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 2 163130334 163130334 + Missense_Mutation SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr2:163130334G>A c.2425C>T c.(2425-2427)Ctc>Ttc p.L809F BLCA 2 163133412 163133412 + Nonsense_Mutation SNP C C A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr2:163133412C>A c.2089G>T c.(2089-2091)Gaa>Taa p.E697* BLCA 2 163136547 163136547 + Missense_Mutation SNP C C G TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr2:163136547C>G c.1600G>C c.(1600-1602)Gag>Cag p.E534Q BLCA 2 163136571 163136571 + Missense_Mutation SNP C C A TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr2:163136571C>A c.1576G>T c.(1576-1578)Gat>Tat p.D526Y BLCA 2 163136595 163136595 + Missense_Mutation SNP T T C TCGA-K4-A5RI-01A-11D-A289-08 TCGA-K4-A5RI-10A-01D-A289-08 g.chr2:163136595T>C c.1552A>G c.(1552-1554)Att>Gtt p.I518V BLCA 2 163144771 163144771 + Silent SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr2:163144771C>T c.969G>A c.(967-969)aaG>aaA p.K323K BLCA 2 163144789 163144789 + Missense_Mutation SNP C C G TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr2:163144789C>G c.951G>C c.(949-951)caG>caC p.Q317H BLCA 2 163167353 163167353 + Silent SNP G G A TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr2:163167353G>A c.544C>T c.(544-546)Ctg>Ttg p.L182L BLCA 2 163174371 163174372 + Frame_Shift_Del DEL TC TC - TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr2:163174371_163174372delTC c.446_447delGA c.(445-447)agafs p.R149fs BLCA 2 163174805 163174806 + Frame_Shift_Ins INS - - CC TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr2:163174805_163174806insCC c.12_13insGG c.(10-15)gggtatfs p.Y5fs BRCA 2 163128799 163128799 + Missense_Mutation SNP C C G TCGA-B6-A0RV-01A-11D-A099-09 TCGA-B6-A0RV-10A-01D-A099-09 g.chr2:163128799C>G c.2553G>C c.(2551-2553)gaG>gaC p.E851D BRCA 2 163130328 163130328 + Missense_Mutation SNP T T C TCGA-EW-A1IZ-01A-11D-A188-09 TCGA-EW-A1IZ-10A-01D-A13O-09 g.chr2:163130328T>C c.2431A>G c.(2431-2433)Acc>Gcc p.T811A BRCA 2 163130442 163130442 + Missense_Mutation SNP C C T TCGA-LL-A5YM-01A-11D-A28B-09 TCGA-LL-A5YM-10A-01D-A28E-09 g.chr2:163130442C>T c.2317G>A c.(2317-2319)Gaa>Aaa p.E773K BRCA 2 163174697 163174697 + Missense_Mutation SNP C C G TCGA-C8-A274-01A-11D-A16D-09 TCGA-C8-A274-10A-01D-A16D-09 g.chr2:163174697C>G c.121G>C c.(121-123)Gag>Cag p.E41Q CESC 2 163124713 163124713 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr2:163124713C>A c.2691G>T c.(2689-2691)aaG>aaT p.K897N CESC 2 163128822 163128822 + Missense_Mutation SNP C C G TCGA-EK-A3GM-01A-11D-A20U-09 TCGA-EK-A3GM-10A-01D-A20U-09 g.chr2:163128822C>G c.2530G>C c.(2530-2532)Gag>Cag p.E844Q COAD 2 163124065 163124065 + Missense_Mutation SNP A A G TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr2:163124065A>G c.2822T>C c.(2821-2823)gTa>gCa p.V941A COAD 2 163124632 163124632 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:163124632C>A c.2772G>T c.(2770-2772)gaG>gaT p.E924D COAD 2 163130424 163130424 + Missense_Mutation SNP G G A TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr2:163130424G>A c.2335C>T c.(2335-2337)Cgc>Tgc p.R779C COAD 2 163130424 163130424 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:163130424G>A c.2335C>T c.(2335-2337)Cgc>Tgc p.R779C COAD 2 163130446 163130446 + Missense_Mutation SNP T T G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr2:163130446T>G c.2313A>C c.(2311-2313)caA>caC p.Q771H COAD 2 163130455 163130455 + Splice_Site SNP C C A TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr2:163130455C>A c.e12-1 COAD 2 163133222 163133222 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr2:163133222C>A c.2279G>T c.(2278-2280)aGc>aTc p.S760I COAD 2 163134104 163134104 + Missense_Mutation SNP G G A TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr2:163134104G>A c.1865C>T c.(1864-1866)gCg>gTg p.A622V COAD 2 163134117 163134117 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:163134117G>A c.1852C>T c.(1852-1854)Cga>Tga p.R618* COAD 2 163134131 163134131 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:163134131A>C c.1838T>G c.(1837-1839)aTt>aGt p.I613S COAD 2 163134133 163134133 + Silent SNP T T C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr2:163134133T>C c.1836A>G c.(1834-1836)caA>caG p.Q612Q COAD 2 163134140 163134140 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:163134140G>A c.1829C>T c.(1828-1830)gCc>gTc p.A610V COAD 2 163134723 163134723 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr2:163134723T>C c.1757A>G c.(1756-1758)gAa>gGa p.E586G COAD 2 163136588 163136588 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:163136588G>T c.1559C>A c.(1558-1560)aCt>aAt p.T520N COAD 2 163136602 163136602 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr2:163136602T>C c.1545A>G c.(1543-1545)gcA>gcG p.A515A COAD 2 163144663 163144663 + Silent SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:163144663A>C c.1077T>G c.(1075-1077)gtT>gtG p.V359V COAD 2 163144687 163144687 + Silent SNP T T C TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr2:163144687T>C c.1053A>G c.(1051-1053)aaA>aaG p.K351K COAD 2 163144688 163144688 + Missense_Mutation SNP T T C TCGA-CA-5254-01A-21D-1835-10 TCGA-CA-5254-10A-01D-1835-10 g.chr2:163144688T>C c.1052A>G c.(1051-1053)aAa>aGa p.K351R COAD 2 163144689 163144689 + Missense_Mutation SNP T T C TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr2:163144689T>C c.1051A>G c.(1051-1053)Aaa>Gaa p.K351E COAD 2 163144790 163144790 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr2:163144790T>C c.950A>G c.(949-951)cAg>cGg p.Q317R COADREAD 2 163124065 163124065 + Missense_Mutation SNP A A G TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr2:163124065A>G c.2822T>C c.(2821-2823)gTa>gCa p.V941A COADREAD 2 163124632 163124632 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:163124632C>A c.2772G>T c.(2770-2772)gaG>gaT p.E924D COADREAD 2 163130424 163130424 + Missense_Mutation SNP G G A TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr2:163130424G>A c.2335C>T c.(2335-2337)Cgc>Tgc p.R779C COADREAD 2 163130424 163130424 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:163130424G>A c.2335C>T c.(2335-2337)Cgc>Tgc p.R779C COADREAD 2 163130446 163130446 + Missense_Mutation SNP T T G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr2:163130446T>G c.2313A>C c.(2311-2313)caA>caC p.Q771H COADREAD 2 163130455 163130455 + Splice_Site SNP C C A TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr2:163130455C>A c.e12-1 COADREAD 2 163133222 163133222 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr2:163133222C>A c.2279G>T c.(2278-2280)aGc>aTc p.S760I COADREAD 2 163134104 163134104 + Missense_Mutation SNP G G A TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr2:163134104G>A c.1865C>T c.(1864-1866)gCg>gTg p.A622V COADREAD 2 163134117 163134117 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr2:163134117G>A c.1852C>T c.(1852-1854)Cga>Tga p.R618* COADREAD 2 163134131 163134131 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr2:163134131A>C c.1838T>G c.(1837-1839)aTt>aGt p.I613S COADREAD 2 163134133 163134133 + Silent SNP T T C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr2:163134133T>C c.1836A>G c.(1834-1836)caA>caG p.Q612Q COADREAD 2 163134140 163134140 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr2:163134140G>A c.1829C>T c.(1828-1830)gCc>gTc p.A610V COADREAD 2 163134723 163134723 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr2:163134723T>C c.1757A>G c.(1756-1758)gAa>gGa p.E586G COADREAD 2 163136588 163136588 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr2:163136588G>T c.1559C>A c.(1558-1560)aCt>aAt p.T520N COADREAD 2 163136602 163136602 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr2:163136602T>C c.1545A>G c.(1543-1545)gcA>gcG p.A515A COADREAD 2 163137949 163137950 + Frame_Shift_Del DEL GA GA - TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr2:163137949_163137950delGA c.1412_1413delTC c.(1411-1413)ctcfs p.L471fs COADREAD 2 163144663 163144663 + Silent SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr2:163144663A>C c.1077T>G c.(1075-1077)gtT>gtG p.V359V COADREAD 2 163144687 163144687 + Silent SNP T T C TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr2:163144687T>C c.1053A>G c.(1051-1053)aaA>aaG p.K351K COADREAD 2 163144688 163144688 + Missense_Mutation SNP T T C TCGA-CA-5254-01A-21D-1835-10 TCGA-CA-5254-10A-01D-1835-10 g.chr2:163144688T>C c.1052A>G c.(1051-1053)aAa>aGa p.K351R COADREAD 2 163144688 163144688 + Missense_Mutation SNP T T C TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr2:163144688T>C c.1052A>G c.(1051-1053)aAa>aGa p.K351R COADREAD 2 163144689 163144689 + Missense_Mutation SNP T T C TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr2:163144689T>C c.1051A>G c.(1051-1053)Aaa>Gaa p.K351E COADREAD 2 163144790 163144790 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr2:163144790T>C c.950A>G c.(949-951)cAg>cGg p.Q317R DLBC 2 163124637 163124637 + Missense_Mutation SNP T T C TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr2:163124637T>C c.2767A>G c.(2767-2769)Att>Gtt p.I923V DLBC 2 163128883 163128883 + Silent SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr2:163128883G>A c.2469C>T c.(2467-2469)gcC>gcT p.A823A DLBC 2 163144683 163144684 + Frame_Shift_Ins INS - - T TCGA-GS-A9TW-01A-11D-A382-10 TCGA-GS-A9TW-10A-01D-A385-10 g.chr2:163144683_163144684insT c.1056_1057insA c.(1054-1059)aaagcafs p.A353fs ESCA 2 163128830 163128830 + Missense_Mutation SNP A A T TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr2:163128830A>T c.2522T>A c.(2521-2523)aTc>aAc p.I841N ESCA 2 163133265 163133265 + Missense_Mutation SNP C C T TCGA-L5-A8NK-01A-21D-A37C-09 TCGA-L5-A8NK-11A-11D-A37F-09 g.chr2:163133265C>T c.2236G>A c.(2236-2238)Gaa>Aaa p.E746K ESCA 2 163134715 163134716 + Splice_Site INS - - T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr2:163134715_163134716insT c.1764_1765insA c.(1762-1767)aaagct>aaaAgct p.A589fs GBMLGG 2 163124612 163124612 + Missense_Mutation SNP A A T TCGA-HW-A5KM-01A-11D-A27K-08 TCGA-HW-A5KM-10A-01D-A27N-08 g.chr2:163124612A>T c.2792T>A c.(2791-2793)aTg>aAg p.M931K GBMLGG 2 163124706 163124706 + Missense_Mutation SNP G G T TCGA-S9-A7IY-01A-11D-A34A-08 TCGA-S9-A7IY-10A-01D-A34A-08 g.chr2:163124706G>T c.2698C>A c.(2698-2700)Cca>Aca p.P900T GBMLGG 2 163133214 163133214 + Missense_Mutation SNP A A C TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr2:163133214A>C c.2287T>G c.(2287-2289)Ttc>Gtc p.F763V GBMLGG 2 163134056 163134056 + Missense_Mutation SNP A A C TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr2:163134056A>C c.1913T>G c.(1912-1914)tTt>tGt p.F638C GBMLGG 2 163136557 163136557 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:163136557G>A c.1590C>T c.(1588-1590)aaC>aaT p.N530N HNSC 2 163128753 163128753 + Missense_Mutation SNP C C G TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr2:163128753C>G c.2599G>C c.(2599-2601)Gag>Cag p.E867Q HNSC 2 163133239 163133239 + Silent SNP C C G TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr2:163133239C>G c.2262G>C c.(2260-2262)ctG>ctC p.L754L HNSC 2 163133418 163133418 + Nonsense_Mutation SNP C C A TCGA-CN-6013-01A-11D-1683-08 TCGA-CN-6013-10A-01D-1683-08 g.chr2:163133418C>A c.2083G>T c.(2083-2085)Gaa>Taa p.E695* HNSC 2 163134157 163134157 + Missense_Mutation SNP C C G TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chr2:163134157C>G c.1812G>C c.(1810-1812)ttG>ttC p.L604F HNSC 2 163134806 163134806 + Missense_Mutation SNP C C A TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr2:163134806C>A c.1674G>T c.(1672-1674)atG>atT p.M558I HNSC 2 163144671 163144671 + Missense_Mutation SNP C C T TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr2:163144671C>T c.1069G>A c.(1069-1071)Gga>Aga p.G357R HNSC 2 163144765 163144765 + Silent SNP G G A TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr2:163144765G>A c.975C>T c.(973-975)atC>atT p.I325I HNSC 2 163163360 163163360 + Missense_Mutation SNP C C G TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr2:163163360C>G c.628G>C c.(628-630)Gag>Cag p.E210Q HNSC 2 163167287 163167287 + Missense_Mutation SNP C C G TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chr2:163167287C>G c.610G>C c.(610-612)Gaa>Caa p.E204Q KIPAN 2 163144684 163144684 + Missense_Mutation SNP T T G TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr2:163144684T>G c.1056A>C c.(1054-1056)aaA>aaC p.K352N KIPAN 2 163167397 163167397 + Missense_Mutation SNP A A G TCGA-DW-7834-01A-11D-2136-08 TCGA-DW-7834-10A-01D-2136-08 g.chr2:163167397A>G c.500T>C c.(499-501)cTa>cCa p.L167P KIRC 2 163144684 163144684 + Missense_Mutation SNP T T G TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr2:163144684T>G c.1056A>C c.(1054-1056)aaA>aaC p.K352N KIRP 2 163167397 163167397 + Missense_Mutation SNP A A G TCGA-DW-7834-01A-11D-2136-08 TCGA-DW-7834-10A-01D-2136-08 g.chr2:163167397A>G c.500T>C c.(499-501)cTa>cCa p.L167P LGG 2 163124612 163124612 + Missense_Mutation SNP A A T TCGA-HW-A5KM-01A-11D-A27K-08 TCGA-HW-A5KM-10A-01D-A27N-08 g.chr2:163124612A>T c.2792T>A c.(2791-2793)aTg>aAg p.M931K LGG 2 163124706 163124706 + Missense_Mutation SNP G G T TCGA-S9-A7IY-01A-11D-A34A-08 TCGA-S9-A7IY-10A-01D-A34A-08 g.chr2:163124706G>T c.2698C>A c.(2698-2700)Cca>Aca p.P900T LGG 2 163133214 163133214 + Missense_Mutation SNP A A C TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr2:163133214A>C c.2287T>G c.(2287-2289)Ttc>Gtc p.F763V LGG 2 163134056 163134056 + Missense_Mutation SNP A A C TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr2:163134056A>C c.1913T>G c.(1912-1914)tTt>tGt p.F638C LGG 2 163136557 163136557 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr2:163136557G>A c.1590C>T c.(1588-1590)aaC>aaT p.N530N LIHC 2 163124064 163124064 + Silent SNP T T C TCGA-CC-A5UD-01A-11D-A28X-10 TCGA-CC-A5UD-10A-01D-A28X-10 g.chr2:163124064T>C c.2823A>G c.(2821-2823)gtA>gtG p.V941V LIHC 2 163139081 163139081 + Silent SNP C C A TCGA-DD-AAW2-01A-11D-A40P-10 TCGA-DD-AAW2-10A-01D-A40P-10 g.chr2:163139081C>A c.1101G>T c.(1099-1101)ctG>ctT p.L367L LUAD 2 163124634 163124634 + Missense_Mutation SNP C C G TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr2:163124634C>G c.2770G>C c.(2770-2772)Gag>Cag p.E924Q LUAD 2 163124717 163124717 + Missense_Mutation SNP T T C TCGA-L9-A443-01A-12D-A24D-08 TCGA-L9-A443-10A-01D-A24F-08 g.chr2:163124717T>C c.2687A>G c.(2686-2688)tAc>tGc p.Y896C LUAD 2 163128776 163128776 + Missense_Mutation SNP T T A TCGA-69-8253-01A-11D-2284-08 TCGA-69-8253-10A-01D-2284-08 g.chr2:163128776T>A c.2576A>T c.(2575-2577)cAt>cTt p.H859L LUAD 2 163130423 163130423 + Missense_Mutation SNP C C T TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr2:163130423C>T c.2336G>A c.(2335-2337)cGc>cAc p.R779H LUAD 2 163133265 163133265 + Missense_Mutation SNP C C T TCGA-80-5607-01A-31D-1945-08 TCGA-80-5607-10A-01D-1946-08 g.chr2:163133265C>T c.2236G>A c.(2236-2238)Gaa>Aaa p.E746K LUAD 2 163133358 163133358 + Missense_Mutation SNP T T G TCGA-97-7547-01A-11D-2036-08 TCGA-97-7547-10A-01D-2036-08 g.chr2:163133358T>G c.2143A>C c.(2143-2145)Act>Cct p.T715P LUAD 2 163133379 163133379 + Missense_Mutation SNP T T C TCGA-17-Z052-01A-01W-0747-08 TCGA-17-Z052-11A-01W-0747-08 g.chr2:163133379T>C c.2122A>G c.(2122-2124)Ata>Gta p.I708V LUAD 2 163133444 163133444 + Missense_Mutation SNP A A G TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr2:163133444A>G c.2057T>C c.(2056-2058)aTg>aCg p.M686T LUAD 2 163134108 163134108 + Missense_Mutation SNP C C G TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr2:163134108C>G c.1861G>C c.(1861-1863)Gat>Cat p.D621H LUAD 2 163134144 163134144 + Missense_Mutation SNP C C T TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr2:163134144C>T c.1825G>A c.(1825-1827)Gag>Aag p.E609K LUAD 2 163144753 163144753 + Silent SNP G G T TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr2:163144753G>T c.987C>A c.(985-987)ctC>ctA p.L329L LUAD 2 163174536 163174536 + Silent SNP G G A TCGA-86-8673-01A-11D-2393-08 TCGA-86-8673-10A-01D-2393-08 g.chr2:163174536G>A c.282C>T c.(280-282)taC>taT p.Y94Y LUAD 2 163174656 163174656 + Silent SNP C C A TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr2:163174656C>A c.162G>T c.(160-162)ggG>ggT p.G54G LUSC 2 163130385 163130385 + Missense_Mutation SNP C C T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr2:163130385C>T c.2374G>A c.(2374-2376)Gca>Aca p.A792T LUSC 2 163133387 163133387 + Missense_Mutation SNP C C A TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr2:163133387C>A c.2114G>T c.(2113-2115)aGa>aTa p.R705I LUSC 2 163144789 163144789 + Missense_Mutation SNP C C G TCGA-33-4533-01A-01D-1267-08 TCGA-33-4533-11A-01D-1267-08 g.chr2:163144789C>G c.951G>C c.(949-951)caG>caC p.Q317H LUSC 2 163174519 163174519 + Missense_Mutation SNP G G A TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr2:163174519G>A c.299C>T c.(298-300)aCg>aTg p.T100M LUSC 2 163174569 163174569 + Silent SNP G G T TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr2:163174569G>T c.249C>A c.(247-249)ctC>ctA p.L83L LUSC 2 163174644 163174644 + Silent SNP T T C TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr2:163174644T>C c.174A>G c.(172-174)gcA>gcG p.A58A OV 2 163144689 163144689 + Missense_Mutation SNP T T C TCGA-24-2267-01A-01W-0799-08 TCGA-24-2267-11A-01W-0799-08 g.chr2:163144689T>C c.1051A>G c.(1051-1053)Aaa>Gaa p.K351E OV 2 163144770 163144770 + Missense_Mutation SNP T T A TCGA-29-1761-01A-01W-0633-09 TCGA-29-1761-10A-01W-0633-09 g.chr2:163144770T>A c.970A>T c.(970-972)Aat>Tat p.N324Y OV 2 163163342 163163342 + Missense_Mutation SNP C C G TCGA-36-2534-01A-01D-1526-09 TCGA-36-2534-10A-01D-1526-09 g.chr2:163163342C>G c.646G>C c.(646-648)Gat>Cat p.D216H PAAD 2 163124694 163124694 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:163124694T>C c.2710A>G c.(2710-2712)Act>Gct p.T904A PAAD 2 163130398 163130398 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:163130398G>A c.2361C>T c.(2359-2361)atC>atT p.I787I PAAD 2 163134021 163134021 + Missense_Mutation SNP C C A TCGA-HZ-A8P1-01A-11D-A377-08 TCGA-HZ-A8P1-10A-01D-A37A-08 g.chr2:163134021C>A c.1948G>T c.(1948-1950)Gat>Tat p.D650Y PAAD 2 163134176 163134176 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:163134176C>T c.1793G>A c.(1792-1794)cGt>cAt p.R598H PAAD 2 163134715 163134716 + Splice_Site INS - - T TCGA-3A-A9IJ-01A-11D-A397-08 TCGA-3A-A9IJ-10A-01D-A39A-08 g.chr2:163134715_163134716insT c.1764_1765insA c.(1762-1767)aaagct>aaaAgct p.A589fs PAAD 2 163144827 163144827 + Missense_Mutation SNP C C T TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr2:163144827C>T c.913G>A c.(913-915)Gaa>Aaa p.E305K PAAD 2 163174679 163174679 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr2:163174679G>A c.139C>T c.(139-141)Cag>Tag p.Q47* READ 2 163137949 163137950 + Frame_Shift_Del DEL GA GA - TCGA-AH-6644-01A-21D-1826-10 TCGA-AH-6644-10A-01D-1826-10 g.chr2:163137949_163137950delGA c.1412_1413delTC c.(1411-1413)ctcfs p.L471fs READ 2 163144688 163144688 + Missense_Mutation SNP T T C TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr2:163144688T>C c.1052A>G c.(1051-1053)aAa>aGa p.K351R SARC 2 163136618 163136618 + Missense_Mutation SNP C C T TCGA-QQ-A8VH-01A-11D-A37C-09 TCGA-QQ-A8VH-10A-01D-A37F-09 g.chr2:163136618C>T c.1529G>A c.(1528-1530)tGt>tAt p.C510Y SKCM 2 163124026 163124026 + Missense_Mutation SNP T T A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr2:163124026T>A c.2861A>T c.(2860-2862)tAt>tTt p.Y954F SKCM 2 163124040 163124040 + Silent SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr2:163124040C>T c.2847G>A c.(2845-2847)aaG>aaA p.K949K SKCM 2 163124599 163124599 + Silent SNP G G A TCGA-D3-A1Q5-06A-11D-A196-08 TCGA-D3-A1Q5-10A-01D-A198-08 g.chr2:163124599G>A c.2805C>T c.(2803-2805)ttC>ttT p.F935F SKCM 2 163128755 163128755 + Missense_Mutation SNP G G A TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr2:163128755G>A c.2597C>T c.(2596-2598)cCa>cTa p.P866L SKCM 2 163128858 163128858 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr2:163128858G>A c.2494C>T c.(2494-2496)Ctg>Ttg p.L832L SKCM 2 163130398 163130398 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr2:163130398G>A c.2361C>T c.(2359-2361)atC>atT p.I787I SKCM 2 163133297 163133297 + Missense_Mutation SNP G G A TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr2:163133297G>A c.2204C>T c.(2203-2205)tCc>tTc p.S735F SKCM 2 163133442 163133442 + Silent SNP A A G TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr2:163133442A>G c.2059T>C c.(2059-2061)Ttg>Ctg p.L687L SKCM 2 163134116 163134116 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr2:163134116C>T c.1853G>A c.(1852-1854)cGa>cAa p.R618Q SKCM 2 163134154 163134154 + Silent SNP C C T TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr2:163134154C>T c.1815G>A c.(1813-1815)agG>agA p.R605R SKCM 2 163134738 163134738 + Nonsense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr2:163134738C>T c.1742G>A c.(1741-1743)tGg>tAg p.W581* SKCM 2 163134828 163134828 + Missense_Mutation SNP T T A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr2:163134828T>A c.1652A>T c.(1651-1653)aAa>aTa p.K551I SKCM 2 163136531 163136531 + Missense_Mutation SNP A A G TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr2:163136531A>G c.1616T>C c.(1615-1617)tTt>tCt p.F539S SKCM 2 163138964 163138964 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr2:163138964G>A c.1218C>T c.(1216-1218)tcC>tcT p.S406S SKCM 2 163139026 163139026 + Missense_Mutation SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr2:163139026G>A c.1156C>T c.(1156-1158)Cgt>Tgt p.R386C SKCM 2 163144699 163144699 + Silent SNP T T C TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr2:163144699T>C c.1041A>G c.(1039-1041)ttA>ttG p.L347L SKCM 2 163163287 163163287 + Missense_Mutation SNP T T C TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr2:163163287T>C c.701A>G c.(700-702)gAg>gGg p.E234G SKCM 2 163163336 163163336 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr2:163163336G>A c.652C>T c.(652-654)Cct>Tct p.P218S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 2 163133303 163133303 single base substitution G A missense_variant A733V 2198C>T BLCA-CN 2 163144730 163144730 single base substitution C G missense_variant R337T 1010G>C BLCA-CN 2 163144863 163144863 single base substitution C T missense_variant E293K 877G>A BLCA-US 2 163136571 163136571 single base substitution C A missense_variant D526Y 1576G>T BLCA-US 2 163144789 163144789 single base substitution C G missense_variant Q317H 951G>C BLCA-US 2 163174805 163174805 insertion of <=200bp - CC frameshift_variant Y5W? BOCA-UK 2 163174407 163174407 single base substitution C T synonymous_variant K137K 411G>A BRCA-EU 2 163120718 163120718 single base substitution C T downstream_gene_variant BRCA-EU 2 163121453 163121453 single base substitution C G downstream_gene_variant BRCA-EU 2 163121762 163121762 single base substitution G A downstream_gene_variant BRCA-EU 2 163121964 163121964 single base substitution T C downstream_gene_variant BRCA-EU 2 163122496 163122496 single base substitution C G downstream_gene_variant BRCA-EU 2 163122779 163122779 single base substitution T A downstream_gene_variant BRCA-EU 2 163123209 163123209 single base substitution G T downstream_gene_variant BRCA-EU 2 163123465 163123465 single base substitution C T downstream_gene_variant BRCA-EU 2 163124107 163124107 single base substitution C T intron_variant BRCA-EU 2 163125168 163125168 single base substitution C T intron_variant BRCA-EU 2 163125996 163125996 single base substitution C T intron_variant BRCA-EU 2 163126549 163126549 deletion of <=200bp A - intron_variant BRCA-EU 2 163126639 163126639 single base substitution G T intron_variant BRCA-EU 2 163127973 163127973 deletion of <=200bp G - intron_variant BRCA-EU 2 163128796 163128796 single base substitution C G missense_variant K852N 2556G>C BRCA-EU 2 163129806 163129806 single base substitution C G intron_variant BRCA-EU 2 163131983 163131983 deletion of <=200bp C - intron_variant BRCA-EU 2 163134716 163134716 deletion of <=200bp T - frameshift_variant K588 BRCA-EU 2 163135709 163135709 single base substitution G A intron_variant BRCA-EU 2 163136455 163136455 single base substitution C G intron_variant BRCA-EU 2 163137511 163137511 single base substitution C T intron_variant BRCA-EU 2 163137728 163137728 single base substitution C G intron_variant BRCA-EU 2 163138589 163138589 single base substitution A G intron_variant BRCA-EU 2 163139695 163139695 single base substitution G C intron_variant BRCA-EU 2 163141235 163141235 single base substitution C T intron_variant BRCA-EU 2 163142582 163142582 single base substitution C G intron_variant BRCA-EU 2 163142716 163142716 insertion of <=200bp - A intron_variant BRCA-EU 2 163143177 163143177 single base substitution G T intron_variant BRCA-EU 2 163143795 163143795 deletion of <=200bp T - intron_variant BRCA-EU 2 163143871 163143871 single base substitution T C intron_variant BRCA-EU 2 163147775 163147775 single base substitution G C downstream_gene_variant BRCA-EU 2 163147775 163147775 single base substitution G C intron_variant BRCA-EU 2 163150606 163150606 single base substitution T A intron_variant BRCA-EU 2 163151218 163151218 single base substitution C A intron_variant BRCA-EU 2 163152808 163152808 single base substitution G C intron_variant BRCA-EU 2 163153426 163153426 single base substitution G A intron_variant BRCA-EU 2 163153686 163153686 single base substitution G A intron_variant BRCA-EU 2 163154001 163154001 single base substitution G T intron_variant BRCA-EU 2 163154343 163154343 single base substitution C T intron_variant BRCA-EU 2 163154752 163154752 single base substitution A G intron_variant BRCA-EU 2 163154756 163154756 single base substitution C A intron_variant BRCA-EU 2 163156199 163156199 single base substitution C A intron_variant BRCA-EU 2 163156837 163156837 deletion of <=200bp A - intron_variant BRCA-EU 2 163157116 163157116 single base substitution C G intron_variant BRCA-EU 2 163157901 163157901 single base substitution T G intron_variant BRCA-EU 2 163160382 163160382 single base substitution A G intron_variant BRCA-EU 2 163160796 163160796 single base substitution C G intron_variant BRCA-EU 2 163161303 163161303 single base substitution C G intron_variant BRCA-EU 2 163164524 163164524 single base substitution C T downstream_gene_variant BRCA-EU 2 163164524 163164524 single base substitution C T intron_variant BRCA-EU 2 163164524 163164524 single base substitution C T upstream_gene_variant BRCA-EU 2 163164958 163164958 single base substitution C A downstream_gene_variant BRCA-EU 2 163164958 163164958 single base substitution C A intron_variant BRCA-EU 2 163164958 163164958 single base substitution C A upstream_gene_variant BRCA-EU 2 163164990 163164990 single base substitution G C downstream_gene_variant BRCA-EU 2 163164990 163164990 single base substitution G C intron_variant BRCA-EU 2 163164990 163164990 single base substitution G C upstream_gene_variant BRCA-EU 2 163165442 163165442 single base substitution G T downstream_gene_variant BRCA-EU 2 163165442 163165442 single base substitution G T intron_variant BRCA-EU 2 163165442 163165442 single base substitution G T upstream_gene_variant BRCA-EU 2 163165837 163165837 single base substitution C T downstream_gene_variant BRCA-EU 2 163165837 163165837 single base substitution C T intron_variant BRCA-EU 2 163165837 163165837 single base substitution C T upstream_gene_variant BRCA-EU 2 163168412 163168412 deletion of <=200bp A - intron_variant BRCA-EU 2 163168412 163168412 deletion of <=200bp A - upstream_gene_variant BRCA-EU 2 163169187 163169187 insertion of <=200bp - T intron_variant BRCA-EU 2 163169463 163169463 single base substitution T G intron_variant BRCA-EU 2 163169730 163169730 single base substitution T A intron_variant BRCA-EU 2 163170269 163170269 single base substitution T G intron_variant BRCA-EU 2 163170864 163170864 single base substitution C T intron_variant BRCA-EU 2 163170902 163170902 single base substitution C T intron_variant BRCA-EU 2 163172384 163172384 single base substitution C T intron_variant BRCA-EU 2 163172432 163172432 single base substitution T A intron_variant BRCA-EU 2 163173367 163173367 single base substitution G A intron_variant BRCA-EU 2 163174345 163174345 single base substitution C G intron_variant BRCA-EU 2 163174593 163174593 single base substitution C A missense_variant W75C 225G>T BRCA-EU 2 163174665 163174665 single base substitution G T synonymous_variant A51A 153C>A BRCA-EU 2 163176108 163176108 insertion of <=200bp - A upstream_gene_variant BRCA-EU 2 163177665 163177665 insertion of <=200bp - T upstream_gene_variant BRCA-FR 2 163124107 163124107 single base substitution C T intron_variant BRCA-FR 2 163125168 163125168 single base substitution C T intron_variant BRCA-FR 2 163125534 163125534 single base substitution T C intron_variant BRCA-FR 2 163138589 163138589 single base substitution A G intron_variant BRCA-FR 2 163148504 163148504 single base substitution G A downstream_gene_variant BRCA-FR 2 163148504 163148504 single base substitution G A intron_variant BRCA-FR 2 163153426 163153426 single base substitution G A intron_variant BRCA-FR 2 163161303 163161303 single base substitution C G intron_variant BRCA-KR 2 163174473 163174473 single base substitution G A synonymous_variant L115L 345C>T BRCA-UK 2 163124737 163124737 single base substitution C A missense_variant K889N 2667G>T BRCA-US 2 163128799 163128799 single base substitution C G missense_variant E851D 2553G>C BRCA-US 2 163130328 163130328 single base substitution T C missense_variant T811A 2431A>G BRCA-US 2 163130442 163130442 single base substitution C T missense_variant E773K 2317G>A BRCA-US 2 163134716 163134716 deletion of <=200bp T - frameshift_variant K588 BRCA-US 2 163174697 163174697 single base substitution C G missense_variant E41Q 121G>C BTCA-JP 2 163130394 163130394 single base substitution T A missense_variant T789S 2365A>T BTCA-JP 2 163136372 163136372 deletion of <=200bp A - intron_variant BTCA-JP 2 163150042 163150042 deletion of <=200bp T - downstream_gene_variant BTCA-JP 2 163150042 163150042 deletion of <=200bp T - intron_variant BTCA-JP 2 163175552 163175552 single base substitution C A upstream_gene_variant CESC-US 2 163124713 163124713 single base substitution C A missense_variant K897N 2691G>T CESC-US 2 163128822 163128822 single base substitution C G missense_variant E844Q 2530G>C CLLE-ES 2 163151468 163151468 insertion of <=200bp - C intron_variant CLLE-ES 2 163160771 163160771 single base substitution G A intron_variant COAD-US 2 163124632 163124632 single base substitution C A missense_variant E924D 2772G>T COAD-US 2 163130424 163130424 single base substitution G A missense_variant R779C 2335C>T COAD-US 2 163130446 163130446 single base substitution T G missense_variant Q771H 2313A>C COAD-US 2 163130455 163130455 single base substitution C A splice_acceptor_variant COAD-US 2 163133222 163133222 single base substitution C A missense_variant S760I 2279G>T COAD-US 2 163134131 163134131 single base substitution A C missense_variant I613S 1838T>G COAD-US 2 163134133 163134133 single base substitution T C synonymous_variant Q612Q 1836A>G COAD-US 2 163134723 163134723 single base substitution T C missense_variant E586G 1757A>G COAD-US 2 163136588 163136588 single base substitution G T missense_variant T520N 1559C>A COAD-US 2 163136602 163136602 single base substitution T C synonymous_variant A515A 1545A>G COAD-US 2 163144790 163144790 single base substitution T C missense_variant Q317R 950A>G COCA-CN 2 163128824 163128824 single base substitution T C missense_variant H843R 2528A>G COCA-CN 2 163128956 163128956 single base substitution G T intron_variant COCA-CN 2 163133319 163133319 single base substitution G A stop_gained R728* 2182C>T COCA-CN 2 163134117 163134117 single base substitution G A stop_gained R618* 1852C>T COCA-CN 2 163136528 163136528 single base substitution G A missense_variant A540V 1619C>T COCA-CN 2 163138852 163138852 single base substitution A T intron_variant COCA-CN 2 163149896 163149896 single base substitution G T downstream_gene_variant COCA-CN 2 163149896 163149896 single base substitution G T intron_variant COCA-CN 2 163149961 163149961 single base substitution G A downstream_gene_variant COCA-CN 2 163149961 163149961 single base substitution G A intron_variant COCA-CN 2 163149961 163149961 single base substitution G T downstream_gene_variant COCA-CN 2 163149961 163149961 single base substitution G T intron_variant EOPC-DE 2 163153232 163153232 single base substitution T C intron_variant ESAD-UK 2 163118590 163118590 single base substitution C T downstream_gene_variant ESAD-UK 2 163119251 163119251 single base substitution C T downstream_gene_variant ESAD-UK 2 163120237 163120237 single base substitution T G downstream_gene_variant ESAD-UK 2 163122246 163122246 single base substitution A G downstream_gene_variant ESAD-UK 2 163122558 163122558 single base substitution C T downstream_gene_variant ESAD-UK 2 163127404 163127404 single base substitution T G intron_variant ESAD-UK 2 163127883 163127883 single base substitution C T intron_variant ESAD-UK 2 163128799 163128799 single base substitution C T synonymous_variant E851E 2553G>A ESAD-UK 2 163131337 163131337 single base substitution C T intron_variant ESAD-UK 2 163131699 163131699 single base substitution T G intron_variant ESAD-UK 2 163133071 163133071 single base substitution T C intron_variant ESAD-UK 2 163133977 163133977 single base substitution C A missense_variant K664N 1992G>T ESAD-UK 2 163134369 163134369 single base substitution T G intron_variant ESAD-UK 2 163138851 163138851 single base substitution T A intron_variant ESAD-UK 2 163138922 163138922 single base substitution G A synonymous_variant S420S 1260C>T ESAD-UK 2 163139932 163139932 single base substitution C A intron_variant ESAD-UK 2 163140007 163140007 single base substitution G A intron_variant ESAD-UK 2 163145309 163145309 single base substitution G A downstream_gene_variant ESAD-UK 2 163145309 163145309 single base substitution G A intron_variant ESAD-UK 2 163151621 163151621 single base substitution C T intron_variant ESAD-UK 2 163154001 163154001 single base substitution G T intron_variant ESAD-UK 2 163154363 163154363 single base substitution G A intron_variant ESAD-UK 2 163154566 163154566 insertion of <=200bp - A intron_variant ESAD-UK 2 163155291 163155291 single base substitution C T intron_variant ESAD-UK 2 163155413 163155413 single base substitution T A intron_variant ESAD-UK 2 163156495 163156495 single base substitution T A intron_variant ESAD-UK 2 163156837 163156837 deletion of <=200bp A - intron_variant ESAD-UK 2 163157295 163157295 insertion of <=200bp - T intron_variant ESAD-UK 2 163157901 163157901 single base substitution T G intron_variant ESAD-UK 2 163159373 163159373 single base substitution C T intron_variant ESAD-UK 2 163159692 163159692 single base substitution T G intron_variant ESAD-UK 2 163159808 163159808 single base substitution T C intron_variant ESAD-UK 2 163160392 163160392 single base substitution G T intron_variant ESAD-UK 2 163163901 163163901 deletion of <=200bp C - downstream_gene_variant ESAD-UK 2 163163901 163163901 deletion of <=200bp C - intron_variant ESAD-UK 2 163163901 163163901 deletion of <=200bp C - upstream_gene_variant ESAD-UK 2 163168053 163168053 deletion of <=200bp T - intron_variant ESAD-UK 2 163168053 163168053 deletion of <=200bp T - upstream_gene_variant ESAD-UK 2 163169649 163169649 single base substitution A C intron_variant ESAD-UK 2 163169892 163169892 single base substitution G A intron_variant ESAD-UK 2 163170932 163170934 deletion of <=200bp TTC - intron_variant ESAD-UK 2 163172713 163172713 single base substitution G A intron_variant ESAD-UK 2 163175044 163175044 single base substitution C G 5_prime_UTR_variant ESAD-UK 2 163175360 163175361 deletion of <=200bp TC - upstream_gene_variant ESAD-UK 2 163175800 163175800 single base substitution T C upstream_gene_variant ESAD-UK 2 163178628 163178628 single base substitution G T upstream_gene_variant ESCA-CN 2 163123838 163123838 single base substitution T A missense_variant I984L 2950A>T ESCA-CN 2 163134000 163134000 single base substitution C A missense_variant D657Y 1969G>T ESCA-CN 2 163149896 163149896 single base substitution G T downstream_gene_variant ESCA-CN 2 163149896 163149896 single base substitution G T intron_variant ESCA-CN 2 163163342 163163342 single base substitution C T downstream_gene_variant ESCA-CN 2 163163342 163163342 single base substitution C T exon_variant ESCA-CN 2 163163342 163163342 single base substitution C T missense_variant D216N 646G>A KIRC-US 2 163144684 163144684 single base substitution T G missense_variant K352N 1056A>C KIRC-US 2 163150172 163150172 single base substitution T C exon_variant KIRC-US 2 163150172 163150172 single base substitution T C missense_variant D259G 776A>G KIRP-US 2 163167397 163167397 single base substitution A G missense_variant L167P 500T>C KIRP-US 2 163167397 163167397 single base substitution A G upstream_gene_variant LAML-KR 2 163136727 163136727 single base substitution G C intron_variant LAML-KR 2 163149949 163149949 single base substitution C T downstream_gene_variant LAML-KR 2 163149949 163149949 single base substitution C T intron_variant LGG-US 2 163133214 163133214 single base substitution A C missense_variant F763V 2287T>G LGG-US 2 163134056 163134056 single base substitution A C missense_variant F638C 1913T>G LIAD-FR 2 163130325 163130325 single base substitution T A missense_variant N812Y 2434A>T LICA-CN 2 163128831 163128831 single base substitution T A missense_variant I841F 2521A>T LICA-FR 2 163167427 163167427 deletion of <=200bp T - frameshift_variant N157 LICA-FR 2 163167427 163167427 deletion of <=200bp T - upstream_gene_variant LICA-FR 2 163167691 163167691 insertion of <=200bp - T intron_variant LICA-FR 2 163167691 163167691 insertion of <=200bp - T upstream_gene_variant LICA-FR 2 163168489 163168489 single base substitution G A intron_variant LICA-FR 2 163168489 163168489 single base substitution G A upstream_gene_variant LINC-JP 2 163124572 163124572 single base substitution T C intron_variant LINC-JP 2 163133767 163133767 single base substitution T C intron_variant LINC-JP 2 163138124 163138124 single base substitution C A intron_variant LINC-JP 2 163138875 163138875 single base substitution C A splice_donor_variant LINC-JP 2 163145545 163145545 single base substitution G C downstream_gene_variant LINC-JP 2 163145545 163145545 single base substitution G C intron_variant LINC-JP 2 163154222 163154222 single base substitution T C intron_variant LIRI-JP 2 163119934 163119934 single base substitution C A downstream_gene_variant LIRI-JP 2 163120048 163120048 single base substitution T C downstream_gene_variant LIRI-JP 2 163121061 163121061 single base substitution T A downstream_gene_variant LIRI-JP 2 163123014 163123014 single base substitution A C downstream_gene_variant LIRI-JP 2 163125556 163125556 single base substitution C A intron_variant LIRI-JP 2 163125786 163125786 single base substitution C A intron_variant LIRI-JP 2 163127641 163127641 single base substitution C A intron_variant LIRI-JP 2 163128973 163128973 single base substitution T C intron_variant LIRI-JP 2 163128998 163129005 deletion of <=200bp TTGGGTTG - intron_variant LIRI-JP 2 163129705 163129705 single base substitution G A intron_variant LIRI-JP 2 163134193 163134193 single base substitution T C synonymous_variant E592E 1776A>G LIRI-JP 2 163135026 163135026 single base substitution A G intron_variant LIRI-JP 2 163135444 163135444 single base substitution T C intron_variant LIRI-JP 2 163135725 163135725 single base substitution T C intron_variant LIRI-JP 2 163136690 163136690 single base substitution T A intron_variant LIRI-JP 2 163139164 163139164 single base substitution G C intron_variant LIRI-JP 2 163140732 163140732 single base substitution T C intron_variant LIRI-JP 2 163142835 163142835 single base substitution G C intron_variant LIRI-JP 2 163144835 163144835 single base substitution G A missense_variant P302L 905C>T LIRI-JP 2 163145152 163145152 single base substitution G A downstream_gene_variant LIRI-JP 2 163145152 163145152 single base substitution G A intron_variant LIRI-JP 2 163146204 163146204 single base substitution A G downstream_gene_variant LIRI-JP 2 163146204 163146204 single base substitution A G intron_variant LIRI-JP 2 163146756 163146756 single base substitution A G downstream_gene_variant LIRI-JP 2 163146756 163146756 single base substitution A G intron_variant LIRI-JP 2 163147190 163147193 deletion of <=200bp AGAT - downstream_gene_variant LIRI-JP 2 163147190 163147193 deletion of <=200bp AGAT - intron_variant LIRI-JP 2 163149195 163149195 single base substitution A C downstream_gene_variant LIRI-JP 2 163149195 163149195 single base substitution A C intron_variant LIRI-JP 2 163151128 163151128 single base substitution T C intron_variant LIRI-JP 2 163151664 163151664 single base substitution T C intron_variant LIRI-JP 2 163152220 163152220 single base substitution T C intron_variant LIRI-JP 2 163154157 163154157 single base substitution A T intron_variant LIRI-JP 2 163154356 163154356 single base substitution A G intron_variant LIRI-JP 2 163156662 163156662 single base substitution T G intron_variant LIRI-JP 2 163157326 163157326 single base substitution T C intron_variant LIRI-JP 2 163157551 163157551 single base substitution T A intron_variant LIRI-JP 2 163157839 163157844 deletion of <=200bp ACGCTG - intron_variant LIRI-JP 2 163158786 163158786 single base substitution G T intron_variant LIRI-JP 2 163161456 163161456 single base substitution T C intron_variant LIRI-JP 2 163162864 163162864 single base substitution T C downstream_gene_variant LIRI-JP 2 163162864 163162864 single base substitution T C intron_variant LIRI-JP 2 163163609 163163609 single base substitution T A downstream_gene_variant LIRI-JP 2 163163609 163163609 single base substitution T A exon_variant LIRI-JP 2 163163609 163163609 single base substitution T A intron_variant LIRI-JP 2 163164217 163164217 single base substitution T C downstream_gene_variant LIRI-JP 2 163164217 163164217 single base substitution T C intron_variant LIRI-JP 2 163164217 163164217 single base substitution T C upstream_gene_variant LIRI-JP 2 163164364 163164364 single base substitution A G downstream_gene_variant LIRI-JP 2 163164364 163164364 single base substitution A G intron_variant LIRI-JP 2 163164364 163164364 single base substitution A G upstream_gene_variant LIRI-JP 2 163168644 163168644 single base substitution C A intron_variant LIRI-JP 2 163168644 163168644 single base substitution C A upstream_gene_variant LIRI-JP 2 163169658 163169658 single base substitution A C intron_variant LIRI-JP 2 163171422 163171422 single base substitution C T intron_variant LIRI-JP 2 163173332 163173332 single base substitution T C intron_variant LIRI-JP 2 163173859 163173859 single base substitution G T intron_variant LIRI-JP 2 163176243 163176243 single base substitution G A upstream_gene_variant LIRI-JP 2 163176588 163176588 single base substitution A T upstream_gene_variant LIRI-JP 2 163179510 163179510 single base substitution T C upstream_gene_variant LUSC-KR 2 163119612 163119612 single base substitution C A downstream_gene_variant LUSC-KR 2 163120938 163120938 single base substitution T C downstream_gene_variant LUSC-KR 2 163128362 163128362 single base substitution C T intron_variant LUSC-KR 2 163129167 163129167 single base substitution C A intron_variant LUSC-KR 2 163129934 163129934 single base substitution C G intron_variant LUSC-KR 2 163130165 163130165 single base substitution T C intron_variant LUSC-KR 2 163131276 163131276 single base substitution C A intron_variant LUSC-KR 2 163131337 163131337 single base substitution C G intron_variant LUSC-KR 2 163132050 163132050 single base substitution A G intron_variant LUSC-KR 2 163132540 163132540 single base substitution C T intron_variant LUSC-KR 2 163132691 163132691 single base substitution T G intron_variant LUSC-KR 2 163135923 163135923 single base substitution A G intron_variant LUSC-KR 2 163136848 163136848 single base substitution T C intron_variant LUSC-KR 2 163137395 163137395 single base substitution T C intron_variant LUSC-KR 2 163141488 163141488 single base substitution C G intron_variant LUSC-KR 2 163142163 163142163 single base substitution T A intron_variant LUSC-KR 2 163142618 163142618 single base substitution C A intron_variant LUSC-KR 2 163142974 163142974 single base substitution G A intron_variant LUSC-KR 2 163144224 163144224 single base substitution A G intron_variant LUSC-KR 2 163153926 163153926 single base substitution C A intron_variant LUSC-KR 2 163157464 163157464 single base substitution T A intron_variant LUSC-KR 2 163157888 163157888 single base substitution C T intron_variant LUSC-KR 2 163158339 163158339 single base substitution T A intron_variant LUSC-KR 2 163162703 163162703 single base substitution T C downstream_gene_variant LUSC-KR 2 163162703 163162703 single base substitution T C intron_variant LUSC-KR 2 163165964 163165964 single base substitution T A downstream_gene_variant LUSC-KR 2 163165964 163165964 single base substitution T A intron_variant LUSC-KR 2 163165964 163165964 single base substitution T A upstream_gene_variant LUSC-KR 2 163167526 163167526 single base substitution G A intron_variant LUSC-KR 2 163167526 163167526 single base substitution G A upstream_gene_variant LUSC-KR 2 163167963 163167963 single base substitution T A intron_variant LUSC-KR 2 163167963 163167963 single base substitution T A upstream_gene_variant LUSC-KR 2 163173604 163173604 single base substitution T C intron_variant LUSC-KR 2 163180100 163180100 single base substitution G T upstream_gene_variant LUSC-KR 2 163180202 163180202 single base substitution C G upstream_gene_variant LUSC-US 2 163130385 163130385 single base substitution C T missense_variant A792T 2374G>A LUSC-US 2 163133387 163133387 single base substitution C A missense_variant R705I 2114G>T LUSC-US 2 163144789 163144789 single base substitution C G missense_variant Q317H 951G>C LUSC-US 2 163174519 163174519 single base substitution G A missense_variant T100M 299C>T LUSC-US 2 163174569 163174569 single base substitution G T synonymous_variant L83L 249C>A LUSC-US 2 163174644 163174644 single base substitution T C synonymous_variant A58A 174A>G MALY-DE 2 163122029 163122029 single base substitution C T downstream_gene_variant MALY-DE 2 163123063 163123063 single base substitution G A downstream_gene_variant MALY-DE 2 163124199 163124199 single base substitution T A intron_variant MALY-DE 2 163124407 163124407 single base substitution T G intron_variant MALY-DE 2 163124665 163124665 single base substitution T C synonymous_variant L913L 2739A>G MALY-DE 2 163124766 163124766 single base substitution T C missense_variant S880G 2638A>G MALY-DE 2 163126191 163126196 deletion of <=200bp TTTTCT - intron_variant MALY-DE 2 163128956 163128956 single base substitution G T intron_variant MALY-DE 2 163133708 163133708 single base substitution A T intron_variant MALY-DE 2 163153448 163153448 single base substitution T A intron_variant MALY-DE 2 163161086 163161086 single base substitution G A intron_variant MALY-DE 2 163164642 163164642 single base substitution T C downstream_gene_variant MALY-DE 2 163164642 163164642 single base substitution T C intron_variant MALY-DE 2 163164642 163164642 single base substitution T C upstream_gene_variant MALY-DE 2 163167215 163167215 single base substitution A G 3_prime_UTR_variant MALY-DE 2 163167215 163167215 single base substitution A G intron_variant MALY-DE 2 163167215 163167215 single base substitution A G upstream_gene_variant MALY-DE 2 163170932 163170934 deletion of <=200bp TTC - intron_variant MALY-DE 2 163171660 163171660 single base substitution T C intron_variant MALY-DE 2 163173170 163173170 single base substitution G A intron_variant MALY-DE 2 163178126 163178126 single base substitution G C upstream_gene_variant MELA-AU 2 163118911 163118911 single base substitution C T downstream_gene_variant MELA-AU 2 163118956 163118956 single base substitution T G downstream_gene_variant MELA-AU 2 163119263 163119263 single base substitution G A downstream_gene_variant MELA-AU 2 163119366 163119366 single base substitution G A downstream_gene_variant MELA-AU 2 163119377 163119377 single base substitution G A downstream_gene_variant MELA-AU 2 163119877 163119877 single base substitution C T downstream_gene_variant MELA-AU 2 163120534 163120534 single base substitution A T downstream_gene_variant MELA-AU 2 163121029 163121030 multiple base substitution (>=2bp and <=200bp) AA TT downstream_gene_variant MELA-AU 2 163121136 163121136 single base substitution C T downstream_gene_variant MELA-AU 2 163121502 163121502 single base substitution C T downstream_gene_variant MELA-AU 2 163121676 163121676 single base substitution G A downstream_gene_variant MELA-AU 2 163122809 163122809 single base substitution A G downstream_gene_variant MELA-AU 2 163123001 163123001 single base substitution G A downstream_gene_variant MELA-AU 2 163123002 163123002 single base substitution G A downstream_gene_variant MELA-AU 2 163123170 163123170 single base substitution G A downstream_gene_variant MELA-AU 2 163123504 163123504 single base substitution G A downstream_gene_variant MELA-AU 2 163123514 163123514 single base substitution G A downstream_gene_variant MELA-AU 2 163123524 163123524 single base substitution C T downstream_gene_variant MELA-AU 2 163123537 163123537 single base substitution C A downstream_gene_variant MELA-AU 2 163123640 163123640 single base substitution A T 3_prime_UTR_variant MELA-AU 2 163124026 163124026 single base substitution T A missense_variant Y954F 2861A>T MELA-AU 2 163126211 163126211 single base substitution G A intron_variant MELA-AU 2 163127061 163127061 single base substitution G A intron_variant MELA-AU 2 163127423 163127423 single base substitution C T intron_variant MELA-AU 2 163128081 163128081 single base substitution C T intron_variant MELA-AU 2 163128287 163128287 single base substitution G A intron_variant MELA-AU 2 163128391 163128391 single base substitution G A intron_variant MELA-AU 2 163128572 163128572 single base substitution G A intron_variant MELA-AU 2 163128715 163128715 single base substitution T G intron_variant MELA-AU 2 163129243 163129243 single base substitution G A intron_variant MELA-AU 2 163129668 163129668 single base substitution G A intron_variant MELA-AU 2 163129998 163129998 single base substitution G A intron_variant MELA-AU 2 163130186 163130186 single base substitution A G intron_variant MELA-AU 2 163130307 163130307 single base substitution G A stop_gained Q818* 2452C>T MELA-AU 2 163130519 163130519 single base substitution G A intron_variant MELA-AU 2 163130745 163130745 single base substitution G A intron_variant MELA-AU 2 163130789 163130789 single base substitution G A intron_variant MELA-AU 2 163131088 163131088 single base substitution G A intron_variant MELA-AU 2 163132396 163132396 single base substitution G A intron_variant MELA-AU 2 163132710 163132710 single base substitution G A intron_variant MELA-AU 2 163132755 163132755 single base substitution G A intron_variant MELA-AU 2 163133127 163133127 single base substitution A G intron_variant MELA-AU 2 163133186 163133186 single base substitution G A intron_variant MELA-AU 2 163133621 163133621 single base substitution G A intron_variant MELA-AU 2 163133814 163133814 single base substitution G A intron_variant MELA-AU 2 163134356 163134356 single base substitution G A intron_variant MELA-AU 2 163134515 163134515 single base substitution G A intron_variant MELA-AU 2 163134730 163134730 single base substitution G A stop_gained Q584* 1750C>T MELA-AU 2 163135061 163135061 single base substitution G A intron_variant MELA-AU 2 163135097 163135097 single base substitution T A intron_variant MELA-AU 2 163135282 163135282 single base substitution G A intron_variant MELA-AU 2 163136166 163136166 single base substitution G A intron_variant MELA-AU 2 163136326 163136326 single base substitution C A intron_variant MELA-AU 2 163136556 163136556 single base substitution G A stop_gained Q531* 1591C>T MELA-AU 2 163137245 163137245 single base substitution G A intron_variant MELA-AU 2 163137636 163137636 single base substitution G A intron_variant MELA-AU 2 163137923 163137923 single base substitution G A missense_variant P480L 1439C>T MELA-AU 2 163138276 163138276 single base substitution C T intron_variant MELA-AU 2 163138627 163138627 single base substitution G A intron_variant MELA-AU 2 163138746 163138746 single base substitution G A intron_variant MELA-AU 2 163138760 163138760 single base substitution C T intron_variant MELA-AU 2 163138820 163138820 single base substitution T G intron_variant MELA-AU 2 163139340 163139340 single base substitution C T intron_variant MELA-AU 2 163139361 163139361 single base substitution G A intron_variant MELA-AU 2 163139388 163139388 single base substitution C T intron_variant MELA-AU 2 163139470 163139470 single base substitution G A intron_variant MELA-AU 2 163139498 163139498 single base substitution C T intron_variant MELA-AU 2 163139751 163139751 single base substitution G A intron_variant MELA-AU 2 163139970 163139970 single base substitution G A intron_variant MELA-AU 2 163140065 163140065 single base substitution G A intron_variant MELA-AU 2 163140337 163140337 single base substitution G A intron_variant MELA-AU 2 163140614 163140614 single base substitution G A intron_variant MELA-AU 2 163141003 163141003 single base substitution G A intron_variant MELA-AU 2 163141161 163141161 single base substitution G A intron_variant MELA-AU 2 163141760 163141760 single base substitution G A intron_variant MELA-AU 2 163141843 163141843 single base substitution G A intron_variant MELA-AU 2 163141982 163141982 single base substitution G T intron_variant MELA-AU 2 163142068 163142068 single base substitution C A intron_variant MELA-AU 2 163142360 163142360 single base substitution T C intron_variant MELA-AU 2 163142378 163142378 single base substitution G A intron_variant MELA-AU 2 163142925 163142925 single base substitution G A intron_variant MELA-AU 2 163142942 163142942 single base substitution G A intron_variant MELA-AU 2 163143097 163143097 single base substitution G A intron_variant MELA-AU 2 163143675 163143675 single base substitution C T intron_variant MELA-AU 2 163143845 163143845 single base substitution G A intron_variant MELA-AU 2 163144021 163144021 single base substitution A T intron_variant MELA-AU 2 163144181 163144181 single base substitution G A intron_variant MELA-AU 2 163144368 163144368 single base substitution G A intron_variant MELA-AU 2 163144672 163144672 single base substitution A C synonymous_variant P356P 1068T>G MELA-AU 2 163144775 163144775 single base substitution C T missense_variant G322E 965G>A MELA-AU 2 163145121 163145121 single base substitution A T downstream_gene_variant MELA-AU 2 163145121 163145121 single base substitution A T intron_variant MELA-AU 2 163145165 163145165 single base substitution G A downstream_gene_variant MELA-AU 2 163145165 163145165 single base substitution G A intron_variant MELA-AU 2 163145753 163145753 single base substitution G A downstream_gene_variant MELA-AU 2 163145753 163145753 single base substitution G A intron_variant MELA-AU 2 163145870 163145870 single base substitution C T downstream_gene_variant MELA-AU 2 163145870 163145870 single base substitution C T intron_variant MELA-AU 2 163145998 163145998 single base substitution G A downstream_gene_variant MELA-AU 2 163145998 163145998 single base substitution G A intron_variant MELA-AU 2 163146392 163146392 single base substitution G A downstream_gene_variant MELA-AU 2 163146392 163146392 single base substitution G A intron_variant MELA-AU 2 163146568 163146568 single base substitution G A downstream_gene_variant MELA-AU 2 163146568 163146568 single base substitution G A intron_variant MELA-AU 2 163147231 163147231 single base substitution G A downstream_gene_variant MELA-AU 2 163147231 163147231 single base substitution G A intron_variant MELA-AU 2 163147282 163147282 single base substitution G A downstream_gene_variant MELA-AU 2 163147282 163147282 single base substitution G A intron_variant MELA-AU 2 163149085 163149085 single base substitution G A downstream_gene_variant MELA-AU 2 163149085 163149085 single base substitution G A intron_variant MELA-AU 2 163149578 163149578 single base substitution G A downstream_gene_variant MELA-AU 2 163149578 163149578 single base substitution G A intron_variant MELA-AU 2 163149845 163149845 single base substitution C T downstream_gene_variant MELA-AU 2 163149845 163149845 single base substitution C T intron_variant MELA-AU 2 163150577 163150577 single base substitution G A intron_variant MELA-AU 2 163152138 163152138 single base substitution T C intron_variant MELA-AU 2 163152392 163152392 single base substitution G A intron_variant MELA-AU 2 163152514 163152514 single base substitution G A intron_variant MELA-AU 2 163152794 163152794 single base substitution G A intron_variant MELA-AU 2 163152882 163152882 single base substitution C T intron_variant MELA-AU 2 163153545 163153545 single base substitution G A intron_variant MELA-AU 2 163153662 163153662 insertion of <=200bp - AC intron_variant MELA-AU 2 163154003 163154003 single base substitution G A intron_variant MELA-AU 2 163154077 163154077 single base substitution G A intron_variant MELA-AU 2 163154104 163154104 single base substitution G A intron_variant MELA-AU 2 163154176 163154176 single base substitution G A intron_variant MELA-AU 2 163154304 163154304 single base substitution G A intron_variant MELA-AU 2 163155084 163155084 single base substitution G A intron_variant MELA-AU 2 163155111 163155111 single base substitution G A intron_variant MELA-AU 2 163155236 163155236 single base substitution G A intron_variant MELA-AU 2 163155346 163155346 single base substitution C T intron_variant MELA-AU 2 163155455 163155455 single base substitution G A intron_variant MELA-AU 2 163155691 163155691 single base substitution G A intron_variant MELA-AU 2 163155902 163155902 single base substitution G A intron_variant MELA-AU 2 163158532 163158532 single base substitution G A intron_variant MELA-AU 2 163159242 163159242 single base substitution G A intron_variant MELA-AU 2 163159644 163159644 single base substitution G A intron_variant MELA-AU 2 163159896 163159896 single base substitution G A intron_variant MELA-AU 2 163160097 163160097 single base substitution G A intron_variant MELA-AU 2 163160127 163160127 single base substitution G A intron_variant MELA-AU 2 163160160 163160160 single base substitution G A intron_variant MELA-AU 2 163160584 163160584 single base substitution G A intron_variant MELA-AU 2 163161004 163161004 single base substitution A T intron_variant MELA-AU 2 163161202 163161202 single base substitution G A intron_variant MELA-AU 2 163161226 163161226 single base substitution G A intron_variant MELA-AU 2 163161825 163161825 single base substitution A T downstream_gene_variant MELA-AU 2 163161825 163161825 single base substitution A T intron_variant MELA-AU 2 163161842 163161843 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 2 163161842 163161843 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 2 163161866 163161866 single base substitution G A downstream_gene_variant MELA-AU 2 163161866 163161866 single base substitution G A intron_variant MELA-AU 2 163162315 163162315 single base substitution A G downstream_gene_variant MELA-AU 2 163162315 163162315 single base substitution A G intron_variant MELA-AU 2 163164072 163164072 single base substitution G A downstream_gene_variant MELA-AU 2 163164072 163164072 single base substitution G A intron_variant MELA-AU 2 163164072 163164072 single base substitution G A upstream_gene_variant MELA-AU 2 163164540 163164540 single base substitution G A downstream_gene_variant MELA-AU 2 163164540 163164540 single base substitution G A intron_variant MELA-AU 2 163164540 163164540 single base substitution G A upstream_gene_variant MELA-AU 2 163164971 163164971 single base substitution C T downstream_gene_variant MELA-AU 2 163164971 163164971 single base substitution C T intron_variant MELA-AU 2 163164971 163164971 single base substitution C T upstream_gene_variant MELA-AU 2 163165053 163165053 single base substitution A G downstream_gene_variant MELA-AU 2 163165053 163165053 single base substitution A G intron_variant MELA-AU 2 163165053 163165053 single base substitution A G upstream_gene_variant MELA-AU 2 163165555 163165555 single base substitution G A downstream_gene_variant MELA-AU 2 163165555 163165555 single base substitution G A intron_variant MELA-AU 2 163165555 163165555 single base substitution G A upstream_gene_variant MELA-AU 2 163166015 163166015 single base substitution G A downstream_gene_variant MELA-AU 2 163166015 163166015 single base substitution G A intron_variant MELA-AU 2 163166015 163166015 single base substitution G A upstream_gene_variant MELA-AU 2 163166222 163166222 single base substitution G A downstream_gene_variant MELA-AU 2 163166222 163166222 single base substitution G A intron_variant MELA-AU 2 163166222 163166222 single base substitution G A upstream_gene_variant MELA-AU 2 163166226 163166227 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 2 163166226 163166227 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 2 163166226 163166227 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 2 163166232 163166232 single base substitution G A downstream_gene_variant MELA-AU 2 163166232 163166232 single base substitution G A intron_variant MELA-AU 2 163166232 163166232 single base substitution G A upstream_gene_variant MELA-AU 2 163167066 163167066 single base substitution G A 3_prime_UTR_variant MELA-AU 2 163167066 163167066 single base substitution G A intron_variant MELA-AU 2 163167066 163167066 single base substitution G A upstream_gene_variant MELA-AU 2 163167112 163167112 single base substitution C T 3_prime_UTR_variant MELA-AU 2 163167112 163167112 single base substitution C T intron_variant MELA-AU 2 163167112 163167112 single base substitution C T upstream_gene_variant MELA-AU 2 163167903 163167903 single base substitution C T intron_variant MELA-AU 2 163167903 163167903 single base substitution C T upstream_gene_variant MELA-AU 2 163168473 163168473 single base substitution G A intron_variant MELA-AU 2 163168473 163168473 single base substitution G A upstream_gene_variant MELA-AU 2 163168747 163168747 single base substitution G A intron_variant MELA-AU 2 163169855 163169855 single base substitution T A intron_variant MELA-AU 2 163170121 163170121 single base substitution C T intron_variant MELA-AU 2 163170719 163170719 single base substitution G A intron_variant MELA-AU 2 163170998 163170998 single base substitution T C intron_variant MELA-AU 2 163171000 163171000 single base substitution C T intron_variant MELA-AU 2 163171569 163171569 deletion of <=200bp T - intron_variant MELA-AU 2 163173304 163173304 single base substitution C G intron_variant MELA-AU 2 163173875 163173875 single base substitution A T intron_variant MELA-AU 2 163177374 163177374 single base substitution C A upstream_gene_variant MELA-AU 2 163178678 163178678 deletion of <=200bp A - upstream_gene_variant MELA-AU 2 163179073 163179073 single base substitution C T upstream_gene_variant MELA-AU 2 163179127 163179127 single base substitution C T upstream_gene_variant MELA-AU 2 163179476 163179476 single base substitution C T upstream_gene_variant MELA-AU 2 163179907 163179907 single base substitution A T upstream_gene_variant ORCA-IN 2 163134104 163134104 single base substitution G A missense_variant A622V 1865C>T ORCA-IN 2 163142376 163142376 single base substitution C G intron_variant ORCA-IN 2 163171537 163171537 single base substitution C T intron_variant OV-AU 2 163121451 163121451 single base substitution G A downstream_gene_variant OV-AU 2 163130843 163130843 single base substitution T A intron_variant OV-AU 2 163147126 163147126 single base substitution C T downstream_gene_variant OV-AU 2 163147126 163147126 single base substitution C T intron_variant OV-AU 2 163148907 163148907 single base substitution G T downstream_gene_variant OV-AU 2 163148907 163148907 single base substitution G T intron_variant OV-AU 2 163149673 163149673 single base substitution C A downstream_gene_variant OV-AU 2 163149673 163149673 single base substitution C A intron_variant OV-AU 2 163152436 163152436 single base substitution T A intron_variant OV-AU 2 163155282 163155282 single base substitution A C intron_variant OV-AU 2 163156993 163156993 single base substitution A T intron_variant OV-AU 2 163163080 163163080 single base substitution C A downstream_gene_variant OV-AU 2 163163080 163163080 single base substitution C A intron_variant OV-AU 2 163172182 163172182 single base substitution G T intron_variant OV-AU 2 163177975 163177975 single base substitution G A upstream_gene_variant PACA-AU 2 163122247 163122247 single base substitution T A downstream_gene_variant PACA-AU 2 163125807 163125807 single base substitution T A intron_variant PACA-AU 2 163127735 163127735 single base substitution A T intron_variant PACA-AU 2 163137714 163137714 single base substitution G A intron_variant PACA-AU 2 163141289 163141289 single base substitution T C intron_variant PACA-AU 2 163142705 163142705 single base substitution C T intron_variant PACA-AU 2 163147694 163147694 single base substitution A C downstream_gene_variant PACA-AU 2 163147694 163147694 single base substitution A C intron_variant PACA-AU 2 163147843 163147843 single base substitution A T downstream_gene_variant PACA-AU 2 163147843 163147843 single base substitution A T intron_variant PACA-AU 2 163151823 163151823 single base substitution T A intron_variant PACA-AU 2 163155774 163155774 insertion of <=200bp - C intron_variant PACA-AU 2 163155926 163155926 single base substitution A G intron_variant PACA-AU 2 163157995 163157995 single base substitution A C intron_variant PACA-AU 2 163159178 163159178 single base substitution C A intron_variant PACA-AU 2 163160662 163160662 single base substitution G C intron_variant PACA-AU 2 163166323 163166323 single base substitution G A downstream_gene_variant PACA-AU 2 163166323 163166323 single base substitution G A intron_variant PACA-AU 2 163166323 163166323 single base substitution G A upstream_gene_variant PACA-AU 2 163169447 163169447 single base substitution C T intron_variant PACA-AU 2 163171485 163171485 single base substitution G A intron_variant PACA-AU 2 163176133 163176133 single base substitution A T upstream_gene_variant PACA-AU 2 163176366 163176366 single base substitution A T upstream_gene_variant PACA-AU 2 163178979 163178979 single base substitution C T upstream_gene_variant PACA-CA 2 163119715 163119715 single base substitution G A downstream_gene_variant PACA-CA 2 163121625 163121625 single base substitution G A downstream_gene_variant PACA-CA 2 163129875 163129875 single base substitution A C intron_variant PACA-CA 2 163131803 163131803 single base substitution T G intron_variant PACA-CA 2 163138468 163138468 single base substitution T C intron_variant PACA-CA 2 163142162 163142162 single base substitution T G intron_variant PACA-CA 2 163154000 163154003 deletion of <=200bp AGAG - intron_variant PACA-CA 2 163155300 163155300 single base substitution G A intron_variant PACA-CA 2 163155302 163155302 single base substitution A G intron_variant PACA-CA 2 163163024 163163024 single base substitution C T downstream_gene_variant PACA-CA 2 163163024 163163024 single base substitution C T intron_variant PACA-CA 2 163163751 163163751 single base substitution A G downstream_gene_variant PACA-CA 2 163163751 163163751 single base substitution A G intron_variant PACA-CA 2 163163751 163163751 single base substitution A G upstream_gene_variant PACA-CA 2 163164494 163164494 single base substitution C G downstream_gene_variant PACA-CA 2 163164494 163164494 single base substitution C G intron_variant PACA-CA 2 163164494 163164494 single base substitution C G upstream_gene_variant PACA-CA 2 163164773 163164773 single base substitution C T downstream_gene_variant PACA-CA 2 163164773 163164773 single base substitution C T intron_variant PACA-CA 2 163164773 163164773 single base substitution C T upstream_gene_variant PACA-CA 2 163165327 163165327 single base substitution T A downstream_gene_variant PACA-CA 2 163165327 163165327 single base substitution T A intron_variant PACA-CA 2 163165327 163165327 single base substitution T A upstream_gene_variant PACA-CA 2 163165412 163165412 single base substitution C T downstream_gene_variant PACA-CA 2 163165412 163165412 single base substitution C T intron_variant PACA-CA 2 163165412 163165412 single base substitution C T upstream_gene_variant PACA-CA 2 163167341 163167341 single base substitution G C missense_variant R186G 556C>G PACA-CA 2 163167341 163167341 single base substitution G C upstream_gene_variant PACA-CA 2 163167641 163167641 single base substitution A T intron_variant PACA-CA 2 163167641 163167641 single base substitution A T upstream_gene_variant PACA-CA 2 163168236 163168236 single base substitution C G intron_variant PACA-CA 2 163168236 163168236 single base substitution C G upstream_gene_variant PACA-CA 2 163169135 163169135 single base substitution G A intron_variant PACA-CA 2 163169269 163169269 single base substitution T G intron_variant PACA-CA 2 163169962 163169962 single base substitution G A intron_variant PACA-CA 2 163170208 163170208 single base substitution A T intron_variant PACA-CA 2 163170950 163170950 single base substitution C A intron_variant PACA-CA 2 163171732 163171732 single base substitution G A intron_variant PACA-CA 2 163174520 163174520 single base substitution T C missense_variant T100A 298A>G PACA-CA 2 163177210 163177210 single base substitution A G upstream_gene_variant PACA-CA 2 163178443 163178443 single base substitution T C upstream_gene_variant PACA-CA 2 163179995 163179995 single base substitution T C upstream_gene_variant PACA-CA 2 163180083 163180083 single base substitution A G upstream_gene_variant PAEN-IT 2 163170536 163170536 single base substitution C A intron_variant PAEN-IT 2 163176794 163176794 single base substitution G A upstream_gene_variant PBCA-DE 2 163125016 163125016 single base substitution C T intron_variant PBCA-DE 2 163126264 163126264 single base substitution T A intron_variant PBCA-DE 2 163139260 163139260 single base substitution A C intron_variant PBCA-DE 2 163140493 163140493 deletion of <=200bp T - intron_variant PBCA-DE 2 163145639 163145639 single base substitution G T downstream_gene_variant PBCA-DE 2 163145639 163145639 single base substitution G T intron_variant PBCA-DE 2 163155301 163155302 deletion of <=200bp CA - intron_variant PBCA-DE 2 163171201 163171201 single base substitution T C intron_variant PBCA-DE 2 163173527 163173528 deletion of <=200bp GT - intron_variant PBCA-DE 2 163174931 163174931 single base substitution C A 5_prime_UTR_variant PRAD-CA 2 163127740 163127740 single base substitution C A intron_variant PRAD-CA 2 163128824 163128824 single base substitution T C missense_variant H843R 2528A>G PRAD-CA 2 163131571 163131571 single base substitution T G intron_variant PRAD-CA 2 163142283 163142283 single base substitution A T intron_variant PRAD-CA 2 163144938 163144938 single base substitution C T intron_variant PRAD-CA 2 163178711 163178711 single base substitution A G upstream_gene_variant PRAD-UK 2 163125934 163125934 single base substitution G A intron_variant PRAD-UK 2 163126316 163126316 single base substitution T G intron_variant PRAD-UK 2 163126661 163126661 deletion of <=200bp A - intron_variant PRAD-UK 2 163142591 163142591 single base substitution G A intron_variant PRAD-UK 2 163142721 163142721 single base substitution A C intron_variant PRAD-UK 2 163150300 163150300 single base substitution A C intron_variant PRAD-UK 2 163150940 163150940 single base substitution C T intron_variant PRAD-UK 2 163150979 163150979 deletion of <=200bp G - intron_variant PRAD-UK 2 163155062 163155062 single base substitution C T intron_variant PRAD-UK 2 163160270 163160270 single base substitution A T intron_variant READ-US 2 163133977 163133977 single base substitution C A missense_variant K664N 1992G>T READ-US 2 163134117 163134117 single base substitution G A stop_gained R618* 1852C>T READ-US 2 163137949 163137950 deletion of <=200bp GA - frameshift_variant L471 RECA-EU 2 163121955 163121955 single base substitution G A downstream_gene_variant RECA-EU 2 163126044 163126044 single base substitution T C intron_variant RECA-EU 2 163126300 163126300 single base substitution G A intron_variant RECA-EU 2 163127386 163127386 single base substitution G T intron_variant RECA-EU 2 163128491 163128491 single base substitution G C intron_variant RECA-EU 2 163130568 163130568 single base substitution C T intron_variant RECA-EU 2 163133116 163133116 single base substitution A C intron_variant RECA-EU 2 163136622 163136622 single base substitution G C missense_variant L509V 1525C>G RECA-EU 2 163136623 163136623 single base substitution C T splice_acceptor_variant RECA-EU 2 163145216 163145216 single base substitution C T downstream_gene_variant RECA-EU 2 163145216 163145216 single base substitution C T intron_variant RECA-EU 2 163154902 163154902 single base substitution A T intron_variant RECA-EU 2 163163214 163163214 single base substitution A C downstream_gene_variant RECA-EU 2 163163214 163163214 single base substitution A C intron_variant RECA-EU 2 163163214 163163214 single base substitution A C splice_region_variant SKCA-BR 2 163121215 163121215 insertion of <=200bp - TTAC downstream_gene_variant SKCA-BR 2 163123975 163123975 single base substitution A T intron_variant SKCA-BR 2 163126167 163126167 single base substitution A T intron_variant SKCA-BR 2 163127720 163127720 single base substitution C T intron_variant SKCA-BR 2 163128824 163128824 single base substitution T C missense_variant H843R 2528A>G SKCA-BR 2 163135128 163135128 single base substitution G A intron_variant SKCA-BR 2 163136503 163136503 single base substitution T C splice_region_variant SKCA-BR 2 163138115 163138115 single base substitution G A intron_variant SKCA-BR 2 163140114 163140114 single base substitution C T intron_variant SKCA-BR 2 163140296 163140296 single base substitution G A intron_variant SKCA-BR 2 163140383 163140383 single base substitution G A intron_variant SKCA-BR 2 163145202 163145202 single base substitution T G downstream_gene_variant SKCA-BR 2 163145202 163145202 single base substitution T G intron_variant SKCA-BR 2 163149895 163149895 insertion of <=200bp - AC downstream_gene_variant SKCA-BR 2 163149895 163149895 insertion of <=200bp - AC intron_variant SKCA-BR 2 163149924 163149924 single base substitution G A downstream_gene_variant SKCA-BR 2 163149924 163149924 single base substitution G A intron_variant SKCA-BR 2 163153239 163153239 single base substitution G A intron_variant SKCA-BR 2 163153636 163153661 deletion of <=200bp CACTTTAAAAACCGTATTACACACAA - intron_variant SKCA-BR 2 163160056 163160056 single base substitution A T intron_variant SKCA-BR 2 163160743 163160743 single base substitution G A intron_variant SKCA-BR 2 163165762 163165762 single base substitution G A downstream_gene_variant SKCA-BR 2 163165762 163165762 single base substitution G A intron_variant SKCA-BR 2 163165762 163165762 single base substitution G A upstream_gene_variant SKCA-BR 2 163166358 163166358 single base substitution G A downstream_gene_variant SKCA-BR 2 163166358 163166358 single base substitution G A intron_variant SKCA-BR 2 163166358 163166358 single base substitution G A upstream_gene_variant SKCA-BR 2 163168735 163168735 single base substitution G A intron_variant SKCA-BR 2 163170908 163170908 insertion of <=200bp - CCTTT intron_variant SKCA-BR 2 163178417 163178445 deletion of <=200bp TATATATATATATATATATATATATATAC - upstream_gene_variant SKCA-BR 2 163178427 163178445 deletion of <=200bp TATATATATATATATATAC - upstream_gene_variant SKCA-BR 2 163178445 163178445 single base substitution C T upstream_gene_variant SKCA-BR 2 163179425 163179425 single base substitution A G upstream_gene_variant SKCA-BR 2 163179528 163179528 single base substitution C T upstream_gene_variant SKCM-US 2 163124007 163124007 single base substitution G A synonymous_variant I960I 2880C>T SKCM-US 2 163124026 163124026 single base substitution T A missense_variant Y954F 2861A>T SKCM-US 2 163124040 163124040 single base substitution C T synonymous_variant K949K 2847G>A SKCM-US 2 163124599 163124599 single base substitution G A splice_region_variant SKCM-US 2 163128755 163128755 single base substitution G A missense_variant P866L 2597C>T SKCM-US 2 163128858 163128858 single base substitution G A synonymous_variant L832L 2494C>T SKCM-US 2 163130398 163130398 single base substitution G A synonymous_variant I787I 2361C>T SKCM-US 2 163133297 163133297 single base substitution G A missense_variant S735F 2204C>T SKCM-US 2 163134116 163134116 single base substitution C T missense_variant R618Q 1853G>A SKCM-US 2 163134154 163134154 single base substitution C T synonymous_variant R605R 1815G>A SKCM-US 2 163134738 163134738 single base substitution C T stop_gained W581* 1742G>A SKCM-US 2 163134828 163134828 single base substitution T A missense_variant K551I 1652A>T SKCM-US 2 163136531 163136531 single base substitution A G missense_variant F539S 1616T>C SKCM-US 2 163138964 163138964 single base substitution G A synonymous_variant S406S 1218C>T SKCM-US 2 163139026 163139026 single base substitution G A missense_variant R386C 1156C>T SKCM-US 2 163144699 163144699 single base substitution T C synonymous_variant L347L 1041A>G SKCM-US 2 163144837 163144837 single base substitution G A synonymous_variant S301S 903C>T SKCM-US 2 163163287 163163287 single base substitution T C downstream_gene_variant SKCM-US 2 163163287 163163287 single base substitution T C exon_variant SKCM-US 2 163163287 163163287 single base substitution T C missense_variant E234G 701A>G SKCM-US 2 163163336 163163336 single base substitution G A downstream_gene_variant SKCM-US 2 163163336 163163336 single base substitution G A exon_variant SKCM-US 2 163163336 163163336 single base substitution G A missense_variant P218S 652C>T STAD-US 2 163128888 163128888 single base substitution G A stop_gained R822* 2464C>T STAD-US 2 163134117 163134117 single base substitution G A stop_gained R618* 1852C>T STAD-US 2 163134716 163134716 insertion of <=200bp - T frameshift_variant K588K? STAD-US 2 163138979 163138979 single base substitution T C synonymous_variant P401P 1203A>G STAD-US 2 163163274 163163274 single base substitution C A downstream_gene_variant STAD-US 2 163163274 163163274 single base substitution C A exon_variant STAD-US 2 163163274 163163274 single base substitution C A missense_variant W238C 714G>T STAD-US 2 163174369 163174369 single base substitution T G missense_variant N150T 449A>C STAD-US 2 163174424 163174424 single base substitution T G synonymous_variant R132R 394A>C STAD-US 2 163174504 163174504 single base substitution G A missense_variant P105L 314C>T STAD-US 2 163174673 163174673 single base substitution T C missense_variant T49A 145A>G UCEC-US 2 163123734 163123734 single base substitution G A synonymous_variant C1018C 3054C>T UCEC-US 2 163123794 163123794 deletion of <=200bp T - frameshift_variant K998 UCEC-US 2 163130343 163130343 single base substitution G A missense_variant R806C 2416C>T UCEC-US 2 163130406 163130406 single base substitution G T missense_variant L785M 2353C>A UCEC-US 2 163134170 163134170 single base substitution C T missense_variant C600Y 1799G>A UCEC-US 2 163137871 163137871 single base substitution C T synonymous_variant T497T 1491G>A UCEC-US 2 163144679 163144679 single base substitution G A missense_variant S354F 1061C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3080 COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - PAPNNX COSM5004676 c.1490C>T p.T497M Substitution - Missense 2:162281362-162281362 - LPJ041 COSM1316024 c.913G>C p.E305Q Substitution - Missense 2:162288317-162288317 - LUAD-S01345 COSM397172 c.1036C>T p.H346Y Substitution - Missense 2:162288194-162288194 - S00472 COSM311916 c.2071G>T p.A691S Substitution - Missense 2:162276920-162276920 - TCGA-AZ-6601-01 COSM1400470 c.2279G>T p.S760I Substitution - Missense 2:162276712-162276712 - Pat_40_B COSM3837174 c.2317G>A p.E773K Substitution - Missense 2:162273932-162273932 - PDA_067 COSM5001499 c.391G>T p.V131F Substitution - Missense 2:162317917-162317917 - TCGA-CG-4305-01 COSM4086015 c.714G>T p.W238C Substitution - Missense 2:162306764-162306764 - CHEWS002 COSM4582747 c.829A>T p.N277Y Substitution - Missense 2:162293609-162293609 - SNUH_G76_S1 COSM4418116 c.2528A>G p.H843R Substitution - Missense 2:162272314-162272314 - TCGA-EE-A2MS-06 COSM3568535 c.652C>T p.P218S Substitution - Missense 2:162306826-162306826 - RMS80_ COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - pfg019T COSM1641679 c.874+7C>T p.? Unknown 2:162293557-162293557 - ESCC-148T COSM3938576 c.1969G>T p.D657Y Substitution - Missense 2:162277490-162277490 - KPOPBR-32-T COSM5964374 c.345C>T p.L115L Substitution - coding silent 2:162317963-162317963 - TCGA-AZ-6598-01 COSM1400479 c.950A>G p.Q317R Substitution - Missense 2:162288280-162288280 - LC_C21 COSM1186043 c.1220G>T p.C407F Substitution - Missense 2:162282452-162282452 - TCGA-CA-6717-01 COSM1400471 c.1838T>G p.I613S Substitution - Missense 2:162277621-162277621 - TCGA-EB-A5SE-01 COSM3311375 c.903C>T p.S301S Substitution - coding silent 2:162288327-162288327 - BN42 COSM1613579 c.1306+1G>T p.? Unknown 2:162282365-162282365 - RK119_C01 COSM3743949 c.905C>T p.P302L Substitution - Missense 2:162288325-162288325 - TCGA-36-2534-01 COSM1325826 c.646G>C p.D216H Substitution - Missense 2:162306832-162306832 - 02-P170 COSM4582748 c.420G>A p.E140E Substitution - coding silent 2:162317888-162317888 - CSCC-31-T COSM4536389 c.2298G>A p.M766I Substitution - Missense 2:162276693-162276693 - ZZUFHECRKL-G034T COSM5440269 c.2950A>T p.I984L Substitution - Missense 2:162267328-162267328 - TCGA-CJ-5682-01 COSM476107 c.1353A>G p.E451E Substitution - coding silent 2:162281499-162281499 - TCGA-FW-A3R5-06 COSM3895088 c.1218C>T p.S406S Substitution - coding silent 2:162282454-162282454 - S02351 COSM5695099 c.2346A>T p.K782N Substitution - Missense 2:162273903-162273903 - RKO COSM3311346 c.2215A>G p.T739A Substitution - Missense 2:162276776-162276776 - HDC82 COSM4636679 c.2210G>A p.W737* Substitution - Nonsense 2:162276781-162276781 - TCGA-AA-A010-01 COSM281851 c.1852C>T p.R618* Substitution - Nonsense 2:162277607-162277607 - PCSI_0504_Pa_P_526 COSM4806657 c.556C>G p.R186G Substitution - Missense 2:162310831-162310831 - Gp5D COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - TCGA-66-2770-01 COSM717203 c.299C>T p.T100M Substitution - Missense 2:162318009-162318009 - B89-10 COSM1752073 c.877G>A p.E293K Substitution - Missense 2:162288353-162288353 - RMS88_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-AP-A056-01 COSM1008378 c.1491G>A p.T497T Substitution - coding silent 2:162281361-162281361 - CSCC-27-T COSM4464070 c.1317C>T p.L439L Substitution - coding silent 2:162281535-162281535 - Pat_41_B COSM5860390 c.2127G>A p.M709I Substitution - Missense 2:162276864-162276864 - RMS110_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - YUGISMO COSM1691223 c.1444C>T p.P482S Substitution - Missense 2:162281408-162281408 - HT115 COSM3311361 c.1589A>G p.N530S Substitution - Missense 2:162280048-162280048 - TCGA-AP-A059-01 COSM244992 c.1799G>A p.C600Y Substitution - Missense 2:162277660-162277660 - TCGA-AS-3778-01 COSM1494669 c.1603C>A p.P535T Substitution - Missense 2:162280034-162280034 - MO_1012 COSM5552439 c.1952A>C p.D651A Substitution - Missense 2:162277507-162277507 - MO_1012 COSM207537 c.1865C>T p.A622V Substitution - Missense 2:162277594-162277594 - 255 COSM3732024 c.2827G>A p.E943K Substitution - Missense 2:162267550-162267550 - C135 COSM4618124 c.539C>T p.A180V Substitution - Missense 2:162310848-162310848 - TCGA-EE-A3AC-06 COSM3568524 c.2494C>T p.L832L Substitution - coding silent 2:162272348-162272348 - sysucc-274T COSM3311360 c.1619C>T p.A540V Substitution - Missense 2:162280018-162280018 - TCGA-EK-A3GM-01 COSM4823296 c.2530G>C p.E844Q Substitution - Missense 2:162272312-162272312 - RMS85_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-BR-8680-01 COSM281851 c.1852C>T p.R618* Substitution - Nonsense 2:162277607-162277607 - 409 COSM4430712 c.2236G>T p.E746* Substitution - Nonsense 2:162276755-162276755 - TCGA-AA-3663-01 COSM1400474 c.1757A>G p.E586G Substitution - Missense 2:162278213-162278213 - Pat_41_B COSM5860391 c.1463C>T p.T488I Substitution - Missense 2:162281389-162281389 - SNU-C4 COSM4653357 c.2548C>T p.R850* Substitution - Nonsense 2:162272294-162272294 - ATL043 COSM5707822 c.1967G>A p.G656D Substitution - Missense 2:162277492-162277492 - TCGA-DW-7834-01 COSM3990688 c.500T>C p.L167P Substitution - Missense 2:162310887-162310887 - RMS66_ COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - CT-TC COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - LUAD-S00488 COSM395212 c.1907A>C p.K636T Substitution - Missense 2:162277552-162277552 - YUKLAB COSM1686400 c.1095+2T>G p.? Unknown 2:162288133-162288133 - TCGA-F1-A448-01 COSM4086020 c.314C>T p.P105L Substitution - Missense 2:162317994-162317994 - SCMC_RM2_ COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - RH30SJ_ COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - sysucc-1038T COSM4418116 c.2528A>G p.H843R Substitution - Missense 2:162272314-162272314 - TCGA-D3-A1Q5-06 COSM3568522 c.2805C>T p.F935F Substitution - coding silent 2:162268089-162268089 - WA51 COSM240196 c.69A>C p.K23N Substitution - Missense 2:162318239-162318239 - BN42T COSM1613579 c.1306+1G>T p.? Unknown 2:162282365-162282365 - LS174T COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - PD4127a COSM161661 c.2667G>T p.K889N Substitution - Missense 2:162268227-162268227 - SNU-175 COSM3311374 c.904C>T p.P302S Substitution - Missense 2:162288326-162288326 - TCGA-F5-6814-01 COSM281851 c.1852C>T p.R618* Substitution - Nonsense 2:162277607-162277607 - PT14_1 COSM5896612 c.1510G>A p.E504K Substitution - Missense 2:162281342-162281342 - 10-P1058 COSM4582746 c.2304G>A p.Q768Q Substitution - coding silent 2:162276687-162276687 - TCGA-EE-A3AE-06 COSM3568533 c.1041A>G p.L347L Substitution - coding silent 2:162288189-162288189 - SWE-39 COSM1179905 c.816A>C p.E272D Substitution - Missense 2:162293622-162293622 - RMS112_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-BR-8680-01 COSM4086022 c.145A>G p.T49A Substitution - Missense 2:162318163-162318163 - RMS105_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - B89-10-Tumor COSM1752073 c.877G>A p.E293K Substitution - Missense 2:162288353-162288353 - Case3a COSM1717491 c.776A>T p.D259V Substitution - Missense 2:162293662-162293662 - TCGA-ER-A193-06 COSM3568529 c.1742G>A p.W581* Substitution - Nonsense 2:162278228-162278228 - TCGA-ER-A195-06 COSM3568531 c.1616T>C p.F539S Substitution - Missense 2:162280021-162280021 - D6 COSM5007222 c.2199G>A p.A733A Substitution - coding silent 2:162276792-162276792 - TCGA-A6-6654-01 COSM275529 c.2335C>T p.R779C Substitution - Missense 2:162273914-162273914 - RH18C COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - TCGA-33-4533-01 COSM717204 c.951G>C p.Q317H Substitution - Missense 2:162288279-162288279 - S00472 COSM311916 c.2071G>T p.A691S Substitution - Missense 2:162276920-162276920 - LUAD-YINHD COSM350397 c.454-1G>C p.? Unknown 2:162310934-162310934 - C0063T COSM4154562 c.1525-1G>A p.? Unknown 2:162280113-162280113 - ESO01T COSM1172812 c.2916G>T p.M972I Substitution - Missense 2:162267362-162267362 - TCGA-AZ-5403-01 COSM1400468 c.2313A>C p.Q771H Substitution - Missense 2:162273936-162273936 - TCGA-D5-6928-01 COSM1400472 c.1836A>G p.Q612Q Substitution - coding silent 2:162277623-162277623 - LUAD-F00162 COSM366339 c.841G>T p.G281C Substitution - Missense 2:162293597-162293597 - PT46 COSM3568532 c.1156C>T p.R386C Substitution - Missense 2:162282516-162282516 - LAU63 COSM232521 c.143G>A p.R48K Substitution - Missense 2:162318165-162318165 - 019T COSM1727929 c.1598A>T p.Q533L Substitution - Missense 2:162280039-162280039 - Case3c COSM1717491 c.776A>T p.D259V Substitution - Missense 2:162293662-162293662 - RH18C COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - HX19T COSM1613579 c.1306+1G>T p.? Unknown 2:162282365-162282365 - LS180 COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - PCSI_0062_Pa_X COSM3379818 c.298A>G p.T100A Substitution - Missense 2:162318010-162318010 - S02292 COSM5687738 c.453+3_453+8delAGGTGT p.? Unknown 2:162317847-162317852 - GHE0955 COSM5714879 c.2726A>C p.N909T Substitution - Missense 2:162268168-162268168 - TCGA-DK-A1AD-01 COSM717204 c.951G>C p.Q317H Substitution - Missense 2:162288279-162288279 - PD6728b COSM5781816 c.153C>A p.A51A Substitution - coding silent 2:162318155-162318155 - T3670 COSM4691799 c.1866G>A p.A622A Substitution - coding silent 2:162277593-162277593 - SNU-283 COSM3311358 c.1701G>A p.M567I Substitution - Missense 2:162278269-162278269 - T3090 COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - RMS77_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - LUAD-YINHD COSM350396 c.1047G>C p.K349N Substitution - Missense 2:162288183-162288183 - TCGA-AZ-4315-01 COSM1400475 c.1559C>A p.T520N Substitution - Missense 2:162280078-162280078 - Case3b COSM1717491 c.776A>T p.D259V Substitution - Missense 2:162293662-162293662 - BK0012 COSM4185737 c.3040G>C p.D1014H Substitution - Missense 2:162267238-162267238 - cSCCP1 COSM134041 c.1057G>A p.A353T Substitution - Missense 2:162288173-162288173 - TCGA-DU-5855-01 COSM3971664 c.1913T>G p.F638C Substitution - Missense 2:162277546-162277546 - TCGA-B5-A11N-01 COSM1008379 c.1061C>T p.S354F Substitution - Missense 2:162288169-162288169 - RMS66_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - Pat_40_A COSM3837174 c.2317G>A p.E773K Substitution - Missense 2:162273932-162273932 - TCGA-AH-6644-01 COSM1564734 c.1412_1413delTC p.L471fs*32 Deletion - Frameshift 2:162281439-162281440 - 18 COSM5744743 c.1871C>T p.T624I Substitution - Missense 2:162277588-162277588 - TCGA-EB-A3Y7-01 COSM3568519 c.2880C>T p.I960I Substitution - coding silent 2:162267497-162267497 - TCGA-FS-A1ZC-06 COSM3568523 c.2597C>T p.P866L Substitution - Missense 2:162272245-162272245 - YUKSI COSM5394658 c.962A>G p.E321G Substitution - Missense 2:162288268-162288268 - CHC976T COSM3668543 c.2434A>T p.N812Y Substitution - Missense 2:162273815-162273815 - Pat_59_B COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - B86 COSM1752072 c.1010G>C p.R337T Substitution - Missense 2:162288220-162288220 - TCGA-FS-A1ZK-06 COSM3568527 c.1853G>A p.R618Q Substitution - Missense 2:162277606-162277606 - TCGA-66-2782-01 COSM717205 c.2114G>T p.R705I Substitution - Missense 2:162276877-162276877 - sysucc-834T COSM5486187 c.2182C>T p.R728* Substitution - Nonsense 2:162276809-162276809 - HCA7 COSM4612123 c.1764_1765insA p.A589fs*21 Insertion - Frameshift 2:162278205-162278206 - TCGA-EE-A29M-06 COSM3568534 c.701A>G p.E234G Substitution - Missense 2:162306777-162306777 - TCGA-BR-6452-01 COSM4086016 c.449A>C p.N150T Substitution - Missense 2:162317859-162317859 - C0063T COSM4154561 c.1525C>G p.L509V Substitution - Missense 2:162280112-162280112 - HT115 COSM3311327 c.2937G>A p.L979L Substitution - coding silent 2:162267341-162267341 - 1_RESISTANT COSM1719116 c.1096-6_1096-5insC p.? Unknown 2:162282581-162282582 - B86-Tumor COSM1752072 c.1010G>C p.R337T Substitution - Missense 2:162288220-162288220 - TCGA-AP-A059-01 COSM1008377 c.2353C>A p.L785M Substitution - Missense 2:162273896-162273896 - LUAD-D01751 COSM338293 c.2116A>G p.N706D Substitution - Missense 2:162276875-162276875 - SJMB008 COSM255464 c.2616+6G>T p.? Unknown 2:162272220-162272220 - UM-SCC-47 COSM4599978 c.971A>G p.N324S Substitution - Missense 2:162288259-162288259 - OSCC-GB_00140111 COSM207537 c.1865C>T p.A622V Substitution - Missense 2:162277594-162277594 - TCGA-AP-A051-01 COSM1008372 c.3054C>T p.C1018C Substitution - coding silent 2:162267224-162267224 - TCGA-EW-A1IZ-01 COSM1482093 c.2431A>G p.T811A Substitution - Missense 2:162273818-162273818 - SC_9010 COSM5552329 c.1642G>T p.D548Y Substitution - Missense 2:162278328-162278328 - RMS10_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-LL-A5YM-01 COSM3837174 c.2317G>A p.E773K Substitution - Missense 2:162273932-162273932 - TCGA-EE-A3AA-06 COSM3568520 c.2861A>T p.Y954F Substitution - Missense 2:162267516-162267516 - TCGA-B8-4153-01 COSM476106 c.1484G>T p.G495V Substitution - Missense 2:162281368-162281368 - PT21_2 COSM5901139 c.2089G>A p.E697K Substitution - Missense 2:162276902-162276902 - TARGET-30-PARBLH COSM1285470 c.1843G>A p.D615N Substitution - Missense 2:162277616-162277616 - PASLZM COSM3311347 c.2198C>T p.A733V Substitution - Missense 2:162276793-162276793 - SNUH_G73_S1 COSM4415003 c.229C>T p.R77W Substitution - Missense 2:162318079-162318079 - TCGA-EE-A3AC-06 COSM3568525 c.2361C>T p.I787I Substitution - coding silent 2:162273888-162273888 - TCGA-24-2267-01 COSM71129 c.1051A>G p.K351E Substitution - Missense 2:162288179-162288179 - SJHGG041_D COSM4969632 c.1224_1226delTAT p.I411delI Deletion - In frame 2:162282446-162282448 - ML_97_T_01 COSM4418116 c.2528A>G p.H843R Substitution - Missense 2:162272314-162272314 - T155 COSM1176637 c.1908G>T p.K636N Substitution - Missense 2:162277551-162277551 - SNB75 COSM1683876 c.392delT p.R132fs*13 Deletion - Frameshift 2:162317916-162317916 - TCGA-FU-A3HZ-01 COSM4840310 c.2691G>T p.K897N Substitution - Missense 2:162268203-162268203 - 1_PRE-TREATMENT COSM1719116 c.1096-6_1096-5insC p.? Unknown 2:162282581-162282582 - TCGA-BG-A0M7-01 COSM1008375 c.2417G>A p.R806H Substitution - Missense 2:162273832-162273832 - TCGA-22-4599-01 COSM717201 c.174A>G p.A58A Substitution - coding silent 2:162318134-162318134 - YUTRAIN COSM4464070 c.1317C>T p.L439L Substitution - coding silent 2:162281535-162281535 - TCGA-ER-A19D-06 COSM3568528 c.1815G>A p.R605R Substitution - coding silent 2:162277644-162277644 - C0015T COSM4154563 c.769+5T>G p.? Unknown 2:162306704-162306704 - SS6003305 COSM3414179 c.1992G>T p.K664N Substitution - Missense 2:162277467-162277467 - PA195 COSM1162649 c.1282G>T p.E428* Substitution - Nonsense 2:162282390-162282390 - pfg038T COSM4763307 c.1386G>C p.L462F Substitution - Missense 2:162281466-162281466 - PD13299a COSM5776722 c.2556G>C p.K852N Substitution - Missense 2:162272286-162272286 - C086 COSM5532549 c.2715C>T p.F905F Substitution - coding silent 2:162268179-162268179 - RK214_C01 COSM3743948 c.1776A>G p.E592E Substitution - coding silent 2:162277683-162277683 - TCGA-B0-4713-01 COSM3364340 c.776A>G p.D259G Substitution - Missense 2:162293662-162293662 - LUAD-B00859 COSM332393 c.1684C>G p.Q562E Substitution - Missense 2:162278286-162278286 - 14T COSM207537 c.1865C>T p.A622V Substitution - Missense 2:162277594-162277594 - PR-09-2517 COSM244992 c.1799G>A p.C600Y Substitution - Missense 2:162277660-162277660 - TCGA-AA-A00N-01 COSM275530 c.1829C>T p.A610V Substitution - Missense 2:162277630-162277630 - PT34 COSM5910286 c.2080C>T p.P694S Substitution - Missense 2:162276911-162276911 - PTC-7C COSM4133204 c.583C>A p.Q195K Substitution - Missense 2:162310804-162310804 - TCGA-CA-5796-01 COSM1400469 c.2305-1G>T p.? Unknown 2:162273945-162273945 - TCGA-A3-3357-01 COSM476108 c.1056A>C p.K352N Substitution - Missense 2:162288174-162288174 - ME037T COSM227706 c.988C>T p.P330S Substitution - Missense 2:162288242-162288242 - S02248 COSM5679611 c.2903G>T p.W968L Substitution - Missense 2:162267375-162267375 - RD COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-C8-A274-01 COSM1482094 c.121G>C p.E41Q Substitution - Missense 2:162318187-162318187 - TCGA-AB-2841-03 COSM1318161 c.151G>A p.A51T Substitution - Missense 2:162318157-162318157 - 587228 COSM1210264 c.1924G>T p.E642* Substitution - Nonsense 2:162277535-162277535 - TCGA-46-3767-01 COSM717202 c.249C>A p.L83L Substitution - coding silent 2:162318059-162318059 - TCGA-AA-3663-01 COSM1400476 c.1545A>G p.A515A Substitution - coding silent 2:162280092-162280092 - CSCC-27-T COSM275529 c.2335C>T p.R779C Substitution - Missense 2:162273914-162273914 - RMS80_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - TCGA-EE-A2MJ-06 COSM3568521 c.2847G>A p.K949K Substitution - coding silent 2:162267530-162267530 - PT55 COSM5941654 c.2899-1G>A p.? Unknown 2:162267380-162267380 - RMS106_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - RMS109_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - 585270 COSM320918 c.921G>T p.Q307H Substitution - Missense 2:162288309-162288309 - SNUH_G76_S1 COSM4418325 c.1379A>G p.H460R Substitution - Missense 2:162281473-162281473 - 3N21-VS-3T21 COSM4979362 c.605G>C p.C202S Substitution - Missense 2:162310782-162310782 - TCGA-AA-A00N-01 COSM275529 c.2335C>T p.R779C Substitution - Missense 2:162273914-162273914 - TCGA-HU-A4H8-01 COSM4086014 c.1203A>G p.P401P Substitution - coding silent 2:162282469-162282469 - CSCC-31-T COSM4468958 c.1572C>T p.N524N Substitution - coding silent 2:162280065-162280065 - PD9582a COSM5769738 c.225G>T p.W75C Substitution - Missense 2:162318083-162318083 - CSCC-27-T COSM3568525 c.2361C>T p.I787I Substitution - coding silent 2:162273888-162273888 - TCGA-HJ-7597-01 COSM4086013 c.2464C>T p.R822* Substitution - Nonsense 2:162272378-162272378 - TCGA-F5-6814-01 COSM3414179 c.1992G>T p.K664N Substitution - Missense 2:162277467-162277467 - TCGA-AN-A0AK-01 COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - TCGA-CA-6717-01 COSM1400467 c.2772G>T p.E924D Substitution - Missense 2:162268122-162268122 - TCGA-D1-A17D-01 COSM1008373 c.2994delA p.K998fs*7 Deletion - Frameshift 2:162267284-162267284 - PDA_087 COSM5002870 c.1294G>T p.V432F Substitution - Missense 2:162282378-162282378 - Gp2D COSM1400473 c.1764delA p.A589fs*16 Deletion - Frameshift 2:162278206-162278206 - STC232 COSM1400474 c.1757A>G p.E586G Substitution - Missense 2:162278213-162278213 - 2492729 COSM5727912 c.995G>A p.G332E Substitution - Missense 2:162288235-162288235 - cSCCP4 COSM138326 c.2527C>A p.H843N Substitution - Missense 2:162272315-162272315 - In-8 COSM144853 c.817_818insA p.S273fs*5 Insertion - Frameshift 2:162293620-162293621 - TCGA-GN-A266-06 COSM3568530 c.1652A>T p.K551I Substitution - Missense 2:162278318-162278318 - CHC1594T COSM5348020 c.470delA p.N157fs*8 Deletion - Frameshift 2:162310917-162310917 - PD6761a COSM1638019 c.411G>A p.K137K Substitution - coding silent 2:162317897-162317897 - TCGA-B5-A11O-01 COSM1008380 c.823G>T p.G275* Substitution - Nonsense 2:162293615-162293615 - BD114T COSM5502551 c.2365A>T p.T789S Substitution - Missense 2:162273884-162273884 - C709 COSM4443977 c.1240G>A p.A414T Substitution - Missense 2:162282432-162282432 - TCGA-DK-A1A7-01 COSM418523 c.1576G>T p.D526Y Substitution - Missense 2:162280061-162280061 - ESCC_158 COSM5646787 c.1725T>G p.T575T Substitution - coding silent 2:162278245-162278245 - TCGA-EE-A2GP-06 COSM3568526 c.2204C>T p.S735F Substitution - Missense 2:162276787-162276787 - TCGA-D1-A174-01 COSM1008374 c.2490C>A p.Y830* Substitution - Nonsense 2:162272352-162272352 - SNUH_G76_S1 COSM4416722 c.1491G>C p.T497T Substitution - coding silent 2:162281361-162281361 - HCC147T COSM5811642 c.2521A>T p.I841F Substitution - Missense 2:162272321-162272321 - TCGA-EQ-8122-01 COSM4086018 c.394A>C p.R132R Substitution - coding silent 2:162317914-162317914 - TCGA-29-1761-01 COSM1325827 c.970A>T p.N324Y Substitution - Missense 2:162288260-162288260 - 587342 COSM1008375 c.2417G>A p.R806H Substitution - Missense 2:162273832-162273832 - RMS111_ COSM4984995 c.2836G>A p.A946T Substitution - Missense 2:162267541-162267541 - LC_C4 COSM1186042 c.2336G>C p.R779P Substitution - Missense 2:162273913-162273913 - TCGA-EE-A3AG-06 COSM3568532 c.1156C>T p.R386C Substitution - Missense 2:162282516-162282516 - ESCC_BICR_008T COSM5428883 c.646G>A p.D216N Substitution - Missense 2:162306832-162306832 - TCGA-DH-A66B-01 COSM3971663 c.2287T>G p.F763V Substitution - Missense 2:162276704-162276704 - SJMB008 COSM255464 c.2616+6G>T p.? Unknown 2:162272220-162272220 - TCGA-AX-A0J1-01 COSM1008376 c.2416C>T p.R806C Substitution - Missense 2:162273833-162273833 - CPCG0117-F1 COSM4418116 c.2528A>G p.H843R Substitution - Missense 2:162272314-162272314 - TCGA-B6-A0RV-01 COSM441323 c.2553G>C p.E851D Substitution - Missense 2:162272289-162272289 - TCGA-DI-A0WH-01 COSM281851 c.1852C>T p.R618* Substitution - Nonsense 2:162277607-162277607 - 7b COSM4657689 c.2913G>C p.M971I Substitution - Missense 2:162267365-162267365 - TCGA-66-2773-01 COSM717207 c.2374G>A p.A792T Substitution - Missense 2:162273875-162273875 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.163173 2q24 606951

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F638C c.1913T>G 2 163134056 LGG A G IntronicSNV . c.622+60T>C 2 163167215 DLBCL A G Missense p.F539S c.1616T>C 2 163136531 CM A G Missense p.M686T c.2057T>C 2 163133444 LUAD A G Missense p.V941A c.2822T>C 2 163124065 COREAD A G Synonymous p.F987F c.2961T>C 2 163123827 CM C A Missense p.A691S c.2071G>T 2 163133430 SCLC C A Missense p.D526Y c.1576G>T 2 163136571 BLCA C A Missense p.K889N c.2667G>T 2 163124737 BRCA C A Missense p.M558I c.1674G>T 2 163134806 HNSC C A Missense p.Q307H c.921G>T 2 163144819 SCLC C A Missense p.R705I c.2114G>T 2 163133387 LUSC C A Missense p.W238C c.714G>T 2 163163274 STAD C A Nonsense p.E695* c.2083G>T 2 163133418 HNSC - CC Frameshift p.Y5Gfs*19 c.11_12dupGG 2 163174806 BLCA CG AT SpliceDonorBlockSubstitution . c.451_452delinsAT 2 163174366 CM C G Missense p.D621H c.1861G>C 2 163134108 LUAD C G Missense p.E204Q c.610G>C 2 163167287 HNSC C G Missense p.E210Q c.628G>C 2 163163360 HNSC C G Missense p.E41Q c.121G>C 2 163174697 BRCA C G Missense p.E851D c.2553G>C 2 163128799 BRCA C G Missense p.E867Q c.2599G>C 2 163128753 HNSC C G Missense p.Q317H c.951G>C 2 163144789 BLCA C G Missense p.Q317H c.951G>C 2 163144789 LUSC C G Synonymous p.L754L c.2262G>C 2 163133239 HNSC C T Missense p.A792T c.2374G>A 2 163130385 LUSC C T Missense p.D615N c.1843G>A 2 163134126 NB C T Missense p.E609K c.1825G>A 2 163134144 LUAD C T Missense p.M882I c.2646G>A 2 163124758 BRCA C T Missense p.M971I c.2913G>A 2 163123875 MM C T Missense p.R618Q c.1853G>A 2 163134116 CM C T Nonsense p.W581* c.1742G>A 2 163134738 CM C T Synonymous p.K949K c.2847G>A 2 163124040 CM C T Synonymous p.R605R c.1815G>A 2 163134154 CM G A IntronicSNV . c.769+2448C>T 2 163160771 CLL G A IntronicSNV . c.874+7C>T 2 163150067 STAD G A Missense p.P218S c.652C>T 2 163163336 CM G A Missense p.P866L c.2597C>T 2 163128755 CM G A Missense p.R386C c.1156C>T 2 163139026 CM G A Missense p.S735F c.2204C>T 2 163133297 CM G A Missense p.T100M c.299C>T 2 163174519 LUSC G A Missense p.T707I c.2120C>T 2 163133381 CM G A Synonymous p.F79F c.237C>T 2 163174581 CM G A Synonymous p.F935F c.2805C>T 2 163124599 CM G A Synonymous p.I325I c.975C>T 2 163144765 HNSC G A Synonymous p.I787I c.2361C>T 2 163130398 CM G A Synonymous p.L421L c.1263C>T 2 163138919 CM G A Synonymous p.L832L c.2494C>T 2 163128858 CM G C Missense p.R77G c.229C>G 2 163174589 LUAD G T IntronicSNV . c.1095+1243C>A 2 163143402 PIA G T Missense p.R93S c.277C>A 2 163174541 STAD G T Synonymous p.L83L c.249C>A 2 163174569 LUSC T A IntronicSNV . c.623-110A>T 2 163163475 CM T A Missense p.Y954F c.2861A>T 2 163124026 CM - TCCC IntronicInsertion . c.770-1290_770-1289insGGAG 2 163151468 CLL T C Missense p.D259G c.776A>G 2 163150172 RCCC T C Missense p.E234G c.701A>G 2 163163287 CM T C Missense p.I708V c.2122A>G 2 163133379 LUAD T C Missense p.K351E c.1051A>G 2 163144689 OV T C Synonymous p.A58A c.174A>G 2 163174644 LUSC T C Synonymous p.L347L c.1041A>G 2 163144699 CM T - Frameshift p.A589Lfs*16 c.1764delA 2 163134716 STAD T - Frameshift p.K998Nfs*7 c.2994delA 2 163123794 UCEC TGGTGGG - Frameshift p.A751Vfs*2 c.2252_2258delCCCACCA 2 163133243 STAD T G Missense p.K352N c.1056A>C 2 163144684 RCCC