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 19 39876663 39876663 + IGR SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr19:39876663C>T BLCA 19 39876761 39876761 + IGR SNP C C G TCGA-CU-A0YO-01A-11D-A10S-08 TCGA-CU-A0YO-10A-01D-A10S-08 g.chr19:39876761C>G BLCA 19 39877398 39877398 + IGR SNP G G A TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr19:39877398G>A BLCA 19 39879228 39879228 + 5'Flank SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:39879228C>T BLCA 19 39879261 39879261 + 5'Flank SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:39879261C>T BLCA 19 39880146 39880146 + 5'Flank SNP C C G TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr19:39880146C>G BLCA 19 39880314 39880314 + 5'Flank SNP G G A TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr19:39880314G>A BRCA 19 39877359 39877359 + IGR SNP A A G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr19:39877359A>G BRCA 19 39880904 39880904 + 5'Flank SNP C C A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr19:39880904C>A CESC 19 39876993 39876993 + IGR SNP C C G TCGA-DG-A2KH-01A-21D-A22X-09 TCGA-DG-A2KH-10A-01D-A22X-09 g.chr19:39876993C>G CESC 19 39877206 39877206 + IGR SNP G G A TCGA-C5-A1BN-01B-11D-A14W-08 TCGA-C5-A1BN-10A-01D-A14W-08 g.chr19:39877206G>A CESC 19 39879479 39879479 + 5'Flank SNP C C T TCGA-LP-A7HU-01A-11D-A33O-09 TCGA-LP-A7HU-10A-01D-A33O-09 g.chr19:39879479C>T CESC 19 39879801 39879801 + 5'Flank SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr19:39879801C>T CESC 19 39880311 39880311 + 5'Flank SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr19:39880311G>C COAD 19 39877361 39877361 + IGR SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr19:39877361G>A COAD 19 39879034 39879034 + Missense_Mutation SNP A A G TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr19:39879034A>G c.931T>C c.(931-933)Tac>Cac p.Y311H COAD 19 39879772 39879772 + 5'Flank SNP G G A TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr19:39879772G>A COAD 19 39879774 39879774 + 5'Flank SNP T T G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:39879774T>G COAD 19 39880316 39880316 + 5'Flank SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr19:39880316G>A COADREAD 19 39877361 39877361 + IGR SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr19:39877361G>A COADREAD 19 39877397 39877397 + IGR SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr19:39877397T>C COADREAD 19 39879034 39879034 + Missense_Mutation SNP A A G TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr19:39879034A>G c.931T>C c.(931-933)Tac>Cac p.Y311H COADREAD 19 39879772 39879772 + 5'Flank SNP G G A TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr19:39879772G>A COADREAD 19 39879774 39879774 + 5'Flank SNP T T G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:39879774T>G COADREAD 19 39880316 39880316 + 5'Flank SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr19:39880316G>A ESCA 19 39876775 39876775 + IGR SNP G G A TCGA-L5-A8NG-01A-11D-A37C-09 TCGA-L5-A8NG-11A-11D-A37F-09 g.chr19:39876775G>A GBMLGG 19 39879756 39879758 + 5'Flank DEL TCT TCT - TCGA-FG-5964-01A-11D-1705-08 TCGA-FG-5964-10A-01D-1705-08 g.chr19:39879756_39879758delTCT GBMLGG 19 39880395 39880395 + 5'Flank SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:39880395G>A GBMLGG 19 39880742 39880742 + 5'Flank SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:39880742G>T HNSC 19 39876966 39876966 + IGR DEL C C - TCGA-CV-7097-01A-11D-2012-08 TCGA-CV-7097-10A-01D-2013-08 g.chr19:39876966delC HNSC 19 39879272 39879272 + 5'Flank SNP A A T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr19:39879272A>T HNSC 19 39879407 39879407 + 5'Flank SNP C C G TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chr19:39879407C>G HNSC 19 39879807 39879807 + 5'Flank SNP C C A TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chr19:39879807C>A HNSC 19 39879970 39879970 + 5'Flank SNP G G A TCGA-CV-7413-01A-11D-2078-08 TCGA-CV-7413-10A-01D-2078-08 g.chr19:39879970G>A HNSC 19 39880374 39880374 + 5'Flank SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr19:39880374C>T HNSC 19 39880712 39880712 + 5'Flank SNP T T C TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr19:39880712T>C HNSC 19 39880720 39880720 + 5'Flank SNP G G A TCGA-CV-5444-01A-02D-1512-08 TCGA-CV-5444-11A-01D-1512-08 g.chr19:39880720G>A KIPAN 19 39876968 39876968 + IGR SNP C C T TCGA-B0-4839-01A-01D-1373-10 TCGA-B0-4839-11A-01D-1373-10 g.chr19:39876968C>T KIPAN 19 39879309 39879309 + 5'Flank SNP T T C TCGA-B1-A47O-01A-11D-A25F-10 TCGA-B1-A47O-10A-01D-A25F-10 g.chr19:39879309T>C KIPAN 19 39880356 39880356 + 5'Flank SNP A A G TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr19:39880356A>G KIPAN 19 39880362 39880362 + 5'Flank SNP G G C TCGA-CJ-4899-01A-01D-1462-08 TCGA-CJ-4899-11A-01D-1462-08 g.chr19:39880362G>C KIRC 19 39876968 39876968 + IGR SNP C C T TCGA-B0-4839-01A-01D-1373-10 TCGA-B0-4839-11A-01D-1373-10 g.chr19:39876968C>T KIRC 19 39880356 39880356 + 5'Flank SNP A A G TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr19:39880356A>G KIRC 19 39880362 39880362 + 5'Flank SNP G G C TCGA-CJ-4899-01A-01D-1462-08 TCGA-CJ-4899-11A-01D-1462-08 g.chr19:39880362G>C KIRP 19 39879309 39879309 + 5'Flank SNP T T C TCGA-B1-A47O-01A-11D-A25F-10 TCGA-B1-A47O-10A-01D-A25F-10 g.chr19:39879309T>C LGG 19 39879756 39879758 + 5'Flank DEL TCT TCT - TCGA-FG-5964-01A-11D-1705-08 TCGA-FG-5964-10A-01D-1705-08 g.chr19:39879756_39879758delTCT LGG 19 39880395 39880395 + 5'Flank SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:39880395G>A LGG 19 39880742 39880742 + 5'Flank SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:39880742G>T LIHC 19 39880716 39880716 + 5'Flank SNP G G T TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr19:39880716G>T LUAD 19 39876663 39876663 + IGR SNP C C T TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr19:39876663C>T LUAD 19 39876822 39876822 + IGR SNP C C T TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr19:39876822C>T LUAD 19 39879075 39879075 + 5'Flank SNP C C A TCGA-67-3773-01A-01D-1040-01 TCGA-67-3773-10A-01D-1489-08 g.chr19:39879075C>A LUAD 19 39879634 39879634 + 5'Flank SNP G G T TCGA-78-7143-01A-11D-2036-08 TCGA-78-7143-10A-01D-2036-08 g.chr19:39879634G>T LUSC 19 39880797 39880797 + 5'Flank SNP C C A TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr19:39880797C>A PAAD 19 39879412 39879412 + 5'Flank SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:39879412C>T PAAD 19 39880299 39880299 + 5'Flank SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:39880299G>T PRAD 19 39876748 39876748 + IGR SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:39876748G>A PRAD 19 39879256 39879256 + 5'Flank SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:39879256C>T PRAD 19 39879989 39879989 + 5'Flank SNP G G A TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr19:39879989G>A READ 19 39877397 39877397 + IGR SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr19:39877397T>C SARC 19 39880307 39880307 + 5'Flank SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr19:39880307G>A SKCM 19 39876822 39876822 + IGR SNP C C A TCGA-D3-A1Q8-06A-11D-A19A-08 TCGA-D3-A1Q8-10A-01D-A19A-08 g.chr19:39876822C>A SKCM 19 39877418 39877418 + IGR SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr19:39877418C>T SKCM 19 39879204 39879204 + 5'Flank SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr19:39879204C>T SKCM 19 39879777 39879777 + 5'Flank SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:39879777G>A SKCM 19 39879778 39879778 + 5'Flank SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:39879778G>A SKCM 19 39879936 39879936 + 5'Flank SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr19:39879936C>T SKCM 19 39880154 39880154 + 5'Flank SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr19:39880154C>T BLCA 8 77895784 77895784 + Frame_Shift_Del DEL T T - TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr8:77895784delT c.631delA c.(631-633)atcfs p.I211fs BRCA 8 77895511 77895511 + Missense_Mutation SNP C C T TCGA-AO-A0JF-01A-11W-A071-09 TCGA-AO-A0JF-10A-01W-A071-09 g.chr8:77895511C>T c.904G>A c.(904-906)Gta>Ata p.V302I BRCA 8 77895909 77895909 + Missense_Mutation SNP C C T TCGA-A7-A13F-01A-11D-A12Q-09 TCGA-A7-A13F-11A-42D-A12Q-09 g.chr8:77895909C>T c.506G>A c.(505-507)cGt>cAt p.R169H BRCA 8 77896091 77896091 + Silent SNP A A G TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr8:77896091A>G c.324T>C c.(322-324)gtT>gtC p.V108V CESC 8 77895827 77895827 + Silent SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr8:77895827G>C c.588C>G c.(586-588)ctC>ctG p.L196L COAD 8 77895523 77895523 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr8:77895523C>T c.892G>A c.(892-894)Gag>Aag p.E298K COAD 8 77895524 77895524 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr8:77895524G>A c.891C>T c.(889-891)atC>atT p.I297I COAD 8 77895575 77895575 + Silent SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr8:77895575A>G c.840T>C c.(838-840)tgT>tgC p.C280C COAD 8 77895826 77895826 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr8:77895826A>G c.589T>C c.(589-591)Tgg>Cgg p.W197R COAD 8 77895991 77895992 + Frame_Shift_Ins INS - - A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr8:77895991_77895992insA c.423_424insT c.(421-426)tttgtgfs p.V142fs COAD 8 77896008 77896008 + Missense_Mutation SNP T T C TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr8:77896008T>C c.407A>G c.(406-408)aAg>aGg p.K136R COAD 8 77896009 77896009 + Missense_Mutation SNP T T C TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr8:77896009T>C c.406A>G c.(406-408)Aag>Gag p.K136E COAD 8 77896062 77896062 + Missense_Mutation SNP T T G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr8:77896062T>G c.353A>C c.(352-354)gAa>gCa p.E118A COAD 8 77896147 77896147 + Frame_Shift_Del DEL A A - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr8:77896147delA c.268delT c.(268-270)tccfs p.S90fs COAD 8 77896210 77896210 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr8:77896210T>C c.205A>G c.(205-207)Atc>Gtc p.I69V COAD 8 77896405 77896405 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr8:77896405T>C c.10A>G c.(10-12)Aga>Gga p.R4G COADREAD 8 77895523 77895523 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr8:77895523C>T c.892G>A c.(892-894)Gag>Aag p.E298K COADREAD 8 77895524 77895524 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr8:77895524G>A c.891C>T c.(889-891)atC>atT p.I297I COADREAD 8 77895575 77895575 + Silent SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr8:77895575A>G c.840T>C c.(838-840)tgT>tgC p.C280C COADREAD 8 77895826 77895826 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr8:77895826A>G c.589T>C c.(589-591)Tgg>Cgg p.W197R COADREAD 8 77895991 77895992 + Frame_Shift_Ins INS - - A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr8:77895991_77895992insA c.423_424insT c.(421-426)tttgtgfs p.V142fs COADREAD 8 77896008 77896008 + Missense_Mutation SNP T T C TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr8:77896008T>C c.407A>G c.(406-408)aAg>aGg p.K136R COADREAD 8 77896008 77896008 + Missense_Mutation SNP T T C TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr8:77896008T>C c.407A>G c.(406-408)aAg>aGg p.K136R COADREAD 8 77896009 77896009 + Missense_Mutation SNP T T C TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr8:77896009T>C c.406A>G c.(406-408)Aag>Gag p.K136E COADREAD 8 77896062 77896062 + Missense_Mutation SNP T T G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr8:77896062T>G c.353A>C c.(352-354)gAa>gCa p.E118A COADREAD 8 77896147 77896147 + Frame_Shift_Del DEL A A - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr8:77896147delA c.268delT c.(268-270)tccfs p.S90fs COADREAD 8 77896210 77896210 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr8:77896210T>C c.205A>G c.(205-207)Atc>Gtc p.I69V COADREAD 8 77896405 77896405 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr8:77896405T>C c.10A>G c.(10-12)Aga>Gga p.R4G DLBC 8 77896279 77896279 + Missense_Mutation SNP G G A TCGA-FA-A4BB-01A-11D-A31X-10 TCGA-FA-A4BB-10A-01D-A31X-10 g.chr8:77896279G>A c.136C>T c.(136-138)Cct>Tct p.P46S ESCA 8 77895531 77895531 + Nonsense_Mutation SNP G G C TCGA-Q9-A6FU-01A-11D-A31U-09 TCGA-Q9-A6FU-10A-01D-A31U-09 g.chr8:77895531G>C c.884C>G c.(883-885)tCa>tGa p.S295* ESCA 8 77895540 77895540 + Missense_Mutation SNP G G T TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr8:77895540G>T c.875C>A c.(874-876)cCa>cAa p.P292Q ESCA 8 77895549 77895549 + Missense_Mutation SNP C C T TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr8:77895549C>T c.866G>A c.(865-867)aGt>aAt p.S289N ESCA 8 77896250 77896250 + Silent SNP C C T TCGA-IG-A8O2-01A-11D-A36J-09 TCGA-IG-A8O2-10A-01D-A36M-09 g.chr8:77896250C>T c.165G>A c.(163-165)gaG>gaA p.E55E HNSC 8 77895656 77895657 + Frame_Shift_Ins INS - - A TCGA-CV-7415-01A-11D-2078-08 TCGA-CV-7415-10A-01D-2078-08 g.chr8:77895656_77895657insA c.758_759insT c.(757-759)atgfs p.M253fs HNSC 8 77896111 77896111 + Missense_Mutation SNP G G T TCGA-BB-4228-01A-01D-1434-08 TCGA-BB-4228-10A-01D-1434-08 g.chr8:77896111G>T c.304C>A c.(304-306)Caa>Aaa p.Q102K HNSC 8 77896226 77896226 + Silent SNP G G A TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr8:77896226G>A c.189C>T c.(187-189)ttC>ttT p.F63F HNSC 8 77896342 77896342 + Missense_Mutation SNP G G T TCGA-CV-7261-01A-11D-2012-08 TCGA-CV-7261-10A-01D-2013-08 g.chr8:77896342G>T c.73C>A c.(73-75)Cta>Ata p.L25I HNSC 8 77896369 77896369 + Nonsense_Mutation SNP T T A TCGA-CN-6010-01A-11D-1683-08 TCGA-CN-6010-10A-01D-1683-08 g.chr8:77896369T>A c.46A>T c.(46-48)Aga>Tga p.R16* KIPAN 8 77896064 77896064 + Missense_Mutation SNP T T A TCGA-BP-5176-01A-01D-1429-08 TCGA-BP-5176-11A-01D-1429-08 g.chr8:77896064T>A c.351A>T c.(349-351)gaA>gaT p.E117D KIPAN 8 77896129 77896129 + Nonsense_Mutation SNP G G A TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr8:77896129G>A c.286C>T c.(286-288)Cag>Tag p.Q96* KIRC 8 77896064 77896064 + Missense_Mutation SNP T T A TCGA-BP-5176-01A-01D-1429-08 TCGA-BP-5176-11A-01D-1429-08 g.chr8:77896064T>A c.351A>T c.(349-351)gaA>gaT p.E117D KIRP 8 77896129 77896129 + Nonsense_Mutation SNP G G A TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr8:77896129G>A c.286C>T c.(286-288)Cag>Tag p.Q96* LIHC 8 77895734 77895734 + Silent SNP A A T TCGA-LG-A6GG-01A-11D-A30V-10 TCGA-LG-A6GG-10A-01D-A30V-10 g.chr8:77895734A>T c.681T>A c.(679-681)ctT>ctA p.L227L LIHC 8 77895736 77895737 + Missense_Mutation DNP GA GA AT TCGA-LG-A6GG-01A-11D-A30V-10 TCGA-LG-A6GG-10A-01D-A30V-10 g.chr8:77895736_77895737GA>AT c.678_679TC>AT c.(676-681)ccTCtt>ccATtt p.L227F LIHC 8 77895811 77895811 + Missense_Mutation SNP C C T TCGA-DD-A3A8-01A-11D-A22F-10 TCGA-DD-A3A8-11A-11D-A22F-10 g.chr8:77895811C>T c.604G>A c.(604-606)Gaa>Aaa p.E202K LUAD 8 77895554 77895554 + Silent SNP T T G TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr8:77895554T>G c.861A>C c.(859-861)gtA>gtC p.V287V LUAD 8 77895569 77895569 + Missense_Mutation SNP C C A TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chr8:77895569C>A c.846G>T c.(844-846)aaG>aaT p.K282N LUAD 8 77895673 77895673 + Nonsense_Mutation SNP C C A TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr8:77895673C>A c.742G>T c.(742-744)Gga>Tga p.G248* LUAD 8 77895675 77895675 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr8:77895675C>A c.740G>T c.(739-741)tGt>tTt p.C247F LUAD 8 77895700 77895700 + Missense_Mutation SNP T T A TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr8:77895700T>A c.715A>T c.(715-717)Acc>Tcc p.T239S LUAD 8 77895970 77895970 + Missense_Mutation SNP C C A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr8:77895970C>A c.445G>T c.(445-447)Ggt>Tgt p.G149C LUAD 8 77896274 77896274 + Silent SNP C C A TCGA-44-A47A-01A-21D-A24D-08 TCGA-44-A47A-10A-01D-A24F-08 g.chr8:77896274C>A c.141G>T c.(139-141)ggG>ggT p.G47G LUAD 8 77896354 77896354 + Missense_Mutation SNP C C T TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr8:77896354C>T c.61G>A c.(61-63)Gat>Aat p.D21N LUSC 8 77895774 77895774 + Missense_Mutation SNP T T A TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr8:77895774T>A c.641A>T c.(640-642)cAg>cTg p.Q214L LUSC 8 77895842 77895842 + Missense_Mutation SNP C C A TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr8:77895842C>A c.573G>T c.(571-573)atG>atT p.M191I OV 8 77896009 77896009 + Nonsense_Mutation SNP T T A TCGA-13-1495-01A-01W-0545-08 TCGA-13-1495-10A-01D-0472-08 g.chr8:77896009T>A c.406A>T c.(406-408)Aag>Tag p.K136* PRAD 8 77895648 77895648 + Missense_Mutation SNP G G A TCGA-YL-A8HM-01A-11D-A364-08 TCGA-YL-A8HM-10A-01D-A362-08 g.chr8:77895648G>A c.767C>T c.(766-768)aCc>aTc p.T256I PRAD 8 77895775 77895775 + Nonsense_Mutation SNP G G A TCGA-J9-A52B-01A-11D-A26M-08 TCGA-J9-A52B-10A-01D-A26K-08 g.chr8:77895775G>A c.640C>T c.(640-642)Cag>Tag p.Q214* READ 8 77896008 77896008 + Missense_Mutation SNP T T C TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr8:77896008T>C c.407A>G c.(406-408)aAg>aGg p.K136R SKCM 8 77895647 77895647 + Silent SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr8:77895647G>A c.768C>T c.(766-768)acC>acT p.T256T SKCM 8 77895753 77895753 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr8:77895753G>A c.662C>T c.(661-663)tCt>tTt p.S221F SKCM 8 77895944 77895944 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr8:77895944G>A c.471C>T c.(469-471)ttC>ttT p.F157F SKCM 8 77896041 77896041 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr8:77896041C>T c.374G>A c.(373-375)cGa>cAa p.R125Q SKCM 8 77896146 77896146 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr8:77896146G>A c.269C>T c.(268-270)tCc>tTc p.S90F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BRCA-EU 8 77888153 77888156 deletion of <=200bp TGGT - downstream_gene_variant BRCA-EU 8 77888438 77888438 single base substitution C T downstream_gene_variant BRCA-EU 8 77889851 77889851 single base substitution G C downstream_gene_variant BRCA-EU 8 77890096 77890099 deletion of <=200bp AGTT - downstream_gene_variant BRCA-EU 8 77890417 77890417 single base substitution T G downstream_gene_variant BRCA-EU 8 77890823 77890823 single base substitution G A downstream_gene_variant BRCA-EU 8 77891885 77891885 single base substitution C T downstream_gene_variant BRCA-EU 8 77892050 77892050 single base substitution C T downstream_gene_variant BRCA-EU 8 77893560 77893560 single base substitution T C 3_prime_UTR_variant BRCA-EU 8 77893560 77893560 single base substitution T C downstream_gene_variant BRCA-EU 8 77893997 77893997 insertion of <=200bp - T 3_prime_UTR_variant BRCA-EU 8 77893997 77893997 insertion of <=200bp - T downstream_gene_variant BRCA-EU 8 77894344 77894344 insertion of <=200bp - T 3_prime_UTR_variant BRCA-EU 8 77894344 77894344 insertion of <=200bp - T downstream_gene_variant BRCA-EU 8 77894643 77894643 single base substitution C T 3_prime_UTR_variant BRCA-EU 8 77894643 77894643 single base substitution C T downstream_gene_variant BRCA-EU 8 77895103 77895103 single base substitution A C 3_prime_UTR_variant BRCA-EU 8 77895103 77895103 single base substitution A C downstream_gene_variant BRCA-EU 8 77895683 77895683 single base substitution G A downstream_gene_variant BRCA-EU 8 77895683 77895683 single base substitution G A synonymous_variant C244C 732C>T BRCA-EU 8 77896269 77896269 single base substitution A C downstream_gene_variant BRCA-EU 8 77896269 77896269 single base substitution A C stop_gained L49* 146T>G BRCA-EU 8 77897870 77897870 insertion of <=200bp - A downstream_gene_variant BRCA-EU 8 77897870 77897870 insertion of <=200bp - A intron_variant BRCA-EU 8 77898518 77898518 single base substitution C T 5_prime_UTR_variant BRCA-EU 8 77898518 77898518 single base substitution C T downstream_gene_variant BRCA-EU 8 77898518 77898518 single base substitution C T intron_variant BRCA-EU 8 77899811 77899811 single base substitution G A downstream_gene_variant BRCA-EU 8 77899811 77899811 single base substitution G A intron_variant BRCA-EU 8 77899811 77899811 single base substitution G A upstream_gene_variant BRCA-EU 8 77900738 77900738 deletion of <=200bp A - intron_variant BRCA-EU 8 77900738 77900738 deletion of <=200bp A - upstream_gene_variant BRCA-EU 8 77901927 77901927 single base substitution A T intron_variant BRCA-EU 8 77901927 77901927 single base substitution A T upstream_gene_variant BRCA-EU 8 77903130 77903130 single base substitution A T intron_variant BRCA-EU 8 77903130 77903130 single base substitution A T upstream_gene_variant BRCA-EU 8 77903558 77903558 single base substitution C A intron_variant BRCA-EU 8 77903558 77903558 single base substitution C A upstream_gene_variant BRCA-EU 8 77904193 77904193 single base substitution G A intron_variant BRCA-EU 8 77904531 77904531 single base substitution T A intron_variant BRCA-EU 8 77904700 77904700 single base substitution C A intron_variant BRCA-EU 8 77905871 77905871 single base substitution A T intron_variant BRCA-EU 8 77905880 77905880 single base substitution C T intron_variant BRCA-EU 8 77906841 77906841 single base substitution C G intron_variant BRCA-EU 8 77908193 77908193 single base substitution C G intron_variant BRCA-EU 8 77908586 77908586 single base substitution C T intron_variant BRCA-EU 8 77908715 77908715 single base substitution A G intron_variant BRCA-EU 8 77909384 77909384 single base substitution C T intron_variant BRCA-EU 8 77909640 77909640 single base substitution A G intron_variant BRCA-EU 8 77909674 77909674 single base substitution G T intron_variant BRCA-EU 8 77909863 77909863 single base substitution G A intron_variant BRCA-EU 8 77910082 77910082 single base substitution T C intron_variant BRCA-EU 8 77911595 77911595 single base substitution A C intron_variant BRCA-EU 8 77911905 77911905 single base substitution C A intron_variant BRCA-EU 8 77912583 77912583 single base substitution C T intron_variant BRCA-EU 8 77912583 77912583 single base substitution C T upstream_gene_variant BRCA-EU 8 77913690 77913690 single base substitution A T upstream_gene_variant BRCA-EU 8 77913802 77913802 deletion of <=200bp A - upstream_gene_variant BRCA-EU 8 77913947 77913947 single base substitution G C upstream_gene_variant BRCA-EU 8 77914105 77914105 single base substitution C A upstream_gene_variant BRCA-EU 8 77916219 77916219 single base substitution C G upstream_gene_variant BRCA-EU 8 77916473 77916486 multiple base substitution (>=2bp and <=200bp) TGCTATCTCCTTTC TATTAAA upstream_gene_variant BRCA-EU 8 77916702 77916702 single base substitution T C upstream_gene_variant BRCA-EU 8 77916794 77916794 single base substitution C T upstream_gene_variant BRCA-EU 8 77917097 77917097 single base substitution C G upstream_gene_variant BRCA-EU 8 77917540 77917540 single base substitution G A upstream_gene_variant BRCA-EU 8 77917741 77917741 single base substitution C G upstream_gene_variant BRCA-EU 8 77917935 77917935 single base substitution A C upstream_gene_variant BRCA-EU 8 77918111 77918111 single base substitution C G upstream_gene_variant BRCA-FR 8 77890417 77890417 single base substitution T G downstream_gene_variant BRCA-FR 8 77899676 77899676 single base substitution C T downstream_gene_variant BRCA-FR 8 77899676 77899676 single base substitution C T intron_variant BRCA-FR 8 77899676 77899676 single base substitution C T upstream_gene_variant BRCA-FR 8 77901927 77901927 single base substitution A T intron_variant BRCA-FR 8 77901927 77901927 single base substitution A T upstream_gene_variant BRCA-FR 8 77905871 77905871 single base substitution A T intron_variant BRCA-FR 8 77905880 77905880 single base substitution C T intron_variant BRCA-FR 8 77907843 77907843 single base substitution C G intron_variant BRCA-FR 8 77909384 77909384 single base substitution C T intron_variant BRCA-FR 8 77911905 77911905 single base substitution C A intron_variant BRCA-FR 8 77912583 77912583 single base substitution C T intron_variant BRCA-FR 8 77912583 77912583 single base substitution C T upstream_gene_variant BRCA-FR 8 77916015 77916015 single base substitution G A upstream_gene_variant BRCA-FR 8 77917180 77917180 single base substitution G T upstream_gene_variant BRCA-UK 8 77894643 77894643 single base substitution C T 3_prime_UTR_variant BRCA-UK 8 77894643 77894643 single base substitution C T downstream_gene_variant BRCA-UK 8 77896269 77896269 single base substitution A C downstream_gene_variant BRCA-UK 8 77896269 77896269 single base substitution A C stop_gained L49* 146T>G BRCA-UK 8 77904193 77904193 single base substitution G A intron_variant BRCA-UK 8 77916474 77916486 multiple base substitution (>=2bp and <=200bp) GCTATCTCCTTTC ATTAAA upstream_gene_variant BRCA-US 8 77895511 77895511 single base substitution C T downstream_gene_variant BRCA-US 8 77895511 77895511 single base substitution C T missense_variant V302I 904G>A BRCA-US 8 77895909 77895909 single base substitution C T downstream_gene_variant BRCA-US 8 77895909 77895909 single base substitution C T missense_variant R169H 506G>A BRCA-US 8 77896091 77896091 single base substitution A G downstream_gene_variant BRCA-US 8 77896091 77896091 single base substitution A G synonymous_variant V108V 324T>C BTCA-JP 8 77895466 77895466 deletion of <=200bp T - 3_prime_UTR_variant BTCA-JP 8 77895466 77895466 deletion of <=200bp T - downstream_gene_variant CESC-US 8 77895827 77895827 single base substitution G C downstream_gene_variant CESC-US 8 77895827 77895827 single base substitution G C synonymous_variant L196L 588C>G CESC-US 8 77912230 77912230 single base substitution G T 5_prime_UTR_variant CESC-US 8 77912230 77912230 single base substitution G T exon_variant CLLE-ES 8 77897153 77897153 single base substitution G A downstream_gene_variant CLLE-ES 8 77897153 77897153 single base substitution G A intron_variant CLLE-ES 8 77911403 77911403 single base substitution T C intron_variant CLLE-ES 8 77912416 77912416 single base substitution G T 5_prime_UTR_variant CLLE-ES 8 77912416 77912416 single base substitution G T exon_variant CLLE-ES 8 77912416 77912416 single base substitution G T intron_variant COAD-US 8 77895523 77895523 single base substitution C T downstream_gene_variant COAD-US 8 77895523 77895523 single base substitution C T missense_variant E298K 892G>A COAD-US 8 77895826 77895826 single base substitution A G downstream_gene_variant COAD-US 8 77895826 77895826 single base substitution A G missense_variant W197R 589T>C COAD-US 8 77895991 77895991 insertion of <=200bp - A downstream_gene_variant COAD-US 8 77895991 77895991 insertion of <=200bp - A frameshift_variant V142V? COAD-US 8 77896147 77896147 deletion of <=200bp A - downstream_gene_variant COAD-US 8 77896147 77896147 deletion of <=200bp A - frameshift_variant S90 COAD-US 8 77896210 77896210 single base substitution T C downstream_gene_variant COAD-US 8 77896210 77896210 single base substitution T C missense_variant I69V 205A>G COCA-CN 8 77893588 77893588 single base substitution C A 3_prime_UTR_variant COCA-CN 8 77893588 77893588 single base substitution C A downstream_gene_variant COCA-CN 8 77895833 77895833 single base substitution T C downstream_gene_variant COCA-CN 8 77895833 77895833 single base substitution T C synonymous_variant E194E 582A>G COCA-CN 8 77901916 77901916 single base substitution A G intron_variant COCA-CN 8 77901916 77901916 single base substitution A G upstream_gene_variant COCA-CN 8 77903674 77903674 single base substitution C T intron_variant COCA-CN 8 77903674 77903674 single base substitution C T upstream_gene_variant COCA-CN 8 77912154 77912154 single base substitution G T intron_variant COCA-CN 8 77912887 77912887 single base substitution T A intron_variant COCA-CN 8 77912887 77912887 single base substitution T A upstream_gene_variant EOPC-DE 8 77903757 77903757 single base substitution T C intron_variant EOPC-DE 8 77903757 77903757 single base substitution T C upstream_gene_variant EOPC-DE 8 77914346 77914346 single base substitution C T upstream_gene_variant ESAD-UK 8 77887831 77887831 single base substitution C T downstream_gene_variant ESAD-UK 8 77888936 77888936 single base substitution G A downstream_gene_variant ESAD-UK 8 77889827 77889827 single base substitution C A downstream_gene_variant ESAD-UK 8 77890207 77890207 single base substitution C T downstream_gene_variant ESAD-UK 8 77891665 77891665 single base substitution G A downstream_gene_variant ESAD-UK 8 77892140 77892140 single base substitution C T downstream_gene_variant ESAD-UK 8 77892152 77892152 single base substitution C T downstream_gene_variant ESAD-UK 8 77893522 77893522 single base substitution C T 3_prime_UTR_variant ESAD-UK 8 77893522 77893522 single base substitution C T downstream_gene_variant ESAD-UK 8 77893718 77893718 insertion of <=200bp - ACAC 3_prime_UTR_variant ESAD-UK 8 77893718 77893718 insertion of <=200bp - ACAC downstream_gene_variant ESAD-UK 8 77897158 77897158 single base substitution A G downstream_gene_variant ESAD-UK 8 77897158 77897158 single base substitution A G intron_variant ESAD-UK 8 77897912 77897912 single base substitution C T downstream_gene_variant ESAD-UK 8 77897912 77897912 single base substitution C T intron_variant ESAD-UK 8 77898133 77898133 single base substitution T C downstream_gene_variant ESAD-UK 8 77898133 77898133 single base substitution T C intron_variant ESAD-UK 8 77898441 77898441 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 8 77898441 77898441 single base substitution G A downstream_gene_variant ESAD-UK 8 77898441 77898441 single base substitution G A intron_variant ESAD-UK 8 77901025 77901025 single base substitution C T intron_variant ESAD-UK 8 77901025 77901025 single base substitution C T upstream_gene_variant ESAD-UK 8 77901936 77901936 single base substitution G T intron_variant ESAD-UK 8 77901936 77901936 single base substitution G T upstream_gene_variant ESAD-UK 8 77903241 77903241 single base substitution C T intron_variant ESAD-UK 8 77903241 77903241 single base substitution C T upstream_gene_variant ESAD-UK 8 77903523 77903523 single base substitution C G intron_variant ESAD-UK 8 77903523 77903523 single base substitution C G upstream_gene_variant ESAD-UK 8 77903756 77903756 insertion of <=200bp - T intron_variant ESAD-UK 8 77903756 77903756 insertion of <=200bp - T upstream_gene_variant ESAD-UK 8 77905132 77905132 single base substitution T C intron_variant ESAD-UK 8 77905948 77905948 single base substitution A G intron_variant ESAD-UK 8 77906627 77906627 single base substitution C A intron_variant ESAD-UK 8 77907870 77907870 insertion of <=200bp - T intron_variant ESAD-UK 8 77908784 77908784 single base substitution A C intron_variant ESAD-UK 8 77909587 77909587 single base substitution C A intron_variant ESAD-UK 8 77912608 77912608 single base substitution A T intron_variant ESAD-UK 8 77912608 77912608 single base substitution A T upstream_gene_variant ESAD-UK 8 77912949 77912949 single base substitution C T intron_variant ESAD-UK 8 77912949 77912949 single base substitution C T upstream_gene_variant ESAD-UK 8 77913776 77913776 single base substitution C A upstream_gene_variant ESAD-UK 8 77915482 77915482 single base substitution T A upstream_gene_variant ESAD-UK 8 77915515 77915515 single base substitution G T upstream_gene_variant ESAD-UK 8 77915753 77915753 single base substitution G A upstream_gene_variant ESAD-UK 8 77917049 77917049 single base substitution A T upstream_gene_variant ESAD-UK 8 77917159 77917159 single base substitution C T upstream_gene_variant KIRC-US 8 77896064 77896064 single base substitution T A downstream_gene_variant KIRC-US 8 77896064 77896064 single base substitution T A missense_variant E117D 351A>T LAML-KR 8 77904788 77904788 single base substitution A G intron_variant LICA-CN 8 77895767 77895767 single base substitution C T downstream_gene_variant LICA-CN 8 77895767 77895767 single base substitution C T synonymous_variant L216L 648G>A LICA-FR 8 77893895 77893895 single base substitution T C 3_prime_UTR_variant LICA-FR 8 77893895 77893895 single base substitution T C downstream_gene_variant LICA-FR 8 77895994 77895994 single base substitution A T downstream_gene_variant LICA-FR 8 77895994 77895994 single base substitution A T missense_variant F141I 421T>A LICA-FR 8 77896024 77896024 single base substitution A T downstream_gene_variant LICA-FR 8 77896024 77896024 single base substitution A T missense_variant S131T 391T>A LICA-FR 8 77896233 77896233 single base substitution C T downstream_gene_variant LICA-FR 8 77896233 77896233 single base substitution C T stop_gained W61* 182G>A LICA-FR 8 77899735 77899735 single base substitution T C downstream_gene_variant LICA-FR 8 77899735 77899735 single base substitution T C intron_variant LICA-FR 8 77899735 77899735 single base substitution T C upstream_gene_variant LIHC-US 8 77895734 77895734 single base substitution A T downstream_gene_variant LIHC-US 8 77895734 77895734 single base substitution A T synonymous_variant L227L 681T>A LIHC-US 8 77895736 77895736 single base substitution G A downstream_gene_variant LIHC-US 8 77895736 77895736 single base substitution G A missense_variant L227F 679C>T LIHC-US 8 77895737 77895737 single base substitution A T downstream_gene_variant LIHC-US 8 77895737 77895737 single base substitution A T synonymous_variant P226P 678T>A LIHC-US 8 77895811 77895811 single base substitution C T downstream_gene_variant LIHC-US 8 77895811 77895811 single base substitution C T missense_variant E202K 604G>A LINC-JP 8 77892192 77892192 single base substitution T C downstream_gene_variant LINC-JP 8 77892203 77892203 single base substitution T C downstream_gene_variant LINC-JP 8 77898465 77898465 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 8 77898465 77898465 single base substitution T C downstream_gene_variant LINC-JP 8 77898465 77898465 single base substitution T C intron_variant LINC-JP 8 77904295 77904295 single base substitution C T intron_variant LINC-JP 8 77905528 77905528 single base substitution G A intron_variant LINC-JP 8 77905533 77905533 single base substitution G A intron_variant LINC-JP 8 77913396 77913396 single base substitution G T upstream_gene_variant LIRI-JP 8 77890096 77890099 deletion of <=200bp AGTT - downstream_gene_variant LIRI-JP 8 77890242 77890242 single base substitution C A downstream_gene_variant LIRI-JP 8 77890337 77890337 single base substitution T C downstream_gene_variant LIRI-JP 8 77890966 77890966 single base substitution T C downstream_gene_variant LIRI-JP 8 77892817 77892817 single base substitution T G 3_prime_UTR_variant LIRI-JP 8 77892817 77892817 single base substitution T G downstream_gene_variant LIRI-JP 8 77894683 77894683 single base substitution C T 3_prime_UTR_variant LIRI-JP 8 77894683 77894683 single base substitution C T downstream_gene_variant LIRI-JP 8 77894785 77894785 single base substitution C T 3_prime_UTR_variant LIRI-JP 8 77894785 77894785 single base substitution C T downstream_gene_variant LIRI-JP 8 77895268 77895268 single base substitution T C 3_prime_UTR_variant LIRI-JP 8 77895268 77895268 single base substitution T C downstream_gene_variant LIRI-JP 8 77895325 77895325 single base substitution T C 3_prime_UTR_variant LIRI-JP 8 77895325 77895325 single base substitution T C downstream_gene_variant LIRI-JP 8 77896358 77896358 single base substitution C A downstream_gene_variant LIRI-JP 8 77896358 77896358 single base substitution C A missense_variant Q19H 57G>T LIRI-JP 8 77896431 77896431 single base substitution T G downstream_gene_variant LIRI-JP 8 77896431 77896431 single base substitution T G splice_region_variant LIRI-JP 8 77896835 77896835 single base substitution A C downstream_gene_variant LIRI-JP 8 77896835 77896835 single base substitution A C intron_variant LIRI-JP 8 77897793 77897793 single base substitution C T downstream_gene_variant LIRI-JP 8 77897793 77897793 single base substitution C T intron_variant LIRI-JP 8 77900111 77900111 single base substitution T C downstream_gene_variant LIRI-JP 8 77900111 77900111 single base substitution T C intron_variant LIRI-JP 8 77900111 77900111 single base substitution T C upstream_gene_variant LIRI-JP 8 77900171 77900171 single base substitution G A exon_variant LIRI-JP 8 77900171 77900171 single base substitution G A intron_variant LIRI-JP 8 77900171 77900171 single base substitution G A upstream_gene_variant LIRI-JP 8 77900508 77900508 single base substitution G A exon_variant LIRI-JP 8 77900508 77900508 single base substitution G A intron_variant LIRI-JP 8 77900508 77900508 single base substitution G A upstream_gene_variant LIRI-JP 8 77901332 77901332 single base substitution T A intron_variant LIRI-JP 8 77901332 77901332 single base substitution T A upstream_gene_variant LIRI-JP 8 77901651 77901651 single base substitution T C intron_variant LIRI-JP 8 77901651 77901651 single base substitution T C upstream_gene_variant LIRI-JP 8 77901828 77901828 single base substitution T A intron_variant LIRI-JP 8 77901828 77901828 single base substitution T A upstream_gene_variant LIRI-JP 8 77902510 77902510 single base substitution T G intron_variant LIRI-JP 8 77902510 77902510 single base substitution T G upstream_gene_variant LIRI-JP 8 77903674 77903674 single base substitution C G intron_variant LIRI-JP 8 77903674 77903674 single base substitution C G upstream_gene_variant LIRI-JP 8 77904080 77904080 single base substitution G A intron_variant LIRI-JP 8 77904780 77904780 single base substitution T C intron_variant LIRI-JP 8 77905178 77905178 single base substitution A G intron_variant LIRI-JP 8 77906533 77906533 single base substitution A G intron_variant LIRI-JP 8 77907505 77907505 single base substitution T C intron_variant LIRI-JP 8 77907994 77907994 single base substitution T C intron_variant LIRI-JP 8 77908164 77908164 single base substitution A C intron_variant LIRI-JP 8 77910815 77910815 single base substitution T A intron_variant LIRI-JP 8 77911189 77911199 deletion of <=200bp TTCTATTTTTT - intron_variant LIRI-JP 8 77911363 77911363 single base substitution T C intron_variant LIRI-JP 8 77912523 77912523 single base substitution T G intron_variant LIRI-JP 8 77912523 77912523 single base substitution T G upstream_gene_variant LIRI-JP 8 77914122 77914122 single base substitution A G upstream_gene_variant LIRI-JP 8 77916359 77916359 single base substitution A T upstream_gene_variant LIRI-JP 8 77916837 77916837 single base substitution C T upstream_gene_variant LIRI-JP 8 77917055 77917055 single base substitution A G upstream_gene_variant LIRI-JP 8 77917965 77917965 single base substitution A G upstream_gene_variant LUSC-KR 8 77887983 77887983 single base substitution C A downstream_gene_variant LUSC-KR 8 77888312 77888312 single base substitution C A downstream_gene_variant LUSC-KR 8 77890357 77890357 single base substitution C A downstream_gene_variant LUSC-KR 8 77890814 77890814 single base substitution C T downstream_gene_variant LUSC-KR 8 77893081 77893081 single base substitution T A 3_prime_UTR_variant LUSC-KR 8 77893081 77893081 single base substitution T A downstream_gene_variant LUSC-KR 8 77893090 77893090 single base substitution C A 3_prime_UTR_variant LUSC-KR 8 77893090 77893090 single base substitution C A downstream_gene_variant LUSC-KR 8 77894680 77894680 single base substitution A G 3_prime_UTR_variant LUSC-KR 8 77894680 77894680 single base substitution A G downstream_gene_variant LUSC-KR 8 77894780 77894780 single base substitution G A 3_prime_UTR_variant LUSC-KR 8 77894780 77894780 single base substitution G A downstream_gene_variant LUSC-KR 8 77897075 77897075 single base substitution T C downstream_gene_variant LUSC-KR 8 77897075 77897075 single base substitution T C intron_variant LUSC-KR 8 77897541 77897541 single base substitution G A downstream_gene_variant LUSC-KR 8 77897541 77897541 single base substitution G A intron_variant LUSC-KR 8 77899616 77899616 single base substitution C A downstream_gene_variant LUSC-KR 8 77899616 77899616 single base substitution C A intron_variant LUSC-KR 8 77899616 77899616 single base substitution C A upstream_gene_variant LUSC-KR 8 77900337 77900337 single base substitution C T exon_variant LUSC-KR 8 77900337 77900337 single base substitution C T intron_variant LUSC-KR 8 77900337 77900337 single base substitution C T upstream_gene_variant LUSC-KR 8 77902482 77902482 single base substitution C A intron_variant LUSC-KR 8 77902482 77902482 single base substitution C A upstream_gene_variant LUSC-KR 8 77903422 77903422 single base substitution C A intron_variant LUSC-KR 8 77903422 77903422 single base substitution C A upstream_gene_variant LUSC-KR 8 77904152 77904152 single base substitution A G intron_variant LUSC-KR 8 77909308 77909308 single base substitution C T intron_variant LUSC-KR 8 77910576 77910576 single base substitution A T intron_variant LUSC-KR 8 77910708 77910708 single base substitution T C intron_variant LUSC-KR 8 77911526 77911526 single base substitution A G intron_variant LUSC-KR 8 77912267 77912267 single base substitution C G 5_prime_UTR_variant LUSC-KR 8 77912267 77912267 single base substitution C G exon_variant LUSC-KR 8 77915946 77915946 single base substitution A T upstream_gene_variant LUSC-KR 8 77915947 77915947 single base substitution G T upstream_gene_variant LUSC-KR 8 77917269 77917269 single base substitution T C upstream_gene_variant LUSC-US 8 77895774 77895774 single base substitution T A downstream_gene_variant LUSC-US 8 77895774 77895774 single base substitution T A missense_variant Q214L 641A>T LUSC-US 8 77895842 77895842 single base substitution C A downstream_gene_variant LUSC-US 8 77895842 77895842 single base substitution C A missense_variant M191I 573G>T MALY-DE 8 77888627 77888627 single base substitution T C downstream_gene_variant MALY-DE 8 77896147 77896147 single base substitution A G downstream_gene_variant MALY-DE 8 77896147 77896147 single base substitution A G missense_variant S90P 268T>C MALY-DE 8 77897860 77897860 single base substitution A G downstream_gene_variant MALY-DE 8 77897860 77897860 single base substitution A G intron_variant MALY-DE 8 77905982 77905982 single base substitution A G intron_variant MALY-DE 8 77907950 77907950 single base substitution C T intron_variant MALY-DE 8 77909075 77909075 single base substitution A C intron_variant MALY-DE 8 77909180 77909180 single base substitution G A intron_variant MALY-DE 8 77912192 77912192 single base substitution G T intron_variant MALY-DE 8 77917678 77917678 single base substitution T A upstream_gene_variant MELA-AU 8 77887781 77887781 single base substitution T C downstream_gene_variant MELA-AU 8 77887957 77887957 single base substitution G A downstream_gene_variant MELA-AU 8 77888127 77888127 single base substitution G A downstream_gene_variant MELA-AU 8 77888128 77888128 single base substitution G A downstream_gene_variant MELA-AU 8 77888261 77888261 single base substitution T C downstream_gene_variant MELA-AU 8 77888509 77888509 single base substitution A C downstream_gene_variant MELA-AU 8 77888750 77888750 single base substitution G A downstream_gene_variant MELA-AU 8 77888776 77888776 single base substitution G A downstream_gene_variant MELA-AU 8 77889051 77889051 single base substitution G A downstream_gene_variant MELA-AU 8 77889791 77889791 single base substitution G A downstream_gene_variant MELA-AU 8 77890045 77890045 single base substitution G A downstream_gene_variant MELA-AU 8 77890132 77890132 single base substitution G A downstream_gene_variant MELA-AU 8 77890676 77890676 single base substitution G A downstream_gene_variant MELA-AU 8 77890718 77890718 single base substitution G A downstream_gene_variant MELA-AU 8 77890807 77890807 single base substitution G A downstream_gene_variant MELA-AU 8 77891643 77891643 single base substitution G A downstream_gene_variant MELA-AU 8 77892711 77892711 single base substitution G A 3_prime_UTR_variant MELA-AU 8 77892711 77892711 single base substitution G A downstream_gene_variant MELA-AU 8 77892815 77892815 single base substitution G A 3_prime_UTR_variant MELA-AU 8 77892815 77892815 single base substitution G A downstream_gene_variant MELA-AU 8 77892892 77892892 single base substitution G A 3_prime_UTR_variant MELA-AU 8 77892892 77892892 single base substitution G A downstream_gene_variant MELA-AU 8 77893257 77893257 single base substitution A G 3_prime_UTR_variant MELA-AU 8 77893257 77893257 single base substitution A G downstream_gene_variant MELA-AU 8 77893659 77893659 single base substitution A C 3_prime_UTR_variant MELA-AU 8 77893659 77893659 single base substitution A C downstream_gene_variant MELA-AU 8 77893869 77893869 single base substitution G A 3_prime_UTR_variant MELA-AU 8 77893869 77893869 single base substitution G A downstream_gene_variant MELA-AU 8 77893881 77893881 single base substitution T A 3_prime_UTR_variant MELA-AU 8 77893881 77893881 single base substitution T A downstream_gene_variant MELA-AU 8 77894387 77894387 single base substitution C T 3_prime_UTR_variant MELA-AU 8 77894387 77894387 single base substitution C T downstream_gene_variant MELA-AU 8 77896042 77896042 single base substitution G A downstream_gene_variant MELA-AU 8 77896042 77896042 single base substitution G A stop_gained R125* 373C>T MELA-AU 8 77896653 77896653 single base substitution C T downstream_gene_variant MELA-AU 8 77896653 77896653 single base substitution C T intron_variant MELA-AU 8 77897079 77897079 single base substitution G A downstream_gene_variant MELA-AU 8 77897079 77897079 single base substitution G A intron_variant MELA-AU 8 77897196 77897196 single base substitution G A downstream_gene_variant MELA-AU 8 77897196 77897196 single base substitution G A intron_variant MELA-AU 8 77897669 77897669 single base substitution C T downstream_gene_variant MELA-AU 8 77897669 77897669 single base substitution C T intron_variant MELA-AU 8 77898341 77898341 single base substitution G A downstream_gene_variant MELA-AU 8 77898341 77898341 single base substitution G A intron_variant MELA-AU 8 77898505 77898505 single base substitution G A 5_prime_UTR_variant MELA-AU 8 77898505 77898505 single base substitution G A downstream_gene_variant MELA-AU 8 77898505 77898505 single base substitution G A intron_variant MELA-AU 8 77899474 77899474 single base substitution G A downstream_gene_variant MELA-AU 8 77899474 77899474 single base substitution G A intron_variant MELA-AU 8 77899474 77899474 single base substitution G A upstream_gene_variant MELA-AU 8 77899607 77899607 single base substitution G A downstream_gene_variant MELA-AU 8 77899607 77899607 single base substitution G A intron_variant MELA-AU 8 77899607 77899607 single base substitution G A upstream_gene_variant MELA-AU 8 77899653 77899654 multiple base substitution (>=2bp and <=200bp) AG TA downstream_gene_variant MELA-AU 8 77899653 77899654 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 8 77899653 77899654 multiple base substitution (>=2bp and <=200bp) AG TA upstream_gene_variant MELA-AU 8 77899683 77899683 single base substitution G A downstream_gene_variant MELA-AU 8 77899683 77899683 single base substitution G A intron_variant MELA-AU 8 77899683 77899683 single base substitution G A upstream_gene_variant MELA-AU 8 77900122 77900122 single base substitution T G downstream_gene_variant MELA-AU 8 77900122 77900122 single base substitution T G intron_variant MELA-AU 8 77900122 77900122 single base substitution T G upstream_gene_variant MELA-AU 8 77900143 77900143 single base substitution G A exon_variant MELA-AU 8 77900143 77900143 single base substitution G A intron_variant MELA-AU 8 77900143 77900143 single base substitution G A upstream_gene_variant MELA-AU 8 77900922 77900922 single base substitution A G intron_variant MELA-AU 8 77900922 77900922 single base substitution A G upstream_gene_variant MELA-AU 8 77901988 77901988 single base substitution G A intron_variant MELA-AU 8 77901988 77901988 single base substitution G A upstream_gene_variant MELA-AU 8 77902428 77902428 single base substitution T G intron_variant MELA-AU 8 77902428 77902428 single base substitution T G upstream_gene_variant MELA-AU 8 77902495 77902495 single base substitution G A intron_variant MELA-AU 8 77902495 77902495 single base substitution G A upstream_gene_variant MELA-AU 8 77903483 77903483 single base substitution G A intron_variant MELA-AU 8 77903483 77903483 single base substitution G A upstream_gene_variant MELA-AU 8 77903891 77903891 single base substitution T C intron_variant MELA-AU 8 77905749 77905749 single base substitution G A intron_variant MELA-AU 8 77906137 77906137 single base substitution G C intron_variant MELA-AU 8 77906462 77906462 single base substitution C G intron_variant MELA-AU 8 77906567 77906567 single base substitution G C intron_variant MELA-AU 8 77906698 77906698 single base substitution G A intron_variant MELA-AU 8 77906735 77906735 single base substitution C A intron_variant MELA-AU 8 77908156 77908156 single base substitution G C intron_variant MELA-AU 8 77908164 77908164 single base substitution A C intron_variant MELA-AU 8 77908421 77908421 single base substitution C T intron_variant MELA-AU 8 77908571 77908571 single base substitution T A intron_variant MELA-AU 8 77909461 77909461 single base substitution G A intron_variant MELA-AU 8 77910047 77910047 single base substitution C T intron_variant MELA-AU 8 77910496 77910496 single base substitution G A intron_variant MELA-AU 8 77910882 77910882 single base substitution C T intron_variant MELA-AU 8 77912470 77912470 single base substitution G A 5_prime_UTR_variant MELA-AU 8 77912470 77912470 single base substitution G A intron_variant MELA-AU 8 77912470 77912470 single base substitution G A upstream_gene_variant MELA-AU 8 77913023 77913023 single base substitution C T intron_variant MELA-AU 8 77913023 77913023 single base substitution C T upstream_gene_variant MELA-AU 8 77913957 77913957 single base substitution G A upstream_gene_variant MELA-AU 8 77914083 77914083 single base substitution A G upstream_gene_variant MELA-AU 8 77914190 77914190 single base substitution C T upstream_gene_variant MELA-AU 8 77914252 77914252 single base substitution A T upstream_gene_variant MELA-AU 8 77915568 77915568 single base substitution C T upstream_gene_variant MELA-AU 8 77915837 77915837 single base substitution G T upstream_gene_variant MELA-AU 8 77915963 77915963 single base substitution A G upstream_gene_variant MELA-AU 8 77915963 77915963 single base substitution A T upstream_gene_variant MELA-AU 8 77916183 77916183 single base substitution T G upstream_gene_variant MELA-AU 8 77916719 77916719 single base substitution C T upstream_gene_variant MELA-AU 8 77917013 77917013 single base substitution T G upstream_gene_variant MELA-AU 8 77917288 77917288 single base substitution G A upstream_gene_variant MELA-AU 8 77917836 77917836 single base substitution C T upstream_gene_variant ORCA-IN 8 77892478 77892478 single base substitution C G downstream_gene_variant ORCA-IN 8 77898397 77898397 single base substitution C T downstream_gene_variant ORCA-IN 8 77898397 77898397 single base substitution C T intron_variant ORCA-IN 8 77899907 77899907 single base substitution A G downstream_gene_variant ORCA-IN 8 77899907 77899907 single base substitution A G intron_variant ORCA-IN 8 77899907 77899907 single base substitution A G upstream_gene_variant ORCA-IN 8 77903401 77903402 multiple base substitution (>=2bp and <=200bp) TG GT intron_variant ORCA-IN 8 77903401 77903402 multiple base substitution (>=2bp and <=200bp) TG GT upstream_gene_variant ORCA-IN 8 77910482 77910482 single base substitution C G intron_variant ORCA-IN 8 77912151 77912151 single base substitution C T intron_variant OV-AU 8 77888841 77888841 single base substitution A C downstream_gene_variant OV-AU 8 77892333 77892333 single base substitution C G downstream_gene_variant OV-AU 8 77892619 77892619 single base substitution T A 3_prime_UTR_variant OV-AU 8 77892619 77892619 single base substitution T A downstream_gene_variant OV-AU 8 77892758 77892758 single base substitution A G 3_prime_UTR_variant OV-AU 8 77892758 77892758 single base substitution A G downstream_gene_variant OV-AU 8 77894110 77894110 single base substitution C T 3_prime_UTR_variant OV-AU 8 77894110 77894110 single base substitution C T downstream_gene_variant OV-AU 8 77895179 77895179 single base substitution C G 3_prime_UTR_variant OV-AU 8 77895179 77895179 single base substitution C G downstream_gene_variant OV-AU 8 77896879 77896879 single base substitution T C downstream_gene_variant OV-AU 8 77896879 77896879 single base substitution T C intron_variant OV-AU 8 77897693 77897693 single base substitution C A downstream_gene_variant OV-AU 8 77897693 77897693 single base substitution C A intron_variant OV-AU 8 77902943 77902943 single base substitution A T intron_variant OV-AU 8 77902943 77902943 single base substitution A T upstream_gene_variant OV-AU 8 77906237 77906237 single base substitution T A intron_variant OV-AU 8 77906705 77906705 single base substitution A G intron_variant OV-AU 8 77913631 77913631 single base substitution C T upstream_gene_variant OV-AU 8 77913989 77913989 single base substitution T C upstream_gene_variant OV-AU 8 77915440 77915440 single base substitution G C upstream_gene_variant PACA-AU 8 77887905 77887905 deletion of <=200bp A - downstream_gene_variant PACA-AU 8 77891266 77891266 single base substitution A C downstream_gene_variant PACA-AU 8 77891282 77891282 single base substitution A G downstream_gene_variant PACA-AU 8 77893734 77893734 single base substitution T A 3_prime_UTR_variant PACA-AU 8 77893734 77893734 single base substitution T A downstream_gene_variant PACA-AU 8 77896638 77896638 deletion of <=200bp T - downstream_gene_variant PACA-AU 8 77896638 77896638 deletion of <=200bp T - intron_variant PACA-AU 8 77896994 77896994 single base substitution T A downstream_gene_variant PACA-AU 8 77896994 77896994 single base substitution T A intron_variant PACA-AU 8 77903749 77903749 single base substitution C A intron_variant PACA-AU 8 77903749 77903749 single base substitution C A upstream_gene_variant PACA-AU 8 77908742 77908742 single base substitution C T intron_variant PACA-AU 8 77910572 77910572 single base substitution C T intron_variant PACA-AU 8 77912367 77912367 deletion of <=200bp G - 5_prime_UTR_variant PACA-AU 8 77912367 77912367 deletion of <=200bp G - exon_variant PACA-AU 8 77912367 77912367 deletion of <=200bp G - splice_region_variant PACA-AU 8 77917063 77917063 single base substitution T A upstream_gene_variant PACA-CA 8 77887844 77887844 single base substitution C T downstream_gene_variant PACA-CA 8 77888055 77888055 single base substitution G A downstream_gene_variant PACA-CA 8 77888106 77888106 single base substitution A C downstream_gene_variant PACA-CA 8 77890792 77890792 single base substitution T C downstream_gene_variant PACA-CA 8 77893869 77893869 single base substitution G A 3_prime_UTR_variant PACA-CA 8 77893869 77893869 single base substitution G A downstream_gene_variant PACA-CA 8 77900059 77900059 single base substitution C T downstream_gene_variant PACA-CA 8 77900059 77900059 single base substitution C T intron_variant PACA-CA 8 77900059 77900059 single base substitution C T upstream_gene_variant PACA-CA 8 77900570 77900570 single base substitution G C 5_prime_UTR_variant PACA-CA 8 77900570 77900570 single base substitution G C exon_variant PACA-CA 8 77900570 77900570 single base substitution G C intron_variant PACA-CA 8 77900570 77900570 single base substitution G C upstream_gene_variant PACA-CA 8 77902487 77902487 single base substitution G A intron_variant PACA-CA 8 77902487 77902487 single base substitution G A upstream_gene_variant PACA-CA 8 77903048 77903048 deletion of <=200bp A - intron_variant PACA-CA 8 77903048 77903048 deletion of <=200bp A - upstream_gene_variant PACA-CA 8 77903596 77903596 insertion of <=200bp - T intron_variant PACA-CA 8 77903596 77903596 insertion of <=200bp - T upstream_gene_variant PACA-CA 8 77903607 77903607 insertion of <=200bp - CC intron_variant PACA-CA 8 77903607 77903607 insertion of <=200bp - CC upstream_gene_variant PACA-CA 8 77904345 77904345 single base substitution C T intron_variant PACA-CA 8 77908951 77908951 single base substitution C A intron_variant PACA-CA 8 77914407 77914407 single base substitution C T upstream_gene_variant PACA-CA 8 77916740 77916740 single base substitution G A upstream_gene_variant PAEN-AU 8 77889671 77889671 single base substitution G A downstream_gene_variant PAEN-AU 8 77910708 77910708 single base substitution T C intron_variant PAEN-IT 8 77910573 77910573 single base substitution G A intron_variant PBCA-DE 8 77896324 77896324 single base substitution G A downstream_gene_variant PBCA-DE 8 77896324 77896324 single base substitution G A stop_gained Q31* 91C>T PRAD-CA 8 77892712 77892712 single base substitution G A 3_prime_UTR_variant PRAD-CA 8 77892712 77892712 single base substitution G A downstream_gene_variant PRAD-CA 8 77898212 77898212 single base substitution C T downstream_gene_variant PRAD-CA 8 77898212 77898212 single base substitution C T intron_variant PRAD-CA 8 77905555 77905555 single base substitution C A intron_variant PRAD-UK 8 77889165 77889165 single base substitution A G downstream_gene_variant PRAD-UK 8 77889231 77889231 single base substitution G A downstream_gene_variant PRAD-UK 8 77891424 77891424 single base substitution C T downstream_gene_variant PRAD-UK 8 77896715 77896715 single base substitution C G downstream_gene_variant PRAD-UK 8 77896715 77896715 single base substitution C G intron_variant PRAD-UK 8 77897982 77897982 single base substitution T C downstream_gene_variant PRAD-UK 8 77897982 77897982 single base substitution T C intron_variant PRAD-US 8 77895775 77895775 single base substitution G A downstream_gene_variant PRAD-US 8 77895775 77895775 single base substitution G A stop_gained Q214* 640C>T RECA-EU 8 77887496 77887496 single base substitution A T downstream_gene_variant RECA-EU 8 77901331 77901331 single base substitution C T intron_variant RECA-EU 8 77901331 77901331 single base substitution C T upstream_gene_variant RECA-EU 8 77903058 77903058 single base substitution C T intron_variant RECA-EU 8 77903058 77903058 single base substitution C T upstream_gene_variant RECA-EU 8 77904535 77904535 single base substitution G A intron_variant RECA-EU 8 77910076 77910076 single base substitution C T intron_variant RECA-EU 8 77912098 77912098 single base substitution G T intron_variant RECA-EU 8 77916761 77916761 single base substitution A C upstream_gene_variant SKCA-BR 8 77892817 77892817 single base substitution T G 3_prime_UTR_variant SKCA-BR 8 77892817 77892817 single base substitution T G downstream_gene_variant SKCA-BR 8 77899402 77899402 single base substitution G A downstream_gene_variant SKCA-BR 8 77899402 77899402 single base substitution G A intron_variant SKCA-BR 8 77899402 77899402 single base substitution G A upstream_gene_variant SKCA-BR 8 77899752 77899752 single base substitution C T downstream_gene_variant SKCA-BR 8 77899752 77899752 single base substitution C T intron_variant SKCA-BR 8 77899752 77899752 single base substitution C T upstream_gene_variant SKCA-BR 8 77900603 77900603 single base substitution T A intron_variant SKCA-BR 8 77900603 77900603 single base substitution T A upstream_gene_variant SKCA-BR 8 77900857 77900857 single base substitution T G intron_variant SKCA-BR 8 77900857 77900857 single base substitution T G upstream_gene_variant SKCA-BR 8 77901220 77901220 single base substitution G A intron_variant SKCA-BR 8 77901220 77901220 single base substitution G A upstream_gene_variant SKCA-BR 8 77902510 77902510 single base substitution T G intron_variant SKCA-BR 8 77902510 77902510 single base substitution T G upstream_gene_variant SKCA-BR 8 77908940 77908940 single base substitution C T intron_variant SKCA-BR 8 77915730 77915730 single base substitution C T upstream_gene_variant SKCA-BR 8 77916045 77916045 single base substitution C T upstream_gene_variant SKCA-BR 8 77916482 77916482 single base substitution C T upstream_gene_variant SKCM-US 8 77895647 77895647 single base substitution G A downstream_gene_variant SKCM-US 8 77895647 77895647 single base substitution G A synonymous_variant T256T 768C>T SKCM-US 8 77895753 77895753 single base substitution G A downstream_gene_variant SKCM-US 8 77895753 77895753 single base substitution G A missense_variant S221F 662C>T SKCM-US 8 77895944 77895944 single base substitution G A downstream_gene_variant SKCM-US 8 77895944 77895944 single base substitution G A synonymous_variant F157F 471C>T SKCM-US 8 77896041 77896041 single base substitution C T downstream_gene_variant SKCM-US 8 77896041 77896041 single base substitution C T missense_variant R125Q 374G>A SKCM-US 8 77896063 77896063 single base substitution C T downstream_gene_variant SKCM-US 8 77896063 77896063 single base substitution C T missense_variant E118K 352G>A SKCM-US 8 77896146 77896146 single base substitution G A downstream_gene_variant SKCM-US 8 77896146 77896146 single base substitution G A missense_variant S90F 269C>T STAD-US 8 77895611 77895611 single base substitution A G downstream_gene_variant STAD-US 8 77895611 77895611 single base substitution A G synonymous_variant A268A 804T>C STAD-US 8 77895873 77895873 single base substitution T C downstream_gene_variant STAD-US 8 77895873 77895873 single base substitution T C missense_variant Q181R 542A>G STAD-US 8 77895910 77895910 single base substitution G A downstream_gene_variant STAD-US 8 77895910 77895910 single base substitution G A missense_variant R169C 505C>T STAD-US 8 77896243 77896243 single base substitution C T downstream_gene_variant STAD-US 8 77896243 77896243 single base substitution C T missense_variant A58T 172G>A STAD-US 8 77896329 77896329 single base substitution A G downstream_gene_variant STAD-US 8 77896329 77896329 single base substitution A G missense_variant L29P 86T>C THCA-SA 8 77912230 77912230 single base substitution G T 5_prime_UTR_variant THCA-SA 8 77912230 77912230 single base substitution G T exon_variant UCEC-US 8 77895794 77895794 single base substitution G A downstream_gene_variant UCEC-US 8 77895794 77895794 single base substitution G A synonymous_variant L207L 621C>T UCEC-US 8 77896041 77896041 single base substitution C T downstream_gene_variant UCEC-US 8 77896041 77896041 single base substitution C T missense_variant R125Q 374G>A UCEC-US 8 77896042 77896042 single base substitution G A downstream_gene_variant UCEC-US 8 77896042 77896042 single base substitution G A stop_gained R125* 373C>T UCEC-US 8 77896103 77896103 single base substitution G T downstream_gene_variant UCEC-US 8 77896103 77896103 single base substitution G T synonymous_variant I104I 312C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T1154 COSM4710822 c.1258C>T p.R420W Substitution - Missense 19:39386329-39386329 - TCGA-DD-A3A8-01 COSM4934825 c.604G>A p.E202K Substitution - Missense 8:76983575-76983575 - CHC1148T COSM5348437 c.1219_1220insAG p.G408fs*>125 Insertion - Frameshift 19:39386367-39386368 - LOXIMVI COSM1673979 c.8C>T p.S3F Substitution - Missense 8:76984171-76984171 - TCGA-FW-A3R5-06 COSM1101867 c.374G>A p.R125Q Substitution - Missense 8:76983805-76983805 - QC2-39-T2 COSM5655597 c.311T>G p.I104S Substitution - Missense 8:76983868-76983868 - PCSI_0081_Pa_X COSM3378730 c.986+7A>G p.? Unknown 19:39388332-39388332 - TCGA-CG-4442-01 COSM3901677 c.172G>A p.A58T Substitution - Missense 8:76984007-76984007 - TCGA-CJ-4899-01 COSM474705 c.210C>G p.H70Q Substitution - Missense 19:39389722-39389722 - 2492729 COSM5727173 c.494C>T p.T165I Substitution - Missense 8:76983685-76983685 - TCGA-AA-3492-01 COSM1393538 c.526A>C p.I176L Substitution - Missense 19:39389134-39389134 - T2940 COSM4713663 c.232C>T p.Q78* Substitution - Nonsense 8:76983947-76983947 - TCGA-CU-A0YO-01 COSM418266 c.1466G>C p.G489A Substitution - Missense 19:39386121-39386121 - TCGA-LG-A6GG-01 COSM4939577 c.678T>A p.P226P Substitution - coding silent 8:76983501-76983501 - TCGA-D1-A15X-01 COSM996282 c.32G>T p.R11L Substitution - Missense 19:39390833-39390833 - B55-Tumor COSM3933030 c.1477A>G p.S493G Substitution - Missense 19:39386110-39386110 - T3503 COSM4710820 c.1474C>T p.R492W Substitution - Missense 19:39386113-39386113 - S02352 COSM5695407 c.631A>G p.I211V Substitution - Missense 8:76983548-76983548 - TCGA-D1-A168-01 COSM1101866 c.621C>T p.L207L Substitution - coding silent 8:76983558-76983558 - I2L-P10-Tumor-Organoid COSM5364813 c.253G>A p.D85N Substitution - Missense 19:39389679-39389679 - SNU-175 COSM3223791 c.1524G>A p.E508E Substitution - coding silent 19:39386063-39386063 - SC_9047 COSM2876485 c.781C>T p.H261Y Substitution - Missense 8:76983398-76983398 - PD4107a COSM163412 c.146T>G p.L49* Substitution - Nonsense 8:76984033-76984033 - TCGA-EJ-7782-01 COSM3783238 c.394C>T p.R132* Substitution - Nonsense 19:39389349-39389349 - ESO-0029 COSM1260822 c.282C>T p.I94I Substitution - coding silent 19:39389650-39389650 - SNU-175 COSM3223811 c.917G>A p.G306D Substitution - Missense 19:39388408-39388408 - CHC1747T COSM4788058 c.421T>A p.F141I Substitution - Missense 8:76983758-76983758 - PD9761a COSM5776087 c.267T>C p.P89P Substitution - coding silent 19:39389665-39389665 - HCC142 COSM1612225 c.1442A>C p.D481A Substitution - Missense 19:39386145-39386145 - TCGA-19-2629 COSM2156314 c.222C>G p.L74L Substitution - coding silent 19:39389710-39389710 - TCGA-BH-A0HA-01 COSM454865 c.324T>C p.V108V Substitution - coding silent 8:76983855-76983855 - S02242 COSM3745673 c.57G>T p.Q19H Substitution - Missense 8:76984122-76984122 - TCGA-B5-A11E-01 COSM996274 c.1414G>T p.G472* Substitution - Nonsense 19:39386173-39386173 - TCGA-19-2629 COSM2156280 c.217G>C p.D73H Substitution - Missense 19:39389715-39389715 - TCGA-13-1495-01 COSM79031 c.406A>T p.K136* Substitution - Nonsense 8:76983773-76983773 - TCGA-AO-A0JF-01 COSM454863 c.904G>A p.V302I Substitution - Missense 8:76983275-76983275 - HCC038T COSM5820436 c.1076A>C p.K359T Substitution - Missense 19:39386710-39386710 - T2944 COSM4713662 c.646T>C p.L216L Substitution - coding silent 8:76983533-76983533 - GC_359T-GC_359N COSM4774744 c.1292A>G p.K431R Substitution - Missense 19:39386295-39386295 - CSCC-31-T COSM4504467 c.665C>T p.S222L Substitution - Missense 8:76983514-76983514 - CSCC-38-T COSM4462337 c.1241C>T p.S414L Substitution - Missense 19:39386346-39386346 - LUAD-E00918 COSM365413 c.314G>C p.W105S Substitution - Missense 8:76983865-76983865 - T3021 COSM4710825 c.1039G>A p.A347T Substitution - Missense 19:39386747-39386747 - WA16 COSM241037 c.683delC p.K230fs*11 Deletion - Frameshift 19:39388819-39388819 - A549 COSM1683706 c.1192_1193insAGGAGAAG p.G401fs*>134 Insertion - Frameshift 19:39386394-39386395 - TCGA-19-2629 COSM2156296 c.215A>G p.H72R Substitution - Missense 19:39389717-39389717 - TCGA-GN-A266-06 COSM3651202 c.768C>T p.T256T Substitution - coding silent 8:76983411-76983411 - 10 COSM87803 c.1312G>A p.E438K Substitution - Missense 19:39386275-39386275 - TCGA-AO-A128-01 COSM3378728 c.1067T>C p.M356T Substitution - Missense 19:39386719-39386719 - BCM723T COSM4956450 c.391T>A p.S131T Substitution - Missense 8:76983788-76983788 - TCGA-EY-A1GS-01 COSM996277 c.818G>A p.R273Q Substitution - Missense 19:39388599-39388599 - TCGA-CG-4465-01 COSM4077959 c.741-1G>A p.? Unknown 19:39388677-39388677 - TCGA-A6-5661-01 COSM1458312 c.268delT p.S90fs*4 Deletion - Frameshift 8:76983911-76983911 - PCSI_0090_Pa_P COSM3378728 c.1067T>C p.M356T Substitution - Missense 19:39386719-39386719 - CHC2216T COSM4805963 c.182G>A p.W61* Substitution - Nonsense 8:76983997-76983997 - TCGA-ER-A193-06 COSM3533699 c.853G>A p.D285N Substitution - Missense 19:39388564-39388564 - LUAD-YINHD COSM349577 c.1072G>A p.E358K Substitution - Missense 19:39386714-39386714 - B89-12 COSM1750881 c.1293G>C p.K431N Substitution - Missense 19:39386294-39386294 - CSCC-54-T COSM4526633 c.1408G>A p.D470N Substitution - Missense 19:39386179-39386179 - 2277217 COSM4422903 c.1387G>A p.D463N Substitution - Missense 19:39386200-39386200 - TCGA-LG-A6GG-01 COSM4939371 c.681T>A p.L227L Substitution - coding silent 8:76983498-76983498 - TCGA-AY-6197-01 COSM1458313 c.205A>G p.I69V Substitution - Missense 8:76983974-76983974 - HCC142 COSM1612227 c.1413A>C p.R471S Substitution - Missense 19:39386174-39386174 - LC_S3 COSM1187566 c.635A>G p.N212S Substitution - Missense 8:76983544-76983544 - RKO COSM3223795 c.1423delC p.Q475fs*>57 Deletion - Frameshift 19:39386164-39386164 - HCC142T COSM1612224 c.1446A>G p.S482S Substitution - coding silent 19:39386141-39386141 - Pat_06_B COSM5855717 c.31C>T p.R11W Substitution - Missense 19:39390834-39390834 - TCGA-B1-A47O-01 COSM4908384 c.748A>G p.M250V Substitution - Missense 19:39388669-39388669 - CSCC-54-T COSM3533693 c.1405G>T p.E469* Substitution - Nonsense 19:39386182-39386182 - CSCC-37-T COSM4522151 c.1149G>A p.E383E Substitution - coding silent 19:39386516-39386516 - PT23_1 COSM5902876 c.524C>T p.S175F Substitution - Missense 8:76983655-76983655 - 587238 COSM1219111 c.113G>T p.S38I Substitution - Missense 19:39390126-39390126 - BZ15 COSM5758363 c.431G>C p.G144A Substitution - Missense 8:76983748-76983748 - 587238 COSM1220221 c.851G>A p.G284D Substitution - Missense 8:76983328-76983328 - T3058 COSM4710827 c.373G>A p.A125T Substitution - Missense 19:39389370-39389370 - CSCC-29-T COSM4448929 c.1454delG p.G485fs*>47 Deletion - Frameshift 19:39386133-39386133 - TCGA-HU-A4H8-01 COSM3901676 c.542A>G p.Q181R Substitution - Missense 8:76983637-76983637 - RK122_C01 COSM3745673 c.57G>T p.Q19H Substitution - Missense 8:76984122-76984122 - CN-AML-NR-08-Dx COSM5426128 c.568-8T>C p.? Unknown 19:39389023-39389023 - C0026T COSM4154211 c.568-8T>G p.? Unknown 19:39389023-39389023 - TCGA-B0-5707-01 COSM474704 c.212A>G p.K71R Substitution - Missense 19:39389720-39389720 - TCGA-FS-A1ZZ-06 COSM3533697 c.1008G>A p.R336R Substitution - coding silent 19:39386778-39386778 - 40M COSM5586192 c.136C>T p.P46S Substitution - Missense 8:76984043-76984043 - PD4107a COSM163412 c.146T>G p.L49* Substitution - Nonsense 8:76984033-76984033 - BCM723T COSM4956450 c.391T>A p.S131T Substitution - Missense 8:76983788-76983788 - TCGA-AZ-6598-01 COSM1458309 c.423_424insT p.V142fs*12 Insertion - Frameshift 8:76983755-76983756 - ESCC_45 COSM5630325 c.1579G>A p.D527N Substitution - Missense 19:39386008-39386008 - TCGA-D1-A103-01 COSM996281 c.222C>T p.L74L Substitution - coding silent 19:39389710-39389710 - TCGA-DK-A2I4-01 COSM3797067 c.829G>A p.E277K Substitution - Missense 19:39388588-39388588 - CHC1182T COSM4788742 c.1594T>G p.*532G Nonstop extension 19:39385993-39385993 - TCGA-B0-4839-01 COSM3223800 c.1259G>A p.R420Q Substitution - Missense 19:39386328-39386328 - PCSI_0175_Pa_P_526 COSM4422903 c.1387G>A p.D463N Substitution - Missense 19:39386200-39386200 - TCGA-18-3421-01 COSM711501 c.82G>T p.G28* Substitution - Nonsense 19:39390157-39390157 - MD-319 COSM302851 c.401C>T p.T134I Substitution - Missense 19:39389342-39389342 - PT45 COSM5927515 c.472C>A p.L158I Substitution - Missense 8:76983707-76983707 - TCGA-HU-8602-01 COSM3901675 c.804T>C p.A268A Substitution - coding silent 8:76983375-76983375 - 260211 COSM3725838 c.826G>T p.V276L Substitution - Missense 8:76983353-76983353 - 2492730 COSM5728489 c.1591G>A p.D531N Substitution - Missense 19:39385996-39385996 - CSCC-60-T COSM4446764 c.568-3C>T p.? Unknown 19:39389018-39389018 - PT34 COSM5911038 c.760G>A p.G254R Substitution - Missense 19:39388657-39388657 - TCGA-F4-6570-01 COSM1393536 c.1065C>T p.D355D Substitution - coding silent 19:39386721-39386721 - TCGA-EE-A29D-06 COSM3651204 c.269C>T p.S90F Substitution - Missense 8:76983910-76983910 - TCGA-CG-5721-01 COSM2876494 c.505C>T p.R169C Substitution - Missense 8:76983674-76983674 - TCGA-LP-A7HU-01 COSM4825775 c.663G>A p.V221V Substitution - coding silent 19:39388839-39388839 - TCGA-19-2629 COSM2156313 c.220C>A p.L74I Substitution - Missense 19:39389712-39389712 - 457 COSM4436166 c.1216_1218delAAG p.K406delK Deletion - In frame 19:39386369-39386371 - PD4120a COSM163234 c.445G>A p.E149K Substitution - Missense 19:39389298-39389298 - TCGA-D1-A17H-01 COSM996279 c.602C>T p.P201L Substitution - Missense 19:39388981-39388981 - T70 COSM1177674 c.107A>T p.Q36L Substitution - Missense 8:76984072-76984072 - T3225 COSM4710823 c.1233T>C p.D411D Substitution - coding silent 19:39386354-39386354 - TCGA-DG-A2KH-01 COSM4851283 c.1234G>C p.E412Q Substitution - Missense 19:39386353-39386353 - TCGA-IR-A3LK-01 COSM4817304 c.261C>G p.I87M Substitution - Missense 19:39389671-39389671 - ESCC_BICR_060T COSM5434972 c.1434T>C p.S478S Substitution - coding silent 19:39386153-39386153 - HCC153T COSM5823279 c.648G>A p.L216L Substitution - coding silent 8:76983531-76983531 - SNUH_G76_S1 COSM4417557 c.1492C>T p.R498C Substitution - Missense 19:39386095-39386095 - TCGA-G4-6297-01 COSM3692748 c.609G>T p.E203D Substitution - Missense 19:39388974-39388974 - B100-Tumor COSM3933030 c.1477A>G p.S493G Substitution - Missense 19:39386110-39386110 - TCGA-AX-A0J0-01 COSM1101868 c.373C>T p.R125* Substitution - Nonsense 8:76983806-76983806 - PTC-14C COSM4163081 c.772G>T p.G258* Substitution - Nonsense 8:76983407-76983407 - TCGA-19-2629 COSM2156294 c.214C>A p.H72N Substitution - Missense 19:39389718-39389718 - TCGA-CD-8535-01 COSM4077957 c.1353G>A p.E451E Substitution - coding silent 19:39386234-39386234 - T3658 COSM4710829 c.159C>T p.F53F Substitution - coding silent 19:39390080-39390080 - C84 COSM4620079 c.963T>C p.V321V Substitution - coding silent 19:39388362-39388362 - TCGA-66-2734-01 COSM751674 c.573G>T p.M191I Substitution - Missense 8:76983606-76983606 - PCSI_0081_Pa_P_526 COSM3378730 c.986+7A>G p.? Unknown 19:39388332-39388332 - TCGA-D1-A17Q-01 COSM1101868 c.373C>T p.R125* Substitution - Nonsense 8:76983806-76983806 - CSCC-16-T COSM4543669 c.341G>A p.R114K Substitution - Missense 8:76983838-76983838 - ICGC_MB126 COSM302851 c.401C>T p.T134I Substitution - Missense 19:39389342-39389342 - TCGA-GF-A6C9-06 COSM4902873 c.662C>T p.S221F Substitution - Missense 8:76983517-76983517 - TCGA-37-4135-01 COSM751675 c.641A>T p.Q214L Substitution - Missense 8:76983538-76983538 - HCC142T COSM1612227 c.1413A>C p.R471S Substitution - Missense 19:39386174-39386174 - TCGA-C5-A1BN-01 COSM4837246 c.1099C>T p.R367W Substitution - Missense 19:39386566-39386566 - 40M COSM4788058 c.421T>A p.F141I Substitution - Missense 8:76983758-76983758 - TCGA-D5-6540-01 COSM1458306 c.892G>A p.E298K Substitution - Missense 8:76983287-76983287 - CHC2216T COSM4805963 c.182G>A p.W61* Substitution - Nonsense 8:76983997-76983997 - HCC49T COSM1612228 c.227_230delCTGA p.T76fs*24 Deletion - Frameshift 19:39389702-39389705 - HCC142 COSM1612226 c.1424A>T p.Q475L Substitution - Missense 19:39386163-39386163 - B74-Tumor COSM3933032 c.1467T>G p.G489G Substitution - coding silent 19:39386120-39386120 - TCGA-CM-6171-01 COSM1458308 c.589T>C p.W197R Substitution - Missense 8:76983590-76983590 - B89-12-Tumor COSM1750881 c.1293G>C p.K431N Substitution - Missense 19:39386294-39386294 - TCGA-A3-3357-01 COSM474703 c.216T>C p.H72H Substitution - coding silent 19:39389716-39389716 - TCGA-DK-A2I4-01 COSM3797069 c.796G>A p.E266K Substitution - Missense 19:39388621-39388621 - TCGA-CG-5721-01 COSM4077961 c.711G>A p.A237A Substitution - coding silent 19:39388791-39388791 - LFS_MB3 COSM216112 c.91C>T p.Q31* Substitution - Nonsense 8:76984088-76984088 - 1N31-VS-1T31 COSM4974450 c.312C>T p.I104I Substitution - coding silent 8:76983867-76983867 - Au3 COSM5602066 c.472C>T p.L158F Substitution - Missense 8:76983707-76983707 - TCGA-F5-6814-01 COSM3422791 c.901A>C p.N301H Substitution - Missense 19:39388424-39388424 - TCGA-19-2629 COSM2156281 c.218A>T p.D73V Substitution - Missense 19:39389714-39389714 - TCGA-BR-4361-01 COSM4077958 c.1248C>T p.S416S Substitution - coding silent 19:39386339-39386339 - LUAD-5V8LT COSM403022 c.502G>T p.E168* Substitution - Nonsense 8:76983677-76983677 - TCGA-JX-A3Q0-01 COSM4824828 c.499G>A p.E167K Substitution - Missense 19:39389161-39389161 - C608 COSM4443096 c.5C>A p.A2D Substitution - Missense 8:76984174-76984174 - SNU-C4 COSM4653129 c.525G>A p.Q175Q Substitution - coding silent 19:39389135-39389135 - STC291 COSM5063348 c.596G>T p.G199V Substitution - Missense 8:76983583-76983583 - 44 COSM5734207 c.952G>T p.G318C Substitution - Missense 19:39388373-39388373 - TCGA-CG-4306-01 COSM3901678 c.86T>C p.L29P Substitution - Missense 8:76984093-76984093 - HCC142T COSM1612225 c.1442A>C p.D481A Substitution - Missense 19:39386145-39386145 - TCGA-D3-A51G-06 COSM3533705 c.325G>A p.E109K Substitution - Missense 19:39389514-39389514 - TCGA-D8-A27G-01 COSM3823010 c.73G>T p.E25* Substitution - Nonsense 19:39390264-39390264 - TCGA-Q1-A73O-01 COSM4835263 c.588C>G p.L196L Substitution - coding silent 8:76983591-76983591 - TCGA-19-2629 COSM2156295 c.216T>G p.H72Q Substitution - Missense 19:39389716-39389716 - Pat_06_A COSM5855715 c.520delA p.S174fs*48 Deletion - Frameshift 19:39389140-39389140 - PTC-7C COSM4163082 c.68T>C p.L23P Substitution - Missense 8:76984111-76984111 - S00946 COSM314620 c.128G>T p.G43V Substitution - Missense 8:76984051-76984051 - pfg311T COSM4757844 c.438G>T p.L146F Substitution - Missense 8:76983741-76983741 - SWE-4A COSM1179504 c.1035C>A p.T345T Substitution - coding silent 19:39386751-39386751 - TCGA-AP-A059-01 COSM1101869 c.312C>A p.I104I Substitution - coding silent 8:76983867-76983867 - B62-0-Tumor COSM3933030 c.1477A>G p.S493G Substitution - Missense 19:39386110-39386110 - TCGA-J9-A52B-01 COSM4876968 c.640C>T p.Q214* Substitution - Nonsense 8:76983539-76983539 - SNUH_G26_S1 COSM3680907 c.372C>T p.H124H Substitution - coding silent 19:39389371-39389371 - TCGA-EE-A2MR-06 COSM3651203 c.471C>T p.F157F Substitution - coding silent 8:76983708-76983708 - CHC1182T COSM4788742 c.1594T>G p.*532G Nonstop extension 19:39385993-39385993 - Pat_06_B COSM5855713 c.1579G>C p.D527H Substitution - Missense 19:39386008-39386008 - PD5947a COSM5781620 c.987-10C>A p.? Unknown 19:39386809-39386809 - TCGA-CM-6162-01 COSM1393539 c.256C>T p.L86F Substitution - Missense 19:39389676-39389676 - TCGA-19-2629 COSM2156315 c.221T>G p.L74R Substitution - Missense 19:39389711-39389711 - B99-Tumor COSM3933032 c.1467T>G p.G489G Substitution - coding silent 19:39386120-39386120 - TCGA-D9-A4Z5-01 COSM3533695 c.1127C>T p.P376L Substitution - Missense 19:39386538-39386538 - RK280_C01 COSM4944357 c.782T>C p.F261S Substitution - Missense 19:39388635-39388635 - T613 COSM4710824 c.1206C>T p.S402S Substitution - coding silent 19:39386381-39386381 - ESCC_44 COSM5630201 c.27G>C p.K9N Substitution - Missense 8:76984152-76984152 - LUAD-S01405 COSM398985 c.375G>A p.A125A Substitution - coding silent 19:39389368-39389368 - CRC-06T COSM5457405 c.582A>G p.E194E Substitution - coding silent 8:76983597-76983597 - TCGA-DK-A1A7-01 COSM418265 c.1028C>T p.S343L Substitution - Missense 19:39386758-39386758 - TCGA-D1-A176-01 COSM996276 c.1100G>A p.R367Q Substitution - Missense 19:39386565-39386565 - BCM723T COSM4956656 c.1365C>T p.G455G Substitution - coding silent 19:39386222-39386222 - LUAD_E00565 COSM389659 c.633C>T p.I211I Substitution - coding silent 8:76983546-76983546 - TCGA-D3-A3MR-06 COSM3533701 c.447G>A p.E149E Substitution - coding silent 19:39389296-39389296 - TCGA-BP-5176-01 COSM486682 c.351A>T p.E117D Substitution - Missense 8:76983828-76983828 - CN-AML-08-T COSM5426128 c.568-8T>C p.? Unknown 19:39389023-39389023 - BCM723T COSM4956656 c.1365C>T p.G455G Substitution - coding silent 19:39386222-39386222 - TCGA-CA-5797-01 COSM1393537 c.528C>T p.I176I Substitution - coding silent 19:39389132-39389132 - CRC-06T COSM5456726 c.991C>T p.R331C Substitution - Missense 19:39386795-39386795 - TCGA-D1-A15X-01 COSM996275 c.1321G>A p.E441K Substitution - Missense 19:39386266-39386266 - BK0043 COSM4187600 c.390G>A p.W130* Substitution - Nonsense 19:39389353-39389353 - TCGA-D3-A1Q8-06 COSM3533693 c.1405G>T p.E469* Substitution - Nonsense 19:39386182-39386182 - HCC142 COSM1612224 c.1446A>G p.S482S Substitution - coding silent 19:39386141-39386141 - CHC1747T COSM4788058 c.421T>A p.F141I Substitution - Missense 8:76983758-76983758 - TCGA-BR-6566-01 COSM4077963 c.51C>A p.P17P Substitution - coding silent 19:39390286-39390286 - PT36 COSM5915799 c.778G>A p.E260K Substitution - Missense 8:76983401-76983401 - PD5935a COSM5771972 c.1545C>T p.G515G Substitution - coding silent 19:39386042-39386042 - TCGA-EB-A5SE-01 COSM3925617 c.352G>A p.E118K Substitution - Missense 8:76983827-76983827 - PD4107a COSM163412 c.146T>G p.L49* Substitution - Nonsense 8:76984033-76984033 - TCGA-AX-A060-01 COSM87803 c.1312G>A p.E438K Substitution - Missense 19:39386275-39386275 - TCGA-DK-A3IU-01 COSM3797071 c.258C>T p.L86L Substitution - coding silent 19:39389674-39389674 - 07-P1079 COSM3223803 c.1195_1197delGAG p.E399delE Deletion - In frame 19:39386390-39386392 - H1155 COSM1195565 c.1060C>T p.R354W Substitution - Missense 19:39386726-39386726 - 070T COSM1730569 c.456T>G p.I152M Substitution - Missense 8:76983723-76983723 - TCGA-A7-A13F-01 COSM454864 c.506G>A p.R169H Substitution - Missense 8:76983673-76983673 - TCGA-AX-A05Z-01 COSM1101867 c.374G>A p.R125Q Substitution - Missense 8:76983805-76983805 - TCGA-AP-A056-01 COSM398985 c.375G>A p.A125A Substitution - coding silent 19:39389368-39389368 - LUAD-RT-S01709 COSM380015 c.747G>A p.E249E Substitution - coding silent 8:76983432-76983432 - B83 COSM1745323 c.1556_1579del24 p.A519_A526delAASDSSEA Deletion - In frame 19:39386008-39386031 - H650 COSM1194426 c.283G>T p.D95Y Substitution - Missense 19:39389649-39389649 - TCGA-AX-A05Z-01 COSM996280 c.315G>T p.E105D Substitution - Missense 19:39389524-39389524 - TCGA-BF-A1Q0-01 COSM3533703 c.399G>C p.K133N Substitution - Missense 19:39389344-39389344 - J73_T COSM3960048 c.1004G>A p.R335H Substitution - Missense 19:39386782-39386782 - pfg143T COSM4757845 c.313T>C p.W105R Substitution - Missense 8:76983866-76983866 - TCGA-BS-A0UF-01 COSM996278 c.812G>A p.R271Q Substitution - Missense 19:39388605-39388605 - 8068564 COSM3771060 c.800C>T p.T267M Substitution - Missense 19:39388617-39388617 - B19-Tumor COSM3933030 c.1477A>G p.S493G Substitution - Missense 19:39386110-39386110 - TCGA-LG-A6GG-01 COSM4939383 c.679C>T p.L227F Substitution - Missense 8:76983500-76983500 - HCC142T COSM1612226 c.1424A>T p.Q475L Substitution - Missense 19:39386163-39386163 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.437966 8q21.1 170993 Hs.466714 19q13.1 610506

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Synonymous p.H72H c.216T>C 19 39880356 RCCC C A Missense p.W297L c.890G>T 19 39879075 LUAD C A Nonsense p.E165* c.493G>T 19 39879807 HNSC C A Nonsense p.E469* c.1405G>T 19 39876822 CM C A Nonsense p.G28* c.82G>T 19 39880797 LUSC C - Frameshift p.E421Rfs*192 c.1261delG 19 39876966 HNSC C G Missense p.G489A c.1466G>C 19 39876761 BLCA C G Missense p.K133N c.399G>C 19 39879984 CM C G Missense p.M245I c.735G>C 19 39879407 HNSC C T Missense p.D285N c.853G>A 19 39879204 CM C T Missense p.D522N c.1564G>A 19 39876663 LUAD C T Missense p.E149K c.445G>A 19 39879938 BRCA C T Missense p.E266K c.796G>A 19 39879261 BLCA C T Missense p.E277K c.829G>A 19 39879228 BLCA C T Missense p.E438K c.1312G>A 19 39876915 UCEC C T Missense p.G485S c.1453G>A 19 39876774 CM C T Missense p.R273Q c.818G>A 19 39879239 UCEC C T Missense p.R367Q c.1100G>A 19 39877205 UCEC C T Missense p.R420Q c.1259G>A 19 39876968 RCCC C T SpliceAcceptorSNV . c.741-1G>A 19 39879317 STAD C T Synonymous p.E149E c.447G>A 19 39879936 CM C T Synonymous p.R336R c.1008G>A 19 39877418 CM G A Missense p.P201L c.602C>T 19 39879621 UCEC G A Missense p.S138F c.413C>T 19 39879970 HNSC G A Missense p.S343L c.1028C>T 19 39877398 BLCA G A Missense p.T134I c.401C>T 19 39879982 MB G A Synonymous p.I94I c.282C>T 19 39880290 ESCA G A Synonymous p.L86L c.258C>T 19 39880314 BLCA G C Missense p.H70Q c.210C>G 19 39880362 RCCC GG AA Missense p.Q175* c.522_523delinsTT 19 39879777 CM TCT - InFrameDeletion p.K181delK c.542_544delAGA 19 39879756 LGG A C Nonsense p.L49* c.146T>G 8 77896269 BRCA - A Frameshift p.M253Ifs*8 c.758dupT 8 77895657 HNSC A G Missense p.L29P c.86T>C 8 77896329 STAD C A Missense p.G149C c.445G>T 8 77895970 LUAD C A Missense p.G43V c.128G>T 8 77896287 SCLC C A Missense p.K282N c.846G>T 8 77895569 LUAD C A Missense p.M191I c.573G>T 8 77895842 LUSC C G Missense p.D275H c.823G>C 8 77895592 CM C T Missense p.C283Y c.848G>A 8 77895567 STAD C T Missense p.D21N c.61G>A 8 77896354 LUAD C T Missense p.R169H c.506G>A 8 77895909 BRCA C T Missense p.V302I c.904G>A 8 77895511 BRCA G A 3-UTRSNV . c.915+126C>T 8 77895374 CM G A Nonsense p.Q214* c.640C>T 8 77895775 PRAD G A Nonsense p.Q31* c.91C>T 8 77896324 MB G A Synonymous p.L207L c.621C>T 8 77895794 UCEC G T Missense p.L25I c.73C>A 8 77896342 HNSC G T Missense p.Q102K c.304C>A 8 77896111 HNSC T A Missense p.E117D c.351A>T 8 77896064 RCCC T A Missense p.Q214L c.641A>T 8 77895774 LUSC T A Nonsense p.K136* c.406A>T 8 77896009 OV T A Nonsense p.R16* c.46A>T 8 77896369 HNSC T G Missense p.E118A c.353A>C 8 77896062 COREAD