Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 15 28377252 28377252 + Silent SNP A A G TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr15:28377252A>G c.12564T>C c.(12562-12564)ccT>ccC p.P4188P ACC 15 28408358 28408358 + Missense_Mutation SNP G G A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr15:28408358G>A c.10628C>T c.(10627-10629)gCg>gTg p.A3543V ACC 15 28422657 28422657 + Splice_Site SNP T T C TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr15:28422657T>C c.e60-2 ACC 15 28441707 28441707 + Missense_Mutation SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr15:28441707C>A c.8020G>T c.(8020-8022)Gcc>Tcc p.A2674S ACC 15 28443647 28443647 + Missense_Mutation SNP A A G TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr15:28443647A>G c.7888T>C c.(7888-7890)Tat>Cat p.Y2630H ACC 15 28473416 28473416 + Silent SNP A A G TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr15:28473416A>G c.5412T>C c.(5410-5412)ctT>ctC p.L1804L BLCA 15 28358394 28358394 + Silent SNP G G C TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr15:28358394G>C c.14055C>G c.(14053-14055)ctC>ctG p.L4685L BLCA 15 28358811 28358811 + Missense_Mutation SNP C C G TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr15:28358811C>G c.13927G>C c.(13927-13929)Gat>Cat p.D4643H BLCA 15 28361860 28361860 + Silent SNP G G A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr15:28361860G>A c.13560C>T c.(13558-13560)ctC>ctT p.L4520L BLCA 15 28362244 28362244 + Silent SNP G G A TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr15:28362244G>A c.13329C>T c.(13327-13329)gtC>gtT p.V4443V BLCA 15 28375377 28375377 + Missense_Mutation SNP C C G TCGA-E7-A4IJ-01A-31D-A26M-08 TCGA-E7-A4IJ-10A-01D-A26K-08 g.chr15:28375377C>G c.12734G>C c.(12733-12735)gGg>gCg p.G4245A BLCA 15 28375399 28375399 + Nonsense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:28375399G>A c.12712C>T c.(12712-12714)Cga>Tga p.R4238* BLCA 15 28375401 28375401 + Missense_Mutation SNP A A G TCGA-FJ-A3ZF-01A-11D-A23M-08 TCGA-FJ-A3ZF-10A-01D-A23K-08 g.chr15:28375401A>G c.12710T>C c.(12709-12711)gTt>gCt p.V4237A BLCA 15 28377404 28377404 + Missense_Mutation SNP C C G TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr15:28377404C>G c.12412G>C c.(12412-12414)Gag>Cag p.E4138Q BLCA 15 28377945 28377945 + Missense_Mutation SNP G G C TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr15:28377945G>C c.12262C>G c.(12262-12264)Ctg>Gtg p.L4088V BLCA 15 28387389 28387389 + Missense_Mutation SNP C C G TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr15:28387389C>G c.11695G>C c.(11695-11697)Gat>Cat p.D3899H BLCA 15 28389103 28389103 + Silent SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr15:28389103C>T c.11334G>A c.(11332-11334)ctG>ctA p.L3778L BLCA 15 28408319 28408319 + Missense_Mutation SNP G G A TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr15:28408319G>A c.10667C>T c.(10666-10668)tCa>tTa p.S3556L BLCA 15 28408392 28408392 + Nonsense_Mutation SNP G G A TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr15:28408392G>A c.10594C>T c.(10594-10596)Cag>Tag p.Q3532* BLCA 15 28413643 28413643 + Silent SNP C C T TCGA-ZF-AA5H-01A-11D-A391-08 TCGA-ZF-AA5H-10A-01D-A394-08 g.chr15:28413643C>T c.10323G>A c.(10321-10323)gcG>gcA p.A3441A BLCA 15 28419570 28419570 + Missense_Mutation SNP G G A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr15:28419570G>A c.10028C>T c.(10027-10029)gCa>gTa p.A3343V BLCA 15 28420727 28420727 + Silent SNP C C G TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr15:28420727C>G c.9762G>C c.(9760-9762)ctG>ctC p.L3254L BLCA 15 28421740 28421740 + Missense_Mutation SNP C C A TCGA-CU-A0YN-01A-21D-A10S-08 TCGA-CU-A0YN-11A-11D-A10S-08 g.chr15:28421740C>A c.9520G>T c.(9520-9522)Gta>Tta p.V3174L BLCA 15 28421741 28421741 + Missense_Mutation SNP C C A TCGA-CU-A0YN-01A-21D-A10S-08 TCGA-CU-A0YN-11A-11D-A10S-08 g.chr15:28421741C>A c.9519G>T c.(9517-9519)ttG>ttT p.L3173F BLCA 15 28424337 28424337 + Silent SNP T T C TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr15:28424337T>C c.8970A>G c.(8968-8970)tcA>tcG p.S2990S BLCA 15 28437183 28437183 + Missense_Mutation SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:28437183G>A c.8375C>T c.(8374-8376)tCg>tTg p.S2792L BLCA 15 28441665 28441665 + Missense_Mutation SNP G G A TCGA-G2-AA3F-01A-12D-A42E-08 TCGA-G2-AA3F-10A-01D-A42H-08 g.chr15:28441665G>A c.8062C>T c.(8062-8064)Cac>Tac p.H2688Y BLCA 15 28447299 28447299 + Missense_Mutation SNP T T A TCGA-CF-A47Y-01A-11D-A23U-08 TCGA-CF-A47Y-10A-01D-A23U-08 g.chr15:28447299T>A c.7577A>T c.(7576-7578)gAg>gTg p.E2526V BLCA 15 28456214 28456214 + Missense_Mutation SNP G G T TCGA-GC-A3YS-01A-11D-A23M-08 TCGA-GC-A3YS-10A-01D-A23K-08 g.chr15:28456214G>T c.7003C>A c.(7003-7005)Cac>Aac p.H2335N BLCA 15 28456242 28456242 + Silent SNP G G A TCGA-GV-A40G-01A-11D-A23M-08 TCGA-GV-A40G-10A-01D-A23K-08 g.chr15:28456242G>A c.6975C>T c.(6973-6975)atC>atT p.I2325I BLCA 15 28458889 28458889 + Splice_Site SNP G G A TCGA-GV-A3JW-01A-11D-A20D-08 TCGA-GV-A3JW-10A-01D-A20D-08 g.chr15:28458889G>A c.6785C>T c.(6784-6786)cCa>cTa p.P2262L BLCA 15 28459805 28459805 + Silent SNP G G A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr15:28459805G>A c.6354C>T c.(6352-6354)ctC>ctT p.L2118L BLCA 15 28460863 28460863 + Silent SNP C C T TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr15:28460863C>T c.6114G>A c.(6112-6114)caG>caA p.Q2038Q BLCA 15 28460878 28460878 + Missense_Mutation SNP G G C TCGA-DK-AA6W-01A-12D-A391-08 TCGA-DK-AA6W-10A-01D-A394-08 g.chr15:28460878G>C c.6099C>G c.(6097-6099)atC>atG p.I2033M BLCA 15 28467317 28467317 + Missense_Mutation SNP G G C TCGA-G2-A2EK-01A-22D-A18F-08 TCGA-G2-A2EK-10A-01D-A18F-08 g.chr15:28467317G>C c.5509C>G c.(5509-5511)Caa>Gaa p.Q1837E BLCA 15 28467360 28467360 + Splice_Site SNP G G A TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr15:28467360G>A c.5466C>T c.(5464-5466)ggC>ggT p.G1822G BLCA 15 28475549 28475549 + Silent SNP A A G TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr15:28475549A>G c.4773T>C c.(4771-4773)aaT>aaC p.N1591N BLCA 15 28478351 28478351 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:28478351G>T c.4616C>A c.(4615-4617)tCt>tAt p.S1539Y BLCA 15 28478819 28478819 + Missense_Mutation SNP C C T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr15:28478819C>T c.4342G>A c.(4342-4344)Gaa>Aaa p.E1448K BLCA 15 28483309 28483309 + Missense_Mutation SNP T T C TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr15:28483309T>C c.3803A>G c.(3802-3804)gAa>gGa p.E1268G BLCA 15 28483901 28483901 + Nonsense_Mutation SNP G G A TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr15:28483901G>A c.3595C>T c.(3595-3597)Cag>Tag p.Q1199* BLCA 15 28493829 28493829 + Missense_Mutation SNP G G A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr15:28493829G>A c.3104C>T c.(3103-3105)tCa>tTa p.S1035L BLCA 15 28493883 28493883 + Splice_Site SNP C C G TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr15:28493883C>G c.e21-1 BLCA 15 28501052 28501052 + Missense_Mutation SNP G G A TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr15:28501052G>A c.2837C>T c.(2836-2838)tCa>tTa p.S946L BLCA 15 28501094 28501094 + Missense_Mutation SNP T T A TCGA-BT-A20X-01A-11D-A16O-08 TCGA-BT-A20X-11A-12D-A16O-08 g.chr15:28501094T>A c.2795A>T c.(2794-2796)gAt>gTt p.D932V BLCA 15 28501250 28501250 + Missense_Mutation SNP G G C TCGA-ZF-AA52-01A-12D-A391-08 TCGA-ZF-AA52-10A-01D-A394-08 g.chr15:28501250G>C c.2731C>G c.(2731-2733)Ctc>Gtc p.L911V BLCA 15 28501377 28501377 + Silent SNP C C A TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr15:28501377C>A c.2604G>T c.(2602-2604)acG>acT p.T868T BLCA 15 28508223 28508223 + Missense_Mutation SNP G G C TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr15:28508223G>C c.1963C>G c.(1963-1965)Caa>Gaa p.Q655E BLCA 15 28511100 28511101 + Frame_Shift_Ins INS - - C TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr15:28511100_28511101insC c.1618_1619insG c.(1618-1620)gtgfs p.V540fs BLCA 15 28517458 28517458 + Missense_Mutation SNP G G A TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr15:28517458G>A c.986C>T c.(985-987)tCc>tTc p.S329F BLCA 15 28519521 28519521 + Missense_Mutation SNP G G A TCGA-CU-A5W6-01A-11D-A289-08 TCGA-CU-A5W6-10A-01D-A289-08 g.chr15:28519521G>A c.716C>T c.(715-717)tCg>tTg p.S239L BLCA 15 28525375 28525375 + Silent SNP G G A TCGA-ZF-A9RN-01A-11D-A42E-08 TCGA-ZF-A9RN-10A-01D-A42H-08 g.chr15:28525375G>A c.381C>T c.(379-381)gcC>gcT p.A127A BRCA 15 28357017 28357017 + Silent SNP G G A TCGA-B6-A0IH-01A-11D-A10Y-09 TCGA-B6-A0IH-10A-01D-A110-09 g.chr15:28357017G>A c.14397C>T c.(14395-14397)atC>atT p.I4799I BRCA 15 28369301 28369301 + Missense_Mutation SNP G G C TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr15:28369301G>C c.13070C>G c.(13069-13071)tCc>tGc p.S4357C BRCA 15 28375390 28375390 + Missense_Mutation SNP G G A TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr15:28375390G>A c.12721C>T c.(12721-12723)Cgg>Tgg p.R4241W BRCA 15 28377860 28377860 + Missense_Mutation SNP C C G TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr15:28377860C>G c.12347G>C c.(12346-12348)gGc>gCc p.G4116A BRCA 15 28386674 28386674 + Silent SNP G G T TCGA-GI-A2C9-01A-11D-A21Q-09 TCGA-GI-A2C9-11A-22D-A21Q-09 g.chr15:28386674G>T c.11919C>A c.(11917-11919)gtC>gtA p.V3973V BRCA 15 28387403 28387403 + Missense_Mutation SNP G G C TCGA-C8-A26W-01A-11D-A16D-09 TCGA-C8-A26W-10A-01D-A16D-09 g.chr15:28387403G>C c.11681C>G c.(11680-11682)cCc>cGc p.P3894R BRCA 15 28389261 28389261 + Missense_Mutation SNP G G A TCGA-B6-A0WY-01A-11D-A10G-09 TCGA-B6-A0WY-10A-01D-A10G-09 g.chr15:28389261G>A c.11261C>T c.(11260-11262)gCg>gTg p.A3754V BRCA 15 28389827 28389828 + Frame_Shift_Del DEL GG GG - TCGA-A2-A0CP-01A-11W-A050-09 TCGA-A2-A0CP-10A-01W-A055-09 g.chr15:28389827_28389828delGG c.11131_11132delCC c.(11131-11133)ccafs p.P3711fs BRCA 15 28389831 28389834 + Frame_Shift_Del DEL TGAT TGAT - TCGA-A2-A0CP-01A-11W-A050-09 TCGA-A2-A0CP-10A-01W-A055-09 g.chr15:28389831_28389834delTGAT c.11125_11128delATCA c.(11125-11130)atcatgfs p.IM3709fs BRCA 15 28391398 28391398 + Missense_Mutation SNP C C T TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr15:28391398C>T c.10993G>A c.(10993-10995)Gtc>Atc p.V3665I BRCA 15 28408347 28408347 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:28408347G>A c.10639C>T c.(10639-10641)Cgt>Tgt p.R3547C BRCA 15 28408363 28408363 + Silent SNP C C T TCGA-A1-A0SI-01A-11D-A142-09 TCGA-A1-A0SI-10B-01D-A142-09 g.chr15:28408363C>T c.10623G>A c.(10621-10623)ctG>ctA p.L3541L BRCA 15 28414741 28414741 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:28414741G>T c.10118C>A c.(10117-10119)tCt>tAt p.S3373Y BRCA 15 28419644 28419644 + Silent SNP C C A TCGA-C8-A12P-01A-11D-A10Y-09 TCGA-C8-A12P-10A-01D-A110-09 g.chr15:28419644C>A c.9954G>T c.(9952-9954)tcG>tcT p.S3318S BRCA 15 28421694 28421694 + Missense_Mutation SNP C C T TCGA-A8-A06U-01A-11W-A019-09 TCGA-A8-A06U-10A-01W-A021-09 g.chr15:28421694C>T c.9566G>A c.(9565-9567)gGa>gAa p.G3189E BRCA 15 28421867 28421867 + Silent SNP A A G TCGA-A8-A0AB-01A-11W-A050-09 TCGA-A8-A0AB-10A-01W-A055-09 g.chr15:28421867A>G c.9480T>C c.(9478-9480)agT>agC p.S3160S BRCA 15 28431765 28431765 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:28431765G>A c.8783C>T c.(8782-8784)tCg>tTg p.S2928L BRCA 15 28436126 28436126 + Silent SNP C C T TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr15:28436126C>T c.8634G>A c.(8632-8634)ctG>ctA p.L2878L BRCA 15 28436380 28436380 + Missense_Mutation SNP C C G TCGA-E2-A574-01A-11D-A29N-09 TCGA-E2-A574-10A-01D-A29N-09 g.chr15:28436380C>G c.8462G>C c.(8461-8463)cGt>cCt p.R2821P BRCA 15 28441424 28441424 + Missense_Mutation SNP C C T TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr15:28441424C>T c.8197G>A c.(8197-8199)Gaa>Aaa p.E2733K BRCA 15 28446656 28446656 + Silent SNP T T A TCGA-AR-A0TU-01A-31D-A10G-09 TCGA-AR-A0TU-10A-01D-A10G-09 g.chr15:28446656T>A c.7662A>T c.(7660-7662)cgA>cgT p.R2554R BRCA 15 28451475 28451475 + Nonsense_Mutation SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr15:28451475G>A c.7123C>T c.(7123-7125)Cag>Tag p.Q2375* BRCA 15 28474383 28474383 + Nonsense_Mutation SNP G G A TCGA-A1-A0SI-01A-11D-A142-09 TCGA-A1-A0SI-10B-01D-A142-09 g.chr15:28474383G>A c.5230C>T c.(5230-5232)Cga>Tga p.R1744* BRCA 15 28478454 28478454 + Missense_Mutation SNP C C A TCGA-A8-A08L-01A-11W-A019-09 TCGA-A8-A08L-10A-01W-A021-09 g.chr15:28478454C>A c.4513G>T c.(4513-4515)Gtc>Ttc p.V1505F BRCA 15 28478469 28478469 + Missense_Mutation SNP G G A TCGA-AO-A12E-01A-11D-A10M-09 TCGA-AO-A12E-10A-01D-A10M-09 g.chr15:28478469G>A c.4498C>T c.(4498-4500)Cgt>Tgt p.R1500C BRCA 15 28479350 28479350 + Missense_Mutation SNP C C G TCGA-E9-A1RH-01A-21D-A167-09 TCGA-E9-A1RH-10A-01D-A167-09 g.chr15:28479350C>G c.4084G>C c.(4084-4086)Gac>Cac p.D1362H BRCA 15 28483866 28483866 + Missense_Mutation SNP T T C TCGA-A7-A26I-01A-11D-A167-09 TCGA-A7-A26I-10A-01D-A167-09 g.chr15:28483866T>C c.3630A>G c.(3628-3630)atA>atG p.I1210M BRCA 15 28493757 28493757 + Missense_Mutation SNP C C T TCGA-AR-A1AJ-01A-21D-A12Q-09 TCGA-AR-A1AJ-10A-01D-A12Q-09 g.chr15:28493757C>T c.3176G>A c.(3175-3177)cGt>cAt p.R1059H BRCA 15 28501072 28501072 + Missense_Mutation SNP C C T TCGA-OL-A5RW-01A-11D-A28B-09 TCGA-OL-A5RW-10A-01D-A28E-09 g.chr15:28501072C>T c.2817G>A c.(2815-2817)atG>atA p.M939I BRCA 15 28501091 28501092 + Frame_Shift_Del DEL AG AG - TCGA-AN-A0AT-01A-11D-A045-09 TCGA-AN-A0AT-10A-01W-A055-09 g.chr15:28501091_28501092delAG c.2797_2798delCT c.(2797-2799)cttfs p.L934fs BRCA 15 28501279 28501279 + Missense_Mutation SNP G G A TCGA-E2-A56Z-01A-12D-A29N-09 TCGA-E2-A56Z-10A-01D-A29N-09 g.chr15:28501279G>A c.2702C>T c.(2701-2703)gCg>gTg p.A901V BRCA 15 28515846 28515846 + Missense_Mutation SNP G G A TCGA-D8-A1JJ-01A-31D-A14K-09 TCGA-D8-A1JJ-10A-01D-A14K-09 g.chr15:28515846G>A c.1252C>T c.(1252-1254)Cat>Tat p.H418Y BRCA 15 28517375 28517375 + Missense_Mutation SNP C C T TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr15:28517375C>T c.1069G>A c.(1069-1071)Gag>Aag p.E357K BRCA 15 28519482 28519482 + Missense_Mutation SNP T T C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr15:28519482T>C c.755A>G c.(754-756)gAg>gGg p.E252G BRCA 15 28525309 28525309 + Silent SNP G G A TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr15:28525309G>A c.447C>T c.(445-447)cgC>cgT p.R149R CESC 15 28358750 28358750 + Missense_Mutation SNP G G C TCGA-EK-A2H1-01A-11D-A17W-09 TCGA-EK-A2H1-10A-01D-A17W-09 g.chr15:28358750G>C c.13988C>G c.(13987-13989)tCt>tGt p.S4663C CESC 15 28387979 28387979 + Silent SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr15:28387979G>A c.11538C>T c.(11536-11538)ttC>ttT p.F3846F CESC 15 28422657 28422657 + Splice_Site SNP T T C TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr15:28422657T>C c.e60-2 CESC 15 28436121 28436121 + Missense_Mutation SNP T T C TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr15:28436121T>C c.8639A>G c.(8638-8640)gAc>gGc p.D2880G CESC 15 28437168 28437168 + Missense_Mutation SNP T T C TCGA-DS-A5RQ-01A-11D-A28B-09 TCGA-DS-A5RQ-10A-01D-A28E-09 g.chr15:28437168T>C c.8390A>G c.(8389-8391)cAg>cGg p.Q2797R CESC 15 28443555 28443555 + Silent SNP A A T TCGA-DS-A3LQ-01A-21D-A21Q-09 TCGA-DS-A3LQ-10A-01D-A21Q-09 g.chr15:28443555A>T c.7980T>A c.(7978-7980)tcT>tcA p.S2660S CESC 15 28463704 28463704 + Missense_Mutation SNP T T G TCGA-LP-A4AU-01A-32D-A243-09 TCGA-LP-A4AU-10A-01D-A243-09 g.chr15:28463704T>G c.5959A>C c.(5959-5961)Agc>Cgc p.S1987R CESC 15 28510988 28510988 + Silent SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr15:28510988G>A c.1731C>T c.(1729-1731)cgC>cgT p.R577R CESC 15 28515957 28515957 + Missense_Mutation SNP G G C TCGA-C5-A1M7-01A-11D-A13W-08 TCGA-C5-A1M7-10A-01D-A13W-08 g.chr15:28515957G>C c.1141C>G c.(1141-1143)Caa>Gaa p.Q381E CESC 15 28517458 28517458 + Missense_Mutation SNP G G A TCGA-FU-A23K-01A-11D-A16O-08 TCGA-FU-A23K-10A-01D-A16O-08 g.chr15:28517458G>A c.986C>T c.(985-987)tCc>tTc p.S329F CESC 15 28517458 28517458 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr15:28517458G>A c.986C>T c.(985-987)tCc>tTc p.S329F CESC 15 28525273 28525273 + Silent SNP C C T TCGA-C5-A1MJ-01A-11D-A14W-08 TCGA-C5-A1MJ-10A-01D-A14W-08 g.chr15:28525273C>T c.483G>A c.(481-483)gaG>gaA p.E161E CESC 15 28566548 28566548 + Missense_Mutation SNP T T C TCGA-C5-A1ML-01A-11D-A14W-08 TCGA-C5-A1ML-10A-01D-A14W-08 g.chr15:28566548T>C c.32A>G c.(31-33)cAg>cGg p.Q11R CHOL 15 28375649 28375649 + Splice_Site SNP C C A TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr15:28375649C>A c.12662G>T c.(12661-12663)tGg>tTg p.W4221L CHOL 15 28492030 28492030 + Missense_Mutation SNP C C A TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr15:28492030C>A c.3249G>T c.(3247-3249)atG>atT p.M1083I COAD 15 28358283 28358283 + Silent SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:28358283G>A c.14166C>T c.(14164-14166)ttC>ttT p.F4722F COAD 15 28359950 28359950 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:28359950T>G c.e90-2 COAD 15 28361942 28361942 + Missense_Mutation SNP A A C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28361942A>C c.13478T>G c.(13477-13479)cTg>cGg p.L4493R COAD 15 28366497 28366497 + Missense_Mutation SNP T T C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr15:28366497T>C c.13267A>G c.(13267-13269)Atc>Gtc p.I4423V COAD 15 28370178 28370178 + Missense_Mutation SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr15:28370178C>T c.12964G>A c.(12964-12966)Gcc>Acc p.A4322T COAD 15 28377284 28377284 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:28377284C>T c.12532G>A c.(12532-12534)Ggc>Agc p.G4178S COAD 15 28377293 28377293 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:28377293C>T c.12523G>A c.(12523-12525)Ggc>Agc p.G4175S COAD 15 28377369 28377369 + Silent SNP G G T TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr15:28377369G>T c.12447C>A c.(12445-12447)gcC>gcA p.A4149A COAD 15 28377372 28377372 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:28377372G>A c.12444C>T c.(12442-12444)atC>atT p.I4148I COAD 15 28386620 28386620 + Silent SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:28386620G>T c.11973C>A c.(11971-11973)atC>atA p.I3991I COAD 15 28389059 28389059 + Missense_Mutation SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr15:28389059T>C c.11378A>G c.(11377-11379)aAt>aGt p.N3793S COAD 15 28389859 28389859 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr15:28389859C>A c.11100G>T c.(11098-11100)tgG>tgT p.W3700C COAD 15 28389862 28389862 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28389862G>A c.11097C>T c.(11095-11097)ggC>ggT p.G3699G COAD 15 28389921 28389921 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:28389921G>A c.11038C>T c.(11038-11040)Ctg>Ttg p.L3680L COAD 15 28391393 28391393 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr15:28391393G>A c.10998C>T c.(10996-10998)tcC>tcT p.S3666S COAD 15 28397918 28397918 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr15:28397918G>A c.10805C>T c.(10804-10806)tCg>tTg p.S3602L COAD 15 28408371 28408371 + Missense_Mutation SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:28408371T>C c.10615A>G c.(10615-10617)Agt>Ggt p.S3539G COAD 15 28412847 28412847 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:28412847T>C c.10540A>G c.(10540-10542)Acc>Gcc p.T3514A COAD 15 28413595 28413595 + Silent SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:28413595G>A c.10371C>T c.(10369-10371)atC>atT p.I3457I COAD 15 28413605 28413605 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr15:28413605G>A c.10361C>T c.(10360-10362)gCt>gTt p.A3454V COAD 15 28419592 28419592 + Missense_Mutation SNP C C T TCGA-AA-A01V-01A-23W-A096-10 TCGA-AA-A01V-11A-11W-A096-10 g.chr15:28419592C>T c.10006G>A c.(10006-10008)Gag>Aag p.E3336K COAD 15 28419659 28419659 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr15:28419659G>A c.9939C>T c.(9937-9939)cgC>cgT p.R3313R COAD 15 28419674 28419674 + Silent SNP G G T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr15:28419674G>T c.9924C>A c.(9922-9924)ggC>ggA p.G3308G COAD 15 28419681 28419681 + Nonsense_Mutation SNP A A C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:28419681A>C c.9917T>G c.(9916-9918)tTa>tGa p.L3306* COAD 15 28419740 28419740 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28419740G>A c.9858C>T c.(9856-9858)caC>caT p.H3286H COAD 15 28422177 28422177 + Silent SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr15:28422177G>A c.9351C>T c.(9349-9351)agC>agT p.S3117S COAD 15 28427597 28427597 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:28427597C>T c.8887G>A c.(8887-8889)Gtg>Atg p.V2963M COAD 15 28431776 28431776 + Silent SNP A A G TCGA-CM-6165-01A-11D-1650-10 TCGA-CM-6165-10A-01D-1650-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COAD 15 28431776 28431776 + Silent SNP A A G TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COAD 15 28431776 28431776 + Silent SNP A A G TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COAD 15 28431776 28431776 + Silent SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COAD 15 28437182 28437182 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:28437182C>T c.8376G>A c.(8374-8376)tcG>tcA p.S2792S COAD 15 28437250 28437250 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr15:28437250A>G c.8308T>C c.(8308-8310)Tgc>Cgc p.C2770R COAD 15 28437272 28437272 + Silent SNP A A G TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr15:28437272A>G c.8286T>C c.(8284-8286)cgT>cgC p.R2762R COAD 15 28441425 28441425 + Silent SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:28441425A>G c.8196T>C c.(8194-8196)tgT>tgC p.C2732C COAD 15 28443535 28443535 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:28443535C>T c.8000G>A c.(7999-8001)gGg>gAg p.G2667E COAD 15 28443624 28443626 + In_Frame_Del DEL AGA AGA - TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr15:28443624_28443626delAGA c.7909_7911delTCT c.(7909-7911)tctdel p.S2637del COAD 15 28443784 28443784 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:28443784G>A c.7848C>T c.(7846-7848)ggC>ggT p.G2616G COAD 15 28446658 28446658 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28446658G>A c.7660C>T c.(7660-7662)Cga>Tga p.R2554* COAD 15 28447529 28447529 + Missense_Mutation SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:28447529G>T c.7444C>A c.(7444-7446)Ctc>Atc p.L2482I COAD 15 28456228 28456228 + Missense_Mutation SNP C C T TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr15:28456228C>T c.6989G>A c.(6988-6990)cGg>cAg p.R2330Q COAD 15 28456241 28456241 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:28456241G>T c.6976C>A c.(6976-6978)Ctg>Atg p.L2326M COAD 15 28456263 28456263 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr15:28456263G>A c.6954C>T c.(6952-6954)tgC>tgT p.C2318C COAD 15 28459069 28459069 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr15:28459069delC c.6605delG c.(6604-6606)ggcfs p.G2202fs COAD 15 28460942 28460942 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:28460942G>T c.6035C>A c.(6034-6036)cCa>cAa p.P2012Q COAD 15 28465671 28465671 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:28465671G>A c.5772C>T c.(5770-5772)taC>taT p.Y1924Y COAD 15 28474407 28474407 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28474407A>G c.5206T>C c.(5206-5208)Tac>Cac p.Y1736H COAD 15 28475600 28475600 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:28475600G>A c.4722C>T c.(4720-4722)aaC>aaT p.N1574N COAD 15 28478824 28478824 + Missense_Mutation SNP T T C TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr15:28478824T>C c.4337A>G c.(4336-4338)aAa>aGa p.K1446R COAD 15 28478848 28478848 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28478848C>T c.4313G>A c.(4312-4314)cGc>cAc p.R1438H COAD 15 28478879 28478879 + Missense_Mutation SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28478879G>A c.4282C>T c.(4282-4284)Ccc>Tcc p.P1428S COAD 15 28483842 28483842 + Silent SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28483842A>G c.3654T>C c.(3652-3654)caT>caC p.H1218H COAD 15 28491948 28491948 + Missense_Mutation SNP C C A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr15:28491948C>A c.3331G>T c.(3331-3333)Gct>Tct p.A1111S COAD 15 28493767 28493767 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr15:28493767G>A c.3166C>T c.(3166-3168)Cgt>Tgt p.R1056C COAD 15 28493767 28493767 + Missense_Mutation SNP G G A TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr15:28493767G>A c.3166C>T c.(3166-3168)Cgt>Tgt p.R1056C COAD 15 28493836 28493836 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:28493836G>A c.3097C>T c.(3097-3099)Cgg>Tgg p.R1033W COAD 15 28499581 28499581 + Silent SNP C C T TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr15:28499581C>T c.2955G>A c.(2953-2955)agG>agA p.R985R COAD 15 28502274 28502274 + Missense_Mutation SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28502274G>A c.2450C>T c.(2449-2451)gCg>gTg p.A817V COAD 15 28502304 28502304 + Missense_Mutation SNP C C A TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr15:28502304C>A c.2420G>T c.(2419-2421)cGg>cTg p.R807L COAD 15 28502305 28502305 + Missense_Mutation SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr15:28502305G>A c.2419C>T c.(2419-2421)Cgg>Tgg p.R807W COAD 15 28508102 28508102 + Missense_Mutation SNP T T A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:28508102T>A c.2084A>T c.(2083-2085)gAa>gTa p.E695V COAD 15 28508136 28508136 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28508136C>A c.2050G>T c.(2050-2052)Ggt>Tgt p.G684C COAD 15 28511069 28511069 + Silent SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr15:28511069C>T c.1650G>A c.(1648-1650)ggG>ggA p.G550G COAD 15 28511071 28511071 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr15:28511071C>A c.1648G>T c.(1648-1650)Ggg>Tgg p.G550W COAD 15 28514429 28514429 + Missense_Mutation SNP G G A TCGA-AA-3814-01A-01W-0900-09 TCGA-AA-3814-10A-01W-0900-09 g.chr15:28514429G>A c.1411C>T c.(1411-1413)Cgc>Tgc p.R471C COAD 15 28515923 28515923 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28515923G>A c.1175C>T c.(1174-1176)aCg>aTg p.T392M COAD 15 28517370 28517370 + Silent SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:28517370G>A c.1074C>T c.(1072-1074)ggC>ggT p.G358G COAD 15 28517371 28517371 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:28517371C>T c.1073G>A c.(1072-1074)gGc>gAc p.G358D COAD 15 28517441 28517441 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:28517441C>A c.1003G>T c.(1003-1005)Gcc>Tcc p.A335S COAD 15 28518050 28518051 + Frame_Shift_Del DEL CT CT - TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28518050_28518051delCT c.900_901delAG c.(898-903)agaggcfs p.G301fs COAD 15 28519445 28519445 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28519445G>A c.792C>T c.(790-792)gtC>gtT p.V264V COAD 15 28519459 28519459 + Missense_Mutation SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr15:28519459A>G c.778T>C c.(778-780)Ttc>Ctc p.F260L COAD 15 28519528 28519528 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:28519528C>T c.709G>A c.(709-711)Gag>Aag p.E237K COAD 15 28519563 28519563 + Missense_Mutation SNP A A G TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr15:28519563A>G c.674T>C c.(673-675)tTg>tCg p.L225S COAD 15 28520068 28520068 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:28520068C>T c.626G>A c.(625-627)cGc>cAc p.R209H COAD 15 28525289 28525289 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:28525289C>A c.467G>T c.(466-468)aGa>aTa p.R156I COAD 15 28544575 28544575 + Frame_Shift_Del DEL G G - TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr15:28544575delG c.160delC c.(160-162)cagfs p.Q54fs COADREAD 15 28358283 28358283 + Silent SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:28358283G>A c.14166C>T c.(14164-14166)ttC>ttT p.F4722F COADREAD 15 28359950 28359950 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:28359950T>G c.e90-2 COADREAD 15 28361942 28361942 + Missense_Mutation SNP A A C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28361942A>C c.13478T>G c.(13477-13479)cTg>cGg p.L4493R COADREAD 15 28366497 28366497 + Missense_Mutation SNP T T C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr15:28366497T>C c.13267A>G c.(13267-13269)Atc>Gtc p.I4423V COADREAD 15 28370178 28370178 + Missense_Mutation SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr15:28370178C>T c.12964G>A c.(12964-12966)Gcc>Acc p.A4322T COADREAD 15 28375399 28375400 + Nonsense_Mutation DNP GA GA AG TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28375399_28375400GA>AG c.12711_12712TC>CT c.(12709-12714)gtTCga>gtCTga p.R4238* COADREAD 15 28377284 28377284 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:28377284C>T c.12532G>A c.(12532-12534)Ggc>Agc p.G4178S COADREAD 15 28377293 28377293 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:28377293C>T c.12523G>A c.(12523-12525)Ggc>Agc p.G4175S COADREAD 15 28377369 28377369 + Silent SNP G G T TCGA-AA-3526-01A-02W-0831-10 TCGA-AA-3526-10A-01W-0831-10 g.chr15:28377369G>T c.12447C>A c.(12445-12447)gcC>gcA p.A4149A COADREAD 15 28377372 28377372 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:28377372G>A c.12444C>T c.(12442-12444)atC>atT p.I4148I COADREAD 15 28386620 28386620 + Silent SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:28386620G>T c.11973C>A c.(11971-11973)atC>atA p.I3991I COADREAD 15 28389059 28389059 + Missense_Mutation SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr15:28389059T>C c.11378A>G c.(11377-11379)aAt>aGt p.N3793S COADREAD 15 28389859 28389859 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr15:28389859C>A c.11100G>T c.(11098-11100)tgG>tgT p.W3700C COADREAD 15 28389862 28389862 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28389862G>A c.11097C>T c.(11095-11097)ggC>ggT p.G3699G COADREAD 15 28389921 28389921 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:28389921G>A c.11038C>T c.(11038-11040)Ctg>Ttg p.L3680L COADREAD 15 28391393 28391393 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr15:28391393G>A c.10998C>T c.(10996-10998)tcC>tcT p.S3666S COADREAD 15 28397918 28397918 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr15:28397918G>A c.10805C>T c.(10804-10806)tCg>tTg p.S3602L COADREAD 15 28408371 28408371 + Missense_Mutation SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:28408371T>C c.10615A>G c.(10615-10617)Agt>Ggt p.S3539G COADREAD 15 28412847 28412847 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:28412847T>C c.10540A>G c.(10540-10542)Acc>Gcc p.T3514A COADREAD 15 28413595 28413595 + Silent SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:28413595G>A c.10371C>T c.(10369-10371)atC>atT p.I3457I COADREAD 15 28413605 28413605 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr15:28413605G>A c.10361C>T c.(10360-10362)gCt>gTt p.A3454V COADREAD 15 28419592 28419592 + Missense_Mutation SNP C C T TCGA-AA-A01V-01A-23W-A096-10 TCGA-AA-A01V-11A-11W-A096-10 g.chr15:28419592C>T c.10006G>A c.(10006-10008)Gag>Aag p.E3336K COADREAD 15 28419659 28419659 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr15:28419659G>A c.9939C>T c.(9937-9939)cgC>cgT p.R3313R COADREAD 15 28419674 28419674 + Silent SNP G G T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr15:28419674G>T c.9924C>A c.(9922-9924)ggC>ggA p.G3308G COADREAD 15 28419681 28419681 + Nonsense_Mutation SNP A A C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:28419681A>C c.9917T>G c.(9916-9918)tTa>tGa p.L3306* COADREAD 15 28419740 28419740 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28419740G>A c.9858C>T c.(9856-9858)caC>caT p.H3286H COADREAD 15 28420712 28420712 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28420712G>A c.9777C>T c.(9775-9777)atC>atT p.I3259I COADREAD 15 28422162 28422162 + Silent SNP G G A TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr15:28422162G>A c.9366C>T c.(9364-9366)acC>acT p.T3122T COADREAD 15 28422177 28422177 + Silent SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr15:28422177G>A c.9351C>T c.(9349-9351)agC>agT p.S3117S COADREAD 15 28427597 28427597 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:28427597C>T c.8887G>A c.(8887-8889)Gtg>Atg p.V2963M COADREAD 15 28431776 28431776 + Silent SNP A A G TCGA-CM-6165-01A-11D-1650-10 TCGA-CM-6165-10A-01D-1650-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COADREAD 15 28431776 28431776 + Silent SNP A A G TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COADREAD 15 28431776 28431776 + Silent SNP A A G TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COADREAD 15 28431776 28431776 + Silent SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:28431776A>G c.8772T>C c.(8770-8772)ccT>ccC p.P2924P COADREAD 15 28437182 28437182 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:28437182C>T c.8376G>A c.(8374-8376)tcG>tcA p.S2792S COADREAD 15 28437250 28437250 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr15:28437250A>G c.8308T>C c.(8308-8310)Tgc>Cgc p.C2770R COADREAD 15 28437272 28437272 + Silent SNP A A G TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr15:28437272A>G c.8286T>C c.(8284-8286)cgT>cgC p.R2762R COADREAD 15 28441425 28441425 + Silent SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:28441425A>G c.8196T>C c.(8194-8196)tgT>tgC p.C2732C COADREAD 15 28443535 28443535 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:28443535C>T c.8000G>A c.(7999-8001)gGg>gAg p.G2667E COADREAD 15 28443624 28443626 + In_Frame_Del DEL AGA AGA - TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr15:28443624_28443626delAGA c.7909_7911delTCT c.(7909-7911)tctdel p.S2637del COADREAD 15 28443784 28443784 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:28443784G>A c.7848C>T c.(7846-7848)ggC>ggT p.G2616G COADREAD 15 28446658 28446658 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28446658G>A c.7660C>T c.(7660-7662)Cga>Tga p.R2554* COADREAD 15 28447529 28447529 + Missense_Mutation SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:28447529G>T c.7444C>A c.(7444-7446)Ctc>Atc p.L2482I COADREAD 15 28456228 28456228 + Missense_Mutation SNP C C T TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr15:28456228C>T c.6989G>A c.(6988-6990)cGg>cAg p.R2330Q COADREAD 15 28456241 28456241 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:28456241G>T c.6976C>A c.(6976-6978)Ctg>Atg p.L2326M COADREAD 15 28456263 28456263 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr15:28456263G>A c.6954C>T c.(6952-6954)tgC>tgT p.C2318C COADREAD 15 28459027 28459027 + Missense_Mutation SNP C C T TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr15:28459027C>T c.6647G>A c.(6646-6648)cGc>cAc p.R2216H COADREAD 15 28459069 28459069 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr15:28459069delC c.6605delG c.(6604-6606)ggcfs p.G2202fs COADREAD 15 28460812 28460812 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28460812G>A c.6165C>T c.(6163-6165)gtC>gtT p.V2055V COADREAD 15 28460942 28460942 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:28460942G>T c.6035C>A c.(6034-6036)cCa>cAa p.P2012Q COADREAD 15 28463812 28463812 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28463812C>T c.5851G>A c.(5851-5853)Gaa>Aaa p.E1951K COADREAD 15 28465671 28465671 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:28465671G>A c.5772C>T c.(5770-5772)taC>taT p.Y1924Y COADREAD 15 28467179 28467179 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28467179C>T c.5647G>A c.(5647-5649)Gat>Aat p.D1883N COADREAD 15 28474407 28474407 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28474407A>G c.5206T>C c.(5206-5208)Tac>Cac p.Y1736H COADREAD 15 28475600 28475600 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:28475600G>A c.4722C>T c.(4720-4722)aaC>aaT p.N1574N COADREAD 15 28478824 28478824 + Missense_Mutation SNP T T C TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr15:28478824T>C c.4337A>G c.(4336-4338)aAa>aGa p.K1446R COADREAD 15 28478848 28478848 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28478848C>T c.4313G>A c.(4312-4314)cGc>cAc p.R1438H COADREAD 15 28478879 28478879 + Missense_Mutation SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28478879G>A c.4282C>T c.(4282-4284)Ccc>Tcc p.P1428S COADREAD 15 28483842 28483842 + Silent SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28483842A>G c.3654T>C c.(3652-3654)caT>caC p.H1218H COADREAD 15 28491948 28491948 + Missense_Mutation SNP C C A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr15:28491948C>A c.3331G>T c.(3331-3333)Gct>Tct p.A1111S COADREAD 15 28492013 28492013 + Missense_Mutation SNP A A T TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chr15:28492013A>T c.3266T>A c.(3265-3267)cTg>cAg p.L1089Q COADREAD 15 28493767 28493767 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr15:28493767G>A c.3166C>T c.(3166-3168)Cgt>Tgt p.R1056C COADREAD 15 28493767 28493767 + Missense_Mutation SNP G G A TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr15:28493767G>A c.3166C>T c.(3166-3168)Cgt>Tgt p.R1056C COADREAD 15 28493836 28493836 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:28493836G>A c.3097C>T c.(3097-3099)Cgg>Tgg p.R1033W COADREAD 15 28499581 28499581 + Silent SNP C C T TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr15:28499581C>T c.2955G>A c.(2953-2955)agG>agA p.R985R COADREAD 15 28502274 28502274 + Missense_Mutation SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:28502274G>A c.2450C>T c.(2449-2451)gCg>gTg p.A817V COADREAD 15 28502304 28502304 + Missense_Mutation SNP C C A TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr15:28502304C>A c.2420G>T c.(2419-2421)cGg>cTg p.R807L COADREAD 15 28502305 28502305 + Missense_Mutation SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr15:28502305G>A c.2419C>T c.(2419-2421)Cgg>Tgg p.R807W COADREAD 15 28508102 28508102 + Missense_Mutation SNP T T A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:28508102T>A c.2084A>T c.(2083-2085)gAa>gTa p.E695V COADREAD 15 28508136 28508136 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28508136C>A c.2050G>T c.(2050-2052)Ggt>Tgt p.G684C COADREAD 15 28511069 28511069 + Silent SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr15:28511069C>T c.1650G>A c.(1648-1650)ggG>ggA p.G550G COADREAD 15 28511071 28511071 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr15:28511071C>A c.1648G>T c.(1648-1650)Ggg>Tgg p.G550W COADREAD 15 28514407 28514407 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:28514407T>G c.1433A>C c.(1432-1434)aAt>aCt p.N478T COADREAD 15 28514429 28514429 + Missense_Mutation SNP G G A TCGA-AA-3814-01A-01W-0900-09 TCGA-AA-3814-10A-01W-0900-09 g.chr15:28514429G>A c.1411C>T c.(1411-1413)Cgc>Tgc p.R471C COADREAD 15 28514475 28514475 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28514475C>T c.1365G>A c.(1363-1365)caG>caA p.Q455Q COADREAD 15 28515923 28515923 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:28515923G>A c.1175C>T c.(1174-1176)aCg>aTg p.T392M COADREAD 15 28517370 28517370 + Silent SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:28517370G>A c.1074C>T c.(1072-1074)ggC>ggT p.G358G COADREAD 15 28517371 28517371 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:28517371C>T c.1073G>A c.(1072-1074)gGc>gAc p.G358D COADREAD 15 28517441 28517441 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:28517441C>A c.1003G>T c.(1003-1005)Gcc>Tcc p.A335S COADREAD 15 28518050 28518051 + Frame_Shift_Del DEL CT CT - TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr15:28518050_28518051delCT c.900_901delAG c.(898-903)agaggcfs p.G301fs COADREAD 15 28519445 28519445 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:28519445G>A c.792C>T c.(790-792)gtC>gtT p.V264V COADREAD 15 28519459 28519459 + Missense_Mutation SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr15:28519459A>G c.778T>C c.(778-780)Ttc>Ctc p.F260L COADREAD 15 28519528 28519528 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:28519528C>T c.709G>A c.(709-711)Gag>Aag p.E237K COADREAD 15 28519563 28519563 + Missense_Mutation SNP A A G TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr15:28519563A>G c.674T>C c.(673-675)tTg>tCg p.L225S COADREAD 15 28520068 28520068 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:28520068C>T c.626G>A c.(625-627)cGc>cAc p.R209H COADREAD 15 28525289 28525289 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:28525289C>A c.467G>T c.(466-468)aGa>aTa p.R156I COADREAD 15 28544575 28544575 + Frame_Shift_Del DEL G G - TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr15:28544575delG c.160delC c.(160-162)cagfs p.Q54fs DLBC 15 28366537 28366537 + Silent SNP T T C TCGA-FM-8000-01A-11D-2210-10 TCGA-FM-8000-10A-01D-2210-10 g.chr15:28366537T>C c.13227A>G c.(13225-13227)gtA>gtG p.V4409V DLBC 15 28389880 28389880 + Silent SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr15:28389880G>A c.11079C>T c.(11077-11079)agC>agT p.S3693S DLBC 15 28420676 28420676 + Silent SNP C C T TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr15:28420676C>T c.9813G>A c.(9811-9813)gcG>gcA p.A3271A DLBC 15 28424100 28424100 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr15:28424100C>T c.9096G>A c.(9094-9096)acG>acA p.T3032T DLBC 15 28459092 28459092 + Silent SNP G G A TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr15:28459092G>A c.6582C>T c.(6580-6582)gaC>gaT p.D2194D DLBC 15 28459325 28459325 + Missense_Mutation SNP C C T TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr15:28459325C>T c.6452G>A c.(6451-6453)cGc>cAc p.R2151H DLBC 15 28459393 28459393 + Silent SNP C C T TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr15:28459393C>T c.6384G>A c.(6382-6384)gtG>gtA p.V2128V ESCA 15 28357144 28357144 + Missense_Mutation SNP G G T TCGA-V5-A7RC-01B-11D-A403-09 TCGA-V5-A7RC-10A-01D-A403-09 g.chr15:28357144G>T c.14270C>A c.(14269-14271)cCt>cAt p.P4757H ESCA 15 28361836 28361836 + Silent SNP C C A TCGA-IG-A51D-01A-11D-A27G-09 TCGA-IG-A51D-10A-01D-A27G-09 g.chr15:28361836C>A c.13584G>T c.(13582-13584)gtG>gtT p.V4528V ESCA 15 28389296 28389296 + Missense_Mutation SNP G G T TCGA-Q9-A6FW-01A-31D-A31U-09 TCGA-Q9-A6FW-10A-01D-A31U-09 g.chr15:28389296G>T c.11226C>A c.(11224-11226)aaC>aaA p.N3742K ESCA 15 28408276 28408276 + Silent SNP G G A TCGA-JY-A6FB-01A-11D-A33E-09 TCGA-JY-A6FB-10A-01D-A33H-09 g.chr15:28408276G>A c.10710C>T c.(10708-10710)tcC>tcT p.S3570S ESCA 15 28419589 28419589 + Missense_Mutation SNP G G A TCGA-L5-A8NQ-01A-11D-A36J-09 TCGA-L5-A8NQ-11A-11D-A36M-09 g.chr15:28419589G>A c.10009C>T c.(10009-10011)Ccc>Tcc p.P3337S ESCA 15 28421704 28421704 + Missense_Mutation SNP C C T TCGA-L5-A8NU-01A-11D-A36J-09 TCGA-L5-A8NU-11A-11D-A36M-09 g.chr15:28421704C>T c.9556G>A c.(9556-9558)Ggc>Agc p.G3186S ESCA 15 28431882 28431882 + Missense_Mutation SNP T T G TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chr15:28431882T>G c.8666A>C c.(8665-8667)gAa>gCa p.E2889A ESCA 15 28437270 28437270 + Missense_Mutation SNP G G A TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr15:28437270G>A c.8288C>T c.(8287-8289)tCt>tTt p.S2763F ESCA 15 28441632 28441632 + Missense_Mutation SNP C C G TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr15:28441632C>G c.8095G>C c.(8095-8097)Gta>Cta p.V2699L ESCA 15 28447658 28447658 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:28447658C>T c.7315G>A c.(7315-7317)Gcc>Acc p.A2439T ESCA 15 28451412 28451412 + Missense_Mutation SNP C C T TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr15:28451412C>T c.7186G>A c.(7186-7188)Gcc>Acc p.A2396T ESCA 15 28451468 28451468 + Missense_Mutation SNP G G A TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr15:28451468G>A c.7130C>T c.(7129-7131)cCc>cTc p.P2377L ESCA 15 28463812 28463812 + Missense_Mutation SNP C C T TCGA-JY-A6FB-01A-11D-A33E-09 TCGA-JY-A6FB-10A-01D-A33H-09 g.chr15:28463812C>T c.5851G>A c.(5851-5853)Gaa>Aaa p.E1951K ESCA 15 28493812 28493812 + Missense_Mutation SNP C C G TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chr15:28493812C>G c.3121G>C c.(3121-3123)Gag>Cag p.E1041Q ESCA 15 28501404 28501404 + Silent SNP G G A TCGA-L5-A8NK-01A-21D-A37C-09 TCGA-L5-A8NK-11A-11D-A37F-09 g.chr15:28501404G>A c.2577C>T c.(2575-2577)agC>agT p.S859S ESCA 15 28514546 28514546 + Nonsense_Mutation SNP C C A TCGA-XP-A8T7-01A-11D-A36J-09 TCGA-XP-A8T7-10A-01D-A36M-09 g.chr15:28514546C>A c.1294G>T c.(1294-1296)Gga>Tga p.G432* GBM 15 28389261 28389261 + Missense_Mutation SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr15:28389261G>A c.11261C>T c.(11260-11262)gCg>gTg p.A3754V GBM 15 28421858 28421858 + Silent SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr15:28421858C>T c.9489G>A c.(9487-9489)gcG>gcA p.A3163A GBM 15 28460793 28460793 + Missense_Mutation SNP A A G TCGA-06-0166-01A-01D-1491-08 TCGA-06-0166-10A-01D-1491-08 g.chr15:28460793A>G c.6184T>C c.(6184-6186)Ttc>Ctc p.F2062L GBM 15 28474893 28474893 + Missense_Mutation SNP C C A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr15:28474893C>A c.4910G>T c.(4909-4911)aGt>aTt p.S1637I GBM 15 28514552 28514553 + Frame_Shift_Ins INS - - C TCGA-41-3392-01A-01D-1495-08 TCGA-41-3392-10A-01D-1495-08 g.chr15:28514552_28514553insC c.1287_1288insG c.(1285-1290)gggttafs p.L430fs GBMLGG 15 28369239 28369239 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28369239G>A c.13132C>T c.(13132-13134)Ctc>Ttc p.L4378F GBMLGG 15 28375699 28375699 + Silent SNP G G A TCGA-TQ-A7RG-01A-11D-A33T-08 TCGA-TQ-A7RG-10A-01D-A33W-08 g.chr15:28375699G>A c.12612C>T c.(12610-12612)tgC>tgT p.C4204C GBMLGG 15 28389059 28389059 + Missense_Mutation SNP T T C TCGA-FG-5962-01B-11D-1893-08 TCGA-FG-5962-10A-01D-1893-08 g.chr15:28389059T>C c.11378A>G c.(11377-11379)aAt>aGt p.N3793S GBMLGG 15 28389261 28389261 + Missense_Mutation SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr15:28389261G>A c.11261C>T c.(11260-11262)gCg>gTg p.A3754V GBMLGG 15 28389916 28389916 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28389916G>A c.11043C>T c.(11041-11043)cgC>cgT p.R3681R GBMLGG 15 28413709 28413709 + Silent SNP C C A TCGA-E1-A7Z3-01A-11D-A34J-08 TCGA-E1-A7Z3-10A-01D-A34M-08 g.chr15:28413709C>A c.10257G>T c.(10255-10257)ccG>ccT p.P3419P GBMLGG 15 28421858 28421858 + Silent SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr15:28421858C>T c.9489G>A c.(9487-9489)gcG>gcA p.A3163A GBMLGG 15 28437207 28437207 + Missense_Mutation SNP C C T TCGA-TQ-A8XE-01A-11D-A36O-08 TCGA-TQ-A8XE-10A-01D-A367-08 g.chr15:28437207C>T c.8351G>A c.(8350-8352)cGc>cAc p.R2784H GBMLGG 15 28447534 28447534 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28447534T>G c.7439A>C c.(7438-7440)aAg>aCg p.K2480T GBMLGG 15 28460793 28460793 + Missense_Mutation SNP A A G TCGA-06-0166-01A-01D-1491-08 TCGA-06-0166-10A-01D-1491-08 g.chr15:28460793A>G c.6184T>C c.(6184-6186)Ttc>Ctc p.F2062L GBMLGG 15 28460828 28460828 + Missense_Mutation SNP G G A TCGA-FG-5962-01B-11D-1893-08 TCGA-FG-5962-10A-01D-1893-08 g.chr15:28460828G>A c.6149C>T c.(6148-6150)aCg>aTg p.T2050M GBMLGG 15 28463781 28463781 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28463781G>A c.5882C>T c.(5881-5883)gCa>gTa p.A1961V GBMLGG 15 28473408 28473408 + Missense_Mutation SNP T T C TCGA-DU-A5TP-01A-11D-A289-08 TCGA-DU-A5TP-10A-01D-A289-08 g.chr15:28473408T>C c.5420A>G c.(5419-5421)aAt>aGt p.N1807S GBMLGG 15 28474893 28474893 + Missense_Mutation SNP C C A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr15:28474893C>A c.4910G>T c.(4909-4911)aGt>aTt p.S1637I GBMLGG 15 28478677 28478677 + Missense_Mutation SNP C C T TCGA-QH-A6CS-01A-11D-A31L-08 TCGA-QH-A6CS-10A-01D-A31J-08 g.chr15:28478677C>T c.4382G>A c.(4381-4383)gGt>gAt p.G1461D GBMLGG 15 28483336 28483336 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28483336A>G c.3776T>C c.(3775-3777)gTa>gCa p.V1259A GBMLGG 15 28491947 28491947 + Missense_Mutation SNP G G A TCGA-DB-A64X-01A-11D-A29Q-08 TCGA-DB-A64X-10A-01D-A29Q-08 g.chr15:28491947G>A c.3332C>T c.(3331-3333)gCt>gTt p.A1111V GBMLGG 15 28514552 28514553 + Frame_Shift_Ins INS - - C TCGA-41-3392-01A-01D-1495-08 TCGA-41-3392-10A-01D-1495-08 g.chr15:28514552_28514553insC c.1287_1288insG c.(1285-1290)gggttafs p.L430fs HNSC 15 28357012 28357012 + Missense_Mutation SNP A A C TCGA-CV-6941-01A-11D-1912-08 TCGA-CV-6941-10A-01D-1912-08 g.chr15:28357012A>C c.14402T>G c.(14401-14403)cTt>cGt p.L4801R HNSC 15 28357065 28357065 + Silent SNP G G A TCGA-UF-A7JC-01A-21D-A34J-08 TCGA-UF-A7JC-10A-01D-A34M-08 g.chr15:28357065G>A c.14349C>T c.(14347-14349)taC>taT p.Y4783Y HNSC 15 28358347 28358347 + Missense_Mutation SNP A A G TCGA-BA-6871-01A-11D-1870-08 TCGA-BA-6871-10A-01D-1870-08 g.chr15:28358347A>G c.14102T>C c.(14101-14103)aTc>aCc p.I4701T HNSC 15 28358821 28358821 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr15:28358821G>A c.13917C>T c.(13915-13917)ctC>ctT p.L4639L HNSC 15 28369194 28369194 + Missense_Mutation SNP A A T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:28369194A>T c.13177T>A c.(13177-13179)Tcc>Acc p.S4393T HNSC 15 28370247 28370247 + Missense_Mutation SNP G G T TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr15:28370247G>T c.12895C>A c.(12895-12897)Cag>Aag p.Q4299K HNSC 15 28375381 28375381 + Nonsense_Mutation SNP G G A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr15:28375381G>A c.12730C>T c.(12730-12732)Caa>Taa p.Q4244* HNSC 15 28375741 28375741 + Splice_Site SNP C C T TCGA-DQ-7591-01A-11D-2078-08 TCGA-DQ-7591-10A-01D-2078-08 g.chr15:28375741C>T c.e82-1 HNSC 15 28380704 28380704 + Missense_Mutation SNP G G C TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr15:28380704G>C c.12150C>G c.(12148-12150)caC>caG p.H4050Q HNSC 15 28380751 28380751 + Nonsense_Mutation SNP G G A TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr15:28380751G>A c.12103C>T c.(12103-12105)Cag>Tag p.Q4035* HNSC 15 28386588 28386588 + Missense_Mutation SNP G G T TCGA-CV-7101-01A-11D-2012-08 TCGA-CV-7101-10A-01D-2013-08 g.chr15:28386588G>T c.12005C>A c.(12004-12006)gCt>gAt p.A4002D HNSC 15 28386662 28386662 + Silent SNP A A C TCGA-CN-6020-01A-11D-1683-08 TCGA-CN-6020-10A-01D-1683-08 g.chr15:28386662A>C c.11931T>G c.(11929-11931)acT>acG p.T3977T HNSC 15 28387409 28387409 + Missense_Mutation SNP G G T TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr15:28387409G>T c.11675C>A c.(11674-11676)cCg>cAg p.P3892Q HNSC 15 28388011 28388011 + Missense_Mutation SNP T T A TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr15:28388011T>A c.11506A>T c.(11506-11508)Agg>Tgg p.R3836W HNSC 15 28389228 28389228 + Missense_Mutation SNP G G A TCGA-CV-7418-01A-11D-2078-08 TCGA-CV-7418-10A-01D-2078-08 g.chr15:28389228G>A c.11294C>T c.(11293-11295)gCc>gTc p.A3765V HNSC 15 28389924 28389924 + Missense_Mutation SNP C C T TCGA-CR-5247-01A-01D-2012-08 TCGA-CR-5247-10A-01D-2013-08 g.chr15:28389924C>T c.11035G>A c.(11035-11037)Gag>Aag p.E3679K HNSC 15 28389948 28389948 + Nonsense_Mutation SNP G G A TCGA-CN-A640-01A-21D-A30E-08 TCGA-CN-A640-10A-01D-A30H-08 g.chr15:28389948G>A c.11011C>T c.(11011-11013)Cga>Tga p.R3671* HNSC 15 28391388 28391388 + Missense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:28391388C>T c.11003G>A c.(11002-11004)cGg>cAg p.R3668Q HNSC 15 28408263 28408263 + Missense_Mutation SNP C C T TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr15:28408263C>T c.10723G>A c.(10723-10725)Ggc>Agc p.G3575S HNSC 15 28408273 28408273 + Silent SNP C C A TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr15:28408273C>A c.10713G>T c.(10711-10713)gcG>gcT p.A3571A HNSC 15 28408274 28408274 + Missense_Mutation SNP G G A TCGA-MT-A51X-01A-11D-A25Y-08 TCGA-MT-A51X-10A-01D-A25Y-08 g.chr15:28408274G>A c.10712C>T c.(10711-10713)gCg>gTg p.A3571V HNSC 15 28408307 28408307 + Missense_Mutation SNP C C T TCGA-F7-8298-01A-11D-2394-08 TCGA-F7-8298-10A-01D-2394-08 g.chr15:28408307C>T c.10679G>A c.(10678-10680)cGg>cAg p.R3560Q HNSC 15 28413555 28413555 + Missense_Mutation SNP C C G TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr15:28413555C>G c.10411G>C c.(10411-10413)Gag>Cag p.E3471Q HNSC 15 28413737 28413737 + Splice_Site SNP C C G TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr15:28413737C>G c.e67-1 HNSC 15 28419625 28419625 + Missense_Mutation SNP T T G TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr15:28419625T>G c.9973A>C c.(9973-9975)Aca>Cca p.T3325P HNSC 15 28420789 28420789 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:28420789A>G c.9700T>C c.(9700-9702)Tac>Cac p.Y3234H HNSC 15 28421842 28421842 + Missense_Mutation SNP T T A TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chr15:28421842T>A c.9505A>T c.(9505-9507)Acc>Tcc p.T3169S HNSC 15 28446658 28446659 + Frame_Shift_Ins INS - - T TCGA-HD-7753-01A-11D-2078-08 TCGA-HD-7753-10A-01D-2078-08 g.chr15:28446658_28446659insT c.7659_7660insA c.(7657-7662)aaacgafs p.R2554fs HNSC 15 28447508 28447508 + Missense_Mutation SNP C C T TCGA-CV-A45O-01A-21D-A24D-08 TCGA-CV-A45O-10A-01D-A24F-08 g.chr15:28447508C>T c.7465G>A c.(7465-7467)Gca>Aca p.A2489T HNSC 15 28447555 28447555 + Missense_Mutation SNP C C A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr15:28447555C>A c.7418G>T c.(7417-7419)aGg>aTg p.R2473M HNSC 15 28458989 28458989 + Nonsense_Mutation SNP C C A TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chr15:28458989C>A c.6685G>T c.(6685-6687)Gga>Tga p.G2229* HNSC 15 28459109 28459109 + Missense_Mutation SNP C C T TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chr15:28459109C>T c.6565G>A c.(6565-6567)Gag>Aag p.E2189K HNSC 15 28459835 28459835 + Silent SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr15:28459835G>A c.6324C>T c.(6322-6324)ctC>ctT p.L2108L HNSC 15 28463722 28463722 + Missense_Mutation SNP G G A TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr15:28463722G>A c.5941C>T c.(5941-5943)Cat>Tat p.H1981Y HNSC 15 28465693 28465693 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr15:28465693C>T c.5750G>A c.(5749-5751)aGg>aAg p.R1917K HNSC 15 28467346 28467346 + Missense_Mutation SNP T T C TCGA-CV-6950-01A-11D-1912-08 TCGA-CV-6950-10A-01D-1912-08 g.chr15:28467346T>C c.5480A>G c.(5479-5481)aAc>aGc p.N1827S HNSC 15 28473446 28473446 + Silent SNP G G A TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr15:28473446G>A c.5382C>T c.(5380-5382)acC>acT p.T1794T HNSC 15 28483355 28483355 + Missense_Mutation SNP C C A TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr15:28483355C>A c.3757G>T c.(3757-3759)Gca>Tca p.A1253S HNSC 15 28483835 28483835 + Missense_Mutation SNP C C T TCGA-CQ-6223-01A-11D-1912-08 TCGA-CQ-6223-10A-01D-1912-08 g.chr15:28483835C>T c.3661G>A c.(3661-3663)Gat>Aat p.D1221N HNSC 15 28491924 28491924 + Missense_Mutation SNP C C T TCGA-CV-6945-01A-11D-1912-08 TCGA-CV-6945-10A-01D-1912-08 g.chr15:28491924C>T c.3355G>A c.(3355-3357)Gcg>Acg p.A1119T HNSC 15 28493761 28493761 + Missense_Mutation SNP G G C TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr15:28493761G>C c.3172C>G c.(3172-3174)Caa>Gaa p.Q1058E HNSC 15 28502276 28502276 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:28502276G>A c.2448C>T c.(2446-2448)tcC>tcT p.S816S HNSC 15 28502312 28502312 + Silent SNP G G C TCGA-KU-A66T-01A-11D-A30E-08 TCGA-KU-A66T-10A-01D-A30H-08 g.chr15:28502312G>C c.2412C>G c.(2410-2412)ctC>ctG p.L804L HNSC 15 28515878 28515878 + Missense_Mutation SNP C C T TCGA-IQ-A6SG-01A-12D-A34J-08 TCGA-IQ-A6SG-10A-01D-A34M-08 g.chr15:28515878C>T c.1220G>A c.(1219-1221)tGt>tAt p.C407Y HNSC 15 28517376 28517376 + Silent SNP G G A TCGA-CV-7416-01A-11D-2078-08 TCGA-CV-7416-10A-01D-2078-08 g.chr15:28517376G>A c.1068C>T c.(1066-1068)tcC>tcT p.S356S HNSC 15 28538128 28538128 + Silent SNP C C T TCGA-CR-7397-01A-11D-2012-08 TCGA-CR-7397-10A-01D-2013-08 g.chr15:28538128C>T c.228G>A c.(226-228)ctG>ctA p.L76L KICH 15 28427617 28427617 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:28427617G>A c.8867C>T c.(8866-8868)aCg>aTg p.T2956M KICH 15 28447318 28447318 + Missense_Mutation SNP A A G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr15:28447318A>G c.7558T>C c.(7558-7560)Tcc>Ccc p.S2520P KICH 15 28456246 28456246 + Missense_Mutation SNP T T A TCGA-KO-8416-01A-11D-2310-10 TCGA-KO-8416-11A-01D-2311-10 g.chr15:28456246T>A c.6971A>T c.(6970-6972)tAc>tTc p.Y2324F KICH 15 28478879 28478879 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:28478879G>A c.4282C>T c.(4282-4284)Ccc>Tcc p.P1428S KICH 15 28482158 28482158 + Silent SNP C C G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr15:28482158C>G c.3954G>C c.(3952-3954)tcG>tcC p.S1318S KIPAN 15 28366558 28366558 + Missense_Mutation SNP T T G TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr15:28366558T>G c.13206A>C c.(13204-13206)aaA>aaC p.K4402N KIPAN 15 28369256 28369256 + Missense_Mutation SNP G G A TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr15:28369256G>A c.13115C>T c.(13114-13116)tCg>tTg p.S4372L KIPAN 15 28375699 28375699 + Silent SNP G G A TCGA-BP-4760-01A-02D-1421-08 TCGA-BP-4760-11A-01D-1421-08 g.chr15:28375699G>A c.12612C>T c.(12610-12612)tgC>tgT p.C4204C KIPAN 15 28377879 28377879 + Missense_Mutation SNP C C T TCGA-5P-A9JZ-01A-11D-A42J-10 TCGA-5P-A9JZ-10A-01D-A42M-10 g.chr15:28377879C>T c.12328G>A c.(12328-12330)Ggg>Agg p.G4110R KIPAN 15 28380665 28380665 + Missense_Mutation SNP C C G TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr15:28380665C>G c.12189G>C c.(12187-12189)tgG>tgC p.W4063C KIPAN 15 28386944 28386944 + Missense_Mutation SNP C C A TCGA-B0-5083-01A-02D-1421-08 TCGA-B0-5083-11A-01D-1421-08 g.chr15:28386944C>A c.11749G>T c.(11749-11751)Gtt>Ttt p.V3917F KIPAN 15 28387457 28387457 + Missense_Mutation SNP C C A TCGA-B0-5695-01A-11D-1534-10 TCGA-B0-5695-11A-01D-1534-10 g.chr15:28387457C>A c.11627G>T c.(11626-11628)aGg>aTg p.R3876M KIPAN 15 28414709 28414709 + Missense_Mutation SNP G G C TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:28414709G>C c.10150C>G c.(10150-10152)Ctc>Gtc p.L3384V KIPAN 15 28414719 28414719 + Silent SNP A A G TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:28414719A>G c.10140T>C c.(10138-10140)ctT>ctC p.L3380L KIPAN 15 28427617 28427617 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:28427617G>A c.8867C>T c.(8866-8868)aCg>aTg p.T2956M KIPAN 15 28431846 28431846 + Missense_Mutation SNP T T A TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr15:28431846T>A c.8702A>T c.(8701-8703)gAt>gTt p.D2901V KIPAN 15 28436294 28436294 + Missense_Mutation SNP C C A TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr15:28436294C>A c.8548G>T c.(8548-8550)Gta>Tta p.V2850L KIPAN 15 28437274 28437274 + Missense_Mutation SNP G G C TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr15:28437274G>C c.8284C>G c.(8284-8286)Cgt>Ggt p.R2762G KIPAN 15 28446698 28446698 + Silent SNP A A G TCGA-AK-3429-01A-02D-1386-10 TCGA-AK-3429-10A-01D-1251-10 g.chr15:28446698A>G c.7620T>C c.(7618-7620)tcT>tcC p.S2540S KIPAN 15 28447318 28447318 + Missense_Mutation SNP A A G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr15:28447318A>G c.7558T>C c.(7558-7560)Tcc>Ccc p.S2520P KIPAN 15 28456246 28456246 + Missense_Mutation SNP T T A TCGA-KO-8416-01A-11D-2310-10 TCGA-KO-8416-11A-01D-2311-10 g.chr15:28456246T>A c.6971A>T c.(6970-6972)tAc>tTc p.Y2324F KIPAN 15 28457714 28457714 + Missense_Mutation SNP A A G TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr15:28457714A>G c.6802T>C c.(6802-6804)Ttt>Ctt p.F2268L KIPAN 15 28459417 28459417 + Splice_Site SNP C C G TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr15:28459417C>G c.6360G>C c.(6358-6360)gaG>gaC p.E2120D KIPAN 15 28473477 28473477 + Missense_Mutation SNP C C A TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr15:28473477C>A c.5351G>T c.(5350-5352)cGc>cTc p.R1784L KIPAN 15 28478879 28478879 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:28478879G>A c.4282C>T c.(4282-4284)Ccc>Tcc p.P1428S KIPAN 15 28482158 28482158 + Silent SNP C C G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr15:28482158C>G c.3954G>C c.(3952-3954)tcG>tcC p.S1318S KIPAN 15 28491151 28491151 + Silent SNP G G A TCGA-AK-3440-01A-01D-0966-08 TCGA-AK-3440-10A-01D-0966-08 g.chr15:28491151G>A c.3453C>T c.(3451-3453)ctC>ctT p.L1151L KIPAN 15 28499508 28499508 + Missense_Mutation SNP G G C TCGA-CJ-5682-01A-11D-1534-10 TCGA-CJ-5682-11A-01D-1535-10 g.chr15:28499508G>C c.3028C>G c.(3028-3030)Cag>Gag p.Q1010E KIPAN 15 28499655 28499655 + Missense_Mutation SNP C C T TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr15:28499655C>T c.2881G>A c.(2881-2883)Gcc>Acc p.A961T KIPAN 15 28501377 28501377 + Silent SNP C C T TCGA-BP-4983-01A-01D-1462-08 TCGA-BP-4983-11A-01D-1462-08 g.chr15:28501377C>T c.2604G>A c.(2602-2604)acG>acA p.T868T KIPAN 15 28510872 28510872 + Missense_Mutation SNP T T A TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr15:28510872T>A c.1762A>T c.(1762-1764)Agt>Tgt p.S588C KIPAN 15 28514431 28514431 + Missense_Mutation SNP C C A TCGA-A3-3317-01A-01D-0966-08 TCGA-A3-3317-11A-01D-0966-08 g.chr15:28514431C>A c.1409G>T c.(1408-1410)gGc>gTc p.G470V KIPAN 15 28515959 28515959 + Missense_Mutation SNP G G A TCGA-AK-3458-01A-01D-1501-10 TCGA-AK-3458-10A-01D-1501-10 g.chr15:28515959G>A c.1139C>T c.(1138-1140)cCa>cTa p.P380L KIRC 15 28366558 28366558 + Missense_Mutation SNP T T G TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr15:28366558T>G c.13206A>C c.(13204-13206)aaA>aaC p.K4402N KIRC 15 28375699 28375699 + Silent SNP G G A TCGA-BP-4760-01A-02D-1421-08 TCGA-BP-4760-11A-01D-1421-08 g.chr15:28375699G>A c.12612C>T c.(12610-12612)tgC>tgT p.C4204C KIRC 15 28386944 28386944 + Missense_Mutation SNP C C A TCGA-B0-5083-01A-02D-1421-08 TCGA-B0-5083-11A-01D-1421-08 g.chr15:28386944C>A c.11749G>T c.(11749-11751)Gtt>Ttt p.V3917F KIRC 15 28387457 28387457 + Missense_Mutation SNP C C A TCGA-B0-5695-01A-11D-1534-10 TCGA-B0-5695-11A-01D-1534-10 g.chr15:28387457C>A c.11627G>T c.(11626-11628)aGg>aTg p.R3876M KIRC 15 28414709 28414709 + Missense_Mutation SNP G G C TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:28414709G>C c.10150C>G c.(10150-10152)Ctc>Gtc p.L3384V KIRC 15 28414719 28414719 + Silent SNP A A G TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:28414719A>G c.10140T>C c.(10138-10140)ctT>ctC p.L3380L KIRC 15 28436294 28436294 + Missense_Mutation SNP C C A TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr15:28436294C>A c.8548G>T c.(8548-8550)Gta>Tta p.V2850L KIRC 15 28446698 28446698 + Silent SNP A A G TCGA-AK-3429-01A-02D-1386-10 TCGA-AK-3429-10A-01D-1251-10 g.chr15:28446698A>G c.7620T>C c.(7618-7620)tcT>tcC p.S2540S KIRC 15 28473477 28473477 + Missense_Mutation SNP C C A TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr15:28473477C>A c.5351G>T c.(5350-5352)cGc>cTc p.R1784L KIRC 15 28491151 28491151 + Silent SNP G G A TCGA-AK-3440-01A-01D-0966-08 TCGA-AK-3440-10A-01D-0966-08 g.chr15:28491151G>A c.3453C>T c.(3451-3453)ctC>ctT p.L1151L KIRC 15 28499508 28499508 + Missense_Mutation SNP G G C TCGA-CJ-5682-01A-11D-1534-10 TCGA-CJ-5682-11A-01D-1535-10 g.chr15:28499508G>C c.3028C>G c.(3028-3030)Cag>Gag p.Q1010E KIRC 15 28501377 28501377 + Silent SNP C C T TCGA-BP-4983-01A-01D-1462-08 TCGA-BP-4983-11A-01D-1462-08 g.chr15:28501377C>T c.2604G>A c.(2602-2604)acG>acA p.T868T KIRC 15 28514431 28514431 + Missense_Mutation SNP C C A TCGA-A3-3317-01A-01D-0966-08 TCGA-A3-3317-11A-01D-0966-08 g.chr15:28514431C>A c.1409G>T c.(1408-1410)gGc>gTc p.G470V KIRC 15 28515959 28515959 + Missense_Mutation SNP G G A TCGA-AK-3458-01A-01D-1501-10 TCGA-AK-3458-10A-01D-1501-10 g.chr15:28515959G>A c.1139C>T c.(1138-1140)cCa>cTa p.P380L KIRP 15 28369256 28369256 + Missense_Mutation SNP G G A TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr15:28369256G>A c.13115C>T c.(13114-13116)tCg>tTg p.S4372L KIRP 15 28377879 28377879 + Missense_Mutation SNP C C T TCGA-5P-A9JZ-01A-11D-A42J-10 TCGA-5P-A9JZ-10A-01D-A42M-10 g.chr15:28377879C>T c.12328G>A c.(12328-12330)Ggg>Agg p.G4110R KIRP 15 28380665 28380665 + Missense_Mutation SNP C C G TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr15:28380665C>G c.12189G>C c.(12187-12189)tgG>tgC p.W4063C KIRP 15 28431846 28431846 + Missense_Mutation SNP T T A TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr15:28431846T>A c.8702A>T c.(8701-8703)gAt>gTt p.D2901V KIRP 15 28437274 28437274 + Missense_Mutation SNP G G C TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr15:28437274G>C c.8284C>G c.(8284-8286)Cgt>Ggt p.R2762G KIRP 15 28457714 28457714 + Missense_Mutation SNP A A G TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr15:28457714A>G c.6802T>C c.(6802-6804)Ttt>Ctt p.F2268L KIRP 15 28459417 28459417 + Splice_Site SNP C C G TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr15:28459417C>G c.6360G>C c.(6358-6360)gaG>gaC p.E2120D KIRP 15 28499655 28499655 + Missense_Mutation SNP C C T TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr15:28499655C>T c.2881G>A c.(2881-2883)Gcc>Acc p.A961T KIRP 15 28510872 28510872 + Missense_Mutation SNP T T A TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr15:28510872T>A c.1762A>T c.(1762-1764)Agt>Tgt p.S588C LAML 15 28389253 28389253 + Missense_Mutation SNP G G T TCGA-AB-2935-03A-01W-0755-09 TCGA-AB-2935-11A-01W-0755-09 g.chr15:28389253G>T c.11269C>A c.(11269-11271)Ctg>Atg p.L3757M LGG 15 28369239 28369239 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28369239G>A c.13132C>T c.(13132-13134)Ctc>Ttc p.L4378F LGG 15 28375699 28375699 + Silent SNP G G A TCGA-TQ-A7RG-01A-11D-A33T-08 TCGA-TQ-A7RG-10A-01D-A33W-08 g.chr15:28375699G>A c.12612C>T c.(12610-12612)tgC>tgT p.C4204C LGG 15 28389059 28389059 + Missense_Mutation SNP T T C TCGA-FG-5962-01B-11D-1893-08 TCGA-FG-5962-10A-01D-1893-08 g.chr15:28389059T>C c.11378A>G c.(11377-11379)aAt>aGt p.N3793S LGG 15 28389916 28389916 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28389916G>A c.11043C>T c.(11041-11043)cgC>cgT p.R3681R LGG 15 28413709 28413709 + Silent SNP C C A TCGA-E1-A7Z3-01A-11D-A34J-08 TCGA-E1-A7Z3-10A-01D-A34M-08 g.chr15:28413709C>A c.10257G>T c.(10255-10257)ccG>ccT p.P3419P LGG 15 28437207 28437207 + Missense_Mutation SNP C C T TCGA-TQ-A8XE-01A-11D-A36O-08 TCGA-TQ-A8XE-10A-01D-A367-08 g.chr15:28437207C>T c.8351G>A c.(8350-8352)cGc>cAc p.R2784H LGG 15 28447534 28447534 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28447534T>G c.7439A>C c.(7438-7440)aAg>aCg p.K2480T LGG 15 28460828 28460828 + Missense_Mutation SNP G G A TCGA-FG-5962-01B-11D-1893-08 TCGA-FG-5962-10A-01D-1893-08 g.chr15:28460828G>A c.6149C>T c.(6148-6150)aCg>aTg p.T2050M LGG 15 28463781 28463781 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28463781G>A c.5882C>T c.(5881-5883)gCa>gTa p.A1961V LGG 15 28473408 28473408 + Missense_Mutation SNP T T C TCGA-DU-A5TP-01A-11D-A289-08 TCGA-DU-A5TP-10A-01D-A289-08 g.chr15:28473408T>C c.5420A>G c.(5419-5421)aAt>aGt p.N1807S LGG 15 28478677 28478677 + Missense_Mutation SNP C C T TCGA-QH-A6CS-01A-11D-A31L-08 TCGA-QH-A6CS-10A-01D-A31J-08 g.chr15:28478677C>T c.4382G>A c.(4381-4383)gGt>gAt p.G1461D LGG 15 28483336 28483336 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:28483336A>G c.3776T>C c.(3775-3777)gTa>gCa p.V1259A LGG 15 28491947 28491947 + Missense_Mutation SNP G G A TCGA-DB-A64X-01A-11D-A29Q-08 TCGA-DB-A64X-10A-01D-A29Q-08 g.chr15:28491947G>A c.3332C>T c.(3331-3333)gCt>gTt p.A1111V LIHC 15 28366565 28366565 + Frame_Shift_Del DEL A A - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr15:28366565delA c.13199delT c.(13198-13200)ttcfs p.F4400fs LIHC 15 28377352 28377352 + Missense_Mutation SNP G G A TCGA-CC-A7IG-01A-11D-A33K-10 TCGA-CC-A7IG-10A-01D-A33K-10 g.chr15:28377352G>A c.12464C>T c.(12463-12465)gCc>gTc p.A4155V LIHC 15 28412958 28412958 + Missense_Mutation SNP C C A TCGA-DD-AAVQ-01A-11D-A40R-10 TCGA-DD-AAVQ-10A-01D-A40U-10 g.chr15:28412958C>A c.10429G>T c.(10429-10431)Gac>Tac p.D3477Y LIHC 15 28419597 28419597 + Missense_Mutation SNP A A C TCGA-K7-A6G5-01A-11D-A30V-10 TCGA-K7-A6G5-10A-01D-A30V-10 g.chr15:28419597A>C c.10001T>G c.(10000-10002)gTc>gGc p.V3334G LIHC 15 28419679 28419679 + Missense_Mutation SNP C C T TCGA-2Y-A9H1-01A-11D-A382-10 TCGA-2Y-A9H1-10A-01D-A385-10 g.chr15:28419679C>T c.9919G>A c.(9919-9921)Gaa>Aaa p.E3307K LIHC 15 28419719 28419729 + Frame_Shift_Del DEL CGTGCCATTGC CGTGCCATTGC - TCGA-ZP-A9D4-01A-11D-A36X-10 TCGA-ZP-A9D4-10A-01D-A370-10 g.chr15:28419719_28419729delCGTGCCATTGC c.9869_9879delGCAATGGCACG c.(9868-9879)ggcaatggcacgfs p.GNGT3290fs LIHC 15 28421641 28421641 + Frame_Shift_Del DEL C C - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr15:28421641delC c.9619delG c.(9619-9621)gtgfs p.V3207fs LIHC 15 28421672 28421672 + Silent SNP G G A TCGA-DD-AAE0-01A-11D-A40R-10 TCGA-DD-AAE0-10A-01D-A40U-10 g.chr15:28421672G>A c.9588C>T c.(9586-9588)ccC>ccT p.P3196P LIHC 15 28422626 28422626 + Missense_Mutation SNP C C A TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr15:28422626C>A c.9193G>T c.(9193-9195)Gat>Tat p.D3065Y LIHC 15 28436339 28436339 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr15:28436339delT c.8503delA c.(8503-8505)atgfs p.M2835fs LIHC 15 28437148 28437148 + Missense_Mutation SNP C C A TCGA-2Y-A9GW-01A-11D-A382-10 TCGA-2Y-A9GW-10A-01D-A385-10 g.chr15:28437148C>A c.8410G>T c.(8410-8412)Ggc>Tgc p.G2804C LIHC 15 28443868 28443868 + Missense_Mutation SNP T T G TCGA-DD-AAD1-01A-11D-A40R-10 TCGA-DD-AAD1-10A-01D-A40U-10 g.chr15:28443868T>G c.7764A>C c.(7762-7764)gaA>gaC p.E2588D LIHC 15 28446674 28446674 + Missense_Mutation SNP G G C TCGA-DD-A1EA-01A-11D-A12Z-10 TCGA-DD-A1EA-10A-01D-A12Z-10 g.chr15:28446674G>C c.7644C>G c.(7642-7644)agC>agG p.S2548R LIHC 15 28446674 28446674 + Missense_Mutation SNP G G C TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr15:28446674G>C c.7644C>G c.(7642-7644)agC>agG p.S2548R LIHC 15 28457606 28457606 + Nonsense_Mutation SNP T T A TCGA-DD-A11A-01A-11D-A12Z-10 TCGA-DD-A11A-10A-01D-A12Z-10 g.chr15:28457606T>A c.6910A>T c.(6910-6912)Aaa>Taa p.K2304* LIHC 15 28460799 28460799 + Missense_Mutation SNP C C G TCGA-ED-A7PZ-01A-11D-A33Q-10 TCGA-ED-A7PZ-10A-01D-A33Q-10 g.chr15:28460799C>G c.6178G>C c.(6178-6180)Gca>Cca p.A2060P LIHC 15 28465614 28465614 + Missense_Mutation SNP G G T TCGA-G3-A25Z-01A-11D-A16V-10 TCGA-G3-A25Z-10A-01D-A16V-10 g.chr15:28465614G>T c.5829C>A c.(5827-5829)gaC>gaA p.D1943E LIHC 15 28474355 28474355 + Missense_Mutation SNP T T C TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr15:28474355T>C c.5258A>G c.(5257-5259)aAa>aGa p.K1753R LIHC 15 28482110 28482110 + Splice_Site SNP G G A TCGA-G3-A3CK-01A-11D-A20W-10 TCGA-G3-A3CK-10A-01D-A20W-10 g.chr15:28482110G>A c.4002C>T c.(4000-4002)gcC>gcT p.A1334A LIHC 15 28491165 28491165 + Missense_Mutation SNP T T C TCGA-DD-A4NF-01A-11D-A27I-10 TCGA-DD-A4NF-10A-01D-A27I-10 g.chr15:28491165T>C c.3439A>G c.(3439-3441)Aaa>Gaa p.K1147E LIHC 15 28493786 28493786 + Silent SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr15:28493786A>G c.3147T>C c.(3145-3147)gcT>gcC p.A1049A LIHC 15 28501325 28501325 + Missense_Mutation SNP C C A TCGA-DD-AACM-01A-11D-A40R-10 TCGA-DD-AACM-10A-01D-A40U-10 g.chr15:28501325C>A c.2656G>T c.(2656-2658)Gcc>Tcc p.A886S LIHC 15 28516001 28516001 + Missense_Mutation SNP G G A TCGA-DD-AAW0-01A-11D-A40R-10 TCGA-DD-AAW0-10A-01D-A40U-10 g.chr15:28516001G>A c.1097C>T c.(1096-1098)cCt>cTt p.P366L LIHC 15 28518063 28518063 + Silent SNP C C A TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chr15:28518063C>A c.888G>T c.(886-888)ctG>ctT p.L296L LUAD 15 28356949 28356949 + Missense_Mutation SNP A A T TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr15:28356949A>T c.14465T>A c.(14464-14466)tTt>tAt p.F4822Y LUAD 15 28356956 28356956 + Frame_Shift_Del DEL C C - TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr15:28356956delC c.14458delG c.(14458-14460)gacfs p.D4820fs LUAD 15 28356962 28356962 + Missense_Mutation SNP C C T TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr15:28356962C>T c.14452G>A c.(14452-14454)Gat>Aat p.D4818N LUAD 15 28358240 28358240 + Missense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr15:28358240G>A c.14209C>T c.(14209-14211)Cgg>Tgg p.R4737W LUAD 15 28358796 28358796 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr15:28358796C>A c.13942G>T c.(13942-13944)Gct>Tct p.A4648S LUAD 15 28359782 28359782 + Missense_Mutation SNP T T C TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr15:28359782T>C c.13889A>G c.(13888-13890)tAc>tGc p.Y4630C LUAD 15 28359842 28359842 + Missense_Mutation SNP C C G TCGA-62-A470-01A-11D-A24D-08 TCGA-62-A470-10A-01D-A24F-08 g.chr15:28359842C>G c.13829G>C c.(13828-13830)gGc>gCc p.G4610A LUAD 15 28360587 28360587 + Silent SNP C C T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr15:28360587C>T c.13710G>A c.(13708-13710)gcG>gcA p.A4570A LUAD 15 28361810 28361810 + Splice_Site SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr15:28361810C>A c.e88+1 LUAD 15 28361852 28361852 + Missense_Mutation SNP G G A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr15:28361852G>A c.13568C>T c.(13567-13569)gCc>gTc p.A4523V LUAD 15 28362196 28362196 + Silent SNP G G A TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chr15:28362196G>A c.13377C>T c.(13375-13377)ctC>ctT p.L4459L LUAD 15 28366563 28366563 + Missense_Mutation SNP G G A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr15:28366563G>A c.13201C>T c.(13201-13203)Cgg>Tgg p.R4401W LUAD 15 28369251 28369251 + Missense_Mutation SNP C C A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr15:28369251C>A c.13120G>T c.(13120-13122)Gac>Tac p.D4374Y LUAD 15 28375308 28375308 + Splice_Site SNP C C T TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr15:28375308C>T c.e83+1 LUAD 15 28375358 28375358 + Silent SNP G G A TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr15:28375358G>A c.12753C>T c.(12751-12753)gtC>gtT p.V4251V LUAD 15 28377245 28377245 + Splice_Site SNP C C T TCGA-75-5125-01A-01D-1753-08 TCGA-75-5125-10A-01D-1753-08 g.chr15:28377245C>T c.e81+1 LUAD 15 28377876 28377876 + Frame_Shift_Del DEL C C - TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr15:28377876delC c.12331delG c.(12331-12333)gacfs p.D4111fs LUAD 15 28380792 28380792 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:28380792C>A c.12062G>T c.(12061-12063)gGg>gTg p.G4021V LUAD 15 28386775 28386775 + Splice_Site SNP G G A TCGA-17-Z048-01A-01W-0746-08 TCGA-17-Z048-11A-01W-0746-08 g.chr15:28386775G>A c.11818C>T c.(11818-11820)Cga>Tga p.R3940* LUAD 15 28387460 28387460 + Missense_Mutation SNP C C A TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr15:28387460C>A c.11624G>T c.(11623-11625)cGg>cTg p.R3875L LUAD 15 28387465 28387465 + Nonsense_Mutation SNP C C T TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr15:28387465C>T c.11619G>A c.(11617-11619)tgG>tgA p.W3873* LUAD 15 28388005 28388005 + Missense_Mutation SNP C C A TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr15:28388005C>A c.11512G>T c.(11512-11514)Ggc>Tgc p.G3838C LUAD 15 28389237 28389237 + Missense_Mutation SNP T T A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr15:28389237T>A c.11285A>T c.(11284-11286)cAg>cTg p.Q3762L LUAD 15 28389295 28389295 + Missense_Mutation SNP G G A TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr15:28389295G>A c.11227C>T c.(11227-11229)Ctt>Ttt p.L3743F LUAD 15 28389852 28389852 + Missense_Mutation SNP G G C TCGA-78-7147-01A-11D-2036-08 TCGA-78-7147-10A-01D-2036-08 g.chr15:28389852G>C c.11107C>G c.(11107-11109)Cgc>Ggc p.R3703G LUAD 15 28391471 28391471 + Silent SNP T T A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:28391471T>A c.10920A>T c.(10918-10920)gtA>gtT p.V3640V LUAD 15 28408392 28408392 + Missense_Mutation SNP G G C TCGA-86-8278-01A-11D-2284-08 TCGA-86-8278-10A-01D-2284-08 g.chr15:28408392G>C c.10594C>G c.(10594-10596)Cag>Gag p.Q3532E LUAD 15 28413618 28413618 + Missense_Mutation SNP C C T TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chr15:28413618C>T c.10348G>A c.(10348-10350)Gaa>Aaa p.E3450K LUAD 15 28413635 28413635 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:28413635C>A c.10331G>T c.(10330-10332)aGt>aTt p.S3444I LUAD 15 28414753 28414753 + Missense_Mutation SNP C C A TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr15:28414753C>A c.10106G>T c.(10105-10107)gGt>gTt p.G3369V LUAD 15 28414754 28414754 + Missense_Mutation SNP C C A TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr15:28414754C>A c.10105G>T c.(10105-10107)Ggt>Tgt p.G3369C LUAD 15 28419689 28419689 + Silent SNP C C T TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr15:28419689C>T c.9909G>A c.(9907-9909)gtG>gtA p.V3303V LUAD 15 28420692 28420692 + Missense_Mutation SNP G G A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr15:28420692G>A c.9797C>T c.(9796-9798)gCc>gTc p.A3266V LUAD 15 28422209 28422209 + Missense_Mutation SNP C C A TCGA-75-6211-01A-11D-1753-08 TCGA-75-6211-10A-01D-1753-08 g.chr15:28422209C>A c.9319G>T c.(9319-9321)Ggg>Tgg p.G3107W LUAD 15 28422230 28422230 + Missense_Mutation SNP G G T TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr15:28422230G>T c.9298C>A c.(9298-9300)Cgt>Agt p.R3100S LUAD 15 28424087 28424087 + Missense_Mutation SNP G G A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr15:28424087G>A c.9109C>T c.(9109-9111)Cgg>Tgg p.R3037W LUAD 15 28424305 28424305 + Missense_Mutation SNP G G T TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr15:28424305G>T c.9002C>A c.(9001-9003)tCt>tAt p.S3001Y LUAD 15 28424369 28424369 + Splice_Site SNP T T C TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr15:28424369T>C c.8938A>G c.(8938-8940)Ata>Gta p.I2980V LUAD 15 28427567 28427567 + Missense_Mutation SNP C C A TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr15:28427567C>A c.8917G>T c.(8917-8919)Ggc>Tgc p.G2973C LUAD 15 28436363 28436363 + Missense_Mutation SNP C C A TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr15:28436363C>A c.8479G>T c.(8479-8481)Gat>Tat p.D2827Y LUAD 15 28437249 28437249 + Missense_Mutation SNP C C A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-11A-01D-2036-08 g.chr15:28437249C>A c.8309G>T c.(8308-8310)tGc>tTc p.C2770F LUAD 15 28441684 28441684 + Silent SNP G G A TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr15:28441684G>A c.8043C>T c.(8041-8043)gtC>gtT p.V2681V LUAD 15 28443559 28443559 + Missense_Mutation SNP C C A TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chr15:28443559C>A c.7976G>T c.(7975-7977)gGa>gTa p.G2659V LUAD 15 28443806 28443806 + Missense_Mutation SNP C C A TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr15:28443806C>A c.7826G>T c.(7825-7827)tGt>tTt p.C2609F LUAD 15 28443874 28443874 + Silent SNP C C A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr15:28443874C>A c.7758G>T c.(7756-7758)gtG>gtT p.V2586V LUAD 15 28447338 28447338 + Missense_Mutation SNP A A G TCGA-75-7025-01A-12D-1945-08 TCGA-75-7025-10A-01D-1946-08 g.chr15:28447338A>G c.7538T>C c.(7537-7539)cTc>cCc p.L2513P LUAD 15 28447502 28447502 + Missense_Mutation SNP T T C TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr15:28447502T>C c.7471A>G c.(7471-7473)Agc>Ggc p.S2491G LUAD 15 28447506 28447506 + Silent SNP T T C TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr15:28447506T>C c.7467A>G c.(7465-7467)gcA>gcG p.A2489A LUAD 15 28456198 28456198 + Missense_Mutation SNP C C G TCGA-73-4659-01A-01D-1265-08 TCGA-73-4659-11A-01D-1265-08 g.chr15:28456198C>G c.7019G>C c.(7018-7020)cGg>cCg p.R2340P LUAD 15 28457617 28457617 + Missense_Mutation SNP T T C TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr15:28457617T>C c.6899A>G c.(6898-6900)aAg>aGg p.K2300R LUAD 15 28458894 28458894 + Silent SNP C C T TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr15:28458894C>T c.6780G>A c.(6778-6780)ctG>ctA p.L2260L LUAD 15 28458898 28458898 + Missense_Mutation SNP T T A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr15:28458898T>A c.6776A>T c.(6775-6777)cAg>cTg p.Q2259L LUAD 15 28458980 28458980 + Missense_Mutation SNP T T C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr15:28458980T>C c.6694A>G c.(6694-6696)Act>Gct p.T2232A LUAD 15 28459224 28459224 + Missense_Mutation SNP C C A TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chr15:28459224C>A c.6553G>T c.(6553-6555)Ggg>Tgg p.G2185W LUAD 15 28459892 28459892 + Missense_Mutation SNP C C A TCGA-38-4629-01A-02D-1265-08 TCGA-38-4629-11A-01D-1265-08 g.chr15:28459892C>A c.6267G>T c.(6265-6267)agG>agT p.R2089S LUAD 15 28460848 28460848 + Silent SNP G G A TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr15:28460848G>A c.6129C>T c.(6127-6129)ctC>ctT p.L2043L LUAD 15 28463681 28463681 + Silent SNP G G A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr15:28463681G>A c.5982C>T c.(5980-5982)tgC>tgT p.C1994C LUAD 15 28465650 28465650 + Silent SNP C C T TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr15:28465650C>T c.5793G>A c.(5791-5793)ctG>ctA p.L1931L LUAD 15 28465739 28465739 + Nonsense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:28465739C>A c.5704G>T c.(5704-5706)Gga>Tga p.G1902* LUAD 15 28465776 28465776 + Silent SNP T T A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr15:28465776T>A c.5667A>T c.(5665-5667)ccA>ccT p.P1889P LUAD 15 28465785 28465785 + Frame_Shift_Del DEL C C - TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr15:28465785delC c.5658delG c.(5656-5658)gggfs p.G1886fs LUAD 15 28467327 28467327 + Missense_Mutation SNP A A C TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr15:28467327A>C c.5499T>G c.(5497-5499)aaT>aaG p.N1833K LUAD 15 28467330 28467330 + Missense_Mutation SNP C C A TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chr15:28467330C>A c.5496G>T c.(5494-5496)atG>atT p.M1832I LUAD 15 28473435 28473435 + Missense_Mutation SNP C C A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr15:28473435C>A c.5393G>T c.(5392-5394)gGc>gTc p.G1798V LUAD 15 28474639 28474639 + Missense_Mutation SNP C C A TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr15:28474639C>A c.5087G>T c.(5086-5088)tGg>tTg p.W1696L LUAD 15 28478365 28478365 + Silent SNP A A G TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr15:28478365A>G c.4602T>C c.(4600-4602)ttT>ttC p.F1534F LUAD 15 28482184 28482184 + Missense_Mutation SNP C C A TCGA-97-A4M0-01A-11D-A24P-08 TCGA-97-A4M0-10A-01D-A24P-08 g.chr15:28482184C>A c.3928G>T c.(3928-3930)Ggc>Tgc p.G1310C LUAD 15 28482208 28482208 + Missense_Mutation SNP G G C TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr15:28482208G>C c.3904C>G c.(3904-3906)Ctg>Gtg p.L1302V LUAD 15 28483351 28483351 + Missense_Mutation SNP C C A TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr15:28483351C>A c.3761G>T c.(3760-3762)gGg>gTg p.G1254V LUAD 15 28491134 28491134 + Missense_Mutation SNP G G C TCGA-49-4487-01A-21D-1855-08 TCGA-49-4487-11A-01D-1855-08 g.chr15:28491134G>C c.3470C>G c.(3469-3471)gCt>gGt p.A1157G LUAD 15 28493761 28493761 + Nonsense_Mutation SNP G G A TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr15:28493761G>A c.3172C>T c.(3172-3174)Caa>Taa p.Q1058* LUAD 15 28493784 28493784 + Missense_Mutation SNP G G A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr15:28493784G>A c.3149C>T c.(3148-3150)tCa>tTa p.S1050L LUAD 15 28493803 28493803 + Missense_Mutation SNP T T A TCGA-55-8097-01A-11D-2238-08 TCGA-55-8097-10A-01D-2238-08 g.chr15:28493803T>A c.3130A>T c.(3130-3132)Agt>Tgt p.S1044C LUAD 15 28499514 28499514 + Missense_Mutation SNP G G C TCGA-55-A48Y-01A-11D-A24D-08 TCGA-55-A48Y-10A-01D-A24F-08 g.chr15:28499514G>C c.3022C>G c.(3022-3024)Ctg>Gtg p.L1008V LUAD 15 28501138 28501138 + Silent SNP T T A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr15:28501138T>A c.2751A>T c.(2749-2751)tcA>tcT p.S917S LUAD 15 28501352 28501352 + Missense_Mutation SNP C C T TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr15:28501352C>T c.2629G>A c.(2629-2631)Ggc>Agc p.G877S LUAD 15 28502359 28502359 + Missense_Mutation SNP G G A TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr15:28502359G>A c.2365C>T c.(2365-2367)Cct>Tct p.P789S LUAD 15 28508179 28508179 + Silent SNP G G A TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr15:28508179G>A c.2007C>T c.(2005-2007)tcC>tcT p.S669S LUAD 15 28508211 28508211 + Missense_Mutation SNP C C G TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr15:28508211C>G c.1975G>C c.(1975-1977)Gtg>Ctg p.V659L LUAD 15 28510962 28510962 + Splice_Site SNP C C T TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr15:28510962C>T c.e13+1 LUAD 15 28510997 28510997 + Silent SNP G G A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:28510997G>A c.1722C>T c.(1720-1722)acC>acT p.T574T LUAD 15 28511033 28511033 + Silent SNP G G A TCGA-95-7944-01A-11D-2184-08 TCGA-95-7944-10A-01D-2184-08 g.chr15:28511033G>A c.1686C>T c.(1684-1686)taC>taT p.Y562Y LUAD 15 28511043 28511043 + Missense_Mutation SNP C C T TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr15:28511043C>T c.1676G>A c.(1675-1677)gGg>gAg p.G559E LUAD 15 28513632 28513632 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr15:28513632C>A c.1577G>T c.(1576-1578)cGg>cTg p.R526L LUAD 15 28513742 28513742 + Silent SNP G G T TCGA-97-8174-01A-11D-2284-08 TCGA-97-8174-10A-01D-2284-08 g.chr15:28513742G>T c.1467C>A c.(1465-1467)ggC>ggA p.G489G LUAD 15 28514451 28514451 + Silent SNP G G A TCGA-97-A4M7-01A-11D-A24P-08 TCGA-97-A4M7-10A-01D-A24P-08 g.chr15:28514451G>A c.1389C>T c.(1387-1389)ttC>ttT p.F463F LUAD 15 28515907 28515907 + Missense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr15:28515907C>A c.1191G>T c.(1189-1191)atG>atT p.M397I LUAD 15 28517458 28517458 + Missense_Mutation SNP G G C TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr15:28517458G>C c.986C>G c.(985-987)tCc>tGc p.S329C LUAD 15 28520107 28520107 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr15:28520107C>A c.587G>T c.(586-588)gGa>gTa p.G196V LUAD 15 28538048 28538048 + Missense_Mutation SNP C C A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr15:28538048C>A c.308G>T c.(307-309)tGg>tTg p.W103L LUAD 15 28538091 28538091 + Missense_Mutation SNP C C A TCGA-55-8203-01A-11D-2238-08 TCGA-55-8203-10A-01D-2238-08 g.chr15:28538091C>A c.265G>T c.(265-267)Gca>Tca p.A89S LUAD 15 28544618 28544618 + Missense_Mutation SNP C C A TCGA-17-Z056-01A-01W-0747-08 TCGA-17-Z056-11A-01W-0747-08 g.chr15:28544618C>A c.117G>T c.(115-117)atG>atT p.M39I LUSC 15 28357016 28357016 + Missense_Mutation SNP C C T TCGA-22-4593-01A-21D-1817-08 TCGA-22-4593-11A-01D-1817-08 g.chr15:28357016C>T c.14398G>A c.(14398-14400)Gca>Aca p.A4800T LUSC 15 28358790 28358790 + Missense_Mutation SNP G G A TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr15:28358790G>A c.13948C>T c.(13948-13950)Cgg>Tgg p.R4650W LUSC 15 28370265 28370265 + Silent SNP G G T TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr15:28370265G>T c.12877C>A c.(12877-12879)Cgg>Agg p.R4293R LUSC 15 28377918 28377918 + Missense_Mutation SNP C C T TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chr15:28377918C>T c.12289G>A c.(12289-12291)Gct>Act p.A4097T LUSC 15 28380782 28380782 + Silent SNP C C T TCGA-70-6723-01A-11D-1817-08 TCGA-70-6723-10A-01D-1817-08 g.chr15:28380782C>T c.12072G>A c.(12070-12072)tcG>tcA p.S4024S LUSC 15 28386602 28386602 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:28386602G>A c.11991C>T c.(11989-11991)ctC>ctT p.L3997L LUSC 15 28386674 28386674 + Silent SNP G G C TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr15:28386674G>C c.11919C>G c.(11917-11919)gtC>gtG p.V3973V LUSC 15 28389936 28389936 + Missense_Mutation SNP C C G TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr15:28389936C>G c.11023G>C c.(11023-11025)Gac>Cac p.D3675H LUSC 15 28391399 28391399 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:28391399G>A c.10992C>T c.(10990-10992)atC>atT p.I3664I LUSC 15 28391416 28391416 + Missense_Mutation SNP C C T TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr15:28391416C>T c.10975G>A c.(10975-10977)Gac>Aac p.D3659N LUSC 15 28413656 28413656 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:28413656G>A c.10310C>T c.(10309-10311)tCc>tTc p.S3437F LUSC 15 28419575 28419575 + Missense_Mutation SNP C C G TCGA-56-6545-01A-11D-1817-08 TCGA-56-6545-10A-01D-1817-08 g.chr15:28419575C>G c.10023G>C c.(10021-10023)caG>caC p.Q3341H LUSC 15 28419668 28419668 + Missense_Mutation SNP C C G TCGA-60-2720-01A-01D-1522-08 TCGA-60-2720-11A-01D-1522-08 g.chr15:28419668C>G c.9930G>C c.(9928-9930)aaG>aaC p.K3310N LUSC 15 28421627 28421627 + Missense_Mutation SNP C C A TCGA-60-2711-01A-01D-1522-08 TCGA-60-2711-11A-01D-1522-08 g.chr15:28421627C>A c.9633G>T c.(9631-9633)gaG>gaT p.E3211D LUSC 15 28436333 28436333 + Missense_Mutation SNP C C A TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr15:28436333C>A c.8509G>T c.(8509-8511)Gta>Tta p.V2837L LUSC 15 28456229 28456229 + Missense_Mutation SNP G G A TCGA-39-5021-01A-01D-1441-08 TCGA-39-5021-11A-01D-1441-08 g.chr15:28456229G>A c.6988C>T c.(6988-6990)Cgg>Tgg p.R2330W LUSC 15 28459024 28459024 + Missense_Mutation SNP A A T TCGA-56-1622-01A-01D-1521-08 TCGA-56-1622-11A-01D-1521-08 g.chr15:28459024A>T c.6650T>A c.(6649-6651)cTg>cAg p.L2217Q LUSC 15 28460816 28460816 + Missense_Mutation SNP T T G TCGA-18-4086-01A-01D-1352-08 TCGA-18-4086-11A-01D-1352-08 g.chr15:28460816T>G c.6161A>C c.(6160-6162)aAg>aCg p.K2054T LUSC 15 28460911 28460911 + Silent SNP C C G TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr15:28460911C>G c.6066G>C c.(6064-6066)cgG>cgC p.R2022R LUSC 15 28465667 28465667 + Missense_Mutation SNP G G A TCGA-34-5927-01A-11D-1817-08 TCGA-34-5927-10A-01D-1817-08 g.chr15:28465667G>A c.5776C>T c.(5776-5778)Ctc>Ttc p.L1926F LUSC 15 28478864 28478864 + Missense_Mutation SNP C C A TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr15:28478864C>A c.4297G>T c.(4297-4299)Gtg>Ttg p.V1433L LUSC 15 28483881 28483881 + Silent SNP C C T TCGA-39-5037-01A-01D-1441-08 TCGA-39-5037-11A-01D-1441-08 g.chr15:28483881C>T c.3615G>A c.(3613-3615)gaG>gaA p.E1205E LUSC 15 28491051 28491051 + Missense_Mutation SNP C C T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr15:28491051C>T c.3553G>A c.(3553-3555)Gag>Aag p.E1185K LUSC 15 28491925 28491925 + Silent SNP G G A TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr15:28491925G>A c.3354C>T c.(3352-3354)ttC>ttT p.F1118F LUSC 15 28492038 28492038 + Missense_Mutation SNP C C G TCGA-34-5234-01A-01D-1632-08 TCGA-34-5234-10A-01D-1632-08 g.chr15:28492038C>G c.3241G>C c.(3241-3243)Gag>Cag p.E1081Q LUSC 15 28493709 28493709 + Nonsense_Mutation SNP G G C TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr15:28493709G>C c.3224C>G c.(3223-3225)tCa>tGa p.S1075* LUSC 15 28501024 28501025 + Missense_Mutation DNP CT CT TC TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr15:28501024_28501025CT>TC c.2864_2865AG>GA c.(2863-2865)gAG>gGA p.E955G LUSC 15 28502333 28502333 + Missense_Mutation SNP C C T TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr15:28502333C>T c.2391G>A c.(2389-2391)atG>atA p.M797I LUSC 15 28506002 28506002 + Missense_Mutation SNP C C A TCGA-18-5592-01A-01D-1632-08 TCGA-18-5592-11A-11D-1632-08 g.chr15:28506002C>A c.2237G>T c.(2236-2238)cGc>cTc p.R746L LUSC 15 28508279 28508279 + Missense_Mutation SNP T T A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:28508279T>A c.1907A>T c.(1906-1908)aAa>aTa p.K636I LUSC 15 28513702 28513702 + Missense_Mutation SNP C C T TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr15:28513702C>T c.1507G>A c.(1507-1509)Gat>Aat p.D503N LUSC 15 28518105 28518105 + Silent SNP G G T TCGA-60-2707-01A-01D-1522-08 TCGA-60-2707-11A-01D-1522-08 g.chr15:28518105G>T c.846C>A c.(844-846)ccC>ccA p.P282P LUSC 15 28520140 28520140 + Missense_Mutation SNP G G A TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr15:28520140G>A c.554C>T c.(553-555)gCg>gTg p.A185V LUSC 15 28544607 28544608 + Missense_Mutation DNP CC CC AT TCGA-33-4533-01A-01D-1267-08 TCGA-33-4533-11A-01D-1267-08 g.chr15:28544607_28544608CC>AT c.127_128GG>AT c.(127-129)GGa>ATa p.G43I OV 15 28408371 28408371 + Missense_Mutation SNP T T A TCGA-61-1736-01B-01W-0722-08 TCGA-61-1736-11A-01W-0722-08 g.chr15:28408371T>A c.10615A>T c.(10615-10617)Agt>Tgt p.S3539C OV 15 28414686 28414686 + Silent SNP C C A TCGA-20-1685-01A-01W-0633-09 TCGA-20-1685-10A-01W-0633-09 g.chr15:28414686C>A c.10173G>T c.(10171-10173)ctG>ctT p.L3391L OV 15 28437274 28437274 + Missense_Mutation SNP G G C TCGA-13-0800-01A-01W-0372-09 TCGA-13-0800-10A-01W-0372-09 g.chr15:28437274G>C c.8284C>G c.(8284-8286)Cgt>Ggt p.R2762G OV 15 28459291 28459291 + Silent SNP G G A TCGA-24-1469-01A-01W-0553-09 TCGA-24-1469-10A-01W-0553-09 g.chr15:28459291G>A c.6486C>T c.(6484-6486)ctC>ctT p.L2162L OV 15 28474390 28474390 + Silent SNP C C T TCGA-29-2429-01A-01D-1526-09 TCGA-29-2429-10A-01D-1526-09 g.chr15:28474390C>T c.5223G>A c.(5221-5223)caG>caA p.Q1741Q OV 15 28508281 28508281 + Silent SNP C C G TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr15:28508281C>G c.1905G>C c.(1903-1905)ggG>ggC p.G635G OV 15 28511071 28511071 + Missense_Mutation SNP C C T TCGA-24-0966-01A-01W-0977-09 TCGA-24-0966-10A-01W-0421-09 g.chr15:28511071C>T c.1648G>A c.(1648-1650)Ggg>Agg p.G550R PAAD 15 28357165 28357165 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28357165T>C c.14249A>G c.(14248-14250)aAc>aGc p.N4750S PAAD 15 28358303 28358303 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28358303G>A c.14146C>T c.(14146-14148)Cgc>Tgc p.R4716C PAAD 15 28358723 28358723 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28358723G>A c.14015C>T c.(14014-14016)aCg>aTg p.T4672M PAAD 15 28360609 28360609 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28360609G>T c.13688C>A c.(13687-13689)gCt>gAt p.A4563D PAAD 15 28370319 28370319 + Missense_Mutation SNP C C A TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr15:28370319C>A c.12823G>T c.(12823-12825)Gac>Tac p.D4275Y PAAD 15 28370319 28370319 + Missense_Mutation SNP C C T TCGA-2J-AABV-01A-12D-A40W-08 TCGA-2J-AABV-10A-01D-A40W-08 g.chr15:28370319C>T c.12823G>A c.(12823-12825)Gac>Aac p.D4275N PAAD 15 28375699 28375699 + Silent SNP G G A TCGA-3A-A9IH-01A-12D-A397-08 TCGA-3A-A9IH-10A-01D-A39A-08 g.chr15:28375699G>A c.12612C>T c.(12610-12612)tgC>tgT p.C4204C PAAD 15 28377840 28377840 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28377840G>T c.12367C>A c.(12367-12369)Ctg>Atg p.L4123M PAAD 15 28377973 28377973 + Silent SNP C C T TCGA-Q3-A5QY-01A-12D-A32N-08 TCGA-Q3-A5QY-10A-01D-A32N-08 g.chr15:28377973C>T c.12234G>A c.(12232-12234)ccG>ccA p.P4078P PAAD 15 28389261 28389261 + Missense_Mutation SNP G G A TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr15:28389261G>A c.11261C>T c.(11260-11262)gCg>gTg p.A3754V PAAD 15 28391388 28391388 + Missense_Mutation SNP C C T TCGA-IB-AAUP-01A-11D-A377-08 TCGA-IB-AAUP-10A-01D-A37A-08 g.chr15:28391388C>T c.11003G>A c.(11002-11004)cGg>cAg p.R3668Q PAAD 15 28413705 28413705 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28413705C>T c.10261G>A c.(10261-10263)Gcc>Acc p.A3421T PAAD 15 28446601 28446601 + Splice_Site SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28446601C>T c.e48+1 PAAD 15 28463640 28463640 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28463640T>G c.6023A>C c.(6022-6024)aAg>aCg p.K2008T PAAD 15 28473421 28473421 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28473421C>T c.5407G>A c.(5407-5409)Gac>Aac p.D1803N PAAD 15 28478313 28478313 + Silent SNP G G T TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr15:28478313G>T c.4654C>A c.(4654-4656)Cga>Aga p.R1552R PAAD 15 28510844 28510844 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28510844A>G c.1790T>C c.(1789-1791)gTa>gCa p.V597A PAAD 15 28510973 28510973 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28510973C>T c.1746G>A c.(1744-1746)cgG>cgA p.R582R PAAD 15 28514426 28514426 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:28514426C>T c.1414G>A c.(1414-1416)Gtg>Atg p.V472M PAAD 15 28515875 28515876 + Frame_Shift_Ins INS - - TC TCGA-F2-7273-01A-11D-2154-08 TCGA-F2-7273-10A-01D-2154-08 g.chr15:28515875_28515876insTC c.1222_1223insGA c.(1222-1224)atgfs p.M408fs PAAD 15 28515875 28515876 + Frame_Shift_Ins INS - - TC TCGA-FZ-5920-01A-11D-1609-08 TCGA-FZ-5920-11A-01D-1609-08 g.chr15:28515875_28515876insTC c.1222_1223insGA c.(1222-1224)atgfs p.M408fs PAAD 15 28515989 28515989 + Missense_Mutation SNP T T C TCGA-XN-A8T5-01A-12D-A36O-08 TCGA-XN-A8T5-10A-01D-A367-08 g.chr15:28515989T>C c.1109A>G c.(1108-1110)aAt>aGt p.N370S PAAD 15 28517442 28517442 + Silent SNP G G A TCGA-IB-AAUU-01A-11D-A377-08 TCGA-IB-AAUU-10A-01D-A37A-08 g.chr15:28517442G>A c.1002C>T c.(1000-1002)agC>agT p.S334S PAAD 15 28518096 28518096 + Missense_Mutation SNP G G C TCGA-IB-AAUM-01A-11D-A377-08 TCGA-IB-AAUM-10A-01D-A37A-08 g.chr15:28518096G>C c.855C>G c.(853-855)gaC>gaG p.D285E PRAD 15 28359926 28359926 + Missense_Mutation SNP C C T TCGA-FC-A5OB-01A-11D-A29Q-08 TCGA-FC-A5OB-10A-01D-A29Q-08 g.chr15:28359926C>T c.13745G>A c.(13744-13746)gGa>gAa p.G4582E PRAD 15 28369237 28369237 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28369237G>A c.13134C>T c.(13132-13134)ctC>ctT p.L4378L PRAD 15 28386775 28386775 + Splice_Site SNP G G A TCGA-G9-6348-01A-11D-1786-08 TCGA-G9-6348-10A-01D-1786-08 g.chr15:28386775G>A c.11818C>T c.(11818-11820)Cga>Tga p.R3940* PRAD 15 28386876 28386876 + Splice_Site SNP C C A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr15:28386876C>A c.e77+1 PRAD 15 28387490 28387490 + Frame_Shift_Del DEL C C - TCGA-CH-5750-01A-11D-1576-08 TCGA-CH-5750-10A-01D-1576-08 g.chr15:28387490delC c.11594delG c.(11593-11595)tgtfs p.C3865fs PRAD 15 28414705 28414705 + Missense_Mutation SNP A A G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28414705A>G c.10154T>C c.(10153-10155)tTg>tCg p.L3385S PRAD 15 28437220 28437220 + Missense_Mutation SNP C C A TCGA-XQ-A8TA-01A-11D-A364-08 TCGA-XQ-A8TA-10A-01D-A362-08 g.chr15:28437220C>A c.8338G>T c.(8338-8340)Gac>Tac p.D2780Y PRAD 15 28437221 28437221 + Silent SNP C C A TCGA-XQ-A8TA-01A-11D-A364-08 TCGA-XQ-A8TA-10A-01D-A362-08 g.chr15:28437221C>A c.8337G>T c.(8335-8337)ctG>ctT p.L2779L PRAD 15 28463646 28463646 + Missense_Mutation SNP G G A TCGA-V1-A9O7-01A-21D-A41K-08 TCGA-V1-A9O7-10A-01D-A41N-08 g.chr15:28463646G>A c.6017C>T c.(6016-6018)aCg>aTg p.T2006M PRAD 15 28463681 28463681 + Silent SNP G G A TCGA-2A-AAYF-01A-11D-A41K-08 TCGA-2A-AAYF-10A-01D-A41N-08 g.chr15:28463681G>A c.5982C>T c.(5980-5982)tgC>tgT p.C1994C PRAD 15 28473394 28473394 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28473394C>T c.5434G>A c.(5434-5436)Gcc>Acc p.A1812T PRAD 15 28483299 28483299 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28483299C>T c.3813G>A c.(3811-3813)cgG>cgA p.R1271R PRAD 15 28483803 28483803 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28483803C>T c.3693G>A c.(3691-3693)aaG>aaA p.K1231K PRAD 15 28501363 28501363 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28501363G>A c.2618C>T c.(2617-2619)gCc>gTc p.A873V PRAD 15 28502369 28502369 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28502369G>A c.2355C>T c.(2353-2355)ggC>ggT p.G785G PRAD 15 28510859 28510859 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28510859G>A c.1775C>T c.(1774-1776)gCc>gTc p.A592V PRAD 15 28538078 28538078 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:28538078C>A c.278G>T c.(277-279)aGg>aTg p.R93M READ 15 28375399 28375400 + Nonsense_Mutation DNP GA GA AG TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28375399_28375400GA>AG c.12711_12712TC>CT c.(12709-12714)gtTCga>gtCTga p.R4238* READ 15 28420712 28420712 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28420712G>A c.9777C>T c.(9775-9777)atC>atT p.I3259I READ 15 28422162 28422162 + Silent SNP G G A TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr15:28422162G>A c.9366C>T c.(9364-9366)acC>acT p.T3122T READ 15 28459027 28459027 + Missense_Mutation SNP C C T TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr15:28459027C>T c.6647G>A c.(6646-6648)cGc>cAc p.R2216H READ 15 28460812 28460812 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28460812G>A c.6165C>T c.(6163-6165)gtC>gtT p.V2055V READ 15 28463812 28463812 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28463812C>T c.5851G>A c.(5851-5853)Gaa>Aaa p.E1951K READ 15 28467179 28467179 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28467179C>T c.5647G>A c.(5647-5649)Gat>Aat p.D1883N READ 15 28492013 28492013 + Missense_Mutation SNP A A T TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chr15:28492013A>T c.3266T>A c.(3265-3267)cTg>cAg p.L1089Q READ 15 28514407 28514407 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:28514407T>G c.1433A>C c.(1432-1434)aAt>aCt p.N478T READ 15 28514475 28514475 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:28514475C>T c.1365G>A c.(1363-1365)caG>caA p.Q455Q SARC 15 28359945 28359945 + Missense_Mutation SNP C C T TCGA-DX-A6BK-01A-11D-A307-09 TCGA-DX-A6BK-10A-01D-A307-09 g.chr15:28359945C>T c.13726G>A c.(13726-13728)Gat>Aat p.D4576N SARC 15 28380807 28380807 + Missense_Mutation SNP C C T TCGA-FX-A3RE-01A-11D-A228-09 TCGA-FX-A3RE-10A-01D-A22A-09 g.chr15:28380807C>T c.12047G>A c.(12046-12048)aGa>aAa p.R4016K SARC 15 28380835 28380835 + Missense_Mutation SNP A A C TCGA-DX-A1KZ-01A-11D-A24N-09 TCGA-DX-A1KZ-10A-01D-A24N-09 g.chr15:28380835A>C c.12019T>G c.(12019-12021)Tat>Gat p.Y4007D SARC 15 28421691 28421691 + Missense_Mutation SNP C C G TCGA-DX-A6B8-01A-11D-A307-09 TCGA-DX-A6B8-10A-01D-A307-09 g.chr15:28421691C>G c.9569G>C c.(9568-9570)aGt>aCt p.S3190T SARC 15 28474893 28474893 + Missense_Mutation SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr15:28474893C>T c.4910G>A c.(4909-4911)aGt>aAt p.S1637N SARC 15 28478362 28478362 + Silent SNP T T C TCGA-DX-A1KZ-01A-11D-A24N-09 TCGA-DX-A1KZ-10A-01D-A24N-09 g.chr15:28478362T>C c.4605A>G c.(4603-4605)aaA>aaG p.K1535K SARC 15 28501459 28501459 + Missense_Mutation SNP T T G TCGA-IE-A4EI-01A-11D-A24N-09 TCGA-IE-A4EI-10A-01D-A24N-09 g.chr15:28501459T>G c.2522A>C c.(2521-2523)cAt>cCt p.H841P SKCM 15 28358283 28358283 + Silent SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr15:28358283G>A c.14166C>T c.(14164-14166)ttC>ttT p.F4722F SKCM 15 28358292 28358292 + Silent SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr15:28358292G>A c.14157C>T c.(14155-14157)ttC>ttT p.F4719F SKCM 15 28358367 28358367 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr15:28358367G>A c.14082C>T c.(14080-14082)atC>atT p.I4694I SKCM 15 28358776 28358776 + Silent SNP G G A TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr15:28358776G>A c.13962C>T c.(13960-13962)gcC>gcT p.A4654A SKCM 15 28362215 28362215 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28362215G>A c.13358C>T c.(13357-13359)tCg>tTg p.S4453L SKCM 15 28362298 28362298 + Silent SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:28362298G>A c.13275C>T c.(13273-13275)gtC>gtT p.V4425V SKCM 15 28366576 28366576 + Splice_Site SNP C C T TCGA-FS-A1ZD-06A-11D-A197-08 TCGA-FS-A1ZD-10A-01D-A199-08 g.chr15:28366576C>T c.e86-1 SKCM 15 28369256 28369256 + Missense_Mutation SNP G G A TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr15:28369256G>A c.13115C>T c.(13114-13116)tCg>tTg p.S4372L SKCM 15 28370267 28370267 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr15:28370267G>A c.12875C>T c.(12874-12876)cCt>cTt p.P4292L SKCM 15 28375694 28375694 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:28375694G>A c.12617C>T c.(12616-12618)tCc>tTc p.S4206F SKCM 15 28377941 28377941 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:28377941C>T c.12266G>A c.(12265-12267)aGa>aAa p.R4089K SKCM 15 28377943 28377943 + Silent SNP C C A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:28377943C>A c.12264G>T c.(12262-12264)ctG>ctT p.L4088L SKCM 15 28386694 28386694 + Missense_Mutation SNP C C G TCGA-EE-A2M7-06A-11D-A197-08 TCGA-EE-A2M7-10A-01D-A199-08 g.chr15:28386694C>G c.11899G>C c.(11899-11901)Ggc>Cgc p.G3967R SKCM 15 28386959 28386959 + Missense_Mutation SNP T T G TCGA-D9-A149-06A-11D-A196-08 TCGA-D9-A149-10A-01D-A198-08 g.chr15:28386959T>G c.11734A>C c.(11734-11736)Agc>Cgc p.S3912R SKCM 15 28389360 28389360 + Missense_Mutation SNP T T C TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr15:28389360T>C c.11162A>G c.(11161-11163)gAc>gGc p.D3721G SKCM 15 28391446 28391446 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr15:28391446C>T c.10945G>A c.(10945-10947)Gag>Aag p.E3649K SKCM 15 28408265 28408265 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr15:28408265G>A c.10721C>T c.(10720-10722)tCc>tTc p.S3574F SKCM 15 28408299 28408299 + Missense_Mutation SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr15:28408299C>T c.10687G>A c.(10687-10689)Gac>Aac p.D3563N SKCM 15 28408300 28408300 + Silent SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr15:28408300C>T c.10686G>A c.(10684-10686)ggG>ggA p.G3562G SKCM 15 28412933 28412933 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:28412933G>A c.10454C>T c.(10453-10455)aCt>aTt p.T3485I SKCM 15 28412966 28412966 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr15:28412966G>A c.10421C>T c.(10420-10422)tCc>tTc p.S3474F SKCM 15 28413670 28413670 + Silent SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr15:28413670G>A c.10296C>T c.(10294-10296)tcC>tcT p.S3432S SKCM 15 28414666 28414666 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr15:28414666G>A c.10193C>T c.(10192-10194)tCa>tTa p.S3398L SKCM 15 28419645 28419645 + Missense_Mutation SNP G G A TCGA-D3-A1Q5-06A-11D-A196-08 TCGA-D3-A1Q5-10A-01D-A198-08 g.chr15:28419645G>A c.9953C>T c.(9952-9954)tCg>tTg p.S3318L SKCM 15 28419673 28419673 + Nonsense_Mutation SNP G G A TCGA-EE-A3AH-06A-11D-A196-08 TCGA-EE-A3AH-10A-01D-A198-08 g.chr15:28419673G>A c.9925C>T c.(9925-9927)Cag>Tag p.Q3309* SKCM 15 28419674 28419674 + Silent SNP G G A TCGA-EE-A3AH-06A-11D-A196-08 TCGA-EE-A3AH-10A-01D-A198-08 g.chr15:28419674G>A c.9924C>T c.(9922-9924)ggC>ggT p.G3308G SKCM 15 28420712 28420712 + Silent SNP G G A TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr15:28420712G>A c.9777C>T c.(9775-9777)atC>atT p.I3259I SKCM 15 28420712 28420712 + Silent SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:28420712G>A c.9777C>T c.(9775-9777)atC>atT p.I3259I SKCM 15 28421699 28421699 + Silent SNP C C T TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr15:28421699C>T c.9561G>A c.(9559-9561)cgG>cgA p.R3187R SKCM 15 28422225 28422225 + Silent SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr15:28422225G>A c.9303C>T c.(9301-9303)atC>atT p.I3101I SKCM 15 28422610 28422610 + Missense_Mutation SNP G G A TCGA-D3-A2JP-06A-11D-A19A-08 TCGA-D3-A2JP-10A-01D-A19A-08 g.chr15:28422610G>A c.9209C>T c.(9208-9210)tCg>tTg p.S3070L SKCM 15 28424160 28424160 + Silent SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr15:28424160C>T c.9036G>A c.(9034-9036)aaG>aaA p.K3012K SKCM 15 28424362 28424362 + Missense_Mutation SNP A A G TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr15:28424362A>G c.8945T>C c.(8944-8946)gTt>gCt p.V2982A SKCM 15 28436193 28436193 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28436193G>A c.8567C>T c.(8566-8568)tCc>tTc p.S2856F SKCM 15 28436193 28436193 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr15:28436193G>A c.8567C>T c.(8566-8568)tCc>tTc p.S2856F SKCM 15 28436199 28436199 + Missense_Mutation SNP C C G TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr15:28436199C>G c.8561G>C c.(8560-8562)gGa>gCa p.G2854A SKCM 15 28441679 28441679 + Missense_Mutation SNP A A T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28441679A>T c.8048T>A c.(8047-8049)tTt>tAt p.F2683Y SKCM 15 28443628 28443628 + Missense_Mutation SNP G G A TCGA-EE-A2A1-06A-11D-A197-08 TCGA-EE-A2A1-10A-01D-A199-08 g.chr15:28443628G>A c.7907C>T c.(7906-7908)tCt>tTt p.S2636F SKCM 15 28443892 28443892 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:28443892G>A c.7740C>T c.(7738-7740)tgC>tgT p.C2580C SKCM 15 28447305 28447305 + Missense_Mutation SNP G G A TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr15:28447305G>A c.7571C>T c.(7570-7572)tCt>tTt p.S2524F SKCM 15 28447509 28447509 + Missense_Mutation SNP A A T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr15:28447509A>T c.7464T>A c.(7462-7464)aaT>aaA p.N2488K SKCM 15 28457652 28457652 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr15:28457652G>A c.6864C>T c.(6862-6864)aaC>aaT p.N2288N SKCM 15 28458946 28458946 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:28458946G>A c.6728C>T c.(6727-6729)aCc>aTc p.T2243I SKCM 15 28465727 28465727 + Missense_Mutation SNP C C A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:28465727C>A c.5716G>T c.(5716-5718)Gtc>Ttc p.V1906F SKCM 15 28465784 28465784 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28465784G>A c.5659C>T c.(5659-5661)Cct>Tct p.P1887S SKCM 15 28467325 28467325 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28467325G>A c.5501C>T c.(5500-5502)gCt>gTt p.A1834V SKCM 15 28473473 28473473 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr15:28473473G>A c.5355C>T c.(5353-5355)ttC>ttT p.F1785F SKCM 15 28474625 28474625 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28474625G>A c.5101C>T c.(5101-5103)Cct>Tct p.P1701S SKCM 15 28474839 28474839 + Missense_Mutation SNP C C T TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr15:28474839C>T c.4964G>A c.(4963-4965)aGa>aAa p.R1655K SKCM 15 28478684 28478684 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28478684G>A c.4375C>T c.(4375-4377)Cat>Tat p.H1459Y SKCM 15 28478849 28478849 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28478849G>A c.4312C>T c.(4312-4314)Cgc>Tgc p.R1438C SKCM 15 28478878 28478878 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr15:28478878G>A c.4283C>T c.(4282-4284)cCc>cTc p.P1428L SKCM 15 28482110 28482110 + Splice_Site SNP G G A TCGA-D3-A1Q9-06A-11D-A19A-08 TCGA-D3-A1Q9-10A-01D-A19A-08 g.chr15:28482110G>A c.4002C>T c.(4000-4002)gcC>gcT p.A1334A SKCM 15 28491205 28491205 + Silent SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr15:28491205G>A c.3399C>T c.(3397-3399)ctC>ctT p.L1133L SKCM 15 28491994 28491994 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr15:28491994G>A c.3285C>T c.(3283-3285)ctC>ctT p.L1095L SKCM 15 28501248 28501248 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr15:28501248G>A c.2733C>T c.(2731-2733)ctC>ctT p.L911L SKCM 15 28501425 28501425 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28501425G>A c.2556C>T c.(2554-2556)ttC>ttT p.F852F SKCM 15 28502252 28502252 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr15:28502252C>T c.2472G>A c.(2470-2472)gaG>gaA p.E824E SKCM 15 28502277 28502277 + Missense_Mutation SNP G G A TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr15:28502277G>A c.2447C>T c.(2446-2448)tCc>tTc p.S816F SKCM 15 28502305 28502305 + Missense_Mutation SNP G G A TCGA-EE-A3AD-06A-11D-A196-08 TCGA-EE-A3AD-10A-01D-A198-08 g.chr15:28502305G>A c.2419C>T c.(2419-2421)Cgg>Tgg p.R807W SKCM 15 28502311 28502311 + Silent SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:28502311G>A c.2413C>T c.(2413-2415)Ctg>Ttg p.L805L SKCM 15 28502359 28502359 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr15:28502359G>A c.2365C>T c.(2365-2367)Cct>Tct p.P789S SKCM 15 28515964 28515964 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr15:28515964G>A c.1134C>T c.(1132-1134)acC>acT p.T378T SKCM 15 28519439 28519439 + Silent SNP C C T TCGA-FS-A1YY-06A-11D-A197-08 TCGA-FS-A1YY-10A-01D-A199-08 g.chr15:28519439C>T c.798G>A c.(796-798)acG>acA p.T266T SKCM 15 28519449 28519449 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:28519449G>A c.788C>T c.(787-789)tCc>tTc p.S263F SKCM 15 28519457 28519457 + Silent SNP G G A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr15:28519457G>A c.780C>T c.(778-780)ttC>ttT p.F260F SKCM 15 28519529 28519529 + Silent SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr15:28519529G>A c.708C>T c.(706-708)ccC>ccT p.P236P SKCM 15 28525345 28525345 + Silent SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr15:28525345G>A c.411C>T c.(409-411)gcC>gcT p.A137A SKCM 15 28538062 28538062 + Silent SNP C C A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr15:28538062C>A c.294G>T c.(292-294)ctG>ctT p.L98L SKCM 15 28538093 28538093 + Missense_Mutation SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr15:28538093G>A c.263C>T c.(262-264)cCt>cTt p.P88L SKCM 15 28544556 28544556 + Missense_Mutation SNP G G A TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr15:28544556G>A c.179C>T c.(178-180)cCt>cTt p.P60L

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 15 28386936 28386936 single base substitution A G exon_variant ALL-US 15 28386936 28386936 single base substitution A G synonymous_variant H3919H 11757T>C BLCA-CN 15 28357059 28357059 single base substitution G A downstream_gene_variant BLCA-CN 15 28357059 28357059 single base substitution G A exon_variant BLCA-CN 15 28357059 28357059 single base substitution G A synonymous_variant I4785I 14355C>T BLCA-CN 15 28360581 28360581 single base substitution G A exon_variant BLCA-CN 15 28360581 28360581 single base substitution G A synonymous_variant L4572L 13716C>T BLCA-CN 15 28360581 28360581 single base substitution G A upstream_gene_variant BLCA-CN 15 28482208 28482208 single base substitution G C missense_variant L1302V 3904C>G BLCA-US 15 28375401 28375401 single base substitution A G missense_variant V4237A 12710T>C BLCA-US 15 28377404 28377404 single base substitution C G missense_variant E4138Q 12412G>C BLCA-US 15 28408392 28408392 single base substitution G A intron_variant BLCA-US 15 28408392 28408392 single base substitution G A stop_gained Q3532* 10594C>T BLCA-US 15 28437183 28437183 single base substitution G A exon_variant BLCA-US 15 28437183 28437183 single base substitution G A missense_variant S2792L 8375C>T BLCA-US 15 28456214 28456214 single base substitution G T missense_variant H2335N 7003C>A BLCA-US 15 28456242 28456242 single base substitution G A synonymous_variant I2325I 6975C>T BLCA-US 15 28458889 28458889 single base substitution G A missense_variant P2262L 6785C>T BLCA-US 15 28460863 28460863 single base substitution C T synonymous_variant Q2038Q 6114G>A BLCA-US 15 28467317 28467317 single base substitution G C exon_variant BLCA-US 15 28467317 28467317 single base substitution G C missense_variant Q1837E 5509C>G BLCA-US 15 28467360 28467360 single base substitution G A splice_region_variant BLCA-US 15 28511100 28511100 insertion of <=200bp - C 3_prime_UTR_variant BLCA-US 15 28511100 28511100 insertion of <=200bp - C frameshift_variant V540V? BOCA-FR 15 28520137 28520137 single base substitution C T 3_prime_UTR_variant BOCA-FR 15 28520137 28520137 single base substitution C T missense_variant G186D 557G>A BOCA-FR 15 28520137 28520137 single base substitution C T upstream_gene_variant BOCA-UK 15 28408317 28408317 single base substitution C T intron_variant BOCA-UK 15 28408317 28408317 single base substitution C T missense_variant V3557M 10669G>A BRCA-EU 15 28353131 28353131 single base substitution A T downstream_gene_variant BRCA-EU 15 28353197 28353197 single base substitution G A downstream_gene_variant BRCA-EU 15 28353755 28353755 single base substitution G A downstream_gene_variant BRCA-EU 15 28354942 28354942 single base substitution G A downstream_gene_variant BRCA-EU 15 28355587 28355587 single base substitution A G downstream_gene_variant BRCA-EU 15 28357375 28357375 single base substitution C T downstream_gene_variant BRCA-EU 15 28357375 28357375 single base substitution C T intron_variant BRCA-EU 15 28357411 28357411 single base substitution G A downstream_gene_variant BRCA-EU 15 28357411 28357411 single base substitution G A intron_variant BRCA-EU 15 28358579 28358579 single base substitution G A downstream_gene_variant BRCA-EU 15 28358579 28358579 single base substitution G A intron_variant BRCA-EU 15 28358618 28358618 single base substitution C G downstream_gene_variant BRCA-EU 15 28358618 28358618 single base substitution C G intron_variant BRCA-EU 15 28359687 28359687 single base substitution C T downstream_gene_variant BRCA-EU 15 28359687 28359687 single base substitution C T intron_variant BRCA-EU 15 28359687 28359687 single base substitution C T upstream_gene_variant BRCA-EU 15 28362755 28362755 single base substitution A G exon_variant BRCA-EU 15 28362755 28362755 single base substitution A G intron_variant BRCA-EU 15 28362755 28362755 single base substitution A G upstream_gene_variant BRCA-EU 15 28364833 28364833 single base substitution C G intron_variant BRCA-EU 15 28364833 28364833 single base substitution C G upstream_gene_variant BRCA-EU 15 28365916 28365916 single base substitution G T intron_variant BRCA-EU 15 28365916 28365916 single base substitution G T upstream_gene_variant BRCA-EU 15 28366631 28366631 single base substitution G T intron_variant BRCA-EU 15 28366631 28366631 single base substitution G T upstream_gene_variant BRCA-EU 15 28367235 28367235 single base substitution C T intron_variant BRCA-EU 15 28367235 28367235 single base substitution C T upstream_gene_variant BRCA-EU 15 28367295 28367295 single base substitution G T intron_variant BRCA-EU 15 28367295 28367295 single base substitution G T upstream_gene_variant BRCA-EU 15 28367619 28367619 single base substitution C A intron_variant BRCA-EU 15 28367619 28367619 single base substitution C A upstream_gene_variant BRCA-EU 15 28367919 28367919 single base substitution C T intron_variant BRCA-EU 15 28367919 28367919 single base substitution C T upstream_gene_variant BRCA-EU 15 28368916 28368916 single base substitution G A intron_variant BRCA-EU 15 28370465 28370465 single base substitution C T intron_variant BRCA-EU 15 28371051 28371051 single base substitution G A intron_variant BRCA-EU 15 28371330 28371330 single base substitution T C intron_variant BRCA-EU 15 28372107 28372107 single base substitution C T intron_variant BRCA-EU 15 28374382 28374382 single base substitution G A intron_variant BRCA-EU 15 28375677 28375677 single base substitution G C missense_variant L4212V 12634C>G BRCA-EU 15 28375684 28375684 single base substitution A G synonymous_variant S4209S 12627T>C BRCA-EU 15 28376112 28376112 single base substitution C T intron_variant BRCA-EU 15 28377342 28377342 single base substitution G A synonymous_variant L4158L 12474C>T BRCA-EU 15 28377563 28377563 single base substitution G A intron_variant BRCA-EU 15 28378287 28378287 single base substitution A G intron_variant BRCA-EU 15 28380456 28380456 single base substitution C A intron_variant BRCA-EU 15 28383717 28383717 single base substitution T C downstream_gene_variant BRCA-EU 15 28383717 28383717 single base substitution T C intron_variant BRCA-EU 15 28385362 28385362 single base substitution C G downstream_gene_variant BRCA-EU 15 28385362 28385362 single base substitution C G intron_variant BRCA-EU 15 28385392 28385392 single base substitution C T downstream_gene_variant BRCA-EU 15 28385392 28385392 single base substitution C T intron_variant BRCA-EU 15 28385819 28385819 single base substitution C A downstream_gene_variant BRCA-EU 15 28385819 28385819 single base substitution C A intron_variant BRCA-EU 15 28386204 28386204 single base substitution T C downstream_gene_variant BRCA-EU 15 28386204 28386204 single base substitution T C intron_variant BRCA-EU 15 28389100 28389100 single base substitution C T synonymous_variant R3779R 11337G>A BRCA-EU 15 28389100 28389100 single base substitution C T upstream_gene_variant BRCA-EU 15 28389145 28389145 single base substitution G A splice_region_variant BRCA-EU 15 28389145 28389145 single base substitution G A upstream_gene_variant BRCA-EU 15 28389244 28389244 single base substitution A T missense_variant C3760S 11278T>A BRCA-EU 15 28389244 28389244 single base substitution A T upstream_gene_variant BRCA-EU 15 28389747 28389747 single base substitution C T intron_variant BRCA-EU 15 28389747 28389747 single base substitution C T upstream_gene_variant BRCA-EU 15 28390823 28390823 single base substitution G C intron_variant BRCA-EU 15 28390823 28390823 single base substitution G C upstream_gene_variant BRCA-EU 15 28391398 28391398 single base substitution C T missense_variant V3665I 10993G>A BRCA-EU 15 28391398 28391398 single base substitution C T upstream_gene_variant BRCA-EU 15 28393775 28393775 single base substitution G A downstream_gene_variant BRCA-EU 15 28393775 28393775 single base substitution G A intron_variant BRCA-EU 15 28394017 28394017 single base substitution A T downstream_gene_variant BRCA-EU 15 28394017 28394017 single base substitution A T intron_variant BRCA-EU 15 28394125 28394125 insertion of <=200bp - A downstream_gene_variant BRCA-EU 15 28394125 28394125 insertion of <=200bp - A intron_variant BRCA-EU 15 28394277 28394277 insertion of <=200bp - A downstream_gene_variant BRCA-EU 15 28394277 28394277 insertion of <=200bp - A intron_variant BRCA-EU 15 28394330 28394330 single base substitution A C downstream_gene_variant BRCA-EU 15 28394330 28394330 single base substitution A C intron_variant BRCA-EU 15 28394339 28394339 single base substitution C G downstream_gene_variant BRCA-EU 15 28394339 28394339 single base substitution C G intron_variant BRCA-EU 15 28394453 28394453 single base substitution A C downstream_gene_variant BRCA-EU 15 28394453 28394453 single base substitution A C intron_variant BRCA-EU 15 28395003 28395003 single base substitution A T downstream_gene_variant BRCA-EU 15 28395003 28395003 single base substitution A T intron_variant BRCA-EU 15 28395573 28395573 single base substitution G C downstream_gene_variant BRCA-EU 15 28395573 28395573 single base substitution G C intron_variant BRCA-EU 15 28396738 28396738 single base substitution C T downstream_gene_variant BRCA-EU 15 28396738 28396738 single base substitution C T intron_variant BRCA-EU 15 28397144 28397144 single base substitution T G downstream_gene_variant BRCA-EU 15 28397144 28397144 single base substitution T G intron_variant BRCA-EU 15 28397265 28397265 single base substitution T C downstream_gene_variant BRCA-EU 15 28397265 28397265 single base substitution T C intron_variant BRCA-EU 15 28397444 28397444 single base substitution T A downstream_gene_variant BRCA-EU 15 28397444 28397444 single base substitution T A intron_variant BRCA-EU 15 28397917 28397917 single base substitution C T synonymous_variant S195S 585G>A BRCA-EU 15 28397917 28397917 single base substitution C T synonymous_variant S3602S 10806G>A BRCA-EU 15 28398153 28398153 single base substitution G C intron_variant BRCA-EU 15 28402950 28402950 single base substitution G A intron_variant BRCA-EU 15 28403712 28403712 insertion of <=200bp - T intron_variant BRCA-EU 15 28404979 28404979 single base substitution C T intron_variant BRCA-EU 15 28405546 28405546 single base substitution C T intron_variant BRCA-EU 15 28407150 28407150 deletion of <=200bp A - intron_variant BRCA-EU 15 28407442 28407442 single base substitution G T intron_variant BRCA-EU 15 28407443 28407443 single base substitution C T intron_variant BRCA-EU 15 28408339 28408339 single base substitution C A intron_variant BRCA-EU 15 28408339 28408339 single base substitution C A synonymous_variant V3549V 10647G>T BRCA-EU 15 28408394 28408394 single base substitution G A intron_variant BRCA-EU 15 28408394 28408394 single base substitution G A missense_variant P3531L 10592C>T BRCA-EU 15 28408400 28408400 single base substitution G A intron_variant BRCA-EU 15 28408400 28408400 single base substitution G A missense_variant P3529L 10586C>T BRCA-EU 15 28408977 28408977 single base substitution G A intron_variant BRCA-EU 15 28409371 28409371 single base substitution A G intron_variant BRCA-EU 15 28410228 28410228 single base substitution G C intron_variant BRCA-EU 15 28411278 28411278 single base substitution C T intron_variant BRCA-EU 15 28411713 28411713 single base substitution G C intron_variant BRCA-EU 15 28412979 28412979 single base substitution C A splice_region_variant BRCA-EU 15 28413643 28413643 single base substitution C T synonymous_variant A3441A 10323G>A BRCA-EU 15 28413643 28413643 single base substitution C T synonymous_variant A98A 294G>A BRCA-EU 15 28413946 28413946 single base substitution A T intron_variant BRCA-EU 15 28413962 28413962 single base substitution G A intron_variant BRCA-EU 15 28414641 28414641 single base substitution G A synonymous_variant I3406I 10218C>T BRCA-EU 15 28414641 28414641 single base substitution G A synonymous_variant I63I 189C>T BRCA-EU 15 28414707 28414707 single base substitution G C synonymous_variant L3384L 10152C>G BRCA-EU 15 28414707 28414707 single base substitution G C synonymous_variant L41L 123C>G BRCA-EU 15 28415965 28415965 single base substitution C A intron_variant BRCA-EU 15 28416204 28416204 single base substitution G T intron_variant BRCA-EU 15 28418386 28418386 single base substitution A T intron_variant BRCA-EU 15 28419911 28419911 single base substitution A T intron_variant BRCA-EU 15 28419911 28419911 single base substitution A T upstream_gene_variant BRCA-EU 15 28420451 28420451 single base substitution G T intron_variant BRCA-EU 15 28420451 28420451 single base substitution G T upstream_gene_variant BRCA-EU 15 28423702 28423702 single base substitution G C intron_variant BRCA-EU 15 28423702 28423702 single base substitution G C upstream_gene_variant BRCA-EU 15 28424197 28424197 single base substitution G A intron_variant BRCA-EU 15 28424197 28424197 single base substitution G A upstream_gene_variant BRCA-EU 15 28426341 28426341 single base substitution C T intron_variant BRCA-EU 15 28427419 28427419 single base substitution G A intron_variant BRCA-EU 15 28427681 28427681 single base substitution G C intron_variant BRCA-EU 15 28428070 28428070 single base substitution C T intron_variant BRCA-EU 15 28428154 28428154 single base substitution G C intron_variant BRCA-EU 15 28429935 28429935 single base substitution G A intron_variant BRCA-EU 15 28430623 28430623 single base substitution C A downstream_gene_variant BRCA-EU 15 28430623 28430623 single base substitution C A intron_variant BRCA-EU 15 28431748 28431748 single base substitution C T downstream_gene_variant BRCA-EU 15 28431748 28431748 single base substitution C T missense_variant E2934K 8800G>A BRCA-EU 15 28431931 28431931 single base substitution T C downstream_gene_variant BRCA-EU 15 28431931 28431931 single base substitution T C intron_variant BRCA-EU 15 28433950 28433950 single base substitution C T downstream_gene_variant BRCA-EU 15 28433950 28433950 single base substitution C T intron_variant BRCA-EU 15 28434491 28434491 single base substitution T C downstream_gene_variant BRCA-EU 15 28434491 28434491 single base substitution T C intron_variant BRCA-EU 15 28434557 28434557 single base substitution A G downstream_gene_variant BRCA-EU 15 28434557 28434557 single base substitution A G intron_variant BRCA-EU 15 28435501 28435501 single base substitution T C exon_variant BRCA-EU 15 28435501 28435501 single base substitution T C intron_variant BRCA-EU 15 28436952 28436952 single base substitution C G intron_variant BRCA-EU 15 28437275 28437275 single base substitution G C exon_variant BRCA-EU 15 28437275 28437275 single base substitution G C synonymous_variant G2761G 8283C>G BRCA-EU 15 28438670 28438670 single base substitution T C intron_variant BRCA-EU 15 28439328 28439328 single base substitution C T intron_variant BRCA-EU 15 28441456 28441456 single base substitution T C exon_variant BRCA-EU 15 28441456 28441456 single base substitution T C missense_variant K2722R 8165A>G BRCA-EU 15 28442981 28442981 single base substitution G C intron_variant BRCA-EU 15 28443728 28443728 single base substitution G C intron_variant BRCA-EU 15 28444149 28444149 single base substitution C T intron_variant BRCA-EU 15 28444569 28444569 single base substitution G A intron_variant BRCA-EU 15 28445114 28445114 deletion of <=200bp C - intron_variant BRCA-EU 15 28445114 28445114 insertion of <=200bp - C intron_variant BRCA-EU 15 28445970 28445970 single base substitution T C intron_variant BRCA-EU 15 28455049 28455049 deletion of <=200bp A - intron_variant BRCA-EU 15 28455274 28455274 deletion of <=200bp T - intron_variant BRCA-EU 15 28457208 28457208 single base substitution G A intron_variant BRCA-EU 15 28459321 28459321 single base substitution C T synonymous_variant T2152T 6456G>A BRCA-EU 15 28459590 28459590 single base substitution G A intron_variant BRCA-EU 15 28460188 28460188 deletion of <=200bp T - intron_variant BRCA-EU 15 28460476 28460476 single base substitution A T intron_variant BRCA-EU 15 28460899 28460899 single base substitution C T synonymous_variant T2026T 6078G>A BRCA-EU 15 28461375 28461375 single base substitution G A intron_variant BRCA-EU 15 28462147 28462147 single base substitution C T intron_variant BRCA-EU 15 28462422 28462422 single base substitution G A downstream_gene_variant BRCA-EU 15 28462422 28462422 single base substitution G A intron_variant BRCA-EU 15 28462724 28462725 deletion of <=200bp AC - downstream_gene_variant BRCA-EU 15 28462724 28462725 deletion of <=200bp AC - intron_variant BRCA-EU 15 28462740 28462740 single base substitution A T downstream_gene_variant BRCA-EU 15 28462740 28462740 single base substitution A T intron_variant BRCA-EU 15 28462804 28462804 single base substitution G C downstream_gene_variant BRCA-EU 15 28462804 28462804 single base substitution G C intron_variant BRCA-EU 15 28463820 28463820 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 28463820 28463820 deletion of <=200bp A - splice_region_variant BRCA-EU 15 28463857 28463857 single base substitution T A downstream_gene_variant BRCA-EU 15 28463857 28463857 single base substitution T A intron_variant BRCA-EU 15 28464613 28464613 single base substitution G A downstream_gene_variant BRCA-EU 15 28464613 28464613 single base substitution G A intron_variant BRCA-EU 15 28465230 28465230 single base substitution G A downstream_gene_variant BRCA-EU 15 28465230 28465230 single base substitution G A intron_variant BRCA-EU 15 28467936 28467936 single base substitution C T intron_variant BRCA-EU 15 28469979 28469979 deletion of <=200bp A - intron_variant BRCA-EU 15 28471115 28471115 single base substitution G C intron_variant BRCA-EU 15 28471666 28471666 single base substitution C T intron_variant BRCA-EU 15 28472214 28472214 single base substitution A T intron_variant BRCA-EU 15 28473477 28473477 single base substitution C A exon_variant BRCA-EU 15 28473477 28473477 single base substitution C A missense_variant R1784L 5351G>T BRCA-EU 15 28473800 28473800 single base substitution A C intron_variant BRCA-EU 15 28474805 28474805 single base substitution C T intron_variant BRCA-EU 15 28474805 28474805 single base substitution C T upstream_gene_variant BRCA-EU 15 28474810 28474810 single base substitution C A intron_variant BRCA-EU 15 28474810 28474810 single base substitution C A upstream_gene_variant BRCA-EU 15 28475418 28475418 single base substitution C T intron_variant BRCA-EU 15 28475418 28475418 single base substitution C T upstream_gene_variant BRCA-EU 15 28476099 28476099 single base substitution A T intron_variant BRCA-EU 15 28476099 28476099 single base substitution A T upstream_gene_variant BRCA-EU 15 28476115 28476115 single base substitution A G intron_variant BRCA-EU 15 28476115 28476115 single base substitution A G upstream_gene_variant BRCA-EU 15 28476146 28476146 single base substitution A C intron_variant BRCA-EU 15 28476146 28476146 single base substitution A C upstream_gene_variant BRCA-EU 15 28476153 28476153 single base substitution A C intron_variant BRCA-EU 15 28476153 28476153 single base substitution A C upstream_gene_variant BRCA-EU 15 28476389 28476389 single base substitution T A intron_variant BRCA-EU 15 28476389 28476389 single base substitution T A upstream_gene_variant BRCA-EU 15 28476709 28476709 single base substitution A G intron_variant BRCA-EU 15 28476709 28476709 single base substitution A G upstream_gene_variant BRCA-EU 15 28481460 28481460 single base substitution G A intron_variant BRCA-EU 15 28484099 28484099 deletion of <=200bp A - intron_variant BRCA-EU 15 28484142 28484142 single base substitution A G intron_variant BRCA-EU 15 28485802 28485802 single base substitution G C intron_variant BRCA-EU 15 28486695 28486695 single base substitution C A intron_variant BRCA-EU 15 28486981 28486981 single base substitution A G intron_variant BRCA-EU 15 28489257 28489257 single base substitution C T intron_variant BRCA-EU 15 28489311 28489311 deletion of <=200bp A - intron_variant BRCA-EU 15 28489722 28489722 single base substitution T C intron_variant BRCA-EU 15 28492854 28492854 single base substitution G A intron_variant BRCA-EU 15 28493793 28493793 single base substitution C G missense_variant R1047T 3140G>C BRCA-EU 15 28494680 28494680 single base substitution G C downstream_gene_variant BRCA-EU 15 28494680 28494680 single base substitution G C intron_variant BRCA-EU 15 28495653 28495653 single base substitution G C downstream_gene_variant BRCA-EU 15 28495653 28495653 single base substitution G C intron_variant BRCA-EU 15 28495793 28495793 single base substitution T C downstream_gene_variant BRCA-EU 15 28495793 28495793 single base substitution T C intron_variant BRCA-EU 15 28495923 28495923 single base substitution C A downstream_gene_variant BRCA-EU 15 28495923 28495923 single base substitution C A intron_variant BRCA-EU 15 28496929 28496929 single base substitution G C downstream_gene_variant BRCA-EU 15 28496929 28496929 single base substitution G C intron_variant BRCA-EU 15 28496953 28496953 insertion of <=200bp - A downstream_gene_variant BRCA-EU 15 28496953 28496953 insertion of <=200bp - A intron_variant BRCA-EU 15 28500584 28500584 single base substitution A C intron_variant BRCA-EU 15 28500591 28500591 single base substitution A G intron_variant BRCA-EU 15 28501696 28501696 single base substitution G C intron_variant BRCA-EU 15 28502358 28502358 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 28502358 28502358 single base substitution G A missense_variant P789L 2366C>T BRCA-EU 15 28503184 28503184 single base substitution G A intron_variant BRCA-EU 15 28503353 28503353 single base substitution C T intron_variant BRCA-EU 15 28506016 28506016 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 28506016 28506016 single base substitution G A synonymous_variant H741H 2223C>T BRCA-EU 15 28509974 28509974 single base substitution G A intron_variant BRCA-EU 15 28511236 28511236 single base substitution C A intron_variant BRCA-EU 15 28512859 28512859 single base substitution G T downstream_gene_variant BRCA-EU 15 28512859 28512859 single base substitution G T intron_variant BRCA-EU 15 28513091 28513091 single base substitution C T downstream_gene_variant BRCA-EU 15 28513091 28513091 single base substitution C T intron_variant BRCA-EU 15 28513155 28513155 single base substitution C T downstream_gene_variant BRCA-EU 15 28513155 28513155 single base substitution C T intron_variant BRCA-EU 15 28514933 28514933 single base substitution G T downstream_gene_variant BRCA-EU 15 28514933 28514933 single base substitution G T intron_variant BRCA-EU 15 28517456 28517456 single base substitution C T 3_prime_UTR_variant BRCA-EU 15 28517456 28517456 single base substitution C T exon_variant BRCA-EU 15 28517456 28517456 single base substitution C T missense_variant A330T 988G>A BRCA-EU 15 28517461 28517461 single base substitution C T 3_prime_UTR_variant BRCA-EU 15 28517461 28517461 single base substitution C T exon_variant BRCA-EU 15 28517461 28517461 single base substitution C T missense_variant R328H 983G>A BRCA-EU 15 28518817 28518817 single base substitution C T intron_variant BRCA-EU 15 28518817 28518817 single base substitution C T upstream_gene_variant BRCA-EU 15 28518863 28518863 single base substitution G A intron_variant BRCA-EU 15 28518863 28518863 single base substitution G A upstream_gene_variant BRCA-EU 15 28518934 28518934 single base substitution C T intron_variant BRCA-EU 15 28518934 28518934 single base substitution C T upstream_gene_variant BRCA-EU 15 28519620 28519620 deletion of <=200bp C - intron_variant BRCA-EU 15 28519620 28519620 deletion of <=200bp C - upstream_gene_variant BRCA-EU 15 28519674 28519674 insertion of <=200bp - A intron_variant BRCA-EU 15 28519674 28519674 insertion of <=200bp - A upstream_gene_variant BRCA-EU 15 28521646 28521646 single base substitution G A downstream_gene_variant BRCA-EU 15 28521646 28521646 single base substitution G A intron_variant BRCA-EU 15 28521646 28521646 single base substitution G A upstream_gene_variant BRCA-EU 15 28524465 28524465 single base substitution G T downstream_gene_variant BRCA-EU 15 28524465 28524465 single base substitution G T intron_variant BRCA-EU 15 28525926 28525926 single base substitution C A intron_variant BRCA-EU 15 28527628 28527628 deletion of <=200bp A - intron_variant BRCA-EU 15 28527785 28527785 single base substitution T A intron_variant BRCA-EU 15 28528868 28528868 single base substitution T A intron_variant BRCA-EU 15 28532077 28532077 deletion of <=200bp A - intron_variant BRCA-EU 15 28534744 28534744 single base substitution G A intron_variant BRCA-EU 15 28535444 28535444 single base substitution C T intron_variant BRCA-EU 15 28535472 28535472 single base substitution C T intron_variant BRCA-EU 15 28535509 28535509 single base substitution A G intron_variant BRCA-EU 15 28536382 28536382 deletion of <=200bp T - intron_variant BRCA-EU 15 28536587 28536587 deletion of <=200bp A - intron_variant BRCA-EU 15 28536774 28536774 deletion of <=200bp A - intron_variant BRCA-EU 15 28536907 28536907 single base substitution C T intron_variant BRCA-EU 15 28536959 28536959 single base substitution G C intron_variant BRCA-EU 15 28537413 28537413 single base substitution T C intron_variant BRCA-EU 15 28538565 28538565 single base substitution G T intron_variant BRCA-EU 15 28538622 28538622 single base substitution G C intron_variant BRCA-EU 15 28539341 28539341 single base substitution A G intron_variant BRCA-EU 15 28540618 28540618 single base substitution C T intron_variant BRCA-EU 15 28541973 28541973 single base substitution G A intron_variant BRCA-EU 15 28542549 28542549 single base substitution G A intron_variant BRCA-EU 15 28544589 28544589 single base substitution C A exon_variant BRCA-EU 15 28544589 28544589 single base substitution C A missense_variant G49V 146G>T BRCA-EU 15 28544590 28544590 single base substitution C A exon_variant BRCA-EU 15 28544590 28544590 single base substitution C A stop_gained G49* 145G>T BRCA-EU 15 28546012 28546012 single base substitution G C intron_variant BRCA-EU 15 28546012 28546012 single base substitution G C upstream_gene_variant BRCA-EU 15 28546623 28546623 single base substitution T C intron_variant BRCA-EU 15 28546623 28546623 single base substitution T C upstream_gene_variant BRCA-EU 15 28546828 28546828 single base substitution C A intron_variant BRCA-EU 15 28546828 28546828 single base substitution C A upstream_gene_variant BRCA-EU 15 28548501 28548501 single base substitution T C intron_variant BRCA-EU 15 28548501 28548501 single base substitution T C upstream_gene_variant BRCA-EU 15 28548782 28548782 single base substitution G C intron_variant BRCA-EU 15 28548782 28548782 single base substitution G C upstream_gene_variant BRCA-EU 15 28550686 28550686 single base substitution A G intron_variant BRCA-EU 15 28552844 28552844 single base substitution G A intron_variant BRCA-EU 15 28553635 28553635 single base substitution C T intron_variant BRCA-EU 15 28554176 28554176 deletion of <=200bp T - intron_variant BRCA-EU 15 28554958 28554958 single base substitution G C intron_variant BRCA-EU 15 28555277 28555277 single base substitution C G intron_variant BRCA-EU 15 28555952 28555952 single base substitution G A intron_variant BRCA-EU 15 28556419 28556419 single base substitution A G intron_variant BRCA-EU 15 28557114 28557114 single base substitution C A intron_variant BRCA-EU 15 28557339 28557339 single base substitution C A intron_variant BRCA-EU 15 28557884 28557884 single base substitution C T intron_variant BRCA-EU 15 28558388 28558388 single base substitution G C intron_variant BRCA-EU 15 28559800 28559800 single base substitution A C intron_variant BRCA-EU 15 28559915 28559915 single base substitution G A intron_variant BRCA-EU 15 28560385 28560385 single base substitution G A downstream_gene_variant BRCA-EU 15 28560385 28560385 single base substitution G A intron_variant BRCA-EU 15 28561199 28561199 single base substitution G A downstream_gene_variant BRCA-EU 15 28561199 28561199 single base substitution G A intron_variant BRCA-EU 15 28561432 28561432 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 28561432 28561432 deletion of <=200bp T - intron_variant BRCA-EU 15 28561985 28561985 single base substitution C T downstream_gene_variant BRCA-EU 15 28561985 28561985 single base substitution C T intron_variant BRCA-EU 15 28563754 28563754 single base substitution G T downstream_gene_variant BRCA-EU 15 28563754 28563754 single base substitution G T intron_variant BRCA-EU 15 28564605 28564605 single base substitution C G downstream_gene_variant BRCA-EU 15 28564605 28564605 single base substitution C G intron_variant BRCA-EU 15 28571869 28571869 single base substitution G A upstream_gene_variant BRCA-EU 15 28572135 28572135 single base substitution A G upstream_gene_variant BRCA-FR 15 28363222 28363222 single base substitution G A exon_variant BRCA-FR 15 28363222 28363222 single base substitution G A intron_variant BRCA-FR 15 28363222 28363222 single base substitution G A upstream_gene_variant BRCA-FR 15 28365916 28365916 single base substitution G T intron_variant BRCA-FR 15 28365916 28365916 single base substitution G T upstream_gene_variant BRCA-FR 15 28375684 28375684 single base substitution A G synonymous_variant S4209S 12627T>C BRCA-FR 15 28389145 28389145 single base substitution G A splice_region_variant BRCA-FR 15 28389145 28389145 single base substitution G A upstream_gene_variant BRCA-FR 15 28398153 28398153 single base substitution G C intron_variant BRCA-FR 15 28402950 28402950 single base substitution G A intron_variant BRCA-FR 15 28404979 28404979 single base substitution C T intron_variant BRCA-FR 15 28406659 28406659 single base substitution C T intron_variant BRCA-FR 15 28411713 28411713 single base substitution G C intron_variant BRCA-FR 15 28414707 28414707 single base substitution G C synonymous_variant L3384L 10152C>G BRCA-FR 15 28414707 28414707 single base substitution G C synonymous_variant L41L 123C>G BRCA-FR 15 28419113 28419113 single base substitution A G intron_variant BRCA-FR 15 28419587 28419587 single base substitution G A synonymous_variant P3337P 10011C>T BRCA-FR 15 28419587 28419587 single base substitution G A upstream_gene_variant BRCA-FR 15 28422676 28422676 single base substitution C T intron_variant BRCA-FR 15 28422676 28422676 single base substitution C T upstream_gene_variant BRCA-FR 15 28429935 28429935 single base substitution G A intron_variant BRCA-FR 15 28431748 28431748 single base substitution C T downstream_gene_variant BRCA-FR 15 28431748 28431748 single base substitution C T missense_variant E2934K 8800G>A BRCA-FR 15 28434557 28434557 single base substitution A G downstream_gene_variant BRCA-FR 15 28434557 28434557 single base substitution A G intron_variant BRCA-FR 15 28439211 28439211 single base substitution G T intron_variant BRCA-FR 15 28439328 28439328 single base substitution C T intron_variant BRCA-FR 15 28445579 28445579 single base substitution C A intron_variant BRCA-FR 15 28456036 28456036 single base substitution C T intron_variant BRCA-FR 15 28462640 28462640 single base substitution C T downstream_gene_variant BRCA-FR 15 28462640 28462640 single base substitution C T intron_variant BRCA-FR 15 28462804 28462804 single base substitution G C downstream_gene_variant BRCA-FR 15 28462804 28462804 single base substitution G C intron_variant BRCA-FR 15 28463476 28463476 single base substitution G A downstream_gene_variant BRCA-FR 15 28463476 28463476 single base substitution G A intron_variant BRCA-FR 15 28467936 28467936 single base substitution C T intron_variant BRCA-FR 15 28485802 28485802 single base substitution G C intron_variant BRCA-FR 15 28494680 28494680 single base substitution G C downstream_gene_variant BRCA-FR 15 28494680 28494680 single base substitution G C intron_variant BRCA-FR 15 28501696 28501696 single base substitution G C intron_variant BRCA-FR 15 28514933 28514933 single base substitution G T downstream_gene_variant BRCA-FR 15 28514933 28514933 single base substitution G T intron_variant BRCA-FR 15 28521646 28521646 single base substitution G A downstream_gene_variant BRCA-FR 15 28521646 28521646 single base substitution G A intron_variant BRCA-FR 15 28521646 28521646 single base substitution G A upstream_gene_variant BRCA-FR 15 28536959 28536959 single base substitution G C intron_variant BRCA-FR 15 28537413 28537413 single base substitution T C intron_variant BRCA-FR 15 28542282 28542282 single base substitution C G intron_variant BRCA-FR 15 28546623 28546623 single base substitution T C intron_variant BRCA-FR 15 28546623 28546623 single base substitution T C upstream_gene_variant BRCA-FR 15 28548782 28548782 single base substitution G C intron_variant BRCA-FR 15 28548782 28548782 single base substitution G C upstream_gene_variant BRCA-FR 15 28552684 28552684 single base substitution T C intron_variant BRCA-FR 15 28561199 28561199 single base substitution G A downstream_gene_variant BRCA-FR 15 28561199 28561199 single base substitution G A intron_variant BRCA-KR 15 28421780 28421780 single base substitution G A intron_variant BRCA-KR 15 28421780 28421780 single base substitution G A upstream_gene_variant BRCA-UK 15 28394453 28394453 single base substitution A C downstream_gene_variant BRCA-UK 15 28394453 28394453 single base substitution A C intron_variant BRCA-UK 15 28402435 28402435 single base substitution C G intron_variant BRCA-UK 15 28441240 28441240 single base substitution C T intron_variant BRCA-UK 15 28445361 28445361 single base substitution G A intron_variant BRCA-UK 15 28462640 28462640 single base substitution C T downstream_gene_variant BRCA-UK 15 28462640 28462640 single base substitution C T intron_variant BRCA-UK 15 28463865 28463865 single base substitution G A downstream_gene_variant BRCA-UK 15 28463865 28463865 single base substitution G A intron_variant BRCA-UK 15 28474805 28474805 single base substitution C T intron_variant BRCA-UK 15 28474805 28474805 single base substitution C T upstream_gene_variant BRCA-UK 15 28481583 28481583 single base substitution C G intron_variant BRCA-UK 15 28493793 28493793 single base substitution C G missense_variant R1047T 3140G>C BRCA-UK 15 28535870 28535870 single base substitution G A intron_variant BRCA-US 15 28357017 28357017 single base substitution G A downstream_gene_variant BRCA-US 15 28357017 28357017 single base substitution G A exon_variant BRCA-US 15 28357017 28357017 single base substitution G A synonymous_variant I4799I 14397C>T BRCA-US 15 28369301 28369301 single base substitution G C missense_variant S4357C 13070C>G BRCA-US 15 28375390 28375390 single base substitution G A missense_variant R4241W 12721C>T BRCA-US 15 28377860 28377860 single base substitution C G missense_variant G4116A 12347G>C BRCA-US 15 28386674 28386674 single base substitution G T downstream_gene_variant BRCA-US 15 28386674 28386674 single base substitution G T synonymous_variant V3973V 11919C>A BRCA-US 15 28387403 28387403 single base substitution G C exon_variant BRCA-US 15 28387403 28387403 single base substitution G C missense_variant P3894R 11681C>G BRCA-US 15 28389261 28389261 single base substitution G A missense_variant A3754V 11261C>T BRCA-US 15 28389261 28389261 single base substitution G A upstream_gene_variant BRCA-US 15 28389827 28389828 deletion of <=200bp GG - frameshift_variant P3711 BRCA-US 15 28389827 28389828 deletion of <=200bp GG - upstream_gene_variant BRCA-US 15 28389831 28389834 deletion of <=200bp TGAT - frameshift_variant IM3709 BRCA-US 15 28389831 28389834 deletion of <=200bp TGAT - upstream_gene_variant BRCA-US 15 28391398 28391398 single base substitution C T missense_variant V3665I 10993G>A BRCA-US 15 28391398 28391398 single base substitution C T upstream_gene_variant BRCA-US 15 28408347 28408347 single base substitution G A intron_variant BRCA-US 15 28408347 28408347 single base substitution G A missense_variant R3547C 10639C>T BRCA-US 15 28408363 28408363 single base substitution C T intron_variant BRCA-US 15 28408363 28408363 single base substitution C T synonymous_variant L3541L 10623G>A BRCA-US 15 28414741 28414741 single base substitution G T missense_variant S30Y 89C>A BRCA-US 15 28414741 28414741 single base substitution G T missense_variant S3373Y 10118C>A BRCA-US 15 28419587 28419587 single base substitution G A synonymous_variant P3337P 10011C>T BRCA-US 15 28419587 28419587 single base substitution G A upstream_gene_variant BRCA-US 15 28419644 28419644 single base substitution C A synonymous_variant S3318S 9954G>T BRCA-US 15 28419644 28419644 single base substitution C A upstream_gene_variant BRCA-US 15 28421694 28421694 single base substitution C T missense_variant G3189E 9566G>A BRCA-US 15 28421694 28421694 single base substitution C T upstream_gene_variant BRCA-US 15 28421867 28421867 single base substitution A G synonymous_variant S3160S 9480T>C BRCA-US 15 28421867 28421867 single base substitution A G upstream_gene_variant BRCA-US 15 28431765 28431765 single base substitution G A downstream_gene_variant BRCA-US 15 28431765 28431765 single base substitution G A missense_variant S2928L 8783C>T BRCA-US 15 28436126 28436126 single base substitution C T exon_variant BRCA-US 15 28436126 28436126 single base substitution C T synonymous_variant L2878L 8634G>A BRCA-US 15 28436380 28436380 single base substitution C G exon_variant BRCA-US 15 28436380 28436380 single base substitution C G missense_variant R2821P 8462G>C BRCA-US 15 28441424 28441424 single base substitution C T exon_variant BRCA-US 15 28441424 28441424 single base substitution C T missense_variant E2733K 8197G>A BRCA-US 15 28446656 28446656 single base substitution T A exon_variant BRCA-US 15 28446656 28446656 single base substitution T A synonymous_variant R2554R 7662A>T BRCA-US 15 28451475 28451475 single base substitution G A stop_gained Q2375* 7123C>T BRCA-US 15 28451475 28451475 single base substitution G A upstream_gene_variant BRCA-US 15 28474383 28474383 single base substitution G A exon_variant BRCA-US 15 28474383 28474383 single base substitution G A stop_gained R1744* 5230C>T BRCA-US 15 28478454 28478454 single base substitution C A missense_variant V1505F 4513G>T BRCA-US 15 28478454 28478454 single base substitution C A upstream_gene_variant BRCA-US 15 28478469 28478469 single base substitution G A missense_variant R1500C 4498C>T BRCA-US 15 28478469 28478469 single base substitution G A upstream_gene_variant BRCA-US 15 28479350 28479350 single base substitution C G missense_variant D1362H 4084G>C BRCA-US 15 28479350 28479350 single base substitution C G upstream_gene_variant BRCA-US 15 28483866 28483866 single base substitution T C missense_variant I1210M 3630A>G BRCA-US 15 28493757 28493757 single base substitution C T missense_variant R1059H 3176G>A BRCA-US 15 28501072 28501072 single base substitution C T 3_prime_UTR_variant BRCA-US 15 28501072 28501072 single base substitution C T missense_variant M939I 2817G>A BRCA-US 15 28501091 28501092 deletion of <=200bp AG - 3_prime_UTR_variant BRCA-US 15 28501091 28501092 deletion of <=200bp AG - frameshift_variant L933 BRCA-US 15 28501279 28501279 single base substitution G A 3_prime_UTR_variant BRCA-US 15 28501279 28501279 single base substitution G A missense_variant A901V 2702C>T BRCA-US 15 28515846 28515846 single base substitution G A 3_prime_UTR_variant BRCA-US 15 28515846 28515846 single base substitution G A downstream_gene_variant BRCA-US 15 28515846 28515846 single base substitution G A missense_variant H418Y 1252C>T BRCA-US 15 28517375 28517375 single base substitution C T 3_prime_UTR_variant BRCA-US 15 28517375 28517375 single base substitution C T exon_variant BRCA-US 15 28517375 28517375 single base substitution C T missense_variant E357K 1069G>A BRCA-US 15 28518115 28518115 single base substitution C A 3_prime_UTR_variant BRCA-US 15 28518115 28518115 single base substitution C A exon_variant BRCA-US 15 28518115 28518115 single base substitution C A missense_variant G279V 836G>T BRCA-US 15 28519482 28519482 single base substitution T C 3_prime_UTR_variant BRCA-US 15 28519482 28519482 single base substitution T C missense_variant E252G 755A>G BRCA-US 15 28519482 28519482 single base substitution T C upstream_gene_variant BRCA-US 15 28525309 28525309 single base substitution G A 3_prime_UTR_variant BRCA-US 15 28525309 28525309 single base substitution G A exon_variant BRCA-US 15 28525309 28525309 single base substitution G A synonymous_variant R149R 447C>T BTCA-JP 15 28359890 28359890 single base substitution T C downstream_gene_variant BTCA-JP 15 28359890 28359890 single base substitution T C exon_variant BTCA-JP 15 28359890 28359890 single base substitution T C missense_variant E4594G 13781A>G BTCA-JP 15 28359890 28359890 single base substitution T C upstream_gene_variant BTCA-JP 15 28362213 28362213 single base substitution A G exon_variant BTCA-JP 15 28362213 28362213 single base substitution A G missense_variant F4454L 13360T>C BTCA-JP 15 28362213 28362213 single base substitution A G upstream_gene_variant BTCA-JP 15 28414915 28414915 single base substitution T C intron_variant BTCA-JP 15 28420749 28420749 single base substitution T A missense_variant K3247I 9740A>T BTCA-JP 15 28420749 28420749 single base substitution T A upstream_gene_variant BTCA-JP 15 28421548 28421548 single base substitution G T intron_variant BTCA-JP 15 28421548 28421548 single base substitution G T upstream_gene_variant BTCA-JP 15 28422229 28422229 single base substitution C A missense_variant R3100L 9299G>T BTCA-JP 15 28422229 28422229 single base substitution C A upstream_gene_variant BTCA-JP 15 28422444 28422444 single base substitution A T intron_variant BTCA-JP 15 28422444 28422444 single base substitution A T upstream_gene_variant BTCA-JP 15 28443857 28443857 single base substitution C T exon_variant BTCA-JP 15 28443857 28443857 single base substitution C T missense_variant G2592D 7775G>A BTCA-JP 15 28473433 28473433 single base substitution C T exon_variant BTCA-JP 15 28473433 28473433 single base substitution C T missense_variant A1799T 5395G>A BTCA-JP 15 28478666 28478666 single base substitution T A missense_variant I1465F 4393A>T BTCA-JP 15 28478666 28478666 single base substitution T A upstream_gene_variant BTCA-JP 15 28478780 28478780 single base substitution C G intron_variant BTCA-JP 15 28478780 28478780 single base substitution C G upstream_gene_variant BTCA-JP 15 28493704 28493704 single base substitution T C missense_variant I1077V 3229A>G BTCA-JP 15 28493838 28493838 single base substitution C T missense_variant R1032H 3095G>A BTCA-JP 15 28513637 28513637 single base substitution G A 3_prime_UTR_variant BTCA-JP 15 28513637 28513637 single base substitution G A downstream_gene_variant BTCA-JP 15 28513637 28513637 single base substitution G A synonymous_variant G524G 1572C>T BTCA-JP 15 28519620 28519620 deletion of <=200bp C - intron_variant BTCA-JP 15 28519620 28519620 deletion of <=200bp C - upstream_gene_variant BTCA-JP 15 28520117 28520117 single base substitution C T 3_prime_UTR_variant BTCA-JP 15 28520117 28520117 single base substitution C T missense_variant A193T 577G>A BTCA-JP 15 28520117 28520117 single base substitution C T upstream_gene_variant BTCA-JP 15 28544603 28544603 single base substitution T G exon_variant BTCA-JP 15 28544603 28544603 single base substitution T G missense_variant E44D 132A>C CESC-US 15 28358750 28358750 single base substitution G C downstream_gene_variant CESC-US 15 28358750 28358750 single base substitution G C exon_variant CESC-US 15 28358750 28358750 single base substitution G C missense_variant S4663C 13988C>G CESC-US 15 28387979 28387979 single base substitution G A synonymous_variant F3846F 11538C>T CESC-US 15 28387979 28387979 single base substitution G A upstream_gene_variant CESC-US 15 28422657 28422657 single base substitution T C splice_acceptor_variant CESC-US 15 28422657 28422657 single base substitution T C upstream_gene_variant CESC-US 15 28436121 28436121 single base substitution T C exon_variant CESC-US 15 28436121 28436121 single base substitution T C missense_variant D2880G 8639A>G CESC-US 15 28437168 28437168 single base substitution T C exon_variant CESC-US 15 28437168 28437168 single base substitution T C missense_variant Q2797R 8390A>G CESC-US 15 28443555 28443555 single base substitution A T exon_variant CESC-US 15 28443555 28443555 single base substitution A T synonymous_variant S2660S 7980T>A CESC-US 15 28463704 28463704 single base substitution T G downstream_gene_variant CESC-US 15 28463704 28463704 single base substitution T G missense_variant S1987R 5959A>C CESC-US 15 28510988 28510988 single base substitution G A 3_prime_UTR_variant CESC-US 15 28510988 28510988 single base substitution G A synonymous_variant R577R 1731C>T CESC-US 15 28515957 28515957 single base substitution G C 3_prime_UTR_variant CESC-US 15 28515957 28515957 single base substitution G C downstream_gene_variant CESC-US 15 28515957 28515957 single base substitution G C missense_variant Q381E 1141C>G CESC-US 15 28517458 28517458 single base substitution G A 3_prime_UTR_variant CESC-US 15 28517458 28517458 single base substitution G A exon_variant CESC-US 15 28517458 28517458 single base substitution G A missense_variant S329F 986C>T CESC-US 15 28525273 28525273 single base substitution C T 3_prime_UTR_variant CESC-US 15 28525273 28525273 single base substitution C T exon_variant CESC-US 15 28525273 28525273 single base substitution C T synonymous_variant E161E 483G>A CESC-US 15 28566548 28566548 single base substitution T C exon_variant CESC-US 15 28566548 28566548 single base substitution T C missense_variant Q11R 32A>G CLLE-ES 15 28355864 28355864 single base substitution T C downstream_gene_variant CLLE-ES 15 28359174 28359174 single base substitution C A downstream_gene_variant CLLE-ES 15 28359174 28359174 single base substitution C A intron_variant CLLE-ES 15 28359174 28359174 single base substitution C A upstream_gene_variant CLLE-ES 15 28365505 28365505 single base substitution A C intron_variant CLLE-ES 15 28365505 28365505 single base substitution A C upstream_gene_variant CLLE-ES 15 28372838 28372838 single base substitution G A intron_variant CLLE-ES 15 28379271 28379271 single base substitution A C intron_variant CLLE-ES 15 28392665 28392665 single base substitution T C intron_variant CLLE-ES 15 28398738 28398738 single base substitution A C intron_variant CLLE-ES 15 28401693 28401693 single base substitution C T intron_variant CLLE-ES 15 28435422 28435422 single base substitution C T exon_variant CLLE-ES 15 28435422 28435422 single base substitution C T intron_variant CLLE-ES 15 28505709 28505709 single base substitution G A intron_variant CLLE-ES 15 28510245 28510245 single base substitution A T intron_variant CLLE-ES 15 28516098 28516098 single base substitution T G downstream_gene_variant CLLE-ES 15 28516098 28516098 single base substitution T G intron_variant CLLE-ES 15 28518485 28518485 single base substitution T A intron_variant CLLE-ES 15 28518485 28518485 single base substitution T A upstream_gene_variant CLLE-ES 15 28536327 28536327 single base substitution T C intron_variant CLLE-ES 15 28544782 28544782 single base substitution T C intron_variant CLLE-ES 15 28544782 28544782 single base substitution T C upstream_gene_variant CLLE-ES 15 28544989 28544989 single base substitution G C intron_variant CLLE-ES 15 28544989 28544989 single base substitution G C upstream_gene_variant COAD-US 15 28370178 28370178 single base substitution C T missense_variant A4322T 12964G>A COAD-US 15 28377284 28377284 single base substitution C T missense_variant G4178S 12532G>A COAD-US 15 28377293 28377293 single base substitution C T missense_variant G4175S 12523G>A COAD-US 15 28377372 28377372 single base substitution G A synonymous_variant I4148I 12444C>T COAD-US 15 28386620 28386620 single base substitution G T downstream_gene_variant COAD-US 15 28386620 28386620 single base substitution G T synonymous_variant I3991I 11973C>A COAD-US 15 28387409 28387409 single base substitution G A exon_variant COAD-US 15 28387409 28387409 single base substitution G A missense_variant P3892L 11675C>T COAD-US 15 28389059 28389059 single base substitution T C missense_variant N3793S 11378A>G COAD-US 15 28389059 28389059 single base substitution T C upstream_gene_variant COAD-US 15 28389862 28389862 single base substitution G A synonymous_variant G3699G 11097C>T COAD-US 15 28389862 28389862 single base substitution G A upstream_gene_variant COAD-US 15 28389921 28389921 single base substitution G A synonymous_variant L3680L 11038C>T COAD-US 15 28389921 28389921 single base substitution G A upstream_gene_variant COAD-US 15 28391393 28391393 single base substitution G A synonymous_variant S3666S 10998C>T COAD-US 15 28391393 28391393 single base substitution G A upstream_gene_variant COAD-US 15 28397918 28397918 single base substitution G A missense_variant S195L 584C>T COAD-US 15 28397918 28397918 single base substitution G A missense_variant S3602L 10805C>T COAD-US 15 28412847 28412847 single base substitution T C missense_variant T171A 511A>G COAD-US 15 28412847 28412847 single base substitution T C missense_variant T3514A 10540A>G COAD-US 15 28412872 28412872 single base substitution G A synonymous_variant A162A 486C>T COAD-US 15 28412872 28412872 single base substitution G A synonymous_variant A3505A 10515C>T COAD-US 15 28413595 28413595 single base substitution G A synonymous_variant I114I 342C>T COAD-US 15 28413595 28413595 single base substitution G A synonymous_variant I3457I 10371C>T COAD-US 15 28413605 28413605 single base substitution G A missense_variant A111V 332C>T COAD-US 15 28413605 28413605 single base substitution G A missense_variant A3454V 10361C>T COAD-US 15 28419740 28419740 single base substitution G A synonymous_variant H3286H 9858C>T COAD-US 15 28419740 28419740 single base substitution G A upstream_gene_variant COAD-US 15 28421907 28421907 single base substitution A T missense_variant V3147D 9440T>A COAD-US 15 28421907 28421907 single base substitution A T upstream_gene_variant COAD-US 15 28422177 28422177 single base substitution G A synonymous_variant S3117S 9351C>T COAD-US 15 28422177 28422177 single base substitution G A upstream_gene_variant COAD-US 15 28437182 28437182 single base substitution C T exon_variant COAD-US 15 28437182 28437182 single base substitution C T synonymous_variant S2792S 8376G>A COAD-US 15 28437250 28437250 single base substitution A G exon_variant COAD-US 15 28437250 28437250 single base substitution A G missense_variant C2770R 8308T>C COAD-US 15 28443535 28443535 single base substitution C T exon_variant COAD-US 15 28443535 28443535 single base substitution C T missense_variant G2667E 8000G>A COAD-US 15 28443784 28443784 single base substitution G A exon_variant COAD-US 15 28443784 28443784 single base substitution G A synonymous_variant G2616G 7848C>T COAD-US 15 28456241 28456241 single base substitution G T missense_variant L2326M 6976C>A COAD-US 15 28457699 28457699 single base substitution G T missense_variant L2273M 6817C>A COAD-US 15 28459069 28459069 deletion of <=200bp C - frameshift_variant G2202 COAD-US 15 28460942 28460942 single base substitution G T missense_variant P2012Q 6035C>A COAD-US 15 28474407 28474407 single base substitution A G exon_variant COAD-US 15 28474407 28474407 single base substitution A G missense_variant Y1736H 5206T>C COAD-US 15 28478848 28478848 single base substitution C T missense_variant R1438H 4313G>A COAD-US 15 28478848 28478848 single base substitution C T upstream_gene_variant COAD-US 15 28493767 28493767 single base substitution G A missense_variant R1056C 3166C>T COAD-US 15 28499581 28499581 single base substitution C T downstream_gene_variant COAD-US 15 28499581 28499581 single base substitution C T synonymous_variant R985R 2955G>A COAD-US 15 28502274 28502274 single base substitution G A 3_prime_UTR_variant COAD-US 15 28502274 28502274 single base substitution G A missense_variant A817V 2450C>T COAD-US 15 28508102 28508102 single base substitution T A 3_prime_UTR_variant COAD-US 15 28508102 28508102 single base substitution T A missense_variant E695V 2084A>T COAD-US 15 28508195 28508195 single base substitution C T 3_prime_UTR_variant COAD-US 15 28508195 28508195 single base substitution C T missense_variant C664Y 1991G>A COAD-US 15 28515923 28515923 single base substitution G A 3_prime_UTR_variant COAD-US 15 28515923 28515923 single base substitution G A downstream_gene_variant COAD-US 15 28515923 28515923 single base substitution G A missense_variant T392M 1175C>T COAD-US 15 28517370 28517370 single base substitution G A 3_prime_UTR_variant COAD-US 15 28517370 28517370 single base substitution G A exon_variant COAD-US 15 28517370 28517370 single base substitution G A synonymous_variant G358G 1074C>T COAD-US 15 28519459 28519459 single base substitution A G 3_prime_UTR_variant COAD-US 15 28519459 28519459 single base substitution A G missense_variant F260L 778T>C COAD-US 15 28519459 28519459 single base substitution A G upstream_gene_variant COAD-US 15 28519528 28519528 single base substitution C T 3_prime_UTR_variant COAD-US 15 28519528 28519528 single base substitution C T missense_variant E237K 709G>A COAD-US 15 28519528 28519528 single base substitution C T upstream_gene_variant COAD-US 15 28519563 28519563 single base substitution A G 3_prime_UTR_variant COAD-US 15 28519563 28519563 single base substitution A G missense_variant L225S 674T>C COAD-US 15 28519563 28519563 single base substitution A G upstream_gene_variant COAD-US 15 28544575 28544575 deletion of <=200bp G - exon_variant COAD-US 15 28544575 28544575 deletion of <=200bp G - frameshift_variant Q54 COCA-CN 15 28358249 28358249 single base substitution C T downstream_gene_variant COCA-CN 15 28358249 28358249 single base substitution C T exon_variant COCA-CN 15 28358249 28358249 single base substitution C T missense_variant A4734T 14200G>A COCA-CN 15 28358387 28358387 single base substitution C T downstream_gene_variant COCA-CN 15 28358387 28358387 single base substitution C T exon_variant COCA-CN 15 28358387 28358387 single base substitution C T missense_variant V4688M 14062G>A COCA-CN 15 28358790 28358790 single base substitution G A downstream_gene_variant COCA-CN 15 28358790 28358790 single base substitution G A exon_variant COCA-CN 15 28358790 28358790 single base substitution G A missense_variant R4650W 13948C>T COCA-CN 15 28360609 28360609 single base substitution G A exon_variant COCA-CN 15 28360609 28360609 single base substitution G A missense_variant A4563V 13688C>T COCA-CN 15 28360609 28360609 single base substitution G A upstream_gene_variant COCA-CN 15 28360659 28360659 single base substitution G A exon_variant COCA-CN 15 28360659 28360659 single base substitution G A synonymous_variant T4546T 13638C>T COCA-CN 15 28360659 28360659 single base substitution G A upstream_gene_variant COCA-CN 15 28377249 28377249 single base substitution C A missense_variant M4189I 12567G>T COCA-CN 15 28386847 28386847 single base substitution G A downstream_gene_variant COCA-CN 15 28386847 28386847 single base substitution G A intron_variant COCA-CN 15 28386852 28386852 single base substitution T G downstream_gene_variant COCA-CN 15 28386852 28386852 single base substitution T G intron_variant COCA-CN 15 28386977 28386977 single base substitution G A exon_variant COCA-CN 15 28386977 28386977 single base substitution G A missense_variant R3906C 11716C>T COCA-CN 15 28387475 28387475 single base substitution T G exon_variant COCA-CN 15 28387475 28387475 single base substitution T G missense_variant K3870T 11609A>C COCA-CN 15 28408229 28408229 single base substitution C A intron_variant COCA-CN 15 28413524 28413524 single base substitution A T intron_variant COCA-CN 15 28414709 28414709 single base substitution G T missense_variant L3384I 10150C>A COCA-CN 15 28414709 28414709 single base substitution G T missense_variant L41I 121C>A COCA-CN 15 28419526 28419526 single base substitution A G intron_variant COCA-CN 15 28419566 28419566 single base substitution T C synonymous_variant R1R 3A>G COCA-CN 15 28419566 28419566 single base substitution T C synonymous_variant R3344R 10032A>G COCA-CN 15 28419587 28419587 single base substitution G A synonymous_variant P3337P 10011C>T COCA-CN 15 28419587 28419587 single base substitution G A upstream_gene_variant COCA-CN 15 28419779 28419779 single base substitution A G intron_variant COCA-CN 15 28419779 28419779 single base substitution A G upstream_gene_variant COCA-CN 15 28419786 28419786 single base substitution A T intron_variant COCA-CN 15 28419786 28419786 single base substitution A T upstream_gene_variant COCA-CN 15 28424289 28424289 single base substitution T G splice_region_variant COCA-CN 15 28424289 28424289 single base substitution T G upstream_gene_variant COCA-CN 15 28436254 28436254 single base substitution T C intron_variant COCA-CN 15 28443908 28443908 single base substitution A G exon_variant COCA-CN 15 28443908 28443908 single base substitution A G missense_variant M2575T 7724T>C COCA-CN 15 28444005 28444005 single base substitution G T intron_variant COCA-CN 15 28447322 28447322 single base substitution C T exon_variant COCA-CN 15 28447322 28447322 single base substitution C T synonymous_variant T2518T 7554G>A COCA-CN 15 28447462 28447462 single base substitution T C intron_variant COCA-CN 15 28447463 28447463 single base substitution A G intron_variant COCA-CN 15 28447464 28447464 single base substitution C T intron_variant COCA-CN 15 28447562 28447562 single base substitution A G exon_variant COCA-CN 15 28447562 28447562 single base substitution A G missense_variant S2471P 7411T>C COCA-CN 15 28458947 28458947 single base substitution T C missense_variant T2243A 6727A>G COCA-CN 15 28459290 28459290 single base substitution T C missense_variant I2163V 6487A>G COCA-CN 15 28462095 28462095 single base substitution G A intron_variant COCA-CN 15 28483903 28483903 single base substitution C A missense_variant G1198V 3593G>T COCA-CN 15 28491953 28491953 single base substitution C T missense_variant S1109N 3326G>A COCA-CN 15 28492050 28492050 single base substitution G A splice_region_variant COCA-CN 15 28507991 28507991 single base substitution A C intron_variant COCA-CN 15 28510759 28510759 single base substitution C T splice_region_variant COCA-CN 15 28510961 28510961 single base substitution A G splice_donor_variant COCA-CN 15 28515869 28515869 single base substitution G A 3_prime_UTR_variant COCA-CN 15 28515869 28515869 single base substitution G A downstream_gene_variant COCA-CN 15 28515869 28515869 single base substitution G A missense_variant P410L 1229C>T COCA-CN 15 28517282 28517282 single base substitution T G exon_variant COCA-CN 15 28517282 28517282 single base substitution T G intron_variant COCA-CN 15 28517283 28517283 single base substitution G C exon_variant COCA-CN 15 28517283 28517283 single base substitution G C intron_variant COCA-CN 15 28517287 28517287 single base substitution T A exon_variant COCA-CN 15 28517287 28517287 single base substitution T A intron_variant COCA-CN 15 28517291 28517291 single base substitution T C exon_variant COCA-CN 15 28517291 28517291 single base substitution T C intron_variant COCA-CN 15 28517295 28517295 single base substitution A G exon_variant COCA-CN 15 28517295 28517295 single base substitution A G intron_variant COCA-CN 15 28517303 28517303 single base substitution T G exon_variant COCA-CN 15 28517303 28517303 single base substitution T G intron_variant COCA-CN 15 28517305 28517305 single base substitution T A exon_variant COCA-CN 15 28517305 28517305 single base substitution T A intron_variant COCA-CN 15 28517310 28517310 single base substitution G A exon_variant COCA-CN 15 28517310 28517310 single base substitution G A intron_variant COCA-CN 15 28517441 28517441 single base substitution C T 3_prime_UTR_variant COCA-CN 15 28517441 28517441 single base substitution C T exon_variant COCA-CN 15 28517441 28517441 single base substitution C T missense_variant A335T 1003G>A COCA-CN 15 28517454 28517454 single base substitution G T 3_prime_UTR_variant COCA-CN 15 28517454 28517454 single base substitution G T exon_variant COCA-CN 15 28517454 28517454 single base substitution G T synonymous_variant A330A 990C>A COCA-CN 15 28517512 28517512 single base substitution A G 3_prime_UTR_variant COCA-CN 15 28517512 28517512 single base substitution A G exon_variant COCA-CN 15 28517512 28517512 single base substitution A G missense_variant L311P 932T>C COCA-CN 15 28517539 28517539 single base substitution G A intron_variant COCA-CN 15 28517539 28517539 single base substitution G A splice_region_variant COCA-CN 15 28517546 28517546 single base substitution G C intron_variant COCA-CN 15 28517587 28517587 single base substitution C T intron_variant COCA-CN 15 28517588 28517588 single base substitution A G intron_variant COCA-CN 15 28517611 28517611 single base substitution T C intron_variant COCA-CN 15 28517616 28517616 single base substitution G A intron_variant COCA-CN 15 28517629 28517629 single base substitution C G intron_variant COCA-CN 15 28518126 28518126 single base substitution G A 3_prime_UTR_variant COCA-CN 15 28518126 28518126 single base substitution G A exon_variant COCA-CN 15 28518126 28518126 single base substitution G A synonymous_variant T275T 825C>T COCA-CN 15 28518130 28518130 single base substitution G C 3_prime_UTR_variant COCA-CN 15 28518130 28518130 single base substitution G C exon_variant COCA-CN 15 28518130 28518130 single base substitution G C missense_variant A274G 821C>G COCA-CN 15 28518135 28518135 single base substitution C T 3_prime_UTR_variant COCA-CN 15 28518135 28518135 single base substitution C T exon_variant COCA-CN 15 28518135 28518135 single base substitution C T synonymous_variant T272T 816G>A COCA-CN 15 28518136 28518136 single base substitution G A 3_prime_UTR_variant COCA-CN 15 28518136 28518136 single base substitution G A exon_variant COCA-CN 15 28518136 28518136 single base substitution G A missense_variant T272M 815C>T COCA-CN 15 28518162 28518162 single base substitution G A exon_variant COCA-CN 15 28518162 28518162 single base substitution G A intron_variant COCA-CN 15 28518179 28518179 single base substitution A G exon_variant COCA-CN 15 28518179 28518179 single base substitution A G intron_variant COCA-CN 15 28518184 28518184 single base substitution A G exon_variant COCA-CN 15 28518184 28518184 single base substitution A G intron_variant COCA-CN 15 28520090 28520090 single base substitution A G 3_prime_UTR_variant COCA-CN 15 28520090 28520090 single base substitution A G missense_variant S202P 604T>C COCA-CN 15 28520090 28520090 single base substitution A G upstream_gene_variant COCA-CN 15 28525246 28525246 single base substitution G A 3_prime_UTR_variant COCA-CN 15 28525246 28525246 single base substitution G A exon_variant COCA-CN 15 28525246 28525246 single base substitution G A synonymous_variant S170S 510C>T COCA-CN 15 28533868 28533868 single base substitution C T intron_variant COCA-CN 15 28539093 28539093 single base substitution G A intron_variant COCA-CN 15 28539094 28539094 single base substitution T C intron_variant COCA-CN 15 28539167 28539167 single base substitution C T intron_variant COCA-CN 15 28539211 28539211 single base substitution G T intron_variant COCA-CN 15 28560804 28560804 single base substitution G A downstream_gene_variant COCA-CN 15 28560804 28560804 single base substitution G A intron_variant COCA-CN 15 28570765 28570765 single base substitution C T upstream_gene_variant EOPC-DE 15 28362793 28362793 single base substitution C T exon_variant EOPC-DE 15 28362793 28362793 single base substitution C T intron_variant EOPC-DE 15 28362793 28362793 single base substitution C T upstream_gene_variant EOPC-DE 15 28378555 28378555 single base substitution A G intron_variant EOPC-DE 15 28394542 28394542 single base substitution C T downstream_gene_variant EOPC-DE 15 28394542 28394542 single base substitution C T intron_variant EOPC-DE 15 28394559 28394559 single base substitution A G downstream_gene_variant EOPC-DE 15 28394559 28394559 single base substitution A G intron_variant EOPC-DE 15 28394711 28394711 single base substitution G A downstream_gene_variant EOPC-DE 15 28394711 28394711 single base substitution G A intron_variant EOPC-DE 15 28394759 28394759 single base substitution A G downstream_gene_variant EOPC-DE 15 28394759 28394759 single base substitution A G intron_variant EOPC-DE 15 28517212 28517212 single base substitution C A exon_variant EOPC-DE 15 28517212 28517212 single base substitution C A intron_variant EOPC-DE 15 28523486 28523486 single base substitution C T downstream_gene_variant EOPC-DE 15 28523486 28523486 single base substitution C T intron_variant EOPC-DE 15 28536470 28536470 single base substitution A C intron_variant ESAD-UK 15 28351871 28351871 single base substitution G A downstream_gene_variant ESAD-UK 15 28352730 28352730 single base substitution T C downstream_gene_variant ESAD-UK 15 28354422 28354422 single base substitution C G downstream_gene_variant ESAD-UK 15 28357790 28357790 single base substitution G A downstream_gene_variant ESAD-UK 15 28357790 28357790 single base substitution G A intron_variant ESAD-UK 15 28358598 28358598 single base substitution C A downstream_gene_variant ESAD-UK 15 28358598 28358598 single base substitution C A intron_variant ESAD-UK 15 28359037 28359037 single base substitution C G downstream_gene_variant ESAD-UK 15 28359037 28359037 single base substitution C G intron_variant ESAD-UK 15 28359037 28359037 single base substitution C G upstream_gene_variant ESAD-UK 15 28361175 28361175 single base substitution G C intron_variant ESAD-UK 15 28361175 28361175 single base substitution G C upstream_gene_variant ESAD-UK 15 28364208 28364208 single base substitution G A intron_variant ESAD-UK 15 28364208 28364208 single base substitution G A upstream_gene_variant ESAD-UK 15 28365515 28365515 single base substitution T A intron_variant ESAD-UK 15 28365515 28365515 single base substitution T A upstream_gene_variant ESAD-UK 15 28369419 28369419 single base substitution A G intron_variant ESAD-UK 15 28371399 28371401 deletion of <=200bp AAC - intron_variant ESAD-UK 15 28373350 28373355 deletion of <=200bp AGTGTC - intron_variant ESAD-UK 15 28374119 28374119 single base substitution C T intron_variant ESAD-UK 15 28376919 28376919 single base substitution T A intron_variant ESAD-UK 15 28377805 28377805 single base substitution C T synonymous_variant P4134P 12402G>A ESAD-UK 15 28379078 28379078 single base substitution T A intron_variant ESAD-UK 15 28379812 28379812 single base substitution G C intron_variant ESAD-UK 15 28379956 28379956 single base substitution A G intron_variant ESAD-UK 15 28380414 28380414 deletion of <=200bp T - intron_variant ESAD-UK 15 28381648 28381648 single base substitution C T intron_variant ESAD-UK 15 28387678 28387678 single base substitution G A intron_variant ESAD-UK 15 28387678 28387678 single base substitution G A upstream_gene_variant ESAD-UK 15 28388144 28388144 single base substitution G A intron_variant ESAD-UK 15 28388144 28388144 single base substitution G A upstream_gene_variant ESAD-UK 15 28388385 28388385 single base substitution G A intron_variant ESAD-UK 15 28388385 28388385 single base substitution G A upstream_gene_variant ESAD-UK 15 28388881 28388881 single base substitution C T intron_variant ESAD-UK 15 28388881 28388881 single base substitution C T upstream_gene_variant ESAD-UK 15 28389329 28389329 single base substitution G C missense_variant D3731E 11193C>G ESAD-UK 15 28389329 28389329 single base substitution G C upstream_gene_variant ESAD-UK 15 28395020 28395020 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 28395020 28395020 deletion of <=200bp A - intron_variant ESAD-UK 15 28395906 28395906 single base substitution G A downstream_gene_variant ESAD-UK 15 28395906 28395906 single base substitution G A intron_variant ESAD-UK 15 28398314 28398314 single base substitution A G intron_variant ESAD-UK 15 28401361 28401361 single base substitution C G intron_variant ESAD-UK 15 28402211 28402211 single base substitution T G intron_variant ESAD-UK 15 28405590 28405590 deletion of <=200bp C - intron_variant ESAD-UK 15 28406019 28406019 single base substitution A T intron_variant ESAD-UK 15 28406096 28406096 single base substitution G A intron_variant ESAD-UK 15 28406189 28406189 single base substitution A G intron_variant ESAD-UK 15 28406285 28406285 single base substitution C T intron_variant ESAD-UK 15 28407344 28407344 single base substitution C T intron_variant ESAD-UK 15 28407669 28407669 insertion of <=200bp - T intron_variant ESAD-UK 15 28408766 28408766 single base substitution C T intron_variant ESAD-UK 15 28410999 28410999 single base substitution C T intron_variant ESAD-UK 15 28411375 28411375 single base substitution G A intron_variant ESAD-UK 15 28414556 28414556 single base substitution C T intron_variant ESAD-UK 15 28414763 28414763 single base substitution T C missense_variant K23E 67A>G ESAD-UK 15 28414763 28414763 single base substitution T C missense_variant K3366E 10096A>G ESAD-UK 15 28414964 28414964 single base substitution A C intron_variant ESAD-UK 15 28416788 28416788 single base substitution A T intron_variant ESAD-UK 15 28417273 28417273 single base substitution G C intron_variant ESAD-UK 15 28418192 28418192 single base substitution A T intron_variant ESAD-UK 15 28418193 28418193 single base substitution G A intron_variant ESAD-UK 15 28418235 28418235 single base substitution G A intron_variant ESAD-UK 15 28418712 28418712 single base substitution A C intron_variant ESAD-UK 15 28421491 28421491 single base substitution C T intron_variant ESAD-UK 15 28421491 28421491 single base substitution C T upstream_gene_variant ESAD-UK 15 28421858 28421858 single base substitution C T synonymous_variant A3163A 9489G>A ESAD-UK 15 28421858 28421858 single base substitution C T upstream_gene_variant ESAD-UK 15 28421950 28421950 single base substitution C A intron_variant ESAD-UK 15 28421950 28421950 single base substitution C A upstream_gene_variant ESAD-UK 15 28424075 28424075 single base substitution C T missense_variant A3041T 9121G>A ESAD-UK 15 28424075 28424075 single base substitution C T upstream_gene_variant ESAD-UK 15 28424099 28424099 single base substitution C G missense_variant V3033L 9097G>C ESAD-UK 15 28424099 28424099 single base substitution C G upstream_gene_variant ESAD-UK 15 28428102 28428102 single base substitution G A intron_variant ESAD-UK 15 28428103 28428103 single base substitution C A intron_variant ESAD-UK 15 28430899 28430899 single base substitution C T downstream_gene_variant ESAD-UK 15 28430899 28430899 single base substitution C T intron_variant ESAD-UK 15 28431605 28431605 single base substitution T C downstream_gene_variant ESAD-UK 15 28431605 28431605 single base substitution T C intron_variant ESAD-UK 15 28432331 28432331 single base substitution A G downstream_gene_variant ESAD-UK 15 28432331 28432331 single base substitution A G intron_variant ESAD-UK 15 28434985 28434985 single base substitution T A downstream_gene_variant ESAD-UK 15 28434985 28434985 single base substitution T A intron_variant ESAD-UK 15 28436053 28436053 single base substitution A G exon_variant ESAD-UK 15 28436053 28436053 single base substitution A G intron_variant ESAD-UK 15 28436650 28436650 single base substitution A C intron_variant ESAD-UK 15 28437668 28437668 single base substitution C A intron_variant ESAD-UK 15 28438699 28438699 single base substitution G T intron_variant ESAD-UK 15 28440288 28440288 single base substitution G C intron_variant ESAD-UK 15 28441231 28441231 single base substitution C T intron_variant ESAD-UK 15 28442469 28442469 single base substitution C G intron_variant ESAD-UK 15 28443347 28443347 insertion of <=200bp - TC intron_variant ESAD-UK 15 28444104 28444104 single base substitution G C intron_variant ESAD-UK 15 28446533 28446533 single base substitution T C intron_variant ESAD-UK 15 28449510 28449510 single base substitution G C intron_variant ESAD-UK 15 28449510 28449510 single base substitution G C upstream_gene_variant ESAD-UK 15 28454242 28454242 single base substitution T A intron_variant ESAD-UK 15 28455401 28455401 single base substitution T A intron_variant ESAD-UK 15 28455608 28455608 single base substitution T C intron_variant ESAD-UK 15 28458045 28458045 insertion of <=200bp - A intron_variant ESAD-UK 15 28458941 28458941 single base substitution G A stop_gained Q2245* 6733C>T ESAD-UK 15 28459069 28459069 deletion of <=200bp C - frameshift_variant G2202 ESAD-UK 15 28459137 28459137 single base substitution C T intron_variant ESAD-UK 15 28459391 28459391 single base substitution C T missense_variant R2129H 6386G>A ESAD-UK 15 28459497 28459497 single base substitution A C intron_variant ESAD-UK 15 28459728 28459728 single base substitution A C intron_variant ESAD-UK 15 28460168 28460168 single base substitution C G intron_variant ESAD-UK 15 28462414 28462414 single base substitution G A downstream_gene_variant ESAD-UK 15 28462414 28462414 single base substitution G A intron_variant ESAD-UK 15 28463159 28463159 single base substitution A T downstream_gene_variant ESAD-UK 15 28463159 28463159 single base substitution A T intron_variant ESAD-UK 15 28467280 28467280 single base substitution T A downstream_gene_variant ESAD-UK 15 28467280 28467280 single base substitution T A missense_variant K1849M 5546A>T ESAD-UK 15 28468043 28468043 single base substitution G A intron_variant ESAD-UK 15 28468508 28468508 single base substitution G A intron_variant ESAD-UK 15 28468570 28468570 single base substitution A G intron_variant ESAD-UK 15 28469313 28469313 insertion of <=200bp - ACACACACACAG intron_variant ESAD-UK 15 28472823 28472823 single base substitution C G intron_variant ESAD-UK 15 28473812 28473812 single base substitution T C intron_variant ESAD-UK 15 28480470 28480470 single base substitution G A intron_variant ESAD-UK 15 28480880 28480880 single base substitution T C intron_variant ESAD-UK 15 28481458 28481458 single base substitution C T intron_variant ESAD-UK 15 28482472 28482472 single base substitution A G intron_variant ESAD-UK 15 28483285 28483285 single base substitution G A missense_variant A1276V 3827C>T ESAD-UK 15 28484533 28484533 single base substitution C T intron_variant ESAD-UK 15 28485098 28485098 deletion of <=200bp A - intron_variant ESAD-UK 15 28485263 28485263 single base substitution A C intron_variant ESAD-UK 15 28485283 28485283 single base substitution C T intron_variant ESAD-UK 15 28488230 28488230 single base substitution G C intron_variant ESAD-UK 15 28488718 28488718 single base substitution T A intron_variant ESAD-UK 15 28492234 28492234 single base substitution C T intron_variant ESAD-UK 15 28494150 28494150 single base substitution C T intron_variant ESAD-UK 15 28494863 28494863 single base substitution G A downstream_gene_variant ESAD-UK 15 28494863 28494863 single base substitution G A intron_variant ESAD-UK 15 28495097 28495097 single base substitution G A downstream_gene_variant ESAD-UK 15 28495097 28495097 single base substitution G A intron_variant ESAD-UK 15 28496689 28496689 single base substitution G A downstream_gene_variant ESAD-UK 15 28496689 28496689 single base substitution G A intron_variant ESAD-UK 15 28498738 28498738 single base substitution C T downstream_gene_variant ESAD-UK 15 28498738 28498738 single base substitution C T intron_variant ESAD-UK 15 28498951 28498951 insertion of <=200bp - G downstream_gene_variant ESAD-UK 15 28498951 28498951 insertion of <=200bp - G intron_variant ESAD-UK 15 28499023 28499023 single base substitution G A downstream_gene_variant ESAD-UK 15 28499023 28499023 single base substitution G A intron_variant ESAD-UK 15 28499169 28499169 single base substitution C A downstream_gene_variant ESAD-UK 15 28499169 28499169 single base substitution C A intron_variant ESAD-UK 15 28499443 28499443 single base substitution G A downstream_gene_variant ESAD-UK 15 28499443 28499443 single base substitution G A intron_variant ESAD-UK 15 28499450 28499450 single base substitution A C downstream_gene_variant ESAD-UK 15 28499450 28499450 single base substitution A C intron_variant ESAD-UK 15 28499557 28499557 single base substitution A T downstream_gene_variant ESAD-UK 15 28499557 28499557 single base substitution A T synonymous_variant I993I 2979T>A ESAD-UK 15 28500732 28500732 single base substitution G A intron_variant ESAD-UK 15 28502190 28502190 single base substitution A C intron_variant ESAD-UK 15 28502533 28502533 single base substitution G C intron_variant ESAD-UK 15 28503778 28503778 deletion of <=200bp A - intron_variant ESAD-UK 15 28505298 28505298 single base substitution C A intron_variant ESAD-UK 15 28505956 28505956 single base substitution T C 3_prime_UTR_variant ESAD-UK 15 28505956 28505956 single base substitution T C synonymous_variant K761K 2283A>G ESAD-UK 15 28507357 28507357 single base substitution G A intron_variant ESAD-UK 15 28507791 28507791 single base substitution T G intron_variant ESAD-UK 15 28508362 28508362 single base substitution C T intron_variant ESAD-UK 15 28508425 28508425 single base substitution G C intron_variant ESAD-UK 15 28511190 28511202 deletion of <=200bp GAAATTCACTATC - intron_variant ESAD-UK 15 28511780 28511780 single base substitution C G intron_variant ESAD-UK 15 28512705 28512705 single base substitution A G downstream_gene_variant ESAD-UK 15 28512705 28512705 single base substitution A G intron_variant ESAD-UK 15 28514628 28514628 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 28514628 28514628 deletion of <=200bp A - intron_variant ESAD-UK 15 28516918 28516918 single base substitution G C downstream_gene_variant ESAD-UK 15 28516918 28516918 single base substitution G C intron_variant ESAD-UK 15 28518530 28518530 single base substitution A G intron_variant ESAD-UK 15 28518530 28518530 single base substitution A G upstream_gene_variant ESAD-UK 15 28520516 28520516 single base substitution G A downstream_gene_variant ESAD-UK 15 28520516 28520516 single base substitution G A intron_variant ESAD-UK 15 28520516 28520516 single base substitution G A upstream_gene_variant ESAD-UK 15 28528260 28528260 single base substitution G A intron_variant ESAD-UK 15 28529457 28529457 single base substitution G C intron_variant ESAD-UK 15 28529537 28529537 single base substitution G A intron_variant ESAD-UK 15 28530215 28530215 single base substitution G A intron_variant ESAD-UK 15 28532194 28532194 single base substitution C T intron_variant ESAD-UK 15 28534976 28534976 single base substitution G A intron_variant ESAD-UK 15 28537620 28537620 single base substitution A G intron_variant ESAD-UK 15 28537717 28537717 single base substitution C A intron_variant ESAD-UK 15 28540692 28540692 single base substitution G A intron_variant ESAD-UK 15 28542225 28542225 single base substitution C T intron_variant ESAD-UK 15 28548696 28548696 single base substitution C A intron_variant ESAD-UK 15 28548696 28548696 single base substitution C A upstream_gene_variant ESAD-UK 15 28552699 28552699 single base substitution A T intron_variant ESAD-UK 15 28552738 28552738 single base substitution T C intron_variant ESAD-UK 15 28553445 28553445 single base substitution A G intron_variant ESAD-UK 15 28553552 28553552 single base substitution A G intron_variant ESAD-UK 15 28554404 28554404 single base substitution G A intron_variant ESAD-UK 15 28555598 28555598 single base substitution T A intron_variant ESAD-UK 15 28560734 28560734 single base substitution T A downstream_gene_variant ESAD-UK 15 28560734 28560734 single base substitution T A intron_variant ESAD-UK 15 28561654 28561654 single base substitution C T downstream_gene_variant ESAD-UK 15 28561654 28561654 single base substitution C T intron_variant ESAD-UK 15 28561934 28561934 insertion of <=200bp - T downstream_gene_variant ESAD-UK 15 28561934 28561934 insertion of <=200bp - T intron_variant ESAD-UK 15 28566663 28566663 single base substitution G A intron_variant ESCA-CN 15 28356878 28356878 single base substitution G A 3_prime_UTR_variant ESCA-CN 15 28356878 28356878 single base substitution G A downstream_gene_variant ESCA-CN 15 28356878 28356878 single base substitution G A exon_variant ESCA-CN 15 28370389 28370389 single base substitution C T intron_variant ESCA-CN 15 28414729 28414729 single base substitution C T missense_variant R3377H 10130G>A ESCA-CN 15 28414729 28414729 single base substitution C T missense_variant R34H 101G>A ESCA-CN 15 28424070 28424070 single base substitution G C synonymous_variant L3042L 9126C>G ESCA-CN 15 28424070 28424070 single base substitution G C upstream_gene_variant ESCA-CN 15 28458991 28458991 single base substitution A C missense_variant F2228C 6683T>G ESCA-CN 15 28459497 28459497 single base substitution A G intron_variant ESCA-CN 15 28459551 28459551 single base substitution G C intron_variant ESCA-CN 15 28465967 28465967 single base substitution C G downstream_gene_variant ESCA-CN 15 28465967 28465967 single base substitution C G intron_variant ESCA-CN 15 28474358 28474358 single base substitution G A exon_variant ESCA-CN 15 28474358 28474358 single base substitution G A missense_variant A1752V 5255C>T ESCA-CN 15 28514398 28514398 single base substitution G A 3_prime_UTR_variant ESCA-CN 15 28514398 28514398 single base substitution G A downstream_gene_variant ESCA-CN 15 28514398 28514398 single base substitution G A missense_variant T481M 1442C>T ESCA-CN 15 28515848 28515848 single base substitution G A 3_prime_UTR_variant ESCA-CN 15 28515848 28515848 single base substitution G A downstream_gene_variant ESCA-CN 15 28515848 28515848 single base substitution G A missense_variant S417F 1250C>T GBM-US 15 28389261 28389261 single base substitution G A missense_variant A3754V 11261C>T GBM-US 15 28389261 28389261 single base substitution G A upstream_gene_variant GBM-US 15 28421858 28421858 single base substitution C T synonymous_variant A3163A 9489G>A GBM-US 15 28421858 28421858 single base substitution C T upstream_gene_variant GBM-US 15 28460793 28460793 single base substitution A G missense_variant F2062L 6184T>C GBM-US 15 28474893 28474893 single base substitution C A missense_variant S1637I 4910G>T GBM-US 15 28474893 28474893 single base substitution C A upstream_gene_variant GBM-US 15 28514552 28514552 insertion of <=200bp - C 3_prime_UTR_variant GBM-US 15 28514552 28514552 insertion of <=200bp - C downstream_gene_variant GBM-US 15 28514552 28514552 insertion of <=200bp - C frameshift_variant L430C? GBM-US 15 28518115 28518115 deletion of <=200bp C - 3_prime_UTR_variant GBM-US 15 28518115 28518115 deletion of <=200bp C - exon_variant GBM-US 15 28518115 28518115 deletion of <=200bp C - frameshift_variant G279 KIRC-US 15 28366558 28366558 single base substitution T G missense_variant K4402N 13206A>C KIRC-US 15 28366558 28366558 single base substitution T G upstream_gene_variant KIRC-US 15 28387457 28387457 single base substitution C A exon_variant KIRC-US 15 28387457 28387457 single base substitution C A missense_variant R3876M 11627G>T KIRC-US 15 28414709 28414709 single base substitution G C missense_variant L3384V 10150C>G KIRC-US 15 28414709 28414709 single base substitution G C missense_variant L41V 121C>G KIRC-US 15 28414719 28414719 single base substitution A G synonymous_variant L3380L 10140T>C KIRC-US 15 28414719 28414719 single base substitution A G synonymous_variant L37L 111T>C KIRC-US 15 28420762 28420762 single base substitution C G missense_variant V3243L 9727G>C KIRC-US 15 28420762 28420762 single base substitution C G upstream_gene_variant KIRC-US 15 28436294 28436294 single base substitution C A exon_variant KIRC-US 15 28436294 28436294 single base substitution C A missense_variant V2850L 8548G>T KIRC-US 15 28446698 28446698 single base substitution A G splice_region_variant KIRC-US 15 28473477 28473477 single base substitution C A exon_variant KIRC-US 15 28473477 28473477 single base substitution C A missense_variant R1784L 5351G>T KIRC-US 15 28499508 28499508 single base substitution G C downstream_gene_variant KIRC-US 15 28499508 28499508 single base substitution G C missense_variant Q1010E 3028C>G KIRC-US 15 28501377 28501377 single base substitution C T 3_prime_UTR_variant KIRC-US 15 28501377 28501377 single base substitution C T synonymous_variant T868T 2604G>A KIRC-US 15 28515959 28515959 single base substitution G A 3_prime_UTR_variant KIRC-US 15 28515959 28515959 single base substitution G A downstream_gene_variant KIRC-US 15 28515959 28515959 single base substitution G A missense_variant P380L 1139C>T KIRP-US 15 28370205 28370205 single base substitution T G missense_variant T4313P 12937A>C KIRP-US 15 28431846 28431846 single base substitution T A downstream_gene_variant KIRP-US 15 28431846 28431846 single base substitution T A missense_variant D2901V 8702A>T KIRP-US 15 28437274 28437274 single base substitution G C exon_variant KIRP-US 15 28437274 28437274 single base substitution G C missense_variant R2762G 8284C>G KIRP-US 15 28460930 28460930 single base substitution A C missense_variant V2016G 6047T>G KIRP-US 15 28510872 28510872 single base substitution T A 3_prime_UTR_variant KIRP-US 15 28510872 28510872 single base substitution T A missense_variant S588C 1762A>T LAML-KR 15 28374944 28374944 single base substitution G T intron_variant LAML-KR 15 28394691 28394691 single base substitution G A downstream_gene_variant LAML-KR 15 28394691 28394691 single base substitution G A intron_variant LAML-KR 15 28414940 28414940 single base substitution T C intron_variant LAML-KR 15 28419526 28419526 single base substitution A G intron_variant LAML-KR 15 28419853 28419853 single base substitution C T intron_variant LAML-KR 15 28419853 28419853 single base substitution C T upstream_gene_variant LAML-KR 15 28419862 28419862 single base substitution C T intron_variant LAML-KR 15 28419862 28419862 single base substitution C T upstream_gene_variant LAML-KR 15 28419864 28419864 single base substitution G A intron_variant LAML-KR 15 28419864 28419864 single base substitution G A upstream_gene_variant LAML-KR 15 28437061 28437061 single base substitution A G intron_variant LAML-KR 15 28447282 28447282 single base substitution C T exon_variant LAML-KR 15 28447282 28447282 single base substitution C T missense_variant V2532M 7594G>A LAML-KR 15 28447283 28447283 single base substitution G A exon_variant LAML-KR 15 28447283 28447283 single base substitution G A synonymous_variant D2531D 7593C>T LAML-KR 15 28447322 28447322 single base substitution C T exon_variant LAML-KR 15 28447322 28447322 single base substitution C T synonymous_variant T2518T 7554G>A LAML-KR 15 28447562 28447562 single base substitution A G exon_variant LAML-KR 15 28447562 28447562 single base substitution A G missense_variant S2471P 7411T>C LAML-KR 15 28451276 28451276 single base substitution T C intron_variant LAML-KR 15 28451276 28451276 single base substitution T C upstream_gene_variant LAML-KR 15 28455917 28455917 single base substitution G A intron_variant LAML-KR 15 28456220 28456220 single base substitution G A missense_variant L2333F 6997C>T LAML-KR 15 28457540 28457540 single base substitution G C intron_variant LAML-KR 15 28465959 28465959 single base substitution A G downstream_gene_variant LAML-KR 15 28465959 28465959 single base substitution A G intron_variant LAML-KR 15 28466021 28466021 single base substitution C G downstream_gene_variant LAML-KR 15 28466021 28466021 single base substitution C G intron_variant LAML-KR 15 28466044 28466044 single base substitution A G downstream_gene_variant LAML-KR 15 28466044 28466044 single base substitution A G intron_variant LAML-KR 15 28466152 28466152 single base substitution G A downstream_gene_variant LAML-KR 15 28466152 28466152 single base substitution G A intron_variant LAML-KR 15 28467246 28467246 single base substitution T C downstream_gene_variant LAML-KR 15 28467246 28467246 single base substitution T C synonymous_variant G1860G 5580A>G LAML-KR 15 28470862 28470862 single base substitution G A intron_variant LAML-KR 15 28473291 28473291 single base substitution G A intron_variant LAML-KR 15 28473296 28473296 single base substitution G A intron_variant LAML-KR 15 28475806 28475806 single base substitution A G intron_variant LAML-KR 15 28475806 28475806 single base substitution A G upstream_gene_variant LAML-KR 15 28479308 28479308 single base substitution G A stop_gained R1376* 4126C>T LAML-KR 15 28479308 28479308 single base substitution G A upstream_gene_variant LAML-KR 15 28483416 28483416 single base substitution G A intron_variant LAML-KR 15 28483655 28483655 single base substitution A G intron_variant LAML-KR 15 28483865 28483865 single base substitution G A missense_variant R1211C 3631C>T LAML-KR 15 28483903 28483903 single base substitution C A missense_variant G1198V 3593G>T LAML-KR 15 28509151 28509151 single base substitution C A intron_variant LAML-KR 15 28517310 28517310 single base substitution G A exon_variant LAML-KR 15 28517310 28517310 single base substitution G A intron_variant LAML-KR 15 28517436 28517436 single base substitution T C 3_prime_UTR_variant LAML-KR 15 28517436 28517436 single base substitution T C exon_variant LAML-KR 15 28517436 28517436 single base substitution T C synonymous_variant P336P 1008A>G LAML-KR 15 28517454 28517454 single base substitution G T 3_prime_UTR_variant LAML-KR 15 28517454 28517454 single base substitution G T exon_variant LAML-KR 15 28517454 28517454 single base substitution G T synonymous_variant A330A 990C>A LAML-KR 15 28517539 28517539 single base substitution G A intron_variant LAML-KR 15 28517539 28517539 single base substitution G A splice_region_variant LAML-KR 15 28517546 28517546 single base substitution G C intron_variant LAML-KR 15 28517577 28517577 single base substitution C T intron_variant LAML-KR 15 28543341 28543341 single base substitution C T intron_variant LAML-KR 15 28548013 28548013 single base substitution T C intron_variant LAML-KR 15 28548013 28548013 single base substitution T C upstream_gene_variant LAML-KR 15 28548021 28548021 single base substitution G T intron_variant LAML-KR 15 28548021 28548021 single base substitution G T upstream_gene_variant LAML-KR 15 28566630 28566630 single base substitution C T intron_variant LAML-KR 15 28567867 28567867 single base substitution G A upstream_gene_variant LAML-KR 15 28568057 28568057 single base substitution C T upstream_gene_variant LAML-KR 15 28570264 28570264 single base substitution T G upstream_gene_variant LAML-KR 15 28570516 28570516 single base substitution T G upstream_gene_variant LAML-KR 15 28570815 28570815 single base substitution A T upstream_gene_variant LAML-KR 15 28570852 28570852 single base substitution C T upstream_gene_variant LAML-KR 15 28570853 28570853 single base substitution G A upstream_gene_variant LGG-US 15 28389059 28389059 single base substitution T C missense_variant N3793S 11378A>G LGG-US 15 28389059 28389059 single base substitution T C upstream_gene_variant LGG-US 15 28460828 28460828 single base substitution G A missense_variant T2050M 6149C>T LGG-US 15 28473408 28473408 single base substitution T C exon_variant LGG-US 15 28473408 28473408 single base substitution T C missense_variant N1807S 5420A>G LGG-US 15 28491947 28491947 single base substitution G A missense_variant A1111V 3332C>T LIAD-FR 15 28460863 28460863 single base substitution C T synonymous_variant Q2038Q 6114G>A LICA-CN 15 28387531 28387531 single base substitution T A exon_variant LICA-CN 15 28387531 28387531 single base substitution T A synonymous_variant V3851V 11553A>T LICA-CN 15 28427558 28427558 single base substitution T A stop_gained K2976* 8926A>T LICA-CN 15 28436348 28436348 single base substitution T A exon_variant LICA-CN 15 28436348 28436348 single base substitution T A stop_gained R2832* 8494A>T LICA-CN 15 28463803 28463803 single base substitution C T downstream_gene_variant LICA-CN 15 28463803 28463803 single base substitution C T missense_variant E1954K 5860G>A LICA-CN 15 28491060 28491060 single base substitution C A missense_variant D1182Y 3544G>T LICA-CN 15 28499541 28499541 single base substitution C T downstream_gene_variant LICA-CN 15 28499541 28499541 single base substitution C T missense_variant E999K 2995G>A LICA-CN 15 28511038 28511038 single base substitution T C 3_prime_UTR_variant LICA-CN 15 28511038 28511038 single base substitution T C missense_variant T561A 1681A>G LICA-CN 15 28519538 28519538 single base substitution T A 3_prime_UTR_variant LICA-CN 15 28519538 28519538 single base substitution T A synonymous_variant R233R 699A>T LICA-CN 15 28519538 28519538 single base substitution T A upstream_gene_variant LICA-FR 15 28354059 28354059 single base substitution C T downstream_gene_variant LICA-FR 15 28354848 28354848 single base substitution A G downstream_gene_variant LICA-FR 15 28369096 28369096 single base substitution T C intron_variant LICA-FR 15 28377262 28377262 single base substitution C T missense_variant C4185Y 12554G>A LICA-FR 15 28386655 28386655 single base substitution C A downstream_gene_variant LICA-FR 15 28386655 28386655 single base substitution C A stop_gained E3980* 11938G>T LICA-FR 15 28389034 28389034 single base substitution C G synonymous_variant G3801G 11403G>C LICA-FR 15 28389034 28389034 single base substitution C G upstream_gene_variant LICA-FR 15 28392356 28392356 single base substitution A G intron_variant LICA-FR 15 28392356 28392356 single base substitution A G upstream_gene_variant LICA-FR 15 28395494 28395494 single base substitution A C downstream_gene_variant LICA-FR 15 28395494 28395494 single base substitution A C intron_variant LICA-FR 15 28396080 28396080 single base substitution C A downstream_gene_variant LICA-FR 15 28396080 28396080 single base substitution C A intron_variant LICA-FR 15 28396201 28396201 single base substitution T C downstream_gene_variant LICA-FR 15 28396201 28396201 single base substitution T C intron_variant LICA-FR 15 28397926 28397926 single base substitution G A synonymous_variant A192A 576C>T LICA-FR 15 28397926 28397926 single base substitution G A synonymous_variant A3599A 10797C>T LICA-FR 15 28402894 28402894 single base substitution T A intron_variant LICA-FR 15 28404064 28404064 single base substitution T C intron_variant LICA-FR 15 28414680 28414680 single base substitution T C synonymous_variant K3393K 10179A>G LICA-FR 15 28414680 28414680 single base substitution T C synonymous_variant K50K 150A>G LICA-FR 15 28424169 28424169 single base substitution C A synonymous_variant V3009V 9027G>T LICA-FR 15 28424169 28424169 single base substitution C A upstream_gene_variant LICA-FR 15 28427562 28427562 single base substitution C T synonymous_variant G2974G 8922G>A LICA-FR 15 28435158 28435158 insertion of <=200bp - T downstream_gene_variant LICA-FR 15 28435158 28435158 insertion of <=200bp - T intron_variant LICA-FR 15 28447282 28447282 single base substitution C T exon_variant LICA-FR 15 28447282 28447282 single base substitution C T missense_variant V2532M 7594G>A LICA-FR 15 28455086 28455086 single base substitution C T intron_variant LICA-FR 15 28456036 28456036 single base substitution C T intron_variant LICA-FR 15 28460347 28460347 single base substitution C T intron_variant LICA-FR 15 28460387 28460387 single base substitution C T intron_variant LICA-FR 15 28462059 28462059 single base substitution C T intron_variant LICA-FR 15 28462120 28462120 single base substitution C A intron_variant LICA-FR 15 28462241 28462241 single base substitution C T intron_variant LICA-FR 15 28470862 28470862 single base substitution G A intron_variant LICA-FR 15 28470866 28470866 single base substitution G A intron_variant LICA-FR 15 28473501 28473501 single base substitution C T exon_variant LICA-FR 15 28473501 28473501 single base substitution C T missense_variant S1776N 5327G>A LICA-FR 15 28474349 28474349 single base substitution T C exon_variant LICA-FR 15 28474349 28474349 single base substitution T C missense_variant K1755R 5264A>G LICA-FR 15 28483894 28483894 single base substitution C A missense_variant C1201F 3602G>T LICA-FR 15 28495044 28495044 single base substitution A C downstream_gene_variant LICA-FR 15 28495044 28495044 single base substitution A C intron_variant LICA-FR 15 28517430 28517430 single base substitution C G 3_prime_UTR_variant LICA-FR 15 28517430 28517430 single base substitution C G exon_variant LICA-FR 15 28517430 28517430 single base substitution C G missense_variant L338F 1014G>C LICA-FR 15 28517454 28517454 single base substitution G T 3_prime_UTR_variant LICA-FR 15 28517454 28517454 single base substitution G T exon_variant LICA-FR 15 28517454 28517454 single base substitution G T synonymous_variant A330A 990C>A LICA-FR 15 28517492 28517492 single base substitution C A 3_prime_UTR_variant LICA-FR 15 28517492 28517492 single base substitution C A exon_variant LICA-FR 15 28517492 28517492 single base substitution C A missense_variant D318Y 952G>T LICA-FR 15 28520137 28520137 single base substitution C A 3_prime_UTR_variant LICA-FR 15 28520137 28520137 single base substitution C A missense_variant G186V 557G>T LICA-FR 15 28520137 28520137 single base substitution C A upstream_gene_variant LICA-FR 15 28533682 28533682 deletion of <=200bp A - intron_variant LICA-FR 15 28533868 28533868 single base substitution C T intron_variant LICA-FR 15 28535012 28535012 single base substitution A C intron_variant LICA-FR 15 28539093 28539093 single base substitution G A intron_variant LICA-FR 15 28539167 28539167 single base substitution C T intron_variant LICA-FR 15 28539196 28539196 single base substitution C G intron_variant LICA-FR 15 28539211 28539211 single base substitution G T intron_variant LICA-FR 15 28558272 28558272 single base substitution C T intron_variant LICA-FR 15 28558468 28558468 single base substitution C T intron_variant LICA-FR 15 28561473 28561473 single base substitution C T downstream_gene_variant LICA-FR 15 28561473 28561473 single base substitution C T intron_variant LICA-FR 15 28564688 28564688 single base substitution G A downstream_gene_variant LICA-FR 15 28564688 28564688 single base substitution G A intron_variant LICA-FR 15 28572215 28572215 single base substitution A G upstream_gene_variant LIHC-US 15 28377352 28377352 single base substitution G A missense_variant A4155V 12464C>T LIHC-US 15 28386583 28386583 single base substitution C T downstream_gene_variant LIHC-US 15 28386583 28386583 single base substitution C T missense_variant G4004R 12010G>A LIHC-US 15 28419597 28419597 single base substitution A C missense_variant V3334G 10001T>G LIHC-US 15 28419597 28419597 single base substitution A C upstream_gene_variant LIHC-US 15 28421656 28421656 single base substitution G C missense_variant L3202V 9604C>G LIHC-US 15 28421656 28421656 single base substitution G C upstream_gene_variant LIHC-US 15 28422626 28422626 single base substitution C A missense_variant D3065Y 9193G>T LIHC-US 15 28422626 28422626 single base substitution C A upstream_gene_variant LIHC-US 15 28427625 28427625 single base substitution T C synonymous_variant S2953S 8859A>G LIHC-US 15 28446674 28446674 single base substitution G C exon_variant LIHC-US 15 28446674 28446674 single base substitution G C missense_variant S2548R 7644C>G LIHC-US 15 28457606 28457606 single base substitution T A stop_gained K2304* 6910A>T LIHC-US 15 28460799 28460799 single base substitution C G missense_variant A2060P 6178G>C LIHC-US 15 28465614 28465614 single base substitution G T downstream_gene_variant LIHC-US 15 28465614 28465614 single base substitution G T missense_variant D1943E 5829C>A LIHC-US 15 28482110 28482110 single base substitution G A splice_region_variant LIHC-US 15 28491165 28491165 single base substitution T C missense_variant K1147E 3439A>G LIHC-US 15 28493786 28493786 single base substitution A G synonymous_variant A1049A 3147T>C LIHC-US 15 28518063 28518063 single base substitution C A 3_prime_UTR_variant LIHC-US 15 28518063 28518063 single base substitution C A exon_variant LIHC-US 15 28518063 28518063 single base substitution C A synonymous_variant L296L 888G>T LINC-JP 15 28356296 28356296 single base substitution A C 3_prime_UTR_variant LINC-JP 15 28356296 28356296 single base substitution A C downstream_gene_variant LINC-JP 15 28360053 28360053 single base substitution T G downstream_gene_variant LINC-JP 15 28360053 28360053 single base substitution T G intron_variant LINC-JP 15 28360053 28360053 single base substitution T G upstream_gene_variant LINC-JP 15 28360592 28360592 single base substitution T C exon_variant LINC-JP 15 28360592 28360592 single base substitution T C missense_variant I4569V 13705A>G LINC-JP 15 28360592 28360592 single base substitution T C upstream_gene_variant LINC-JP 15 28362528 28362528 single base substitution G A exon_variant LINC-JP 15 28362528 28362528 single base substitution G A intron_variant LINC-JP 15 28362528 28362528 single base substitution G A upstream_gene_variant LINC-JP 15 28375609 28375609 single base substitution T A intron_variant LINC-JP 15 28375958 28375958 single base substitution C A intron_variant LINC-JP 15 28376534 28376534 single base substitution G T intron_variant LINC-JP 15 28376645 28376645 single base substitution C T intron_variant LINC-JP 15 28385101 28385101 single base substitution C T downstream_gene_variant LINC-JP 15 28385101 28385101 single base substitution C T intron_variant LINC-JP 15 28385527 28385527 single base substitution G A downstream_gene_variant LINC-JP 15 28385527 28385527 single base substitution G A intron_variant LINC-JP 15 28386928 28386928 single base substitution T C exon_variant LINC-JP 15 28386928 28386928 single base substitution T C missense_variant H3922R 11765A>G LINC-JP 15 28389535 28389535 single base substitution C T intron_variant LINC-JP 15 28389535 28389535 single base substitution C T upstream_gene_variant LINC-JP 15 28397371 28397371 single base substitution G A downstream_gene_variant LINC-JP 15 28397371 28397371 single base substitution G A intron_variant LINC-JP 15 28399746 28399746 single base substitution C T intron_variant LINC-JP 15 28403099 28403099 single base substitution T C intron_variant LINC-JP 15 28408353 28408353 single base substitution C A intron_variant LINC-JP 15 28408353 28408353 single base substitution C A missense_variant D3545Y 10633G>T LINC-JP 15 28408562 28408562 single base substitution T A intron_variant LINC-JP 15 28416634 28416634 single base substitution C A intron_variant LINC-JP 15 28419473 28419473 single base substitution T G intron_variant LINC-JP 15 28420589 28420589 single base substitution G A intron_variant LINC-JP 15 28420589 28420589 single base substitution G A upstream_gene_variant LINC-JP 15 28421911 28421911 single base substitution T C missense_variant K3146E 9436A>G LINC-JP 15 28421911 28421911 single base substitution T C upstream_gene_variant LINC-JP 15 28427586 28427586 single base substitution C G synonymous_variant L2966L 8898G>C LINC-JP 15 28429637 28429637 single base substitution A C intron_variant LINC-JP 15 28434738 28434738 single base substitution T A downstream_gene_variant LINC-JP 15 28434738 28434738 single base substitution T A intron_variant LINC-JP 15 28459700 28459700 single base substitution C A intron_variant LINC-JP 15 28464227 28464227 single base substitution T C downstream_gene_variant LINC-JP 15 28464227 28464227 single base substitution T C intron_variant LINC-JP 15 28470862 28470862 single base substitution G A intron_variant LINC-JP 15 28472614 28472614 single base substitution G A intron_variant LINC-JP 15 28486298 28486298 single base substitution G A intron_variant LINC-JP 15 28492027 28492027 single base substitution A T synonymous_variant G1084G 3252T>A LINC-JP 15 28505857 28505857 single base substitution T C intron_variant LINC-JP 15 28506054 28506054 single base substitution C G 3_prime_UTR_variant LINC-JP 15 28506054 28506054 single base substitution C G missense_variant E729Q 2185G>C LINC-JP 15 28517185 28517185 single base substitution G C downstream_gene_variant LINC-JP 15 28517185 28517185 single base substitution G C intron_variant LINC-JP 15 28517295 28517295 single base substitution A G exon_variant LINC-JP 15 28517295 28517295 single base substitution A G intron_variant LINC-JP 15 28517837 28517837 insertion of <=200bp - G intron_variant LINC-JP 15 28517938 28517938 single base substitution T C intron_variant LINC-JP 15 28517946 28517946 single base substitution G A intron_variant LINC-JP 15 28518433 28518433 single base substitution A C intron_variant LINC-JP 15 28518433 28518433 single base substitution A C upstream_gene_variant LINC-JP 15 28518441 28518441 single base substitution A G intron_variant LINC-JP 15 28518441 28518441 single base substitution A G upstream_gene_variant LINC-JP 15 28518447 28518447 single base substitution A G intron_variant LINC-JP 15 28518447 28518447 single base substitution A G upstream_gene_variant LINC-JP 15 28529192 28529192 single base substitution T C intron_variant LINC-JP 15 28538117 28538117 single base substitution T C 3_prime_UTR_variant LINC-JP 15 28538117 28538117 single base substitution T C exon_variant LINC-JP 15 28538117 28538117 single base substitution T C missense_variant E80G 239A>G LINC-JP 15 28538734 28538734 single base substitution T A intron_variant LINC-JP 15 28559069 28559069 single base substitution C A intron_variant LIRI-JP 15 28355269 28355269 single base substitution G A downstream_gene_variant LIRI-JP 15 28359596 28359596 single base substitution C T downstream_gene_variant LIRI-JP 15 28359596 28359596 single base substitution C T intron_variant LIRI-JP 15 28359596 28359596 single base substitution C T upstream_gene_variant LIRI-JP 15 28360632 28360632 single base substitution G A exon_variant LIRI-JP 15 28360632 28360632 single base substitution G A synonymous_variant A4555A 13665C>T LIRI-JP 15 28360632 28360632 single base substitution G A upstream_gene_variant LIRI-JP 15 28361319 28361319 deletion of <=200bp C - intron_variant LIRI-JP 15 28361319 28361319 deletion of <=200bp C - upstream_gene_variant LIRI-JP 15 28362092 28362092 single base substitution T C exon_variant LIRI-JP 15 28362092 28362092 single base substitution T C intron_variant LIRI-JP 15 28362092 28362092 single base substitution T C upstream_gene_variant LIRI-JP 15 28366144 28366144 single base substitution C T intron_variant LIRI-JP 15 28366144 28366144 single base substitution C T upstream_gene_variant LIRI-JP 15 28367680 28367680 single base substitution C T intron_variant LIRI-JP 15 28367680 28367680 single base substitution C T upstream_gene_variant LIRI-JP 15 28367785 28367785 single base substitution G T intron_variant LIRI-JP 15 28367785 28367785 single base substitution G T upstream_gene_variant LIRI-JP 15 28369235 28369235 single base substitution C G missense_variant G4379A 13136G>C LIRI-JP 15 28374367 28374367 single base substitution T C intron_variant LIRI-JP 15 28376456 28376456 single base substitution C T intron_variant LIRI-JP 15 28377229 28377232 deletion of <=200bp GAAA - intron_variant LIRI-JP 15 28377262 28377265 deletion of <=200bp CAGC - frameshift_variant GC4184 LIRI-JP 15 28381079 28381079 single base substitution T C intron_variant LIRI-JP 15 28382845 28382845 single base substitution C A downstream_gene_variant LIRI-JP 15 28382845 28382845 single base substitution C A intron_variant LIRI-JP 15 28384472 28384472 single base substitution C T downstream_gene_variant LIRI-JP 15 28384472 28384472 single base substitution C T intron_variant LIRI-JP 15 28385637 28385637 single base substitution T C downstream_gene_variant LIRI-JP 15 28385637 28385637 single base substitution T C intron_variant LIRI-JP 15 28388388 28388388 single base substitution C T intron_variant LIRI-JP 15 28388388 28388388 single base substitution C T upstream_gene_variant LIRI-JP 15 28391162 28391162 single base substitution C T intron_variant LIRI-JP 15 28391162 28391162 single base substitution C T upstream_gene_variant LIRI-JP 15 28393141 28393141 single base substitution C T downstream_gene_variant LIRI-JP 15 28393141 28393141 single base substitution C T intron_variant LIRI-JP 15 28398840 28398840 deletion of <=200bp C - intron_variant LIRI-JP 15 28398856 28398856 single base substitution T C intron_variant LIRI-JP 15 28399485 28399485 single base substitution A G intron_variant LIRI-JP 15 28400009 28400009 single base substitution C A intron_variant LIRI-JP 15 28400336 28400336 single base substitution A C intron_variant LIRI-JP 15 28402330 28402330 single base substitution A G intron_variant LIRI-JP 15 28402812 28402812 single base substitution T G intron_variant LIRI-JP 15 28406348 28406348 single base substitution G A intron_variant LIRI-JP 15 28407402 28407402 single base substitution G C intron_variant LIRI-JP 15 28408766 28408766 single base substitution C T intron_variant LIRI-JP 15 28410046 28410046 single base substitution T C intron_variant LIRI-JP 15 28410217 28410217 single base substitution G C intron_variant LIRI-JP 15 28411201 28411201 single base substitution G T intron_variant LIRI-JP 15 28414064 28414064 single base substitution T C intron_variant LIRI-JP 15 28418183 28418183 single base substitution A G intron_variant LIRI-JP 15 28418903 28418903 single base substitution C T intron_variant LIRI-JP 15 28421088 28421088 single base substitution C T intron_variant LIRI-JP 15 28421088 28421088 single base substitution C T upstream_gene_variant LIRI-JP 15 28421341 28421341 single base substitution T C intron_variant LIRI-JP 15 28421341 28421341 single base substitution T C upstream_gene_variant LIRI-JP 15 28421611 28421611 deletion of <=200bp A - frameshift_variant S3217 LIRI-JP 15 28421611 28421611 deletion of <=200bp A - upstream_gene_variant LIRI-JP 15 28423182 28423182 single base substitution C T intron_variant LIRI-JP 15 28423182 28423182 single base substitution C T upstream_gene_variant LIRI-JP 15 28425936 28425936 single base substitution C T intron_variant LIRI-JP 15 28426151 28426151 single base substitution T C intron_variant LIRI-JP 15 28426859 28426859 single base substitution A G intron_variant LIRI-JP 15 28426933 28426933 single base substitution C G intron_variant LIRI-JP 15 28427254 28427254 single base substitution G A intron_variant LIRI-JP 15 28429642 28429642 single base substitution A C intron_variant LIRI-JP 15 28430870 28430870 single base substitution C A downstream_gene_variant LIRI-JP 15 28430870 28430870 single base substitution C A intron_variant LIRI-JP 15 28436464 28436464 single base substitution T C intron_variant LIRI-JP 15 28439029 28439029 single base substitution A G intron_variant LIRI-JP 15 28441601 28441601 single base substitution A C splice_region_variant LIRI-JP 15 28443761 28443761 single base substitution T C exon_variant LIRI-JP 15 28443761 28443761 single base substitution T C missense_variant H2624R 7871A>G LIRI-JP 15 28444091 28444091 single base substitution T C intron_variant LIRI-JP 15 28444572 28444572 single base substitution T A intron_variant LIRI-JP 15 28450195 28450195 single base substitution T C intron_variant LIRI-JP 15 28450195 28450195 single base substitution T C upstream_gene_variant LIRI-JP 15 28451772 28451772 single base substitution T G intron_variant LIRI-JP 15 28451772 28451772 single base substitution T G upstream_gene_variant LIRI-JP 15 28451776 28451776 single base substitution A G intron_variant LIRI-JP 15 28451776 28451776 single base substitution A G upstream_gene_variant LIRI-JP 15 28452657 28452657 single base substitution C A intron_variant LIRI-JP 15 28452657 28452657 single base substitution C A upstream_gene_variant LIRI-JP 15 28453415 28453415 single base substitution C G intron_variant LIRI-JP 15 28453415 28453415 single base substitution C G upstream_gene_variant LIRI-JP 15 28453908 28453908 single base substitution C T intron_variant LIRI-JP 15 28453908 28453908 single base substitution C T upstream_gene_variant LIRI-JP 15 28455114 28455114 single base substitution A T intron_variant LIRI-JP 15 28460383 28460383 single base substitution T C intron_variant LIRI-JP 15 28462360 28462360 single base substitution T C downstream_gene_variant LIRI-JP 15 28462360 28462360 single base substitution T C intron_variant LIRI-JP 15 28462383 28462383 single base substitution A G downstream_gene_variant LIRI-JP 15 28462383 28462383 single base substitution A G intron_variant LIRI-JP 15 28463870 28463870 single base substitution T C downstream_gene_variant LIRI-JP 15 28463870 28463870 single base substitution T C intron_variant LIRI-JP 15 28469218 28469218 single base substitution T C intron_variant LIRI-JP 15 28469497 28469497 single base substitution A G intron_variant LIRI-JP 15 28471129 28471129 single base substitution G C intron_variant LIRI-JP 15 28472014 28472014 single base substitution A G intron_variant LIRI-JP 15 28473395 28473395 single base substitution C T exon_variant LIRI-JP 15 28473395 28473395 single base substitution C T synonymous_variant L1811L 5433G>A LIRI-JP 15 28473893 28473893 single base substitution G A intron_variant LIRI-JP 15 28474108 28474108 single base substitution T C intron_variant LIRI-JP 15 28474768 28474768 single base substitution A T intron_variant LIRI-JP 15 28474768 28474768 single base substitution A T upstream_gene_variant LIRI-JP 15 28475348 28475348 deletion of <=200bp G - intron_variant LIRI-JP 15 28475348 28475348 deletion of <=200bp G - upstream_gene_variant LIRI-JP 15 28475973 28475973 single base substitution A C intron_variant LIRI-JP 15 28475973 28475973 single base substitution A C upstream_gene_variant LIRI-JP 15 28476379 28476379 single base substitution C T intron_variant LIRI-JP 15 28476379 28476379 single base substitution C T upstream_gene_variant LIRI-JP 15 28477252 28477252 single base substitution T C intron_variant LIRI-JP 15 28477252 28477252 single base substitution T C upstream_gene_variant LIRI-JP 15 28478077 28478077 insertion of <=200bp - A intron_variant LIRI-JP 15 28478077 28478077 insertion of <=200bp - A upstream_gene_variant LIRI-JP 15 28480826 28480826 single base substitution C A intron_variant LIRI-JP 15 28483903 28483903 single base substitution C A missense_variant G1198V 3593G>T LIRI-JP 15 28483921 28483921 single base substitution G C splice_region_variant LIRI-JP 15 28483923 28483923 single base substitution A G splice_region_variant LIRI-JP 15 28484074 28484074 single base substitution A C intron_variant LIRI-JP 15 28485468 28485468 single base substitution G A intron_variant LIRI-JP 15 28488593 28488593 single base substitution C A intron_variant LIRI-JP 15 28488594 28488594 single base substitution C A intron_variant LIRI-JP 15 28488919 28488919 single base substitution C T intron_variant LIRI-JP 15 28489049 28489049 single base substitution G A intron_variant LIRI-JP 15 28498976 28498976 single base substitution C T downstream_gene_variant LIRI-JP 15 28498976 28498976 single base substitution C T intron_variant LIRI-JP 15 28500336 28500336 single base substitution A C intron_variant LIRI-JP 15 28501478 28501478 single base substitution A G intron_variant LIRI-JP 15 28501983 28501983 single base substitution A G intron_variant LIRI-JP 15 28503740 28503740 single base substitution A G intron_variant LIRI-JP 15 28506100 28506100 single base substitution A T 3_prime_UTR_variant LIRI-JP 15 28506100 28506100 single base substitution A T missense_variant D713E 2139T>A LIRI-JP 15 28506477 28506477 single base substitution T C intron_variant LIRI-JP 15 28508538 28508538 single base substitution T C intron_variant LIRI-JP 15 28509277 28509277 single base substitution A C intron_variant LIRI-JP 15 28510718 28510718 single base substitution T C intron_variant LIRI-JP 15 28512019 28512019 single base substitution C T intron_variant LIRI-JP 15 28514504 28514504 single base substitution C G 3_prime_UTR_variant LIRI-JP 15 28514504 28514504 single base substitution C G downstream_gene_variant LIRI-JP 15 28514504 28514504 single base substitution C G missense_variant E446Q 1336G>C LIRI-JP 15 28514657 28514657 single base substitution C A downstream_gene_variant LIRI-JP 15 28514657 28514657 single base substitution C A intron_variant LIRI-JP 15 28514659 28514659 single base substitution A G downstream_gene_variant LIRI-JP 15 28514659 28514659 single base substitution A G intron_variant LIRI-JP 15 28515416 28515416 single base substitution C T downstream_gene_variant LIRI-JP 15 28515416 28515416 single base substitution C T intron_variant LIRI-JP 15 28515420 28515420 single base substitution C A downstream_gene_variant LIRI-JP 15 28515420 28515420 single base substitution C A intron_variant LIRI-JP 15 28516018 28516018 single base substitution G C downstream_gene_variant LIRI-JP 15 28516018 28516018 single base substitution G C splice_region_variant LIRI-JP 15 28517859 28517859 single base substitution C A intron_variant LIRI-JP 15 28517898 28517898 single base substitution A C intron_variant LIRI-JP 15 28518115 28518115 deletion of <=200bp C - 3_prime_UTR_variant LIRI-JP 15 28518115 28518115 deletion of <=200bp C - exon_variant LIRI-JP 15 28518115 28518115 deletion of <=200bp C - frameshift_variant G279 LIRI-JP 15 28518373 28518373 single base substitution A G intron_variant LIRI-JP 15 28518373 28518373 single base substitution A G upstream_gene_variant LIRI-JP 15 28521682 28521682 single base substitution A G downstream_gene_variant LIRI-JP 15 28521682 28521682 single base substitution A G intron_variant LIRI-JP 15 28521682 28521682 single base substitution A G upstream_gene_variant LIRI-JP 15 28522231 28522231 single base substitution A G downstream_gene_variant LIRI-JP 15 28522231 28522231 single base substitution A G intron_variant LIRI-JP 15 28522231 28522231 single base substitution A G upstream_gene_variant LIRI-JP 15 28522796 28522796 single base substitution T C downstream_gene_variant LIRI-JP 15 28522796 28522796 single base substitution T C intron_variant LIRI-JP 15 28522796 28522796 single base substitution T C upstream_gene_variant LIRI-JP 15 28526687 28526687 single base substitution G A intron_variant LIRI-JP 15 28528612 28528612 single base substitution C T intron_variant LIRI-JP 15 28530184 28530184 single base substitution C A intron_variant LIRI-JP 15 28530329 28530329 single base substitution T C intron_variant LIRI-JP 15 28530651 28530651 single base substitution T C intron_variant LIRI-JP 15 28532236 28532236 single base substitution A T intron_variant LIRI-JP 15 28534437 28534437 single base substitution A C intron_variant LIRI-JP 15 28535978 28535978 single base substitution T C intron_variant LIRI-JP 15 28536294 28536294 single base substitution G A intron_variant LIRI-JP 15 28536539 28536539 single base substitution C A intron_variant LIRI-JP 15 28536637 28536637 single base substitution A G intron_variant LIRI-JP 15 28537762 28537762 single base substitution G A intron_variant LIRI-JP 15 28538437 28538437 single base substitution A T intron_variant LIRI-JP 15 28538957 28538957 single base substitution A C intron_variant LIRI-JP 15 28538981 28538981 single base substitution C G intron_variant LIRI-JP 15 28539316 28539316 single base substitution G A intron_variant LIRI-JP 15 28539325 28539325 single base substitution A G intron_variant LIRI-JP 15 28548473 28548473 single base substitution C G intron_variant LIRI-JP 15 28548473 28548473 single base substitution C G upstream_gene_variant LIRI-JP 15 28549270 28549270 single base substitution C T intron_variant LIRI-JP 15 28549270 28549270 single base substitution C T upstream_gene_variant LIRI-JP 15 28553546 28553546 single base substitution T C intron_variant LIRI-JP 15 28555193 28555193 single base substitution C T intron_variant LIRI-JP 15 28558823 28558823 single base substitution A G intron_variant LIRI-JP 15 28558839 28558839 single base substitution A G intron_variant LIRI-JP 15 28566411 28566411 single base substitution A T intron_variant LUSC-KR 15 28355833 28355833 single base substitution C G downstream_gene_variant LUSC-KR 15 28360677 28360677 single base substitution C A exon_variant LUSC-KR 15 28360677 28360677 single base substitution C A synonymous_variant L4540L 13620G>T LUSC-KR 15 28360677 28360677 single base substitution C A upstream_gene_variant LUSC-KR 15 28361220 28361220 single base substitution G C intron_variant LUSC-KR 15 28361220 28361220 single base substitution G C upstream_gene_variant LUSC-KR 15 28362342 28362342 single base substitution G C exon_variant LUSC-KR 15 28362342 28362342 single base substitution G C intron_variant LUSC-KR 15 28362342 28362342 single base substitution G C upstream_gene_variant LUSC-KR 15 28363318 28363318 single base substitution G T exon_variant LUSC-KR 15 28363318 28363318 single base substitution G T intron_variant LUSC-KR 15 28363318 28363318 single base substitution G T upstream_gene_variant LUSC-KR 15 28368140 28368140 single base substitution A G intron_variant LUSC-KR 15 28368140 28368140 single base substitution A G upstream_gene_variant LUSC-KR 15 28374600 28374600 single base substitution C A intron_variant LUSC-KR 15 28375617 28375617 single base substitution T C intron_variant LUSC-KR 15 28377772 28377772 single base substitution C T intron_variant LUSC-KR 15 28388274 28388274 single base substitution G A intron_variant LUSC-KR 15 28388274 28388274 single base substitution G A upstream_gene_variant LUSC-KR 15 28391559 28391559 single base substitution C T intron_variant LUSC-KR 15 28391559 28391559 single base substitution C T upstream_gene_variant LUSC-KR 15 28391692 28391692 single base substitution G C intron_variant LUSC-KR 15 28391692 28391692 single base substitution G C upstream_gene_variant LUSC-KR 15 28391758 28391758 single base substitution C T intron_variant LUSC-KR 15 28391758 28391758 single base substitution C T upstream_gene_variant LUSC-KR 15 28391759 28391759 single base substitution A C intron_variant LUSC-KR 15 28391759 28391759 single base substitution A C upstream_gene_variant LUSC-KR 15 28392263 28392263 single base substitution G T intron_variant LUSC-KR 15 28392263 28392263 single base substitution G T upstream_gene_variant LUSC-KR 15 28392356 28392356 single base substitution A G intron_variant LUSC-KR 15 28392356 28392356 single base substitution A G upstream_gene_variant LUSC-KR 15 28394531 28394531 single base substitution G A downstream_gene_variant LUSC-KR 15 28394531 28394531 single base substitution G A intron_variant LUSC-KR 15 28394711 28394711 single base substitution G A downstream_gene_variant LUSC-KR 15 28394711 28394711 single base substitution G A intron_variant LUSC-KR 15 28396614 28396614 single base substitution C G downstream_gene_variant LUSC-KR 15 28396614 28396614 single base substitution C G intron_variant LUSC-KR 15 28396677 28396677 single base substitution C T downstream_gene_variant LUSC-KR 15 28396677 28396677 single base substitution C T intron_variant LUSC-KR 15 28397206 28397206 single base substitution G C downstream_gene_variant LUSC-KR 15 28397206 28397206 single base substitution G C intron_variant LUSC-KR 15 28398625 28398625 single base substitution C T intron_variant LUSC-KR 15 28399990 28399990 single base substitution C T intron_variant LUSC-KR 15 28400073 28400073 single base substitution C A intron_variant LUSC-KR 15 28401638 28401638 single base substitution T C intron_variant LUSC-KR 15 28401909 28401909 single base substitution C A intron_variant LUSC-KR 15 28403791 28403791 single base substitution G T intron_variant LUSC-KR 15 28403805 28403805 single base substitution C T intron_variant LUSC-KR 15 28403860 28403860 single base substitution T C intron_variant LUSC-KR 15 28407074 28407074 single base substitution C A intron_variant LUSC-KR 15 28407643 28407643 single base substitution C G intron_variant LUSC-KR 15 28411376 28411376 single base substitution C A intron_variant LUSC-KR 15 28411671 28411671 single base substitution C A intron_variant LUSC-KR 15 28413823 28413823 single base substitution G A intron_variant LUSC-KR 15 28415221 28415221 single base substitution C T intron_variant LUSC-KR 15 28416473 28416473 single base substitution C A intron_variant LUSC-KR 15 28418715 28418715 single base substitution T A intron_variant LUSC-KR 15 28419526 28419526 single base substitution A G intron_variant LUSC-KR 15 28419644 28419644 single base substitution C T synonymous_variant S3318S 9954G>A LUSC-KR 15 28419644 28419644 single base substitution C T upstream_gene_variant LUSC-KR 15 28419695 28419695 single base substitution T C synonymous_variant T3301T 9903A>G LUSC-KR 15 28419695 28419695 single base substitution T C upstream_gene_variant LUSC-KR 15 28419746 28419746 single base substitution G A synonymous_variant N3284N 9852C>T LUSC-KR 15 28419746 28419746 single base substitution G A upstream_gene_variant LUSC-KR 15 28419867 28419867 single base substitution G T intron_variant LUSC-KR 15 28419867 28419867 single base substitution G T upstream_gene_variant LUSC-KR 15 28422026 28422026 single base substitution T C intron_variant LUSC-KR 15 28422026 28422026 single base substitution T C upstream_gene_variant LUSC-KR 15 28422471 28422471 single base substitution C G intron_variant LUSC-KR 15 28422471 28422471 single base substitution C G upstream_gene_variant LUSC-KR 15 28424100 28424100 single base substitution C T synonymous_variant T3032T 9096G>A LUSC-KR 15 28424100 28424100 single base substitution C T upstream_gene_variant LUSC-KR 15 28430233 28430233 single base substitution G C intron_variant LUSC-KR 15 28430250 28430250 single base substitution G C intron_variant LUSC-KR 15 28430307 28430307 single base substitution C A intron_variant LUSC-KR 15 28434562 28434562 single base substitution C A downstream_gene_variant LUSC-KR 15 28434562 28434562 single base substitution C A intron_variant LUSC-KR 15 28435754 28435754 single base substitution C A exon_variant LUSC-KR 15 28435754 28435754 single base substitution C A intron_variant LUSC-KR 15 28436164 28436164 single base substitution T C exon_variant LUSC-KR 15 28436164 28436164 single base substitution T C missense_variant I2866V 8596A>G LUSC-KR 15 28436869 28436869 single base substitution C A intron_variant LUSC-KR 15 28437441 28437441 single base substitution T C intron_variant LUSC-KR 15 28439115 28439115 single base substitution A G intron_variant LUSC-KR 15 28441817 28441817 single base substitution G T intron_variant LUSC-KR 15 28442431 28442431 single base substitution C A intron_variant LUSC-KR 15 28443474 28443474 single base substitution G A intron_variant LUSC-KR 15 28443682 28443682 single base substitution A G intron_variant LUSC-KR 15 28444266 28444266 single base substitution C A intron_variant LUSC-KR 15 28444536 28444536 single base substitution T C intron_variant LUSC-KR 15 28445082 28445082 single base substitution G A intron_variant LUSC-KR 15 28446178 28446178 single base substitution C A intron_variant LUSC-KR 15 28446658 28446658 single base substitution G T exon_variant LUSC-KR 15 28446658 28446658 single base substitution G T synonymous_variant R2554R 7660C>A LUSC-KR 15 28447243 28447243 single base substitution C A intron_variant LUSC-KR 15 28447282 28447282 single base substitution C T exon_variant LUSC-KR 15 28447282 28447282 single base substitution C T missense_variant V2532M 7594G>A LUSC-KR 15 28447283 28447283 single base substitution G A exon_variant LUSC-KR 15 28447283 28447283 single base substitution G A synonymous_variant D2531D 7593C>T LUSC-KR 15 28447322 28447322 single base substitution C T exon_variant LUSC-KR 15 28447322 28447322 single base substitution C T synonymous_variant T2518T 7554G>A LUSC-KR 15 28447562 28447562 single base substitution A G exon_variant LUSC-KR 15 28447562 28447562 single base substitution A G missense_variant S2471P 7411T>C LUSC-KR 15 28449534 28449534 single base substitution G A intron_variant LUSC-KR 15 28449534 28449534 single base substitution G A upstream_gene_variant LUSC-KR 15 28449573 28449573 single base substitution C A intron_variant LUSC-KR 15 28449573 28449573 single base substitution C A upstream_gene_variant LUSC-KR 15 28450564 28450564 single base substitution T C intron_variant LUSC-KR 15 28450564 28450564 single base substitution T C upstream_gene_variant LUSC-KR 15 28450598 28450598 single base substitution T G intron_variant LUSC-KR 15 28450598 28450598 single base substitution T G upstream_gene_variant LUSC-KR 15 28451339 28451339 single base substitution A C intron_variant LUSC-KR 15 28451339 28451339 single base substitution A C upstream_gene_variant LUSC-KR 15 28451718 28451718 single base substitution G A intron_variant LUSC-KR 15 28451718 28451718 single base substitution G A upstream_gene_variant LUSC-KR 15 28452182 28452182 single base substitution T C intron_variant LUSC-KR 15 28452182 28452182 single base substitution T C upstream_gene_variant LUSC-KR 15 28454197 28454197 single base substitution G C intron_variant LUSC-KR 15 28454633 28454633 single base substitution G A intron_variant LUSC-KR 15 28454992 28454992 single base substitution C A intron_variant LUSC-KR 15 28455884 28455884 single base substitution A G intron_variant LUSC-KR 15 28455905 28455905 single base substitution C A intron_variant LUSC-KR 15 28455917 28455917 single base substitution G A intron_variant LUSC-KR 15 28459728 28459728 single base substitution A G intron_variant LUSC-KR 15 28459835 28459835 single base substitution G A synonymous_variant L2108L 6324C>T LUSC-KR 15 28461962 28461962 single base substitution C G intron_variant LUSC-KR 15 28462096 28462096 single base substitution C T intron_variant LUSC-KR 15 28462554 28462554 single base substitution G A downstream_gene_variant LUSC-KR 15 28462554 28462554 single base substitution G A intron_variant LUSC-KR 15 28462760 28462760 single base substitution G T downstream_gene_variant LUSC-KR 15 28462760 28462760 single base substitution G T intron_variant LUSC-KR 15 28463026 28463026 single base substitution G T downstream_gene_variant LUSC-KR 15 28463026 28463026 single base substitution G T intron_variant LUSC-KR 15 28465913 28465913 single base substitution G C downstream_gene_variant LUSC-KR 15 28465913 28465913 single base substitution G C intron_variant LUSC-KR 15 28466072 28466072 single base substitution C A downstream_gene_variant LUSC-KR 15 28466072 28466072 single base substitution C A intron_variant LUSC-KR 15 28467246 28467246 single base substitution T C downstream_gene_variant LUSC-KR 15 28467246 28467246 single base substitution T C synonymous_variant G1860G 5580A>G LUSC-KR 15 28468042 28468042 single base substitution A G intron_variant LUSC-KR 15 28469045 28469045 single base substitution T A intron_variant LUSC-KR 15 28470862 28470862 single base substitution G A intron_variant LUSC-KR 15 28472137 28472137 single base substitution C T intron_variant LUSC-KR 15 28472525 28472525 single base substitution T G intron_variant LUSC-KR 15 28473209 28473209 single base substitution C T intron_variant LUSC-KR 15 28473697 28473697 single base substitution G A intron_variant LUSC-KR 15 28473746 28473746 single base substitution T C intron_variant LUSC-KR 15 28474058 28474058 single base substitution C A intron_variant LUSC-KR 15 28475370 28475370 single base substitution C T intron_variant LUSC-KR 15 28475370 28475370 single base substitution C T upstream_gene_variant LUSC-KR 15 28475633 28475633 single base substitution T C synonymous_variant P1563P 4689A>G LUSC-KR 15 28475633 28475633 single base substitution T C upstream_gene_variant LUSC-KR 15 28476011 28476011 single base substitution C A intron_variant LUSC-KR 15 28476011 28476011 single base substitution C A upstream_gene_variant LUSC-KR 15 28478272 28478272 single base substitution C T intron_variant LUSC-KR 15 28478272 28478272 single base substitution C T upstream_gene_variant LUSC-KR 15 28478323 28478323 single base substitution T C synonymous_variant Q1548Q 4644A>G LUSC-KR 15 28478323 28478323 single base substitution T C upstream_gene_variant LUSC-KR 15 28478351 28478351 single base substitution G T missense_variant S1539Y 4616C>A LUSC-KR 15 28478351 28478351 single base substitution G T upstream_gene_variant LUSC-KR 15 28479779 28479779 single base substitution A T intron_variant LUSC-KR 15 28479861 28479861 single base substitution G T intron_variant LUSC-KR 15 28481551 28481551 single base substitution C A intron_variant LUSC-KR 15 28491335 28491335 single base substitution T G intron_variant LUSC-KR 15 28494938 28494938 single base substitution C G downstream_gene_variant LUSC-KR 15 28494938 28494938 single base substitution C G intron_variant LUSC-KR 15 28495198 28495198 single base substitution A C downstream_gene_variant LUSC-KR 15 28495198 28495198 single base substitution A C intron_variant LUSC-KR 15 28495937 28495937 single base substitution A G downstream_gene_variant LUSC-KR 15 28495937 28495937 single base substitution A G intron_variant LUSC-KR 15 28496483 28496483 single base substitution G A downstream_gene_variant LUSC-KR 15 28496483 28496483 single base substitution G A intron_variant LUSC-KR 15 28496576 28496576 single base substitution G A downstream_gene_variant LUSC-KR 15 28496576 28496576 single base substitution G A intron_variant LUSC-KR 15 28499330 28499330 single base substitution G A downstream_gene_variant LUSC-KR 15 28499330 28499330 single base substitution G A intron_variant LUSC-KR 15 28500110 28500110 single base substitution C T intron_variant LUSC-KR 15 28500236 28500236 single base substitution C A intron_variant LUSC-KR 15 28501279 28501279 single base substitution G A 3_prime_UTR_variant LUSC-KR 15 28501279 28501279 single base substitution G A missense_variant A901V 2702C>T LUSC-KR 15 28501287 28501287 single base substitution C A 3_prime_UTR_variant LUSC-KR 15 28501287 28501287 single base substitution C A synonymous_variant L898L 2694G>T LUSC-KR 15 28502279 28502279 single base substitution A G 3_prime_UTR_variant LUSC-KR 15 28502279 28502279 single base substitution A G synonymous_variant G815G 2445T>C LUSC-KR 15 28508740 28508740 single base substitution C A intron_variant LUSC-KR 15 28508989 28508989 single base substitution G A intron_variant LUSC-KR 15 28510655 28510655 single base substitution G A intron_variant LUSC-KR 15 28511093 28511093 single base substitution G A 3_prime_UTR_variant LUSC-KR 15 28511093 28511093 single base substitution G A synonymous_variant S542S 1626C>T LUSC-KR 15 28513529 28513529 single base substitution A G downstream_gene_variant LUSC-KR 15 28513529 28513529 single base substitution A G intron_variant LUSC-KR 15 28513702 28513702 single base substitution C T 3_prime_UTR_variant LUSC-KR 15 28513702 28513702 single base substitution C T downstream_gene_variant LUSC-KR 15 28513702 28513702 single base substitution C T missense_variant D503N 1507G>A LUSC-KR 15 28514094 28514094 single base substitution C T downstream_gene_variant LUSC-KR 15 28514094 28514094 single base substitution C T intron_variant LUSC-KR 15 28514223 28514223 single base substitution C A downstream_gene_variant LUSC-KR 15 28514223 28514223 single base substitution C A intron_variant LUSC-KR 15 28516084 28516084 single base substitution C T downstream_gene_variant LUSC-KR 15 28516084 28516084 single base substitution C T intron_variant LUSC-KR 15 28517539 28517539 single base substitution G A intron_variant LUSC-KR 15 28517539 28517539 single base substitution G A splice_region_variant LUSC-KR 15 28517546 28517546 single base substitution G C intron_variant LUSC-KR 15 28517577 28517577 single base substitution C T intron_variant LUSC-KR 15 28517588 28517588 single base substitution A G intron_variant LUSC-KR 15 28517611 28517611 single base substitution T C intron_variant LUSC-KR 15 28517616 28517616 single base substitution G A intron_variant LUSC-KR 15 28517643 28517643 single base substitution T A intron_variant LUSC-KR 15 28517659 28517659 single base substitution C G intron_variant LUSC-KR 15 28517940 28517940 single base substitution T G intron_variant LUSC-KR 15 28517946 28517946 single base substitution G A intron_variant LUSC-KR 15 28526408 28526408 single base substitution C A intron_variant LUSC-KR 15 28529366 28529366 single base substitution A G intron_variant LUSC-KR 15 28534093 28534093 single base substitution G T intron_variant LUSC-KR 15 28534350 28534350 single base substitution T A intron_variant LUSC-KR 15 28534744 28534744 single base substitution G C intron_variant LUSC-KR 15 28535432 28535432 single base substitution A C intron_variant LUSC-KR 15 28540210 28540210 single base substitution G A intron_variant LUSC-KR 15 28541332 28541332 single base substitution C A intron_variant LUSC-KR 15 28542872 28542872 single base substitution G C intron_variant LUSC-KR 15 28543259 28543259 single base substitution A G intron_variant LUSC-KR 15 28546051 28546051 single base substitution C A intron_variant LUSC-KR 15 28546051 28546051 single base substitution C A upstream_gene_variant LUSC-KR 15 28546308 28546308 single base substitution C T intron_variant LUSC-KR 15 28546308 28546308 single base substitution C T upstream_gene_variant LUSC-KR 15 28547254 28547254 single base substitution C G intron_variant LUSC-KR 15 28547254 28547254 single base substitution C G upstream_gene_variant LUSC-KR 15 28547441 28547441 single base substitution C T intron_variant LUSC-KR 15 28547441 28547441 single base substitution C T upstream_gene_variant LUSC-KR 15 28547926 28547926 single base substitution C T intron_variant LUSC-KR 15 28547926 28547926 single base substitution C T upstream_gene_variant LUSC-KR 15 28548013 28548013 single base substitution T C intron_variant LUSC-KR 15 28548013 28548013 single base substitution T C upstream_gene_variant LUSC-KR 15 28548021 28548021 single base substitution G T intron_variant LUSC-KR 15 28548021 28548021 single base substitution G T upstream_gene_variant LUSC-KR 15 28549358 28549358 single base substitution T A intron_variant LUSC-KR 15 28549358 28549358 single base substitution T A upstream_gene_variant LUSC-KR 15 28550014 28550014 single base substitution A C intron_variant LUSC-KR 15 28550235 28550235 single base substitution C T intron_variant LUSC-KR 15 28551314 28551314 single base substitution C T intron_variant LUSC-KR 15 28553710 28553710 single base substitution T A intron_variant LUSC-KR 15 28554054 28554054 single base substitution T A intron_variant LUSC-KR 15 28556387 28556387 single base substitution G C intron_variant LUSC-KR 15 28557710 28557710 single base substitution G C intron_variant LUSC-KR 15 28558474 28558474 single base substitution C A intron_variant LUSC-KR 15 28558516 28558516 single base substitution G A intron_variant LUSC-KR 15 28559529 28559529 single base substitution G A intron_variant LUSC-KR 15 28559583 28559583 single base substitution T A intron_variant LUSC-KR 15 28560459 28560459 single base substitution T A downstream_gene_variant LUSC-KR 15 28560459 28560459 single base substitution T A intron_variant LUSC-KR 15 28561049 28561049 single base substitution G A downstream_gene_variant LUSC-KR 15 28561049 28561049 single base substitution G A intron_variant LUSC-KR 15 28564330 28564330 single base substitution G A downstream_gene_variant LUSC-KR 15 28564330 28564330 single base substitution G A intron_variant LUSC-KR 15 28565720 28565720 single base substitution C A intron_variant LUSC-KR 15 28566548 28566548 single base substitution T C exon_variant LUSC-KR 15 28566548 28566548 single base substitution T C missense_variant Q11R 32A>G LUSC-KR 15 28566562 28566562 single base substitution G C exon_variant LUSC-KR 15 28566562 28566562 single base substitution G C missense_variant F6L 18C>G LUSC-KR 15 28566630 28566630 single base substitution C T intron_variant LUSC-KR 15 28566742 28566742 single base substitution G A intron_variant LUSC-KR 15 28566757 28566757 single base substitution G C intron_variant LUSC-KR 15 28567813 28567813 single base substitution C G upstream_gene_variant LUSC-KR 15 28567840 28567840 single base substitution A G upstream_gene_variant LUSC-KR 15 28567867 28567867 single base substitution G A upstream_gene_variant LUSC-KR 15 28568057 28568057 single base substitution C T upstream_gene_variant LUSC-KR 15 28569903 28569903 single base substitution G A upstream_gene_variant LUSC-KR 15 28570183 28570183 single base substitution C G upstream_gene_variant LUSC-KR 15 28570272 28570272 single base substitution G C upstream_gene_variant LUSC-KR 15 28570276 28570276 single base substitution C T upstream_gene_variant LUSC-KR 15 28570516 28570516 single base substitution T G upstream_gene_variant LUSC-KR 15 28570536 28570536 single base substitution C T upstream_gene_variant LUSC-KR 15 28570853 28570853 single base substitution G A upstream_gene_variant LUSC-KR 15 28571611 28571611 single base substitution A G upstream_gene_variant LUSC-KR 15 28571670 28571670 single base substitution G T upstream_gene_variant LUSC-US 15 28357016 28357016 single base substitution C T downstream_gene_variant LUSC-US 15 28357016 28357016 single base substitution C T exon_variant LUSC-US 15 28357016 28357016 single base substitution C T missense_variant A4800T 14398G>A LUSC-US 15 28358790 28358790 single base substitution G A downstream_gene_variant LUSC-US 15 28358790 28358790 single base substitution G A exon_variant LUSC-US 15 28358790 28358790 single base substitution G A missense_variant R4650W 13948C>T LUSC-US 15 28370265 28370265 single base substitution G T synonymous_variant R4293R 12877C>A LUSC-US 15 28377918 28377918 single base substitution C T missense_variant A4097T 12289G>A LUSC-US 15 28380782 28380782 single base substitution C T synonymous_variant S4024S 12072G>A LUSC-US 15 28386602 28386602 single base substitution G A downstream_gene_variant LUSC-US 15 28386602 28386602 single base substitution G A synonymous_variant L3997L 11991C>T LUSC-US 15 28386674 28386674 single base substitution G C downstream_gene_variant LUSC-US 15 28386674 28386674 single base substitution G C synonymous_variant V3973V 11919C>G LUSC-US 15 28389936 28389936 single base substitution C G missense_variant D3675H 11023G>C LUSC-US 15 28389936 28389936 single base substitution C G upstream_gene_variant LUSC-US 15 28391399 28391399 single base substitution G A synonymous_variant I3664I 10992C>T LUSC-US 15 28391399 28391399 single base substitution G A upstream_gene_variant LUSC-US 15 28391416 28391416 single base substitution C T missense_variant D3659N 10975G>A LUSC-US 15 28391416 28391416 single base substitution C T upstream_gene_variant LUSC-US 15 28413656 28413656 single base substitution G A missense_variant S3437F 10310C>T LUSC-US 15 28413656 28413656 single base substitution G A missense_variant S94F 281C>T LUSC-US 15 28419575 28419575 single base substitution C G missense_variant Q3341H 10023G>C LUSC-US 15 28419575 28419575 single base substitution C G upstream_gene_variant LUSC-US 15 28419668 28419668 single base substitution C G missense_variant K3310N 9930G>C LUSC-US 15 28419668 28419668 single base substitution C G upstream_gene_variant LUSC-US 15 28421627 28421627 single base substitution C A missense_variant E3211D 9633G>T LUSC-US 15 28421627 28421627 single base substitution C A upstream_gene_variant LUSC-US 15 28436333 28436333 single base substitution C A exon_variant LUSC-US 15 28436333 28436333 single base substitution C A missense_variant V2837L 8509G>T LUSC-US 15 28456229 28456229 single base substitution G A missense_variant R2330W 6988C>T LUSC-US 15 28459024 28459024 single base substitution A T missense_variant L2217Q 6650T>A LUSC-US 15 28460816 28460816 single base substitution T G missense_variant K2054T 6161A>C LUSC-US 15 28460911 28460911 single base substitution C G synonymous_variant R2022R 6066G>C LUSC-US 15 28465667 28465667 single base substitution G A downstream_gene_variant LUSC-US 15 28465667 28465667 single base substitution G A missense_variant L1926F 5776C>T LUSC-US 15 28478864 28478864 single base substitution C A missense_variant V1433L 4297G>T LUSC-US 15 28478864 28478864 single base substitution C A upstream_gene_variant LUSC-US 15 28483881 28483881 single base substitution C T synonymous_variant E1205E 3615G>A LUSC-US 15 28491051 28491051 single base substitution C T missense_variant E1185K 3553G>A LUSC-US 15 28491925 28491925 single base substitution G A synonymous_variant F1118F 3354C>T LUSC-US 15 28492038 28492038 single base substitution C G missense_variant E1081Q 3241G>C LUSC-US 15 28493709 28493709 single base substitution G C stop_gained S1075* 3224C>G LUSC-US 15 28501024 28501024 single base substitution C T 3_prime_UTR_variant LUSC-US 15 28501024 28501024 single base substitution C T synonymous_variant E955E 2865G>A LUSC-US 15 28501025 28501025 single base substitution T C 3_prime_UTR_variant LUSC-US 15 28501025 28501025 single base substitution T C missense_variant E955G 2864A>G LUSC-US 15 28502333 28502333 single base substitution C T 3_prime_UTR_variant LUSC-US 15 28502333 28502333 single base substitution C T missense_variant M797I 2391G>A LUSC-US 15 28506002 28506002 single base substitution C A 3_prime_UTR_variant LUSC-US 15 28506002 28506002 single base substitution C A missense_variant R746L 2237G>T LUSC-US 15 28508279 28508279 single base substitution T A 3_prime_UTR_variant LUSC-US 15 28508279 28508279 single base substitution T A missense_variant K636I 1907A>T LUSC-US 15 28513702 28513702 single base substitution C T 3_prime_UTR_variant LUSC-US 15 28513702 28513702 single base substitution C T downstream_gene_variant LUSC-US 15 28513702 28513702 single base substitution C T missense_variant D503N 1507G>A LUSC-US 15 28518105 28518105 single base substitution G T 3_prime_UTR_variant LUSC-US 15 28518105 28518105 single base substitution G T exon_variant LUSC-US 15 28518105 28518105 single base substitution G T synonymous_variant P282P 846C>A LUSC-US 15 28520140 28520140 single base substitution G A 3_prime_UTR_variant LUSC-US 15 28520140 28520140 single base substitution G A missense_variant A185V 554C>T LUSC-US 15 28520140 28520140 single base substitution G A upstream_gene_variant LUSC-US 15 28544607 28544607 single base substitution C A exon_variant LUSC-US 15 28544607 28544607 single base substitution C A missense_variant G43V 128G>T LUSC-US 15 28544608 28544608 single base substitution C T exon_variant LUSC-US 15 28544608 28544608 single base substitution C T missense_variant G43R 127G>A MALY-DE 15 28353254 28353254 single base substitution A G downstream_gene_variant MALY-DE 15 28356829 28356829 single base substitution C T 3_prime_UTR_variant MALY-DE 15 28356829 28356829 single base substitution C T downstream_gene_variant MALY-DE 15 28356829 28356829 single base substitution C T exon_variant MALY-DE 15 28358211 28358211 single base substitution G A downstream_gene_variant MALY-DE 15 28358211 28358211 single base substitution G A splice_region_variant MALY-DE 15 28372570 28372570 single base substitution G T intron_variant MALY-DE 15 28388604 28388604 insertion of <=200bp - T intron_variant MALY-DE 15 28388604 28388604 insertion of <=200bp - T upstream_gene_variant MALY-DE 15 28391735 28391735 single base substitution C T intron_variant MALY-DE 15 28391735 28391735 single base substitution C T upstream_gene_variant MALY-DE 15 28408263 28408263 single base substitution C T intron_variant MALY-DE 15 28408263 28408263 single base substitution C T missense_variant G3575S 10723G>A MALY-DE 15 28419619 28419619 single base substitution C T missense_variant V3327M 9979G>A MALY-DE 15 28419619 28419619 single base substitution C T upstream_gene_variant MALY-DE 15 28428531 28428531 insertion of <=200bp - T intron_variant MALY-DE 15 28433179 28433179 single base substitution G A downstream_gene_variant MALY-DE 15 28433179 28433179 single base substitution G A intron_variant MALY-DE 15 28437968 28437968 single base substitution G A intron_variant MALY-DE 15 28438224 28438224 single base substitution C G intron_variant MALY-DE 15 28475412 28475412 single base substitution G A intron_variant MALY-DE 15 28475412 28475412 single base substitution G A upstream_gene_variant MALY-DE 15 28481069 28481069 single base substitution G A intron_variant MALY-DE 15 28493725 28493725 single base substitution T A missense_variant S1070C 3208A>T MALY-DE 15 28505360 28505360 single base substitution A G intron_variant MALY-DE 15 28506340 28506340 single base substitution T C intron_variant MALY-DE 15 28509142 28509142 single base substitution G A intron_variant MALY-DE 15 28510529 28510529 single base substitution T G intron_variant MALY-DE 15 28511039 28511039 single base substitution G C 3_prime_UTR_variant MALY-DE 15 28511039 28511039 single base substitution G C missense_variant S560R 1680C>G MALY-DE 15 28511061 28511061 single base substitution A C 3_prime_UTR_variant MALY-DE 15 28511061 28511061 single base substitution A C missense_variant V553G 1658T>G MALY-DE 15 28511149 28511149 single base substitution G T intron_variant MALY-DE 15 28522117 28522117 single base substitution A T downstream_gene_variant MALY-DE 15 28522117 28522117 single base substitution A T intron_variant MALY-DE 15 28522117 28522117 single base substitution A T upstream_gene_variant MALY-DE 15 28524473 28524473 single base substitution C T downstream_gene_variant MALY-DE 15 28524473 28524473 single base substitution C T intron_variant MELA-AU 15 28351538 28351539 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 28351709 28351709 single base substitution C T downstream_gene_variant MELA-AU 15 28351749 28351749 single base substitution G A downstream_gene_variant MELA-AU 15 28352751 28352751 single base substitution C T downstream_gene_variant MELA-AU 15 28352957 28352958 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 28353779 28353779 single base substitution C T downstream_gene_variant MELA-AU 15 28354170 28354170 single base substitution G A downstream_gene_variant MELA-AU 15 28355016 28355016 single base substitution G A downstream_gene_variant MELA-AU 15 28355342 28355342 single base substitution G A downstream_gene_variant MELA-AU 15 28355975 28355975 single base substitution G A downstream_gene_variant MELA-AU 15 28355982 28355982 single base substitution G A downstream_gene_variant MELA-AU 15 28356108 28356108 single base substitution G C downstream_gene_variant MELA-AU 15 28356511 28356511 single base substitution C T 3_prime_UTR_variant MELA-AU 15 28356511 28356511 single base substitution C T downstream_gene_variant MELA-AU 15 28356511 28356511 single base substitution C T exon_variant MELA-AU 15 28356528 28356528 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28356528 28356528 single base substitution G A downstream_gene_variant MELA-AU 15 28356528 28356528 single base substitution G A exon_variant MELA-AU 15 28357701 28357701 single base substitution G A downstream_gene_variant MELA-AU 15 28357701 28357701 single base substitution G A intron_variant MELA-AU 15 28357963 28357963 single base substitution G A downstream_gene_variant MELA-AU 15 28357963 28357963 single base substitution G A intron_variant MELA-AU 15 28358288 28358288 single base substitution G A downstream_gene_variant MELA-AU 15 28358288 28358288 single base substitution G A exon_variant MELA-AU 15 28358288 28358288 single base substitution G A missense_variant R4721C 14161C>T MELA-AU 15 28358291 28358291 single base substitution G A downstream_gene_variant MELA-AU 15 28358291 28358291 single base substitution G A exon_variant MELA-AU 15 28358291 28358291 single base substitution G A missense_variant L4720F 14158C>T MELA-AU 15 28358430 28358430 single base substitution C T downstream_gene_variant MELA-AU 15 28358430 28358430 single base substitution C T splice_acceptor_variant MELA-AU 15 28358444 28358444 single base substitution C T downstream_gene_variant MELA-AU 15 28358444 28358444 single base substitution C T intron_variant MELA-AU 15 28358457 28358458 multiple base substitution (>=2bp and <=200bp) GT AA downstream_gene_variant MELA-AU 15 28358457 28358458 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 15 28358491 28358491 single base substitution C T downstream_gene_variant MELA-AU 15 28358491 28358491 single base substitution C T intron_variant MELA-AU 15 28358727 28358727 single base substitution C T downstream_gene_variant MELA-AU 15 28358727 28358727 single base substitution C T exon_variant MELA-AU 15 28358727 28358727 single base substitution C T missense_variant E4671K 14011G>A MELA-AU 15 28359185 28359185 single base substitution C T downstream_gene_variant MELA-AU 15 28359185 28359185 single base substitution C T intron_variant MELA-AU 15 28359185 28359185 single base substitution C T upstream_gene_variant MELA-AU 15 28359321 28359321 single base substitution G A downstream_gene_variant MELA-AU 15 28359321 28359321 single base substitution G A intron_variant MELA-AU 15 28359321 28359321 single base substitution G A upstream_gene_variant MELA-AU 15 28359756 28359756 single base substitution A G downstream_gene_variant MELA-AU 15 28359756 28359756 single base substitution A G splice_donor_variant MELA-AU 15 28359756 28359756 single base substitution A G upstream_gene_variant MELA-AU 15 28361450 28361450 single base substitution C G intron_variant MELA-AU 15 28361450 28361450 single base substitution C G upstream_gene_variant MELA-AU 15 28361632 28361632 single base substitution G C intron_variant MELA-AU 15 28361632 28361632 single base substitution G C upstream_gene_variant MELA-AU 15 28361797 28361797 single base substitution G A intron_variant MELA-AU 15 28361797 28361797 single base substitution G A upstream_gene_variant MELA-AU 15 28364218 28364218 single base substitution A G intron_variant MELA-AU 15 28364218 28364218 single base substitution A G upstream_gene_variant MELA-AU 15 28365009 28365009 single base substitution T A intron_variant MELA-AU 15 28365009 28365009 single base substitution T A upstream_gene_variant MELA-AU 15 28366058 28366058 single base substitution A G intron_variant MELA-AU 15 28366058 28366058 single base substitution A G upstream_gene_variant MELA-AU 15 28367797 28367797 single base substitution T C intron_variant MELA-AU 15 28367797 28367797 single base substitution T C upstream_gene_variant MELA-AU 15 28368132 28368132 single base substitution T G intron_variant MELA-AU 15 28368132 28368132 single base substitution T G upstream_gene_variant MELA-AU 15 28368768 28368768 single base substitution G A intron_variant MELA-AU 15 28369453 28369453 single base substitution G A intron_variant MELA-AU 15 28369853 28369853 single base substitution A C intron_variant MELA-AU 15 28370703 28370703 single base substitution G A intron_variant MELA-AU 15 28371093 28371093 single base substitution G A intron_variant MELA-AU 15 28371264 28371264 single base substitution G A intron_variant MELA-AU 15 28371635 28371635 single base substitution C T intron_variant MELA-AU 15 28371778 28371779 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28371857 28371857 single base substitution G A intron_variant MELA-AU 15 28372444 28372444 single base substitution C T intron_variant MELA-AU 15 28372450 28372450 single base substitution G A intron_variant MELA-AU 15 28373056 28373056 single base substitution T G intron_variant MELA-AU 15 28373405 28373405 single base substitution A C intron_variant MELA-AU 15 28374524 28374524 single base substitution G A intron_variant MELA-AU 15 28376521 28376521 single base substitution G A intron_variant MELA-AU 15 28376970 28376971 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28377002 28377002 single base substitution A C intron_variant MELA-AU 15 28377098 28377098 single base substitution G A intron_variant MELA-AU 15 28378486 28378486 single base substitution T C intron_variant MELA-AU 15 28378744 28378744 single base substitution G A intron_variant MELA-AU 15 28379322 28379322 single base substitution G A intron_variant MELA-AU 15 28380049 28380049 single base substitution G A intron_variant MELA-AU 15 28380358 28380358 single base substitution G A intron_variant MELA-AU 15 28382289 28382289 single base substitution G A downstream_gene_variant MELA-AU 15 28382289 28382289 single base substitution G A intron_variant MELA-AU 15 28382365 28382365 single base substitution G A downstream_gene_variant MELA-AU 15 28382365 28382365 single base substitution G A intron_variant MELA-AU 15 28383902 28383902 single base substitution T C downstream_gene_variant MELA-AU 15 28383902 28383902 single base substitution T C intron_variant MELA-AU 15 28384612 28384612 single base substitution G A downstream_gene_variant MELA-AU 15 28384612 28384612 single base substitution G A intron_variant MELA-AU 15 28385073 28385073 single base substitution G A downstream_gene_variant MELA-AU 15 28385073 28385073 single base substitution G A intron_variant MELA-AU 15 28385692 28385692 single base substitution G A downstream_gene_variant MELA-AU 15 28385692 28385692 single base substitution G A intron_variant MELA-AU 15 28386014 28386014 single base substitution G T downstream_gene_variant MELA-AU 15 28386014 28386014 single base substitution G T intron_variant MELA-AU 15 28387745 28387745 single base substitution C A intron_variant MELA-AU 15 28387745 28387745 single base substitution C A upstream_gene_variant MELA-AU 15 28388465 28388465 single base substitution C T intron_variant MELA-AU 15 28388465 28388465 single base substitution C T upstream_gene_variant MELA-AU 15 28388937 28388937 single base substitution G A intron_variant MELA-AU 15 28388937 28388937 single base substitution G A upstream_gene_variant MELA-AU 15 28389971 28389972 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 28389971 28389972 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 28389974 28389974 single base substitution G A intron_variant MELA-AU 15 28389974 28389974 single base substitution G A upstream_gene_variant MELA-AU 15 28390188 28390188 single base substitution G A intron_variant MELA-AU 15 28390188 28390188 single base substitution G A upstream_gene_variant MELA-AU 15 28390412 28390412 single base substitution G A intron_variant MELA-AU 15 28390412 28390412 single base substitution G A upstream_gene_variant MELA-AU 15 28390952 28390952 single base substitution G A intron_variant MELA-AU 15 28390952 28390952 single base substitution G A upstream_gene_variant MELA-AU 15 28390963 28390963 single base substitution G A intron_variant MELA-AU 15 28390963 28390963 single base substitution G A upstream_gene_variant MELA-AU 15 28392572 28392572 single base substitution A C intron_variant MELA-AU 15 28392572 28392572 single base substitution A C upstream_gene_variant MELA-AU 15 28392914 28392914 single base substitution C T downstream_gene_variant MELA-AU 15 28392914 28392914 single base substitution C T intron_variant MELA-AU 15 28392926 28392926 single base substitution G A downstream_gene_variant MELA-AU 15 28392926 28392926 single base substitution G A intron_variant MELA-AU 15 28393143 28393143 single base substitution A G downstream_gene_variant MELA-AU 15 28393143 28393143 single base substitution A G intron_variant MELA-AU 15 28394126 28394126 insertion of <=200bp - C downstream_gene_variant MELA-AU 15 28394126 28394126 insertion of <=200bp - C intron_variant MELA-AU 15 28394126 28394126 single base substitution A C downstream_gene_variant MELA-AU 15 28394126 28394126 single base substitution A C intron_variant MELA-AU 15 28394224 28394224 single base substitution C T downstream_gene_variant MELA-AU 15 28394224 28394224 single base substitution C T intron_variant MELA-AU 15 28394403 28394403 single base substitution G A downstream_gene_variant MELA-AU 15 28394403 28394403 single base substitution G A intron_variant MELA-AU 15 28394451 28394451 single base substitution G A downstream_gene_variant MELA-AU 15 28394451 28394451 single base substitution G A intron_variant MELA-AU 15 28394767 28394767 single base substitution G A downstream_gene_variant MELA-AU 15 28394767 28394767 single base substitution G A intron_variant MELA-AU 15 28394823 28394823 single base substitution C T downstream_gene_variant MELA-AU 15 28394823 28394823 single base substitution C T intron_variant MELA-AU 15 28395317 28395317 single base substitution T G downstream_gene_variant MELA-AU 15 28395317 28395317 single base substitution T G intron_variant MELA-AU 15 28395321 28395321 single base substitution G A downstream_gene_variant MELA-AU 15 28395321 28395321 single base substitution G A intron_variant MELA-AU 15 28395487 28395487 single base substitution G A downstream_gene_variant MELA-AU 15 28395487 28395487 single base substitution G A intron_variant MELA-AU 15 28395698 28395698 single base substitution G A downstream_gene_variant MELA-AU 15 28395698 28395698 single base substitution G A intron_variant MELA-AU 15 28396659 28396659 single base substitution G A downstream_gene_variant MELA-AU 15 28396659 28396659 single base substitution G A intron_variant MELA-AU 15 28398842 28398842 single base substitution C T intron_variant MELA-AU 15 28399038 28399038 single base substitution A G intron_variant MELA-AU 15 28399093 28399093 single base substitution G A intron_variant MELA-AU 15 28399222 28399222 single base substitution G A intron_variant MELA-AU 15 28400474 28400474 single base substitution G A intron_variant MELA-AU 15 28401164 28401164 single base substitution G A intron_variant MELA-AU 15 28401506 28401506 single base substitution G A intron_variant MELA-AU 15 28402412 28402412 single base substitution G A intron_variant MELA-AU 15 28404540 28404540 single base substitution C G intron_variant MELA-AU 15 28405474 28405474 single base substitution G A intron_variant MELA-AU 15 28405794 28405794 single base substitution A T intron_variant MELA-AU 15 28406559 28406559 single base substitution G A intron_variant MELA-AU 15 28406606 28406606 single base substitution G A intron_variant MELA-AU 15 28407193 28407194 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28407284 28407284 single base substitution G A intron_variant MELA-AU 15 28407661 28407661 single base substitution G A intron_variant MELA-AU 15 28407796 28407796 single base substitution G A intron_variant MELA-AU 15 28410417 28410417 single base substitution G A intron_variant MELA-AU 15 28410703 28410703 single base substitution T C intron_variant MELA-AU 15 28411203 28411203 single base substitution G A intron_variant MELA-AU 15 28411297 28411297 single base substitution G A intron_variant MELA-AU 15 28411734 28411734 single base substitution G A intron_variant MELA-AU 15 28411786 28411786 single base substitution G A intron_variant MELA-AU 15 28411898 28411898 single base substitution G A intron_variant MELA-AU 15 28411934 28411934 single base substitution G A intron_variant MELA-AU 15 28412250 28412250 single base substitution G A intron_variant MELA-AU 15 28412263 28412263 single base substitution G A intron_variant MELA-AU 15 28415075 28415075 single base substitution C A intron_variant MELA-AU 15 28416331 28416331 single base substitution G A intron_variant MELA-AU 15 28417101 28417101 single base substitution G A intron_variant MELA-AU 15 28417482 28417482 single base substitution G C intron_variant MELA-AU 15 28418807 28418807 single base substitution G A intron_variant MELA-AU 15 28418863 28418863 single base substitution C G intron_variant MELA-AU 15 28418942 28418942 single base substitution A T intron_variant MELA-AU 15 28419404 28419404 single base substitution A G intron_variant MELA-AU 15 28419673 28419674 multiple base substitution (>=2bp and <=200bp) GG AA stop_gained GQ3308G* MELA-AU 15 28419673 28419674 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 28420559 28420559 single base substitution A T intron_variant MELA-AU 15 28420559 28420559 single base substitution A T upstream_gene_variant MELA-AU 15 28420801 28420801 single base substitution C T missense_variant G3230R 9688G>A MELA-AU 15 28420801 28420801 single base substitution C T upstream_gene_variant MELA-AU 15 28422141 28422141 single base substitution G A synonymous_variant G3129G 9387C>T MELA-AU 15 28422141 28422141 single base substitution G A upstream_gene_variant MELA-AU 15 28422331 28422331 single base substitution G A intron_variant MELA-AU 15 28422331 28422331 single base substitution G A upstream_gene_variant MELA-AU 15 28422529 28422529 single base substitution C T intron_variant MELA-AU 15 28422529 28422529 single base substitution C T upstream_gene_variant MELA-AU 15 28422593 28422593 single base substitution C T missense_variant D3076N 9226G>A MELA-AU 15 28422593 28422593 single base substitution C T upstream_gene_variant MELA-AU 15 28422695 28422695 single base substitution G A intron_variant MELA-AU 15 28422695 28422695 single base substitution G A upstream_gene_variant MELA-AU 15 28422942 28422942 single base substitution G A intron_variant MELA-AU 15 28422942 28422942 single base substitution G A upstream_gene_variant MELA-AU 15 28423034 28423034 single base substitution C T intron_variant MELA-AU 15 28423034 28423034 single base substitution C T upstream_gene_variant MELA-AU 15 28423124 28423124 single base substitution G A intron_variant MELA-AU 15 28423124 28423124 single base substitution G A upstream_gene_variant MELA-AU 15 28423245 28423245 single base substitution A G intron_variant MELA-AU 15 28423245 28423245 single base substitution A G upstream_gene_variant MELA-AU 15 28423661 28423661 single base substitution C A intron_variant MELA-AU 15 28423661 28423661 single base substitution C A upstream_gene_variant MELA-AU 15 28423760 28423760 single base substitution G A intron_variant MELA-AU 15 28423760 28423760 single base substitution G A upstream_gene_variant MELA-AU 15 28423953 28423953 single base substitution G A intron_variant MELA-AU 15 28423953 28423953 single base substitution G A upstream_gene_variant MELA-AU 15 28424184 28424184 single base substitution G A splice_region_variant MELA-AU 15 28424184 28424184 single base substitution G A upstream_gene_variant MELA-AU 15 28424549 28424549 single base substitution C T intron_variant MELA-AU 15 28424549 28424549 single base substitution C T upstream_gene_variant MELA-AU 15 28424990 28424990 single base substitution A G intron_variant MELA-AU 15 28425533 28425533 single base substitution C T intron_variant MELA-AU 15 28426333 28426333 single base substitution G A intron_variant MELA-AU 15 28427655 28427655 single base substitution G A synonymous_variant L2943L 8829C>T MELA-AU 15 28428260 28428260 single base substitution G A intron_variant MELA-AU 15 28428943 28428943 single base substitution G A intron_variant MELA-AU 15 28429202 28429202 single base substitution T C intron_variant MELA-AU 15 28429471 28429471 single base substitution G A intron_variant MELA-AU 15 28429711 28429711 single base substitution T C intron_variant MELA-AU 15 28429767 28429767 single base substitution G A intron_variant MELA-AU 15 28429984 28429984 single base substitution G A intron_variant MELA-AU 15 28430626 28430626 single base substitution G A downstream_gene_variant MELA-AU 15 28430626 28430626 single base substitution G A intron_variant MELA-AU 15 28431052 28431052 single base substitution G A downstream_gene_variant MELA-AU 15 28431052 28431052 single base substitution G A intron_variant MELA-AU 15 28431309 28431309 single base substitution T C downstream_gene_variant MELA-AU 15 28431309 28431309 single base substitution T C intron_variant MELA-AU 15 28431566 28431566 single base substitution A T downstream_gene_variant MELA-AU 15 28431566 28431566 single base substitution A T intron_variant MELA-AU 15 28431722 28431722 single base substitution C A downstream_gene_variant MELA-AU 15 28431722 28431722 single base substitution C A splice_donor_variant MELA-AU 15 28431725 28431725 single base substitution T C downstream_gene_variant MELA-AU 15 28431725 28431725 single base substitution T C splice_region_variant MELA-AU 15 28432123 28432123 single base substitution G A downstream_gene_variant MELA-AU 15 28432123 28432123 single base substitution G A intron_variant MELA-AU 15 28432177 28432177 single base substitution G A downstream_gene_variant MELA-AU 15 28432177 28432177 single base substitution G A intron_variant MELA-AU 15 28432460 28432460 single base substitution G A downstream_gene_variant MELA-AU 15 28432460 28432460 single base substitution G A intron_variant MELA-AU 15 28432572 28432572 single base substitution G A downstream_gene_variant MELA-AU 15 28432572 28432572 single base substitution G A intron_variant MELA-AU 15 28433528 28433560 deletion of <=200bp TACAAAAACAAAATTAGCCAGGCATGGTGGCAG - downstream_gene_variant MELA-AU 15 28433528 28433560 deletion of <=200bp TACAAAAACAAAATTAGCCAGGCATGGTGGCAG - intron_variant MELA-AU 15 28433790 28433790 single base substitution G A downstream_gene_variant MELA-AU 15 28433790 28433790 single base substitution G A intron_variant MELA-AU 15 28435802 28435802 single base substitution C A exon_variant MELA-AU 15 28435802 28435802 single base substitution C A intron_variant MELA-AU 15 28436017 28436017 single base substitution G A exon_variant MELA-AU 15 28436017 28436017 single base substitution G A intron_variant MELA-AU 15 28436199 28436199 single base substitution C G exon_variant MELA-AU 15 28436199 28436199 single base substitution C G missense_variant G2854A 8561G>C MELA-AU 15 28436589 28436589 single base substitution C G intron_variant MELA-AU 15 28437073 28437073 single base substitution A G intron_variant MELA-AU 15 28437525 28437525 single base substitution G A intron_variant MELA-AU 15 28439285 28439285 single base substitution C T intron_variant MELA-AU 15 28439346 28439346 single base substitution G A intron_variant MELA-AU 15 28440515 28440515 single base substitution G A intron_variant MELA-AU 15 28440691 28440691 single base substitution G A intron_variant MELA-AU 15 28440691 28440691 single base substitution G T intron_variant MELA-AU 15 28441817 28441817 deletion of <=200bp G - intron_variant MELA-AU 15 28442458 28442458 single base substitution G A intron_variant MELA-AU 15 28444688 28444688 single base substitution G A intron_variant MELA-AU 15 28444902 28444902 single base substitution G T intron_variant MELA-AU 15 28445073 28445074 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28445311 28445311 single base substitution G T intron_variant MELA-AU 15 28446736 28446736 single base substitution G A intron_variant MELA-AU 15 28447486 28447486 single base substitution G A intron_variant MELA-AU 15 28447486 28447486 single base substitution G A splice_region_variant MELA-AU 15 28449263 28449263 single base substitution C T intron_variant MELA-AU 15 28449263 28449263 single base substitution C T upstream_gene_variant MELA-AU 15 28449450 28449450 single base substitution A C intron_variant MELA-AU 15 28449450 28449450 single base substitution A C upstream_gene_variant MELA-AU 15 28450392 28450392 single base substitution G A intron_variant MELA-AU 15 28450392 28450392 single base substitution G A upstream_gene_variant MELA-AU 15 28450458 28450458 single base substitution T A intron_variant MELA-AU 15 28450458 28450458 single base substitution T A upstream_gene_variant MELA-AU 15 28450506 28450506 single base substitution G A intron_variant MELA-AU 15 28450506 28450506 single base substitution G A upstream_gene_variant MELA-AU 15 28453380 28453380 single base substitution T C intron_variant MELA-AU 15 28453380 28453380 single base substitution T C upstream_gene_variant MELA-AU 15 28453845 28453845 single base substitution C A intron_variant MELA-AU 15 28453845 28453845 single base substitution C A upstream_gene_variant MELA-AU 15 28454442 28454442 single base substitution T C intron_variant MELA-AU 15 28454923 28454923 single base substitution G A intron_variant MELA-AU 15 28455985 28455985 single base substitution G A intron_variant MELA-AU 15 28456074 28456074 single base substitution A G intron_variant MELA-AU 15 28456967 28456967 single base substitution C A intron_variant MELA-AU 15 28457067 28457067 single base substitution T G intron_variant MELA-AU 15 28457332 28457332 single base substitution G A intron_variant MELA-AU 15 28459297 28459297 single base substitution A T missense_variant N2160K 6480T>A MELA-AU 15 28459540 28459540 single base substitution G A intron_variant MELA-AU 15 28459657 28459657 single base substitution G A intron_variant MELA-AU 15 28460280 28460280 single base substitution C T intron_variant MELA-AU 15 28460828 28460828 single base substitution G C missense_variant T2050R 6149C>G MELA-AU 15 28461176 28461176 single base substitution G A intron_variant MELA-AU 15 28461257 28461257 single base substitution G A intron_variant MELA-AU 15 28462941 28462941 single base substitution T C downstream_gene_variant MELA-AU 15 28462941 28462941 single base substitution T C intron_variant MELA-AU 15 28463436 28463436 single base substitution G C downstream_gene_variant MELA-AU 15 28463436 28463436 single base substitution G C intron_variant MELA-AU 15 28464122 28464122 single base substitution G A downstream_gene_variant MELA-AU 15 28464122 28464122 single base substitution G A intron_variant MELA-AU 15 28465518 28465518 single base substitution G A downstream_gene_variant MELA-AU 15 28465518 28465518 single base substitution G A intron_variant MELA-AU 15 28465610 28465610 single base substitution C T downstream_gene_variant MELA-AU 15 28465610 28465610 single base substitution C T missense_variant E1945K 5833G>A MELA-AU 15 28465724 28465724 single base substitution G A downstream_gene_variant MELA-AU 15 28465724 28465724 single base substitution G A stop_gained Q1907* 5719C>T MELA-AU 15 28465747 28465747 single base substitution C A downstream_gene_variant MELA-AU 15 28465747 28465747 single base substitution C A missense_variant G1899V 5696G>T MELA-AU 15 28466075 28466075 single base substitution C G downstream_gene_variant MELA-AU 15 28466075 28466075 single base substitution C G intron_variant MELA-AU 15 28466096 28466096 single base substitution G C downstream_gene_variant MELA-AU 15 28466096 28466096 single base substitution G C intron_variant MELA-AU 15 28466104 28466104 single base substitution C A downstream_gene_variant MELA-AU 15 28466104 28466104 single base substitution C A intron_variant MELA-AU 15 28467415 28467415 single base substitution T C intron_variant MELA-AU 15 28468131 28468131 single base substitution T A intron_variant MELA-AU 15 28468484 28468484 single base substitution G A intron_variant MELA-AU 15 28468966 28468966 single base substitution A G intron_variant MELA-AU 15 28470068 28470068 single base substitution G A intron_variant MELA-AU 15 28470377 28470377 single base substitution G A intron_variant MELA-AU 15 28470378 28470378 single base substitution G A intron_variant MELA-AU 15 28471707 28471707 single base substitution G A intron_variant MELA-AU 15 28471811 28471811 single base substitution G A intron_variant MELA-AU 15 28471966 28471966 single base substitution C A intron_variant MELA-AU 15 28472018 28472018 single base substitution G A intron_variant MELA-AU 15 28472196 28472196 single base substitution A C intron_variant MELA-AU 15 28472402 28472402 single base substitution C T intron_variant MELA-AU 15 28472679 28472679 single base substitution C T intron_variant MELA-AU 15 28473012 28473023 deletion of <=200bp AAATGGTATGAT - intron_variant MELA-AU 15 28473983 28473983 single base substitution C T intron_variant MELA-AU 15 28474724 28474724 single base substitution G A missense_variant R1668C 5002C>T MELA-AU 15 28474724 28474724 single base substitution G A upstream_gene_variant MELA-AU 15 28476986 28476986 single base substitution A T intron_variant MELA-AU 15 28476986 28476986 single base substitution A T upstream_gene_variant MELA-AU 15 28477029 28477029 single base substitution C T intron_variant MELA-AU 15 28477029 28477029 single base substitution C T upstream_gene_variant MELA-AU 15 28477092 28477093 multiple base substitution (>=2bp and <=200bp) GC TT intron_variant MELA-AU 15 28477092 28477093 multiple base substitution (>=2bp and <=200bp) GC TT upstream_gene_variant MELA-AU 15 28477141 28477141 single base substitution C T intron_variant MELA-AU 15 28477141 28477141 single base substitution C T upstream_gene_variant MELA-AU 15 28477609 28477609 single base substitution C T intron_variant MELA-AU 15 28477609 28477609 single base substitution C T upstream_gene_variant MELA-AU 15 28478069 28478069 single base substitution C T intron_variant MELA-AU 15 28478069 28478069 single base substitution C T upstream_gene_variant MELA-AU 15 28478102 28478102 single base substitution C A intron_variant MELA-AU 15 28478102 28478102 single base substitution C A upstream_gene_variant MELA-AU 15 28478332 28478332 single base substitution C A missense_variant R1545S 4635G>T MELA-AU 15 28478332 28478332 single base substitution C A upstream_gene_variant MELA-AU 15 28478338 28478338 single base substitution C G missense_variant W1543C 4629G>C MELA-AU 15 28478338 28478338 single base substitution C G upstream_gene_variant MELA-AU 15 28478668 28478668 single base substitution C A missense_variant G1464V 4391G>T MELA-AU 15 28478668 28478668 single base substitution C A upstream_gene_variant MELA-AU 15 28478840 28478840 single base substitution A G synonymous_variant L1441L 4321T>C MELA-AU 15 28478840 28478840 single base substitution A G upstream_gene_variant MELA-AU 15 28478858 28478858 single base substitution C G missense_variant E1435Q 4303G>C MELA-AU 15 28478858 28478858 single base substitution C G upstream_gene_variant MELA-AU 15 28478992 28478992 single base substitution C A intron_variant MELA-AU 15 28478992 28478992 single base substitution C A upstream_gene_variant MELA-AU 15 28480201 28480201 single base substitution G A intron_variant MELA-AU 15 28480663 28480663 deletion of <=200bp C - intron_variant MELA-AU 15 28482173 28482173 single base substitution G A synonymous_variant L1313L 3939C>T MELA-AU 15 28482401 28482401 single base substitution G A intron_variant MELA-AU 15 28483010 28483010 single base substitution G A intron_variant MELA-AU 15 28483865 28483865 single base substitution G A missense_variant R1211C 3631C>T MELA-AU 15 28483903 28483903 single base substitution C A missense_variant G1198V 3593G>T MELA-AU 15 28484192 28484192 single base substitution A T intron_variant MELA-AU 15 28486090 28486090 single base substitution A G intron_variant MELA-AU 15 28486443 28486443 single base substitution G A intron_variant MELA-AU 15 28486728 28486728 single base substitution G A intron_variant MELA-AU 15 28486984 28486984 single base substitution A G intron_variant MELA-AU 15 28487656 28487656 single base substitution A T intron_variant MELA-AU 15 28487890 28487890 single base substitution G A intron_variant MELA-AU 15 28487985 28487985 single base substitution G A intron_variant MELA-AU 15 28488536 28488536 single base substitution G A intron_variant MELA-AU 15 28489623 28489623 single base substitution G A intron_variant MELA-AU 15 28489881 28489882 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 15 28489896 28489896 single base substitution A C intron_variant MELA-AU 15 28489954 28489954 single base substitution C T intron_variant MELA-AU 15 28489980 28489980 single base substitution G A intron_variant MELA-AU 15 28490368 28490368 single base substitution G A intron_variant MELA-AU 15 28490511 28490512 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28491698 28491698 single base substitution A C intron_variant MELA-AU 15 28492058 28492058 single base substitution G A intron_variant MELA-AU 15 28494064 28494064 single base substitution G A intron_variant MELA-AU 15 28494420 28494420 single base substitution G A intron_variant MELA-AU 15 28494466 28494466 single base substitution G A intron_variant MELA-AU 15 28494690 28494690 single base substitution G A downstream_gene_variant MELA-AU 15 28494690 28494690 single base substitution G A intron_variant MELA-AU 15 28494896 28494896 single base substitution G A downstream_gene_variant MELA-AU 15 28494896 28494896 single base substitution G A intron_variant MELA-AU 15 28495311 28495311 single base substitution G A downstream_gene_variant MELA-AU 15 28495311 28495311 single base substitution G A intron_variant MELA-AU 15 28495814 28495814 single base substitution G A downstream_gene_variant MELA-AU 15 28495814 28495814 single base substitution G A intron_variant MELA-AU 15 28495851 28495851 single base substitution G A downstream_gene_variant MELA-AU 15 28495851 28495851 single base substitution G A intron_variant MELA-AU 15 28496225 28496225 single base substitution G A downstream_gene_variant MELA-AU 15 28496225 28496225 single base substitution G A intron_variant MELA-AU 15 28496348 28496348 single base substitution G A downstream_gene_variant MELA-AU 15 28496348 28496348 single base substitution G A intron_variant MELA-AU 15 28496380 28496380 single base substitution G A downstream_gene_variant MELA-AU 15 28496380 28496380 single base substitution G A intron_variant MELA-AU 15 28496676 28496676 single base substitution G A downstream_gene_variant MELA-AU 15 28496676 28496676 single base substitution G A intron_variant MELA-AU 15 28497801 28497801 single base substitution C T downstream_gene_variant MELA-AU 15 28497801 28497801 single base substitution C T intron_variant MELA-AU 15 28498718 28498718 single base substitution T A downstream_gene_variant MELA-AU 15 28498718 28498718 single base substitution T A intron_variant MELA-AU 15 28498782 28498782 single base substitution A T downstream_gene_variant MELA-AU 15 28498782 28498782 single base substitution A T intron_variant MELA-AU 15 28499095 28499095 single base substitution G A downstream_gene_variant MELA-AU 15 28499095 28499095 single base substitution G A intron_variant MELA-AU 15 28499118 28499118 single base substitution T A downstream_gene_variant MELA-AU 15 28499118 28499118 single base substitution T A intron_variant MELA-AU 15 28499417 28499417 single base substitution G A downstream_gene_variant MELA-AU 15 28499417 28499417 single base substitution G A intron_variant MELA-AU 15 28499518 28499518 single base substitution C T downstream_gene_variant MELA-AU 15 28499518 28499518 single base substitution C T synonymous_variant L1006L 3018G>A MELA-AU 15 28499671 28499671 single base substitution T A intron_variant MELA-AU 15 28499671 28499671 single base substitution T A splice_region_variant MELA-AU 15 28500562 28500562 single base substitution G A intron_variant MELA-AU 15 28500765 28500765 single base substitution A G intron_variant MELA-AU 15 28501059 28501059 single base substitution A G 3_prime_UTR_variant MELA-AU 15 28501059 28501059 single base substitution A G synonymous_variant L944L 2830T>C MELA-AU 15 28501266 28501267 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 15 28501266 28501267 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant A905V 2714CC>TT MELA-AU 15 28501425 28501425 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28501425 28501425 single base substitution G A synonymous_variant F852F 2556C>T MELA-AU 15 28501962 28501962 single base substitution G A intron_variant MELA-AU 15 28502007 28502007 single base substitution C T intron_variant MELA-AU 15 28502118 28502118 single base substitution A C intron_variant MELA-AU 15 28502359 28502359 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28502359 28502359 single base substitution G A missense_variant P789S 2365C>T MELA-AU 15 28502693 28502693 single base substitution G A intron_variant MELA-AU 15 28502922 28502922 single base substitution C A intron_variant MELA-AU 15 28503169 28503169 single base substitution G A intron_variant MELA-AU 15 28503434 28503434 single base substitution G A intron_variant MELA-AU 15 28503922 28503922 single base substitution A T intron_variant MELA-AU 15 28504044 28504044 single base substitution G A intron_variant MELA-AU 15 28504331 28504331 single base substitution C T intron_variant MELA-AU 15 28504344 28504344 single base substitution G A intron_variant MELA-AU 15 28504376 28504376 single base substitution G A intron_variant MELA-AU 15 28504498 28504498 single base substitution C T intron_variant MELA-AU 15 28505508 28505508 single base substitution C G intron_variant MELA-AU 15 28506660 28506660 single base substitution G A intron_variant MELA-AU 15 28507114 28507114 single base substitution C T intron_variant MELA-AU 15 28507907 28507907 single base substitution A C intron_variant MELA-AU 15 28508199 28508199 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28508199 28508199 single base substitution G A missense_variant R663C 1987C>T MELA-AU 15 28508511 28508511 single base substitution G A intron_variant MELA-AU 15 28509403 28509403 single base substitution G A intron_variant MELA-AU 15 28510031 28510031 single base substitution G A intron_variant MELA-AU 15 28510864 28510864 single base substitution G C 3_prime_UTR_variant MELA-AU 15 28510864 28510864 single base substitution G C missense_variant D590E 1770C>G MELA-AU 15 28510958 28510958 single base substitution C A splice_region_variant MELA-AU 15 28511189 28511189 single base substitution G A intron_variant MELA-AU 15 28511532 28511532 single base substitution G A intron_variant MELA-AU 15 28511743 28511743 single base substitution G A intron_variant MELA-AU 15 28511945 28511945 single base substitution G A intron_variant MELA-AU 15 28511995 28511995 single base substitution T C intron_variant MELA-AU 15 28512652 28512652 single base substitution C T downstream_gene_variant MELA-AU 15 28512652 28512652 single base substitution C T intron_variant MELA-AU 15 28512843 28512843 single base substitution G A downstream_gene_variant MELA-AU 15 28512843 28512843 single base substitution G A intron_variant MELA-AU 15 28513306 28513306 single base substitution A T downstream_gene_variant MELA-AU 15 28513306 28513306 single base substitution A T intron_variant MELA-AU 15 28513461 28513461 single base substitution G A downstream_gene_variant MELA-AU 15 28513461 28513461 single base substitution G A intron_variant MELA-AU 15 28513628 28513628 single base substitution C A 3_prime_UTR_variant MELA-AU 15 28513628 28513628 single base substitution C A downstream_gene_variant MELA-AU 15 28513628 28513628 single base substitution C A synonymous_variant L527L 1581G>T MELA-AU 15 28515201 28515201 single base substitution G A downstream_gene_variant MELA-AU 15 28515201 28515201 single base substitution G A intron_variant MELA-AU 15 28515241 28515242 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 28515241 28515242 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28516023 28516023 single base substitution G A downstream_gene_variant MELA-AU 15 28516023 28516023 single base substitution G A intron_variant MELA-AU 15 28516632 28516632 single base substitution G A downstream_gene_variant MELA-AU 15 28516632 28516632 single base substitution G A intron_variant MELA-AU 15 28516837 28516837 single base substitution T A downstream_gene_variant MELA-AU 15 28516837 28516837 single base substitution T A intron_variant MELA-AU 15 28516942 28516942 single base substitution G A downstream_gene_variant MELA-AU 15 28516942 28516942 single base substitution G A intron_variant MELA-AU 15 28517101 28517101 single base substitution C T downstream_gene_variant MELA-AU 15 28517101 28517101 single base substitution C T intron_variant MELA-AU 15 28517164 28517164 single base substitution G A downstream_gene_variant MELA-AU 15 28517164 28517164 single base substitution G A intron_variant MELA-AU 15 28517457 28517457 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28517457 28517457 single base substitution G A exon_variant MELA-AU 15 28517457 28517457 single base substitution G A synonymous_variant S329S 987C>T MELA-AU 15 28517992 28517992 single base substitution C A intron_variant MELA-AU 15 28519457 28519457 single base substitution G A 3_prime_UTR_variant MELA-AU 15 28519457 28519457 single base substitution G A synonymous_variant F260F 780C>T MELA-AU 15 28519457 28519457 single base substitution G A upstream_gene_variant MELA-AU 15 28519529 28519530 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 15 28519529 28519530 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P236L 707CC>TT MELA-AU 15 28519529 28519530 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 28520505 28520505 single base substitution G A downstream_gene_variant MELA-AU 15 28520505 28520505 single base substitution G A intron_variant MELA-AU 15 28520505 28520505 single base substitution G A upstream_gene_variant MELA-AU 15 28521569 28521569 single base substitution G A downstream_gene_variant MELA-AU 15 28521569 28521569 single base substitution G A intron_variant MELA-AU 15 28521569 28521569 single base substitution G A upstream_gene_variant MELA-AU 15 28521776 28521776 single base substitution G A downstream_gene_variant MELA-AU 15 28521776 28521776 single base substitution G A intron_variant MELA-AU 15 28521776 28521776 single base substitution G A upstream_gene_variant MELA-AU 15 28522011 28522011 single base substitution G A downstream_gene_variant MELA-AU 15 28522011 28522011 single base substitution G A intron_variant MELA-AU 15 28522011 28522011 single base substitution G A upstream_gene_variant MELA-AU 15 28522407 28522407 single base substitution G A downstream_gene_variant MELA-AU 15 28522407 28522407 single base substitution G A intron_variant MELA-AU 15 28522407 28522407 single base substitution G A upstream_gene_variant MELA-AU 15 28525805 28525805 single base substitution C T intron_variant MELA-AU 15 28526921 28526921 insertion of <=200bp - T intron_variant MELA-AU 15 28527281 28527281 single base substitution A T intron_variant MELA-AU 15 28527500 28527500 single base substitution G A intron_variant MELA-AU 15 28527802 28527802 single base substitution G A intron_variant MELA-AU 15 28527839 28527840 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28528062 28528062 single base substitution G A intron_variant MELA-AU 15 28528094 28528094 single base substitution G A intron_variant MELA-AU 15 28528104 28528104 single base substitution G A intron_variant MELA-AU 15 28528113 28528113 single base substitution G A intron_variant MELA-AU 15 28528114 28528114 single base substitution G A intron_variant MELA-AU 15 28528481 28528481 single base substitution T A intron_variant MELA-AU 15 28528753 28528753 single base substitution G A intron_variant MELA-AU 15 28529613 28529613 single base substitution G A intron_variant MELA-AU 15 28530046 28530046 single base substitution G A intron_variant MELA-AU 15 28531225 28531225 single base substitution G T intron_variant MELA-AU 15 28531234 28531235 multiple base substitution (>=2bp and <=200bp) CA GC intron_variant MELA-AU 15 28531817 28531817 single base substitution G A intron_variant MELA-AU 15 28533365 28533365 single base substitution G A intron_variant MELA-AU 15 28533888 28533888 single base substitution G A intron_variant MELA-AU 15 28533901 28533901 single base substitution G A intron_variant MELA-AU 15 28534172 28534172 single base substitution G A intron_variant MELA-AU 15 28534293 28534293 single base substitution A C intron_variant MELA-AU 15 28534933 28534933 single base substitution G A intron_variant MELA-AU 15 28535074 28535074 single base substitution G A intron_variant MELA-AU 15 28535170 28535170 single base substitution G A intron_variant MELA-AU 15 28536349 28536349 single base substitution G A intron_variant MELA-AU 15 28536379 28536379 single base substitution G A intron_variant MELA-AU 15 28536585 28536585 single base substitution G A intron_variant MELA-AU 15 28536616 28536616 single base substitution G A intron_variant MELA-AU 15 28536899 28536899 single base substitution G A intron_variant MELA-AU 15 28536984 28536984 single base substitution G A intron_variant MELA-AU 15 28537134 28537134 single base substitution G A intron_variant MELA-AU 15 28537493 28537493 single base substitution G A intron_variant MELA-AU 15 28537584 28537584 single base substitution G A intron_variant MELA-AU 15 28537587 28537587 single base substitution G A intron_variant MELA-AU 15 28538415 28538415 single base substitution G A intron_variant MELA-AU 15 28538522 28538522 single base substitution C A intron_variant MELA-AU 15 28540408 28540409 multiple base substitution (>=2bp and <=200bp) AA TC intron_variant MELA-AU 15 28540555 28540555 single base substitution G A intron_variant MELA-AU 15 28540802 28540802 single base substitution C T intron_variant MELA-AU 15 28541341 28541341 single base substitution G A intron_variant MELA-AU 15 28541351 28541351 single base substitution G A intron_variant MELA-AU 15 28542714 28542714 single base substitution G A intron_variant MELA-AU 15 28543570 28543570 single base substitution G A intron_variant MELA-AU 15 28544372 28544372 single base substitution A T intron_variant MELA-AU 15 28545957 28545957 single base substitution G A intron_variant MELA-AU 15 28545957 28545957 single base substitution G A upstream_gene_variant MELA-AU 15 28550484 28550484 single base substitution C T intron_variant MELA-AU 15 28551014 28551014 single base substitution G A intron_variant MELA-AU 15 28551478 28551478 single base substitution G A intron_variant MELA-AU 15 28552025 28552025 single base substitution G A intron_variant MELA-AU 15 28552338 28552338 single base substitution G A intron_variant MELA-AU 15 28553609 28553609 single base substitution T C intron_variant MELA-AU 15 28553646 28553646 single base substitution G A intron_variant MELA-AU 15 28554592 28554593 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28555384 28555384 single base substitution G A intron_variant MELA-AU 15 28556430 28556430 single base substitution G A intron_variant MELA-AU 15 28556536 28556536 single base substitution G A intron_variant MELA-AU 15 28556903 28556903 single base substitution G A intron_variant MELA-AU 15 28558984 28558984 single base substitution G A intron_variant MELA-AU 15 28560326 28560326 single base substitution G A downstream_gene_variant MELA-AU 15 28560326 28560326 single base substitution G A intron_variant MELA-AU 15 28560919 28560919 single base substitution C T downstream_gene_variant MELA-AU 15 28560919 28560919 single base substitution C T intron_variant MELA-AU 15 28561652 28561652 single base substitution C T downstream_gene_variant MELA-AU 15 28561652 28561652 single base substitution C T intron_variant MELA-AU 15 28562505 28562505 single base substitution G A downstream_gene_variant MELA-AU 15 28562505 28562505 single base substitution G A intron_variant MELA-AU 15 28563175 28563175 single base substitution G A downstream_gene_variant MELA-AU 15 28563175 28563175 single base substitution G A intron_variant MELA-AU 15 28564379 28564379 single base substitution C T downstream_gene_variant MELA-AU 15 28564379 28564379 single base substitution C T intron_variant MELA-AU 15 28564384 28564384 single base substitution G A downstream_gene_variant MELA-AU 15 28564384 28564384 single base substitution G A intron_variant MELA-AU 15 28564511 28564511 single base substitution C T downstream_gene_variant MELA-AU 15 28564511 28564511 single base substitution C T intron_variant MELA-AU 15 28564706 28564706 single base substitution G A downstream_gene_variant MELA-AU 15 28564706 28564706 single base substitution G A intron_variant MELA-AU 15 28566009 28566009 single base substitution C G intron_variant MELA-AU 15 28566255 28566256 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 28570865 28570865 single base substitution G A upstream_gene_variant MELA-AU 15 28572011 28572017 deletion of <=200bp TCTCTAC - upstream_gene_variant ORCA-IN 15 28359789 28359789 single base substitution C T downstream_gene_variant ORCA-IN 15 28359789 28359789 single base substitution C T exon_variant ORCA-IN 15 28359789 28359789 single base substitution C T missense_variant A4628T 13882G>A ORCA-IN 15 28359789 28359789 single base substitution C T upstream_gene_variant ORCA-IN 15 28368725 28368725 single base substitution C T intron_variant ORCA-IN 15 28383143 28383143 single base substitution G C downstream_gene_variant ORCA-IN 15 28383143 28383143 single base substitution G C intron_variant ORCA-IN 15 28392471 28392471 single base substitution C A intron_variant ORCA-IN 15 28392471 28392471 single base substitution C A upstream_gene_variant ORCA-IN 15 28398400 28398400 single base substitution G A intron_variant ORCA-IN 15 28421639 28421639 single base substitution C A synonymous_variant V3207V 9621G>T ORCA-IN 15 28421639 28421639 single base substitution C A upstream_gene_variant ORCA-IN 15 28461318 28461318 single base substitution C T intron_variant ORCA-IN 15 28472290 28472290 single base substitution G A intron_variant ORCA-IN 15 28482832 28482832 single base substitution G A intron_variant ORCA-IN 15 28509166 28509166 deletion of <=200bp C - intron_variant ORCA-IN 15 28515389 28515390 multiple base substitution (>=2bp and <=200bp) TT AG downstream_gene_variant ORCA-IN 15 28515389 28515390 multiple base substitution (>=2bp and <=200bp) TT AG intron_variant ORCA-IN 15 28531751 28531751 single base substitution C G intron_variant ORCA-IN 15 28545096 28545096 single base substitution A C intron_variant ORCA-IN 15 28545096 28545096 single base substitution A C upstream_gene_variant OV-AU 15 28351239 28351239 single base substitution T G downstream_gene_variant OV-AU 15 28352036 28352036 single base substitution C A downstream_gene_variant OV-AU 15 28352181 28352181 single base substitution C G downstream_gene_variant OV-AU 15 28354671 28354671 single base substitution T C downstream_gene_variant OV-AU 15 28360485 28360485 single base substitution G A exon_variant OV-AU 15 28360485 28360485 single base substitution G A intron_variant OV-AU 15 28360485 28360485 single base substitution G A upstream_gene_variant OV-AU 15 28360487 28360487 single base substitution C A exon_variant OV-AU 15 28360487 28360487 single base substitution C A intron_variant OV-AU 15 28360487 28360487 single base substitution C A upstream_gene_variant OV-AU 15 28371558 28371558 single base substitution T A intron_variant OV-AU 15 28373666 28373666 single base substitution C G intron_variant OV-AU 15 28374305 28374305 single base substitution T G intron_variant OV-AU 15 28376885 28376885 single base substitution C T intron_variant OV-AU 15 28379113 28379113 single base substitution G A intron_variant OV-AU 15 28384726 28384726 single base substitution T G downstream_gene_variant OV-AU 15 28384726 28384726 single base substitution T G intron_variant OV-AU 15 28385360 28385360 single base substitution C T downstream_gene_variant OV-AU 15 28385360 28385360 single base substitution C T intron_variant OV-AU 15 28399288 28399288 single base substitution A G intron_variant OV-AU 15 28422427 28422427 single base substitution A T intron_variant OV-AU 15 28422427 28422427 single base substitution A T upstream_gene_variant OV-AU 15 28428315 28428315 single base substitution C T intron_variant OV-AU 15 28440424 28440424 single base substitution C G intron_variant OV-AU 15 28454154 28454154 single base substitution G A intron_variant OV-AU 15 28459092 28459092 single base substitution G A synonymous_variant D2194D 6582C>T OV-AU 15 28459095 28459095 single base substitution G A synonymous_variant P2193P 6579C>T OV-AU 15 28462829 28462829 single base substitution G A downstream_gene_variant OV-AU 15 28462829 28462829 single base substitution G A intron_variant OV-AU 15 28463344 28463344 single base substitution A C downstream_gene_variant OV-AU 15 28463344 28463344 single base substitution A C intron_variant OV-AU 15 28464262 28464262 single base substitution G C downstream_gene_variant OV-AU 15 28464262 28464262 single base substitution G C intron_variant OV-AU 15 28483792 28483792 single base substitution A G missense_variant I1235T 3704T>C OV-AU 15 28488634 28488634 single base substitution G A intron_variant OV-AU 15 28489886 28489886 single base substitution G A intron_variant OV-AU 15 28492122 28492122 single base substitution A G intron_variant OV-AU 15 28495198 28495198 single base substitution A C downstream_gene_variant OV-AU 15 28495198 28495198 single base substitution A C intron_variant OV-AU 15 28495312 28495312 single base substitution T A downstream_gene_variant OV-AU 15 28495312 28495312 single base substitution T A intron_variant OV-AU 15 28495595 28495595 single base substitution T A downstream_gene_variant OV-AU 15 28495595 28495595 single base substitution T A intron_variant OV-AU 15 28498830 28498830 single base substitution G A downstream_gene_variant OV-AU 15 28498830 28498830 single base substitution G A intron_variant OV-AU 15 28500716 28500716 single base substitution G A intron_variant OV-AU 15 28500767 28500767 single base substitution C T intron_variant OV-AU 15 28507509 28507509 single base substitution C A intron_variant OV-AU 15 28520890 28520890 single base substitution C T downstream_gene_variant OV-AU 15 28520890 28520890 single base substitution C T intron_variant OV-AU 15 28520890 28520890 single base substitution C T upstream_gene_variant OV-AU 15 28537757 28537757 single base substitution T A intron_variant OV-AU 15 28540614 28540614 single base substitution C A intron_variant OV-AU 15 28543994 28543994 single base substitution A G intron_variant OV-AU 15 28551682 28551682 single base substitution T C intron_variant OV-AU 15 28555782 28555782 single base substitution G A intron_variant OV-US 15 28437274 28437274 single base substitution G C exon_variant OV-US 15 28437274 28437274 single base substitution G C missense_variant R2762G 8284C>G OV-US 15 28459291 28459291 single base substitution G A synonymous_variant L2162L 6486C>T OV-US 15 28511071 28511071 single base substitution C T 3_prime_UTR_variant OV-US 15 28511071 28511071 single base substitution C T missense_variant G550R 1648G>A PACA-AU 15 28353443 28353443 single base substitution C A downstream_gene_variant PACA-AU 15 28367472 28367472 single base substitution G C intron_variant PACA-AU 15 28367472 28367472 single base substitution G C upstream_gene_variant PACA-AU 15 28373829 28373829 single base substitution C T intron_variant PACA-AU 15 28378931 28378931 single base substitution C A intron_variant PACA-AU 15 28379475 28379475 single base substitution A G intron_variant PACA-AU 15 28380623 28380623 single base substitution C A splice_donor_variant PACA-AU 15 28384491 28384491 single base substitution G A downstream_gene_variant PACA-AU 15 28384491 28384491 single base substitution G A intron_variant PACA-AU 15 28388302 28388302 single base substitution A G intron_variant PACA-AU 15 28388302 28388302 single base substitution A G upstream_gene_variant PACA-AU 15 28389359 28389359 single base substitution G T missense_variant D3721E 11163C>A PACA-AU 15 28389359 28389359 single base substitution G T upstream_gene_variant PACA-AU 15 28389505 28389505 single base substitution C G intron_variant PACA-AU 15 28389505 28389505 single base substitution C G upstream_gene_variant PACA-AU 15 28390044 28390044 single base substitution G A intron_variant PACA-AU 15 28390044 28390044 single base substitution G A upstream_gene_variant PACA-AU 15 28395108 28395108 single base substitution C T downstream_gene_variant PACA-AU 15 28395108 28395108 single base substitution C T intron_variant PACA-AU 15 28401395 28401395 single base substitution C T intron_variant PACA-AU 15 28404827 28404827 single base substitution C G intron_variant PACA-AU 15 28405018 28405018 single base substitution T C intron_variant PACA-AU 15 28408036 28408036 single base substitution C T intron_variant PACA-AU 15 28411125 28411125 single base substitution G A intron_variant PACA-AU 15 28419991 28419991 single base substitution A C intron_variant PACA-AU 15 28419991 28419991 single base substitution A C upstream_gene_variant PACA-AU 15 28420441 28420441 single base substitution C A intron_variant PACA-AU 15 28420441 28420441 single base substitution C A upstream_gene_variant PACA-AU 15 28422548 28422548 deletion of <=200bp A - intron_variant PACA-AU 15 28422548 28422548 deletion of <=200bp A - upstream_gene_variant PACA-AU 15 28425936 28425936 single base substitution C A intron_variant PACA-AU 15 28427718 28427718 insertion of <=200bp - A intron_variant PACA-AU 15 28429326 28429326 single base substitution G A intron_variant PACA-AU 15 28436178 28436178 single base substitution A G exon_variant PACA-AU 15 28436178 28436178 single base substitution A G missense_variant I2861T 8582T>C PACA-AU 15 28438558 28438558 single base substitution C A intron_variant PACA-AU 15 28441768 28441768 single base substitution C G intron_variant PACA-AU 15 28441817 28441817 deletion of <=200bp G - intron_variant PACA-AU 15 28442695 28442695 single base substitution C T intron_variant PACA-AU 15 28444139 28444139 insertion of <=200bp - A intron_variant PACA-AU 15 28446644 28446644 single base substitution C T exon_variant PACA-AU 15 28446644 28446644 single base substitution C T synonymous_variant L2558L 7674G>A PACA-AU 15 28453992 28453992 single base substitution G A intron_variant PACA-AU 15 28453992 28453992 single base substitution G A upstream_gene_variant PACA-AU 15 28456250 28456250 single base substitution G T missense_variant L2323I 6967C>A PACA-AU 15 28459634 28459634 single base substitution A G intron_variant PACA-AU 15 28460216 28460216 single base substitution A G intron_variant PACA-AU 15 28460242 28460242 single base substitution C T intron_variant PACA-AU 15 28462360 28462360 single base substitution T C downstream_gene_variant PACA-AU 15 28462360 28462360 single base substitution T C intron_variant PACA-AU 15 28465560 28465560 single base substitution G A downstream_gene_variant PACA-AU 15 28465560 28465560 single base substitution G A intron_variant PACA-AU 15 28467979 28467979 single base substitution G A intron_variant PACA-AU 15 28469540 28469540 single base substitution G A intron_variant PACA-AU 15 28474440 28474440 single base substitution G A exon_variant PACA-AU 15 28474440 28474440 single base substitution G A missense_variant R1725W 5173C>T PACA-AU 15 28476099 28476099 single base substitution A T intron_variant PACA-AU 15 28476099 28476099 single base substitution A T upstream_gene_variant PACA-AU 15 28486707 28486707 deletion of <=200bp C - intron_variant PACA-AU 15 28490711 28490726 deletion of <=200bp ATACACACACACACAC - intron_variant PACA-AU 15 28498476 28498476 single base substitution A C downstream_gene_variant PACA-AU 15 28498476 28498476 single base substitution A C intron_variant PACA-AU 15 28502869 28502871 deletion of <=200bp CAA - intron_variant PACA-AU 15 28510924 28510924 single base substitution C A intron_variant PACA-AU 15 28513635 28513635 single base substitution C A 3_prime_UTR_variant PACA-AU 15 28513635 28513635 single base substitution C A downstream_gene_variant PACA-AU 15 28513635 28513635 single base substitution C A missense_variant G525V 1574G>T PACA-AU 15 28514275 28514275 single base substitution C A downstream_gene_variant PACA-AU 15 28514275 28514275 single base substitution C A intron_variant PACA-AU 15 28515371 28515371 single base substitution C T downstream_gene_variant PACA-AU 15 28515371 28515371 single base substitution C T intron_variant PACA-AU 15 28517010 28517010 single base substitution G A downstream_gene_variant PACA-AU 15 28517010 28517010 single base substitution G A intron_variant PACA-AU 15 28517715 28517715 single base substitution C T intron_variant PACA-AU 15 28519479 28519479 single base substitution A C 3_prime_UTR_variant PACA-AU 15 28519479 28519479 single base substitution A C missense_variant V253G 758T>G PACA-AU 15 28519479 28519479 single base substitution A C upstream_gene_variant PACA-AU 15 28527718 28527718 single base substitution G A intron_variant PACA-AU 15 28530393 28530393 single base substitution C G intron_variant PACA-AU 15 28535472 28535472 single base substitution C T intron_variant PACA-AU 15 28542836 28542836 single base substitution A G intron_variant PACA-AU 15 28543259 28543259 single base substitution A G intron_variant PACA-AU 15 28545210 28545210 single base substitution A G intron_variant PACA-AU 15 28545210 28545210 single base substitution A G upstream_gene_variant PACA-AU 15 28555601 28555601 single base substitution T A intron_variant PACA-AU 15 28560919 28560919 single base substitution C T downstream_gene_variant PACA-AU 15 28560919 28560919 single base substitution C T intron_variant PACA-AU 15 28563315 28563315 single base substitution T C downstream_gene_variant PACA-AU 15 28563315 28563315 single base substitution T C intron_variant PACA-AU 15 28566301 28566301 single base substitution C A intron_variant PACA-CA 15 28353727 28353727 single base substitution G A downstream_gene_variant PACA-CA 15 28357735 28357735 single base substitution T C downstream_gene_variant PACA-CA 15 28357735 28357735 single base substitution T C intron_variant PACA-CA 15 28359180 28359180 single base substitution C T downstream_gene_variant PACA-CA 15 28359180 28359180 single base substitution C T intron_variant PACA-CA 15 28359180 28359180 single base substitution C T upstream_gene_variant PACA-CA 15 28361492 28361492 single base substitution T G intron_variant PACA-CA 15 28361492 28361492 single base substitution T G upstream_gene_variant PACA-CA 15 28365840 28365840 single base substitution G A intron_variant PACA-CA 15 28365840 28365840 single base substitution G A upstream_gene_variant PACA-CA 15 28368811 28368811 single base substitution G A intron_variant PACA-CA 15 28369289 28369289 single base substitution C A missense_variant C4361F 13082G>T PACA-CA 15 28371243 28371243 single base substitution C A intron_variant PACA-CA 15 28371562 28371562 single base substitution A G intron_variant PACA-CA 15 28373249 28373249 deletion of <=200bp A - intron_variant PACA-CA 15 28373336 28373336 single base substitution C G intron_variant PACA-CA 15 28373829 28373829 single base substitution C T intron_variant PACA-CA 15 28375710 28375710 single base substitution T A stop_gained K4201* 12601A>T PACA-CA 15 28376885 28376885 single base substitution C T intron_variant PACA-CA 15 28382085 28382085 single base substitution T G downstream_gene_variant PACA-CA 15 28382085 28382085 single base substitution T G intron_variant PACA-CA 15 28382973 28382973 single base substitution A C downstream_gene_variant PACA-CA 15 28382973 28382973 single base substitution A C intron_variant PACA-CA 15 28385055 28385055 single base substitution A G downstream_gene_variant PACA-CA 15 28385055 28385055 single base substitution A G intron_variant PACA-CA 15 28385295 28385295 single base substitution G A downstream_gene_variant PACA-CA 15 28385295 28385295 single base substitution G A intron_variant PACA-CA 15 28386513 28386513 single base substitution A G downstream_gene_variant PACA-CA 15 28386513 28386513 single base substitution A G intron_variant PACA-CA 15 28386769 28386769 single base substitution C A downstream_gene_variant PACA-CA 15 28386769 28386769 single base substitution C A missense_variant D3942Y 11824G>T PACA-CA 15 28388715 28388715 single base substitution C T intron_variant PACA-CA 15 28388715 28388715 single base substitution C T upstream_gene_variant PACA-CA 15 28389365 28389365 single base substitution G C synonymous_variant L3719L 11157C>G PACA-CA 15 28389365 28389365 single base substitution G C upstream_gene_variant PACA-CA 15 28390194 28390194 single base substitution G A intron_variant PACA-CA 15 28390194 28390194 single base substitution G A upstream_gene_variant PACA-CA 15 28390211 28390211 single base substitution G T intron_variant PACA-CA 15 28390211 28390211 single base substitution G T upstream_gene_variant PACA-CA 15 28391023 28391023 single base substitution G A intron_variant PACA-CA 15 28391023 28391023 single base substitution G A upstream_gene_variant PACA-CA 15 28391348 28391348 single base substitution G T intron_variant PACA-CA 15 28391348 28391348 single base substitution G T upstream_gene_variant PACA-CA 15 28391428 28391428 single base substitution G A missense_variant L3655F 10963C>T PACA-CA 15 28391428 28391428 single base substitution G A upstream_gene_variant PACA-CA 15 28393709 28393709 single base substitution G A downstream_gene_variant PACA-CA 15 28393709 28393709 single base substitution G A intron_variant PACA-CA 15 28396110 28396110 single base substitution G T downstream_gene_variant PACA-CA 15 28396110 28396110 single base substitution G T intron_variant PACA-CA 15 28396186 28396186 single base substitution C G downstream_gene_variant PACA-CA 15 28396186 28396186 single base substitution C G intron_variant PACA-CA 15 28400709 28400709 single base substitution T G intron_variant PACA-CA 15 28406666 28406666 single base substitution T C intron_variant PACA-CA 15 28407679 28407679 single base substitution G A intron_variant PACA-CA 15 28408640 28408640 single base substitution T C intron_variant PACA-CA 15 28410666 28410666 single base substitution G A intron_variant PACA-CA 15 28411375 28411375 single base substitution G A intron_variant PACA-CA 15 28412382 28412382 single base substitution A T intron_variant PACA-CA 15 28413758 28413758 single base substitution C A intron_variant PACA-CA 15 28413981 28413981 single base substitution A G intron_variant PACA-CA 15 28416780 28416780 insertion of <=200bp - T intron_variant PACA-CA 15 28416824 28416824 single base substitution G C intron_variant PACA-CA 15 28417280 28417280 single base substitution A G intron_variant PACA-CA 15 28418244 28418244 single base substitution A G intron_variant PACA-CA 15 28418365 28418365 single base substitution G A intron_variant PACA-CA 15 28419462 28419462 single base substitution T C intron_variant PACA-CA 15 28420046 28420046 single base substitution C A intron_variant PACA-CA 15 28420046 28420046 single base substitution C A upstream_gene_variant PACA-CA 15 28420047 28420047 single base substitution T G intron_variant PACA-CA 15 28420047 28420047 single base substitution T G upstream_gene_variant PACA-CA 15 28421492 28421492 single base substitution G A intron_variant PACA-CA 15 28421492 28421492 single base substitution G A upstream_gene_variant PACA-CA 15 28421607 28421607 single base substitution A G missense_variant L3218P 9653T>C PACA-CA 15 28421607 28421607 single base substitution A G upstream_gene_variant PACA-CA 15 28421959 28421959 single base substitution A G intron_variant PACA-CA 15 28421959 28421959 single base substitution A G upstream_gene_variant PACA-CA 15 28423759 28423759 single base substitution G T intron_variant PACA-CA 15 28423759 28423759 single base substitution G T upstream_gene_variant PACA-CA 15 28425589 28425589 single base substitution A C intron_variant PACA-CA 15 28428236 28428236 single base substitution G A intron_variant PACA-CA 15 28428573 28428573 single base substitution G A intron_variant PACA-CA 15 28430156 28430156 single base substitution T C intron_variant PACA-CA 15 28430233 28430233 single base substitution G C intron_variant PACA-CA 15 28434777 28434777 single base substitution T A downstream_gene_variant PACA-CA 15 28434777 28434777 single base substitution T A intron_variant PACA-CA 15 28439713 28439713 single base substitution G A intron_variant PACA-CA 15 28441049 28441049 single base substitution C T intron_variant PACA-CA 15 28441229 28441229 single base substitution C T intron_variant PACA-CA 15 28442125 28442125 single base substitution C T intron_variant PACA-CA 15 28443598 28443598 single base substitution C T exon_variant PACA-CA 15 28443598 28443598 single base substitution C T missense_variant R2646Q 7937G>A PACA-CA 15 28449985 28449985 single base substitution A G intron_variant PACA-CA 15 28449985 28449985 single base substitution A G upstream_gene_variant PACA-CA 15 28450267 28450267 single base substitution G T intron_variant PACA-CA 15 28450267 28450267 single base substitution G T upstream_gene_variant PACA-CA 15 28453897 28453897 single base substitution C T intron_variant PACA-CA 15 28453897 28453897 single base substitution C T upstream_gene_variant PACA-CA 15 28457531 28457531 single base substitution T A intron_variant PACA-CA 15 28459383 28459383 single base substitution C A missense_variant A2132S 6394G>T PACA-CA 15 28460015 28460015 deletion of <=200bp T - intron_variant PACA-CA 15 28462241 28462241 single base substitution C T intron_variant PACA-CA 15 28462408 28462408 single base substitution C A downstream_gene_variant PACA-CA 15 28462408 28462408 single base substitution C A intron_variant PACA-CA 15 28463738 28463738 single base substitution A G downstream_gene_variant PACA-CA 15 28463738 28463738 single base substitution A G synonymous_variant C1975C 5925T>C PACA-CA 15 28467273 28467273 single base substitution C T downstream_gene_variant PACA-CA 15 28467273 28467273 single base substitution C T synonymous_variant T1851T 5553G>A PACA-CA 15 28468427 28468427 single base substitution G A intron_variant PACA-CA 15 28468833 28468833 single base substitution T A intron_variant PACA-CA 15 28472345 28472345 single base substitution C T intron_variant PACA-CA 15 28473341 28473341 single base substitution C T intron_variant PACA-CA 15 28474081 28474081 single base substitution A T intron_variant PACA-CA 15 28476099 28476099 single base substitution A T intron_variant PACA-CA 15 28476099 28476099 single base substitution A T upstream_gene_variant PACA-CA 15 28477610 28477610 single base substitution G A intron_variant PACA-CA 15 28477610 28477610 single base substitution G A upstream_gene_variant PACA-CA 15 28478796 28478796 single base substitution A G intron_variant PACA-CA 15 28478796 28478796 single base substitution A G upstream_gene_variant PACA-CA 15 28483285 28483285 single base substitution G A missense_variant A1276V 3827C>T PACA-CA 15 28485223 28485223 single base substitution T G intron_variant PACA-CA 15 28489011 28489011 single base substitution G A intron_variant PACA-CA 15 28489597 28489597 single base substitution T C intron_variant PACA-CA 15 28494062 28494062 single base substitution A G intron_variant PACA-CA 15 28494851 28494851 single base substitution G A downstream_gene_variant PACA-CA 15 28494851 28494851 single base substitution G A intron_variant PACA-CA 15 28496469 28496469 single base substitution G C downstream_gene_variant PACA-CA 15 28496469 28496469 single base substitution G C intron_variant PACA-CA 15 28496759 28496759 single base substitution C A downstream_gene_variant PACA-CA 15 28496759 28496759 single base substitution C A intron_variant PACA-CA 15 28500765 28500765 single base substitution A G intron_variant PACA-CA 15 28501223 28501223 single base substitution C A intron_variant PACA-CA 15 28503636 28503636 single base substitution A C intron_variant PACA-CA 15 28506899 28506899 single base substitution C A intron_variant PACA-CA 15 28509196 28509196 deletion of <=200bp A - intron_variant PACA-CA 15 28511221 28511221 single base substitution G A intron_variant PACA-CA 15 28513606 28513606 single base substitution C T downstream_gene_variant PACA-CA 15 28513606 28513606 single base substitution C T splice_region_variant PACA-CA 15 28517925 28517926 deletion of <=200bp AC - intron_variant PACA-CA 15 28520937 28520937 single base substitution T A downstream_gene_variant PACA-CA 15 28520937 28520937 single base substitution T A intron_variant PACA-CA 15 28520937 28520937 single base substitution T A upstream_gene_variant PACA-CA 15 28522624 28522624 single base substitution A G downstream_gene_variant PACA-CA 15 28522624 28522624 single base substitution A G intron_variant PACA-CA 15 28522624 28522624 single base substitution A G upstream_gene_variant PACA-CA 15 28526120 28526120 single base substitution C A intron_variant PACA-CA 15 28529246 28529246 single base substitution G A intron_variant PACA-CA 15 28529474 28529474 single base substitution A G intron_variant PACA-CA 15 28532387 28532387 single base substitution G T intron_variant PACA-CA 15 28534738 28534738 single base substitution C T intron_variant PACA-CA 15 28535257 28535257 single base substitution T A intron_variant PACA-CA 15 28536092 28536092 insertion of <=200bp - A intron_variant PACA-CA 15 28536199 28536199 single base substitution G A intron_variant PACA-CA 15 28537547 28537547 single base substitution G T intron_variant PACA-CA 15 28537628 28537628 single base substitution A G intron_variant PACA-CA 15 28541236 28541236 single base substitution C T intron_variant PACA-CA 15 28543954 28543954 single base substitution G A intron_variant PACA-CA 15 28544107 28544107 single base substitution C A intron_variant PACA-CA 15 28548658 28548658 single base substitution G A intron_variant PACA-CA 15 28548658 28548658 single base substitution G A upstream_gene_variant PACA-CA 15 28548812 28548812 single base substitution T C intron_variant PACA-CA 15 28548812 28548812 single base substitution T C upstream_gene_variant PACA-CA 15 28556491 28556491 single base substitution G C intron_variant PACA-CA 15 28557021 28557021 single base substitution T A intron_variant PACA-CA 15 28557022 28557022 single base substitution T A intron_variant PACA-CA 15 28559031 28559031 single base substitution A T intron_variant PACA-CA 15 28560785 28560785 single base substitution A G downstream_gene_variant PACA-CA 15 28560785 28560785 single base substitution A G intron_variant PACA-CA 15 28562312 28562312 single base substitution C T downstream_gene_variant PACA-CA 15 28562312 28562312 single base substitution C T intron_variant PACA-CA 15 28564363 28564363 single base substitution C T downstream_gene_variant PACA-CA 15 28564363 28564363 single base substitution C T intron_variant PACA-CA 15 28564408 28564408 single base substitution A G downstream_gene_variant PACA-CA 15 28564408 28564408 single base substitution A G intron_variant PACA-CA 15 28572014 28572014 single base substitution C G upstream_gene_variant PAEN-AU 15 28490711 28490726 deletion of <=200bp ATACACACACACACAC - intron_variant PAEN-AU 15 28515389 28515389 single base substitution T A downstream_gene_variant PAEN-AU 15 28515389 28515389 single base substitution T A intron_variant PAEN-AU 15 28534601 28534601 single base substitution C G intron_variant PAEN-AU 15 28543954 28543954 single base substitution G A intron_variant PAEN-IT 15 28375354 28375354 single base substitution C T missense_variant A4253T 12757G>A PAEN-IT 15 28493612 28493612 single base substitution T C intron_variant PBCA-DE 15 28360759 28360759 single base substitution G A intron_variant PBCA-DE 15 28360759 28360759 single base substitution G A upstream_gene_variant PBCA-DE 15 28366746 28366746 single base substitution G A intron_variant PBCA-DE 15 28366746 28366746 single base substitution G A upstream_gene_variant PBCA-DE 15 28376840 28376840 single base substitution C A intron_variant PBCA-DE 15 28389565 28389565 single base substitution C G intron_variant PBCA-DE 15 28389565 28389565 single base substitution C G upstream_gene_variant PBCA-DE 15 28397571 28397571 single base substitution G C downstream_gene_variant PBCA-DE 15 28397571 28397571 single base substitution G C intron_variant PBCA-DE 15 28406400 28406400 insertion of <=200bp - T intron_variant PBCA-DE 15 28428531 28428531 insertion of <=200bp - T intron_variant PBCA-DE 15 28436410 28436410 single base substitution C A intron_variant PBCA-DE 15 28437274 28437274 single base substitution G C exon_variant PBCA-DE 15 28437274 28437274 single base substitution G C missense_variant R2762G 8284C>G PBCA-DE 15 28444293 28444293 insertion of <=200bp - A intron_variant PBCA-DE 15 28462261 28462261 insertion of <=200bp - C intron_variant PBCA-DE 15 28515391 28515391 insertion of <=200bp - ATAG downstream_gene_variant PBCA-DE 15 28515391 28515391 insertion of <=200bp - ATAG intron_variant PBCA-DE 15 28529686 28529686 deletion of <=200bp A - intron_variant PBCA-DE 15 28538710 28538710 deletion of <=200bp C - intron_variant PBCA-DE 15 28538744 28538744 deletion of <=200bp A - intron_variant PBCA-DE 15 28554673 28554673 single base substitution G A intron_variant PBCA-DE 15 28566677 28566677 insertion of <=200bp - GTT intron_variant PBCA-DE 15 28566678 28566678 insertion of <=200bp - AATG intron_variant PRAD-CA 15 28372873 28372873 single base substitution G C intron_variant PRAD-CA 15 28387667 28387667 single base substitution C T intron_variant PRAD-CA 15 28387667 28387667 single base substitution C T upstream_gene_variant PRAD-CA 15 28419695 28419695 single base substitution T C synonymous_variant T3301T 9903A>G PRAD-CA 15 28419695 28419695 single base substitution T C upstream_gene_variant PRAD-CA 15 28447034 28447034 single base substitution T C intron_variant PRAD-CA 15 28462341 28462341 single base substitution C T downstream_gene_variant PRAD-CA 15 28462341 28462341 single base substitution C T intron_variant PRAD-CA 15 28472376 28472376 single base substitution G A intron_variant PRAD-CA 15 28472614 28472614 single base substitution G A intron_variant PRAD-CA 15 28474627 28474627 single base substitution A G exon_variant PRAD-CA 15 28474627 28474627 single base substitution A G missense_variant I1700T 5099T>C PRAD-CA 15 28490708 28490708 single base substitution T A intron_variant PRAD-CA 15 28490712 28490712 single base substitution T C intron_variant PRAD-CA 15 28500765 28500765 single base substitution A G intron_variant PRAD-CA 15 28520095 28520095 single base substitution G A 3_prime_UTR_variant PRAD-CA 15 28520095 28520095 single base substitution G A missense_variant A200V 599C>T PRAD-CA 15 28520095 28520095 single base substitution G A upstream_gene_variant PRAD-CA 15 28534186 28534186 single base substitution A G intron_variant PRAD-CA 15 28534605 28534605 single base substitution A G intron_variant PRAD-CA 15 28566684 28566684 single base substitution A G intron_variant PRAD-UK 15 28390598 28390598 single base substitution C T intron_variant PRAD-UK 15 28390598 28390598 single base substitution C T upstream_gene_variant PRAD-UK 15 28397030 28397030 single base substitution C T downstream_gene_variant PRAD-UK 15 28397030 28397030 single base substitution C T intron_variant PRAD-UK 15 28423540 28423540 single base substitution C A intron_variant PRAD-UK 15 28423540 28423540 single base substitution C A upstream_gene_variant PRAD-UK 15 28426114 28426114 single base substitution G A intron_variant PRAD-UK 15 28427671 28427671 single base substitution A G intron_variant PRAD-UK 15 28428710 28428710 single base substitution A C intron_variant PRAD-UK 15 28428832 28428832 single base substitution A C intron_variant PRAD-UK 15 28428950 28428950 single base substitution A C intron_variant PRAD-UK 15 28428990 28428990 single base substitution A G intron_variant PRAD-UK 15 28429041 28429041 single base substitution A C intron_variant PRAD-UK 15 28434725 28434740 deletion of <=200bp ATTATGAAATAGTTCC - downstream_gene_variant PRAD-UK 15 28434725 28434740 deletion of <=200bp ATTATGAAATAGTTCC - intron_variant PRAD-UK 15 28436556 28436556 single base substitution G A intron_variant PRAD-UK 15 28437861 28437861 single base substitution A T intron_variant PRAD-UK 15 28441607 28441607 single base substitution G A missense_variant T2707M 8120C>T PRAD-UK 15 28441607 28441607 single base substitution G A splice_region_variant PRAD-UK 15 28453190 28453190 single base substitution G T intron_variant PRAD-UK 15 28453190 28453190 single base substitution G T upstream_gene_variant PRAD-UK 15 28462734 28462734 insertion of <=200bp - CACA downstream_gene_variant PRAD-UK 15 28462734 28462734 insertion of <=200bp - CACA intron_variant PRAD-UK 15 28466105 28466105 single base substitution C A downstream_gene_variant PRAD-UK 15 28466105 28466105 single base substitution C A intron_variant PRAD-UK 15 28474905 28474905 single base substitution G A missense_variant S1633F 4898C>T PRAD-UK 15 28474905 28474905 single base substitution G A upstream_gene_variant PRAD-UK 15 28501297 28501297 single base substitution G A 3_prime_UTR_variant PRAD-UK 15 28501297 28501297 single base substitution G A missense_variant S895F 2684C>T PRAD-UK 15 28501787 28501787 single base substitution A C intron_variant PRAD-UK 15 28502602 28502602 single base substitution C G intron_variant PRAD-UK 15 28516407 28516407 single base substitution A G downstream_gene_variant PRAD-UK 15 28516407 28516407 single base substitution A G intron_variant PRAD-UK 15 28548005 28548005 insertion of <=200bp - ATT intron_variant PRAD-UK 15 28548005 28548005 insertion of <=200bp - ATT upstream_gene_variant PRAD-UK 15 28570449 28570449 single base substitution C A upstream_gene_variant PRAD-UK 15 28572011 28572017 deletion of <=200bp TCTCTAC - upstream_gene_variant PRAD-US 15 28359926 28359926 single base substitution C T downstream_gene_variant PRAD-US 15 28359926 28359926 single base substitution C T exon_variant PRAD-US 15 28359926 28359926 single base substitution C T missense_variant G4582E 13745G>A PRAD-US 15 28359926 28359926 single base substitution C T upstream_gene_variant PRAD-US 15 28386775 28386775 single base substitution G A downstream_gene_variant PRAD-US 15 28386775 28386775 single base substitution G A stop_gained R3940* 11818C>T PRAD-US 15 28386876 28386876 single base substitution C A downstream_gene_variant PRAD-US 15 28386876 28386876 single base substitution C A splice_donor_variant PRAD-US 15 28387490 28387490 deletion of <=200bp C - exon_variant PRAD-US 15 28387490 28387490 deletion of <=200bp C - frameshift_variant C3865 READ-US 15 28358790 28358790 single base substitution G A downstream_gene_variant READ-US 15 28358790 28358790 single base substitution G A exon_variant READ-US 15 28358790 28358790 single base substitution G A missense_variant R4650W 13948C>T READ-US 15 28377391 28377391 single base substitution C T missense_variant G4142D 12425G>A READ-US 15 28422162 28422162 single base substitution G A synonymous_variant T3122T 9366C>T READ-US 15 28422162 28422162 single base substitution G A upstream_gene_variant READ-US 15 28431765 28431765 single base substitution G A downstream_gene_variant READ-US 15 28431765 28431765 single base substitution G A missense_variant S2928L 8783C>T READ-US 15 28459027 28459027 single base substitution C T missense_variant R2216H 6647G>A READ-US 15 28499628 28499628 single base substitution C A downstream_gene_variant READ-US 15 28499628 28499628 single base substitution C A stop_gained E970* 2908G>T READ-US 15 28502333 28502333 single base substitution C A 3_prime_UTR_variant READ-US 15 28502333 28502333 single base substitution C A missense_variant M797I 2391G>T READ-US 15 28517361 28517361 single base substitution G A exon_variant READ-US 15 28517361 28517361 single base substitution G A splice_region_variant RECA-CN 15 28389088 28389088 single base substitution T A synonymous_variant T3783T 11349A>T RECA-CN 15 28389088 28389088 single base substitution T A upstream_gene_variant RECA-CN 15 28483903 28483903 single base substitution C A missense_variant G1198V 3593G>T RECA-EU 15 28355682 28355682 single base substitution A C downstream_gene_variant RECA-EU 15 28365918 28365918 single base substitution A C intron_variant RECA-EU 15 28365918 28365918 single base substitution A C upstream_gene_variant RECA-EU 15 28385059 28385059 single base substitution A G downstream_gene_variant RECA-EU 15 28385059 28385059 single base substitution A G intron_variant RECA-EU 15 28385947 28385947 single base substitution C A downstream_gene_variant RECA-EU 15 28385947 28385947 single base substitution C A intron_variant RECA-EU 15 28387426 28387426 single base substitution G A exon_variant RECA-EU 15 28387426 28387426 single base substitution G A synonymous_variant A3886A 11658C>T RECA-EU 15 28389674 28389674 single base substitution C T intron_variant RECA-EU 15 28389674 28389674 single base substitution C T upstream_gene_variant RECA-EU 15 28400707 28400707 single base substitution C G intron_variant RECA-EU 15 28407386 28407386 single base substitution G A intron_variant RECA-EU 15 28413981 28413981 single base substitution A G intron_variant RECA-EU 15 28419778 28419778 single base substitution G A intron_variant RECA-EU 15 28419778 28419778 single base substitution G A upstream_gene_variant RECA-EU 15 28437247 28437247 single base substitution G C exon_variant RECA-EU 15 28437247 28437247 single base substitution G C missense_variant H2771D 8311C>G RECA-EU 15 28444750 28444750 single base substitution T G intron_variant RECA-EU 15 28448486 28448486 single base substitution C A exon_variant RECA-EU 15 28448486 28448486 single base substitution C A intron_variant RECA-EU 15 28449363 28449363 single base substitution T A intron_variant RECA-EU 15 28449363 28449363 single base substitution T A upstream_gene_variant RECA-EU 15 28452840 28452840 single base substitution C G intron_variant RECA-EU 15 28452840 28452840 single base substitution C G upstream_gene_variant RECA-EU 15 28460102 28460102 single base substitution T A intron_variant RECA-EU 15 28488623 28488623 single base substitution T C intron_variant RECA-EU 15 28516257 28516257 single base substitution C T downstream_gene_variant RECA-EU 15 28516257 28516257 single base substitution C T intron_variant RECA-EU 15 28533857 28533857 single base substitution G A intron_variant RECA-EU 15 28552227 28552227 single base substitution C T intron_variant RECA-EU 15 28562621 28562621 single base substitution G C downstream_gene_variant RECA-EU 15 28562621 28562621 single base substitution G C intron_variant SKCA-BR 15 28353209 28353209 single base substitution G A downstream_gene_variant SKCA-BR 15 28353570 28353570 single base substitution T G downstream_gene_variant SKCA-BR 15 28363430 28363430 single base substitution G C exon_variant SKCA-BR 15 28363430 28363430 single base substitution G C intron_variant SKCA-BR 15 28363430 28363430 single base substitution G C upstream_gene_variant SKCA-BR 15 28364799 28364799 single base substitution C G intron_variant SKCA-BR 15 28364799 28364799 single base substitution C G upstream_gene_variant SKCA-BR 15 28368563 28368563 single base substitution C A intron_variant SKCA-BR 15 28368563 28368563 single base substitution C A upstream_gene_variant SKCA-BR 15 28371990 28371990 single base substitution C T intron_variant SKCA-BR 15 28378467 28378467 single base substitution T C intron_variant SKCA-BR 15 28380887 28380887 single base substitution C T intron_variant SKCA-BR 15 28381143 28381143 single base substitution T A intron_variant SKCA-BR 15 28381774 28381774 single base substitution C A intron_variant SKCA-BR 15 28381995 28381995 single base substitution A G downstream_gene_variant SKCA-BR 15 28381995 28381995 single base substitution A G intron_variant SKCA-BR 15 28391399 28391399 single base substitution G A synonymous_variant I3664I 10992C>T SKCA-BR 15 28391399 28391399 single base substitution G A upstream_gene_variant SKCA-BR 15 28392292 28392292 single base substitution G A intron_variant SKCA-BR 15 28392292 28392292 single base substitution G A upstream_gene_variant SKCA-BR 15 28394696 28394696 single base substitution G A downstream_gene_variant SKCA-BR 15 28394696 28394696 single base substitution G A intron_variant SKCA-BR 15 28395220 28395221 deletion of <=200bp AC - downstream_gene_variant SKCA-BR 15 28395220 28395221 deletion of <=200bp AC - intron_variant SKCA-BR 15 28400069 28400069 single base substitution A C intron_variant SKCA-BR 15 28400738 28400738 single base substitution C T intron_variant SKCA-BR 15 28400740 28400740 single base substitution C T intron_variant SKCA-BR 15 28400747 28400747 single base substitution G T intron_variant SKCA-BR 15 28402491 28402491 single base substitution C A intron_variant SKCA-BR 15 28405291 28405291 single base substitution T G intron_variant SKCA-BR 15 28406795 28406795 single base substitution C T intron_variant SKCA-BR 15 28409189 28409189 single base substitution G A intron_variant SKCA-BR 15 28410428 28410428 single base substitution G A intron_variant SKCA-BR 15 28413963 28413963 single base substitution T G intron_variant SKCA-BR 15 28419012 28419018 deletion of <=200bp GAAATTA - intron_variant SKCA-BR 15 28419423 28419423 single base substitution G T intron_variant SKCA-BR 15 28429181 28429181 single base substitution C A intron_variant SKCA-BR 15 28429328 28429328 single base substitution C A intron_variant SKCA-BR 15 28431891 28431891 single base substitution C A downstream_gene_variant SKCA-BR 15 28431891 28431891 single base substitution C A missense_variant R2886M 8657G>T SKCA-BR 15 28431980 28431980 single base substitution C T downstream_gene_variant SKCA-BR 15 28431980 28431980 single base substitution C T intron_variant SKCA-BR 15 28435435 28435435 single base substitution G A exon_variant SKCA-BR 15 28435435 28435435 single base substitution G A intron_variant SKCA-BR 15 28437280 28437280 single base substitution A T exon_variant SKCA-BR 15 28437280 28437280 single base substitution A T missense_variant C2760S 8278T>A SKCA-BR 15 28440201 28440201 insertion of <=200bp - CA intron_variant SKCA-BR 15 28444802 28444802 single base substitution T C intron_variant SKCA-BR 15 28448907 28448907 single base substitution G A exon_variant SKCA-BR 15 28448907 28448907 single base substitution G A intron_variant SKCA-BR 15 28450073 28450073 single base substitution A G intron_variant SKCA-BR 15 28450073 28450073 single base substitution A G upstream_gene_variant SKCA-BR 15 28450905 28450905 single base substitution G A intron_variant SKCA-BR 15 28450905 28450905 single base substitution G A upstream_gene_variant SKCA-BR 15 28451161 28451161 single base substitution T C intron_variant SKCA-BR 15 28451161 28451161 single base substitution T C upstream_gene_variant SKCA-BR 15 28455722 28455738 deletion of <=200bp ACACCAACTGAAATTCC - intron_variant SKCA-BR 15 28456306 28456306 single base substitution A T intron_variant SKCA-BR 15 28456814 28456814 single base substitution G T intron_variant SKCA-BR 15 28456853 28456853 single base substitution A T intron_variant SKCA-BR 15 28456967 28456967 single base substitution C T intron_variant SKCA-BR 15 28461189 28461204 deletion of <=200bp GTTTCCCAGGCTGGTC - intron_variant SKCA-BR 15 28462263 28462263 single base substitution G A intron_variant SKCA-BR 15 28463447 28463447 single base substitution G A downstream_gene_variant SKCA-BR 15 28463447 28463447 single base substitution G A intron_variant SKCA-BR 15 28465598 28465598 single base substitution C T downstream_gene_variant SKCA-BR 15 28465598 28465598 single base substitution C T missense_variant E1949K 5845G>A SKCA-BR 15 28466122 28466122 single base substitution T C downstream_gene_variant SKCA-BR 15 28466122 28466122 single base substitution T C intron_variant SKCA-BR 15 28469348 28469348 single base substitution T C intron_variant SKCA-BR 15 28475922 28475922 single base substitution C T intron_variant SKCA-BR 15 28475922 28475922 single base substitution C T upstream_gene_variant SKCA-BR 15 28476694 28476694 single base substitution T C intron_variant SKCA-BR 15 28476694 28476694 single base substitution T C upstream_gene_variant SKCA-BR 15 28478250 28478250 single base substitution G A intron_variant SKCA-BR 15 28478250 28478250 single base substitution G A upstream_gene_variant SKCA-BR 15 28479491 28479491 insertion of <=200bp - TA intron_variant SKCA-BR 15 28479491 28479491 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 15 28481297 28481297 single base substitution G C intron_variant SKCA-BR 15 28484266 28484266 single base substitution T G intron_variant SKCA-BR 15 28484447 28484447 single base substitution G A intron_variant SKCA-BR 15 28485578 28485578 insertion of <=200bp - AAAAAT intron_variant SKCA-BR 15 28485814 28485814 single base substitution A G intron_variant SKCA-BR 15 28487205 28487205 single base substitution C T intron_variant SKCA-BR 15 28491174 28491174 single base substitution G A synonymous_variant L1144L 3430C>T SKCA-BR 15 28492567 28492568 deletion of <=200bp CT - intron_variant SKCA-BR 15 28494228 28494228 single base substitution G A intron_variant SKCA-BR 15 28495008 28495008 single base substitution A C downstream_gene_variant SKCA-BR 15 28495008 28495008 single base substitution A C intron_variant SKCA-BR 15 28509185 28509185 single base substitution C A intron_variant SKCA-BR 15 28509189 28509189 single base substitution C A intron_variant SKCA-BR 15 28513305 28513305 single base substitution G A downstream_gene_variant SKCA-BR 15 28513305 28513305 single base substitution G A intron_variant SKCA-BR 15 28513822 28513822 single base substitution C A downstream_gene_variant SKCA-BR 15 28513822 28513822 single base substitution C A intron_variant SKCA-BR 15 28516351 28516351 single base substitution A T downstream_gene_variant SKCA-BR 15 28516351 28516351 single base substitution A T intron_variant SKCA-BR 15 28518248 28518248 single base substitution G A exon_variant SKCA-BR 15 28518248 28518248 single base substitution G A intron_variant SKCA-BR 15 28527365 28527365 single base substitution G A intron_variant SKCA-BR 15 28536671 28536671 single base substitution G A intron_variant SKCA-BR 15 28539919 28539919 single base substitution G A intron_variant SKCA-BR 15 28540476 28540476 single base substitution A G intron_variant SKCA-BR 15 28540479 28540479 single base substitution C G intron_variant SKCA-BR 15 28543259 28543259 single base substitution A G intron_variant SKCA-BR 15 28545215 28545215 single base substitution G A intron_variant SKCA-BR 15 28545215 28545215 single base substitution G A upstream_gene_variant SKCA-BR 15 28545448 28545448 single base substitution G A intron_variant SKCA-BR 15 28545448 28545448 single base substitution G A upstream_gene_variant SKCA-BR 15 28545724 28545724 single base substitution T G intron_variant SKCA-BR 15 28545724 28545724 single base substitution T G upstream_gene_variant SKCA-BR 15 28546879 28546879 single base substitution G A intron_variant SKCA-BR 15 28546879 28546879 single base substitution G A upstream_gene_variant SKCA-BR 15 28546883 28546883 single base substitution A G intron_variant SKCA-BR 15 28546883 28546883 single base substitution A G upstream_gene_variant SKCA-BR 15 28546887 28546887 single base substitution A G intron_variant SKCA-BR 15 28546887 28546887 single base substitution A G upstream_gene_variant SKCA-BR 15 28546947 28546948 deletion of <=200bp CT - intron_variant SKCA-BR 15 28546947 28546948 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 15 28547592 28547592 single base substitution T C intron_variant SKCA-BR 15 28547592 28547592 single base substitution T C upstream_gene_variant SKCA-BR 15 28550809 28550809 single base substitution C A intron_variant SKCA-BR 15 28552220 28552220 single base substitution A C intron_variant SKCA-BR 15 28554227 28554227 single base substitution C T intron_variant SKCA-BR 15 28557287 28557287 single base substitution T A intron_variant SKCA-BR 15 28557694 28557694 single base substitution C T intron_variant SKCA-BR 15 28557910 28557910 single base substitution A C intron_variant SKCA-BR 15 28558396 28558396 single base substitution G A intron_variant SKCA-BR 15 28558568 28558568 single base substitution A C intron_variant SKCA-BR 15 28561611 28561611 single base substitution C T downstream_gene_variant SKCA-BR 15 28561611 28561611 single base substitution C T intron_variant SKCA-BR 15 28561708 28561708 single base substitution A G downstream_gene_variant SKCA-BR 15 28561708 28561708 single base substitution A G intron_variant SKCA-BR 15 28564408 28564408 single base substitution A G downstream_gene_variant SKCA-BR 15 28564408 28564408 single base substitution A G intron_variant SKCA-BR 15 28564428 28564428 single base substitution G A downstream_gene_variant SKCA-BR 15 28564428 28564428 single base substitution G A intron_variant SKCA-BR 15 28564788 28564788 single base substitution A G downstream_gene_variant SKCA-BR 15 28564788 28564788 single base substitution A G intron_variant SKCA-BR 15 28565267 28565267 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 15 28565267 28565267 insertion of <=200bp - CT intron_variant SKCA-BR 15 28566918 28566920 deletion of <=200bp TAC - intron_variant SKCA-BR 15 28570779 28570779 single base substitution G T upstream_gene_variant SKCA-BR 15 28571107 28571107 single base substitution C T upstream_gene_variant SKCA-BR 15 28571147 28571147 single base substitution T C upstream_gene_variant SKCA-BR 15 28572124 28572124 single base substitution T G upstream_gene_variant SKCM-US 15 28358283 28358283 single base substitution G A downstream_gene_variant SKCM-US 15 28358283 28358283 single base substitution G A exon_variant SKCM-US 15 28358283 28358283 single base substitution G A synonymous_variant F4722F 14166C>T SKCM-US 15 28358292 28358292 single base substitution G A downstream_gene_variant SKCM-US 15 28358292 28358292 single base substitution G A exon_variant SKCM-US 15 28358292 28358292 single base substitution G A synonymous_variant F4719F 14157C>T SKCM-US 15 28358367 28358367 single base substitution G A downstream_gene_variant SKCM-US 15 28358367 28358367 single base substitution G A exon_variant SKCM-US 15 28358367 28358367 single base substitution G A synonymous_variant I4694I 14082C>T SKCM-US 15 28362215 28362215 single base substitution G A exon_variant SKCM-US 15 28362215 28362215 single base substitution G A missense_variant S4453L 13358C>T SKCM-US 15 28362215 28362215 single base substitution G A upstream_gene_variant SKCM-US 15 28362298 28362298 single base substitution G A exon_variant SKCM-US 15 28362298 28362298 single base substitution G A splice_region_variant SKCM-US 15 28362298 28362298 single base substitution G A upstream_gene_variant SKCM-US 15 28366576 28366576 single base substitution C T splice_acceptor_variant SKCM-US 15 28366576 28366576 single base substitution C T upstream_gene_variant SKCM-US 15 28369256 28369256 single base substitution G A missense_variant S4372L 13115C>T SKCM-US 15 28370267 28370267 single base substitution G A missense_variant P4292L 12875C>T SKCM-US 15 28375694 28375694 single base substitution G A missense_variant S4206F 12617C>T SKCM-US 15 28377941 28377941 single base substitution C T missense_variant R4089K 12266G>A SKCM-US 15 28377943 28377943 single base substitution C A synonymous_variant L4088L 12264G>T SKCM-US 15 28386694 28386694 single base substitution C G downstream_gene_variant SKCM-US 15 28386694 28386694 single base substitution C G missense_variant G3967R 11899G>C SKCM-US 15 28386959 28386959 single base substitution T G exon_variant SKCM-US 15 28386959 28386959 single base substitution T G missense_variant S3912R 11734A>C SKCM-US 15 28389360 28389360 single base substitution T C missense_variant D3721G 11162A>G SKCM-US 15 28389360 28389360 single base substitution T C upstream_gene_variant SKCM-US 15 28391446 28391446 single base substitution C T missense_variant E3649K 10945G>A SKCM-US 15 28391446 28391446 single base substitution C T upstream_gene_variant SKCM-US 15 28408265 28408265 single base substitution G A intron_variant SKCM-US 15 28408265 28408265 single base substitution G A missense_variant S3574F 10721C>T SKCM-US 15 28408339 28408339 single base substitution C A intron_variant SKCM-US 15 28408339 28408339 single base substitution C A synonymous_variant V3549V 10647G>T SKCM-US 15 28412933 28412933 single base substitution G A missense_variant T142I 425C>T SKCM-US 15 28412933 28412933 single base substitution G A missense_variant T3485I 10454C>T SKCM-US 15 28412966 28412966 single base substitution G A missense_variant S131F 392C>T SKCM-US 15 28412966 28412966 single base substitution G A missense_variant S3474F 10421C>T SKCM-US 15 28413670 28413670 single base substitution G A synonymous_variant S3432S 10296C>T SKCM-US 15 28413670 28413670 single base substitution G A synonymous_variant S89S 267C>T SKCM-US 15 28414666 28414666 single base substitution G A missense_variant S3398L 10193C>T SKCM-US 15 28414666 28414666 single base substitution G A missense_variant S55L 164C>T SKCM-US 15 28419645 28419645 single base substitution G A missense_variant S3318L 9953C>T SKCM-US 15 28419645 28419645 single base substitution G A upstream_gene_variant SKCM-US 15 28420712 28420712 single base substitution G A synonymous_variant I3259I 9777C>T SKCM-US 15 28420712 28420712 single base substitution G A upstream_gene_variant SKCM-US 15 28421699 28421699 single base substitution C T synonymous_variant R3187R 9561G>A SKCM-US 15 28421699 28421699 single base substitution C T upstream_gene_variant SKCM-US 15 28422225 28422225 single base substitution G A synonymous_variant I3101I 9303C>T SKCM-US 15 28422225 28422225 single base substitution G A upstream_gene_variant SKCM-US 15 28422610 28422610 single base substitution G A missense_variant S3070L 9209C>T SKCM-US 15 28422610 28422610 single base substitution G A upstream_gene_variant SKCM-US 15 28424160 28424160 single base substitution C T synonymous_variant K3012K 9036G>A SKCM-US 15 28424160 28424160 single base substitution C T upstream_gene_variant SKCM-US 15 28424362 28424362 single base substitution A G missense_variant V2982A 8945T>C SKCM-US 15 28424362 28424362 single base substitution A G upstream_gene_variant SKCM-US 15 28424363 28424363 single base substitution C T missense_variant V2982I 8944G>A SKCM-US 15 28424363 28424363 single base substitution C T upstream_gene_variant SKCM-US 15 28436193 28436193 single base substitution G A exon_variant SKCM-US 15 28436193 28436193 single base substitution G A missense_variant S2856F 8567C>T SKCM-US 15 28436199 28436199 single base substitution C G exon_variant SKCM-US 15 28436199 28436199 single base substitution C G missense_variant G2854A 8561G>C SKCM-US 15 28441679 28441679 single base substitution A T exon_variant SKCM-US 15 28441679 28441679 single base substitution A T missense_variant F2683Y 8048T>A SKCM-US 15 28443628 28443628 single base substitution G A exon_variant SKCM-US 15 28443628 28443628 single base substitution G A missense_variant S2636F 7907C>T SKCM-US 15 28443892 28443892 single base substitution G A exon_variant SKCM-US 15 28443892 28443892 single base substitution G A synonymous_variant C2580C 7740C>T SKCM-US 15 28447305 28447305 single base substitution G A exon_variant SKCM-US 15 28447305 28447305 single base substitution G A missense_variant S2524F 7571C>T SKCM-US 15 28447509 28447509 single base substitution A T exon_variant SKCM-US 15 28447509 28447509 single base substitution A T missense_variant N2488K 7464T>A SKCM-US 15 28457652 28457652 single base substitution G A synonymous_variant N2288N 6864C>T SKCM-US 15 28458946 28458946 single base substitution G A missense_variant T2243I 6728C>T SKCM-US 15 28459414 28459414 single base substitution G A synonymous_variant S2121S 6363C>T SKCM-US 15 28465727 28465727 single base substitution C A downstream_gene_variant SKCM-US 15 28465727 28465727 single base substitution C A missense_variant V1906F 5716G>T SKCM-US 15 28465784 28465784 single base substitution G A downstream_gene_variant SKCM-US 15 28465784 28465784 single base substitution G A missense_variant P1887S 5659C>T SKCM-US 15 28467325 28467325 single base substitution G A exon_variant SKCM-US 15 28467325 28467325 single base substitution G A missense_variant A1834V 5501C>T SKCM-US 15 28473473 28473473 single base substitution G A exon_variant SKCM-US 15 28473473 28473473 single base substitution G A synonymous_variant F1785F 5355C>T SKCM-US 15 28474625 28474625 single base substitution G A exon_variant SKCM-US 15 28474625 28474625 single base substitution G A missense_variant P1701S 5101C>T SKCM-US 15 28474724 28474724 single base substitution G A missense_variant R1668C 5002C>T SKCM-US 15 28474724 28474724 single base substitution G A upstream_gene_variant SKCM-US 15 28474839 28474839 single base substitution C T missense_variant R1655K 4964G>A SKCM-US 15 28474839 28474839 single base substitution C T upstream_gene_variant SKCM-US 15 28478684 28478684 single base substitution G A missense_variant H1459Y 4375C>T SKCM-US 15 28478684 28478684 single base substitution G A upstream_gene_variant SKCM-US 15 28478849 28478849 single base substitution G A missense_variant R1438C 4312C>T SKCM-US 15 28478849 28478849 single base substitution G A upstream_gene_variant SKCM-US 15 28478878 28478878 single base substitution G A missense_variant P1428L 4283C>T SKCM-US 15 28478878 28478878 single base substitution G A upstream_gene_variant SKCM-US 15 28482110 28482110 single base substitution G A splice_region_variant SKCM-US 15 28491205 28491205 single base substitution G A synonymous_variant L1133L 3399C>T SKCM-US 15 28491994 28491994 single base substitution G A synonymous_variant L1095L 3285C>T SKCM-US 15 28499564 28499564 single base substitution T C downstream_gene_variant SKCM-US 15 28499564 28499564 single base substitution T C missense_variant D991G 2972A>G SKCM-US 15 28501248 28501248 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28501248 28501248 single base substitution G A synonymous_variant L911L 2733C>T SKCM-US 15 28501425 28501425 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28501425 28501425 single base substitution G A synonymous_variant F852F 2556C>T SKCM-US 15 28502252 28502252 single base substitution C T 3_prime_UTR_variant SKCM-US 15 28502252 28502252 single base substitution C T synonymous_variant E824E 2472G>A SKCM-US 15 28502277 28502277 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28502277 28502277 single base substitution G A missense_variant S816F 2447C>T SKCM-US 15 28502305 28502305 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28502305 28502305 single base substitution G A missense_variant R807W 2419C>T SKCM-US 15 28502311 28502311 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28502311 28502311 single base substitution G A synonymous_variant L805L 2413C>T SKCM-US 15 28502359 28502359 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28502359 28502359 single base substitution G A missense_variant P789S 2365C>T SKCM-US 15 28511016 28511016 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28511016 28511016 single base substitution G A missense_variant A568V 1703C>T SKCM-US 15 28515964 28515964 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28515964 28515964 single base substitution G A downstream_gene_variant SKCM-US 15 28515964 28515964 single base substitution G A synonymous_variant T378T 1134C>T SKCM-US 15 28518115 28518115 deletion of <=200bp C - 3_prime_UTR_variant SKCM-US 15 28518115 28518115 deletion of <=200bp C - exon_variant SKCM-US 15 28518115 28518115 deletion of <=200bp C - frameshift_variant G279 SKCM-US 15 28519439 28519439 single base substitution C T splice_region_variant SKCM-US 15 28519439 28519439 single base substitution C T upstream_gene_variant SKCM-US 15 28519449 28519449 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28519449 28519449 single base substitution G A missense_variant S263F 788C>T SKCM-US 15 28519449 28519449 single base substitution G A upstream_gene_variant SKCM-US 15 28519457 28519457 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28519457 28519457 single base substitution G A synonymous_variant F260F 780C>T SKCM-US 15 28519457 28519457 single base substitution G A upstream_gene_variant SKCM-US 15 28519529 28519529 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28519529 28519529 single base substitution G A synonymous_variant P236P 708C>T SKCM-US 15 28519529 28519529 single base substitution G A upstream_gene_variant SKCM-US 15 28525345 28525345 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28525345 28525345 single base substitution G A exon_variant SKCM-US 15 28525345 28525345 single base substitution G A synonymous_variant A137A 411C>T SKCM-US 15 28538062 28538062 single base substitution C A 3_prime_UTR_variant SKCM-US 15 28538062 28538062 single base substitution C A exon_variant SKCM-US 15 28538062 28538062 single base substitution C A synonymous_variant L98L 294G>T SKCM-US 15 28538093 28538093 single base substitution G A 3_prime_UTR_variant SKCM-US 15 28538093 28538093 single base substitution G A exon_variant SKCM-US 15 28538093 28538093 single base substitution G A missense_variant P88L 263C>T SKCM-US 15 28544556 28544556 single base substitution G A exon_variant SKCM-US 15 28544556 28544556 single base substitution G A missense_variant P60L 179C>T STAD-US 15 28357109 28357109 single base substitution G A downstream_gene_variant STAD-US 15 28357109 28357109 single base substitution G A exon_variant STAD-US 15 28357109 28357109 single base substitution G A missense_variant P4769S 14305C>T STAD-US 15 28358272 28358272 single base substitution C T downstream_gene_variant STAD-US 15 28358272 28358272 single base substitution C T exon_variant STAD-US 15 28358272 28358272 single base substitution C T missense_variant R4726Q 14177G>A STAD-US 15 28359775 28359775 single base substitution C T downstream_gene_variant STAD-US 15 28359775 28359775 single base substitution C T exon_variant STAD-US 15 28359775 28359775 single base substitution C T synonymous_variant R4632R 13896G>A STAD-US 15 28359775 28359775 single base substitution C T upstream_gene_variant STAD-US 15 28361831 28361831 single base substitution C T exon_variant STAD-US 15 28361831 28361831 single base substitution C T missense_variant S4530N 13589G>A STAD-US 15 28361831 28361831 single base substitution C T upstream_gene_variant STAD-US 15 28361854 28361854 single base substitution C T exon_variant STAD-US 15 28361854 28361854 single base substitution C T synonymous_variant P4522P 13566G>A STAD-US 15 28361854 28361854 single base substitution C T upstream_gene_variant STAD-US 15 28366498 28366498 single base substitution G A synonymous_variant R4422R 13266C>T STAD-US 15 28366498 28366498 single base substitution G A upstream_gene_variant STAD-US 15 28366538 28366538 single base substitution A G missense_variant V4409A 13226T>C STAD-US 15 28366538 28366538 single base substitution A G upstream_gene_variant STAD-US 15 28366563 28366563 single base substitution G A missense_variant R4401W 13201C>T STAD-US 15 28366563 28366563 single base substitution G A upstream_gene_variant STAD-US 15 28366571 28366571 single base substitution G A missense_variant A4398V 13193C>T STAD-US 15 28366571 28366571 single base substitution G A upstream_gene_variant STAD-US 15 28366578 28366578 deletion of <=200bp A - splice_region_variant STAD-US 15 28366578 28366578 deletion of <=200bp A - upstream_gene_variant STAD-US 15 28369270 28369270 single base substitution G A synonymous_variant F4367F 13101C>T STAD-US 15 28377829 28377829 single base substitution G A synonymous_variant S4126S 12378C>T STAD-US 15 28377925 28377925 single base substitution G A synonymous_variant V4094V 12282C>T STAD-US 15 28380769 28380769 single base substitution T C missense_variant T4029A 12085A>G STAD-US 15 28386594 28386594 single base substitution A G downstream_gene_variant STAD-US 15 28386594 28386594 single base substitution A G missense_variant V4000A 11999T>C STAD-US 15 28386693 28386693 deletion of <=200bp C - downstream_gene_variant STAD-US 15 28386693 28386693 deletion of <=200bp C - frameshift_variant G3967 STAD-US 15 28386775 28386775 single base substitution G A downstream_gene_variant STAD-US 15 28386775 28386775 single base substitution G A stop_gained R3940* 11818C>T STAD-US 15 28386919 28386919 single base substitution A G exon_variant STAD-US 15 28386919 28386919 single base substitution A G missense_variant F3925S 11774T>C STAD-US 15 28386977 28386977 single base substitution G A exon_variant STAD-US 15 28386977 28386977 single base substitution G A missense_variant R3906C 11716C>T STAD-US 15 28389353 28389353 single base substitution G A synonymous_variant C3723C 11169C>T STAD-US 15 28389353 28389353 single base substitution G A upstream_gene_variant STAD-US 15 28389918 28389918 single base substitution G A missense_variant R3681C 11041C>T STAD-US 15 28389918 28389918 single base substitution G A upstream_gene_variant STAD-US 15 28408251 28408251 single base substitution C T intron_variant STAD-US 15 28408251 28408251 single base substitution C T missense_variant A3579T 10735G>A STAD-US 15 28408263 28408263 single base substitution C T intron_variant STAD-US 15 28408263 28408263 single base substitution C T missense_variant G3575S 10723G>A STAD-US 15 28408274 28408274 single base substitution G A intron_variant STAD-US 15 28408274 28408274 single base substitution G A missense_variant A3571V 10712C>T STAD-US 15 28408275 28408275 single base substitution C T intron_variant STAD-US 15 28408275 28408275 single base substitution C T missense_variant A3571T 10711G>A STAD-US 15 28408287 28408287 single base substitution C T intron_variant STAD-US 15 28408287 28408287 single base substitution C T missense_variant D3567N 10699G>A STAD-US 15 28412927 28412927 single base substitution G A missense_variant S144L 431C>T STAD-US 15 28412927 28412927 single base substitution G A missense_variant S3487L 10460C>T STAD-US 15 28412940 28412940 single base substitution C T missense_variant A140T 418G>A STAD-US 15 28412940 28412940 single base substitution C T missense_variant A3483T 10447G>A STAD-US 15 28413568 28413568 single base substitution C T stop_gained W123* 369G>A STAD-US 15 28413568 28413568 single base substitution C T stop_gained W3466* 10398G>A STAD-US 15 28413654 28413654 single base substitution C T missense_variant D3438N 10312G>A STAD-US 15 28413654 28413654 single base substitution C T missense_variant D95N 283G>A STAD-US 15 28413691 28413691 single base substitution C T synonymous_variant P3425P 10275G>A STAD-US 15 28413691 28413691 single base substitution C T synonymous_variant P82P 246G>A STAD-US 15 28419605 28419605 single base substitution C T synonymous_variant T3331T 9993G>A STAD-US 15 28419605 28419605 single base substitution C T upstream_gene_variant STAD-US 15 28420752 28420752 single base substitution C T missense_variant R3246Q 9737G>A STAD-US 15 28420752 28420752 single base substitution C T upstream_gene_variant STAD-US 15 28421604 28421604 single base substitution G A missense_variant A3219V 9656C>T STAD-US 15 28421604 28421604 single base substitution G A upstream_gene_variant STAD-US 15 28421671 28421671 insertion of <=200bp - G frameshift_variant Q3197P? STAD-US 15 28421671 28421671 insertion of <=200bp - G upstream_gene_variant STAD-US 15 28421839 28421839 single base substitution C T missense_variant D3170N 9508G>A STAD-US 15 28421839 28421839 single base substitution C T upstream_gene_variant STAD-US 15 28422219 28422219 single base substitution A G synonymous_variant D3103D 9309T>C STAD-US 15 28422219 28422219 single base substitution A G upstream_gene_variant STAD-US 15 28422236 28422236 single base substitution T C missense_variant T3098A 9292A>G STAD-US 15 28422236 28422236 single base substitution T C upstream_gene_variant STAD-US 15 28422651 28422651 single base substitution G A synonymous_variant G3056G 9168C>T STAD-US 15 28422651 28422651 single base substitution G A upstream_gene_variant STAD-US 15 28427565 28427565 single base substitution G A synonymous_variant G2973G 8919C>T STAD-US 15 28437133 28437133 single base substitution A C exon_variant STAD-US 15 28437133 28437133 single base substitution A C missense_variant W2809G 8425T>G STAD-US 15 28437159 28437159 single base substitution C T exon_variant STAD-US 15 28437159 28437159 single base substitution C T missense_variant R2800H 8399G>A STAD-US 15 28437288 28437288 single base substitution G A exon_variant STAD-US 15 28437288 28437288 single base substitution G A missense_variant A2757V 8270C>T STAD-US 15 28441687 28441687 single base substitution A G exon_variant STAD-US 15 28441687 28441687 single base substitution A G synonymous_variant I2680I 8040T>C STAD-US 15 28441714 28441714 single base substitution A G splice_region_variant STAD-US 15 28443624 28443626 deletion of <=200bp AGA - exon_variant STAD-US 15 28443624 28443626 deletion of <=200bp AGA - inframe_deletion S2637 STAD-US 15 28443768 28443768 single base substitution A T exon_variant STAD-US 15 28443768 28443768 single base substitution A T missense_variant Y2622N 7864T>A STAD-US 15 28443796 28443796 single base substitution C T exon_variant STAD-US 15 28443796 28443796 single base substitution C T synonymous_variant Q2612Q 7836G>A STAD-US 15 28446623 28446623 single base substitution T C exon_variant STAD-US 15 28446623 28446623 single base substitution T C synonymous_variant V2565V 7695A>G STAD-US 15 28446651 28446651 single base substitution T C exon_variant STAD-US 15 28446651 28446651 single base substitution T C missense_variant D2556G 7667A>G STAD-US 15 28446681 28446681 single base substitution G A exon_variant STAD-US 15 28446681 28446681 single base substitution G A missense_variant T2546M 7637C>T STAD-US 15 28447365 28447365 single base substitution T A exon_variant STAD-US 15 28447365 28447365 single base substitution T A missense_variant D2504V 7511A>T STAD-US 15 28447385 28447385 single base substitution G T exon_variant STAD-US 15 28447385 28447385 single base substitution G T synonymous_variant A2497A 7491C>A STAD-US 15 28447491 28447491 single base substitution A G splice_donor_variant STAD-US 15 28447515 28447515 single base substitution G A exon_variant STAD-US 15 28447515 28447515 single base substitution G A synonymous_variant S2486S 7458C>T STAD-US 15 28447538 28447538 single base substitution G C exon_variant STAD-US 15 28447538 28447538 single base substitution G C missense_variant L2479V 7435C>G STAD-US 15 28459021 28459021 single base substitution C T missense_variant R2218H 6653G>A STAD-US 15 28459349 28459349 single base substitution G A missense_variant A2143V 6428C>T STAD-US 15 28460840 28460840 single base substitution G A missense_variant P2046L 6137C>T STAD-US 15 28463820 28463820 deletion of <=200bp A - downstream_gene_variant STAD-US 15 28463820 28463820 deletion of <=200bp A - splice_region_variant STAD-US 15 28465618 28465618 single base substitution G A downstream_gene_variant STAD-US 15 28465618 28465618 single base substitution G A missense_variant S1942L 5825C>T STAD-US 15 28473458 28473458 single base substitution G A exon_variant STAD-US 15 28473458 28473458 single base substitution G A synonymous_variant L1790L 5370C>T STAD-US 15 28473545 28473545 single base substitution C T exon_variant STAD-US 15 28473545 28473545 single base substitution C T synonymous_variant P1761P 5283G>A STAD-US 15 28474412 28474412 single base substitution T C exon_variant STAD-US 15 28474412 28474412 single base substitution T C missense_variant K1734R 5201A>G STAD-US 15 28474714 28474714 single base substitution C A missense_variant G1671V 5012G>T STAD-US 15 28474714 28474714 single base substitution C A upstream_gene_variant STAD-US 15 28474843 28474843 insertion of <=200bp - T frameshift_variant M1654N? STAD-US 15 28474843 28474843 insertion of <=200bp - T upstream_gene_variant STAD-US 15 28478297 28478297 single base substitution T C missense_variant K1557R 4670A>G STAD-US 15 28478297 28478297 single base substitution T C upstream_gene_variant STAD-US 15 28478342 28478342 single base substitution C T missense_variant R1542H 4625G>A STAD-US 15 28478342 28478342 single base substitution C T upstream_gene_variant STAD-US 15 28478854 28478854 single base substitution A G missense_variant V1436A 4307T>C STAD-US 15 28478854 28478854 single base substitution A G upstream_gene_variant STAD-US 15 28482137 28482137 single base substitution C T synonymous_variant P1325P 3975G>A STAD-US 15 28483908 28483908 deletion of <=200bp A - frameshift_variant F1196 STAD-US 15 28493767 28493767 single base substitution G A missense_variant R1056C 3166C>T STAD-US 15 28493822 28493822 single base substitution A G synonymous_variant C1037C 3111T>C STAD-US 15 28499647 28499647 insertion of <=200bp - T 3_prime_UTR_variant STAD-US 15 28499647 28499647 insertion of <=200bp - T frameshift_variant K963K? STAD-US 15 28501287 28501287 single base substitution C T 3_prime_UTR_variant STAD-US 15 28501287 28501287 single base substitution C T synonymous_variant L898L 2694G>A STAD-US 15 28501325 28501325 single base substitution C T 3_prime_UTR_variant STAD-US 15 28501325 28501325 single base substitution C T missense_variant A886T 2656G>A STAD-US 15 28501349 28501349 single base substitution C T 3_prime_UTR_variant STAD-US 15 28501349 28501349 single base substitution C T missense_variant V878M 2632G>A STAD-US 15 28501354 28501354 single base substitution G A 3_prime_UTR_variant STAD-US 15 28501354 28501354 single base substitution G A missense_variant A876V 2627C>T STAD-US 15 28510807 28510807 single base substitution C T 3_prime_UTR_variant STAD-US 15 28510807 28510807 single base substitution C T synonymous_variant A609A 1827G>A STAD-US 15 28511044 28511044 single base substitution C T 3_prime_UTR_variant STAD-US 15 28511044 28511044 single base substitution C T missense_variant G559R 1675G>A STAD-US 15 28511077 28511077 single base substitution G A 3_prime_UTR_variant STAD-US 15 28511077 28511077 single base substitution G A stop_gained Q548* 1642C>T STAD-US 15 28514464 28514464 single base substitution G A 3_prime_UTR_variant STAD-US 15 28514464 28514464 single base substitution G A downstream_gene_variant STAD-US 15 28514464 28514464 single base substitution G A missense_variant A459V 1376C>T STAD-US 15 28515891 28515891 single base substitution G C 3_prime_UTR_variant STAD-US 15 28515891 28515891 single base substitution G C downstream_gene_variant STAD-US 15 28515891 28515891 single base substitution G C missense_variant L403V 1207C>G STAD-US 15 28518100 28518100 single base substitution T C 3_prime_UTR_variant STAD-US 15 28518100 28518100 single base substitution T C exon_variant STAD-US 15 28518100 28518100 single base substitution T C missense_variant Q284R 851A>G STAD-US 15 28525254 28525254 single base substitution T C 3_prime_UTR_variant STAD-US 15 28525254 28525254 single base substitution T C exon_variant STAD-US 15 28525254 28525254 single base substitution T C missense_variant K168E 502A>G STAD-US 15 28538035 28538035 single base substitution T C splice_region_variant STAD-US 15 28538093 28538093 single base substitution G T 3_prime_UTR_variant STAD-US 15 28538093 28538093 single base substitution G T exon_variant STAD-US 15 28538093 28538093 single base substitution G T missense_variant P88H 263C>A STAD-US 15 28538116 28538116 single base substitution C A 3_prime_UTR_variant STAD-US 15 28538116 28538116 single base substitution C A exon_variant STAD-US 15 28538116 28538116 single base substitution C A missense_variant E80D 240G>T THCA-SA 15 28377896 28377897 deletion of <=200bp GC - frameshift_variant A4104 THCA-SA 15 28419619 28419619 single base substitution C T missense_variant V3327M 9979G>A THCA-SA 15 28419619 28419619 single base substitution C T upstream_gene_variant THCA-SA 15 28474421 28474421 single base substitution G A exon_variant THCA-SA 15 28474421 28474421 single base substitution G A missense_variant T1731I 5192C>T THCA-SA 15 28518046 28518046 single base substitution G A 3_prime_UTR_variant THCA-SA 15 28518046 28518046 single base substitution G A exon_variant THCA-SA 15 28518046 28518046 single base substitution G A missense_variant T302M 905C>T THCA-SA 15 28518112 28518112 deletion of <=200bp C - 3_prime_UTR_variant THCA-SA 15 28518112 28518112 deletion of <=200bp C - exon_variant THCA-SA 15 28518112 28518112 deletion of <=200bp C - frameshift_variant S280 THCA-SA 15 28518112 28518112 single base substitution C A 3_prime_UTR_variant THCA-SA 15 28518112 28518112 single base substitution C A exon_variant THCA-SA 15 28518112 28518112 single base substitution C A missense_variant S280I 839G>T THCA-SA 15 28518130 28518130 single base substitution G C 3_prime_UTR_variant THCA-SA 15 28518130 28518130 single base substitution G C exon_variant THCA-SA 15 28518130 28518130 single base substitution G C missense_variant A274G 821C>G THCA-SA 15 28566562 28566562 single base substitution G C exon_variant THCA-SA 15 28566562 28566562 single base substitution G C missense_variant F6L 18C>G UCEC-US 15 28356990 28356990 single base substitution G A downstream_gene_variant UCEC-US 15 28356990 28356990 single base substitution G A exon_variant UCEC-US 15 28356990 28356990 single base substitution G A synonymous_variant D4808D 14424C>T UCEC-US 15 28357109 28357109 single base substitution G A downstream_gene_variant UCEC-US 15 28357109 28357109 single base substitution G A exon_variant UCEC-US 15 28357109 28357109 single base substitution G A missense_variant P4769S 14305C>T UCEC-US 15 28358367 28358367 single base substitution G A downstream_gene_variant UCEC-US 15 28358367 28358367 single base substitution G A exon_variant UCEC-US 15 28358367 28358367 single base substitution G A synonymous_variant I4694I 14082C>T UCEC-US 15 28359943 28359943 single base substitution A G downstream_gene_variant UCEC-US 15 28359943 28359943 single base substitution A G exon_variant UCEC-US 15 28359943 28359943 single base substitution A G synonymous_variant D4576D 13728T>C UCEC-US 15 28359943 28359943 single base substitution A G upstream_gene_variant UCEC-US 15 28360632 28360632 single base substitution G A exon_variant UCEC-US 15 28360632 28360632 single base substitution G A synonymous_variant A4555A 13665C>T UCEC-US 15 28360632 28360632 single base substitution G A upstream_gene_variant UCEC-US 15 28361877 28361877 single base substitution G A exon_variant UCEC-US 15 28361877 28361877 single base substitution G A stop_gained R4515* 13543C>T UCEC-US 15 28361877 28361877 single base substitution G A upstream_gene_variant UCEC-US 15 28361966 28361966 single base substitution G A exon_variant UCEC-US 15 28361966 28361966 single base substitution G A missense_variant S4485F 13454C>T UCEC-US 15 28361966 28361966 single base substitution G A upstream_gene_variant UCEC-US 15 28361972 28361972 single base substitution C A exon_variant UCEC-US 15 28361972 28361972 single base substitution C A missense_variant S4483I 13448G>T UCEC-US 15 28361972 28361972 single base substitution C A upstream_gene_variant UCEC-US 15 28362215 28362215 single base substitution G A exon_variant UCEC-US 15 28362215 28362215 single base substitution G A missense_variant S4453L 13358C>T UCEC-US 15 28362215 28362215 single base substitution G A upstream_gene_variant UCEC-US 15 28362261 28362261 single base substitution C T exon_variant UCEC-US 15 28362261 28362261 single base substitution C T missense_variant D4438N 13312G>A UCEC-US 15 28362261 28362261 single base substitution C T upstream_gene_variant UCEC-US 15 28362399 28362399 single base substitution C T exon_variant UCEC-US 15 28362399 28362399 single base substitution C T intron_variant UCEC-US 15 28362399 28362399 single base substitution C T upstream_gene_variant UCEC-US 15 28366536 28366536 single base substitution G A missense_variant R4410C 13228C>T UCEC-US 15 28366536 28366536 single base substitution G A upstream_gene_variant UCEC-US 15 28369219 28369219 single base substitution G A synonymous_variant F4384F 13152C>T UCEC-US 15 28369299 28369299 single base substitution C T missense_variant E4358K 13072G>A UCEC-US 15 28370199 28370199 single base substitution C T missense_variant A4315T 12943G>A UCEC-US 15 28370293 28370293 single base substitution G A synonymous_variant D4283D 12849C>T UCEC-US 15 28375324 28375324 single base substitution A G missense_variant C4263R 12787T>C UCEC-US 15 28375399 28375399 single base substitution G T synonymous_variant R4238R 12712C>A UCEC-US 15 28377309 28377309 single base substitution C T stop_gained W4169* 12507G>A UCEC-US 15 28377898 28377898 single base substitution G A synonymous_variant S4103S 12309C>T UCEC-US 15 28380624 28380624 single base substitution C A missense_variant S4077I 12230G>T UCEC-US 15 28380658 28380658 single base substitution C T missense_variant A4066T 12196G>A UCEC-US 15 28380783 28380783 single base substitution G A missense_variant S4024L 12071C>T UCEC-US 15 28386774 28386774 single base substitution C T downstream_gene_variant UCEC-US 15 28386774 28386774 single base substitution C T missense_variant R3940Q 11819G>A UCEC-US 15 28386977 28386977 single base substitution G A exon_variant UCEC-US 15 28386977 28386977 single base substitution G A missense_variant R3906C 11716C>T UCEC-US 15 28389028 28389028 single base substitution T C synonymous_variant T3803T 11409A>G UCEC-US 15 28389028 28389028 single base substitution T C upstream_gene_variant UCEC-US 15 28389094 28389094 single base substitution C T synonymous_variant L3781L 11343G>A UCEC-US 15 28389094 28389094 single base substitution C T upstream_gene_variant UCEC-US 15 28389267 28389267 single base substitution C T missense_variant R3752H 11255G>A UCEC-US 15 28389267 28389267 single base substitution C T upstream_gene_variant UCEC-US 15 28389335 28389335 single base substitution G T synonymous_variant S3729S 11187C>A UCEC-US 15 28389335 28389335 single base substitution G T upstream_gene_variant UCEC-US 15 28391434 28391434 single base substitution C T missense_variant D3653N 10957G>A UCEC-US 15 28391434 28391434 single base substitution C T upstream_gene_variant UCEC-US 15 28391470 28391470 single base substitution C A stop_gained E3641* 10921G>T UCEC-US 15 28391470 28391470 single base substitution C A upstream_gene_variant UCEC-US 15 28397830 28397830 single base substitution C A downstream_gene_variant UCEC-US 15 28397830 28397830 single base substitution C A missense_variant K3631N 10893G>T UCEC-US 15 28397857 28397857 single base substitution G A downstream_gene_variant UCEC-US 15 28397857 28397857 single base substitution G A synonymous_variant D3622D 10866C>T UCEC-US 15 28408246 28408246 single base substitution G A intron_variant UCEC-US 15 28408246 28408246 single base substitution G A synonymous_variant Y3580Y 10740C>T UCEC-US 15 28414696 28414696 single base substitution T A missense_variant D3388V 10163A>T UCEC-US 15 28414696 28414696 single base substitution T A missense_variant D45V 134A>T UCEC-US 15 28414721 28414721 single base substitution G A missense_variant L3380F 10138C>T UCEC-US 15 28414721 28414721 single base substitution G A missense_variant L37F 109C>T UCEC-US 15 28419642 28419642 single base substitution G A missense_variant S3319F 9956C>T UCEC-US 15 28419642 28419642 single base substitution G A upstream_gene_variant UCEC-US 15 28419655 28419655 single base substitution C T missense_variant A3315T 9943G>A UCEC-US 15 28419655 28419655 single base substitution C T upstream_gene_variant UCEC-US 15 28422597 28422597 single base substitution A G synonymous_variant G3074G 9222T>C UCEC-US 15 28422597 28422597 single base substitution A G upstream_gene_variant UCEC-US 15 28422639 28422639 single base substitution C T synonymous_variant T3060T 9180G>A UCEC-US 15 28422639 28422639 single base substitution C T upstream_gene_variant UCEC-US 15 28424159 28424159 single base substitution C T missense_variant V3013M 9037G>A UCEC-US 15 28424159 28424159 single base substitution C T upstream_gene_variant UCEC-US 15 28431880 28431880 deletion of <=200bp T - downstream_gene_variant UCEC-US 15 28431880 28431880 deletion of <=200bp T - frameshift_variant I2890 UCEC-US 15 28436162 28436162 single base substitution G T exon_variant UCEC-US 15 28436162 28436162 single base substitution G T synonymous_variant I2866I 8598C>A UCEC-US 15 28436304 28436304 single base substitution C T exon_variant UCEC-US 15 28436304 28436304 single base substitution C T synonymous_variant P2846P 8538G>A UCEC-US 15 28436380 28436380 single base substitution C T exon_variant UCEC-US 15 28436380 28436380 single base substitution C T missense_variant R2821H 8462G>A UCEC-US 15 28437149 28437149 single base substitution G A exon_variant UCEC-US 15 28437149 28437149 single base substitution G A synonymous_variant D2803D 8409C>T UCEC-US 15 28443818 28443818 single base substitution A G exon_variant UCEC-US 15 28443818 28443818 single base substitution A G missense_variant L2605P 7814T>C UCEC-US 15 28446668 28446668 single base substitution C T exon_variant UCEC-US 15 28446668 28446668 single base substitution C T synonymous_variant T2550T 7650G>A UCEC-US 15 28447531 28447531 single base substitution G T exon_variant UCEC-US 15 28447531 28447531 single base substitution G T missense_variant S2481Y 7442C>A UCEC-US 15 28447622 28447622 single base substitution G A exon_variant UCEC-US 15 28447622 28447622 single base substitution G A missense_variant R2451C 7351C>T UCEC-US 15 28458979 28458979 single base substitution G T missense_variant T2232N 6695C>A UCEC-US 15 28458998 28458998 single base substitution C T missense_variant D2226N 6676G>A UCEC-US 15 28459291 28459291 single base substitution G T synonymous_variant L2162L 6486C>A UCEC-US 15 28459326 28459326 single base substitution G A missense_variant R2151C 6451C>T UCEC-US 15 28459411 28459411 single base substitution C T synonymous_variant T2122T 6366G>A UCEC-US 15 28459875 28459875 single base substitution C T missense_variant C2095Y 6284G>A UCEC-US 15 28459906 28459906 single base substitution C T missense_variant D2085N 6253G>A UCEC-US 15 28463709 28463709 single base substitution A G downstream_gene_variant UCEC-US 15 28463709 28463709 single base substitution A G missense_variant M1985T 5954T>C UCEC-US 15 28465764 28465764 single base substitution G A downstream_gene_variant UCEC-US 15 28465764 28465764 single base substitution G A synonymous_variant R1893R 5679C>T UCEC-US 15 28467335 28467335 single base substitution C A exon_variant UCEC-US 15 28467335 28467335 single base substitution C A missense_variant D1831Y 5491G>T UCEC-US 15 28473477 28473477 single base substitution C T exon_variant UCEC-US 15 28473477 28473477 single base substitution C T missense_variant R1784H 5351G>A UCEC-US 15 28473507 28473507 single base substitution C T exon_variant UCEC-US 15 28473507 28473507 single base substitution C T missense_variant G1774E 5321G>A UCEC-US 15 28474382 28474382 single base substitution C T exon_variant UCEC-US 15 28474382 28474382 single base substitution C T missense_variant R1744Q 5231G>A UCEC-US 15 28474383 28474383 single base substitution G A exon_variant UCEC-US 15 28474383 28474383 single base substitution G A stop_gained R1744* 5230C>T UCEC-US 15 28474649 28474649 single base substitution A G exon_variant UCEC-US 15 28474649 28474649 single base substitution A G missense_variant F1693L 5077T>C UCEC-US 15 28474704 28474704 single base substitution T C synonymous_variant T1674T 5022A>G UCEC-US 15 28474704 28474704 single base substitution T C upstream_gene_variant UCEC-US 15 28478402 28478402 single base substitution G T missense_variant P1522H 4565C>A UCEC-US 15 28478402 28478402 single base substitution G T upstream_gene_variant UCEC-US 15 28478848 28478848 single base substitution C T missense_variant R1438H 4313G>A UCEC-US 15 28478848 28478848 single base substitution C T upstream_gene_variant UCEC-US 15 28482250 28482250 single base substitution C A stop_gained E1288* 3862G>T UCEC-US 15 28483763 28483763 single base substitution C A stop_gained G1245* 3733G>T UCEC-US 15 28483809 28483809 single base substitution G A synonymous_variant D1229D 3687C>T UCEC-US 15 28491887 28491887 single base substitution C T splice_donor_variant UCEC-US 15 28491985 28491985 single base substitution C T synonymous_variant T1098T 3294G>A UCEC-US 15 28493707 28493707 single base substitution C T missense_variant D1076N 3226G>A UCEC-US 15 28493757 28493757 single base substitution C T missense_variant R1059H 3176G>A UCEC-US 15 28499552 28499552 single base substitution G A downstream_gene_variant UCEC-US 15 28499552 28499552 single base substitution G A missense_variant T995M 2984C>T UCEC-US 15 28499565 28499565 single base substitution C A downstream_gene_variant UCEC-US 15 28499565 28499565 single base substitution C A missense_variant D991Y 2971G>T UCEC-US 15 28499609 28499609 single base substitution G A downstream_gene_variant UCEC-US 15 28499609 28499609 single base substitution G A missense_variant A976V 2927C>T UCEC-US 15 28499628 28499628 single base substitution C A downstream_gene_variant UCEC-US 15 28499628 28499628 single base substitution C A stop_gained E970* 2908G>T UCEC-US 15 28501281 28501281 single base substitution G A 3_prime_UTR_variant UCEC-US 15 28501281 28501281 single base substitution G A synonymous_variant T900T 2700C>T UCEC-US 15 28501325 28501325 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28501325 28501325 single base substitution C T missense_variant A886T 2656G>A UCEC-US 15 28502228 28502228 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28502228 28502228 single base substitution C T synonymous_variant T832T 2496G>A UCEC-US 15 28502305 28502305 single base substitution G A 3_prime_UTR_variant UCEC-US 15 28502305 28502305 single base substitution G A missense_variant R807W 2419C>T UCEC-US 15 28506000 28506000 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28506000 28506000 single base substitution C T missense_variant V747M 2239G>A UCEC-US 15 28506067 28506067 deletion of <=200bp C - 3_prime_UTR_variant UCEC-US 15 28506067 28506067 deletion of <=200bp C - frameshift_variant L724 UCEC-US 15 28508147 28508147 single base substitution G T 3_prime_UTR_variant UCEC-US 15 28508147 28508147 single base substitution G T stop_gained S680* 2039C>A UCEC-US 15 28508242 28508242 single base substitution T C 3_prime_UTR_variant UCEC-US 15 28508242 28508242 single base substitution T C synonymous_variant P648P 1944A>G UCEC-US 15 28511022 28511022 single base substitution A G 3_prime_UTR_variant UCEC-US 15 28511022 28511022 single base substitution A G missense_variant I566T 1697T>C UCEC-US 15 28511092 28511092 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28511092 28511092 single base substitution C T missense_variant A543T 1627G>A UCEC-US 15 28517370 28517370 single base substitution G A 3_prime_UTR_variant UCEC-US 15 28517370 28517370 single base substitution G A exon_variant UCEC-US 15 28517370 28517370 single base substitution G A synonymous_variant G358G 1074C>T UCEC-US 15 28517496 28517496 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28517496 28517496 single base substitution C T exon_variant UCEC-US 15 28517496 28517496 single base substitution C T synonymous_variant L316L 948G>A UCEC-US 15 28525245 28525245 single base substitution C A 3_prime_UTR_variant UCEC-US 15 28525245 28525245 single base substitution C A exon_variant UCEC-US 15 28525245 28525245 single base substitution C A missense_variant G171C 511G>T UCEC-US 15 28525247 28525247 single base substitution C T 3_prime_UTR_variant UCEC-US 15 28525247 28525247 single base substitution C T exon_variant UCEC-US 15 28525247 28525247 single base substitution C T missense_variant S170N 509G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-39-5022-01 COSM700247 c.1507G>A p.D503N Substitution - Missense 15:28268556-28268556 - TCGA-B6-A0IH-01 COSM4813664 c.14397C>T p.I4799I Substitution - coding silent 15:28111871-28111871 - TCGA-85-6561-01 COSM4861005 c.11919C>G p.V3973V Substitution - coding silent 15:28141528-28141528 - PCSI_0356_Pa_P_526 COSM4809280 c.6394G>T p.A2132S Substitution - Missense 15:28214237-28214237 - TCGA-E2-A574-01 COSM4814833 c.8462G>C p.R2821P Substitution - Missense 15:28191234-28191234 - sysucc-783T COSM5448722 c.1003G>A p.A335T Substitution - Missense 15:28272295-28272295 - I2L-P19Tb-Tumor-Biopsy COSM5362972 c.9859G>A p.G3287S Substitution - Missense 15:28174593-28174593 - MO_1012 COSM5561909 c.6713C>T p.P2238L Substitution - Missense 15:28213815-28213815 - CSCC-27-T COSM960107 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - TCGA-37-5819-01 COSM4862954 c.3354C>T p.F1118F Substitution - coding silent 15:28246779-28246779 - PTC_393 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-A6-2676-01 COSM291138 c.626G>A p.R209H Substitution - Missense 15:28274922-28274922 - TCGA-E9-A1RH-01 COSM4816003 c.4084G>C p.D1362H Substitution - Missense 15:28234204-28234204 - TCGA-D1-A103-01 COSM4875013 c.1697T>C p.I566T Substitution - Missense 15:28265876-28265876 - PTC-7C COSM3999484 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - TCGA-EB-A41A-01 COSM3500311 c.788C>T p.S263F Substitution - Missense 15:28274303-28274303 - Pat_41_A COSM5848944 c.12365G>A p.R4122Q Substitution - Missense 15:28132696-28132696 - PTC_455 COSM5957983 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - TCGA-D3-A51T-06 COSM3500268 c.14166C>T p.F4722F Substitution - coding silent 15:28113137-28113137 - MO_1277 COSM5572206 c.12506G>T p.W4169L Substitution - Missense 15:28132164-28132164 - T578 COSM4690086 c.6738C>A p.F2246L Substitution - Missense 15:28213790-28213790 - sysucc-311T COSM4867491 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - TCGA-AP-A059-01 COSM960239 c.3733G>T p.G1245* Substitution - Nonsense 15:28238617-28238617 - TCGA-AS-3778-01 COSM1493405 c.5685T>G p.I1895M Substitution - Missense 15:28220612-28220612 - SWE-3B COSM1178342 c.146G>T p.G49V Substitution - Missense 15:28299443-28299443 - HCC102 COSM1608219 c.8898G>C p.L2966L Substitution - coding silent 15:28182440-28182440 - HCT116 COSM2083271 c.12492C>T p.D4164D Substitution - coding silent 15:28132178-28132178 - D-03 COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - HCT15 COSM4623070 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - CN-AML-CR-26-Dx COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - 3101B7_041_T COSM5039286 c.1273G>T p.V425F Substitution - Missense 15:28269421-28269421 - C086 COSM5532289 c.9527C>T p.S3176F Substitution - Missense 15:28176587-28176587 - ZZUFHECRKL-G060T COSM5438414 c.5255C>T p.A1752V Substitution - Missense 15:28229212-28229212 - BD124T COSM5493244 c.7775G>A p.G2592D Substitution - Missense 15:28198711-28198711 - TCGA-CU-A3KJ-01 COSM1301014 c.5356C>T p.L1786F Substitution - Missense 15:28228326-28228326 - TCGA-D1-A17S-01 COSM960143 c.11386C>T p.L3796F Substitution - Missense 15:28143905-28143905 - TCGA-EE-A29D-06 COSM4905970 c.7464T>A p.N2488K Substitution - Missense 15:28202363-28202363 - TCGA-AR-A250-01 COSM4594666 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - S02294 COSM5688735 c.9838G>A p.A3280T Substitution - Missense 15:28174614-28174614 - QC2-25-T2 COSM2083365 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - TCGA-HU-A4GX-01 COSM4053867 c.2632G>A p.V878M Substitution - Missense 15:28256203-28256203 - TCGA-A5-A0GP-01 COSM4865968 c.5491G>T p.D1831Y Substitution - Missense 15:28222189-28222189 - TCGA-A5-A0GP-01 COSM960217 c.5491G>T p.D1831Y Substitution - Missense 15:28222189-28222189 - TCGA-B5-A11E-01 COSM960229 c.5022A>G p.T1674T Substitution - coding silent 15:28229558-28229558 - TCGA-EE-A3AE-06 COSM3500314 c.411C>T p.A137A Substitution - coding silent 15:28280199-28280199 - TCGA-EE-A29V-06 COSM3500316 c.263C>T p.P88L Substitution - Missense 15:28292947-28292947 - AML_14y_10_DX COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-AX-A0J0-01 COSM4867157 c.10921G>T p.E3641* Substitution - Nonsense 15:28146324-28146324 - HCC038T COSM5820433 c.1681A>G p.T561A Substitution - Missense 15:28265892-28265892 - CSCC-16-T COSM4465458 c.13850C>T p.S4617F Substitution - Missense 15:28114675-28114675 - SCC-15 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-FW-A3R5-06 COSM3886813 c.4375C>T p.H1459Y Substitution - Missense 15:28233538-28233538 - HCC2998 COSM1678318 c.8461C>T p.R2821C Substitution - Missense 15:28191235-28191235 - S02065 COSM5672617 c.11077A>G p.S3693G Substitution - Missense 15:28144736-28144736 - MZ7-mel COSM23127 c.3099G>A p.R1033R Substitution - coding silent 15:28248688-28248688 - PD4970a COSM5768566 c.145G>T p.G49* Substitution - Nonsense 15:28299444-28299444 - TCGA-DA-A1I1-06 COSM261276 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - RK164_C01 COSM3700931 c.1084-4C>G p.? Unknown 15:28270872-28270872 - C2 COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-AP-A051-01 COSM4872868 c.3391+1G>A p.? Unknown 15:28246741-28246741 - CHC892T COSM4798245 c.10797C>T p.A3599A Substitution - coding silent 15:28152780-28152780 - TCGA-AN-A0AK-01 COSM4814384 c.12347G>C p.G4116A Substitution - Missense 15:28132714-28132714 - TCGA-CD-A486-01 COSM4053870 c.1675G>A p.G559R Substitution - Missense 15:28265898-28265898 - MedB-1 COSM5620949 c.9574G>T p.G3192C Substitution - Missense 15:28176540-28176540 - PTC_455 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - BD152T COSM5507022 c.13781A>G p.E4594G Substitution - Missense 15:28114744-28114744 - TCGA-B0-5695-01 COSM4857833 c.11627G>T p.R3876M Substitution - Missense 15:28142311-28142311 - MO_1277 COSM5572205 c.12506G>T p.W4169L Substitution - Missense 15:28132164-28132164 - 2521252 COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - T20 COSM5065046 c.5656G>A p.G1886R Substitution - Missense 15:28220641-28220641 - UM-SCC-17B COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AU-6004-01 COSM4783362 c.11378A>G p.N3793S Substitution - Missense 15:28143913-28143913 - TCGA-GM-A2D9-01 COSM4815935 c.8197G>A p.E2733K Substitution - Missense 15:28196278-28196278 - TCGA-60-2698-01 COSM4860788 c.3553G>A p.E1185K Substitution - Missense 15:28245905-28245905 - P134 COSM4053813 c.13226T>C p.V4409A Substitution - Missense 15:28121392-28121392 - TCGA-AY-6197-01 COSM4948366 c.11973C>A p.I3991I Substitution - coding silent 15:28141474-28141474 - BD123T COSM5521107 c.3095G>A p.R1032H Substitution - Missense 15:28248692-28248692 - PTC_456 COSM5957984 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - D8 COSM5007567 c.14092G>A p.A4698T Substitution - Missense 15:28113211-28113211 - CHC892T COSM4961173 c.8922G>A p.G2974G Substitution - coding silent 15:28182416-28182416 - WSU-HN30 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - PT35 COSM5913675 c.8558-5C>T p.? Unknown 15:28191061-28191061 - 19 COSM5747624 c.3202G>A p.G1068R Substitution - Missense 15:28248585-28248585 - 2492729 COSM5729568 c.12994C>T p.P4332S Substitution - Missense 15:28124231-28124231 - CSCC-15-T COSM4555543 c.6595G>A p.E2199K Substitution - Missense 15:28213933-28213933 - TCGA-34-5231-01 COSM4862254 c.8509G>T p.V2837L Substitution - Missense 15:28191187-28191187 - TCGA-85-6561-01 COSM700276 c.11919C>G p.V3973V Substitution - coding silent 15:28141528-28141528 - TCGA-EE-A3JD-06 COSM4396030 c.12264G>T p.L4088L Substitution - coding silent 15:28132797-28132797 - A1 COSM4386169 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - T2225 COSM4690082 c.8120C>T p.T2707M Substitution - Missense 15:28196461-28196461 - BK0028 COSM4186712 c.2167G>C p.A723P Substitution - Missense 15:28260926-28260926 - T3021 COSM4690110 c.1414G>A p.V472M Substitution - Missense 15:28269280-28269280 - TCGA-EI-6917-01 COSM4782606 c.12425G>A p.G4142D Substitution - Missense 15:28132245-28132245 - TCGA-AX-A0J1-01 COSM4867812 c.6284G>A p.C2095Y Substitution - Missense 15:28214729-28214729 - ESCC_127 COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - T70 COSM4690060 c.12233C>T p.P4078L Substitution - Missense 15:28132828-28132828 - T3021 COSM4690077 c.9409A>G p.T3137A Substitution - Missense 15:28176973-28176973 - PD11748a COSM5767416 c.11278T>A p.C3760S Substitution - Missense 15:28144098-28144098 - PTC_33 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-66-2782-01 COSM700254 c.2865G>A p.E955E Substitution - coding silent 15:28255878-28255878 - TCGA-FW-A3R5-06 COSM3500311 c.788C>T p.S263F Substitution - Missense 15:28274303-28274303 - S02295 COSM5689104 c.5116A>G p.I1706V Substitution - Missense 15:28229464-28229464 - TCGA-AN-A0AT-01 COSM4578149 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - ESCC_BICR_057T COSM5436787 c.9126C>G p.L3042L Substitution - coding silent 15:28178924-28178924 - P100 COSM5009259 c.2510G>A p.R837Q Substitution - Missense 15:28257068-28257068 - ME009T COSM223741 c.1916G>A p.R639K Substitution - Missense 15:28263124-28263124 - S00935 COSM311753 c.6906G>T p.S2302S Substitution - coding silent 15:28212464-28212464 - D28 COSM3500296 c.5355C>T p.F1785F Substitution - coding silent 15:28228327-28228327 - BRC39 COSM5027935 c.660C>T p.L220L Substitution - coding silent 15:28274431-28274431 - 2492705 COSM5716818 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - TCGA-CH-5738-01 COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - HCC6T COSM1608220 c.2185G>C p.E729Q Substitution - Missense 15:28260908-28260908 - TCGA-AX-A0J0-01 COSM1587793 c.12196G>A p.A4066T Substitution - Missense 15:28135512-28135512 - CSCC-35-T COSM4561615 c.8917G>A p.G2973S Substitution - Missense 15:28182421-28182421 - HCA7 COSM4630104 c.12990G>T p.Q4330H Substitution - Missense 15:28125006-28125006 - HCC079T COSM5808148 c.3544G>T p.D1182Y Substitution - Missense 15:28245914-28245914 - 2492704 COSM5716756 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - CHC796T COSM4949603 c.1014G>C p.L338F Substitution - Missense 15:28272284-28272284 - TCGA-AA-A010-01 COSM281678 c.2050G>T p.G684C Substitution - Missense 15:28262990-28262990 - WSU-HN13 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - BICR_22 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - RKO COSM4647802 c.14311T>C p.Y4771H Substitution - Missense 15:28111957-28111957 - TCGA-60-2707-01 COSM4859378 c.846C>A p.P282P Substitution - coding silent 15:28272959-28272959 - ESO-157 COSM1254128 c.832C>A p.P278T Substitution - Missense 15:28272973-28272973 - TCGA-AP-A051-01 COSM960207 c.6366G>A p.T2122T Substitution - coding silent 15:28214265-28214265 - WSU-HN30 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - 98 COSM5012841 c.215A>T p.K72M Substitution - Missense 15:28292995-28292995 - MO_1012 COSM5561910 c.6714A>G p.P2238P Substitution - coding silent 15:28213814-28213814 - TCGA-AX-A0J0-01 COSM960237 c.3862G>T p.E1288* Substitution - Nonsense 15:28237104-28237104 - TCGA-BR-4361-01 COSM4053820 c.11999T>C p.V4000A Substitution - Missense 15:28141448-28141448 - B70 COSM1749090 c.13716C>T p.L4572L Substitution - coding silent 15:28115435-28115435 - TCGA-BQ-5889-01 COSM4908113 c.1762A>T p.S588C Substitution - Missense 15:28265726-28265726 - CSCC-18-T COSM4470548 c.1668C>T p.I556I Substitution - coding silent 15:28265905-28265905 - TCGA-B5-A11Y-01 COSM4864168 c.3687C>T p.D1229D Substitution - coding silent 15:28238663-28238663 - TCGA-39-5021-01 COSM4862276 c.6988C>T p.R2330W Substitution - Missense 15:28211083-28211083 - TCGA-BR-8680-01 COSM4870586 c.2656G>A p.A886T Substitution - Missense 15:28256179-28256179 - P110 COSM5008121 c.1819G>A p.D607N Substitution - Missense 15:28265669-28265669 - 2521244 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-AA-3715-01 COSM293640 c.4722C>T p.N1574N Substitution - coding silent 15:28230454-28230454 - 35M COSM5581306 c.13384C>T p.P4462S Substitution - Missense 15:28117043-28117043 - TCGA-D1-A15X-01 COSM4871892 c.8409C>T p.D2803D Substitution - coding silent 15:28192003-28192003 - TCGA-18-3409-01 COSM700272 c.10310C>T p.S3437F Substitution - Missense 15:28168510-28168510 - TCGA-EE-A3AE-06 COSM4898025 c.411C>T p.A137A Substitution - coding silent 15:28280199-28280199 - 8057683 COSM4945849 c.7674G>A p.L2558L Substitution - coding silent 15:28201498-28201498 - DN12007 COSM5770144 c.8800G>A p.E2934K Substitution - Missense 15:28186602-28186602 - Pat_45_B COSM5848955 c.2566G>A p.G856S Substitution - Missense 15:28256269-28256269 - TCGA-DM-A28C-01 COSM4783896 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - TCGA-33-4583-01 COSM700275 c.11023G>C p.D3675H Substitution - Missense 15:28144790-28144790 - TCGA-EE-A2MR-06 COSM3500274 c.12617C>T p.S4206F Substitution - Missense 15:28130548-28130548 - DU-145 COSM238584 c.10471G>A p.A3491T Substitution - Missense 15:28167770-28167770 - TCGA-EE-A29E-06 COSM3500287 c.8945T>C p.V2982A Substitution - Missense 15:28179216-28179216 - TCGA-AM-5820-01 COSM3754256 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - RK138_C01 COSM4780156 c.3578-5T>C p.? Unknown 15:28238777-28238777 - sysucc-1370T COSM5470332 c.510C>T p.S170S Substitution - coding silent 15:28280100-28280100 - MedB-1 COSM5620948 c.9574G>T p.G3192C Substitution - Missense 15:28176540-28176540 - PD18264a COSM5794210 c.11337G>A p.R3779R Substitution - coding silent 15:28143954-28143954 - 08-P1004 COSM2083374 c.8097A>G p.V2699V Substitution - coding silent 15:28196484-28196484 - PD6751a COSM4879661 c.10669G>A p.V3557M Substitution - Missense 15:28163171-28163171 - TCGA-AP-A059-01 COSM960280 c.1074C>T p.G358G Substitution - coding silent 15:28272224-28272224 - CAL27 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - LUAD-S01409 COSM346422 c.1354G>T p.G452* Substitution - Nonsense 15:28269340-28269340 - DLD1 COSM4623069 c.10621C>T p.L3541L Substitution - coding silent 15:28163219-28163219 - 587336 COSM1209585 c.8351G>A p.R2784H Substitution - Missense 15:28192061-28192061 - TCGA-D5-6927-01 COSM1372272 c.674T>C p.L225S Substitution - Missense 15:28274417-28274417 - CN-AML-CR-55-Dx COSM5054226 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - TCGA-A6-6781-01 COSM4786519 c.8000G>A p.G2667E Substitution - Missense 15:28198389-28198389 - TCGA-A5-A0VP-01 COSM960197 c.7351C>T p.R2451C Substitution - Missense 15:28202476-28202476 - TCGA-D8-A1J8-01 COSM4815843 c.12721C>T p.R4241W Substitution - Missense 15:28130244-28130244 - T1 COSM5618699 c.14118G>A p.E4706E Substitution - coding silent 15:28113185-28113185 - LUAD-NYU330 COSM373775 c.9938G>A p.R3313H Substitution - Missense 15:28174514-28174514 - K20-Tumor COSM249637 c.11349A>T p.T3783T Substitution - coding silent 15:28143942-28143942 - 523LT COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - 509LT COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - TCGA-BR-8372-01 COSM4906747 c.6137C>T p.P2046L Substitution - Missense 15:28215694-28215694 - CSCC-16-T COSM960129 c.12309C>T p.S4103S Substitution - coding silent 15:28132752-28132752 - TCGA-A6-6653-01 COSM960233 c.4313G>A p.R1438H Substitution - Missense 15:28233702-28233702 - TCGA-FW-A3R5-06 COSM3886810 c.5659C>T p.P1887S Substitution - Missense 15:28220638-28220638 - PTC_456 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-56-6545-01 COSM700271 c.10023G>C p.Q3341H Substitution - Missense 15:28174429-28174429 - TCGA-AN-A0AT-01 COSM4578148 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - sysucc-783T COSM5448721 c.1003G>A p.A335T Substitution - Missense 15:28272295-28272295 - TCGA-E2-A56Z-01 COSM4813286 c.2702C>T p.A901V Substitution - Missense 15:28256133-28256133 - Pat_41_B COSM5848954 c.4948G>A p.D1650N Substitution - Missense 15:28229709-28229709 - 64 COSM5742629 c.14015C>T p.T4672M Substitution - Missense 15:28113577-28113577 - TCGA-A5-A0GW-01 COSM4872136 c.11409A>G p.T3803T Substitution - coding silent 15:28143882-28143882 - TCGA-DM-A1D8-01 COSM1372261 c.2955G>A p.R985R Substitution - coding silent 15:28254435-28254435 - CHC1328T COSM1301012 c.6114G>A p.Q2038Q Substitution - coding silent 15:28215717-28215717 - 2951_PT COSM2083420 c.6440T>C p.V2147A Substitution - Missense 15:28214191-28214191 - TCGA-EI-6917-01 COSM3420220 c.8783C>T p.S2928L Substitution - Missense 15:28186619-28186619 - T207 COSM4690081 c.8953T>C p.F2985L Substitution - Missense 15:28179208-28179208 - PCSI_0218_Pa_P_526 COSM4807333 c.11157C>G p.L3719L Substitution - coding silent 15:28144219-28144219 - S02291 COSM4892303 c.6363C>T p.S2121S Substitution - coding silent 15:28214268-28214268 - TCGA-AX-A063-01 COSM4863943 c.9943G>A p.A3315T Substitution - Missense 15:28174509-28174509 - TCGA-GL-7773-01 COSM4908408 c.8702A>T p.D2901V Substitution - Missense 15:28186700-28186700 - TCGA-BR-6454-01 COSM4906616 c.10460C>T p.S3487L Substitution - Missense 15:28167781-28167781 - CHC796T COSM4949602 c.1014G>C p.L338F Substitution - Missense 15:28272284-28272284 - PD4836a COSM5781429 c.8283C>G p.G2761G Substitution - coding silent 15:28192129-28192129 - TCGA-EJ-7125-01 COSM3672012 c.5331G>T p.L1777L Substitution - coding silent 15:28228351-28228351 - TCGA-AP-A0LM-01 COSM4873865 c.2971G>T p.D991Y Substitution - Missense 15:28254419-28254419 - PD3945a COSM5784881 c.988G>A p.A330T Substitution - Missense 15:28272310-28272310 - TCGA-AX-A05Z-01 COSM960163 c.10138C>T p.L3380F Substitution - Missense 15:28169575-28169575 - HCA7 COSM1209584 c.12990G>T p.Q4330H Substitution - Missense 15:28125006-28125006 - CHC923T COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - sysucc-936T COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-A5-A0VP-01 COSM4874243 c.7351C>T p.R2451C Substitution - Missense 15:28202476-28202476 - RKO COSM4647805 c.8509G>A p.V2837I Substitution - Missense 15:28191187-28191187 - TCGA-AP-A056-01 COSM4868571 c.5231G>A p.R1744Q Substitution - Missense 15:28229236-28229236 - TCGA-D1-A163-01 COSM4875127 c.948G>A p.L316L Substitution - coding silent 15:28272350-28272350 - TCGA-D1-A174-01 COSM960119 c.12849C>T p.D4283D Substitution - coding silent 15:28125147-28125147 - HCC017T COSM5815284 c.699A>T p.R233R Substitution - coding silent 15:28274392-28274392 - CSCC-27-T COSM4554009 c.6088G>T p.V2030L Substitution - Missense 15:28215743-28215743 - T660 COSM4690085 c.6905C>T p.S2302L Substitution - Missense 15:28212465-28212465 - PDA_049 COSM5000649 c.4014G>T p.Q1338H Substitution - Missense 15:28234274-28234274 - CSCC-38-T COSM4448874 c.13914-3delC p.? Unknown 15:28113681-28113681 - TCGA-D5-6540-01 COSM1372246 c.9351C>T p.S3117S Substitution - coding silent 15:28177031-28177031 - 2492705 COSM5716817 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - 169 COSM3729613 c.3020C>A p.P1007H Substitution - Missense 15:28254370-28254370 - PTC_455 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - 587224 COSM1209579 c.1741G>A p.G581S Substitution - Missense 15:28265832-28265832 - CHC1209T COSM4804675 c.11938G>T p.E3980* Substitution - Nonsense 15:28141509-28141509 - TCGA-BR-6452-01 COSM4907469 c.12085A>G p.T4029A Substitution - Missense 15:28135623-28135623 - BRC39 COSM5027934 c.660C>T p.L220L Substitution - coding silent 15:28274431-28274431 - PT49 COSM5729569 c.12994C>T p.P4332S Substitution - Missense 15:28124231-28124231 - TCGA-G4-6309-01 COSM1372239 c.10998C>T p.S3666S Substitution - coding silent 15:28146247-28146247 - TCGA-39-5021-01 COSM700265 c.6988C>T p.R2330W Substitution - Missense 15:28211083-28211083 - PD13766a COSM5786874 c.10218C>T p.I3406I Substitution - coding silent 15:28169495-28169495 - TCGA-22-1012-01 COSM700284 c.13948C>T p.R4650W Substitution - Missense 15:28113644-28113644 - TCGA-BR-8284-01 COSM4907292 c.8040T>C p.I2680I Substitution - coding silent 15:28196541-28196541 - TCGA-AN-A046-01 COSM3815789 c.10639C>T p.R3547C Substitution - Missense 15:28163201-28163201 - S00936 COSM317459 c.6269C>T p.A2090V Substitution - Missense 15:28214744-28214744 - ESCC_60 COSM5632706 c.12344_12345insT p.W4115fs*15 Insertion - Frameshift 15:28132716-28132717 - ESCC_BICR_057T COSM5436788 c.9126C>G p.L3042L Substitution - coding silent 15:28178924-28178924 - HCT15 COSM1678317 c.9324C>A p.S3108R Substitution - Missense 15:28177058-28177058 - PD18264a COSM5794211 c.11337G>A p.R3779R Substitution - coding silent 15:28143954-28143954 - TCGA-BR-4361-01 COSM4053850 c.7480+2T>C p.? Unknown 15:28202345-28202345 - CHC892T COSM4961174 c.8922G>A p.G2974G Substitution - coding silent 15:28182416-28182416 - K20 COSM249637 c.11349A>T p.T3783T Substitution - coding silent 15:28143942-28143942 - BD180T COSM5495161 c.9299G>T p.R3100L Substitution - Missense 15:28177083-28177083 - TCGA-BR-8487-01 COSM4053835 c.9309T>C p.D3103D Substitution - coding silent 15:28177073-28177073 - HCT116 COSM4632085 c.12492C>T p.D4164D Substitution - coding silent 15:28132178-28132178 - BD124T COSM5493249 c.577G>A p.A193T Substitution - Missense 15:28274971-28274971 - BICR_22 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - HT115 COSM4638183 c.8368A>G p.N2790D Substitution - Missense 15:28192044-28192044 - TCGA-BR-4370-01 COSM4053860 c.5012G>T p.G1671V Substitution - Missense 15:28229568-28229568 - Pat_11_A COSM109718 c.7628C>T p.A2543V Substitution - Missense 15:28201544-28201544 - 2_PRE-TREATMENT COSM1640201 c.5846-3delT p.? Unknown 15:28218674-28218674 - WSU-HN30 COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - 49M COSM4891834 c.14157C>T p.F4719F Substitution - coding silent 15:28113146-28113146 - TCGA-18-3409-01 COSM4861111 c.1907A>T p.K636I Substitution - Missense 15:28263133-28263133 - 08-P1177 COSM4578135 c.9358C>T p.L3120L Substitution - coding silent 15:28177024-28177024 - TCGA-EE-A3JI-06 COSM3500313 c.708C>T p.P236P Substitution - coding silent 15:28274383-28274383 - TCGA-BH-A0B6-01 COSM3815791 c.8634G>A p.L2878L Substitution - coding silent 15:28190980-28190980 - B106 COSM1749089 c.14355C>T p.I4785I Substitution - coding silent 15:28111913-28111913 - TCGA-34-5231-01 COSM700267 c.8509G>T p.V2837L Substitution - Missense 15:28191187-28191187 - PTC_448 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - 98 COSM5012842 c.215A>T p.K72M Substitution - Missense 15:28292995-28292995 - TCGA-EK-A2H1-01 COSM4822256 c.13988C>G p.S4663C Substitution - Missense 15:28113604-28113604 - TCGA-B5-A0JY-01 COSM960203 c.6486C>A p.L2162L Substitution - coding silent 15:28214145-28214145 - TCGA-AP-A051-01 COSM4872350 c.12787T>C p.C4263R Substitution - Missense 15:28130178-28130178 - TCGA-A2-A0CP-01 COSM5832858 c.11131_11132delCC p.P3711fs*5 Deletion - Frameshift 15:28144681-28144682 - 587376 COSM1209593 c.3212T>A p.I1071N Substitution - Missense 15:28248575-28248575 - 2521252 COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - sysucc-834T COSM4578152 c.1229C>T p.P410L Substitution - Missense 15:28270723-28270723 - DLD1 COSM4623070 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - TCGA-AK-3429-01 COSM4858235 c.7620T>C p.S2540S Substitution - coding silent 15:28201552-28201552 - TCGA-D1-A17Q-01 COSM4865103 c.10957G>A p.D3653N Substitution - Missense 15:28146288-28146288 - sysucc-1128T COSM5021827 c.912-7C>T p.? Unknown 15:28272393-28272393 - PT34 COSM5021827 c.912-7C>T p.? Unknown 15:28272393-28272393 - TCGA-GV-A40G-01 COSM4810970 c.6975C>T p.I2325I Substitution - coding silent 15:28211096-28211096 - pfg081T COSM4751796 c.2945A>G p.H982R Substitution - Missense 15:28254445-28254445 - TCGA-BR-8680-01 COSM4907114 c.240G>T p.E80D Substitution - Missense 15:28292970-28292970 - B106-Tumor COSM1749089 c.14355C>T p.I4785I Substitution - coding silent 15:28111913-28111913 - TCGA-FW-A3R5-06 COSM3886811 c.5501C>T p.A1834V Substitution - Missense 15:28222179-28222179 - TCGA-ER-A194-01 COSM3500309 c.1703C>T p.A568V Substitution - Missense 15:28265870-28265870 - WSU-HN30 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-G4-6320-01 COSM4783802 c.6817C>A p.L2273M Substitution - Missense 15:28212553-28212553 - P110 COSM5008120 c.1819G>A p.D607N Substitution - Missense 15:28265669-28265669 - BCB109T COSM4798760 c.10179A>G p.K3393K Substitution - coding silent 15:28169534-28169534 - LP6005409-DNA_F02 COSM5032331 c.3827C>T p.A1276V Substitution - Missense 15:28238139-28238139 - ESCC_118 COSM5640186 c.12465C>G p.A4155A Substitution - coding silent 15:28132205-28132205 - TCGA-AA-3510-01 COSM1372234 c.12444C>T p.I4148I Substitution - coding silent 15:28132226-28132226 - TCGA-AG-A002-01 COSM290924 c.12711_12712TC>CT p.V4237>? Complex 15:28130253-28130254 - TCGA-AB-2854-03 COSM1317814 c.903C>T p.G301G Substitution - coding silent 15:28272902-28272902 - TCGA-EE-A3AA-06 COSM3500297 c.5002C>T p.R1668C Substitution - Missense 15:28229578-28229578 - sysucc-936T COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - 4537_T COSM3956508 c.6369G>C p.L2123L Substitution - coding silent 15:28214262-28214262 - V-PH-16T COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - pfg068T COSM4751780 c.12532G>A p.G4178S Substitution - Missense 15:28132138-28132138 - Pat_15_B COSM5848951 c.4960delA p.M1654fs*1 Deletion - Frameshift 15:28229697-28229697 - WSU-HN30 COSM4600675 c.7334C>G p.P2445R Substitution - Missense 15:28202493-28202493 - sysucc-880T COSM5462441 c.932T>C p.L311P Substitution - Missense 15:28272366-28272366 - S02093 COSM5673110 c.3646G>C p.E1216Q Substitution - Missense 15:28238704-28238704 - TCGA-HU-A4G9-01 COSM4907682 c.3111T>C p.C1037C Substitution - coding silent 15:28248676-28248676 - TCGA-BP-4176-01 COSM4856973 c.10140T>C p.L3380L Substitution - coding silent 15:28169573-28169573 - TCGA-AR-A0TU-01 COSM433667 c.7662A>T p.R2554R Substitution - coding silent 15:28201510-28201510 - WSU-HN13 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-FS-A1YY-06 COSM4627310 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - TCGA-BR-4361-01 COSM4907823 c.1642C>T p.Q548* Substitution - Nonsense 15:28265931-28265931 - YURAY COSM5383107 c.11674_11675CC>TT p.P3892L Substitution - Missense 15:28142263-28142264 - BRC50 COSM5027933 c.5340C>G p.I1780M Substitution - Missense 15:28228342-28228342 - D15 COSM1209581 c.14200G>A p.A4734T Substitution - Missense 15:28113103-28113103 - TCGA-BG-A18B-01 COSM960262 c.2496G>A p.T832T Substitution - coding silent 15:28257082-28257082 - TCGA-D3-A3MR-06 COSM3500304 c.2972A>G p.D991G Substitution - Missense 15:28254418-28254418 - CSCC-49-T COSM4458769 c.10997C>T p.S3666F Substitution - Missense 15:28146248-28146248 - NCHP_DIPG103 COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - OSCC-GB_00680111 COSM4887751 c.9621G>T p.V3207V Substitution - coding silent 15:28176493-28176493 - CHC884T COSM4958368 c.11403G>C p.G3801G Substitution - coding silent 15:28143888-28143888 - TCGA-DD-A11A-01 COSM4940478 c.6910A>T p.K2304* Substitution - Nonsense 15:28212460-28212460 - TCGA-D3-A51T-06 COSM3500285 c.9303C>T p.I3101I Substitution - coding silent 15:28177079-28177079 - SCC-25 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - LUAD-D01603 COSM337409 c.13271A>T p.Q4424L Substitution - Missense 15:28121347-28121347 - TCGA-BR-4257-01 COSM4907432 c.9656C>T p.A3219V Substitution - Missense 15:28176458-28176458 - TCGA-AP-A0LM-01 COSM960252 c.2971G>T p.D991Y Substitution - Missense 15:28254419-28254419 - ME030T COSM227113 c.6713_6714CA>TG p.P2238>? Complex 15:28213814-28213815 - CSCC-55-T COSM4474841 c.1948C>T p.L650L Substitution - coding silent 15:28263092-28263092 - TCGA-FW-A3R5-06 COSM3886809 c.8048T>A p.F2683Y Substitution - Missense 15:28196533-28196533 - Gp2D COSM4627309 c.1902T>A p.Y634* Substitution - Nonsense 15:28263138-28263138 - 2250189 COSM5030029 c.557G>A p.G186D Substitution - Missense 15:28274991-28274991 - CRC-03T COSM5451343 c.13638C>T p.T4546T Substitution - coding silent 15:28115513-28115513 - LUAD-NYU259 COSM371748 c.3347G>T p.R1116L Substitution - Missense 15:28246786-28246786 - PD6751a COSM1637765 c.10669G>A p.V3557M Substitution - Missense 15:28163171-28163171 - TCGA-A6-6653-01 COSM4784944 c.11097C>T p.G3699G Substitution - coding silent 15:28144716-28144716 - CHC1209T COSM4804674 c.11938G>T p.E3980* Substitution - Nonsense 15:28141509-28141509 - TCGA-MI-A75G-01 COSM4939958 c.9193G>T p.D3065Y Substitution - Missense 15:28177480-28177480 - LP6005409-DNA_F02 COSM5032330 c.3827C>T p.A1276V Substitution - Missense 15:28238139-28238139 - TCGA-F1-6874-01 COSM4907765 c.263C>A p.P88H Substitution - Missense 15:28292947-28292947 - TCGA-BR-6452-01 COSM4053875 c.502A>G p.K168E Substitution - Missense 15:28280108-28280108 - Pat_11_A COSM1254121 c.13565C>T p.P4522L Substitution - Missense 15:28116709-28116709 - UM-SCC-47 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-EB-A1NK-01 COSM3500280 c.10647G>T p.V3549V Substitution - coding silent 15:28163193-28163193 - TCGA-AP-A0LD-01 COSM960266 c.2239G>A p.V747M Substitution - Missense 15:28260854-28260854 - ESO-1733 COSM1254131 c.14203G>T p.D4735Y Substitution - Missense 15:28113100-28113100 - TCGA-EE-A184-06 COSM3500315 c.294G>T p.L98L Substitution - coding silent 15:28292916-28292916 - PDA_034 COSM4999826 c.8535G>T p.M2845I Substitution - Missense 15:28191161-28191161 - TCGA-B0-4818-01 COSM470470 c.8548G>T p.V2850L Substitution - Missense 15:28191148-28191148 - tumor_4120193 COSM3927503 c.1658T>G p.V553G Substitution - Missense 15:28265915-28265915 - 587226 COSM1209571 c.14125G>A p.E4709K Substitution - Missense 15:28113178-28113178 - HCT-116 COSM1678315 c.9431T>C p.M3144T Substitution - Missense 15:28176951-28176951 - TCGA-EE-A2A1-06 COSM3500290 c.7907C>T p.S2636F Substitution - Missense 15:28198482-28198482 - TCGA-AX-A0J1-01 COSM4867662 c.12943G>A p.A4315T Substitution - Missense 15:28125053-28125053 - TCGA-ER-A194-01 COSM4899375 c.1703C>T p.A568V Substitution - Missense 15:28265870-28265870 - EGC15 COSM5054228 c.2781T>C p.R927R Substitution - coding silent 15:28255962-28255962 - CPCG0001-F1 COSM4880110 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - T3080 COSM4690063 c.11244C>T p.S3748S Substitution - coding silent 15:28144132-28144132 - PTC_415 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - pfg068T COSM1372232 c.12532G>A p.G4178S Substitution - Missense 15:28132138-28132138 - UM-SCC-17B COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - 2492706 COSM5716816 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - P117 COSM5010320 c.11840_11841delCT p.S3947fs*13 Deletion - Frameshift 15:28141606-28141607 - TCGA-CG-5721-01 COSM4053852 c.7435C>G p.L2479V Substitution - Missense 15:28202392-28202392 - pfg072T COSM4751791 c.8671G>T p.A2891S Substitution - Missense 15:28186731-28186731 - TCGA-ER-A198-06 COSM3500317 c.179C>T p.P60L Substitution - Missense 15:28299410-28299410 - RK159_C01 COSM1629490 c.13136G>C p.G4379A Substitution - Missense 15:28124089-28124089 - S01504 COSM4386910 c.2074G>T p.G692* Substitution - Nonsense 15:28262966-28262966 - 1N63-VS-1T63 COSM4977969 c.4642C>T p.Q1548* Substitution - Nonsense 15:28233179-28233179 - 97 COSM3732859 c.3638C>T p.A1213V Substitution - Missense 15:28238712-28238712 - PD11357a COSM5793131 c.983G>A p.R328H Substitution - Missense 15:28272315-28272315 - TCGA-ED-A7PZ-01 COSM4916857 c.6178G>C p.A2060P Substitution - Missense 15:28215653-28215653 - BICR_22 COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - pfg043T COSM4751768 c.14402T>G p.L4801R Substitution - Missense 15:28111866-28111866 - PD11357a COSM5793132 c.983G>A p.R328H Substitution - Missense 15:28272315-28272315 - TCGA-FU-A23K-01 COSM459065 c.986C>T p.S329F Substitution - Missense 15:28272312-28272312 - SCC-25 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-K7-A6G5-01 COSM4939280 c.10001T>G p.V3334G Substitution - Missense 15:28174451-28174451 - TCGA-BR-4184-01 COSM4907244 c.2627C>T p.A876V Substitution - Missense 15:28256208-28256208 - Sample_1 COSM4594491 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - PD6722a COSM5800587 c.12634C>G p.L4212V Substitution - Missense 15:28130531-28130531 - TCGA-AA-3696-01 COSM268498 c.4337A>G p.K1446R Substitution - Missense 15:28233678-28233678 - CHC892T COSM4798244 c.10797C>T p.A3599A Substitution - coding silent 15:28152780-28152780 - CSCC-17-T COSM4053849 c.7491C>A p.A2497A Substitution - coding silent 15:28202239-28202239 - tumor_4191799 COSM4879568 c.14232+6C>T p.? Unknown 15:28113065-28113065 - PCSI_0083_Pa_P_526 COSM3786501 c.1598+5G>A p.? Unknown 15:28268460-28268460 - CSCC-49-T COSM4458768 c.10997C>T p.S3666F Substitution - Missense 15:28146248-28146248 - pfg272T COSM4751775 c.13529A>C p.E4510A Substitution - Missense 15:28116745-28116745 - TCGA-B5-A11X-01 COSM4872299 c.13665C>T p.A4555A Substitution - coding silent 15:28115486-28115486 - TCGA-AP-A051-01 COSM4872830 c.11255G>A p.R3752H Substitution - Missense 15:28144121-28144121 - PT47 COSM5070860 c.9832-8G>A p.? Unknown 15:28174628-28174628 - PD9573a COSM5785950 c.10323G>A p.A3441A Substitution - coding silent 15:28168497-28168497 - TCGA-BR-8487-01 COSM4906961 c.8919C>T p.G2973G Substitution - coding silent 15:28182419-28182419 - ESO-114 COSM1254124 c.6518C>T p.S2173F Substitution - Missense 15:28214113-28214113 - TCGA-EE-A2GJ-06 COSM3500270 c.13275C>T p.V4425V Substitution - coding silent 15:28117152-28117152 - 587376 COSM1209594 c.2093G>A p.R698H Substitution - Missense 15:28262947-28262947 - TCGA-AA-3492-01 COSM4948819 c.9858C>T p.H3286H Substitution - coding silent 15:28174594-28174594 - PCSI_0007_Pa_P COSM5420170 c.10963C>T p.L3655F Substitution - Missense 15:28146282-28146282 - TCGA-BR-8363-01 COSM4053830 c.10312G>A p.D3438N Substitution - Missense 15:28168508-28168508 - T26 COSM5618270 c.7654A>C p.K2552Q Substitution - Missense 15:28201518-28201518 - TCGA-CD-8529-01 COSM4907137 c.1207C>G p.L403V Substitution - Missense 15:28270745-28270745 - TCGA-A2-A0T5-01 COSM3815799 c.755A>G p.E252G Substitution - Missense 15:28274336-28274336 - CN-AML-CR-56-Dx COSM5427070 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - CN-AML-NR-26-Dx COSM4386169 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-DD-A4NF-01 COSM4912684 c.3439A>G p.K1147E Substitution - Missense 15:28246019-28246019 - 6P2-2 COSM3734523 c.8500A>G p.K2834E Substitution - Missense 15:28191196-28191196 - PCSI_0105_Pa_P_526 COSM4962172 c.12601A>T p.K4201* Substitution - Nonsense 15:28130564-28130564 - AML_14y_08_DX COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-AG-3909-01 COSM258840 c.3266T>A p.L1089Q Substitution - Missense 15:28246867-28246867 - TCGA-CD-A4MG-01 COSM2083295 c.11169C>T p.C3723C Substitution - coding silent 15:28144207-28144207 - C086 COSM3500282 c.10296C>T p.S3432S Substitution - coding silent 15:28168524-28168524 - TCGA-BR-8680-01 COSM4053817 c.12378C>T p.S4126S Substitution - coding silent 15:28132683-28132683 - TCGA-BR-8680-01 COSM4053853 c.6653G>A p.R2218H Substitution - Missense 15:28213875-28213875 - C086 COSM5532286 c.6842C>T p.S2281F Substitution - Missense 15:28212528-28212528 - MO_1012 COSM5561908 c.6713C>T p.P2238L Substitution - Missense 15:28213815-28213815 - 2521259 COSM5890849 c.11816+3T>G p.? Unknown 15:28141728-28141728 - TCGA-CM-6162-01 COSM1372240 c.10805C>T p.S3602L Substitution - Missense 15:28152772-28152772 - PCSI_0090_Pa_X COSM5419826 c.11824G>T p.D3942Y Substitution - Missense 15:28141623-28141623 - T3021 COSM4690072 c.9736C>T p.R3246W Substitution - Missense 15:28175607-28175607 - 07-P1079 COSM4578149 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - TCGA-33-4533-01 COSM700244 c.128G>T p.G43V Substitution - Missense 15:28299461-28299461 - CSCC-62-T COSM4461113 c.11932C>T p.P3978S Substitution - Missense 15:28141515-28141515 - TCGA-A8-A06U-01 COSM4814276 c.836G>T p.G279V Substitution - Missense 15:28272969-28272969 - 93VU147T COSM4590646 c.14082C>G p.I4694M Substitution - Missense 15:28113221-28113221 - TCGA-CM-4743-01 COSM1372250 c.8308T>C p.C2770R Substitution - Missense 15:28192104-28192104 - TCGA-B5-A0JY-01 COSM960278 c.1627G>A p.A543T Substitution - Missense 15:28265946-28265946 - CHC923T COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - TCGA-AP-A051-01 COSM4872371 c.11187C>A p.S3729S Substitution - coding silent 15:28144189-28144189 - QC2-09-T2 COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - sysucc-1512T COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - T3152 COSM4690066 c.10059C>T p.G3353G Substitution - coding silent 15:28169654-28169654 - TCGA-DD-A4NF-01 COSM4912683 c.3439A>G p.K1147E Substitution - Missense 15:28246019-28246019 - PD11464a COSM5770145 c.8800G>A p.E2934K Substitution - Missense 15:28186602-28186602 - S0059 COSM5882552 c.1483A>C p.I495L Substitution - Missense 15:28268580-28268580 - PT35 COSM5913676 c.8558-5C>T p.? Unknown 15:28191061-28191061 - PT41 COSM5924637 c.12863C>T p.A4288V Substitution - Missense 15:28125133-28125133 - T3152 COSM4690067 c.10059C>T p.G3353G Substitution - coding silent 15:28169654-28169654 - 01-P1216 COSM4578142 c.6637A>G p.I2213V Substitution - Missense 15:28213891-28213891 - TCGA-AP-A0LM-01 COSM4873402 c.14305C>T p.P4769S Substitution - Missense 15:28111963-28111963 - TCGA-AA-3663-01 COSM1372232 c.12532G>A p.G4178S Substitution - Missense 15:28132138-28132138 - TCGA-A1-A0SI-01 COSM960225 c.5230C>T p.R1744* Substitution - Nonsense 15:28229237-28229237 - PT22_1 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-BR-7707-01 COSM4053872 c.1376C>T p.A459V Substitution - Missense 15:28269318-28269318 - TCGA-BR-4201-01 COSM4053876 c.321A>G p.P107P Substitution - coding silent 15:28292889-28292889 - P95 COSM2083361 c.8509G>A p.V2837I Substitution - Missense 15:28191187-28191187 - TCGA-A5-A0VP-01 COSM4874222 c.3294G>A p.T1098T Substitution - coding silent 15:28246839-28246839 - TCGA-EI-6507-01 COSM3749292 c.1083C>T p.H361H Substitution - coding silent 15:28272215-28272215 - TCGA-DD-A119-01 COSM4919881 c.3147T>C p.A1049A Substitution - coding silent 15:28248640-28248640 - S02294 COSM5688736 c.9838G>A p.A3280T Substitution - Missense 15:28174614-28174614 - TCGA-A8-A08L-01 COSM4816153 c.4513G>T p.V1505F Substitution - Missense 15:28233308-28233308 - 509LT COSM4386169 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - CSCC-38-T COSM4448875 c.13914-3delC p.? Unknown 15:28113681-28113681 - 19 COSM5747622 c.12931G>C p.A4311P Substitution - Missense 15:28125065-28125065 - pfg043T COSM4751769 c.14402T>G p.L4801R Substitution - Missense 15:28111866-28111866 - LIM2551 COSM4643880 c.12690C>T p.G4230G Substitution - coding silent 15:28130275-28130275 - TCGA-AP-A056-01 COSM960223 c.5231G>A p.R1744Q Substitution - Missense 15:28229236-28229236 - 8057676 COSM3386818 c.12230+1G>T p.? Unknown 15:28135477-28135477 - sysucc-809T COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - T3021 COSM4690076 c.9409A>G p.T3137A Substitution - Missense 15:28176973-28176973 - CHC1209T COSM4804675 c.11938G>T p.E3980* Substitution - Nonsense 15:28141509-28141509 - QC2-25-T2 COSM4906408 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - P134 COSM5010114 c.9649T>C p.S3217P Substitution - Missense 15:28176465-28176465 - Pat_11_A COSM5848940 c.13565C>T p.P4522L Substitution - Missense 15:28116709-28116709 - TCGA-FW-A3R5-06 COSM3886814 c.4312C>T p.R1438C Substitution - Missense 15:28233703-28233703 - CHC892T COSM4961418 c.12554G>A p.C4185Y Substitution - Missense 15:28132116-28132116 - PDA_017 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - P134 COSM960266 c.2239G>A p.V747M Substitution - Missense 15:28260854-28260854 - TCGA-B5-A11E-01 COSM960260 c.2656G>A p.A886T Substitution - Missense 15:28256179-28256179 - TCGA-18-4086-01 COSM700263 c.6161A>C p.K2054T Substitution - Missense 15:28215670-28215670 - TCGA-CG-4306-01 COSM4053864 c.3975G>A p.P1325P Substitution - coding silent 15:28236991-28236991 - NOKSI COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-FS-A1ZD-06 COSM4898932 c.13189-1G>A p.? Unknown 15:28121430-28121430 - WSU-HN8 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - N170T COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - sysucc-1397T COSM5473602 c.13688C>T p.A4563V Substitution - Missense 15:28115463-28115463 - RK138_C01 COSM1629492 c.3578-5T>C p.? Unknown 15:28238777-28238777 - HCC58T COSM1608218 c.9436A>G p.K3146E Substitution - Missense 15:28176765-28176765 - TCGA-CI-6624-01 COSM4946129 c.9366C>T p.T3122T Substitution - coding silent 15:28177016-28177016 - Gp5D COSM2083561 c.728A>G p.E243G Substitution - Missense 15:28274363-28274363 - CN-AML-NR-26-Dx COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-AP-A051-01 COSM960103 c.13454C>T p.S4485F Substitution - Missense 15:28116820-28116820 - CCRF-CEM COSM1678319 c.2701G>A p.A901T Substitution - Missense 15:28256134-28256134 - TCGA-CG-5721-01 COSM4053863 c.4307T>C p.V1436A Substitution - Missense 15:28233708-28233708 - ORL-48 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-CC-A5UE-01 COSM4933867 c.888G>T p.L296L Substitution - coding silent 15:28272917-28272917 - ESO-1670 COSM1254130 c.7936C>T p.R2646W Substitution - Missense 15:28198453-28198453 - 67 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-EE-A2GJ-06 COSM4897317 c.2413C>T p.L805L Substitution - coding silent 15:28257165-28257165 - TCGA-AP-A059-01 COSM4866274 c.3733G>T p.G1245* Substitution - Nonsense 15:28238617-28238617 - S39_pre COSM4578148 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - TCGA-66-2773-01 COSM700262 c.6066G>C p.R2022R Substitution - coding silent 15:28215765-28215765 - CSCC-55-T COSM4474842 c.1948C>T p.L650L Substitution - coding silent 15:28263092-28263092 - P134 COSM4874292 c.2239G>A p.V747M Substitution - Missense 15:28260854-28260854 - TCGA-A5-A0VP-01 COSM960245 c.3294G>A p.T1098T Substitution - coding silent 15:28246839-28246839 - TCGA-A2-A0CP-01 COSM5832861 c.11125_11128delATCA p.I3709fs*24 Deletion - Frameshift 15:28144685-28144688 - TCGA-JX-A3Q0-01 COSM1162283 c.1731C>T p.R577R Substitution - coding silent 15:28265842-28265842 - BD217T COSM5495453 c.4393A>T p.I1465F Substitution - Missense 15:28233520-28233520 - TCGA-BR-8680-01 COSM4053846 c.7667A>G p.D2556G Substitution - Missense 15:28201505-28201505 - PCSI_0090_Pa_P COSM5419825 c.11824G>T p.D3942Y Substitution - Missense 15:28141623-28141623 - TCGA-DB-A64X-01 COSM3969052 c.3332C>T p.A1111V Substitution - Missense 15:28246801-28246801 - TCGA-C8-A26W-01 COSM4814607 c.11681C>G p.P3894R Substitution - Missense 15:28142257-28142257 - PT24_1 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AA-3966-01 COSM272771 c.3654T>C p.H1218H Substitution - coding silent 15:28238696-28238696 - 587332 COSM1209587 c.13723-2A>G p.? Unknown 15:28114804-28114804 - RK150_C01 COSM3744540 c.2139T>A p.D713E Substitution - Missense 15:28260954-28260954 - WSU-HN6 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-BR-A4QL-01 COSM4906408 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - EGC15 COSM5054229 c.2781T>C p.R927R Substitution - coding silent 15:28255962-28255962 - sysucc-1317T COSM5448722 c.1003G>A p.A335T Substitution - Missense 15:28272295-28272295 - TCGA-G2-A2EK-01 COSM1301013 c.5509C>G p.Q1837E Substitution - Missense 15:28222171-28222171 - HCC102T COSM4781333 c.8898G>C p.L2966L Substitution - coding silent 15:28182440-28182440 - RK282_C01 COSM4964014 c.7871A>G p.H2624R Substitution - Missense 15:28198615-28198615 - TCGA-GN-A267-06 COSM3500272 c.13115C>T p.S4372L Substitution - Missense 15:28124110-28124110 - PA055 COSM1162283 c.1731C>T p.R577R Substitution - coding silent 15:28265842-28265842 - TCGA-CK-5913-01 COSM1372259 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - CSCC-62-T COSM4503680 c.6465C>T p.S2155S Substitution - coding silent 15:28214166-28214166 - TCGA-DD-A119-01 COSM4919880 c.3147T>C p.A1049A Substitution - coding silent 15:28248640-28248640 - Pat_53_B COSM2083287 c.11791G>A p.E3931K Substitution - Missense 15:28141756-28141756 - TCGA-DM-A1DA-01 COSM1372274 c.160delC p.Q54fs*23 Deletion - Frameshift 15:28299429-28299429 - CSCC-27-T COSM4464461 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - TCGA-EE-A3JD-06 COSM4394928 c.5716G>T p.V1906F Substitution - Missense 15:28220581-28220581 - sysucc-1640T COSM4597961 c.815C>T p.T272M Substitution - Missense 15:28272990-28272990 - HCC017T COSM5815285 c.699A>T p.R233R Substitution - coding silent 15:28274392-28274392 - YUKLAB COSM1707961 c.2053G>C p.D685H Substitution - Missense 15:28262987-28262987 - S00539 COSM317456 c.11866G>T p.G3956* Substitution - Nonsense 15:28141581-28141581 - TCGA-EE-A184-06 COSM4904021 c.294G>T p.L98L Substitution - coding silent 15:28292916-28292916 - TCGA-P4-A5EB-01 COSM74889 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - 2290929 COSM554526 c.5982C>T p.C1994C Substitution - coding silent 15:28218535-28218535 - TCGA-FS-A1ZA-06 COSM3500302 c.3399C>T p.L1133L Substitution - coding silent 15:28246059-28246059 - HT115 COSM2083362 c.8508C>T p.I2836I Substitution - coding silent 15:28191188-28191188 - AOCS-134-3-9 COSM3981438 c.3704T>C p.I1235T Substitution - Missense 15:28238646-28238646 - TCGA-CG-5721-01 COSM4906788 c.5201A>G p.K1734R Substitution - Missense 15:28229266-28229266 - TCGA-HF-7133-01 COSM4907642 c.6428C>T p.A2143V Substitution - Missense 15:28214203-28214203 - ESO-160 COSM1254129 c.6091C>T p.R2031W Substitution - Missense 15:28215740-28215740 - LS411 COSM2083542 c.1570G>A p.G524S Substitution - Missense 15:28268493-28268493 - TCGA-EE-A2GJ-06 COSM3500307 c.2413C>T p.L805L Substitution - coding silent 15:28257165-28257165 - TCGA-D1-A17Q-01 COSM4865486 c.13543C>T p.R4515* Substitution - Nonsense 15:28116731-28116731 - PT47 COSM5930324 c.8437G>A p.G2813R Substitution - Missense 15:28191975-28191975 - WSU-HN8 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - Pat_24_A COSM5848947 c.9432G>A p.M3144I Substitution - Missense 15:28176950-28176950 - TCGA-BR-8680-01 COSM4907337 c.12378C>T p.S4126S Substitution - coding silent 15:28132683-28132683 - PTC-10C COSM2083591 c.46T>A p.S16T Substitution - Missense 15:28321388-28321388 - CSCC-44-T COSM4485448 c.2934C>T p.A978A Substitution - coding silent 15:28254456-28254456 - TCGA-AK-3429-01 COSM470471 c.7620T>C p.S2540S Substitution - coding silent 15:28201552-28201552 - 117 COSM3732869 c.10005C>G p.H3335Q Substitution - Missense 15:28174447-28174447 - TCGA-CU-A0YN-01 COSM416528 c.9520G>T p.V3174L Substitution - Missense 15:28176594-28176594 - TCGA-G4-6588-01 COSM1372254 c.6976C>A p.L2326M Substitution - Missense 15:28211095-28211095 - TCGA-HU-A4GX-01 COSM4053832 c.9993G>A p.T3331T Substitution - coding silent 15:28174459-28174459 - PDA_018 COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - CN-AML-CR-28-Dx COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-DU-A5TP-01 COSM4908686 c.5420A>G p.N1807S Substitution - Missense 15:28228262-28228262 - TCGA-BR-7703-01 COSM4053824 c.10723G>A p.G3575S Substitution - Missense 15:28163117-28163117 - sysucc-1163T COSM5458494 c.604T>C p.S202P Substitution - Missense 15:28274944-28274944 - CSCC-35-T COSM4560444 c.8446G>A p.G2816R Substitution - Missense 15:28191966-28191966 - ESCC_131 COSM5642199 c.13658A>C p.N4553T Substitution - Missense 15:28115493-28115493 - C0007T COSM4150914 c.8311C>G p.H2771D Substitution - Missense 15:28192101-28192101 - C086 COSM4053816 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - TCGA-BR-8680-01 COSM960137 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - CSCC-18-T COSM4470547 c.1668C>T p.I556I Substitution - coding silent 15:28265905-28265905 - 40M COSM4907748 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - TCGA-AA-3492-01 COSM4948853 c.5206T>C p.Y1736H Substitution - Missense 15:28229261-28229261 - TCGA-AP-A056-01 COSM960133 c.12071C>T p.S4024L Substitution - Missense 15:28135637-28135637 - TCGA-AX-A0J1-01 COSM960262 c.2496G>A p.T832T Substitution - coding silent 15:28257082-28257082 - CG-3609 COSM2157535 c.7985C>T p.T2662I Substitution - Missense 15:28198404-28198404 - TCGA-BS-A0UF-01 COSM4875714 c.2039C>A p.S680* Substitution - Nonsense 15:28263001-28263001 - 1862877 COSM1180672 c.6555+3G>A p.? Unknown 15:28214073-28214073 - C2 COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-DA-A1I1-06 COSM4897453 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - 388 COSM97925 c.8424C>A p.C2808* Substitution - Nonsense 15:28191988-28191988 - I2L-P25-Tumor-Organoid COSM5363036 c.5163G>A p.P1721P Substitution - coding silent 15:28229304-28229304 - TCGA-B5-A11X-01 COSM960099 c.13665C>T p.A4555A Substitution - coding silent 15:28115486-28115486 - TCGA-66-2789-01 COSM4859407 c.4297G>T p.V1433L Substitution - Missense 15:28233718-28233718 - LUAD-AEIUF COSM392865 c.6473A>G p.Q2158R Substitution - Missense 15:28214158-28214158 - CSCC-27-T COSM4482827 c.2643C>T p.T881T Substitution - coding silent 15:28256192-28256192 - TCGA-13-1495-01 COSM116806 c.6647G>A p.R2216H Substitution - Missense 15:28213881-28213881 - UM-SCC-4 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - 587342 COSM1209591 c.832C>T p.P278S Substitution - Missense 15:28272973-28272973 - EW8 COSM4578150 c.2743G>T p.A915S Substitution - Missense 15:28256092-28256092 - DLD1 COSM4623068 c.10621C>T p.L3541L Substitution - coding silent 15:28163219-28163219 - TCGA-A6-6653-01 COSM4783282 c.4313G>A p.R1438H Substitution - Missense 15:28233702-28233702 - LUAD-RT-S01810 COSM382803 c.2200G>T p.G734W Substitution - Missense 15:28260893-28260893 - YURAY COSM5383117 c.423G>A p.K141K Substitution - coding silent 15:28280187-28280187 - TCGA-BR-8363-01 COSM4906653 c.10312G>A p.D3438N Substitution - Missense 15:28168508-28168508 - ESO-153 COSM1254126 c.6342C>T p.D2114D Substitution - coding silent 15:28214671-28214671 - TCGA-D3-A5GU-06 COSM4905563 c.10296C>T p.S3432S Substitution - coding silent 15:28168524-28168524 - PTC-28C COSM4909389 c.1709G>T p.G570V Substitution - Missense 15:28265864-28265864 - TCGA-EB-A5UN-06 COSM4897238 c.780C>T p.F260F Substitution - coding silent 15:28274311-28274311 - TCGA-B5-A0JY-01 COSM960256 c.2908G>T p.E970* Substitution - Nonsense 15:28254482-28254482 - TCGA-D1-A16F-01 COSM960219 c.5351G>A p.R1784H Substitution - Missense 15:28228331-28228331 - sysucc-1397T COSM5473601 c.13688C>T p.A4563V Substitution - Missense 15:28115463-28115463 - Pat_15_B COSM5848952 c.4960delA p.M1654fs*1 Deletion - Frameshift 15:28229697-28229697 - TCGA-B5-A11Y-01 COSM960205 c.6451C>T p.R2151C Substitution - Missense 15:28214180-28214180 - 180 COSM3722026 c.3359A>G p.E1120G Substitution - Missense 15:28246774-28246774 - PCSI_0356_Pa_P_526 COSM3786500 c.6394G>T p.A2132S Substitution - Missense 15:28214237-28214237 - BICR_22 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - WSU-HN30 COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-EE-A3JD-06 COSM4396363 c.10454C>T p.T3485I Substitution - Missense 15:28167787-28167787 - T3503 COSM4690113 c.477_478insT p.Q160fs*7 Insertion - Frameshift 15:28280132-28280133 - SNU-175 COSM4650345 c.1345G>A p.A449T Substitution - Missense 15:28269349-28269349 - TCGA-D5-6930-01 COSM4782895 c.10361C>T p.A3454V Substitution - Missense 15:28168459-28168459 - TCGA-HU-8602-01 COSM4906707 c.9737G>A p.R3246Q Substitution - Missense 15:28175606-28175606 - I2L-P7-Tumor-Organoid COSM5363165 c.8117T>C p.V2706A Substitution - Missense 15:28196464-28196464 - 5202_PT COSM5754665 c.958G>A p.G320R Substitution - Missense 15:28272340-28272340 - TCGA-AP-A051-01 COSM960233 c.4313G>A p.R1438H Substitution - Missense 15:28233702-28233702 - TCGA-AP-A051-01 COSM960147 c.11255G>A p.R3752H Substitution - Missense 15:28144121-28144121 - LN229 COSM307015 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - sysucc-715T COSM5054227 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - TCGA-CG-5726-01 COSM4907057 c.7637C>T p.T2546M Substitution - Missense 15:28201535-28201535 - 1N01-VS-1T01 COSM4972381 c.8834G>C p.R2945T Substitution - Missense 15:28182504-28182504 - TCGA-BR-6452-01 COSM4907542 c.502A>G p.K168E Substitution - Missense 15:28280108-28280108 - HCC059T COSM5809753 c.8926A>T p.K2976* Substitution - Nonsense 15:28182412-28182412 - TCGA-D5-6930-01 COSM1372255 c.6605delG p.G2202fs*8 Deletion - Frameshift 15:28213923-28213923 - TCGA-D1-A103-01 COSM960276 c.1697T>C p.I566T Substitution - Missense 15:28265876-28265876 - CRC-31T COSM5457823 c.1870+5G>A p.? Unknown 15:28265613-28265613 - TCGA-FS-A1Z3-06 COSM4906108 c.10421C>T p.S3474F Substitution - Missense 15:28167820-28167820 - K20-Tumor COSM4909225 c.11349A>T p.T3783T Substitution - coding silent 15:28143942-28143942 - TCGA-A6-5665-01 COSM4783317 c.8376G>A p.S2792S Substitution - coding silent 15:28192036-28192036 - TCGA-D5-6930-01 COSM5106397 c.6605delG p.G2202fs*8 Deletion - Frameshift 15:28213923-28213923 - TCGA-CJ-5683-01 COSM470475 c.1967A>G p.D656G Substitution - Missense 15:28263073-28263073 - TCGA-ED-A7PZ-01 COSM317458 c.6178G>C p.A2060P Substitution - Missense 15:28215653-28215653 - TCGA-K7-A6G5-01 COSM4939279 c.10001T>G p.V3334G Substitution - Missense 15:28174451-28174451 - 509LT COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-D3-A5GU-06 COSM3500282 c.10296C>T p.S3432S Substitution - coding silent 15:28168524-28168524 - sysucc-1512T COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - CAL33 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-BR-6452-01 COSM4907475 c.8013T>C p.A2671A Substitution - coding silent 15:28196568-28196568 - TCGA-GD-A3OP-01 COSM4810579 c.10594C>T p.Q3532* Substitution - Nonsense 15:28163246-28163246 - TCGA-D1-A103-01 COSM960157 c.10866C>T p.D3622D Substitution - coding silent 15:28152711-28152711 - CSCC-60-T COSM4497763 c.5049C>T p.F1683F Substitution - coding silent 15:28229531-28229531 - T3503 COSM4690102 c.3356C>T p.A1119V Substitution - Missense 15:28246777-28246777 - TCGA-A5-A0VP-01 COSM4874200 c.14424C>T p.D4808D Substitution - coding silent 15:28111844-28111844 - 1N63-VS-1T63 COSM4977968 c.4642C>T p.Q1548* Substitution - Nonsense 15:28233179-28233179 - 587346 COSM1209580 c.13063C>T p.H4355Y Substitution - Missense 15:28124162-28124162 - HCT116 COSM1678315 c.9431T>C p.M3144T Substitution - Missense 15:28176951-28176951 - TCGA-BR-4257-01 COSM2083333 c.9656C>T p.A3219V Substitution - Missense 15:28176458-28176458 - TCGA-BR-6452-01 COSM4053821 c.11774T>C p.F3925S Substitution - Missense 15:28141773-28141773 - sysucc-809T COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - HCT8 COSM4623070 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - EGC15 COSM4874243 c.7351C>T p.R2451C Substitution - Missense 15:28202476-28202476 - BD173T COSM5500104 c.132A>C p.E44D Substitution - Missense 15:28299457-28299457 - PT26 COSM5905307 c.8653C>T p.H2885Y Substitution - Missense 15:28186749-28186749 - P140 COSM5008285 c.382G>A p.V128I Substitution - Missense 15:28280228-28280228 - P60 COSM5008478 c.9210G>A p.S3070S Substitution - coding silent 15:28177463-28177463 - LUAD-NYU508 COSM374772 c.10587G>C p.P3529P Substitution - coding silent 15:28163253-28163253 - TCGA-AA-3715-01 COSM269305 c.9917T>G p.L3306* Substitution - Nonsense 15:28174535-28174535 - sysucc-1163T COSM5458495 c.604T>C p.S202P Substitution - Missense 15:28274944-28274944 - BCB109T COSM4798760 c.10179A>G p.K3393K Substitution - coding silent 15:28169534-28169534 - sysucc-880T COSM5462436 c.14062G>A p.V4688M Substitution - Missense 15:28113241-28113241 - PCSI_0090_Pa_X COSM5419825 c.11824G>T p.D3942Y Substitution - Missense 15:28141623-28141623 - TCGA-BR-8372-01 COSM4053855 c.6137C>T p.P2046L Substitution - Missense 15:28215694-28215694 - WSU-HN8 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-BR-4184-01 COSM4053822 c.11041C>T p.R3681C Substitution - Missense 15:28144772-28144772 - OST103PT COSM1732357 c.10273C>T p.P3425S Substitution - Missense 15:28168547-28168547 - HCC058T COSM5805401 c.5860G>A p.E1954K Substitution - Missense 15:28218657-28218657 - TCGA-DI-A0WH-01 COSM4870848 c.9037G>A p.V3013M Substitution - Missense 15:28179013-28179013 - TCGA-BR-7703-01 COSM2083365 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - LUAD-5V8LT COSM401531 c.10680G>T p.R3560R Substitution - coding silent 15:28163160-28163160 - TCGA-EJ-5506-01 COSM1129250 c.6550G>A p.E2184K Substitution - Missense 15:28214081-28214081 - 587376 COSM1209592 c.10150C>A p.L3384I Substitution - Missense 15:28169563-28169563 - TCGA-AC-A23H-01 COSM3420220 c.8783C>T p.S2928L Substitution - Missense 15:28186619-28186619 - TCGA-BR-8284-01 COSM4053841 c.8040T>C p.I2680I Substitution - coding silent 15:28196541-28196541 - TCGA-BR-8680-01 COSM4053878 c.240G>T p.E80D Substitution - Missense 15:28292970-28292970 - OSCC-GB_00680111 COSM4887752 c.9621G>T p.V3207V Substitution - coding silent 15:28176493-28176493 - P108 COSM5009550 c.13937T>C p.V4646A Substitution - Missense 15:28113655-28113655 - NOKSI COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-BS-A0UV-01 COSM960225 c.5230C>T p.R1744* Substitution - Nonsense 15:28229237-28229237 - T368 COSM4690101 c.5103T>C p.P1701P Substitution - coding silent 15:28229477-28229477 - TCGA-33-4533-01 COSM700242 c.127G>A p.G43R Substitution - Missense 15:28299462-28299462 - 3206A7_017_T COSM5038931 c.1627G>T p.A543S Substitution - Missense 15:28265946-28265946 - 49M COSM3500269 c.14157C>T p.F4719F Substitution - coding silent 15:28113146-28113146 - ATL030 COSM5705834 c.794T>A p.V265E Substitution - Missense 15:28274297-28274297 - Pat_24_A COSM5848946 c.9432G>A p.M3144I Substitution - Missense 15:28176950-28176950 - TCGA-EE-A2MT-06 COSM3500279 c.10721C>T p.S3574F Substitution - Missense 15:28163119-28163119 - TCGA-CJ-5682-01 COSM4857486 c.3028C>G p.Q1010E Substitution - Missense 15:28254362-28254362 - P134 COSM5010115 c.9649T>C p.S3217P Substitution - Missense 15:28176465-28176465 - 587316 COSM1209581 c.14200G>A p.A4734T Substitution - Missense 15:28113103-28113103 - TCGA-D9-A149-06 COSM3500276 c.11734A>C p.S3912R Substitution - Missense 15:28141813-28141813 - TCGA-AA-A010-01 COSM281679 c.792C>T p.V264V Substitution - coding silent 15:28274299-28274299 - TCGA-FP-A4BE-01 COSM1129252 c.11818C>T p.R3940* Substitution - Nonsense 15:28141629-28141629 - TCGA-D1-A103-01 COSM4874872 c.10866C>T p.D3622D Substitution - coding silent 15:28152711-28152711 - TCGA-B9-5156-01 COSM4908283 c.6047T>G p.V2016G Substitution - Missense 15:28215784-28215784 - CN-AML-CR-25-Dx COSM5021826 c.912-7C>T p.? Unknown 15:28272393-28272393 - 2492729 COSM5729569 c.12994C>T p.P4332S Substitution - Missense 15:28124231-28124231 - TCGA-AP-A0LM-01 COSM960247 c.3226G>A p.D1076N Substitution - Missense 15:28248561-28248561 - OSCC-GB_00970111 COSM4889621 c.13882G>A p.A4628T Substitution - Missense 15:28114643-28114643 - TCGA-D3-A3MR-06 COSM4897932 c.2972A>G p.D991G Substitution - Missense 15:28254418-28254418 - TCGA-KK-A59V-01 COSM4878521 c.11816+1G>T p.? Unknown 15:28141730-28141730 - PTC_456 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - 132 COSM3732919 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - TCGA-39-5037-01 COSM700259 c.3615G>A p.E1205E Substitution - coding silent 15:28238735-28238735 - 587220 COSM1209573 c.14417C>T p.A4806V Substitution - Missense 15:28111851-28111851 - TCGA-HU-A4H8-01 COSM4053816 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - LUAD-U6SJ7 COSM400167 c.10980C>T p.G3660G Substitution - coding silent 15:28146265-28146265 - CRC-21T COSM5479427 c.3236-7C>T p.? Unknown 15:28246904-28246904 - T2417 COSM4690108 c.2018C>T p.T673M Substitution - Missense 15:28263022-28263022 - PDA_013 COSM4998686 c.5447C>T p.T1816M Substitution - Missense 15:28228235-28228235 - UM-SCC-47 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-D1-A103-01 COSM960095 c.14082C>T p.I4694I Substitution - coding silent 15:28113221-28113221 - TCGA-B5-A11E-01 COSM960155 c.10893G>T p.K3631N Substitution - Missense 15:28152684-28152684 - OVCAR-8 COSM1678320 c.1292T>A p.I431K Substitution - Missense 15:28269402-28269402 - TCGA-KK-A59V-01 COSM4878520 c.11816+1G>T p.? Unknown 15:28141730-28141730 - TCGA-AX-A0J0-01 COSM4867400 c.3862G>T p.E1288* Substitution - Nonsense 15:28237104-28237104 - TCGA-D1-A15X-01 COSM4871932 c.10163A>T p.D3388V Substitution - Missense 15:28169550-28169550 - YUKAT COSM5383110 c.10901-1G>A p.? Unknown 15:28146345-28146345 - S02322 COSM5691242 c.5418C>G p.L1806L Substitution - coding silent 15:28228264-28228264 - S02360 COSM5696018 c.4788C>G p.P1596P Substitution - coding silent 15:28230388-28230388 - PT13 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - CSCC-40-T COSM4543406 c.3375G>A p.V1125V Substitution - coding silent 15:28246758-28246758 - PTC_221 COSM5960163 c.12310_12311delGC p.A4104fs*25 Deletion - Frameshift 15:28132750-28132751 - YURAY COSM5383118 c.423G>A p.K141K Substitution - coding silent 15:28280187-28280187 - TCGA-D3-A51T-06 COSM4905493 c.9303C>T p.I3101I Substitution - coding silent 15:28177079-28177079 - 7285 COSM5614202 c.6930A>T p.Q2310H Substitution - Missense 15:28211141-28211141 - HCC58 COSM1608218 c.9436A>G p.K3146E Substitution - Missense 15:28176765-28176765 - BN45T COSM1608216 c.13705A>G p.I4569V Substitution - Missense 15:28115446-28115446 - TCGA-EE-A2MI-06 COSM3500283 c.10193C>T p.S3398L Substitution - Missense 15:28169520-28169520 - UM-SCC-2 COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - PTC_428 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - 228 COSM4426076 c.10730G>A p.G3577E Substitution - Missense 15:28163110-28163110 - TCGA-D3-A1Q9-06 COSM3500300 c.4002C>T p.A1334A Substitution - coding silent 15:28236964-28236964 - TCGA-A8-A06U-01 COSM4814278 c.9566G>A p.G3189E Substitution - Missense 15:28176548-28176548 - T3174 COSM4690057 c.12293C>A p.A4098D Substitution - Missense 15:28132768-28132768 - CHC1061T COSM4799612 c.3602G>T p.C1201F Substitution - Missense 15:28238748-28238748 - 40M COSM4053816 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - P5 COSM5009798 c.12613G>A p.G4205R Substitution - Missense 15:28130552-28130552 - T3021 COSM4690111 c.1414G>A p.V472M Substitution - Missense 15:28269280-28269280 - TCGA-G9-6342-01 COSM3672011 c.7019G>T p.R2340L Substitution - Missense 15:28211052-28211052 - TCGA-A8-A09Z-01 COSM4815011 c.7123C>T p.Q2375* Substitution - Nonsense 15:28206329-28206329 - B70-Tumor COSM1749090 c.13716C>T p.L4572L Substitution - coding silent 15:28115435-28115435 - 2492706 COSM5716757 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - UD-SCC-2 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - YULETA COSM261276 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - TCGA-AY-6197-01 COSM1372235 c.11973C>A p.I3991I Substitution - coding silent 15:28141474-28141474 - TCGA-CG-5721-01 COSM4053859 c.5201A>G p.K1734R Substitution - Missense 15:28229266-28229266 - 2521244 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-B5-A0JY-01 COSM4782472 c.2908G>T p.E970* Substitution - Nonsense 15:28254482-28254482 - C0007T COSM4909237 c.8311C>G p.H2771D Substitution - Missense 15:28192101-28192101 - S00832 COSM5660821 c.6309C>T p.F2103F Substitution - coding silent 15:28214704-28214704 - PDA_035 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - PD4261a COSM5800769 c.8165A>G p.K2722R Substitution - Missense 15:28196310-28196310 - TCGA-BS-A0V7-01 COSM4865663 c.2700C>T p.T900T Substitution - coding silent 15:28256135-28256135 - TCGA-AP-A051-01 COSM960193 c.7650G>A p.T2550T Substitution - coding silent 15:28201522-28201522 - PTC_456 COSM3732919 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - TCGA-G2-A3VY-01 COSM4811484 c.12412G>C p.E4138Q Substitution - Missense 15:28132258-28132258 - TCGA-CD-8529-01 COSM4053808 c.14177G>A p.R4726Q Substitution - Missense 15:28113126-28113126 - TCGA-FG-5962-01 COSM1372236 c.11378A>G p.N3793S Substitution - Missense 15:28143913-28143913 - PT36 COSM5916428 c.812G>A p.G271E Substitution - Missense 15:28272993-28272993 - D15 COSM5006645 c.14200G>A p.A4734T Substitution - Missense 15:28113103-28113103 - 8035567 COSM3386819 c.8582T>C p.I2861T Substitution - Missense 15:28191032-28191032 - 113368 COSM325488 c.6433G>A p.E2145K Substitution - Missense 15:28214198-28214198 - TCGA-EE-A29M-06 COSM261276 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - PTC-10C COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - 523LT COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - HT115 COSM4638181 c.14275T>C p.S4759P Substitution - Missense 15:28111993-28111993 - TCGA-18-3421-01 COSM4859905 c.12877C>A p.R4293R Substitution - coding silent 15:28125119-28125119 - TCGA-60-2711-01 COSM4860801 c.9633G>T p.E3211D Substitution - Missense 15:28176481-28176481 - U2940 COSM4897447 c.6728C>T p.T2243I Substitution - Missense 15:28213800-28213800 - TCGA-DD-A1EA-01 COSM4920156 c.7644C>G p.S2548R Substitution - Missense 15:28201528-28201528 - 2492713 COSM5718994 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - CHC1040T COSM4799598 c.9027G>T p.V3009V Substitution - coding silent 15:28179023-28179023 - P60 COSM5008477 c.9210G>A p.S3070S Substitution - coding silent 15:28177463-28177463 - tumor_4120193 COSM3927502 c.1680C>G p.S560R Substitution - Missense 15:28265893-28265893 - LUAD-B02515 COSM336043 c.8327G>T p.G2776V Substitution - Missense 15:28192085-28192085 - ORL-48 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - WA53 COSM237496 c.10058-3T>A p.? Unknown 15:28169658-28169658 - CSCC-46-T COSM4520203 c.10482G>T p.R3494R Substitution - coding silent 15:28167759-28167759 - TCGA-ER-A19H-06 COSM3500277 c.11162A>G p.D3721G Substitution - Missense 15:28144214-28144214 - TCGA-EE-A182-06 COSM4891819 c.7571C>T p.S2524F Substitution - Missense 15:28202159-28202159 - pfg213T COSM4751793 c.6377G>A p.R2126H Substitution - Missense 15:28214254-28214254 - CSCC-30-T COSM4492160 c.3925C>T p.L1309L Substitution - coding silent 15:28237041-28237041 - TCGA-AX-A0J1-01 COSM960209 c.6284G>A p.C2095Y Substitution - Missense 15:28214729-28214729 - TCGA-D1-A16F-01 COSM249302 c.3176G>A p.R1059H Substitution - Missense 15:28248611-28248611 - HN_00190 COSM123573 c.10592C>A p.P3531H Substitution - Missense 15:28163248-28163248 - TCGA-AP-A051-01 COSM960243 c.3391+1G>A p.? Unknown 15:28246741-28246741 - CRC-19T COSM5481227 c.6727A>G p.T2243A Substitution - Missense 15:28213801-28213801 - ESO-077 COSM1254120 c.14077G>A p.G4693S Substitution - Missense 15:28113226-28113226 - TCGA-BP-4760-01 COSM1493407 c.12612C>T p.C4204C Substitution - coding silent 15:28130553-28130553 - WSU-HN30 COSM4600673 c.7316C>A p.A2439D Substitution - Missense 15:28202511-28202511 - TCGA-EE-A29M-06 COSM4897447 c.6728C>T p.T2243I Substitution - Missense 15:28213800-28213800 - PD8621a COSM5789248 c.6456G>A p.T2152T Substitution - coding silent 15:28214175-28214175 - ZZUFHECRKL-G057T COSM5445515 c.10130G>A p.R3377H Substitution - Missense 15:28169583-28169583 - CSCC-32-T COSM4457869 c.10637C>T p.T3546I Substitution - Missense 15:28163203-28163203 - 2521262 COSM5892259 c.13728T>A p.D4576E Substitution - Missense 15:28114797-28114797 - TCGA-HF-7133-01 COSM4053854 c.6428C>T p.A2143V Substitution - Missense 15:28214203-28214203 - UM-SCC-11B COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - 2492705 COSM5716815 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - PD13771a COSM2083312 c.10414-6G>T p.? Unknown 15:28167833-28167833 - TCGA-F1-6874-01 COSM4507532 c.7491C>A p.A2497A Substitution - coding silent 15:28202239-28202239 - PT23_2 COSM4906108 c.10421C>T p.S3474F Substitution - Missense 15:28167820-28167820 - TCGA-CG-5726-01 COSM4053847 c.7637C>T p.T2546M Substitution - Missense 15:28201535-28201535 - CN-AML-26-T COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-AA-3966-01 COSM272769 c.13478T>G p.L4493R Substitution - Missense 15:28116796-28116796 - ME001T COSM221809 c.7058C>G p.T2353S Substitution - Missense 15:28211013-28211013 - UM-SCC-11B COSM3732920 c.815C>T p.T272M Substitution - Missense 15:28272990-28272990 - TCGA-HU-8602-01 COSM4053874 c.851A>G p.Q284R Substitution - Missense 15:28272954-28272954 - PTC-50C COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - S02294 COSM5688733 c.11619G>T p.W3873C Substitution - Missense 15:28142319-28142319 - PD6722a COSM5800586 c.12634C>G p.L4212V Substitution - Missense 15:28130531-28130531 - TCGA-BP-4983-01 COSM470474 c.2604G>A p.T868T Substitution - coding silent 15:28256231-28256231 - WSU-HN13 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - PTC_386 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - BCB109T COSM4798761 c.10179A>G p.K3393K Substitution - coding silent 15:28169534-28169534 - TCGA-CU-A0YN-01 COSM416526 c.9519G>T p.L3173F Substitution - Missense 15:28176595-28176595 - T3262 COSM4690065 c.10324A>G p.M3442V Substitution - Missense 15:28168496-28168496 - HCC2998 COSM1678318 c.8461C>T p.R2821C Substitution - Missense 15:28191235-28191235 - Gp5D COSM4627310 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - T3202 COSM4690093 c.5393G>A p.G1798D Substitution - Missense 15:28228289-28228289 - HCT15 COSM2083352 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - Pat_14_A COSM5848941 c.12514G>T p.G4172W Substitution - Missense 15:28132156-28132156 - TCGA-EI-6507-01 COSM4945947 c.1083C>T p.H361H Substitution - coding silent 15:28272215-28272215 - XHDG27 COSM4769237 c.12172G>A p.G4058R Substitution - Missense 15:28135536-28135536 - T207 COSM4690107 c.2080G>T p.E694* Substitution - Nonsense 15:28262960-28262960 - SCC-15 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - HN_00190 COSM123574 c.3368A>G p.Y1123C Substitution - Missense 15:28246765-28246765 - IGROV-1 COSM1678316 c.9379G>A p.E3127K Substitution - Missense 15:28177003-28177003 - SCC-15 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - T3262 COSM4690064 c.10324A>G p.M3442V Substitution - Missense 15:28168496-28168496 - TCGA-G3-A25Z-01 COSM4922226 c.5829C>A p.D1943E Substitution - Missense 15:28220468-28220468 - TCGA-AZ-6598-01 COSM4784697 c.1074C>T p.G358G Substitution - coding silent 15:28272224-28272224 - P134 COSM5010110 c.14019+2T>C p.? Unknown 15:28113571-28113571 - HCC2998 COSM1678312 c.12125T>C p.V4042A Substitution - Missense 15:28135583-28135583 - T368 COSM4690100 c.5103T>C p.P1701P Substitution - coding silent 15:28229477-28229477 - WSU-HN8 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-F5-6814-01 COSM960256 c.2908G>T p.E970* Substitution - Nonsense 15:28254482-28254482 - TCGA-34-5234-01 COSM700256 c.3241G>C p.E1081Q Substitution - Missense 15:28246892-28246892 - TCGA-EE-A2MR-06 COSM4904151 c.12617C>T p.S4206F Substitution - Missense 15:28130548-28130548 - 13394 COSM700246 c.846C>A p.P282P Substitution - coding silent 15:28272959-28272959 - TCGA-AD-6889-01 COSM4786695 c.7848C>T p.G2616G Substitution - coding silent 15:28198638-28198638 - BK0097 COSM4188965 c.3689G>A p.G1230E Substitution - Missense 15:28238661-28238661 - P134 COSM5010112 c.10958A>G p.D3653G Substitution - Missense 15:28146287-28146287 - TCGA-EE-A2GO-06 COSM4892008 c.2733C>T p.L911L Substitution - coding silent 15:28256102-28256102 - 134417 COSM320799 c.1750G>A p.G584S Substitution - Missense 15:28265823-28265823 - TCGA-BS-A0V7-01 COSM960258 c.2700C>T p.T900T Substitution - coding silent 15:28256135-28256135 - 509LT COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - PD4970a COSM1178342 c.146G>T p.G49V Substitution - Missense 15:28299443-28299443 - pfg212T COSM1372273 c.541delA p.S181fs*85 Deletion - Frameshift 15:28280069-28280069 - TCGA-AO-A12E-01 COSM3815795 c.4498C>T p.R1500C Substitution - Missense 15:28233323-28233323 - BHY COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-A8-A0AB-01 COSM4815412 c.9480T>C p.S3160S Substitution - coding silent 15:28176721-28176721 - S02397 COSM5699101 c.2306G>T p.G769V Substitution - Missense 15:28260787-28260787 - SCC-15 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-AA-3972-01 COSM297294 c.6989G>A p.R2330Q Substitution - Missense 15:28211082-28211082 - TCGA-EE-A3AD-06 COSM4872986 c.2419C>T p.R807W Substitution - Missense 15:28257159-28257159 - PET124T COSM5825399 c.12757G>A p.A4253T Substitution - Missense 15:28130208-28130208 - TCGA-BR-4184-01 COSM4907243 c.13193C>T p.A4398V Substitution - Missense 15:28121425-28121425 - CSCC-40-T COSM4543407 c.3375G>A p.V1125V Substitution - coding silent 15:28246758-28246758 - YUOTHO COSM5383114 c.741C>T p.S247S Substitution - coding silent 15:28274350-28274350 - 2492713 COSM5718993 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - TCGA-A6-6781-01 COSM1372252 c.8000G>A p.G2667E Substitution - Missense 15:28198389-28198389 - PT40 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - CN-AML-CR-31-Dx COSM4148581 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - TCGA-24-1469-01 COSM4947118 c.6486C>T p.L2162L Substitution - coding silent 15:28214145-28214145 - HN_62338 COSM123575 c.2488G>T p.V830L Substitution - Missense 15:28257090-28257090 - SCC-25 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-18-3421-01 COSM700283 c.12877C>A p.R4293R Substitution - coding silent 15:28125119-28125119 - PTC-14C COSM2149154 c.2683T>G p.S895A Substitution - Missense 15:28256152-28256152 - CSCC-27-T COSM4473466 c.1851C>T p.T617T Substitution - coding silent 15:28265637-28265637 - TCGA-ER-A198-06 COSM4892114 c.179C>T p.P60L Substitution - Missense 15:28299410-28299410 - sysucc-783T COSM5483906 c.6487A>G p.I2163V Substitution - Missense 15:28214144-28214144 - TCGA-BR-8680-01 COSM4053826 c.10699G>A p.D3567N Substitution - Missense 15:28163141-28163141 - CN-AML-CR-26-Dx COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - ATL030 COSM5705835 c.794T>A p.V265E Substitution - Missense 15:28274297-28274297 - TCGA-22-4599-01 COSM700273 c.10975G>A p.D3659N Substitution - Missense 15:28146270-28146270 - 07-P1079 COSM4578148 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - SM-4B296 COSM4411602 c.12402G>A p.P4134P Substitution - coding silent 15:28132659-28132659 - UM-SCC-11B COSM4597963 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - HCT-15 COSM1678314 c.11312G>T p.R3771I Substitution - Missense 15:28143979-28143979 - TCGA-BR-8680-01 COSM4907129 c.10699G>A p.D3567N Substitution - Missense 15:28163141-28163141 - 587352 COSM1209575 c.13901C>T p.A4634V Substitution - Missense 15:28114624-28114624 - YUOTHO COSM5383113 c.741C>T p.S247S Substitution - coding silent 15:28274350-28274350 - Detroit_562 COSM4594917 c.9852C>T p.N3284N Substitution - coding silent 15:28174600-28174600 - BICR_22 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - LUAD-S01345 COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-18-3409-01 COSM700249 c.1907A>T p.K636I Substitution - Missense 15:28263133-28263133 - TCGA-EE-A3JD-06 COSM4396029 c.12264G>T p.L4088L Substitution - coding silent 15:28132797-28132797 - PT34 COSM5021826 c.912-7C>T p.? Unknown 15:28272393-28272393 - WSU-HN8 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - UD-SCC-2 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AP-A059-01 COSM960195 c.7442C>A p.S2481Y Substitution - Missense 15:28202385-28202385 - K216 COSM249302 c.3176G>A p.R1059H Substitution - Missense 15:28248611-28248611 - TCGA-FP-A4BE-01 COSM4876248 c.11818C>T p.R3940* Substitution - Nonsense 15:28141629-28141629 - C135 COSM4617572 c.9487G>A p.A3163T Substitution - Missense 15:28176714-28176714 - J38_T COSM3956500 c.13620G>T p.L4540L Substitution - coding silent 15:28115531-28115531 - TCGA-AX-A0J0-01 COSM960137 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - YURUS COSM1707960 c.9650C>T p.S3217F Substitution - Missense 15:28176464-28176464 - CSCC-5-T COSM4457518 c.10491C>T p.I3497I Substitution - coding silent 15:28167750-28167750 - AML_14y_08_DX COSM4386169 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-FG-5962-01 COSM3969050 c.6149C>T p.T2050M Substitution - Missense 15:28215682-28215682 - 226 COSM3730078 c.10032A>G p.R3344R Substitution - coding silent 15:28174420-28174420 - TCGA-CG-4465-01 COSM4053857 c.5370C>T p.L1790L Substitution - coding silent 15:28228312-28228312 - Br15X COSM39725 c.10152C>T p.L3384L Substitution - coding silent 15:28169561-28169561 - 587226 COSM1209572 c.2237G>A p.R746H Substitution - Missense 15:28260856-28260856 - YUDAB COSM1707959 c.12967A>C p.S4323R Substitution - Missense 15:28125029-28125029 - TCGA-BR-8368-01 COSM4053839 c.8425T>G p.W2809G Substitution - Missense 15:28191987-28191987 - CHEWS025 COSM4578146 c.3629T>C p.I1210T Substitution - Missense 15:28238721-28238721 - TCGA-24-1469-01 COSM81260 c.6486C>T p.L2162L Substitution - coding silent 15:28214145-28214145 - PCA17-1 COSM4053866 c.2694G>A p.L898L Substitution - coding silent 15:28256141-28256141 - CLL115 COSM1290364 c.11148A>T p.K3716N Substitution - Missense 15:28144228-28144228 - TCGA-BR-4201-01 COSM960093 c.14305C>T p.P4769S Substitution - Missense 15:28111963-28111963 - S00539 COSM317456 c.11866G>T p.G3956* Substitution - Nonsense 15:28141581-28141581 - TCGA-CM-6162-01 COSM4949185 c.10805C>T p.S3602L Substitution - Missense 15:28152772-28152772 - T26 COSM5618271 c.7654A>C p.K2552Q Substitution - Missense 15:28201518-28201518 - TCGA-AA-3713-01 COSM1372256 c.6035C>A p.P2012Q Substitution - Missense 15:28215796-28215796 - TCGA-FS-A1ZW-06 COSM4893580 c.10945G>A p.E3649K Substitution - Missense 15:28146300-28146300 - sysucc-1640T COSM289694 c.816G>A p.T272T Substitution - coding silent 15:28272989-28272989 - WSU-HN13 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - Pat_31_B COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-G2-A2EO-01 COSM1301010 c.8375C>T p.S2792L Substitution - Missense 15:28192037-28192037 - LUAD-NYU184 COSM370764 c.7885+1G>C p.? Unknown 15:28198600-28198600 - TCGA-CJ-5682-01 COSM470473 c.3028C>G p.Q1010E Substitution - Missense 15:28254362-28254362 - TCGA-CG-5726-01 COSM4053843 c.7864T>A p.Y2622N Substitution - Missense 15:28198622-28198622 - OSCC-GB_00970111 COSM4889620 c.13882G>A p.A4628T Substitution - Missense 15:28114643-28114643 - TCGA-BP-4176-01 COSM3361307 c.10140T>C p.L3380L Substitution - coding silent 15:28169573-28169573 - EW8 COSM2083520 c.2743G>T p.A915S Substitution - Missense 15:28256092-28256092 - 18 COSM4746854 c.541delA p.S181fs*85 Deletion - Frameshift 15:28280069-28280069 - TCGA-D5-6924-01 COSM3690351 c.9440T>A p.V3147D Substitution - Missense 15:28176761-28176761 - PTC_455 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-BP-4176-01 COSM3361306 c.10150C>G p.L3384V Substitution - Missense 15:28169563-28169563 - CRC-27T COSM5468728 c.10032A>G p.R3344R Substitution - coding silent 15:28174420-28174420 - TCGA-66-2782-01 COSM4861898 c.2864A>G p.E955G Substitution - Missense 15:28255879-28255879 - LUAD-D01603 COSM337410 c.5371A>T p.S1791C Substitution - Missense 15:28228311-28228311 - TCGA-AP-A0LM-01 COSM960231 c.4565C>A p.P1522H Substitution - Missense 15:28233256-28233256 - STC246 COSM5054231 c.558C>T p.G186G Substitution - coding silent 15:28274990-28274990 - ESO-081 COSM1243308 c.10951C>T p.R3651C Substitution - Missense 15:28146294-28146294 - DN12015 COSM1478013 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - tumor_4146289 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-34-5927-01 COSM4858622 c.5776C>T p.L1926F Substitution - Missense 15:28220521-28220521 - TCGA-BS-A0UJ-01 COSM960097 c.13728T>C p.D4576D Substitution - coding silent 15:28114797-28114797 - TCGA-AP-A0LM-01 COSM4872986 c.2419C>T p.R807W Substitution - Missense 15:28257159-28257159 - TCGA-AX-A0J1-01 COSM4867701 c.2496G>A p.T832T Substitution - coding silent 15:28257082-28257082 - TCGA-B5-A11E-01 COSM4870587 c.13152C>T p.F4384F Substitution - coding silent 15:28124073-28124073 - PCA17-1 COSM4907615 c.2694G>A p.L898L Substitution - coding silent 15:28256141-28256141 - T2225 COSM4690083 c.8120C>T p.T2707M Substitution - Missense 15:28196461-28196461 - Sample_1 COSM4594492 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - TCGA-AG-A002-01 COSM261277 c.6165C>T p.V2055V Substitution - coding silent 15:28215666-28215666 - SJRHB011 COSM4776301 c.645C>T p.G215G Substitution - coding silent 15:28274446-28274446 - tumor_4191799 COSM3927501 c.14232+6C>T p.? Unknown 15:28113065-28113065 - 8068563 COSM4388137 c.758T>G p.V253G Substitution - Missense 15:28274333-28274333 - UPCI:SCC090 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-AG-A002-01 COSM289692 c.5851G>A p.E1951K Substitution - Missense 15:28218666-28218666 - TCGA-A2-A0CP-01 COSM5832860 c.11125_11128delATCA p.I3709fs*24 Deletion - Frameshift 15:28144685-28144688 - P5 COSM5009799 c.12613G>A p.G4205R Substitution - Missense 15:28130552-28130552 - S0059 COSM5882553 c.1483A>C p.I495L Substitution - Missense 15:28268580-28268580 - CSCC-16-T COSM4465459 c.13850C>T p.S4617F Substitution - Missense 15:28114675-28114675 - I2L-P7-Tumor-Organoid COSM5363164 c.8117T>C p.V2706A Substitution - Missense 15:28196464-28196464 - WSU-HN30 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-CG-5717-01 COSM4906786 c.9508G>A p.D3170N Substitution - Missense 15:28176693-28176693 - 18 COSM1372273 c.541delA p.S181fs*85 Deletion - Frameshift 15:28280069-28280069 - PCSI_0218_Pa_P_526 COSM3786499 c.11157C>G p.L3719L Substitution - coding silent 15:28144219-28144219 - CN-AML-CR-28-Dx COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - PTC_33 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - B86-Tumor COSM4908937 c.3904C>G p.L1302V Substitution - Missense 15:28237062-28237062 - 35M COSM5581305 c.13384C>T p.P4462S Substitution - Missense 15:28117043-28117043 - 2492705 COSM5716756 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - BN42 COSM1608221 c.239A>G p.E80G Substitution - Missense 15:28292971-28292971 - TCGA-EE-A2GI-06 COSM3500286 c.9036G>A p.K3012K Substitution - coding silent 15:28179014-28179014 - ESO-1059 COSM1254123 c.6385C>T p.R2129C Substitution - Missense 15:28214246-28214246 - UPCI:SCC090 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-06-0166 COSM2150173 c.6184T>C p.F2062L Substitution - Missense 15:28215647-28215647 - TCGA-B5-A0K8-01 COSM960268 c.2172delG p.T725fs*23 Deletion - Frameshift 15:28260921-28260921 - MB54 COSM2157582 c.9080G>A p.G3027D Substitution - Missense 15:28178970-28178970 - TCGA-AP-A0LM-01 COSM960105 c.13448G>T p.S4483I Substitution - Missense 15:28116826-28116826 - CSCC-35-T COSM4560445 c.8446G>A p.G2816R Substitution - Missense 15:28191966-28191966 - 587338 COSM1209586 c.13297G>A p.G4433R Substitution - Missense 15:28117130-28117130 - S01170 COSM5667048 c.14072A>G p.Y4691C Substitution - Missense 15:28113231-28113231 - PT46 COSM5929581 c.1138C>T p.P380S Substitution - Missense 15:28270814-28270814 - TCGA-CZ-4857-01 COSM3361333 c.13206A>C p.K4402N Substitution - Missense 15:28121412-28121412 - TCGA-FU-A3HZ-01 COSM4840138 c.8639A>G p.D2880G Substitution - Missense 15:28190975-28190975 - TCGA-FU-A3HZ-01 COSM4840139 c.8639A>G p.D2880G Substitution - Missense 15:28190975-28190975 - ESCC_BICR_061T COSM5430743 c.1442C>T p.T481M Substitution - Missense 15:28269252-28269252 - TCGA-32-4208-01 COSM4782134 c.4910G>T p.S1637I Substitution - Missense 15:28229747-28229747 - pfg019T COSM1640199 c.13507G>A p.V4503M Substitution - Missense 15:28116767-28116767 - TCGA-G9-6348-01 COSM4876248 c.11818C>T p.R3940* Substitution - Nonsense 15:28141629-28141629 - BICR_22 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - CHC884T COSM4958367 c.11403G>C p.G3801G Substitution - coding silent 15:28143888-28143888 - TCGA-06-0166-01 COSM4782054 c.6184T>C p.F2062L Substitution - Missense 15:28215647-28215647 - pfg127T COSM4751795 c.3098G>A p.R1033Q Substitution - Missense 15:28248689-28248689 - TCGA-AX-A0J0-01 COSM4867491 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - NCI-H1770 COSM23121 c.2420G>A p.R807Q Substitution - Missense 15:28257158-28257158 - TCGA-A8-A09Z-01 COSM3815794 c.7123C>T p.Q2375* Substitution - Nonsense 15:28206329-28206329 - TCGA-FP-A4BE-01 COSM4907186 c.13896G>A p.R4632R Substitution - coding silent 15:28114629-28114629 - C086 COSM5532291 c.11460T>C p.L3820L Substitution - coding silent 15:28142911-28142911 - HCC116T COSM5807110 c.2995G>A p.E999K Substitution - Missense 15:28254395-28254395 - TCGA-BR-4370-01 COSM4053869 c.1827G>A p.A609A Substitution - coding silent 15:28265661-28265661 - HN_00190 COSM123572 c.10700A>T p.D3567V Substitution - Missense 15:28163140-28163140 - TCGA-E2-A56Z-01 COSM3815797 c.2702C>T p.A901V Substitution - Missense 15:28256133-28256133 - D8 COSM5007566 c.14092G>A p.A4698T Substitution - Missense 15:28113211-28113211 - ESCC_150 COSM5644968 c.8106delT p.H2703fs*48 Deletion - Frameshift 15:28196475-28196475 - TCGA-AA-3966-01 COSM297185 c.900_901delAG p.G301fs*24 Deletion - Frameshift 15:28272904-28272905 - TCGA-EE-A2A1-06 COSM4905633 c.7907C>T p.S2636F Substitution - Missense 15:28198482-28198482 - 2492712 COSM5718993 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - 13394 COSM4859378 c.846C>A p.P282P Substitution - coding silent 15:28272959-28272959 - PTC-7C COSM4594608 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - Gp2D COSM4627310 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - Gp2D COSM2083560 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - TCGA-AP-A059-01 COSM4866834 c.12230G>T p.S4077I Substitution - Missense 15:28135478-28135478 - LUAD-CHTN-3090346 COSM356784 c.2975T>G p.L992R Substitution - Missense 15:28254415-28254415 - TCGA-B5-A11E-01 COSM4870325 c.9956C>T p.S3319F Substitution - Missense 15:28174496-28174496 - TCGA-GM-A2D9-01 COSM3815793 c.8197G>A p.E2733K Substitution - Missense 15:28196278-28196278 - TCGA-CD-A4MG-01 COSM4053825 c.10711G>A p.A3571T Substitution - Missense 15:28163129-28163129 - CCK81 COSM4620689 c.13306G>A p.G4436S Substitution - Missense 15:28117121-28117121 - TCGA-D1-A15X-01 COSM4871893 c.1944A>G p.P648P Substitution - coding silent 15:28263096-28263096 - TCGA-22-4599-01 COSM4859480 c.10975G>A p.D3659N Substitution - Missense 15:28146270-28146270 - TCGA-BR-4361-01 COSM4907803 c.11999T>C p.V4000A Substitution - Missense 15:28141448-28141448 - PT46 COSM5929579 c.10628C>G p.A3543G Substitution - Missense 15:28163212-28163212 - TCGA-D1-A103-01 COSM4874890 c.14082C>T p.I4694I Substitution - coding silent 15:28113221-28113221 - ZZUFHECRKL-G060T COSM5438415 c.5255C>T p.A1752V Substitution - Missense 15:28229212-28229212 - CSCC-30-T COSM4492159 c.3925C>T p.L1309L Substitution - coding silent 15:28237041-28237041 - SCC-25 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - CN-AML-CR-62-Dx COSM4594492 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - T3202 COSM4690094 c.5376G>A p.M1792I Substitution - Missense 15:28228306-28228306 - S00833 COSM317457 c.278G>T p.R93M Substitution - Missense 15:28292932-28292932 - TCGA-AP-A0LM-01 COSM960109 c.13312G>A p.D4438N Substitution - Missense 15:28117115-28117115 - TCGA-A6-5665-01 COSM1372249 c.8376G>A p.S2792S Substitution - coding silent 15:28192036-28192036 - 1115157 COSM5548534 c.3791C>A p.A1264D Substitution - Missense 15:28238175-28238175 - TCGA-BR-8589-01 COSM4053861 c.4670A>G p.K1557R Substitution - Missense 15:28233151-28233151 - TCGA-ER-A19N-06 COSM3500298 c.4964G>A p.R1655K Substitution - Missense 15:28229693-28229693 - TCGA-56-1622-01 COSM700264 c.6650T>A p.L2217Q Substitution - Missense 15:28213878-28213878 - BHY COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - RKO COSM4647801 c.14311T>C p.Y4771H Substitution - Missense 15:28111957-28111957 - TCGA-B5-A11E-01 COSM4870378 c.5022A>G p.T1674T Substitution - coding silent 15:28229558-28229558 - TCGA-A1-A0SI-01 COSM4813859 c.5230C>T p.R1744* Substitution - Nonsense 15:28229237-28229237 - TCGA-13-0800-01 COSM4787320 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - TCGA-AN-A046-01 COSM4814321 c.10639C>T p.R3547C Substitution - Missense 15:28163201-28163201 - PTC-88C COSM3999484 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - UD-SCC-2 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-F5-6814-01 COSM700284 c.13948C>T p.R4650W Substitution - Missense 15:28113644-28113644 - 585270 COSM320800 c.861C>A p.H287Q Substitution - Missense 15:28272944-28272944 - TCGA-37-5819-01 COSM700257 c.3354C>T p.F1118F Substitution - coding silent 15:28246779-28246779 - HCC116T COSM5807109 c.2995G>A p.E999K Substitution - Missense 15:28254395-28254395 - S00836 COSM317458 c.6178G>C p.A2060P Substitution - Missense 15:28215653-28215653 - TCGA-AA-3492-01 COSM1372245 c.9858C>T p.H3286H Substitution - coding silent 15:28174594-28174594 - CHC1040T COSM349016 c.9027G>T p.V3009V Substitution - coding silent 15:28179023-28179023 - BN45 COSM1608216 c.13705A>G p.I4569V Substitution - Missense 15:28115446-28115446 - TCGA-D8-A1JJ-01 COSM1478016 c.1252C>T p.H418Y Substitution - Missense 15:28270700-28270700 - TCGA-EE-A2M7-06 COSM3500275 c.11899G>C p.G3967R Substitution - Missense 15:28141548-28141548 - NOKSI COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - TCGA-ER-A19H-06 COSM4892127 c.11162A>G p.D3721G Substitution - Missense 15:28144214-28144214 - TCGA-HU-A4H8-01 COSM4907750 c.4625G>A p.R1542H Substitution - Missense 15:28233196-28233196 - CRC-31T COSM5457824 c.1870+5G>A p.? Unknown 15:28265613-28265613 - TCGA-EW-A1J5-01 COSM1478010 c.13070C>G p.S4357C Substitution - Missense 15:28124155-28124155 - PD4109a COSM4810410 c.3140G>C p.R1047T Substitution - Missense 15:28248647-28248647 - PT35 COSM5913674 c.7990C>T p.Q2664* Substitution - Nonsense 15:28198399-28198399 - PTC_415 COSM3732919 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - PT41 COSM5924638 c.12863C>T p.A4288V Substitution - Missense 15:28125133-28125133 - MOLT-4 COSM1678313 c.11854G>T p.G3952* Substitution - Nonsense 15:28141593-28141593 - TCGA-BS-A0UJ-01 COSM4871356 c.2927C>T p.A976V Substitution - Missense 15:28254463-28254463 - TCGA-EE-A2GI-06 COSM3500273 c.12875C>T p.P4292L Substitution - Missense 15:28125121-28125121 - T1154 COSM4690105 c.2573G>A p.G858D Substitution - Missense 15:28256262-28256262 - TCGA-IR-A3LA-01 COSM4844991 c.11538C>T p.F3846F Substitution - coding silent 15:28142833-28142833 - CSCC-16-T COSM4525835 c.13582G>A p.V4528M Substitution - Missense 15:28116692-28116692 - P46 COSM4785206 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - S00935 COSM5663057 c.6906G>T p.S2302S Substitution - coding silent 15:28212464-28212464 - WSU-HN8 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - CN-AML-CR-5-Dx COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - AML_14y_10_DX COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-AX-A0J0-01 COSM4464461 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - CHC891T COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - PTC-10C COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - CPCG0040-F1 COSM307015 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - pfg317T COSM4053814 c.13201C>T p.R4401W Substitution - Missense 15:28121417-28121417 - TCGA-D9-A149-06 COSM4897218 c.11734A>C p.S3912R Substitution - Missense 15:28141813-28141813 - P134 COSM5010113 c.10958A>G p.D3653G Substitution - Missense 15:28146287-28146287 - CPCG0246-F1 COSM4880279 c.5099T>C p.I1700T Substitution - Missense 15:28229481-28229481 - T55 COSM4690051 c.14019+1G>A p.? Unknown 15:28113572-28113572 - S02375 COSM5702383 c.7617_7617+1GG>AT p.? Unknown 15:28202112-28202113 - TCGA-B0-5083-01 COSM1493406 c.11749G>T p.V3917F Substitution - Missense 15:28141798-28141798 - PD4261a COSM5800768 c.8165A>G p.K2722R Substitution - Missense 15:28196310-28196310 - TCGA-EE-A3AF-06 COSM3500299 c.4283C>T p.P1428L Substitution - Missense 15:28233732-28233732 - TCGA-AA-3966-01 COSM272770 c.4282C>T p.P1428S Substitution - Missense 15:28233733-28233733 - TCGA-09-2051-01 COSM117401 c.5173C>T p.R1725W Substitution - Missense 15:28229294-28229294 - CRC-27T COSM3730078 c.10032A>G p.R3344R Substitution - coding silent 15:28174420-28174420 - TCGA-FG-5962-01 COSM4908709 c.6149C>T p.T2050M Substitution - Missense 15:28215682-28215682 - HCC102T COSM1608219 c.8898G>C p.L2966L Substitution - coding silent 15:28182440-28182440 - CRC-27T COSM1478013 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - J83_T COSM3956505 c.7660C>G p.R2554G Substitution - Missense 15:28201512-28201512 - CSCC-40-T COSM4493183 c.410C>T p.A137V Substitution - Missense 15:28280200-28280200 - CHC891T COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - RK138_C01 COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-CG-4465-01 COSM4907030 c.5370C>T p.L1790L Substitution - coding silent 15:28228312-28228312 - pfg212T COSM4746854 c.541delA p.S181fs*85 Deletion - Frameshift 15:28280069-28280069 - D-09 COSM4766640 c.5162C>T p.P1721L Substitution - Missense 15:28229305-28229305 - P04-1421 COSM244893 c.1205G>A p.R402H Substitution - Missense 15:28270747-28270747 - TCGA-G2-A2EK-01 COSM4811211 c.5509C>G p.Q1837E Substitution - Missense 15:28222171-28222171 - TCGA-AN-A046-01 COSM3815790 c.10118C>A p.S3373Y Substitution - Missense 15:28169595-28169595 - I2L-P25-Tumor-Organoid COSM5363035 c.5163G>A p.P1721P Substitution - coding silent 15:28229304-28229304 - DN12015 COSM4594666 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - TCGA-CA-6718-01 COSM1372243 c.10371C>T p.I3457I Substitution - coding silent 15:28168449-28168449 - PD4970a COSM5768565 c.145G>T p.G49* Substitution - Nonsense 15:28299444-28299444 - ESCC_133 COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - V-PH-16T COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - T3021 COSM4690078 c.9292delA p.T3098fs*43 Deletion - Frameshift 15:28177090-28177090 - sysucc-311T COSM5478838 c.10150C>A p.L3384I Substitution - Missense 15:28169563-28169563 - PT27 COSM5905989 c.7440G>T p.K2480N Substitution - Missense 15:28202387-28202387 - 1N50-VS-1T50 COSM4976531 c.2237G>A p.R746H Substitution - Missense 15:28260856-28260856 - PTC_455 COSM5957984 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - Gp5D COSM4627311 c.728A>G p.E243G Substitution - Missense 15:28274363-28274363 - CHC892T COSM4961417 c.12554G>A p.C4185Y Substitution - Missense 15:28132116-28132116 - TCGA-AX-A05Z-01 COSM4863594 c.5321G>A p.G1774E Substitution - Missense 15:28228361-28228361 - TCGA-AA-3492-01 COSM1372262 c.2450C>T p.A817V Substitution - Missense 15:28257128-28257128 - TCGA-GN-A26A-06 COSM4895046 c.2447C>T p.S816F Substitution - Missense 15:28257131-28257131 - TCGA-A5-A0GW-01 COSM960139 c.11542A>G p.K3848E Substitution - Missense 15:28142829-28142829 - TCGA-D8-A27G-01 COSM4814068 c.1069G>A p.E357K Substitution - Missense 15:28272229-28272229 - RK282_C01 COSM4964013 c.7871A>G p.H2624R Substitution - Missense 15:28198615-28198615 - TCGA-GN-A26C-01 COSM3500288 c.8944G>A p.V2982I Substitution - Missense 15:28179217-28179217 - STC252 COSM5054222 c.11305A>G p.S3769G Substitution - Missense 15:28143986-28143986 - TCGA-BR-A4QL-01 COSM2083365 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - 5202_PT COSM2083556 c.958G>A p.G320R Substitution - Missense 15:28272340-28272340 - pfg054T COSM4751770 c.13946T>C p.V4649A Substitution - Missense 15:28113646-28113646 - T3225 COSM4690088 c.6459G>A p.L2153L Substitution - coding silent 15:28214172-28214172 - TCGA-G3-A3CK-01 COSM4899091 c.4002C>T p.A1334A Substitution - coding silent 15:28236964-28236964 - ESCC_127 COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - CHC884T COSM4958368 c.11403G>C p.G3801G Substitution - coding silent 15:28143888-28143888 - TCGA-D1-A103-01 COSM4875053 c.12712C>A p.R4238R Substitution - coding silent 15:28130253-28130253 - PT40 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - UM-SCC-4 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - I2L-P7-Tumor-Organoid COSM4690068 c.9969G>A p.A3323A Substitution - coding silent 15:28174483-28174483 - P134 COSM5010116 c.6122G>A p.G2041D Substitution - Missense 15:28215709-28215709 - CSCC-20-T COSM4509415 c.8064C>T p.H2688H Substitution - coding silent 15:28196517-28196517 - DLD1 COSM2083352 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - TCGA-AA-3713-01 COSM4786641 c.6035C>A p.P2012Q Substitution - Missense 15:28215796-28215796 - TCGA-EE-A29V-06 COSM4904036 c.263C>T p.P88L Substitution - Missense 15:28292947-28292947 - TCGA-GV-A40G-01 COSM3794053 c.6975C>T p.I2325I Substitution - coding silent 15:28211096-28211096 - 2492704 COSM5716818 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - TCGA-AK-3458-01 COSM470476 c.1139C>T p.P380L Substitution - Missense 15:28270813-28270813 - sysucc-311T COSM1209592 c.10150C>A p.L3384I Substitution - Missense 15:28169563-28169563 - TCGA-HU-A4G8-01 COSM4053851 c.7458C>T p.S2486S Substitution - coding silent 15:28202369-28202369 - EGC3 COSM4623070 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - TCGA-EE-A3JD-06 COSM4396364 c.10454C>T p.T3485I Substitution - Missense 15:28167787-28167787 - sysucc-783T COSM5483907 c.6487A>G p.I2163V Substitution - Missense 15:28214144-28214144 - TCGA-EE-A29M-06 COSM4897453 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - TCGA-CG-4442-01 COSM4907618 c.5825C>T p.S1942L Substitution - Missense 15:28220472-28220472 - TCGA-BR-8680-01 COSM4907336 c.6653G>A p.R2218H Substitution - Missense 15:28213875-28213875 - TCGA-06-0166-01 COSM2150173 c.6184T>C p.F2062L Substitution - Missense 15:28215647-28215647 - TCGA-AX-A0J0-01 COSM4867395 c.5077T>C p.F1693L Substitution - Missense 15:28229503-28229503 - LS411 COSM4646496 c.1570G>A p.G524S Substitution - Missense 15:28268493-28268493 - CRC-19T COSM5481226 c.9018A>C p.A3006A Substitution - coding silent 15:28179143-28179143 - LUAD-CHTN-MAD08-00104 COSM361158 c.12388G>T p.D4130Y Substitution - Missense 15:28132673-28132673 - TCGA-FR-A3YN-06 COSM4898922 c.9561G>A p.R3187R Substitution - coding silent 15:28176553-28176553 - TCGA-DB-A64X-01 COSM4908897 c.3332C>T p.A1111V Substitution - Missense 15:28246801-28246801 - EGC15 COSM960197 c.7351C>T p.R2451C Substitution - Missense 15:28202476-28202476 - 8034048 COSM3386822 c.1574G>T p.G525V Substitution - Missense 15:28268489-28268489 - WSU-HN13 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - CAL27 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AP-A056-01 COSM960201 c.6676G>A p.D2226N Substitution - Missense 15:28213852-28213852 - TCGA-CI-6624-01 COSM1562988 c.9366C>T p.T3122T Substitution - coding silent 15:28177016-28177016 - HCC58T COSM4781469 c.9436A>G p.K3146E Substitution - Missense 15:28176765-28176765 - TCGA-22-1012-01 COSM4860009 c.13948C>T p.R4650W Substitution - Missense 15:28113644-28113644 - T20 COSM5065045 c.5656G>A p.G1886R Substitution - Missense 15:28220641-28220641 - 0060_CRUK_PC_0060_T1_DNA COSM5420686 c.4898C>T p.S1633F Substitution - Missense 15:28229759-28229759 - PD3945a COSM2083554 c.988G>A p.A330T Substitution - Missense 15:28272310-28272310 - 2011-2311:2012-362-T COSM4604313 c.13834G>A p.D4612N Substitution - Missense 15:28114691-28114691 - K48-Tumor COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - T3503 COSM4690103 c.3356C>T p.A1119V Substitution - Missense 15:28246777-28246777 - P30 COSM2083341 c.9375C>T p.L3125L Substitution - coding silent 15:28177007-28177007 - Pat_32_A COSM5848957 c.445C>T p.R149C Substitution - Missense 15:28280165-28280165 - TCGA-AP-A059-01 COSM960183 c.8462G>A p.R2821H Substitution - Missense 15:28191234-28191234 - TCGA-AU-6004-01 COSM1372236 c.11378A>G p.N3793S Substitution - Missense 15:28143913-28143913 - sysucc-1163T COSM5458492 c.11609A>C p.K3870T Substitution - Missense 15:28142329-28142329 - TCGA-GC-A3YS-01 COSM4812712 c.7003C>A p.H2335N Substitution - Missense 15:28211068-28211068 - TCGA-AD-6964-01 COSM1372264 c.2084A>T p.E695V Substitution - Missense 15:28262956-28262956 - 93VU147T COSM4590647 c.14082C>G p.I4694M Substitution - Missense 15:28113221-28113221 - TCGA-EJ-5510-01 COSM1129248 c.6452G>A p.R2151H Substitution - Missense 15:28214179-28214179 - TCGA-56-6545-01 COSM4863076 c.10023G>C p.Q3341H Substitution - Missense 15:28174429-28174429 - LUAD-D00147 COSM362762 c.3749C>T p.A1250V Substitution - Missense 15:28238217-28238217 - LC_S11 COSM1188940 c.2198G>T p.W733L Substitution - Missense 15:28260895-28260895 - pfg127T COSM4751794 c.3098G>A p.R1033Q Substitution - Missense 15:28248689-28248689 - CN-AML-CR-30-Dx COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - TCGA-EW-A1J5-01 COSM4813523 c.10993G>A p.V3665I Substitution - Missense 15:28146252-28146252 - PD9004a COSM4813523 c.10993G>A p.V3665I Substitution - Missense 15:28146252-28146252 - TCGA-CG-4442-01 COSM4907626 c.7511A>T p.D2504V Substitution - Missense 15:28202219-28202219 - P100 COSM5009257 c.8469G>T p.E2823D Substitution - Missense 15:28191227-28191227 - ESO-805 COSM1254133 c.3397C>T p.L1133F Substitution - Missense 15:28246061-28246061 - TCGA-CJ-5680-01 COSM4858182 c.5351G>T p.R1784L Substitution - Missense 15:28228331-28228331 - T3446 COSM4690091 c.6365C>T p.T2122M Substitution - Missense 15:28214266-28214266 - TCGA-D8-A27G-01 COSM3815798 c.1069G>A p.E357K Substitution - Missense 15:28272229-28272229 - 3_RESISTANT COSM1723574 c.8948C>T p.P2983L Substitution - Missense 15:28179213-28179213 - Au9 COSM4905499 c.14166C>T p.F4722F Substitution - coding silent 15:28113137-28113137 - LUAD-S01302 COSM395565 c.5233A>T p.N1745Y Substitution - Missense 15:28229234-28229234 - 64 COSM5742628 c.14015C>T p.T4672M Substitution - Missense 15:28113577-28113577 - TCGA-51-4081-01 COSM700282 c.12289G>A p.A4097T Substitution - Missense 15:28132772-28132772 - UD-SCC-2 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - P134 COSM5010111 c.14019+2T>C p.? Unknown 15:28113571-28113571 - TCGA-AX-A063-01 COSM960167 c.9943G>A p.A3315T Substitution - Missense 15:28174509-28174509 - CG-3609 COSM2157534 c.11572G>A p.E3858K Substitution - Missense 15:28142366-28142366 - sysucc-1038T COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - PTC-28C COSM4148583 c.6685G>C p.G2229R Substitution - Missense 15:28213843-28213843 - CSCC-20-T COSM4554197 c.6150G>A p.T2050T Substitution - coding silent 15:28215681-28215681 - CSCC-27-T COSM4473465 c.1851C>T p.T617T Substitution - coding silent 15:28265637-28265637 - TCGA-GN-A267-06 COSM4897881 c.13115C>T p.S4372L Substitution - Missense 15:28124110-28124110 - C086 COSM5167607 c.7361C>T p.S2454L Substitution - Missense 15:28202466-28202466 - PCSI_0007_Pa_P COSM5420169 c.10963C>T p.L3655F Substitution - Missense 15:28146282-28146282 - TCGA-AP-A051-01 COSM960123 c.12787T>C p.C4263R Substitution - Missense 15:28130178-28130178 - 169 COSM3729612 c.6837G>A p.M2279I Substitution - Missense 15:28212533-28212533 - TCGA-FW-A3R5-06 COSM3886808 c.8567C>T p.S2856F Substitution - Missense 15:28191047-28191047 - sysucc-311T COSM5478836 c.12567G>T p.M4189I Substitution - Missense 15:28132103-28132103 - PDA_049 COSM5000650 c.4014G>T p.Q1338H Substitution - Missense 15:28234274-28234274 - EGC3 COSM2083352 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - sysucc-880T COSM5462439 c.7724T>C p.M2575T Substitution - Missense 15:28198762-28198762 - TCGA-AD-6964-01 COSM1372242 c.10540A>G p.T3514A Substitution - Missense 15:28167701-28167701 - HCT116 COSM4632086 c.9431T>C p.M3144T Substitution - Missense 15:28176951-28176951 - TCGA-CD-8529-01 COSM4053873 c.1207C>G p.L403V Substitution - Missense 15:28270745-28270745 - PT26 COSM5905306 c.8653C>T p.H2885Y Substitution - Missense 15:28186749-28186749 - TCGA-G4-6588-01 COSM4783509 c.6976C>A p.L2326M Substitution - Missense 15:28211095-28211095 - S00501 COSM221809 c.7058C>G p.T2353S Substitution - Missense 15:28211013-28211013 - P46 COSM3754256 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - Gp2D COSM4627307 c.1971G>A p.L657L Substitution - coding silent 15:28263069-28263069 - CHC1209T COSM4804674 c.11938G>T p.E3980* Substitution - Nonsense 15:28141509-28141509 - TCGA-28-5218-01 COSM4781888 c.11261C>T p.A3754V Substitution - Missense 15:28144115-28144115 - S02295 COSM5689105 c.5116A>G p.I1706V Substitution - Missense 15:28229464-28229464 - TCGA-BR-4361-01 COSM4053813 c.13226T>C p.V4409A Substitution - Missense 15:28121392-28121392 - TCGA-BR-4201-01 COSM4873402 c.14305C>T p.P4769S Substitution - Missense 15:28111963-28111963 - CPCG0040-F1 COSM4880110 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - TCGA-28-5218-01 COSM433663 c.11261C>T p.A3754V Substitution - Missense 15:28144115-28144115 - TCGA-RP-A693-06 COSM3886808 c.8567C>T p.S2856F Substitution - Missense 15:28191047-28191047 - TCGA-CD-A4MG-01 COSM4907609 c.11169C>T p.C3723C Substitution - coding silent 15:28144207-28144207 - TCGA-BR-6452-01 COSM4053819 c.12085A>G p.T4029A Substitution - Missense 15:28135623-28135623 - TCGA-EE-A2M7-06 COSM4904074 c.11899G>C p.G3967R Substitution - Missense 15:28141548-28141548 - STC252 COSM5054223 c.11305A>G p.S3769G Substitution - Missense 15:28143986-28143986 - CSCC-29-T COSM4530194 c.1675G>C p.G559R Substitution - Missense 15:28265898-28265898 - HCC058T COSM5805181 c.11553A>T p.V3851V Substitution - coding silent 15:28142385-28142385 - SS6003323 COSM1290365 c.4654C>T p.R1552* Substitution - Nonsense 15:28233167-28233167 - PT47 COSM5070859 c.9832-8G>A p.? Unknown 15:28174628-28174628 - TCGA-BR-4201-01 COSM4053814 c.13201C>T p.R4401W Substitution - Missense 15:28121417-28121417 - CN-AML-CR-17-Dx COSM3999484 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - sysucc-1640T COSM3732919 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - CSCC-5-T COSM4457519 c.10491C>T p.I3497I Substitution - coding silent 15:28167750-28167750 - CHC1714T COSM4148581 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - CHC1714T COSM4148581 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - TCGA-E2-A574-01 COSM3815792 c.8462G>C p.R2821P Substitution - Missense 15:28191234-28191234 - TCGA-CZ-4857-01 COSM4857607 c.13206A>C p.K4402N Substitution - Missense 15:28121412-28121412 - HN_00076 COSM123576 c.790G>A p.V264I Substitution - Missense 15:28274301-28274301 - TCGA-66-2789-01 COSM700260 c.4297G>T p.V1433L Substitution - Missense 15:28233718-28233718 - TC71 COSM4578134 c.13975G>A p.V4659I Substitution - Missense 15:28113617-28113617 - TCGA-FS-A1Z3-06 COSM3500281 c.10421C>T p.S3474F Substitution - Missense 15:28167820-28167820 - P129 COSM3754256 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - TCGA-GV-A3JW-01 COSM4810615 c.6785C>T p.P2262L Substitution - Missense 15:28213743-28213743 - TCGA-A6-6781-01 COSM4948752 c.12523G>A p.G4175S Substitution - Missense 15:28132147-28132147 - PT19_1 COSM5899676 c.9020-8C>T p.? Unknown 15:28179038-28179038 - P9 COSM5008477 c.9210G>A p.S3070S Substitution - coding silent 15:28177463-28177463 - ICGC_MB45 COSM307015 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - TARGET-30-PAPVFD COSM1285356 c.13567G>C p.A4523P Substitution - Missense 15:28116707-28116707 - CSCC-16-T COSM4490980 c.3725C>T p.S1242L Substitution - Missense 15:28238625-28238625 - PT13 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - 93VU147T COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - CHC884T COSM4958367 c.11403G>C p.G3801G Substitution - coding silent 15:28143888-28143888 - BD152T COSM5507023 c.13781A>G p.E4594G Substitution - Missense 15:28114744-28114744 - TCGA-CK-5913-01 COSM4783896 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - 699_T COSM3956502 c.12077C>G p.S4026C Substitution - Missense 15:28135631-28135631 - TCGA-EE-A3AF-06 COSM4898059 c.4283C>T p.P1428L Substitution - Missense 15:28233732-28233732 - CRC-03T COSM5451344 c.13638C>T p.T4546T Substitution - coding silent 15:28115513-28115513 - HT115 COSM4638182 c.8508C>T p.I2836I Substitution - coding silent 15:28191188-28191188 - T3724 COSM4690098 c.5211T>C p.A1737A Substitution - coding silent 15:28229256-28229256 - TCGA-EE-A3AA-06 COSM4904241 c.5002C>T p.R1668C Substitution - Missense 15:28229578-28229578 - 132 COSM3732920 c.815C>T p.T272M Substitution - Missense 15:28272990-28272990 - CN-AML-CR-5-Dx COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - AOCS-141-3-2 COSM4422326 c.6579C>T p.P2193P Substitution - coding silent 15:28213949-28213949 - TCGA-AP-A056-01 COSM4868818 c.6676G>A p.D2226N Substitution - Missense 15:28213852-28213852 - BD230T COSM5496743 c.1572C>T p.G524G Substitution - coding silent 15:28268491-28268491 - 2492712 COSM5718994 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - 2521259 COSM5890850 c.11816+3T>G p.? Unknown 15:28141728-28141728 - CHC1040T COSM4799598 c.9027G>T p.V3009V Substitution - coding silent 15:28179023-28179023 - SCC-9 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-BR-8487-01 COSM4053811 c.13566G>A p.P4522P Substitution - coding silent 15:28116708-28116708 - ZZUFHECRKL-G057T COSM5445514 c.10130G>A p.R3377H Substitution - Missense 15:28169583-28169583 - CSCC-46-T COSM4520204 c.10482G>T p.R3494R Substitution - coding silent 15:28167759-28167759 - TCGA-C5-A1ML-01 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - SC_9032 COSM5551133 c.1047C>T p.C349C Substitution - coding silent 15:28272251-28272251 - TCGA-18-3409-01 COSM700278 c.11991C>T p.L3997L Substitution - coding silent 15:28141456-28141456 - TCGA-HU-A4G8-01 COSM4907667 c.7458C>T p.S2486S Substitution - coding silent 15:28202369-28202369 - 08-P1004 COSM4578138 c.8097A>G p.V2699V Substitution - coding silent 15:28196484-28196484 - TCGA-BR-4361-01 COSM4907811 c.7480+2T>C p.? Unknown 15:28202345-28202345 - I2L-P19Tb-Tumor-Biopsy COSM5362973 c.9859G>A p.G3287S Substitution - Missense 15:28174593-28174593 - UPCI:SCC090 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-A5-A0GB-01 COSM960145 c.11343G>A p.L3781L Substitution - coding silent 15:28143948-28143948 - TCGA-D3-A2JP-06 COSM1180454 c.9209C>T p.S3070L Substitution - Missense 15:28177464-28177464 - TCGA-DD-A11A-01 COSM4940479 c.6910A>T p.K2304* Substitution - Nonsense 15:28212460-28212460 - PCSI_0105_Pa_P_526 COSM4962173 c.12601A>T p.K4201* Substitution - Nonsense 15:28130564-28130564 - SJOS016_D COSM5023145 c.3662A>T p.D1221V Substitution - Missense 15:28238688-28238688 - S02065 COSM5672618 c.11077A>G p.S3693G Substitution - Missense 15:28144736-28144736 - Pat_32_A COSM5848958 c.445C>T p.R149C Substitution - Missense 15:28280165-28280165 - PT19_1 COSM5899677 c.9020-8C>T p.? Unknown 15:28179038-28179038 - NCHP_DIPG103 COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-AX-A0J0-01 COSM960227 c.5077T>C p.F1693L Substitution - Missense 15:28229503-28229503 - PT24_1 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - PD13299a COSM5794889 c.2366C>T p.P789L Substitution - Missense 15:28257212-28257212 - TCGA-FS-A1ZW-06 COSM3500278 c.10945G>A p.E3649K Substitution - Missense 15:28146300-28146300 - T3202 COSM4690092 c.5393G>A p.G1798D Substitution - Missense 15:28228289-28228289 - TCGA-D1-A176-01 COSM960171 c.9222T>C p.G3074G Substitution - coding silent 15:28177451-28177451 - Gp5D COSM2083560 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - TCGA-AA-3510-01 COSM4785868 c.12444C>T p.I4148I Substitution - coding silent 15:28132226-28132226 - PD8621a COSM5789249 c.6456G>A p.T2152T Substitution - coding silent 15:28214175-28214175 - TCGA-G3-A5SK-01 COSM4927475 c.9604C>G p.L3202V Substitution - Missense 15:28176510-28176510 - LUAD-NYU284 COSM372786 c.4964G>T p.R1655I Substitution - Missense 15:28229693-28229693 - S00516 COSM4387048 c.8842G>T p.A2948S Substitution - Missense 15:28182496-28182496 - TCGA-EE-A181-06 COSM3500296 c.5355C>T p.F1785F Substitution - coding silent 15:28228327-28228327 - PD4876a COSM5778173 c.10592C>T p.P3531L Substitution - Missense 15:28163248-28163248 - Gp2D COSM2083252 c.13581C>T p.P4527P Substitution - coding silent 15:28116693-28116693 - 587228 COSM1209578 c.1184T>A p.V395D Substitution - Missense 15:28270768-28270768 - KYSE-150 COSM2083457 c.5281C>T p.P1761S Substitution - Missense 15:28228401-28228401 - PT25 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - KYSE-30 COSM4439665 c.7638G>A p.T2546T Substitution - coding silent 15:28201534-28201534 - TCGA-AX-A05Z-01 COSM4863788 c.10138C>T p.L3380F Substitution - Missense 15:28169575-28169575 - P100 COSM5009253 c.13080C>A p.F4360L Substitution - Missense 15:28124145-28124145 - Sample_1 COSM5021826 c.912-7C>T p.? Unknown 15:28272393-28272393 - I2L-P19Tb-Tumor-Organoid COSM5362940 c.10595A>G p.Q3532R Substitution - Missense 15:28163245-28163245 - 2492711 COSM5718994 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - PCSI_0624_Pa_P_526 COSM5761289 c.5553G>A p.T1851T Substitution - coding silent 15:28222127-28222127 - RK138_C01 COSM4780157 c.3578-3C>G p.? Unknown 15:28238775-28238775 - CHC892T COSM4961173 c.8922G>A p.G2974G Substitution - coding silent 15:28182416-28182416 - YUMUL COSM5383116 c.727G>A p.E243K Substitution - Missense 15:28274364-28274364 - TCGA-EE-A3JD-06 COSM4396891 c.12266G>A p.R4089K Substitution - Missense 15:28132795-28132795 - 8015299 COSM3769564 c.11163C>A p.D3721E Substitution - Missense 15:28144213-28144213 - HCT116 COSM1372246 c.9351C>T p.S3117S Substitution - coding silent 15:28177031-28177031 - TCGA-AG-A002-01 COSM289694 c.816G>A p.T272T Substitution - coding silent 15:28272989-28272989 - sysucc-311T COSM5478837 c.12567G>T p.M4189I Substitution - Missense 15:28132103-28132103 - TCGA-FC-A5OB-01 COSM3672009 c.13745G>A p.G4582E Substitution - Missense 15:28114780-28114780 - CHEWS017 COSM4578153 c.810C>T p.H270H Substitution - coding silent 15:28272995-28272995 - TCGA-ER-A193-06 COSM4905751 c.6864C>T p.N2288N Substitution - coding silent 15:28212506-28212506 - PD4876a COSM5778174 c.10592C>T p.P3531L Substitution - Missense 15:28163248-28163248 - TCGA-G2-A3VY-01 COSM3794051 c.12412G>C p.E4138Q Substitution - Missense 15:28132258-28132258 - 587342 COSM1209589 c.9292A>C p.T3098P Substitution - Missense 15:28177090-28177090 - 256528 COSM3725076 c.2773C>G p.P925A Substitution - Missense 15:28255970-28255970 - PTC-88C COSM4594608 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - 587376 COSM960137 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - RK138_C01 COSM1629491 c.3578-3C>G p.? Unknown 15:28238775-28238775 - LUAD-RT-S01721 COSM380388 c.6143G>T p.W2048L Substitution - Missense 15:28215688-28215688 - 304_T COSM3956510 c.1925G>T p.S642I Substitution - Missense 15:28263115-28263115 - C086 COSM5167608 c.7361C>T p.S2454L Substitution - Missense 15:28202466-28202466 - PTC_393 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-CC-A7IG-01 COSM4943119 c.12464C>T p.A4155V Substitution - Missense 15:28132206-28132206 - T3118 COSM4690097 c.5268G>A p.E1756E Substitution - coding silent 15:28229199-28229199 - SWE-55A COSM1180454 c.9209C>T p.S3070L Substitution - Missense 15:28177464-28177464 - TCGA-HU-A4GX-01 COSM4053812 c.13266C>T p.R4422R Substitution - coding silent 15:28121352-28121352 - TCGA-EE-A3AE-06 COSM3500308 c.2365C>T p.P789S Substitution - Missense 15:28257213-28257213 - P103 COSM5008662 c.8282G>A p.G2761D Substitution - Missense 15:28192130-28192130 - TCGA-18-3409-01 COSM700274 c.10992C>T p.I3664I Substitution - coding silent 15:28146253-28146253 - T3262 COSM4690068 c.9969G>A p.A3323A Substitution - coding silent 15:28174483-28174483 - PD8981a COSM4858182 c.5351G>T p.R1784L Substitution - Missense 15:28228331-28228331 - 587228 COSM1209577 c.5815G>A p.A1939T Substitution - Missense 15:28220482-28220482 - LFS_MB4 COSM74889 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - TCGA-AD-6964-01 COSM4948707 c.2084A>T p.E695V Substitution - Missense 15:28262956-28262956 - CRC-02T COSM5454331 c.1756+2T>C p.? Unknown 15:28265815-28265815 - TCGA-AG-A002-01 COSM289693 c.5647G>A p.D1883N Substitution - Missense 15:28222033-28222033 - TCGA-D1-A17Q-01 COSM960101 c.13543C>T p.R4515* Substitution - Nonsense 15:28116731-28116731 - TCGA-AM-5820-01 COSM4785206 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - TCGA-B9-5156-01 COSM3987889 c.6047T>G p.V2016G Substitution - Missense 15:28215784-28215784 - TCGA-D8-A1J8-01 COSM3815786 c.12721C>T p.R4241W Substitution - Missense 15:28130244-28130244 - TCGA-EE-A2MD-06 COSM4899293 c.8561G>C p.G2854A Substitution - Missense 15:28191053-28191053 - SNU-C1 COSM2083534 c.1702G>T p.A568S Substitution - Missense 15:28265871-28265871 - TCGA-AG-A002-01 COSM261276 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - TCGA-A5-A0GA-01 COSM960284 c.511G>T p.G171C Substitution - Missense 15:28280099-28280099 - WSU-HN8 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-18-3409-01 COSM4458767 c.10992C>T p.I3664I Substitution - coding silent 15:28146253-28146253 - CN-AML-CR-31-Dx COSM5427484 c.7593C>T p.D2531D Substitution - coding silent 15:28202137-28202137 - PT25 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - ESO-1059 COSM1254122 c.11701-1G>C p.? Unknown 15:28141847-28141847 - TCGA-AP-A051-01 COSM960286 c.509G>A p.S170N Substitution - Missense 15:28280101-28280101 - HCT116 COSM4632087 c.9351C>T p.S3117S Substitution - coding silent 15:28177031-28177031 - Detroit_562 COSM3999484 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - TCGA-EE-A3AD-06 COSM960264 c.2419C>T p.R807W Substitution - Missense 15:28257159-28257159 - WSU-HN30 COSM4600672 c.7316C>A p.A2439D Substitution - Missense 15:28202511-28202511 - BK0063 COSM4188425 c.692C>T p.A231V Substitution - Missense 15:28274399-28274399 - TCGA-D5-6924-01 COSM4783739 c.9440T>A p.V3147D Substitution - Missense 15:28176761-28176761 - MO_1012 COSM5561911 c.6714A>G p.P2238P Substitution - coding silent 15:28213814-28213814 - TCGA-D8-A1JJ-01 COSM4814769 c.1252C>T p.H418Y Substitution - Missense 15:28270700-28270700 - CN-AML-CR-30-Dx COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - TCGA-BS-A0UJ-01 COSM4871390 c.13728T>C p.D4576D Substitution - coding silent 15:28114797-28114797 - 1N50-VS-1T50 COSM1209572 c.2237G>A p.R746H Substitution - Missense 15:28260856-28260856 - NCI-H2126 COSM23119 c.10472C>T p.A3491V Substitution - Missense 15:28167769-28167769 - NCHP_DIPG105 COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-A1-A0SI-01 COSM4813858 c.10623G>A p.L3541L Substitution - coding silent 15:28163217-28163217 - TCGA-EE-A3JI-06 COSM4905725 c.708C>T p.P236P Substitution - coding silent 15:28274383-28274383 - CHC796T COSM4949603 c.1014G>C p.L338F Substitution - Missense 15:28272284-28272284 - P95 COSM4647805 c.8509G>A p.V2837I Substitution - Missense 15:28191187-28191187 - TCGA-24-0966-01 COSM74890 c.1648G>A p.G550R Substitution - Missense 15:28265925-28265925 - PDA_043 COSM5000334 c.9347C>T p.S3116F Substitution - Missense 15:28177035-28177035 - CSCC-20-T COSM4554196 c.6150G>A p.T2050T Substitution - coding silent 15:28215681-28215681 - PDA_034 COSM4999827 c.8535G>T p.M2845I Substitution - Missense 15:28191161-28191161 - TCGA-A5-A0VP-01 COSM960091 c.14424C>T p.D4808D Substitution - coding silent 15:28111844-28111844 - 3844_T COSM3956506 c.7122G>T p.P2374P Substitution - coding silent 15:28206330-28206330 - 19 COSM5747623 c.3202G>A p.G1068R Substitution - Missense 15:28248585-28248585 - Gp2D COSM4627305 c.13581C>T p.P4527P Substitution - coding silent 15:28116693-28116693 - TCGA-E9-A1RH-01 COSM1478014 c.4084G>C p.D1362H Substitution - Missense 15:28234204-28234204 - TCGA-32-4208-01 COSM3401661 c.4910G>T p.S1637I Substitution - Missense 15:28229747-28229747 - TCGA-EE-A182-06 COSM3500291 c.7571C>T p.S2524F Substitution - Missense 15:28202159-28202159 - TCGA-EE-A29M-06 COSM3500294 c.6728C>T p.T2243I Substitution - Missense 15:28213800-28213800 - TCGA-AX-A05Z-01 COSM960221 c.5321G>A p.G1774E Substitution - Missense 15:28228361-28228361 - 2492704 COSM5716757 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - 2492706 COSM5716818 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - 587278 COSM1209582 c.9788C>A p.A3263D Substitution - Missense 15:28175555-28175555 - CHC1714T COSM4600773 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - S0029 COSM4459088 c.11114C>T p.T3705I Substitution - Missense 15:28144699-28144699 - UM-SCC-4 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-BR-4201-01 COSM4751778 c.13201C>T p.R4401W Substitution - Missense 15:28121417-28121417 - TCGA-AP-A051-01 COSM4783282 c.4313G>A p.R1438H Substitution - Missense 15:28233702-28233702 - CLL069 COSM1290363 c.12360C>T p.Y4120Y Substitution - coding silent 15:28132701-28132701 - TCGA-61-2095-01 COSM118092 c.4308C>T p.V1436V Substitution - coding silent 15:28233707-28233707 - HCC2998 COSM4631596 c.8461C>T p.R2821C Substitution - Missense 15:28191235-28191235 - CAL33 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-A2-A0T5-01 COSM4814910 c.755A>G p.E252G Substitution - Missense 15:28274336-28274336 - PET124T COSM5825400 c.12757G>A p.A4253T Substitution - Missense 15:28130208-28130208 - 19 COSM5747621 c.12931G>C p.A4311P Substitution - Missense 15:28125065-28125065 - C086 COSM5532287 c.6842C>T p.S2281F Substitution - Missense 15:28212528-28212528 - TCGA-AP-A059-01 COSM4866666 c.8462G>A p.R2821H Substitution - Missense 15:28191234-28191234 - TCGA-BR-8487-01 COSM4053828 c.10447G>A p.A3483T Substitution - Missense 15:28167794-28167794 - BK0055 COSM74889 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - UM-SCC-4 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - ESCC_56 COSM5632159 c.1575A>G p.G525G Substitution - coding silent 15:28268488-28268488 - T3021 COSM4690073 c.9736C>T p.R3246W Substitution - Missense 15:28175607-28175607 - 587228 COSM1209575 c.13901C>T p.A4634V Substitution - Missense 15:28114624-28114624 - TCGA-MI-A75G-01 COSM4939957 c.9193G>T p.D3065Y Substitution - Missense 15:28177480-28177480 - HCC159T COSM3706504 c.10633G>T p.D3545Y Substitution - Missense 15:28163207-28163207 - TCGA-AP-A059-01 COSM4866339 c.6695C>A p.T2232N Substitution - Missense 15:28213833-28213833 - B86-Tumor COSM1516695 c.3904C>G p.L1302V Substitution - Missense 15:28237062-28237062 - PDA_035 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - AOCS-141-3-2 COSM4422328 c.6582C>T p.D2194D Substitution - coding silent 15:28213946-28213946 - TCGA-DD-A1EA-01 COSM4920155 c.7644C>G p.S2548R Substitution - Missense 15:28201528-28201528 - TCGA-DK-A1A7-01 COSM4812521 c.5466C>T p.G1822G Substitution - coding silent 15:28222214-28222214 - 2208 COSM5015270 c.13121A>G p.D4374G Substitution - Missense 15:28124104-28124104 - TCGA-21-1077-01 COSM4862597 c.2391G>A p.M797I Substitution - Missense 15:28257187-28257187 - STC273 COSM5054227 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - YULETA COSM4897453 c.9777C>T p.I3259I Substitution - coding silent 15:28175566-28175566 - SCC-25 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - 2492704 COSM5716815 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - CRC-19T COSM5481225 c.9018A>C p.A3006A Substitution - coding silent 15:28179143-28179143 - 228 COSM4426077 c.10730G>A p.G3577E Substitution - Missense 15:28163110-28163110 - I2L-P19Tb-Tumor-Organoid COSM5362941 c.10595A>G p.Q3532R Substitution - Missense 15:28163245-28163245 - CN-AML-CR-51-Dx COSM5427070 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - 8044424 COSM117401 c.5173C>T p.R1725W Substitution - Missense 15:28229294-28229294 - PD9573a COSM5785949 c.10323G>A p.A3441A Substitution - coding silent 15:28168497-28168497 - TCGA-B5-A11E-01 COSM960111 c.13228C>T p.R4410C Substitution - Missense 15:28121390-28121390 - 254891 COSM3724789 c.8858C>T p.S2953L Substitution - Missense 15:28182480-28182480 - C0035T COSM4150913 c.11658C>T p.A3886A Substitution - coding silent 15:28142280-28142280 - D-03 COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - WSU-HN30 COSM4600773 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - CSCC-32-T COSM4457870 c.10637C>T p.T3546I Substitution - Missense 15:28163203-28163203 - CHC892T COSM4794056 c.5327G>A p.S1776N Substitution - Missense 15:28228355-28228355 - VLTS-7 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - WSU-HN13 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-FW-A3R5-06 COSM3886815 c.2556C>T p.F852F Substitution - coding silent 15:28256279-28256279 - TCGA-AD-6889-01 COSM4948927 c.11038C>T p.L3680L Substitution - coding silent 15:28144775-28144775 - PT47 COSM5930323 c.8437G>A p.G2813R Substitution - Missense 15:28191975-28191975 - P134 COSM4907815 c.13226T>C p.V4409A Substitution - Missense 15:28121392-28121392 - TCGA-FU-A5XV-01 COSM4844216 c.9164-2A>G p.? Unknown 15:28177511-28177511 - TC71 COSM4578133 c.13975G>A p.V4659I Substitution - Missense 15:28113617-28113617 - BD217T COSM5495452 c.4393A>T p.I1465F Substitution - Missense 15:28233520-28233520 - S02299 COSM5690223 c.9068G>T p.R3023L Substitution - Missense 15:28178982-28178982 - S02375 COSM5702384 c.7617_7617+1GG>AT p.? Unknown 15:28202112-28202113 - T3724 COSM4690099 c.5211T>C p.A1737A Substitution - coding silent 15:28229256-28229256 - TCGA-BR-8591-01 COSM4053810 c.13589G>A p.S4530N Substitution - Missense 15:28116685-28116685 - WSU-HN8 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-A6-6781-01 COSM1372233 c.12523G>A p.G4175S Substitution - Missense 15:28132147-28132147 - TCGA-AX-A0IW-01 COSM960127 c.12507G>A p.W4169* Substitution - Nonsense 15:28132163-28132163 - PT35 COSM5913677 c.5708G>A p.W1903* Substitution - Nonsense 15:28220589-28220589 - BD230T COSM5496744 c.1572C>T p.G524G Substitution - coding silent 15:28268491-28268491 - TCGA-20-1685-01 COSM1323253 c.10173G>T p.L3391L Substitution - coding silent 15:28169540-28169540 - TCGA-BQ-5889-01 COSM3987890 c.1762A>T p.S588C Substitution - Missense 15:28265726-28265726 - CSCC-27-T COSM4511518 c.8713C>T p.H2905Y Substitution - Missense 15:28186689-28186689 - TCGA-F1-6874-01 COSM4053849 c.7491C>A p.A2497A Substitution - coding silent 15:28202239-28202239 - TCGA-AA-3814-01 COSM270763 c.1411C>T p.R471C Substitution - Missense 15:28269283-28269283 - NCI-ADR-RES COSM1678320 c.1292T>A p.I431K Substitution - Missense 15:28269402-28269402 - SNU-C4 COSM4053825 c.10711G>A p.A3571T Substitution - Missense 15:28163129-28163129 - BICR_22 COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - TCGA-06-5858-01 COSM4782074 c.9489G>A p.A3163A Substitution - coding silent 15:28176712-28176712 - Sample_1 COSM5021827 c.912-7C>T p.? Unknown 15:28272393-28272393 - S00539 COSM5658737 c.11866G>T p.G3956* Substitution - Nonsense 15:28141581-28141581 - TCGA-HU-A4GX-01 COSM4906334 c.13266C>T p.R4422R Substitution - coding silent 15:28121352-28121352 - TCGA-AP-A051-01 COSM4872785 c.6366G>A p.T2122T Substitution - coding silent 15:28214265-28214265 - S02294 COSM5688734 c.11619G>T p.W3873C Substitution - Missense 15:28142319-28142319 - TCGA-06-5858-01 COSM2083336 c.9489G>A p.A3163A Substitution - coding silent 15:28176712-28176712 - PR-03-1026 COSM244892 c.6719G>A p.G2240D Substitution - Missense 15:28213809-28213809 - TCGA-AD-6964-01 COSM4786452 c.10540A>G p.T3514A Substitution - Missense 15:28167701-28167701 - TCGA-AX-A0J0-01 COSM4867066 c.12196G>A p.A4066T Substitution - Missense 15:28135512-28135512 - TCGA-D1-A16N-01 COSM4876127 c.10740C>T p.Y3580Y Substitution - coding silent 15:28163100-28163100 - TCGA-24-0966-01 COSM4947079 c.1648G>A p.G550R Substitution - Missense 15:28265925-28265925 - TCGA-A8-A08L-01 COSM433668 c.4513G>T p.V1505F Substitution - Missense 15:28233308-28233308 - TCGA-DK-A2I6-01 COSM1301012 c.6114G>A p.Q2038Q Substitution - coding silent 15:28215717-28215717 - CSCC-41-T COSM4459088 c.11114C>T p.T3705I Substitution - Missense 15:28144699-28144699 - EW8 COSM4578143 c.5128C>G p.L1710V Substitution - Missense 15:28229339-28229339 - C658 COSM4443271 c.7999G>T p.G2667W Substitution - Missense 15:28198390-28198390 - TCGA-BP-4983-01 COSM4857404 c.2604G>A p.T868T Substitution - coding silent 15:28256231-28256231 - TCGA-56-1622-01 COSM4862346 c.6650T>A p.L2217Q Substitution - Missense 15:28213878-28213878 - TCGA-AP-A0LM-01 COSM4873548 c.13312G>A p.D4438N Substitution - Missense 15:28117115-28117115 - PARBRK COSM5005442 c.11757T>C p.H3919H Substitution - coding silent 15:28141790-28141790 - sysucc-880T COSM5462438 c.7724T>C p.M2575T Substitution - Missense 15:28198762-28198762 - TCGA-AZ-6598-01 COSM960280 c.1074C>T p.G358G Substitution - coding silent 15:28272224-28272224 - P108 COSM5009551 c.13937T>C p.V4646A Substitution - Missense 15:28113655-28113655 - Pat_41_A COSM5848943 c.12365G>A p.R4122Q Substitution - Missense 15:28132696-28132696 - UM-SCC-2 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-A5-A0GB-01 COSM960213 c.5954T>C p.M1985T Substitution - Missense 15:28218563-28218563 - sysucc-311T COSM960137 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - 06-P036 COSM4578139 c.6651G>A p.L2217L Substitution - coding silent 15:28213877-28213877 - I2L-P19Tb-Tumor-Biopsy COSM5362941 c.10595A>G p.Q3532R Substitution - Missense 15:28163245-28163245 - C086 COSM4907748 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - sysucc-834T COSM4578151 c.1229C>T p.P410L Substitution - Missense 15:28270723-28270723 - NOKSI COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - TCGA-AZ-4615-01 COSM3690350 c.11675C>T p.P3892L Substitution - Missense 15:28142263-28142263 - WSU-HN30 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - PT49 COSM5070859 c.9832-8G>A p.? Unknown 15:28174628-28174628 - TCGA-AA-3492-01 COSM4948814 c.2450C>T p.A817V Substitution - Missense 15:28257128-28257128 - TCGA-RP-A693-06 COSM4895360 c.8567C>T p.S2856F Substitution - Missense 15:28191047-28191047 - TCGA-34-5234-01 COSM4860242 c.3241G>C p.E1081Q Substitution - Missense 15:28246892-28246892 - SCC-25 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - PD4836a COSM5781430 c.8283C>G p.G2761G Substitution - coding silent 15:28192129-28192129 - TCGA-DM-A28C-01 COSM1372259 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - TCGA-B5-A11E-01 COSM960113 c.13152C>T p.F4384F Substitution - coding silent 15:28124073-28124073 - CSCC-62-T COSM4249882 c.11932C>T p.P3978S Substitution - Missense 15:28141515-28141515 - TCGA-BS-A0UJ-01 COSM960254 c.2927C>T p.A976V Substitution - Missense 15:28254463-28254463 - TCGA-D9-A4Z6-01 COSM3500301 c.3811C>T p.R1271W Substitution - Missense 15:28238155-28238155 - T3503 COSM4690112 c.477_478insT p.Q160fs*7 Insertion - Frameshift 15:28280132-28280133 - TCGA-DM-A1D8-01 COSM4784891 c.2955G>A p.R985R Substitution - coding silent 15:28254435-28254435 - TCGA-B5-A0JY-01 COSM4869410 c.1627G>A p.A543T Substitution - Missense 15:28265946-28265946 - CSCC-16-T COSM4525834 c.13582G>A p.V4528M Substitution - Missense 15:28116692-28116692 - BN13T COSM1608217 c.11765A>G p.H3922R Substitution - Missense 15:28141782-28141782 - SM-4B296 COSM4411601 c.12402G>A p.P4134P Substitution - coding silent 15:28132659-28132659 - TCGA-AK-3450-01 COSM3361334 c.9727G>C p.V3243L Substitution - Missense 15:28175616-28175616 - KYSE-150 COSM4439664 c.5281C>T p.P1761S Substitution - Missense 15:28228401-28228401 - CN-AML-CR-41-Dx COSM5427069 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - ESCC_BICR_064T COSM5437091 c.1250C>T p.S417F Substitution - Missense 15:28270702-28270702 - TCGA-33-4583-01 COSM4858574 c.11023G>C p.D3675H Substitution - Missense 15:28144790-28144790 - TCGA-A8-A06U-01 COSM433670 c.836G>T p.G279V Substitution - Missense 15:28272969-28272969 - CHEWS024 COSM4578136 c.8700C>T p.I2900I Substitution - coding silent 15:28186702-28186702 - PTC_456 COSM4597963 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - TCGA-13-0800-01 COSM74889 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - LC_S11 COSM1188939 c.2199G>T p.W733C Substitution - Missense 15:28260894-28260894 - TCGA-IR-A3LA-01 COSM4844990 c.11538C>T p.F3846F Substitution - coding silent 15:28142833-28142833 - TCGA-BR-4184-01 COSM4053815 c.13193C>T p.A4398V Substitution - Missense 15:28121425-28121425 - SCC-25 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - 7285 COSM5614203 c.6930A>T p.Q2310H Substitution - Missense 15:28211141-28211141 - UM-SCC-11B COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - 3_PRE-TREATMENT COSM1723574 c.8948C>T p.P2983L Substitution - Missense 15:28179213-28179213 - TCGA-D1-A17R-01 COSM960235 c.3949G>A p.A1317T Substitution - Missense 15:28237017-28237017 - TCGA-OL-A5RW-01 COSM3815796 c.2817G>A p.M939I Substitution - Missense 15:28255926-28255926 - CHEWS025 COSM4578147 c.3629T>C p.I1210T Substitution - Missense 15:28238721-28238721 - CSCC-35-T COSM4561614 c.8917G>A p.G2973S Substitution - Missense 15:28182421-28182421 - CHEWS035 COSM4578152 c.1229C>T p.P410L Substitution - Missense 15:28270723-28270723 - TCGA-AN-A046-01 COSM4814345 c.10118C>A p.S3373Y Substitution - Missense 15:28169595-28169595 - CHC892T COSM4961418 c.12554G>A p.C4185Y Substitution - Missense 15:28132116-28132116 - ESCC_150 COSM5644969 c.8106delT p.H2703fs*48 Deletion - Frameshift 15:28196475-28196475 - S02093 COSM5673111 c.3646G>C p.E1216Q Substitution - Missense 15:28238704-28238704 - UM-SCC-11B COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - BCB109T COSM4798761 c.10179A>G p.K3393K Substitution - coding silent 15:28169534-28169534 - TCGA-G4-6320-01 COSM3690352 c.6817C>A p.L2273M Substitution - Missense 15:28212553-28212553 - TCGA-CA-6717-01 COSM4783378 c.709G>A p.E237K Substitution - Missense 15:28274382-28274382 - 2293770 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-HU-A4GX-01 COSM4906353 c.9993G>A p.T3331T Substitution - coding silent 15:28174459-28174459 - 3206A7_017_T COSM5038930 c.1627G>T p.A543S Substitution - Missense 15:28265946-28265946 - TCGA-BR-4362-01 COSM4906585 c.10275G>A p.P3425P Substitution - coding silent 15:28168545-28168545 - TCGA-EE-A29D-06 COSM3500292 c.7464T>A p.N2488K Substitution - Missense 15:28202363-28202363 - P134 COSM5010117 c.6122G>A p.G2041D Substitution - Missense 15:28215709-28215709 - 0060_CRUK_PC_0060_T1_DNA COSM5420685 c.4898C>T p.S1633F Substitution - Missense 15:28229759-28229759 - HT115 COSM2083367 c.8368A>G p.N2790D Substitution - Missense 15:28192044-28192044 - TCGA-G4-6309-01 COSM4948084 c.10998C>T p.S3666S Substitution - coding silent 15:28146247-28146247 - TCGA-66-2782-01 COSM700252 c.2864A>G p.E955G Substitution - Missense 15:28255879-28255879 - TCGA-AA-3492-01 COSM1372257 c.5206T>C p.Y1736H Substitution - Missense 15:28229261-28229261 - J65_T COSM3956509 c.6324C>T p.L2108L Substitution - coding silent 15:28214689-28214689 - TCGA-CG-4306-01 COSM4907144 c.3975G>A p.P1325P Substitution - coding silent 15:28236991-28236991 - TCGA-18-3409-01 COSM4861113 c.10310C>T p.S3437F Substitution - Missense 15:28168510-28168510 - WSU-HN30 COSM4600674 c.7334C>G p.P2445R Substitution - Missense 15:28202493-28202493 - S02397 COSM5699102 c.2306G>T p.G769V Substitution - Missense 15:28260787-28260787 - 587356 COSM1209583 c.1881G>A p.W627* Substitution - Nonsense 15:28263159-28263159 - TCGA-F1-6177-01 COSM4053840 c.8270C>T p.A2757V Substitution - Missense 15:28192142-28192142 - TCGA-BR-4256-01 COSM4053836 c.9292A>G p.T3098A Substitution - Missense 15:28177090-28177090 - TCGA-FC-A5OB-01 COSM4878023 c.13745G>A p.G4582E Substitution - Missense 15:28114780-28114780 - LIM2405 COSM2083546 c.1384C>T p.R462C Substitution - Missense 15:28269310-28269310 - 2492706 COSM5716815 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - BRC50 COSM5027932 c.5340C>G p.I1780M Substitution - Missense 15:28228342-28228342 - TCGA-BR-4370-01 COSM4907855 c.1827G>A p.A609A Substitution - coding silent 15:28265661-28265661 - HX19T COSM4781314 c.239A>G p.E80G Substitution - Missense 15:28292971-28292971 - TCGA-A1-A0SI-01 COSM1478012 c.10623G>A p.L3541L Substitution - coding silent 15:28163217-28163217 - HN_62861 COSM123570 c.14392C>T p.R4798C Substitution - Missense 15:28111876-28111876 - TCGA-IR-A3LK-01 COSM459065 c.986C>T p.S329F Substitution - Missense 15:28272312-28272312 - TCGA-GV-A3JW-01 COSM1301011 c.6785C>T p.P2262L Substitution - Missense 15:28213743-28213743 - TCGA-CG-4305-01 COSM4053844 c.7836G>A p.Q2612Q Substitution - coding silent 15:28198650-28198650 - CSCC-27-T COSM4554010 c.6088G>T p.V2030L Substitution - Missense 15:28215743-28215743 - TCGA-BR-7703-01 COSM4906405 c.10723G>A p.G3575S Substitution - Missense 15:28163117-28163117 - EGC3 COSM5054225 c.8419C>A p.P2807T Substitution - Missense 15:28191993-28191993 - AOCS-141-3-2 COSM3981436 c.6582C>T p.D2194D Substitution - coding silent 15:28213946-28213946 - TCGA-BG-A18B-01 COSM4867701 c.2496G>A p.T832T Substitution - coding silent 15:28257082-28257082 - 8034048 COSM4945839 c.1574G>T p.G525V Substitution - Missense 15:28268489-28268489 - CN-AML-CR-56-Dx COSM5427069 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - SS6003317 COSM3983003 c.11193C>G p.D3731E Substitution - Missense 15:28144183-28144183 - TCGA-CM-4743-01 COSM4949054 c.8308T>C p.C2770R Substitution - Missense 15:28192104-28192104 - BD180T COSM5495160 c.9299G>T p.R3100L Substitution - Missense 15:28177083-28177083 - TCGA-CG-5717-01 COSM4053834 c.9508G>A p.D3170N Substitution - Missense 15:28176693-28176693 - pfg081T COSM4751797 c.2945A>G p.H982R Substitution - Missense 15:28254445-28254445 - CSCC-17-T COSM4507532 c.7491C>A p.A2497A Substitution - coding silent 15:28202239-28202239 - TCGA-EI-6917-01 COSM4782525 c.8783C>T p.S2928L Substitution - Missense 15:28186619-28186619 - LUAD-YINHD COSM349016 c.9027G>T p.V3009V Substitution - coding silent 15:28179023-28179023 - LUAD-NYU284 COSM372785 c.5467C>T p.P1823S Substitution - Missense 15:28222213-28222213 - TCGA-D1-A16N-01 COSM960159 c.10740C>T p.Y3580Y Substitution - coding silent 15:28163100-28163100 - PT23_2 COSM3500281 c.10421C>T p.S3474F Substitution - Missense 15:28167820-28167820 - CSCC-7-T COSM4535247 c.216G>T p.K72N Substitution - Missense 15:28292994-28292994 - T3118 COSM4690054 c.13369G>A p.D4457N Substitution - Missense 15:28117058-28117058 - TCGA-EE-A20F-06 COSM4891834 c.14157C>T p.F4719F Substitution - coding silent 15:28113146-28113146 - 8015299 COSM4781696 c.11163C>A p.D3721E Substitution - Missense 15:28144213-28144213 - HCC038T COSM5820434 c.1681A>G p.T561A Substitution - Missense 15:28265892-28265892 - CHC892T COSM4794055 c.5327G>A p.S1776N Substitution - Missense 15:28228355-28228355 - WSU-HN6 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - CPCG0211-F1 COSM4880643 c.599C>T p.A200V Substitution - Missense 15:28274949-28274949 - BD72T COSM5513076 c.13360T>C p.F4454L Substitution - Missense 15:28117067-28117067 - PT42 COSM5925826 c.8435C>T p.S2812L Substitution - Missense 15:28191977-28191977 - C086 COSM4905563 c.10296C>T p.S3432S Substitution - coding silent 15:28168524-28168524 - P100 COSM5009260 c.2510G>A p.R837Q Substitution - Missense 15:28257068-28257068 - TCGA-CG-5723-01 COSM4907913 c.10735G>A p.A3579T Substitution - Missense 15:28163105-28163105 - LIM2551 COSM4643881 c.12690C>T p.G4230G Substitution - coding silent 15:28130275-28130275 - TCGA-34-5927-01 COSM700261 c.5776C>T p.L1926F Substitution - Missense 15:28220521-28220521 - TCGA-FJ-A3ZF-01 COSM3794050 c.12710T>C p.V4237A Substitution - Missense 15:28130255-28130255 - UD-SCC-2 COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - T3090 COSM4690070 c.9835T>C p.Y3279H Substitution - Missense 15:28174617-28174617 - T2940 COSM4690074 c.9657G>A p.A3219A Substitution - coding silent 15:28176457-28176457 - TCGA-JX-A3Q0-01 COSM4824437 c.1731C>T p.R577R Substitution - coding silent 15:28265842-28265842 - TCGA-BR-8372-01 COSM4906746 c.10712C>T p.A3571V Substitution - Missense 15:28163128-28163128 - 2290929 COSM4440378 c.5982C>T p.C1994C Substitution - coding silent 15:28218535-28218535 - PD9600a COSM5779596 c.4983+10G>T p.? Unknown 15:28229664-28229664 - HCC058T COSM5805400 c.5860G>A p.E1954K Substitution - Missense 15:28218657-28218657 - TCGA-D3-A2JP-06 COSM4906209 c.9209C>T p.S3070L Substitution - Missense 15:28177464-28177464 - TCGA-LP-A4AU-01 COSM4855211 c.5959A>C p.S1987R Substitution - Missense 15:28218558-28218558 - HCC058T COSM5805182 c.11553A>T p.V3851V Substitution - coding silent 15:28142385-28142385 - 129 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-BR-4361-01 COSM4907807 c.10398G>A p.W3466* Substitution - Nonsense 15:28168422-28168422 - sysucc-1163T COSM5458493 c.11609A>C p.K3870T Substitution - Missense 15:28142329-28142329 - TCGA-BR-4201-01 COSM4906570 c.321A>G p.P107P Substitution - coding silent 15:28292889-28292889 - TCGA-AP-A059-01 COSM960131 c.12230G>T p.S4077I Substitution - Missense 15:28135478-28135478 - TCGA-A6-5661-01 COSM1372270 c.778T>C p.F260L Substitution - Missense 15:28274313-28274313 - PT35 COSM2083378 c.7990C>T p.Q2664* Substitution - Nonsense 15:28198399-28198399 - TCGA-EB-A431-01 COSM3500295 c.6363C>T p.S2121S Substitution - coding silent 15:28214268-28214268 - TCGA-FW-A3R5-06 COSM3886812 c.5101C>T p.P1701S Substitution - Missense 15:28229479-28229479 - AOCS-141-3-2 COSM3981437 c.6579C>T p.P2193P Substitution - coding silent 15:28213949-28213949 - J87_T COSM3956504 c.8596A>G p.I2866V Substitution - Missense 15:28191018-28191018 - QC2-09-T2 COSM4386229 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - SCC-15 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - T3174 COSM4690056 c.12293C>A p.A4098D Substitution - Missense 15:28132768-28132768 - TCGA-AX-A0J0-01 COSM4867004 c.6253G>A p.D2085N Substitution - Missense 15:28214760-28214760 - CPCG0211-F1 COSM4880644 c.599C>T p.A200V Substitution - Missense 15:28274949-28274949 - CN-AML-CR-25-Dx COSM5021827 c.912-7C>T p.? Unknown 15:28272393-28272393 - PT49 COSM5070860 c.9832-8G>A p.? Unknown 15:28174628-28174628 - sysucc-880T COSM5462437 c.14062G>A p.V4688M Substitution - Missense 15:28113241-28113241 - BN13 COSM1608217 c.11765A>G p.H3922R Substitution - Missense 15:28141782-28141782 - PT35 COSM5913678 c.5708G>A p.W1903* Substitution - Nonsense 15:28220589-28220589 - TCGA-DM-A1DA-01 COSM5167662 c.160delC p.Q54fs*23 Deletion - Frameshift 15:28299429-28299429 - TCGA-BR-8487-01 COSM4053838 c.8919C>T p.G2973G Substitution - coding silent 15:28182419-28182419 - TCGA-29-2429-01 COSM1323252 c.5223G>A p.Q1741Q Substitution - coding silent 15:28229244-28229244 - ESO-143 COSM1254125 c.4966A>T p.K1656* Substitution - Nonsense 15:28229691-28229691 - UM-SCC-17B COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - P100 COSM5009255 c.10952G>A p.R3651H Substitution - Missense 15:28146293-28146293 - BN13T COSM4781400 c.11765A>G p.H3922R Substitution - Missense 15:28141782-28141782 - TCGA-EE-A20F-06 COSM3500269 c.14157C>T p.F4719F Substitution - coding silent 15:28113146-28113146 - sysucc-1370T COSM5470331 c.510C>T p.S170S Substitution - coding silent 15:28280100-28280100 - T3021 COSM4690079 c.9292delA p.T3098fs*43 Deletion - Frameshift 15:28177090-28177090 - CH-60-T2 COSM5651298 c.2936C>G p.S979* Substitution - Nonsense 15:28254454-28254454 - 1115157 COSM5548535 c.3791C>A p.A1264D Substitution - Missense 15:28238175-28238175 - CSCC-41-T COSM4458769 c.10997C>T p.S3666F Substitution - Missense 15:28146248-28146248 - RK138_C01 COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - TCGA-D1-A176-01 COSM4876154 c.9222T>C p.G3074G Substitution - coding silent 15:28177451-28177451 - CRC-12T COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - TCGA-AA-3526-01 COSM291771 c.12447C>A p.A4149A Substitution - coding silent 15:28132223-28132223 - UM-SCC-4 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-AP-A0LM-01 COSM960093 c.14305C>T p.P4769S Substitution - Missense 15:28111963-28111963 - TCGA-CG-5721-01 COSM4906839 c.4307T>C p.V1436A Substitution - Missense 15:28233708-28233708 - 46M COSM5587983 c.14173G>T p.G4725C Substitution - Missense 15:28113130-28113130 - TCGA-B5-A11E-01 COSM4870247 c.8538G>A p.P2846P Substitution - coding silent 15:28191158-28191158 - HCT15 COSM4632658 c.9324C>A p.S3108R Substitution - Missense 15:28177058-28177058 - CHC892T COSM4961417 c.12554G>A p.C4185Y Substitution - Missense 15:28132116-28132116 - TCGA-FS-A1YY-06 COSM2083560 c.798G>A p.T266T Substitution - coding silent 15:28274293-28274293 - TCGA-GC-A3YS-01 COSM3794052 c.7003C>A p.H2335N Substitution - Missense 15:28211068-28211068 - TCGA-B5-A11E-01 COSM960181 c.8538G>A p.P2846P Substitution - coding silent 15:28191158-28191158 - TCGA-GI-A2C9-01 COSM3815788 c.11919C>A p.V3973V Substitution - coding silent 15:28141528-28141528 - TCGA-39-5037-01 COSM4860675 c.3615G>A p.E1205E Substitution - coding silent 15:28238735-28238735 - PD9004a COSM1209576 c.10993G>A p.V3665I Substitution - Missense 15:28146252-28146252 - S02291 COSM3500295 c.6363C>T p.S2121S Substitution - coding silent 15:28214268-28214268 - CSCC-20-T COSM4509416 c.8064C>T p.H2688H Substitution - coding silent 15:28196517-28196517 - T207 COSM4690106 c.2080G>T p.E694* Substitution - Nonsense 15:28262960-28262960 - PCSI_0624_Pa_P_526 COSM5761290 c.5553G>A p.T1851T Substitution - coding silent 15:28222127-28222127 - TCGA-B5-A11Y-01 COSM960241 c.3687C>T p.D1229D Substitution - coding silent 15:28238663-28238663 - TCGA-EE-A181-06 COSM4874890 c.14082C>T p.I4694I Substitution - coding silent 15:28113221-28113221 - TCGA-D1-A16F-01 COSM4812973 c.3176G>A p.R1059H Substitution - Missense 15:28248611-28248611 - T3262 COSM4690069 c.9969G>A p.A3323A Substitution - coding silent 15:28174483-28174483 - TCGA-AP-A0LM-01 COSM4873028 c.13448G>T p.S4483I Substitution - Missense 15:28116826-28116826 - ESCC-243T COSM4909103 c.6683T>G p.F2228C Substitution - Missense 15:28213845-28213845 - 2492704 COSM5716817 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - CHC892T COSM4961174 c.8922G>A p.G2974G Substitution - coding silent 15:28182416-28182416 - 2334194 COSM23122 c.8770C>G p.P2924A Substitution - Missense 15:28186632-28186632 - NCI-H209 COSM23122 c.8770C>G p.P2924A Substitution - Missense 15:28186632-28186632 - LUAD-F00282 COSM367133 c.12694_12695GG>TT p.G4232>? Complex 15:28130270-28130271 - TCGA-CJ-5680-01 COSM470472 c.5351G>T p.R1784L Substitution - Missense 15:28228331-28228331 - HCC2998 COSM4464461 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - TCGA-BS-A0TC-01 COSM4462032 c.12309C>T p.S4103S Substitution - coding silent 15:28132752-28132752 - CSCC-44-T COSM4485449 c.2934C>T p.A978A Substitution - coding silent 15:28254456-28254456 - TCGA-BP-4176-01 COSM4856972 c.10150C>G p.L3384V Substitution - Missense 15:28169563-28169563 - SC_9032 COSM5551134 c.1047C>T p.C349C Substitution - coding silent 15:28272251-28272251 - LN229 COSM4880110 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - UD-SCC-2 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - PCSI_0090_Pa_P COSM5419826 c.11824G>T p.D3942Y Substitution - Missense 15:28141623-28141623 - TCGA-AK-3450-01 COSM4857337 c.9727G>C p.V3243L Substitution - Missense 15:28175616-28175616 - TCGA-BR-6452-01 COSM4907477 c.9168C>T p.G3056G Substitution - coding silent 15:28177505-28177505 - TCGA-AP-A059-01 COSM960199 c.6695C>A p.T2232N Substitution - Missense 15:28213833-28213833 - CHC892T COSM4798244 c.10797C>T p.A3599A Substitution - coding silent 15:28152780-28152780 - WSU-HN30 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - S02322 COSM5691243 c.5418C>G p.L1806L Substitution - coding silent 15:28228264-28228264 - sysucc-1640T COSM5765501 c.825C>T p.T275T Substitution - coding silent 15:28272980-28272980 - SJRHB011 COSM4776300 c.645C>T p.G215G Substitution - coding silent 15:28274446-28274446 - TCGA-AX-A0J0-01 COSM960211 c.6253G>A p.D2085N Substitution - Missense 15:28214760-28214760 - P129 COSM4785206 c.10515C>T p.A3505A Substitution - coding silent 15:28167726-28167726 - TCGA-D3-A51T-06 COSM3500306 c.2472G>A p.E824E Substitution - coding silent 15:28257106-28257106 - TCGA-B5-A11Y-01 COSM4864188 c.6451C>T p.R2151C Substitution - Missense 15:28214180-28214180 - TCGA-BR-4368-01 COSM4907355 c.5283G>A p.P1761P Substitution - coding silent 15:28228399-28228399 - SS6003311 COSM3665084 c.6386G>A p.R2129H Substitution - Missense 15:28214245-28214245 - T2940 COSM4690053 c.13609G>T p.G4537C Substitution - Missense 15:28116665-28116665 - T660 COSM4690084 c.6905C>T p.S2302L Substitution - Missense 15:28212465-28212465 - TCGA-C5-A1MJ-01 COSM4842828 c.483G>A p.E161E Substitution - coding silent 15:28280127-28280127 - S02360 COSM5696017 c.4788C>G p.P1596P Substitution - coding silent 15:28230388-28230388 - PTC-28C COSM4909378 c.6685G>C p.G2229R Substitution - Missense 15:28213843-28213843 - TCGA-BR-4184-01 COSM4053868 c.2627C>T p.A876V Substitution - Missense 15:28256208-28256208 - TCGA-18-4086-01 COSM4861389 c.6161A>C p.K2054T Substitution - Missense 15:28215670-28215670 - TCGA-CK-5916-01 COSM4948018 c.1991G>A p.C664Y Substitution - Missense 15:28263049-28263049 - WSU-HN13 COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-D1-A17Q-01 COSM960151 c.10957G>A p.D3653N Substitution - Missense 15:28146288-28146288 - TCGA-EE-A3AE-06 COSM4898018 c.2365C>T p.P789S Substitution - Missense 15:28257213-28257213 - 2293744 COSM4606586 c.10543A>T p.K3515* Substitution - Nonsense 15:28167698-28167698 - HCC159 COSM3706504 c.10633G>T p.D3545Y Substitution - Missense 15:28163207-28163207 - ESCC_131 COSM5642200 c.13658A>C p.N4553T Substitution - Missense 15:28115493-28115493 - TCGA-G4-6306-01 COSM1372231 c.12964G>A p.A4322T Substitution - Missense 15:28125032-28125032 - 4000_T COSM3956501 c.12383G>T p.S4128I Substitution - Missense 15:28132678-28132678 - TCGA-FG-5962-01 COSM4783362 c.11378A>G p.N3793S Substitution - Missense 15:28143913-28143913 - TCGA-GN-A26C-01 COSM4903868 c.8944G>A p.V2982I Substitution - Missense 15:28179217-28179217 - HCC079T COSM5808149 c.3544G>T p.D1182Y Substitution - Missense 15:28245914-28245914 - TCGA-D1-A16F-01 COSM4870780 c.5351G>A p.R1784H Substitution - Missense 15:28228331-28228331 - BD124T COSM5493245 c.7775G>A p.G2592D Substitution - Missense 15:28198711-28198711 - TCGA-BR-8487-01 COSM4906979 c.13566G>A p.P4522P Substitution - coding silent 15:28116708-28116708 - TCGA-AP-A0LD-01 COSM4874292 c.2239G>A p.V747M Substitution - Missense 15:28260854-28260854 - 16461 COSM5614204 c.1803A>T p.K601N Substitution - Missense 15:28265685-28265685 - EW8 COSM2083462 c.5128C>G p.L1710V Substitution - Missense 15:28229339-28229339 - LUAD-RT-S01709 COSM379872 c.14213G>T p.G4738V Substitution - Missense 15:28113090-28113090 - TCGA-B5-A11E-01 COSM960165 c.9956C>T p.S3319F Substitution - Missense 15:28174496-28174496 - PT19_1 COSM5899674 c.13247C>T p.P4416L Substitution - Missense 15:28121371-28121371 - PD8981a COSM470472 c.5351G>T p.R1784L Substitution - Missense 15:28228331-28228331 - MZ7-mel COSM26915 c.14027G>A p.G4676D Substitution - Missense 15:28113276-28113276 - AOCS-141-8-0 COSM4422326 c.6579C>T p.P2193P Substitution - coding silent 15:28213949-28213949 - CCK81 COSM2083257 c.13306G>A p.G4436S Substitution - Missense 15:28117121-28117121 - P9 COSM5008478 c.9210G>A p.S3070S Substitution - coding silent 15:28177463-28177463 - TCGA-C8-A12P-01 COSM4814562 c.9954G>T p.S3318S Substitution - coding silent 15:28174498-28174498 - TCGA-AP-A0LM-01 COSM4872949 c.4565C>A p.P1522H Substitution - Missense 15:28233256-28233256 - TCGA-BR-8680-01 COSM960260 c.2656G>A p.A886T Substitution - Missense 15:28256179-28256179 - TCGA-18-5592-01 COSM4859961 c.2237G>T p.R746L Substitution - Missense 15:28260856-28260856 - TCGA-CC-A7IG-01 COSM4943118 c.12464C>T p.A4155V Substitution - Missense 15:28132206-28132206 - TCGA-IR-A3LK-01 COSM4817250 c.986C>T p.S329F Substitution - Missense 15:28272312-28272312 - TCGA-BR-6452-01 COSM4053842 c.8013T>C p.A2671A Substitution - coding silent 15:28196568-28196568 - CHEWS035 COSM4578151 c.1229C>T p.P410L Substitution - Missense 15:28270723-28270723 - TCGA-B5-A0JY-01 COSM4869786 c.8598C>A p.I2866I Substitution - coding silent 15:28191016-28191016 - TCGA-D1-A103-01 COSM960191 c.7814T>C p.L2605P Substitution - Missense 15:28198672-28198672 - TCGA-CG-5721-01 COSM4906835 c.7695A>G p.V2565V Substitution - coding silent 15:28201477-28201477 - ESCC_133 COSM4953435 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - LFS_MB4 COSM4787320 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - TCGA-CD-A4MG-01 COSM4053866 c.2694G>A p.L898L Substitution - coding silent 15:28256141-28256141 - 58 COSM5012840 c.12974G>A p.G4325D Substitution - Missense 15:28125022-28125022 - TCGA-AP-A059-01 COSM960173 c.9180G>A p.T3060T Substitution - coding silent 15:28177493-28177493 - CHC1717T COSM4802092 c.557G>T p.G186V Substitution - Missense 15:28274991-28274991 - 2492704 COSM5716816 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - TCGA-F1-6177-01 COSM4783896 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - TCGA-EE-A2MI-06 COSM4892046 c.10193C>T p.S3398L Substitution - Missense 15:28169520-28169520 - 2492706 COSM5716817 c.6659G>A p.G2220D Substitution - Missense 15:28213869-28213869 - 587336 COSM1209584 c.12990G>T p.Q4330H Substitution - Missense 15:28125006-28125006 - ESO-157 COSM1254127 c.13279C>T p.R4427* Substitution - Nonsense 15:28117148-28117148 - sysucc-880T COSM5462442 c.932T>C p.L311P Substitution - Missense 15:28272366-28272366 - SC_9091 COSM5550073 c.1535C>T p.A512V Substitution - Missense 15:28268528-28268528 - CHC1040T COSM349016 c.9027G>T p.V3009V Substitution - coding silent 15:28179023-28179023 - TCGA-G9-6348-01 COSM1129252 c.11818C>T p.R3940* Substitution - Nonsense 15:28141629-28141629 - TCGA-FR-A3YN-06 COSM2083334 c.9561G>A p.R3187R Substitution - coding silent 15:28176553-28176553 - TCGA-BR-6452-01 COSM4053837 c.9168C>T p.G3056G Substitution - coding silent 15:28177505-28177505 - TCGA-AP-A056-01 COSM4868583 c.11819G>A p.R3940Q Substitution - Missense 15:28141628-28141628 - PTC-10C COSM4909295 c.46T>A p.S16T Substitution - Missense 15:28321388-28321388 - 58 COSM5012839 c.12974G>A p.G4325D Substitution - Missense 15:28125022-28125022 - sysucc-1128T COSM5021826 c.912-7C>T p.? Unknown 15:28272393-28272393 - PD4970a COSM5768573 c.146G>T p.G49V Substitution - Missense 15:28299443-28299443 - sysucc-1640T COSM5765500 c.825C>T p.T275T Substitution - coding silent 15:28272980-28272980 - TCGA-CU-A0YN-01 COSM416527 c.9519_9520GG>TT p.L3173>? Complex 15:28176594-28176595 - TCGA-BR-4370-01 COSM4907842 c.5012G>T p.G1671V Substitution - Missense 15:28229568-28229568 - TCGA-EE-A29E-06 COSM3500303 c.3285C>T p.L1095L Substitution - coding silent 15:28246848-28246848 - CSCC-60-T COSM4497762 c.5049C>T p.F1683F Substitution - coding silent 15:28229531-28229531 - TCGA-A7-A26I-01 COSM4813542 c.3630A>G p.I1210M Substitution - Missense 15:28238720-28238720 - TCGA-AZ-4615-01 COSM4784271 c.11675C>T p.P3892L Substitution - Missense 15:28142263-28142263 - 01-P1216 COSM4578141 c.6637A>G p.I2213V Substitution - Missense 15:28213891-28213891 - TCGA-BS-A0UV-01 COSM4864444 c.13072G>A p.E4358K Substitution - Missense 15:28124153-28124153 - STC263 COSM5032331 c.3827C>T p.A1276V Substitution - Missense 15:28238139-28238139 - RK164_C01 COSM4780826 c.1084-4C>G p.? Unknown 15:28270872-28270872 - 2951_PT COSM5754664 c.6440T>C p.V2147A Substitution - Missense 15:28214191-28214191 - CSCC-27-T COSM4482826 c.2643C>T p.T881T Substitution - coding silent 15:28256192-28256192 - STC273 COSM5054226 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - 2293770 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-AG-3892-01 COSM257107 c.1433A>C p.N478T Substitution - Missense 15:28269261-28269261 - NOKSI COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - AOCS-141-8-0 COSM3981437 c.6579C>T p.P2193P Substitution - coding silent 15:28213949-28213949 - CSCC-16-T COSM4462032 c.12309C>T p.S4103S Substitution - coding silent 15:28132752-28132752 - TCGA-B5-A0JY-01 COSM4869317 c.6486C>A p.L2162L Substitution - coding silent 15:28214145-28214145 - TCGA-F5-6814-01 COSM4782472 c.2908G>T p.E970* Substitution - Nonsense 15:28254482-28254482 - TCGA-B5-A11E-01 COSM4869925 c.13228C>T p.R4410C Substitution - Missense 15:28121390-28121390 - TCGA-AP-A0LM-01 COSM4873539 c.3226G>A p.D1076N Substitution - Missense 15:28248561-28248561 - NPC27F COSM4995556 c.9352G>A p.G3118R Substitution - Missense 15:28177030-28177030 - TCGA-BS-A0UM-01 COSM960121 c.12821G>A p.G4274D Substitution - Missense 15:28125175-28125175 - YUMOKI COSM5383112 c.5788G>A p.E1930K Substitution - Missense 15:28220509-28220509 - PTC_455 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-AR-A1AJ-01 COSM4812973 c.3176G>A p.R1059H Substitution - Missense 15:28248611-28248611 - CHEWS024 COSM4578145 c.3669C>T p.G1223G Substitution - coding silent 15:28238681-28238681 - PTC-88C COSM4148581 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - TCGA-CA-6717-01 COSM1372271 c.709G>A p.E237K Substitution - Missense 15:28274382-28274382 - pfg072T COSM4751790 c.8671G>T p.A2891S Substitution - Missense 15:28186731-28186731 - BD124T COSM5493247 c.5395G>A p.A1799T Substitution - Missense 15:28228287-28228287 - TCGA-GI-A2C9-01 COSM4814727 c.11919C>A p.V3973V Substitution - coding silent 15:28141528-28141528 - P100 COSM5009256 c.10952G>A p.R3651H Substitution - Missense 15:28146293-28146293 - CSCC-62-T COSM4503679 c.6465C>T p.S2155S Substitution - coding silent 15:28214166-28214166 - TCGA-AO-A12E-01 COSM4816194 c.4498C>T p.R1500C Substitution - Missense 15:28233323-28233323 - TCGA-GL-7773-01 COSM3987888 c.8702A>T p.D2901V Substitution - Missense 15:28186700-28186700 - 2492706 COSM5716756 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - TCGA-G3-A3CK-01 COSM3500300 c.4002C>T p.A1334A Substitution - coding silent 15:28236964-28236964 - TCGA-G3-A5SK-01 COSM4927474 c.9604C>G p.L3202V Substitution - Missense 15:28176510-28176510 - Pat_05_B COSM5848938 c.13922A>G p.E4641G Substitution - Missense 15:28113670-28113670 - TCGA-D1-A103-01 COSM960125 c.12712C>A p.R4238R Substitution - coding silent 15:28130253-28130253 - TCGA-GD-A3OP-01 COSM1301009 c.10594C>T p.Q3532* Substitution - Nonsense 15:28163246-28163246 - TCGA-AP-A051-01 COSM4872374 c.13454C>T p.S4485F Substitution - Missense 15:28116820-28116820 - PTC_221 COSM5960162 c.12310_12311delGC p.A4104fs*25 Deletion - Frameshift 15:28132750-28132751 - S01563 COSM5669937 c.1459G>T p.V487F Substitution - Missense 15:28268604-28268604 - TCGA-BR-8591-01 COSM4906993 c.13589G>A p.S4530N Substitution - Missense 15:28116685-28116685 - HCT-15 COSM1678317 c.9324C>A p.S3108R Substitution - Missense 15:28177058-28177058 - TCGA-GF-A6C9-06 COSM4903291 c.7740C>T p.C2580C Substitution - coding silent 15:28198746-28198746 - TCGA-EB-A1NK-01 COSM4899209 c.10647G>T p.V3549V Substitution - coding silent 15:28163193-28163193 - HCC053T COSM5803789 c.8494A>T p.R2832* Substitution - Nonsense 15:28191202-28191202 - TCGA-39-5030-01 COSM700255 c.3224C>G p.S1075* Substitution - Nonsense 15:28248563-28248563 - TCGA-A7-A26I-01 COSM1478015 c.3630A>G p.I1210M Substitution - Missense 15:28238720-28238720 - WSU-HN13 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - TCGA-AD-6889-01 COSM1372253 c.7848C>T p.G2616G Substitution - coding silent 15:28198638-28198638 - ESO-105 COSM1254121 c.13565C>T p.P4522L Substitution - Missense 15:28116709-28116709 - HCC6T COSM4781105 c.2185G>C p.E729Q Substitution - Missense 15:28260908-28260908 - ESCC_143 COSM5644066 c.4356T>C p.H1452H Substitution - coding silent 15:28233557-28233557 - TCGA-BR-8487-01 COSM4906953 c.10447G>A p.A3483T Substitution - Missense 15:28167794-28167794 - PD4109a COSM161514 c.3140G>C p.R1047T Substitution - Missense 15:28248647-28248647 - AOCS-134-3-9 COSM4909171 c.3704T>C p.I1235T Substitution - Missense 15:28238646-28238646 - ESCC_143 COSM5644067 c.4356T>C p.H1452H Substitution - coding silent 15:28233557-28233557 - 1N01-VS-1T01 COSM4972382 c.8834G>C p.R2945T Substitution - Missense 15:28182504-28182504 - HCC84T COSM3706505 c.3252T>A p.G1084G Substitution - coding silent 15:28246881-28246881 - TCGA-CC-A3MA-01 COSM4942720 c.8859A>G p.S2953S Substitution - coding silent 15:28182479-28182479 - TCGA-G2-A2EO-01 COSM4812015 c.8375C>T p.S2792L Substitution - Missense 15:28192037-28192037 - NOKSI COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-A5-A0GA-01 COSM4875263 c.511G>T p.G171C Substitution - Missense 15:28280099-28280099 - TCGA-AA-A00N-01 COSM275459 c.8196T>C p.C2732C Substitution - coding silent 15:28196279-28196279 - SJOS016_D COSM5023146 c.3662A>T p.D1221V Substitution - Missense 15:28238688-28238688 - TCGA-CG-4442-01 COSM4053856 c.5825C>T p.S1942L Substitution - Missense 15:28220472-28220472 - 8068563 COSM4388138 c.758T>G p.V253G Substitution - Missense 15:28274333-28274333 - PT49 COSM5729568 c.12994C>T p.P4332S Substitution - Missense 15:28124231-28124231 - PTC_415 COSM5957983 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - CHEWS017 COSM4578154 c.810C>T p.H270H Substitution - coding silent 15:28272995-28272995 - BD123T COSM5521106 c.3095G>A p.R1032H Substitution - Missense 15:28248692-28248692 - TCGA-60-2707-01 COSM700246 c.846C>A p.P282P Substitution - coding silent 15:28272959-28272959 - TCGA-BR-8680-01 COSM4867491 c.11716C>T p.R3906C Substitution - Missense 15:28141831-28141831 - TCGA-C8-A12P-01 COSM433664 c.9954G>T p.S3318S Substitution - coding silent 15:28174498-28174498 - Detroit_562 COSM1478013 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - CHC1061T COSM3667707 c.3602G>T p.C1201F Substitution - Missense 15:28238748-28238748 - PD18279a COSM3770273 c.2184C>G p.S728R Substitution - Missense 15:28260909-28260909 - PTC-88C COSM4600773 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - CHC1717T COSM4802091 c.557G>T p.G186V Substitution - Missense 15:28274991-28274991 - TCGA-66-2782-01 COSM4861907 c.2865G>A p.E955E Substitution - coding silent 15:28255878-28255878 - HCC059T COSM5809752 c.8926A>T p.K2976* Substitution - Nonsense 15:28182412-28182412 - TCGA-FW-A3R5-06 COSM960107 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - T55 COSM4690050 c.14019+1G>A p.? Unknown 15:28113572-28113572 - S02234 COSM5676012 c.5316G>A p.P1772P Substitution - coding silent 15:28228366-28228366 - SCC-15 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - C086 COSM5532285 c.619T>G p.F207V Substitution - Missense 15:28274929-28274929 - PD4109a COSM4810410 c.3140G>C p.R1047T Substitution - Missense 15:28248647-28248647 - 08-P1177 COSM2083342 c.9358C>T p.L3120L Substitution - coding silent 15:28177024-28177024 - TCGA-D3-A1Q5-06 COSM3500284 c.9953C>T p.S3318L Substitution - Missense 15:28174499-28174499 - T2940 COSM4690075 c.9657G>A p.A3219A Substitution - coding silent 15:28176457-28176457 - T3202 COSM4690058 c.12247C>T p.R4083C Substitution - Missense 15:28132814-28132814 - TCGA-F1-6177-01 COSM1372259 c.3166C>T p.R1056C Substitution - Missense 15:28248621-28248621 - 2521262 COSM5892258 c.13728T>A p.D4576E Substitution - Missense 15:28114797-28114797 - XHDG27 COSM4769238 c.12172G>A p.G4058R Substitution - Missense 15:28135536-28135536 - UM-SCC-2 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - EGC3 COSM5054224 c.8419C>A p.P2807T Substitution - Missense 15:28191993-28191993 - CN-AML-CR-31-Dx COSM2083389 c.7593C>T p.D2531D Substitution - coding silent 15:28202137-28202137 - CN-AML-CR-31-Dx COSM4600773 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - TCGA-AP-A051-01 COSM4874053 c.7650G>A p.T2550T Substitution - coding silent 15:28201522-28201522 - I2L-P19Tb-Tumor-Biopsy COSM5362940 c.10595A>G p.Q3532R Substitution - Missense 15:28163245-28163245 - S02234 COSM5676011 c.5316G>A p.P1772P Substitution - coding silent 15:28228366-28228366 - TCGA-D8-A1XK-01 COSM3815800 c.447C>T p.R149R Substitution - coding silent 15:28280163-28280163 - CSCC-16-T COSM4490979 c.3725C>T p.S1242L Substitution - Missense 15:28238625-28238625 - 234 COSM3731151 c.2328G>C p.W776C Substitution - Missense 15:28257250-28257250 - TCGA-BS-A0UV-01 COSM4864825 c.5679C>T p.R1893R Substitution - coding silent 15:28220618-28220618 - PTC_428 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - pfg001T COSM1640200 c.12192_12216del25 p.E4065fs*16 Deletion - Frameshift 15:28135492-28135516 - TCGA-BR-6452-01 COSM4907520 c.11774T>C p.F3925S Substitution - Missense 15:28141773-28141773 - sysucc-1317T COSM5448721 c.1003G>A p.A335T Substitution - Missense 15:28272295-28272295 - T1154 COSM4690104 c.2573G>A p.G858D Substitution - Missense 15:28256262-28256262 - Au9 COSM3500268 c.14166C>T p.F4722F Substitution - coding silent 15:28113137-28113137 - TCGA-A2-A0CP-01 COSM5832859 c.11131_11132delCC p.P3711fs*5 Deletion - Frameshift 15:28144681-28144682 - TCGA-60-2713-01 COSM4860820 c.554C>T p.A185V Substitution - Missense 15:28274994-28274994 - I2L-P19Tb-Tumor-Organoid COSM5362973 c.9859G>A p.G3287S Substitution - Missense 15:28174593-28174593 - 587228 COSM1209576 c.10993G>A p.V3665I Substitution - Missense 15:28146252-28146252 - TCGA-60-2713-01 COSM700245 c.554C>T p.A185V Substitution - Missense 15:28274994-28274994 - 76629543 COSM1582289 c.14224G>A p.V4742I Substitution - Missense 15:28113079-28113079 - TCGA-06-0165 COSM2150154 c.2683_2685delTCC p.S895delS Deletion - In frame 15:28256150-28256152 - sysucc-1038T COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-D3-A1Q9-06 COSM4899091 c.4002C>T p.A1334A Substitution - coding silent 15:28236964-28236964 - CHC892T COSM4794056 c.5327G>A p.S1776N Substitution - Missense 15:28228355-28228355 - TCGA-B5-A11E-01 COSM4870586 c.2656G>A p.A886T Substitution - Missense 15:28256179-28256179 - TCGA-BR-4256-01 COSM4907782 c.9292A>G p.T3098A Substitution - Missense 15:28177090-28177090 - TCGA-LP-A4AU-01 COSM4855212 c.5959A>C p.S1987R Substitution - Missense 15:28218558-28218558 - CPCG0001-F1 COSM307015 c.9903A>G p.T3301T Substitution - coding silent 15:28174549-28174549 - TCGA-61-1740-01 COSM1323251 c.1905G>C p.G635G Substitution - coding silent 15:28263135-28263135 - Gp2D COSM4627311 c.728A>G p.E243G Substitution - Missense 15:28274363-28274363 - TCGA-BR-8589-01 COSM4907418 c.4670A>G p.K1557R Substitution - Missense 15:28233151-28233151 - Pat_31_B COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - PD13299a COSM5794890 c.2366C>T p.P789L Substitution - Missense 15:28257212-28257212 - 587332 COSM1209588 c.8104A>T p.I2702F Substitution - Missense 15:28196477-28196477 - UD-SCC-2 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-33-4533-01 COSM4862143 c.128G>T p.G43V Substitution - Missense 15:28299461-28299461 - TCGA-EE-A2GI-06 COSM4892443 c.12875C>T p.P4292L Substitution - Missense 15:28125121-28125121 - A1 COSM396917 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-CG-5723-01 COSM4053823 c.10735G>A p.A3579T Substitution - Missense 15:28163105-28163105 - K48-Tumor COSM4745969 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - I2L-P19Tb-Tumor-Organoid COSM5362972 c.9859G>A p.G3287S Substitution - Missense 15:28174593-28174593 - BN42T COSM1608221 c.239A>G p.E80G Substitution - Missense 15:28292971-28292971 - HN_62699 COSM123571 c.12260C>T p.S4087F Substitution - Missense 15:28132801-28132801 - TCGA-66-2773-01 COSM4861846 c.6066G>C p.R2022R Substitution - coding silent 15:28215765-28215765 - TCGA-AP-A0LM-01 COSM960264 c.2419C>T p.R807W Substitution - Missense 15:28257159-28257159 - TCGA-FS-A1ZA-06 COSM4897763 c.3399C>T p.L1133L Substitution - coding silent 15:28246059-28246059 - BN42T COSM4781314 c.239A>G p.E80G Substitution - Missense 15:28292971-28292971 - TCGA-D1-A15X-01 COSM960272 c.1944A>G p.P648P Substitution - coding silent 15:28263096-28263096 - TCGA-HU-A4H8-01 COSM4907748 c.13101C>T p.F4367F Substitution - coding silent 15:28124124-28124124 - T207 COSM4690080 c.8953T>C p.F2985L Substitution - Missense 15:28179208-28179208 - TCGA-AA-A010-01 COSM281677 c.7660C>T p.R2554* Substitution - Nonsense 15:28201512-28201512 - 422_T COSM3956503 c.8742T>C p.R2914R Substitution - coding silent 15:28186660-28186660 - CHC923T COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - CHC892T COSM4798245 c.10797C>T p.A3599A Substitution - coding silent 15:28152780-28152780 - TCGA-BS-A0UV-01 COSM4813859 c.5230C>T p.R1744* Substitution - Nonsense 15:28229237-28229237 - TCGA-EI-6917-01 COSM4782541 c.2391G>T p.M797I Substitution - Missense 15:28257187-28257187 - TCGA-B5-A11E-01 COSM4870137 c.10893G>T p.K3631N Substitution - Missense 15:28152684-28152684 - ESO-0013 COSM1254119 c.934T>C p.L312L Substitution - coding silent 15:28272364-28272364 - TCGA-B5-A0JY-01 COSM960179 c.8598C>A p.I2866I Substitution - coding silent 15:28191016-28191016 - BK0027 COSM4186643 c.1996A>G p.S666G Substitution - Missense 15:28263044-28263044 - TCGA-AP-A059-01 COSM4784697 c.1074C>T p.G358G Substitution - coding silent 15:28272224-28272224 - TCGA-D5-6540-01 COSM4632087 c.9351C>T p.S3117S Substitution - coding silent 15:28177031-28177031 - RK308_C01 COSM960099 c.13665C>T p.A4555A Substitution - coding silent 15:28115486-28115486 - ESO-139 COSM1254125 c.4966A>T p.K1656* Substitution - Nonsense 15:28229691-28229691 - 45 COSM3732752 c.11170G>A p.V3724I Substitution - Missense 15:28144206-28144206 - 8057676 COSM4945899 c.12230+1G>T p.? Unknown 15:28135477-28135477 - C086 COSM5532290 c.11460T>C p.L3820L Substitution - coding silent 15:28142911-28142911 - UM-SCC-2 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-FJ-A3ZF-01 COSM4810543 c.12710T>C p.V4237A Substitution - Missense 15:28130255-28130255 - TCGA-GN-A26A-06 COSM3886816 c.2447C>T p.S816F Substitution - Missense 15:28257131-28257131 - S00516 COSM4387047 c.8842G>T p.A2948S Substitution - Missense 15:28182496-28182496 - ESCC_56 COSM5632160 c.1575A>G p.G525G Substitution - coding silent 15:28268488-28268488 - DN12007 COSM5770145 c.8800G>A p.E2934K Substitution - Missense 15:28186602-28186602 - ESCC_BICR_061T COSM5430742 c.1442C>T p.T481M Substitution - Missense 15:28269252-28269252 - LUAD-VUMN6 COSM347860 c.12383G>C p.S4128T Substitution - Missense 15:28132678-28132678 - Pat_41_B COSM5848949 c.9338C>T p.A3113V Substitution - Missense 15:28177044-28177044 - TCGA-HU-8602-01 COSM4053833 c.9737G>A p.R3246Q Substitution - Missense 15:28175606-28175606 - 8035567 COSM4781710 c.8582T>C p.I2861T Substitution - Missense 15:28191032-28191032 - YUKAT COSM5383109 c.10901-1G>A p.? Unknown 15:28146345-28146345 - TCGA-EB-A41A-01 COSM4903979 c.788C>T p.S263F Substitution - Missense 15:28274303-28274303 - PT27 COSM5905990 c.7440G>T p.K2480N Substitution - Missense 15:28202387-28202387 - TCGA-EI-6917-01 COSM3420219 c.12425G>A p.G4142D Substitution - Missense 15:28132245-28132245 - TCGA-EE-A3JD-06 COSM4394929 c.5716G>T p.V1906F Substitution - Missense 15:28220581-28220581 - 67 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - T3446 COSM4690090 c.6365C>T p.T2122M Substitution - Missense 15:28214266-28214266 - NPC27F COSM4995557 c.9352G>A p.G3118R Substitution - Missense 15:28177030-28177030 - Pat_41_B COSM5848948 c.9338C>T p.A3113V Substitution - Missense 15:28177044-28177044 - WSU-HN30 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - HCC2998 COSM960107 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - SCC-25 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-CD-A4MG-01 COSM4652582 c.10711G>A p.A3571T Substitution - Missense 15:28163129-28163129 - CN-AML-CR-51-Dx COSM5427069 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - TCGA-CD-A4MG-01 COSM4907615 c.2694G>A p.L898L Substitution - coding silent 15:28256141-28256141 - TCGA-EB-A5UN-06 COSM3500312 c.780C>T p.F260F Substitution - coding silent 15:28274311-28274311 - 06-P036 COSM4578140 c.6651G>A p.L2217L Substitution - coding silent 15:28213877-28213877 - RKO COSM4647804 c.9376G>A p.G3126S Substitution - Missense 15:28177006-28177006 - 2492705 COSM5716757 c.10941C>T p.S3647S Substitution - coding silent 15:28146304-28146304 - TCGA-D1-A15X-01 COSM960161 c.10163A>T p.D3388V Substitution - Missense 15:28169550-28169550 - sysucc-1640T COSM3732920 c.815C>T p.T272M Substitution - Missense 15:28272990-28272990 - UM-SCC-47 COSM4592934 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - PCSI_0142_Pa_P_526 COSM4808370 c.7937G>A p.R2646Q Substitution - Missense 15:28198452-28198452 - TCGA-F5-6814-01 COSM4860009 c.13948C>T p.R4650W Substitution - Missense 15:28113644-28113644 - BICR_22 COSM4593234 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-AX-A0J0-01 COSM960107 c.13358C>T p.S4453L Substitution - Missense 15:28117069-28117069 - NCHP_DIPG105 COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - HX19T COSM1608221 c.239A>G p.E80G Substitution - Missense 15:28292971-28292971 - YUMOKI COSM5383111 c.5788G>A p.E1930K Substitution - Missense 15:28220509-28220509 - BD124T COSM5493248 c.577G>A p.A193T Substitution - Missense 15:28274971-28274971 - PT19_1 COSM5899675 c.13247C>T p.P4416L Substitution - Missense 15:28121371-28121371 - TCGA-G9-6499-01 COSM3672010 c.9448G>T p.G3150C Substitution - Missense 15:28176753-28176753 - CHC796T COSM4949602 c.1014G>C p.L338F Substitution - Missense 15:28272284-28272284 - TCGA-F1-6177-01 COSM4906300 c.8270C>T p.A2757V Substitution - Missense 15:28192142-28192142 - TCGA-FP-A4BE-01 COSM4053809 c.13896G>A p.R4632R Substitution - coding silent 15:28114629-28114629 - 2250189 COSM5030028 c.557G>A p.G186D Substitution - Missense 15:28274991-28274991 - TCGA-EE-A29E-06 COSM4891909 c.8945T>C p.V2982A Substitution - Missense 15:28179216-28179216 - PDA_005 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - Detroit_562 COSM4594608 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - CN-AML-26-T COSM4386169 c.6997C>T p.L2333F Substitution - Missense 15:28211074-28211074 - TCGA-CG-4442-01 COSM4053848 c.7511A>T p.D2504V Substitution - Missense 15:28202219-28202219 - CHEWS024 COSM4578144 c.3669C>T p.G1223G Substitution - coding silent 15:28238681-28238681 - J38_T COSM700247 c.1507G>A p.D503N Substitution - Missense 15:28268556-28268556 - CHC1061T COSM3667707 c.3602G>T p.C1201F Substitution - Missense 15:28238748-28238748 - HCC84 COSM3706505 c.3252T>A p.G1084G Substitution - coding silent 15:28246881-28246881 - PT36 COSM5916427 c.812G>A p.G271E Substitution - Missense 15:28272993-28272993 - TCGA-EE-A29E-06 COSM4891885 c.3285C>T p.L1095L Substitution - coding silent 15:28246848-28246848 - TCGA-EE-A3JD-06 COSM4396890 c.12266G>A p.R4089K Substitution - Missense 15:28132795-28132795 - TCGA-61-1736-01 COSM71044 c.10615A>T p.S3539C Substitution - Missense 15:28163225-28163225 - WSU-HN13 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - UM-SCC-11B COSM3732919 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - TCGA-AA-3696-01 COSM293460 c.7909_7911delTCT p.S2637delS Deletion - In frame 15:28198478-28198480 - TCGA-AK-3458-01 COSM4856962 c.1139C>T p.P380L Substitution - Missense 15:28270813-28270813 - TCGA-60-2698-01 COSM700258 c.3553G>A p.E1185K Substitution - Missense 15:28245905-28245905 - UPCI:SCC090 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - TCGA-DK-A1A7-01 COSM416525 c.5466C>T p.G1822G Substitution - coding silent 15:28222214-28222214 - TCGA-CC-A3MA-01 COSM4942721 c.8859A>G p.S2953S Substitution - coding silent 15:28182479-28182479 - TCGA-EW-A1J5-01 COSM1209576 c.10993G>A p.V3665I Substitution - Missense 15:28146252-28146252 - PTC_448 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-D3-A51T-06 COSM4905499 c.14166C>T p.F4722F Substitution - coding silent 15:28113137-28113137 - TCGA-BS-A0UV-01 COSM960115 c.13072G>A p.E4358K Substitution - Missense 15:28124153-28124153 - TCGA-DI-A0WH-01 COSM960175 c.9037G>A p.V3013M Substitution - Missense 15:28179013-28179013 - G5 COSM1191818 c.8288C>G p.S2763C Substitution - Missense 15:28192124-28192124 - TCGA-BR-4184-01 COSM4907255 c.11041C>T p.R3681C Substitution - Missense 15:28144772-28144772 - PT42 COSM5925825 c.8435C>T p.S2812L Substitution - Missense 15:28191977-28191977 - CHC1717T COSM4802092 c.557G>T p.G186V Substitution - Missense 15:28274991-28274991 - BD173T COSM5500103 c.132A>C p.E44D Substitution - Missense 15:28299457-28299457 - PT46 COSM5929580 c.1138C>T p.P380S Substitution - Missense 15:28270814-28270814 - TCGA-DU-A5TP-01 COSM3969051 c.5420A>G p.N1807S Substitution - Missense 15:28228262-28228262 - HCC053T COSM5803790 c.8494A>T p.R2832* Substitution - Nonsense 15:28191202-28191202 - PD11464a COSM5770144 c.8800G>A p.E2934K Substitution - Missense 15:28186602-28186602 - TCGA-G4-6306-01 COSM4786914 c.12964G>A p.A4322T Substitution - Missense 15:28125032-28125032 - LUAD-F00257 COSM340074 c.4387C>G p.L1463V Substitution - Missense 15:28233526-28233526 - S00832 COSM5660820 c.6309C>T p.F2103F Substitution - coding silent 15:28214704-28214704 - Gp2D COSM4627306 c.1971G>A p.L657L Substitution - coding silent 15:28263069-28263069 - D28 COSM5545093 c.6103C>T p.L2035F Substitution - Missense 15:28215728-28215728 - Gp2D COSM2083561 c.728A>G p.E243G Substitution - Missense 15:28274363-28274363 - TCGA-AP-A056-01 COSM960135 c.11819G>A p.R3940Q Substitution - Missense 15:28141628-28141628 - ESO-251 COSM1254132 c.11623C>T p.R3875W Substitution - Missense 15:28142315-28142315 - TCGA-AR-A250-01 COSM1478013 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - TCGA-BR-8680-01 COSM4907126 c.7667A>G p.D2556G Substitution - Missense 15:28201505-28201505 - TCGA-EI-6917-01 COSM3420221 c.2391G>T p.M797I Substitution - Missense 15:28257187-28257187 - Pat_41_B COSM5848953 c.4948G>A p.D1650N Substitution - Missense 15:28229709-28229709 - SNU-C4 COSM4652582 c.10711G>A p.A3571T Substitution - Missense 15:28163129-28163129 - UM-SCC-17B COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-C5-A1ML-01 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-60-2720-01 COSM700270 c.9930G>C p.K3310N Substitution - Missense 15:28174522-28174522 - LUAD-RT-S01487 COSM377869 c.3506A>T p.D1169V Substitution - Missense 15:28245952-28245952 - TCGA-F1-6874-01 COSM4053877 c.263C>A p.P88H Substitution - Missense 15:28292947-28292947 - TCGA-FU-A23K-01 COSM4817250 c.986C>T p.S329F Substitution - Missense 15:28272312-28272312 - TCGA-A5-A0R7-01 COSM960189 c.7936C>G p.R2646G Substitution - Missense 15:28198453-28198453 - PT22_1 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-B6-A0IH-01 COSM433661 c.14397C>T p.I4799I Substitution - coding silent 15:28111871-28111871 - TCGA-BS-A0UV-01 COSM960215 c.5679C>T p.R1893R Substitution - coding silent 15:28220618-28220618 - TCGA-21-1077-01 COSM700251 c.2391G>A p.M797I Substitution - Missense 15:28257187-28257187 - ESCC-243T COSM3936712 c.6683T>G p.F2228C Substitution - Missense 15:28213845-28213845 - CHC923T COSM4593462 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - TCGA-AP-A059-01 COSM4866770 c.7442C>A p.S2481Y Substitution - Missense 15:28202385-28202385 - TCGA-D1-A103-01 COSM4874726 c.7814T>C p.L2605P Substitution - Missense 15:28198672-28198672 - TCGA-CD-8529-01 COSM4907138 c.14177G>A p.R4726Q Substitution - Missense 15:28113126-28113126 - TCGA-FV-A23B-01 COSM4914067 c.12010G>A p.G4004R Substitution - Missense 15:28141437-28141437 - PARBRK COSM5005441 c.11757T>C p.H3919H Substitution - coding silent 15:28141790-28141790 - CN-AML-CR-55-Dx COSM5054227 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - TCGA-D1-A17U-01 COSM960169 c.9726C>T p.D3242D Substitution - coding silent 15:28175617-28175617 - LUAD-B02216 COSM335403 c.12843G>T p.L4281L Substitution - coding silent 15:28125153-28125153 - B106-Tumor COSM4908956 c.14355C>T p.I4785I Substitution - coding silent 15:28111913-28111913 - BD124T COSM5493246 c.5395G>A p.A1799T Substitution - Missense 15:28228287-28228287 - UM-SCC-11B COSM236299 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - CRC-02T COSM5454330 c.1756+2T>C p.? Unknown 15:28265815-28265815 - TCGA-C8-A26W-01 COSM1478011 c.11681C>G p.P3894R Substitution - Missense 15:28142257-28142257 - BN45T COSM4781230 c.13705A>G p.I4569V Substitution - Missense 15:28115446-28115446 - TCGA-D8-A1XK-01 COSM4814052 c.447C>T p.R149R Substitution - coding silent 15:28280163-28280163 - NCI-H209 COSM23122 c.8770C>G p.P2924A Substitution - Missense 15:28186632-28186632 - TCGA-EE-A2GI-06 COSM4892435 c.9036G>A p.K3012K Substitution - coding silent 15:28179014-28179014 - STC263 COSM5032330 c.3827C>T p.A1276V Substitution - Missense 15:28238139-28238139 - Pat_45_B COSM5848956 c.2566G>A p.G856S Substitution - Missense 15:28256269-28256269 - PT46 COSM5929578 c.10628C>G p.A3543G Substitution - Missense 15:28163212-28163212 - TCGA-CK-5916-01 COSM3690317 c.1991G>A p.C664Y Substitution - Missense 15:28263049-28263049 - LIM2405 COSM4641912 c.1384C>T p.R462C Substitution - Missense 15:28269310-28269310 - Detroit_562 COSM4594492 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - TCGA-BH-A0B6-01 COSM4815131 c.8634G>A p.L2878L Substitution - coding silent 15:28190980-28190980 - TCGA-39-5022-01 COSM4858699 c.1507G>A p.D503N Substitution - Missense 15:28268556-28268556 - TCGA-AR-A1AJ-01 COSM249302 c.3176G>A p.R1059H Substitution - Missense 15:28248611-28248611 - P140 COSM5008286 c.382G>A p.V128I Substitution - Missense 15:28280228-28280228 - LUAD-CHTN-MAD06-00678 COSM360805 c.14146C>T p.R4716C Substitution - Missense 15:28113157-28113157 - LUAD-E00443 COSM363729 c.9103A>T p.I3035F Substitution - Missense 15:28178947-28178947 - CN-AML-CR-41-Dx COSM5427070 c.4126C>T p.R1376* Substitution - Nonsense 15:28234162-28234162 - C086 COSM5532288 c.9527C>T p.S3176F Substitution - Missense 15:28176587-28176587 - SNU-175 COSM2083547 c.1345G>A p.A449T Substitution - Missense 15:28269349-28269349 - T578 COSM4690087 c.6738C>A p.F2246L Substitution - Missense 15:28213790-28213790 - CRC-12T COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - TCGA-HU-A4GX-01 COSM4053818 c.12282C>T p.V4094V Substitution - coding silent 15:28132779-28132779 - TCGA-CD-A486-01 COSM4907141 c.1675G>A p.G559R Substitution - Missense 15:28265898-28265898 - HT115 COSM2083245 c.14275T>C p.S4759P Substitution - Missense 15:28111993-28111993 - T1 COSM5618700 c.14118G>A p.E4706E Substitution - coding silent 15:28113185-28113185 - I2L-P17-Tumor-Organoid COSM5362864 c.11816G>C p.R3939T Substitution - Missense 15:28141731-28141731 - T2417 COSM4690109 c.2018C>T p.T673M Substitution - Missense 15:28263022-28263022 - TCGA-DI-A0WH-01 COSM960274 c.1828T>C p.C610R Substitution - Missense 15:28265660-28265660 - 16933 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - KYSE-30 COSM4249886 c.7638G>A p.T2546T Substitution - coding silent 15:28201534-28201534 - PD11748a COSM5767417 c.11278T>A p.C3760S Substitution - Missense 15:28144098-28144098 - TCGA-33-4533-01 COSM4862141 c.127G>A p.G43R Substitution - Missense 15:28299462-28299462 - I2L-P7-Tumor-Organoid COSM4690069 c.9969G>A p.A3323A Substitution - coding silent 15:28174483-28174483 - TCGA-AP-A059-01 COSM4866890 c.9180G>A p.T3060T Substitution - coding silent 15:28177493-28177493 - Detroit_562 COSM4594666 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - 16461 COSM5614205 c.1803A>T p.K601N Substitution - Missense 15:28265685-28265685 - TCGA-D3-A1Q5-06 COSM4899073 c.9953C>T p.S3318L Substitution - Missense 15:28174499-28174499 - LUAD-F00170 COSM366802 c.9448G>A p.G3150S Substitution - Missense 15:28176753-28176753 - ME029T COSM226754 c.6197C>T p.S2066L Substitution - Missense 15:28215634-28215634 - TCGA-18-5592-01 COSM700250 c.2237G>T p.R746L Substitution - Missense 15:28260856-28260856 - 587220 COSM1209574 c.1729C>T p.R577C Substitution - Missense 15:28265844-28265844 - sysucc-1465T COSM1478013 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - SCC-9 COSM4594345 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - T3080 COSM4690062 c.11244C>T p.S3748S Substitution - coding silent 15:28144132-28144132 - TCGA-BR-8368-01 COSM4906944 c.8425T>G p.W2809G Substitution - Missense 15:28191987-28191987 - CRC-21T COSM5479426 c.3236-7C>T p.? Unknown 15:28246904-28246904 - PD13771a COSM5780311 c.10414-6G>T p.? Unknown 15:28167833-28167833 - UM-SCC-11B COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-22-4593-01 COSM700286 c.14398G>A p.A4800T Substitution - Missense 15:28111870-28111870 - TCGA-CG-5721-01 COSM4906808 c.7435C>G p.L2479V Substitution - Missense 15:28202392-28202392 - ESCC_60 COSM5632707 c.12344_12345insT p.W4115fs*15 Insertion - Frameshift 15:28132716-28132717 - TCGA-FV-A23B-01 COSM4914066 c.12010G>A p.G4004R Substitution - Missense 15:28141437-28141437 - RKO COSM2083361 c.8509G>A p.V2837I Substitution - Missense 15:28191187-28191187 - PDA_017 COSM3732885 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - T70 COSM4690061 c.12233C>T p.P4078L Substitution - Missense 15:28132828-28132828 - CRC-19T COSM5481228 c.6727A>G p.T2243A Substitution - Missense 15:28213801-28213801 - TCGA-EE-A181-06 COSM4894629 c.5355C>T p.F1785F Substitution - coding silent 15:28228327-28228327 - pfg213T COSM4751792 c.6377G>A p.R2126H Substitution - Missense 15:28214254-28214254 - TCGA-BS-A0UF-01 COSM960270 c.2039C>A p.S680* Substitution - Nonsense 15:28263001-28263001 - TCGA-AN-A0AK-01 COSM3815787 c.12347G>C p.G4116A Substitution - Missense 15:28132714-28132714 - TCGA-HU-A4G9-01 COSM4053865 c.3111T>C p.C1037C Substitution - coding silent 15:28248676-28248676 - TCGA-BR-4361-01 COSM4053871 c.1642C>T p.Q548* Substitution - Nonsense 15:28265931-28265931 - VLTS-7 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - TCGA-BR-7707-01 COSM4907372 c.1376C>T p.A459V Substitution - Missense 15:28269318-28269318 - P117 COSM5010319 c.11840_11841delCT p.S3947fs*13 Deletion - Frameshift 15:28141606-28141607 - PDA_005 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - Detroit_562 COSM4594491 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - UM-SCC-2 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - PTC_415 COSM4597429 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-D1-A103-01 COSM4874864 c.2984C>T p.T995M Substitution - Missense 15:28254406-28254406 - TCGA-B0-5695-01 COSM470469 c.11627G>T p.R3876M Substitution - Missense 15:28142311-28142311 - TCGA-CC-A5UE-01 COSM4933866 c.888G>T p.L296L Substitution - coding silent 15:28272917-28272917 - B70-Tumor COSM4909016 c.13716C>T p.L4572L Substitution - coding silent 15:28115435-28115435 - I2L-P17-Tumor-Organoid COSM5362863 c.11816G>C p.R3939T Substitution - Missense 15:28141731-28141731 - PDA_018 COSM1129246 c.3631C>T p.R1211C Substitution - Missense 15:28238719-28238719 - TCGA-02-2483 COSM2149154 c.2683T>G p.S895A Substitution - Missense 15:28256152-28256152 - WSU-HN30 COSM4148585 c.18C>G p.F6L Substitution - Missense 15:28321416-28321416 - AOCS-141-8-0 COSM4422328 c.6582C>T p.D2194D Substitution - coding silent 15:28213946-28213946 - T3202 COSM4690095 c.5376G>A p.M1792I Substitution - Missense 15:28228306-28228306 - HCC84T COSM4781293 c.3252T>A p.G1084G Substitution - coding silent 15:28246881-28246881 - TCGA-DK-A2I6-01 COSM4812623 c.6114G>A p.Q2038Q Substitution - coding silent 15:28215717-28215717 - WSU-HN30 COSM4593131 c.32A>G p.Q11R Substitution - Missense 15:28321402-28321402 - TCGA-EE-A2MD-06 COSM3500289 c.8561G>C p.G2854A Substitution - Missense 15:28191053-28191053 - 8034061 COSM3386821 c.6967C>A p.L2323I Substitution - Missense 15:28211104-28211104 - sysucc-1640T COSM4597963 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - PTC-14C COSM4909310 c.2683T>G p.S895A Substitution - Missense 15:28256152-28256152 - T3118 COSM4690096 c.5268G>A p.E1756E Substitution - coding silent 15:28229199-28229199 - CRC-27T COSM4594666 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - TCGA-CA-6718-01 COSM4949133 c.10371C>T p.I3457I Substitution - coding silent 15:28168449-28168449 - UM-SCC-4 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - UM-SCC-11B COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AD-6889-01 COSM1372238 c.11038C>T p.L3680L Substitution - coding silent 15:28144775-28144775 - T2940 COSM4690052 c.13609G>T p.G4537C Substitution - Missense 15:28116665-28116665 - TCGA-BQ-5887-01 COSM4908266 c.12937A>C p.T4313P Substitution - Missense 15:28125059-28125059 - 16933 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - TCGA-B6-A0WY-01 COSM433663 c.11261C>T p.A3754V Substitution - Missense 15:28144115-28144115 - CSCC-10-T COSM700274 c.10992C>T p.I3664I Substitution - coding silent 15:28146253-28146253 - S01170 COSM5667049 c.14072A>G p.Y4691C Substitution - Missense 15:28113231-28113231 - PD9600a COSM5779595 c.4983+10G>T p.? Unknown 15:28229664-28229664 - 2492714 COSM5718993 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - TCGA-B0-4818-01 COSM4856970 c.8548G>T p.V2850L Substitution - Missense 15:28191148-28191148 - TCGA-AR-A0TU-01 COSM4813612 c.7662A>T p.R2554R Substitution - coding silent 15:28201510-28201510 - TCGA-BR-4368-01 COSM4053858 c.5283G>A p.P1761P Substitution - coding silent 15:28228399-28228399 - TCGA-EK-A2H1-01 COSM4822257 c.13988C>G p.S4663C Substitution - Missense 15:28113604-28113604 - BD72T COSM5513075 c.13360T>C p.F4454L Substitution - Missense 15:28117067-28117067 - TCGA-BR-6454-01 COSM4053827 c.10460C>T p.S3487L Substitution - Missense 15:28167781-28167781 - CSCC-7-T COSM4535248 c.216G>T p.K72N Substitution - Missense 15:28292994-28292994 - D-09 COSM4766639 c.5162C>T p.P1721L Substitution - Missense 15:28229305-28229305 - 8044424 COSM4945893 c.5173C>T p.R1725W Substitution - Missense 15:28229294-28229294 - TCGA-BR-4361-01 COSM4053829 c.10398G>A p.W3466* Substitution - Nonsense 15:28168422-28168422 - RKO COSM4647803 c.9376G>A p.G3126S Substitution - Missense 15:28177006-28177006 - TCGA-OL-A5RW-01 COSM4815939 c.2817G>A p.M939I Substitution - Missense 15:28255926-28255926 - 388 COSM97925 c.8424C>A p.C2808* Substitution - Nonsense 15:28191988-28191988 - TCGA-A5-A0GW-01 COSM960141 c.11409A>G p.T3803T Substitution - coding silent 15:28143882-28143882 - TCGA-A5-A0GB-01 COSM4874127 c.5954T>C p.M1985T Substitution - Missense 15:28218563-28218563 - WSU-HN30 COSM4148581 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - PDA_043 COSM5000333 c.9347C>T p.S3116F Substitution - Missense 15:28177035-28177035 - PTC-28C COSM4148584 c.1709G>T p.G570V Substitution - Missense 15:28265864-28265864 - S01563 COSM311754 c.1459G>T p.V487F Substitution - Missense 15:28268604-28268604 - TCGA-70-6723-01 COSM4862063 c.12072G>A p.S4024S Substitution - coding silent 15:28135636-28135636 - TCGA-BR-4362-01 COSM4053831 c.10275G>A p.P3425P Substitution - coding silent 15:28168545-28168545 - UM-SCC-47 COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - T3118 COSM4690055 c.13369G>A p.D4457N Substitution - Missense 15:28117058-28117058 - TCGA-AA-3663-01 COSM4751780 c.12532G>A p.G4178S Substitution - Missense 15:28132138-28132138 - TCGA-HU-8602-01 COSM4906719 c.851A>G p.Q284R Substitution - Missense 15:28272954-28272954 - 2011-2311:2012-362-T COSM4604314 c.13834G>A p.D4612N Substitution - Missense 15:28114691-28114691 - TCGA-60-2720-01 COSM4862397 c.9930G>C p.K3310N Substitution - Missense 15:28174522-28174522 - PD13766a COSM5786875 c.10218C>T p.I3406I Substitution - coding silent 15:28169495-28169495 - CN-AML-CR-62-Dx COSM4594491 c.1008A>G p.P336P Substitution - coding silent 15:28272290-28272290 - P100 COSM5009254 c.13080C>A p.F4360L Substitution - Missense 15:28124145-28124145 - 46M COSM5587984 c.14173G>T p.G4725C Substitution - Missense 15:28113130-28113130 - S39_pre COSM4578149 c.2797_2798delCT p.L933fs*8 Deletion - Frameshift 15:28255945-28255946 - Pat_14_A COSM5848942 c.12514G>T p.G4172W Substitution - Missense 15:28132156-28132156 - 93VU147T COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - 12T COSM109718 c.7628C>T p.A2543V Substitution - Missense 15:28201544-28201544 - TCGA-AX-A0J1-01 COSM960117 c.12943G>A p.A4315T Substitution - Missense 15:28125053-28125053 - TCGA-A6-6653-01 COSM1372267 c.1175C>T p.T392M Substitution - Missense 15:28270777-28270777 - ESO-0292 COSM1241251 c.8843C>T p.A2948V Substitution - Missense 15:28182495-28182495 - TCGA-BQ-5887-01 COSM3987887 c.12937A>C p.T4313P Substitution - Missense 15:28125059-28125059 - CSCC-41-T COSM4458768 c.10997C>T p.S3666F Substitution - Missense 15:28146248-28146248 - TCGA-C5-A1MJ-01 COSM4842829 c.483G>A p.E161E Substitution - coding silent 15:28280127-28280127 - TCGA-EB-A431-01 COSM4892303 c.6363C>T p.S2121S Substitution - coding silent 15:28214268-28214268 - TCGA-B6-A0WY-01 COSM4781888 c.11261C>T p.A3754V Substitution - Missense 15:28144115-28144115 - TCGA-A6-6653-01 COSM1372237 c.11097C>T p.G3699G Substitution - coding silent 15:28144716-28144716 - SC_9091 COSM5550074 c.1535C>T p.A512V Substitution - Missense 15:28268528-28268528 - C658 COSM4443272 c.7999G>T p.G2667W Substitution - Missense 15:28198390-28198390 - PCSI_0142_Pa_P_526 COSM4808371 c.7937G>A p.R2646Q Substitution - Missense 15:28198452-28198452 - pfg272T COSM4751774 c.13529A>C p.E4510A Substitution - Missense 15:28116745-28116745 - CHC1061T COSM4799612 c.3602G>T p.C1201F Substitution - Missense 15:28238748-28238748 - CSCC-15-T COSM4555544 c.6595G>A p.E2199K Substitution - Missense 15:28213933-28213933 - P100 COSM5009258 c.8469G>T p.E2823D Substitution - Missense 15:28191227-28191227 - C135 COSM4617573 c.9487G>A p.A3163T Substitution - Missense 15:28176714-28176714 - LUAD-NYU330 COSM373776 c.9906C>T p.L3302L Substitution - coding silent 15:28174546-28174546 - D28 COSM5545092 c.6103C>T p.L2035F Substitution - Missense 15:28215728-28215728 - TCGA-CG-5721-01 COSM4053845 c.7695A>G p.V2565V Substitution - coding silent 15:28201477-28201477 - TCGA-P4-A5EB-01 COSM4787320 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - P103 COSM5008663 c.8282G>A p.G2761D Substitution - Missense 15:28192130-28192130 - TCGA-D5-6930-01 COSM1372244 c.10361C>T p.A3454V Substitution - Missense 15:28168459-28168459 - AOCS-141-8-0 COSM3981436 c.6582C>T p.D2194D Substitution - coding silent 15:28213946-28213946 - TCGA-D1-A163-01 COSM960282 c.948G>A p.L316L Substitution - coding silent 15:28272350-28272350 - UM-SCC-11B COSM4597961 c.815C>T p.T272M Substitution - Missense 15:28272990-28272990 - HCC159T COSM4780926 c.10633G>T p.D3545Y Substitution - Missense 15:28163207-28163207 - 2208 COSM5015271 c.13121A>G p.D4374G Substitution - Missense 15:28124104-28124104 - 2492711 COSM5718993 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - TCGA-A6-6653-01 COSM4783272 c.1175C>T p.T392M Substitution - Missense 15:28270777-28270777 - PTC_456 COSM5957983 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - sysucc-715T COSM5054226 c.7554G>A p.T2518T Substitution - coding silent 15:28202176-28202176 - SNU-C1 COSM4650963 c.1702G>T p.A568S Substitution - Missense 15:28265871-28265871 - Pat_05_B COSM5848939 c.13922A>G p.E4641G Substitution - Missense 15:28113670-28113670 - 2734_T COSM3956507 c.6990G>T p.R2330R Substitution - coding silent 15:28211081-28211081 - TCGA-AF-5654-01 COSM4946243 c.6647G>A p.R2216H Substitution - Missense 15:28213881-28213881 - UD-SCC-2 COSM4593463 c.952G>T p.D318Y Substitution - Missense 15:28272346-28272346 - PT42 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-ER-A193-06 COSM3500293 c.6864C>T p.N2288N Substitution - coding silent 15:28212506-28212506 - CHC1717T COSM4802091 c.557G>T p.G186V Substitution - Missense 15:28274991-28274991 - TCGA-39-5030-01 COSM4859218 c.3224C>G p.S1075* Substitution - Nonsense 15:28248563-28248563 - TCGA-D5-6927-01 COSM4784862 c.674T>C p.L225S Substitution - Missense 15:28274417-28274417 - TCGA-CG-5726-01 COSM4907043 c.7864T>A p.Y2622N Substitution - Missense 15:28198622-28198622 - 2492714 COSM5718994 c.6464C>T p.S2155F Substitution - Missense 15:28214167-28214167 - TCGA-D1-A15X-01 COSM960185 c.8409C>T p.D2803D Substitution - coding silent 15:28192003-28192003 - Detroit_562 COSM4594918 c.9852C>T p.N3284N Substitution - coding silent 15:28174600-28174600 - T3090 COSM4690071 c.9835T>C p.Y3279H Substitution - Missense 15:28174617-28174617 - CH-60-T2 COSM5651299 c.2936C>G p.S979* Substitution - Nonsense 15:28254454-28254454 - CSCC-41-T COSM4459089 c.11114C>T p.T3705I Substitution - Missense 15:28144699-28144699 - TCGA-AP-A051-01 COSM4872701 c.509G>A p.S170N Substitution - Missense 15:28280101-28280101 - TCGA-EE-A2GO-06 COSM3500305 c.2733C>T p.L911L Substitution - coding silent 15:28256102-28256102 - ESO-K08 COSM1254134 c.10178A>C p.K3393T Substitution - Missense 15:28169535-28169535 - PTC_415 COSM4597963 c.821C>G p.A274G Substitution - Missense 15:28272984-28272984 - TCGA-EE-A181-06 COSM3500310 c.1134C>T p.T378T Substitution - coding silent 15:28270818-28270818 - CN-AML-CR-17-Dx COSM4594608 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - T3225 COSM4690089 c.6459G>A p.L2153L Substitution - coding silent 15:28214172-28214172 - TCGA-AF-5654-01 COSM116806 c.6647G>A p.R2216H Substitution - Missense 15:28213881-28213881 - CPCG0246-F1 COSM4880278 c.5099T>C p.I1700T Substitution - Missense 15:28229481-28229481 - WSU-HN30 COSM4590011 c.836delG p.G279fs*25 Deletion - Frameshift 15:28272969-28272969 - U2940 COSM3500294 c.6728C>T p.T2243I Substitution - Missense 15:28213800-28213800 - TCGA-A5-A0GB-01 COSM4874139 c.11343G>A p.L3781L Substitution - coding silent 15:28143948-28143948 - TCGA-60-2711-01 COSM700269 c.9633G>T p.E3211D Substitution - Missense 15:28176481-28176481 - TCGA-AC-A23H-01 COSM4782525 c.8783C>T p.S2928L Substitution - Missense 15:28186619-28186619 - D28 COSM4894629 c.5355C>T p.F1785F Substitution - coding silent 15:28228327-28228327 - TCGA-AX-A0J0-01 COSM960153 c.10921G>T p.E3641* Substitution - Nonsense 15:28146324-28146324 - TCGA-FS-A1ZD-06 COSM3500271 c.13189-1G>A p.? Unknown 15:28121430-28121430 - UM-SCC-2 COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-51-4081-01 COSM4862341 c.12289G>A p.A4097T Substitution - Missense 15:28132772-28132772 - C086 COSM5532284 c.619T>G p.F207V Substitution - Missense 15:28274929-28274929 - CLL030 COSM1290365 c.4654C>T p.R1552* Substitution - Nonsense 15:28233167-28233167 - WSU-HN13 COSM4597430 c.839G>T p.S280I Substitution - Missense 15:28272966-28272966 - Pat_11_A COSM5848950 c.7628C>T p.A2543V Substitution - Missense 15:28201544-28201544 - 3101B7_041_T COSM5039285 c.1273G>T p.V425F Substitution - Missense 15:28269421-28269421 - PT42 COSM4593324 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-AP-A056-01 COSM4869017 c.12071C>T p.S4024L Substitution - Missense 15:28135637-28135637 - YUMUL COSM5383115 c.727G>A p.E243K Substitution - Missense 15:28274364-28274364 - TCGA-D3-A51T-06 COSM4905489 c.2472G>A p.E824E Substitution - coding silent 15:28257106-28257106 - TCGA-ER-A19N-06 COSM4898899 c.4964G>A p.R1655K Substitution - Missense 15:28229693-28229693 - S02299 COSM5690222 c.9068G>T p.R3023L Substitution - Missense 15:28178982-28178982 - TCGA-EE-A2MT-06 COSM4897530 c.10721C>T p.S3574F Substitution - Missense 15:28163119-28163119 - TCGA-B5-A11U-01 COSM960177 c.8668delA p.I2890fs*3 Deletion - Frameshift 15:28186734-28186734 - PD4109a COSM161514 c.3140G>C p.R1047T Substitution - Missense 15:28248647-28248647 - TCGA-A6-5661-01 COSM4784182 c.778T>C p.F260L Substitution - Missense 15:28274313-28274313 - CSCC-40-T COSM2083572 c.410C>T p.A137V Substitution - Missense 15:28280200-28280200 - TCGA-EE-A181-06 COSM4891783 c.1134C>T p.T378T Substitution - coding silent 15:28270818-28270818 - sysucc-1465T COSM4594666 c.10011C>T p.P3337P Substitution - coding silent 15:28174441-28174441 - 8057683 COSM3386820 c.7674G>A p.L2558L Substitution - coding silent 15:28201498-28201498 - CHC891T COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - PTC_386 COSM4593325 c.905C>T p.T302M Substitution - Missense 15:28272900-28272900 - TCGA-A8-A0AB-01 COSM433666 c.9480T>C p.S3160S Substitution - coding silent 15:28176721-28176721 - TCGA-EE-A181-06 COSM960095 c.14082C>T p.I4694I Substitution - coding silent 15:28113221-28113221 - PTC-50C COSM4148582 c.7411T>C p.S2471P Substitution - Missense 15:28202416-28202416 - TCGA-AX-A0IW-01 COSM4866943 c.12507G>A p.W4169* Substitution - Nonsense 15:28132163-28132163 - TCGA-BR-7703-01 COSM4906408 c.8399G>A p.R2800H Substitution - Missense 15:28192013-28192013 - sysucc-1640T COSM5765430 c.816G>A p.T272T Substitution - coding silent 15:28272989-28272989 - P30 COSM5008232 c.9375C>T p.L3125L Substitution - coding silent 15:28177007-28177007 - TCGA-BS-A0TC-01 COSM960129 c.12309C>T p.S4103S Substitution - coding silent 15:28132752-28132752 - CHC892T COSM4794055 c.5327G>A p.S1776N Substitution - Missense 15:28228355-28228355 - Gp2D COSM4627308 c.1902T>A p.Y634* Substitution - Nonsense 15:28263138-28263138 - TCGA-GF-A6C9-06 COSM4903290 c.7740C>T p.C2580C Substitution - coding silent 15:28198746-28198746 - TCGA-BR-8372-01 COSM2083302 c.10712C>T p.A3571V Substitution - Missense 15:28163128-28163128 - S01504 COSM4386909 c.2074G>T p.G692* Substitution - Nonsense 15:28262966-28262966 - 2293744 COSM4606585 c.10543A>T p.K3515* Substitution - Nonsense 15:28167698-28167698 - TCGA-BR-4361-01 COSM4907815 c.13226T>C p.V4409A Substitution - Missense 15:28121392-28121392 - ESCC_BICR_064T COSM5437090 c.1250C>T p.S417F Substitution - Missense 15:28270702-28270702 - CSCC-29-T COSM4530193 c.1675G>C p.G559R Substitution - Missense 15:28265898-28265898 - S01563 COSM311754 c.1459G>T p.V487F Substitution - Missense 15:28268604-28268604 - TCGA-EE-A2GJ-06 COSM4897314 c.13275C>T p.V4425V Substitution - coding silent 15:28117152-28117152 - YURAY COSM5383108 c.11674_11675CC>TT p.P3892L Substitution - Missense 15:28142263-28142264 - TCGA-AP-A051-01 COSM960149 c.11187C>A p.S3729S Substitution - coding silent 15:28144189-28144189 - PDA_013 COSM4998685 c.5447C>T p.T1816M Substitution - Missense 15:28228235-28228235 - TCGA-HU-A4H8-01 COSM4053862 c.4625G>A p.R1542H Substitution - Missense 15:28233196-28233196 - TCGA-70-6723-01 COSM700279 c.12072G>A p.S4024S Substitution - coding silent 15:28135636-28135636 - pfg008T COSM1640201 c.5846-3delT p.? Unknown 15:28218674-28218674 - CHC1714T COSM4600773 c.7594G>A p.V2532M Substitution - Missense 15:28202136-28202136 - CHEWS024 COSM4578137 c.8700C>T p.I2900I Substitution - coding silent 15:28186702-28186702 - CSCC-10-T COSM4458767 c.10992C>T p.I3664I Substitution - coding silent 15:28146253-28146253 - pfg317T COSM4751778 c.13201C>T p.R4401W Substitution - Missense 15:28121417-28121417 - TCGA-HU-A4GX-01 COSM4906352 c.12282C>T p.V4094V Substitution - coding silent 15:28132779-28132779 - STC246 COSM5054230 c.558C>T p.G186G Substitution - coding silent 15:28274990-28274990 - Pat_53_B COSM5848945 c.11791G>A p.E3931K Substitution - Missense 15:28141756-28141756 - TCGA-HU-A4GX-01 COSM4906342 c.2632G>A p.V878M Substitution - Missense 15:28256203-28256203 - LUAD-YINHD COSM349015 c.12299G>T p.G4100V Substitution - Missense 15:28132762-28132762 - S0029 COSM4459089 c.11114C>T p.T3705I Substitution - Missense 15:28144699-28144699 - tumor_4146289 COSM4594346 c.9979G>A p.V3327M Substitution - Missense 15:28174473-28174473 - SNUH_G45_S1 COSM3999484 c.5580A>G p.G1860G Substitution - coding silent 15:28222100-28222100 - TCGA-BR-8487-01 COSM4906955 c.9309T>C p.D3103D Substitution - coding silent 15:28177073-28177073 - HCT8 COSM2083352 c.8794G>A p.E2932K Substitution - Missense 15:28186608-28186608 - CSCC-27-T COSM4511517 c.8713C>T p.H2905Y Substitution - Missense 15:28186689-28186689 - TCGA-FU-A5XV-01 COSM4844215 c.9164-2A>G p.? Unknown 15:28177511-28177511 - pfg054T COSM4751771 c.13946T>C p.V4649A Substitution - Missense 15:28113646-28113646 - TCGA-D1-A174-01 COSM4875149 c.12849C>T p.D4283D Substitution - coding silent 15:28125147-28125147 - TCGA-D1-A103-01 COSM960250 c.2984C>T p.T995M Substitution - Missense 15:28254406-28254406 - CHC891T COSM4953434 c.990C>A p.A330A Substitution - coding silent 15:28272308-28272308 - TCGA-18-3409-01 COSM4861119 c.11991C>T p.L3997L Substitution - coding silent 15:28141456-28141456 - TCGA-EW-A1J5-01 COSM4813508 c.13070C>G p.S4357C Substitution - Missense 15:28124155-28124155 - K48 COSM249246 c.3593G>T p.G1198V Substitution - Missense 15:28238757-28238757 - 587342 COSM1209590 c.6623C>T p.A2208V Substitution - Missense 15:28213905-28213905 - TCGA-G3-A25Z-01 COSM4922225 c.5829C>A p.D1943E Substitution - Missense 15:28220468-28220468 - PTC_415 COSM5957984 c.839delG p.S280fs*24 Deletion - Frameshift 15:28272966-28272966 - 2492705 COSM5716816 c.6711C>T p.T2237T Substitution - coding silent 15:28213817-28213817 - TCGA-CG-4305-01 COSM4906671 c.7836G>A p.Q2612Q Substitution - coding silent 15:28198650-28198650 - TCGA-D1-A17M-01 COSM960187 c.8271G>A p.A2757A Substitution - coding silent 15:28192141-28192141 - TCGA-22-4593-01 COSM4859082 c.14398G>A p.A4800T Substitution - Missense 15:28111870-28111870 - T3202 COSM4690059 c.12247C>T p.R4083C Substitution - Missense 15:28132814-28132814 - MD-330 COSM74889 c.8284C>G p.R2762G Substitution - Missense 15:28192128-28192128 - TCGA-A8-A06U-01 COSM433665 c.9566G>A p.G3189E Substitution - Missense 15:28176548-28176548 - S00935 COSM311753 c.6906G>T p.S2302S Substitution - coding silent 15:28212464-28212464 - pfg017T COSM281677 c.7660C>T p.R2554* Substitution - Nonsense 15:28201512-28201512 - ESCC_118 COSM5640187 c.12465C>G p.A4155A Substitution - coding silent 15:28132205-28132205 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.434889;Hs.434890 15q13 605837 Hs.740983;Hs.740988;Hs.740989;Hs.740992;Hs.740995;Hs.740999;Hs.741000;Hs.741003;Hs.741007;Hs.741009;Hs.741011;Hs.741013;Hs.741014;Hs.741016;Hs.741017;Hs.741018;Hs.741019 15q13 605837

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.13272+987T>G 15 28365505 CLL A C Missense p.L4801R c.14402T>G 15 28357012 HNSC A C Missense p.N1833K c.5499T>G 15 28467327 LUAD A C Synonymous p.T3977T c.11931T>G 15 28386662 HNSC AGA - InFrameDeletion p.S2637delS c.7909_7911delTCT 15 28443624 COREAD A G Missense p.F2062L c.6184T>C 15 28460793 GBM A G Missense p.I4701T c.14102T>C 15 28358347 HNSC A G Missense p.L2263P c.6788T>C 15 28457728 LUAD A G Missense p.M1985T c.5954T>C 15 28463709 UCEC A G Synonymous p.F1534F c.4602T>C 15 28478365 LUAD A G Synonymous p.G3074G c.9222T>C 15 28422597 UCEC A G Synonymous p.L312L c.934T>C 15 28517510 ESCA A G Synonymous p.L3380L c.10140T>C 15 28414719 RCCC A G Synonymous p.S2540S c.7620T>C 15 28446698 RCCC A G Synonymous p.S3160S c.9480T>C 15 28421867 BRCA A - IntronicDeletion . c.5846-3delT 15 28463820 STAD A T Missense p.L1089Q c.3266T>A 15 28492013 COREAD A T Missense p.L2217Q c.6650T>A 15 28459024 LUSC A T Missense p.Y2622N c.7864T>A 15 28443768 STAD C A Missense p.D1256Y c.3766G>T 15 28483346 LUAD C A Missense p.D1831Y c.5491G>T 15 28467335 UCEC C A Missense p.D4735Y c.14203G>T 15 28358246 ESCA C A Missense p.E3211D c.9633G>T 15 28421627 LUSC C A Missense p.G1671V c.5012G>T 15 28474714 STAD C A Missense p.G171C c.511G>T 15 28525245 UCEC C A Missense p.G2185W c.6553G>T 15 28459224 LUAD C A Missense p.G2659V c.7976G>T 15 28443559 LUAD C A Missense p.G279V c.836G>T 15 28518115 BRCA C A Missense p.G3107W c.9319G>T 15 28422209 LUAD C A Missense p.G3150C c.9448G>T 15 28421899 PRAD C A Missense p.G43V c.128G>T 15 28544607 LUSC C A Missense p.G470V c.1409G>T 15 28514431 RCCC C A Missense p.M1832I c.5496G>T 15 28467330 LUAD C A Missense p.M39I c.117G>T 15 28544618 LUAD C A Missense p.R1271L c.3812G>T 15 28483300 LUAD C A Missense p.R1784L c.5351G>T 15 28473477 RCCC C A Missense p.R2089S c.6267G>T 15 28459892 LUAD C A Missense p.R3876M c.11627G>T 15 28387457 RCCC C A Missense p.R746L c.2237G>T 15 28506002 LUSC C A Missense p.R93M c.278G>T 15 28538078 SCLC C A Missense p.S1637I c.4910G>T 15 28474893 GBM C A Missense p.V1433L c.4297G>T 15 28478864 LUSC C A Missense p.V1505F c.4513G>T 15 28478454 BRCA C A Missense p.V1906F c.5716G>T 15 28465727 CM C A Missense p.V2837L c.8509G>T 15 28436333 LUSC C A Missense p.V2850L c.8548G>T 15 28436294 RCCC C A Missense p.V487F c.1459G>T 15 28513750 SCLC C A Missense p.V830L c.2488G>T 15 28502236 HNSC C A Missense p.W1696L c.5087G>T 15 28474639 LUAD C A Nonsense p.G3956* c.11866G>T 15 28386727 SCLC C A SpliceDonorSNV . c.13609+1G>T 15 28361810 LUAD C A SpliceDonorSNV . c.8937+1G>T 15 28427546 STAD C A Synonymous p.L3503L c.10509G>T 15 28412878 LUAD C A Synonymous p.L4088L c.12264G>T 15 28377943 CM C A Synonymous p.L98L c.294G>T 15 28538062 CM C A Synonymous p.S2302S c.6906G>T 15 28457610 SCLC C A Synonymous p.S3318S c.9954G>T 15 28419644 BRCA C A Synonymous p.V3549V c.10647G>T 15 28408339 CM CC AA Missense p.G3369F c.10105_10106delinsTT 15 28414753 LUAD CC AA MultiAAMissense p.L3173_V3174delinsFL c.9519_9520delinsTT 15 28421740 BLCA CCCCAACTTCCCATCTTCTGCCTCA - Frameshift p.E4065Mfs*16 c.12192_12216delTGAGGCAGAAGATGGGAAGTTGGGG 15 28380638 STAD CC TT Missense p.D3563N c.10686_10687delinsAA 15 28408299 CM C - Frameshift p.C3865Lfs*44 c.11594delG 15 28387490 PRAD C - Frameshift p.G279Efs*25 c.836delG 15 28518115 CM C - Frameshift p.G279Efs*25 c.836delG 15 28518115 GBM C - Frameshift p.G279Efs*25 c.836delG 15 28518115 HNSC - C Frameshift p.L430Vfs*49 c.1287dupG 15 28514553 GBM C - Frameshift p.T725Lfs*23 c.2172delG 15 28506067 UCEC C G Missense p.A2060P c.6178G>C 15 28460799 SCLC C G Missense p.A4523P c.13567G>C 15 28361853 NB C G Missense p.D1362H c.4084G>C 15 28479350 BRCA C G Missense p.D3675H c.11023G>C 15 28389936 LUSC C G Missense p.E1081Q c.3241G>C 15 28492038 LUSC C G Missense p.E3471Q c.10411G>C 15 28413555 HNSC C G Missense p.G2854A c.8561G>C 15 28436199 CM C G Missense p.G3967R c.11899G>C 15 28386694 CM C G Missense p.K3310N c.9930G>C 15 28419668 LUSC C G Missense p.Q3341H c.10023G>C 15 28419575 LUSC C G Missense p.R1047T c.3140G>C 15 28493793 BRCA C G Missense p.R2340P c.7019G>C 15 28456198 LUAD C G Missense p.V3243L c.9727G>C 15 28420762 RCCC C G SpliceAcceptorSNV . c.10230-1G>C 15 28413737 HNSC C G SpliceAcceptorSNV . c.11701-1G>C 15 28386993 ESCA C G Synonymous p.R2022R c.6066G>C 15 28460911 LUSC C T IntronicSNV . c.10747-3717G>A 15 28401693 CLL C T IntronicSNV . c.187+1207G>A 15 28543341 CLL C T IntronicSNV . c.72+5036G>A 15 28561472 CLL C T Missense p.A1119T c.3355G>A 15 28491924 HNSC C T Missense p.A3315T c.9943G>A 15 28419655 UCEC C T Missense p.A4097T c.12289G>A 15 28377918 LUSC C T Missense p.A4800T c.14398G>A 15 28357016 LUSC C T Missense p.D1221N c.3661G>A 15 28483835 HNSC C T Missense p.D3659N c.10975G>A 15 28391416 LUSC C T Missense p.D503N c.1507G>A 15 28513702 LUSC C T Missense p.E2145K c.6433G>A 15 28459344 SCLC C T Missense p.E2189K c.6565G>A 15 28459109 HNSC C T Missense p.E3336K c.10006G>A 15 28419592 COREAD C T Missense p.E3649K c.10945G>A 15 28391446 CM C T Missense p.E3679K c.11035G>A 15 28389924 HNSC C T Missense p.G3189E c.9566G>A 15 28421694 BRCA C T Missense p.G3206E c.9617G>A 15 28421643 CM C T Missense p.G43R c.127G>A 15 28544608 LUSC C T Missense p.G4582E c.13745G>A 15 28359926 PRAD C T Missense p.G4693S c.14077G>A 15 28358372 ESCA C T Missense p.G550R c.1648G>A 15 28511071 OV C T Missense p.G584S c.1750G>A 15 28510969 SCLC C T Missense p.G877S c.2629G>A 15 28501352 LUAD C T Missense p.M797I c.2391G>A 15 28502333 LUSC C T Missense p.R1059H c.3176G>A 15 28493757 BRCA C T Missense p.R1059H c.3176G>A 15 28493757 UCEC C T Missense p.R1655K c.4964G>A 15 28474839 CM C T Missense p.R1784H c.5351G>A 15 28473477 UCEC C T Missense p.R2031Q c.6092G>A 15 28460885 BRCA C T Missense p.R2216H c.6647G>A 15 28459027 OV C T Missense p.R2330Q c.6989G>A 15 28456228 COREAD C T Missense p.R2800H c.8399G>A 15 28437159 STAD C T Missense p.R4089K c.12266G>A 15 28377941 CM C T Missense p.R639K c.1916G>A 15 28508270 CM C T Missense p.V264I c.790G>A 15 28519447 HNSC C T Missense p.V2982I c.8944G>A 15 28424363 CM C T Missense p.V3013M c.9037G>A 15 28424159 UCEC C T Missense p.V4503M c.13507G>A 15 28361913 STAD C T Missense p.V747M c.2239G>A 15 28506000 UCEC C T Nonsense p.W4169* c.12507G>A 15 28377309 UCEC C T SpliceAcceptorSNV . c.12571-1G>A 15 28375741 HNSC C T SpliceAcceptorSNV . c.13189-1G>A 15 28366576 CM C T SpliceDonorSNV . c.12570+1G>A 15 28377245 LUAD C T SpliceDonorSNV . c.12802+1G>A 15 28375308 LUAD C T Synonymous p.A609A c.1827G>A 15 28510807 STAD C T Synonymous p.E1205E c.3615G>A 15 28483881 LUSC C T Synonymous p.E955E c.2865G>A 15 28501024 LUSC C T Synonymous p.K3012K c.9036G>A 15 28424160 CM C T Synonymous p.K3257K c.9771G>A 15 28420718 CM C T Synonymous p.L316L c.948G>A 15 28517496 UCEC C T Synonymous p.L3384L c.10152C>T 15 28414707 GBM C T Synonymous p.L3541L c.10623G>A 15 28408363 BRCA C T Synonymous p.L3781L c.11343G>A 15 28389094 UCEC C T Synonymous p.L76L c.228G>A 15 28538128 HNSC C T Synonymous p.P1325P c.3975G>A 15 28482137 STAD C T Synonymous p.P1761P c.5283G>A 15 28473545 STAD C T Synonymous p.Q1815Q c.5445G>A 15 28473383 CM C T Synonymous p.Q2038Q c.6114G>A 15 28460863 BLCA C T Synonymous p.Q2612Q c.7836G>A 15 28443796 STAD C T Synonymous p.Q3776Q c.11328G>A 15 28389109 CM C T Synonymous p.S4024S c.12072G>A 15 28380782 LUSC C T Synonymous p.T1098T c.3294G>A 15 28491985 UCEC C T Synonymous p.T266T c.798G>A 15 28519439 CM C T Synonymous p.T832T c.2496G>A 15 28502228 UCEC C T Synonymous p.T868T c.2604G>A 15 28501377 RCCC G A IntronicSNV . c.12802+2471C>T 15 28372838 CLL G A IntronicSNV . c.3236-11C>T 15 28492054 NSCLC G A IntronicSNV . c.8649+97C>T 15 28436014 CM G A Missense p.A127V c.380C>T 15 28525376 CM G A Missense p.A185V c.554C>T 15 28520140 LUSC G A Missense p.A2090V c.6269C>T 15 28459890 SCLC G A Missense p.A2757V c.8270C>T 15 28437288 STAD G A Missense p.A3219V c.9656C>T 15 28421604 STAD G A Missense p.A3754V c.11261C>T 15 28389261 BRCA G A Missense p.A3754V c.11261C>T 15 28389261 GBM G A Missense p.A3765V c.11294C>T 15 28389228 HNSC G A Missense p.A568V c.1703C>T 15 28511016 CM G A Missense p.H1981Y c.5941C>T 15 28463722 HNSC G A Missense p.H418Y c.1252C>T 15 28515846 BRCA G A Missense p.H555Y c.1663C>T 15 28511056 BRCA G A Missense p.H731Y c.2191C>T 15 28506048 CM G A Missense p.L1133F c.3397C>T 15 28491207 ESCA G A Missense p.L1786F c.5356C>T 15 28473472 BLCA G A Missense p.L1926F c.5776C>T 15 28465667 LUSC G A Missense p.L3743F c.11227C>T 15 28389295 CM G A Missense p.L3743F c.11227C>T 15 28389295 LUAD G A Missense p.P1428L c.4283C>T 15 28478878 CM G A Missense p.P1428S c.4282C>T 15 28478879 CM G A Missense p.P2262L c.6785C>T 15 28458889 BLCA G A Missense p.P380L c.1139C>T 15 28515959 RCCC G A Missense p.P4292L c.12875C>T 15 28370267 CM G A Missense p.P4522L c.13565C>T 15 28361855 ESCA G A Missense p.P4769S c.14305C>T 15 28357109 STAD G A Missense p.P60L c.179C>T 15 28544556 CM G A Missense p.P789S c.2365C>T 15 28502359 CM G A Missense p.P88L c.263C>T 15 28538093 CM G A Missense p.R1056C c.3166C>T 15 28493767 STAD G A Missense p.R1668C c.5002C>T 15 28474724 CM G A Missense p.R1725W c.5173C>T 15 28474440 OV G A Missense p.R2031W c.6091C>T 15 28460886 ESCA G A Missense p.R2129C c.6385C>T 15 28459392 ESCA G A Missense p.R2151C c.6451C>T 15 28459326 UCEC G A Missense p.R2330W c.6988C>T 15 28456229 LUSC G A Missense p.R2451C c.7351C>T 15 28447622 UCEC G A Missense p.R2646W c.7936C>T 15 28443599 ESCA G A Missense p.R2784C c.8350C>T 15 28437208 CM G A Missense p.R3875W c.11623C>T 15 28387461 ESCA G A Missense p.R3906C c.11716C>T 15 28386977 CM G A Missense p.R4401W c.13201C>T 15 28366563 STAD G A Missense p.R4650W c.13948C>T 15 28358790 LUSC G A Missense p.R471C c.1411C>T 15 28514429 COREAD G A Missense p.R4726W c.14176C>T 15 28358273 CM G A Missense p.R4798C c.14392C>T 15 28357022 HNSC G A Missense p.R807W c.2419C>T 15 28502305 CM G A Missense p.S2066L c.6197C>T 15 28460780 CM G A Missense p.S2173F c.6518C>T 15 28459259 ESCA G A Missense p.S2524F c.7571C>T 15 28447305 CM G A Missense p.S2636F c.7907C>T 15 28443628 CM G A Missense p.S2792L c.8375C>T 15 28437183 BLCA G A Missense p.S3070L c.9209C>T 15 28422610 CM G A Missense p.S3318L c.9953C>T 15 28419645 CM G A Missense p.S3398L c.10193C>T 15 28414666 CM G A Missense p.S3474F c.10421C>T 15 28412966 CM G A Missense p.S3487L c.10460C>T 15 28412927 STAD G A Missense p.S3574F c.10721C>T 15 28408265 CM G A Missense p.S4087F c.12260C>T 15 28377947 HNSC G A Missense p.S4372L c.13115C>T 15 28369256 CM G A Missense p.S816F c.2447C>T 15 28502277 CM G A Missense p.T2050M c.6149C>T 15 28460828 LGG G A Missense p.T2243I c.6728C>T 15 28458946 CM G A Missense p.T2546M c.7637C>T 15 28446681 STAD G A Missense p.T3221I c.9662C>T 15 28421598 CM G A Missense p.T3485I c.10454C>T 15 28412933 CM G A Missense p.T4001M c.12002C>T 15 28386591 STAD G A Nonsense p.Q315* c.943C>T 15 28517501 CM G A Nonsense p.Q3532* c.10594C>T 15 28408392 BLCA G A Nonsense p.R1552* c.4654C>T 15 28478313 CLL G A Nonsense p.R1552* c.4654C>T 15 28478313 CM G A Nonsense p.R1744* c.5230C>T 15 28474383 BRCA G A Nonsense p.R2554* c.7660C>T 15 28446658 STAD G A Nonsense p.R3940* c.11818C>T 15 28386775 LUAD G A Nonsense p.R3940* c.11818C>T 15 28386775 PRAD G A Nonsense p.R4427* c.13279C>T 15 28362294 ESCA G A Synonymous p.A1334A c.4002C>T 15 28482110 CM G A Synonymous p.A137A c.411C>T 15 28525345 CM G A Synonymous p.A4555A c.13665C>T 15 28360632 UCEC G A Synonymous p.A771A c.2313C>T 15 28505926 CM G A Synonymous p.C1994C c.5982C>T 15 28463681 LUAD G A Synonymous p.D4283D c.12849C>T 15 28370293 UCEC G A Synonymous p.D4808D c.14424C>T 15 28356990 UCEC G A Synonymous p.F1118F c.3354C>T 15 28491925 LUSC G A Synonymous p.F1785F c.5355C>T 15 28473473 CM G A Synonymous p.F4719F c.14157C>T 15 28358292 CM G A Synonymous p.F4741F c.14223C>T 15 28358226 CM G A Synonymous p.G1822G c.5466C>T 15 28467360 BLCA G A Synonymous p.G4676G c.14028C>T 15 28358421 CM G A Synonymous p.I3259I c.9777C>T 15 28420712 CM G A Synonymous p.I4694I c.14082C>T 15 28358367 CM G A Synonymous p.I4799I c.14397C>T 15 28357017 BRCA G A Synonymous p.L1133L c.3399C>T 15 28491205 CM G A Synonymous p.L1790L c.5370C>T 15 28473458 STAD G A Synonymous p.L2108L c.6324C>T 15 28459835 HNSC G A Synonymous p.L2162L c.6486C>T 15 28459291 OV G A Synonymous p.L220L c.660C>T 15 28519577 BRCA G A Synonymous p.L805L c.2413C>T 15 28502311 CM G A Synonymous p.L911L c.2733C>T 15 28501248 CM G A Synonymous p.N2288N c.6864C>T 15 28457652 CM G A Synonymous p.P236P c.708C>T 15 28519529 CM G A Synonymous p.S1808S c.5424C>T 15 28473404 CM G A Synonymous p.S1987S c.5961C>T 15 28463702 STAD G A Synonymous p.S356S c.1068C>T 15 28517376 HNSC G A Synonymous p.S4103S c.12309C>T 15 28377898 UCEC G A Synonymous p.T378T c.1134C>T 15 28515964 CM G A Synonymous p.T900T c.2700C>T 15 28501281 UCEC G A Synonymous p.V1436V c.4308C>T 15 28478853 OV G A Synonymous p.V1730V c.5190C>T 15 28474423 CM G A Synonymous p.V2681V c.8043C>T 15 28441684 CM G A Synonymous p.V4251V c.12753C>T 15 28375358 LUAD G A Synonymous p.V4425V c.13275C>T 15 28362298 CM G A Synonymous p.Y3580Y c.10740C>T 15 28408246 UCEC G A Synonymous p.Y4120Y c.12360C>T 15 28377847 CLL G A Synonymous p.Y507Y c.1521C>T 15 28513688 CM G C Missense p.A1157G c.3470C>G 15 28491134 LUAD G C Missense p.I1780M c.5340C>G 15 28473488 BRCA G C Missense p.L3384V c.10150C>G 15 28414709 RCCC G C Missense p.P2924A c.8770C>G 15 28431778 SCLC G C Missense p.P3894R c.11681C>G 15 28387403 BRCA G C Missense p.Q1010E c.3028C>G 15 28499508 RCCC G C Missense p.Q1837E c.5509C>G 15 28467317 BLCA G C Missense p.R2762G c.8284C>G 15 28437274 MB G C Missense p.R2762G c.8284C>G 15 28437274 OV G C Missense p.T2353S c.7058C>G 15 28456159 SCLC G C Nonsense p.S1075* c.3224C>G 15 28493709 LUSC G C Nonsense p.S52* c.155C>G 15 28544580 MM G C Synonymous p.V3973V c.11919C>G 15 28386674 LUSC GG AA Missense p.Q3309* c.9924_9925delinsTT 15 28419673 CM GG AA Missense p.R4655C c.13962_13963delinsTT 15 28358775 CM G T Missense p.A4002D c.12005C>A 15 28386588 HNSC G T Missense p.H287Q c.861C>A 15 28518090 SCLC G T Missense p.L3757M c.11269C>A 15 28389253 AML G T Missense p.P1432T c.4294C>A 15 28478867 BRCA G T Missense p.P278T c.832C>A 15 28518119 ESCA G T Missense p.P3531H c.10592C>A 15 28408394 HNSC G T Missense p.P88H c.263C>A 15 28538093 STAD G T Missense p.S3001Y c.9002C>A 15 28424305 LUAD G T Synonymous p.A2497A c.7491C>A 15 28447385 STAD G T Synonymous p.A4149A c.12447C>A 15 28377369 COREAD G T Synonymous p.P282P c.846C>A 15 28518105 LUSC G T Synonymous p.P282P c.846C>A 15 28518105 NSCLC G T Synonymous p.R4293R c.12877C>A 15 28370265 LUSC G T Synonymous p.S3437S c.10311C>A 15 28413655 STAD TACCTCACTGAGGTCCGCGA - SpliceDonorDeletion . c.13706_13722+3delTCGCGGACCTCAGTGAGGTA 15 28360572 BRCA T A Missense p.D3567V c.10700A>T 15 28408286 HNSC T A Missense p.K1064N c.3192A>T 15 28493741 CM T A Missense p.K3716N c.11148A>T 15 28389374 CLL T A Missense p.K601N c.1803A>T 15 28510831 NSCLC T A Missense p.Q2259L c.6776A>T 15 28458898 LUAD T A Missense p.Q2310H c.6930A>T 15 28456287 NSCLC T A Missense p.R3836W c.11506A>T 15 28388011 HNSC T A Missense p.S3539C c.10615A>T 15 28408371 OV T A Nonsense p.K1656* c.4966A>T 15 28474837 ESCA T A Synonymous p.R2554R c.7662A>T 15 28446656 BRCA T C Missense p.D3721G c.11162A>G 15 28389360 CM T C Missense p.D991G c.2972A>G 15 28499564 CM T C Missense p.E955G c.2864A>G 15 28501025 LUSC T C Missense p.I1210M c.3630A>G 15 28483866 BRCA T C Missense p.I152V c.454A>G 15 28525302 LUAD T C Missense p.K1446R c.4337A>G 15 28478824 COREAD T C Missense p.K2300R c.6899A>G 15 28457617 LUAD T C Missense p.N1827S c.5480A>G 15 28467346 HNSC T C Missense p.N3793S c.11378A>G 15 28389059 LGG T C Missense p.T3098A c.9292A>G 15 28422236 STAD T C Missense p.Y1123C c.3368A>G 15 28491911 HNSC T C Missense p.Y4630C c.13889A>G 15 28359782 LUAD T C Synonymous p.P107P c.321A>G 15 28538035 STAD T C Synonymous p.T2988T c.8964A>G 15 28424343 LUAD T C Synonymous p.T3803T c.11409A>G 15 28389028 UCEC T - Frameshift p.I2890Lfs*3 c.8668delA 15 28431880 UCEC - T Frameshift p.R2554Tfs*3 c.7659dupA 15 28446659 HNSC T G Missense p.K2054T c.6161A>C 15 28460816 LUSC T G Missense p.K3393T c.10178A>C 15 28414681 ESCA T G Missense p.K4402N c.13206A>C 15 28366558 RCCC T G Missense p.S3912R c.11734A>C 15 28386959 CM T G Missense p.T3325P c.9973A>C 15 28419625 HNSC - T IntronicInsertion . c.72+1240dupA 15 28565268 STAD