183967-155183967 + TCGA-QU-A6IL-01 COSM4393771 c.153C>T p.N51N Substitution - coding silent 1:155175475-155175475 + CSCC-31-T COSM4486180 c.301C>T p.R101C Substitution - Missense 1:155175623-155175623 + PACA-73-T COSM1158346 c.1083T>C p.G361G Substitution - coding silent 1:155178175-155178175 + Br27P COSM40715 c.2259G>A p.G753G Substitution - coding silent 1:155184169-155184169 + Pat_45_B COSM5843859 c.2141T>G p.L714W Substitution - Missense 1:155184051-155184051 + PCSI_0164_Pa_P_526 COSM3849286 c.1519C>T p.R507C Substitution - Missense 1:155179865-155179865 + CSCC-11-T COSM4548680 c.453G>A p.L151L Substitution - coding silent 1:155176015-155176015 + CSCC-31-T COSM4481963 c.255C>T p.S85S Substitution - coding silent 1:155175577-155175577 + YUOMEGA COSM5377815 c.848G>T p.G283V Substitution - Missense 1:155177229-155177229 + HCT-116 COSM1668022 c.943C>T p.Q315* Substitution - Nonsense 1:155178035-155178035 + TCGA-D1-A101-01 COSM896782 c.631C>T p.H211Y Substitution - Missense 1:155176193-155176193 + UM-SCC-4 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + Pat_41_B COSM5843853 c.146C>T p.T49I Substitution - Missense 1:155175468-155175468 + T26 COSM5341573 c.1606G>A p.D536N Substitution - Missense 1:155181869-155181869 + TCGA-AP-A054-01 COSM896785 c.1058A>G p.H353R Substitution - Missense 1:155178150-155178150 + 3N26-VS-3T26 COSM4980051 c.1761G>A p.V587V Substitution - coding silent 1:155182024-155182024 + LP6005500-DNA_B01 COSM4410004 c.1860G>C p.Q620H Substitution - Missense 1:155182123-155182123 + TCGA-DD-A1EA-01 COSM4920100 c.1285G>T p.V429L Substitution - Missense 1:155178613-155178613 + TCGA-CG-4305-01 COSM4022939 c.311G>A p.R104Q Substitution - Missense 1:155175633-155175633 + HCC111T COSM1600908 c.1716C>T p.T572T Substitution - coding silent 1:155181979-155181979 + T1764 COSM4736117 c.895G>A p.V299M Substitution - Missense 1:155177276-155177276 + Pat_31_A COSM2209991 c.1546G>A p.E516K Substitution - Missense 1:155179892-155179892 + DLD1 COSM2209963 c.394G>T p.A132S Substitution - Missense 1:155175956-155175956 + NOKSI COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + PD7067a COSM5797755 c.894C>G p.A298A Substitution - coding silent 1:155177275-155177275 + KPOPBR-40-T COSM5965916 c.1329T>G p.Y443* Substitution - Nonsense 1:155179675-155179675 + UM-SCC-2 COSM4590233 c.256A>C p.T86P Substitution - Missense 1:155175578-155175578 + TCGA-D3-A1Q5-06 COSM3474863 c.895G>T p.V299L Substitution - Missense 1:155177276-155177276 + UM-SCC-47 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + UM-SCC-2 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + NB2181 COSM5703342 c.1621G>A p.A541T Substitution - Missense 1:155181884-155181884 + ICC012T COSM4439797 c.310C>T p.R104W Substitution - Missense 1:155175632-155175632 + LUAD-F00089 COSM339709 c.1095T>A p.Y365* Substitution - Nonsense 1:155178187-155178187 + TCGA-A8-A08F-01 COSM424032 c.1184delC p.L396fs*23 Deletion - Frameshift 1:155178512-155178512 + LS174T COSM2209992 c.1576delC p.P527fs*45 Deletion - Frameshift 1:155179922-155179922 + Pat_31_A COSM5843855 c.253T>A p.S85T Substitution - Missense 1:155175575-155175575 + 587376 COSM1230346 c.1849G>T p.E617* Substitution - Nonsense 1:155182112-155182112 + 91T COSM108085 c.385C>T p.P129S Substitution - Missense 1:155175947-155175947 + CSCC-31-T COSM4463139 c.1278C>T p.F426F Substitution - coding silent 1:155178606-155178606 + TCGA-AP-A054-01 COSM896783 c.640A>G p.T214A Substitution - Missense 1:155176202-155176202 + LUAD-RT-S01711 COSM380062 c.543G>A p.E181E Substitution - coding silent 1:155176105-155176105 + LOVO COSM2209999 c.1885A>G p.R629G Substitution - Missense 1:155182148-155182148 + ME016T COSM224812 c.1580C>T p.P527L Substitution - Missense 1:155179926-155179926 + HCC111 COSM1600908 c.1716C>T p.T572T Substitution - coding silent 1:155181979-155181979 + TCGA-E2-A1LE-01 COSM3802092 c.1630G>C p.E544Q Substitution - Missense 1:155181893-155181893 + 587278 COSM1230345 c.2131C>T p.R711C Substitution - Missense 1:155184041-155184041 + PCSI_0084_Pa_X COSM2209991 c.1546G>A p.E516K Substitution - Missense 1:155179892-155179892 + SCC-15 COSM4593121 c.247A>C p.T83P Substitution - Missense 1:155175569-155175569 + TCGA-A8-A09A-01 COSM3802089 c.1057C>T p.H353Y Substitution - Missense 1:155178149-155178149 + TCGA-D1-A15X-01 COSM896792 c.2138T>G p.L713R Substitution - Missense 1:155184048-155184048 + pfg065T COSM4762975 c.390C>A p.C130* Substitution - Nonsense 1:155175952-155175952 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.287735 1q22 600986 608618|dbSNP|BC069568|A/G|non-coding||1787|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.H353R c.1058A>G 1 155150626 UCEC A G Missense p.T214A c.640A>G 1 155148678 UCEC A T Missense p.E368D c.1104A>T 1 155150672 CLL A T Missense p.H301L c.902A>T 1 155149759 LUAD A T Synonymous p.T373T c.1119A>T 1 155150687 CM C A Missense p.P228Q c.683C>A 1 155149421 LUAD CC TT Missense p.P628L c.1883_1884delinsTT 1 155154622 CM C - Frameshift p.L396Sfs*23 c.1186delC 1 155150988 BRCA C G Missense p.Q589E c.1765C>G 1 155154504 OV C G Missense p.T302S c.905C>G 1 155149762 BRCA C G Synonymous p.G364G c.1092C>G 1 155150660 BRCA C T Missense p.P527L c.1580C>T 1 155152402 CM C T Missense p.P689L c.2066C>T 1 155156452 LUAD C T Missense p.P726L c.2177C>T 1 155156563 CM C T Missense p.R345C c.1033C>T 1 155150601 UCEC C T Missense p.S703F c.2108C>T 1 155156494 CM C T Missense p.S709F c.2126C>T 1 155156512 CM C T Missense p.T463I c.1388C>T 1 155152210 CM C T Missense p.T680I c.2039C>T 1 155156425 THCA C T Synonymous p.F407F c.1221C>T 1 155151025 CM C T Synonymous p.G515G c.1545C>T 1 155152367 HNSC C T Synonymous p.I731I c.2193C>T 1 155156579 CM C T Synonymous p.N51N c.153C>T 1 155147951 PRAD C T Synonymous p.P689P c.2067C>T 1 155156453 CM G A Missense p.E138K c.412G>A 1 155148450 CM G A Missense p.E188K c.562G>A 1 155148600 LUSC G A Missense p.E747K c.2239G>A 1 155156625 HNSC G A Missense p.G283E c.848G>A 1 155149705 THCA G A Missense p.G515S c.1543G>A 1 155152365 HNSC G A Missense p.G610R c.1828G>A 1 155154567 STAD G A Missense p.G635R c.1903G>A 1 155156289 BRCA G A Missense p.G682S c.2044G>A 1 155156430 UCEC G A Missense p.G734S c.2200G>A 1 155156586 CM G A Missense p.R104Q c.311G>A 1 155148109 STAD G A Missense p.R482Q c.1445G>A 1 155152267 BLCA G A Missense p.R556Q c.1667G>A 1 155154406 CM G A Missense p.R90H c.269G>A 1 155148067 LUSC G A Missense p.S347N c.1040G>A 1 155150608 GBM G A Missense p.V609I c.1825G>A 1 155154564 BLCA G A Synonymous p.E303E c.909G>A 1 155149766 NSCLC G A Synonymous p.G753G c.2259G>A 1 155156645 GBM G A Synonymous p.R300R c.900G>A 1 155149757 CM G C Missense p.D520H c.1558G>C 1 155152380 UCEC G C Missense p.D706H c.2116G>C 1 155156502 HNSC G C Missense p.E747Q c.2239G>C 1 155156625 HNSC - G Frameshift p.A344Gfs*28 c.1030dupG 1 155150597 RCCC GG AA Missense p.D470N c.1407_1408delinsAA 1 155152229 CM G T Missense p.G515C c.1543G>T 1 155152365 BRCA G T Missense p.G732W c.2194G>T 1 155156580 ESCA G T Missense p.R676M c.2027G>T 1 155156413 LUSC G T Missense p.V299L c.895G>T 1 155149752 CM G T Nonsense p.E28* c.82G>T 1 155147880 SCLC T C Missense p.S85P c.253T>C 1 155148051 HNSC T C Missense p.Y113H c.337T>C 1 155148375 LUSC TGGG - IntronicDeletion . c.1589-376_1589-373delTGGG 1 155153952 CLL