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 11 36596616 36596616 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr11:36596616G>T c.1762G>T c.(1762-1764)Gat>Tat p.D588Y ACC 11 36597790 36597790 + Missense_Mutation SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr11:36597790C>A c.2936C>A c.(2935-2937)gCc>gAc p.A979D BLCA 11 36594953 36594953 + Silent SNP C C T TCGA-DK-AA6Q-01A-11D-A391-08 TCGA-DK-AA6Q-10A-01D-A394-08 g.chr11:36594953C>T c.99C>T c.(97-99)ttC>ttT p.F33F BLCA 11 36595001 36595001 + Silent SNP G G A TCGA-BL-A3JM-01A-12D-A21A-08 TCGA-BL-A3JM-11A-31D-A21A-08 g.chr11:36595001G>A c.147G>A c.(145-147)aaG>aaA p.K49K BLCA 11 36595452 36595452 + Missense_Mutation SNP G G A TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr11:36595452G>A c.598G>A c.(598-600)Gtg>Atg p.V200M BLCA 11 36595984 36595984 + Nonsense_Mutation SNP C C G TCGA-GC-A6I3-01A-11D-A31L-08 TCGA-GC-A6I3-10A-01D-A31J-08 g.chr11:36595984C>G c.1130C>G c.(1129-1131)tCa>tGa p.S377* BLCA 11 36596435 36596435 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:36596435G>T c.1581G>T c.(1579-1581)aaG>aaT p.K527N BLCA 11 36597157 36597157 + Missense_Mutation SNP A A G TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr11:36597157A>G c.2303A>G c.(2302-2304)tAc>tGc p.Y768C BLCA 11 36597187 36597187 + Frame_Shift_Del DEL G G - TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr11:36597187delG c.2333delG c.(2332-2334)cggfs p.R778fs BLCA 11 36597335 36597335 + Missense_Mutation SNP G G T TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr11:36597335G>T c.2481G>T c.(2479-2481)gaG>gaT p.E827D BRCA 11 36595236 36595236 + Missense_Mutation SNP C C G TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr11:36595236C>G c.382C>G c.(382-384)Cca>Gca p.P128A BRCA 11 36595756 36595756 + Missense_Mutation SNP C C A TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr11:36595756C>A c.902C>A c.(901-903)gCt>gAt p.A301D BRCA 11 36595870 36595870 + Missense_Mutation SNP A A T TCGA-B6-A0RG-01A-11W-A071-09 TCGA-B6-A0RG-10A-01W-A071-09 g.chr11:36595870A>T c.1016A>T c.(1015-1017)gAc>gTc p.D339V BRCA 11 36596585 36596585 + Silent SNP C C T TCGA-AR-A24Q-01A-12D-A167-09 TCGA-AR-A24Q-10A-01D-A167-09 g.chr11:36596585C>T c.1731C>T c.(1729-1731)atC>atT p.I577I BRCA 11 36597190 36597190 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:36597190T>G c.2336T>G c.(2335-2337)gTg>gGg p.V779G BRCA 11 36597221 36597221 + Silent SNP G G A TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr11:36597221G>A c.2367G>A c.(2365-2367)gaG>gaA p.E789E BRCA 11 36597333 36597333 + Missense_Mutation SNP G G C TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr11:36597333G>C c.2479G>C c.(2479-2481)Gag>Cag p.E827Q BRCA 11 36597340 36597340 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:36597340G>T c.2486G>T c.(2485-2487)aGg>aTg p.R829M BRCA 11 36597453 36597453 + Missense_Mutation SNP G G A TCGA-AR-A1AI-01A-11D-A12Q-09 TCGA-AR-A1AI-10A-01D-A12Q-09 g.chr11:36597453G>A c.2599G>A c.(2599-2601)Gat>Aat p.D867N CESC 11 36595309 36595309 + Missense_Mutation SNP C C T TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr11:36595309C>T c.455C>T c.(454-456)cCg>cTg p.P152L CESC 11 36596661 36596661 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:36596661G>C c.1807G>C c.(1807-1809)Gat>Cat p.D603H CHOL 11 36597457 36597457 + Missense_Mutation SNP C C T TCGA-W5-AA34-01A-11D-A417-09 TCGA-W5-AA34-10A-01D-A41A-09 g.chr11:36597457C>T c.2603C>T c.(2602-2604)gCa>gTa p.A868V COAD 11 36594954 36594954 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:36594954C>T c.100C>T c.(100-102)Cgg>Tgg p.R34W COAD 11 36594979 36594979 + Missense_Mutation SNP C C A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:36594979C>A c.125C>A c.(124-126)cCt>cAt p.P42H COAD 11 36595136 36595136 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr11:36595136C>T c.282C>T c.(280-282)aaC>aaT p.N94N COAD 11 36595417 36595417 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:36595417G>A c.563G>A c.(562-564)aGc>aAc p.S188N COAD 11 36595451 36595451 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:36595451C>T c.597C>T c.(595-597)aaC>aaT p.N199N COAD 11 36596059 36596059 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:36596059T>C c.1205T>C c.(1204-1206)cTg>cCg p.L402P COAD 11 36596344 36596344 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:36596344G>A c.1490G>A c.(1489-1491)aGa>aAa p.R497K COAD 11 36596384 36596384 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:36596384G>A c.1530G>A c.(1528-1530)gaG>gaA p.E510E COAD 11 36596423 36596423 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:36596423G>A c.1569G>A c.(1567-1569)caG>caA p.Q523Q COAD 11 36596580 36596580 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:36596580G>T c.1726G>T c.(1726-1728)Gac>Tac p.D576Y COAD 11 36596672 36596672 + Silent SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COAD 11 36596672 36596672 + Silent SNP A A G TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COAD 11 36596672 36596672 + Silent SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COAD 11 36596672 36596672 + Silent SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COAD 11 36596790 36596790 + Nonsense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:36596790G>T c.1936G>T c.(1936-1938)Gaa>Taa p.E646* COAD 11 36596837 36596837 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:36596837G>A c.1983G>A c.(1981-1983)atG>atA p.M661I COAD 11 36596847 36596847 + Nonsense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:36596847G>T c.1993G>T c.(1993-1995)Gag>Tag p.E665* COAD 11 36596863 36596863 + Missense_Mutation SNP C C T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr11:36596863C>T c.2009C>T c.(2008-2010)aCg>aTg p.T670M COAD 11 36596949 36596949 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:36596949C>T c.2095C>T c.(2095-2097)Cgg>Tgg p.R699W COAD 11 36597197 36597197 + Silent SNP G G C TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr11:36597197G>C c.2343G>C c.(2341-2343)ggG>ggC p.G781G COAD 11 36597544 36597544 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:36597544G>A c.2690G>A c.(2689-2691)cGa>cAa p.R897Q COAD 11 36597631 36597631 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36597631A>C c.2777A>C c.(2776-2778)aAg>aCg p.K926T COADREAD 11 36594954 36594954 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:36594954C>T c.100C>T c.(100-102)Cgg>Tgg p.R34W COADREAD 11 36594979 36594979 + Missense_Mutation SNP C C A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:36594979C>A c.125C>A c.(124-126)cCt>cAt p.P42H COADREAD 11 36595001 36595001 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:36595001G>T c.147G>T c.(145-147)aaG>aaT p.K49N COADREAD 11 36595136 36595136 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr11:36595136C>T c.282C>T c.(280-282)aaC>aaT p.N94N COADREAD 11 36595361 36595361 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:36595361G>A c.507G>A c.(505-507)tcG>tcA p.S169S COADREAD 11 36595417 36595417 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:36595417G>A c.563G>A c.(562-564)aGc>aAc p.S188N COADREAD 11 36595451 36595451 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:36595451C>T c.597C>T c.(595-597)aaC>aaT p.N199N COADREAD 11 36596059 36596059 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:36596059T>C c.1205T>C c.(1204-1206)cTg>cCg p.L402P COADREAD 11 36596344 36596344 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:36596344G>A c.1490G>A c.(1489-1491)aGa>aAa p.R497K COADREAD 11 36596384 36596384 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:36596384G>A c.1530G>A c.(1528-1530)gaG>gaA p.E510E COADREAD 11 36596423 36596423 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:36596423G>A c.1569G>A c.(1567-1569)caG>caA p.Q523Q COADREAD 11 36596514 36596514 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:36596514G>A c.1660G>A c.(1660-1662)Gac>Aac p.D554N COADREAD 11 36596580 36596580 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:36596580G>T c.1726G>T c.(1726-1728)Gac>Tac p.D576Y COADREAD 11 36596672 36596672 + Silent SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COADREAD 11 36596672 36596672 + Silent SNP A A G TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COADREAD 11 36596672 36596672 + Silent SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COADREAD 11 36596672 36596672 + Silent SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COADREAD 11 36596672 36596672 + Silent SNP A A G TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G COADREAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COADREAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COADREAD 11 36596716 36596716 + Missense_Mutation SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr11:36596716A>G c.1862A>G c.(1861-1863)aAg>aGg p.K621R COADREAD 11 36596790 36596790 + Nonsense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:36596790G>T c.1936G>T c.(1936-1938)Gaa>Taa p.E646* COADREAD 11 36596837 36596837 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:36596837G>A c.1983G>A c.(1981-1983)atG>atA p.M661I COADREAD 11 36596847 36596847 + Nonsense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:36596847G>T c.1993G>T c.(1993-1995)Gag>Tag p.E665* COADREAD 11 36596863 36596863 + Missense_Mutation SNP C C T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr11:36596863C>T c.2009C>T c.(2008-2010)aCg>aTg p.T670M COADREAD 11 36596949 36596949 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:36596949C>T c.2095C>T c.(2095-2097)Cgg>Tgg p.R699W COADREAD 11 36596949 36596949 + Missense_Mutation SNP C C T TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr11:36596949C>T c.2095C>T c.(2095-2097)Cgg>Tgg p.R699W COADREAD 11 36597197 36597197 + Silent SNP G G C TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr11:36597197G>C c.2343G>C c.(2341-2343)ggG>ggC p.G781G COADREAD 11 36597544 36597544 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:36597544G>A c.2690G>A c.(2689-2691)cGa>cAa p.R897Q COADREAD 11 36597631 36597631 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36597631A>C c.2777A>C c.(2776-2778)aAg>aCg p.K926T COADREAD 11 36597747 36597747 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:36597747G>T c.2893G>T c.(2893-2895)Gag>Tag p.E965* ESCA 11 36595270 36595270 + Missense_Mutation SNP G G T TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr11:36595270G>T c.416G>T c.(415-417)gGc>gTc p.G139V ESCA 11 36596040 36596040 + Missense_Mutation SNP C C T TCGA-XP-A8T6-01A-11D-A36J-09 TCGA-XP-A8T6-10A-01D-A36M-09 g.chr11:36596040C>T c.1186C>T c.(1186-1188)Cgc>Tgc p.R396C ESCA 11 36596307 36596307 + Missense_Mutation SNP C C A TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr11:36596307C>A c.1453C>A c.(1453-1455)Cac>Aac p.H485N ESCA 11 36596806 36596806 + Missense_Mutation SNP C C G TCGA-IG-A5B8-01A-11D-A28B-09 TCGA-IG-A5B8-10A-01D-A28E-09 g.chr11:36596806C>G c.1952C>G c.(1951-1953)tCt>tGt p.S651C ESCA 11 36596847 36596847 + Nonsense_Mutation SNP G G T TCGA-IG-A6QS-01A-12D-A33E-09 TCGA-IG-A6QS-10B-01D-A33H-09 g.chr11:36596847G>T c.1993G>T c.(1993-1995)Gag>Tag p.E665* ESCA 11 36597527 36597527 + Silent SNP G G A TCGA-L5-A4OU-01A-11D-A28B-09 TCGA-L5-A4OU-11A-11D-A28E-09 g.chr11:36597527G>A c.2673G>A c.(2671-2673)aaG>aaA p.K891K GBM 11 36595309 36595309 + Missense_Mutation SNP C C T TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chr11:36595309C>T c.455C>T c.(454-456)cCg>cTg p.P152L GBM 11 36596029 36596029 + Missense_Mutation SNP G G T TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr11:36596029G>T c.1175G>T c.(1174-1176)gGg>gTg p.G392V GBM 11 36596275 36596275 + Missense_Mutation SNP G G A TCGA-06-0237-01A-02D-1491-08 TCGA-06-0237-10A-01D-1491-08 g.chr11:36596275G>A c.1421G>A c.(1420-1422)cGt>cAt p.R474H GBM 11 36596452 36596452 + Missense_Mutation SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr11:36596452C>T c.1598C>T c.(1597-1599)aCt>aTt p.T533I GBM 11 36596877 36596877 + Silent SNP C C T TCGA-27-1830-01A-01W-0643-08 TCGA-27-1830-10A-01W-0644-08 g.chr11:36596877C>T c.2023C>T c.(2023-2025)Ctg>Ttg p.L675L GBM 11 36597064 36597064 + Missense_Mutation SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr11:36597064G>A c.2210G>A c.(2209-2211)cGt>cAt p.R737H GBMLGG 11 36595107 36595107 + Missense_Mutation SNP C C T TCGA-P5-A730-01A-11D-A32B-08 TCGA-P5-A730-10A-01D-A329-08 g.chr11:36595107C>T c.253C>T c.(253-255)Cct>Tct p.P85S GBMLGG 11 36595309 36595309 + Missense_Mutation SNP C C T TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chr11:36595309C>T c.455C>T c.(454-456)cCg>cTg p.P152L GBMLGG 11 36596029 36596029 + Missense_Mutation SNP G G T TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr11:36596029G>T c.1175G>T c.(1174-1176)gGg>gTg p.G392V GBMLGG 11 36596275 36596275 + Missense_Mutation SNP G G A TCGA-06-0237-01A-02D-1491-08 TCGA-06-0237-10A-01D-1491-08 g.chr11:36596275G>A c.1421G>A c.(1420-1422)cGt>cAt p.R474H GBMLGG 11 36596452 36596452 + Missense_Mutation SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr11:36596452C>T c.1598C>T c.(1597-1599)aCt>aTt p.T533I GBMLGG 11 36596598 36596598 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36596598A>G c.1744A>G c.(1744-1746)Aga>Gga p.R582G GBMLGG 11 36596675 36596675 + Silent SNP C C T TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr11:36596675C>T c.1821C>T c.(1819-1821)gaC>gaT p.D607D GBMLGG 11 36596877 36596877 + Silent SNP C C T TCGA-27-1830-01A-01W-0643-08 TCGA-27-1830-10A-01W-0644-08 g.chr11:36596877C>T c.2023C>T c.(2023-2025)Ctg>Ttg p.L675L GBMLGG 11 36597064 36597064 + Missense_Mutation SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr11:36597064G>A c.2210G>A c.(2209-2211)cGt>cAt p.R737H HNSC 11 36594923 36594923 + Missense_Mutation SNP T T G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:36594923T>G c.69T>G c.(67-69)atT>atG p.I23M HNSC 11 36595094 36595094 + Missense_Mutation SNP G G C TCGA-CQ-6221-01A-11D-2078-08 TCGA-CQ-6221-10A-01D-2078-08 g.chr11:36595094G>C c.240G>C c.(238-240)ttG>ttC p.L80F HNSC 11 36595444 36595444 + Missense_Mutation SNP C C T TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr11:36595444C>T c.590C>T c.(589-591)cCg>cTg p.P197L HNSC 11 36595801 36595801 + Missense_Mutation SNP G G T TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr11:36595801G>T c.947G>T c.(946-948)tGc>tTc p.C316F HNSC 11 36596040 36596040 + Missense_Mutation SNP C C T TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr11:36596040C>T c.1186C>T c.(1186-1188)Cgc>Tgc p.R396C HNSC 11 36596713 36596713 + Missense_Mutation SNP A A G TCGA-MZ-A6I9-01A-11D-A31L-08 TCGA-MZ-A6I9-10A-01D-A31J-08 g.chr11:36596713A>G c.1859A>G c.(1858-1860)gAa>gGa p.E620G HNSC 11 36597294 36597294 + Missense_Mutation SNP G G C TCGA-UF-A7JV-01A-11D-A34J-08 TCGA-UF-A7JV-10A-01D-A34M-08 g.chr11:36597294G>C c.2440G>C c.(2440-2442)Gag>Cag p.E814Q HNSC 11 36597387 36597387 + Missense_Mutation SNP A A T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:36597387A>T c.2533A>T c.(2533-2535)Aac>Tac p.N845Y HNSC 11 36597850 36597850 + Missense_Mutation SNP C C G TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chr11:36597850C>G c.2996C>G c.(2995-2997)tCc>tGc p.S999C HNSC 11 36597916 36597916 + Missense_Mutation SNP C C A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:36597916C>A c.3062C>A c.(3061-3063)cCt>cAt p.P1021H KIPAN 11 36596889 36596889 + Missense_Mutation SNP A A C TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr11:36596889A>C c.2035A>C c.(2035-2037)Att>Ctt p.I679L KIRP 11 36596889 36596889 + Missense_Mutation SNP A A C TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr11:36596889A>C c.2035A>C c.(2035-2037)Att>Ctt p.I679L LGG 11 36595107 36595107 + Missense_Mutation SNP C C T TCGA-P5-A730-01A-11D-A32B-08 TCGA-P5-A730-10A-01D-A329-08 g.chr11:36595107C>T c.253C>T c.(253-255)Cct>Tct p.P85S LGG 11 36596598 36596598 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36596598A>G c.1744A>G c.(1744-1746)Aga>Gga p.R582G LGG 11 36596675 36596675 + Silent SNP C C T TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr11:36596675C>T c.1821C>T c.(1819-1821)gaC>gaT p.D607D LIHC 11 36594873 36594873 + Frame_Shift_Del DEL C C - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr11:36594873delC c.19delC c.(19-21)cccfs p.P7fs LIHC 11 36595110 36595110 + Nonsense_Mutation SNP A A T TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chr11:36595110A>T c.256A>T c.(256-258)Aag>Tag p.K86* LIHC 11 36595488 36595488 + Missense_Mutation SNP G G T TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chr11:36595488G>T c.634G>T c.(634-636)Gac>Tac p.D212Y LIHC 11 36596385 36596385 + Nonsense_Mutation SNP A A T TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr11:36596385A>T c.1531A>T c.(1531-1533)Aag>Tag p.K511* LIHC 11 36596843 36596843 + Silent SNP A A C TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr11:36596843A>C c.1989A>C c.(1987-1989)gcA>gcC p.A663A LIHC 11 36597181 36597181 + Missense_Mutation SNP G G T TCGA-DD-AAD2-01A-11D-A40R-10 TCGA-DD-AAD2-10A-01D-A40U-10 g.chr11:36597181G>T c.2327G>T c.(2326-2328)cGg>cTg p.R776L LIHC 11 36597509 36597509 + Silent SNP G G A TCGA-KR-A7K0-01A-12D-A33Q-10 TCGA-KR-A7K0-10A-01D-A33Q-10 g.chr11:36597509G>A c.2655G>A c.(2653-2655)ctG>ctA p.L885L LIHC 11 36597714 36597714 + Missense_Mutation SNP G G T TCGA-DD-A113-01A-11D-A12Z-10 TCGA-DD-A113-10A-01D-A12Z-10 g.chr11:36597714G>T c.2860G>T c.(2860-2862)Ggc>Tgc p.G954C LUAD 11 36594881 36594881 + Missense_Mutation SNP G G C TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr11:36594881G>C c.27G>C c.(25-27)ttG>ttC p.L9F LUAD 11 36594888 36594888 + Missense_Mutation SNP A A C TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chr11:36594888A>C c.34A>C c.(34-36)Agt>Cgt p.S12R LUAD 11 36594898 36594898 + Missense_Mutation SNP C C T TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr11:36594898C>T c.44C>T c.(43-45)cCa>cTa p.P15L LUAD 11 36594961 36594961 + Missense_Mutation SNP G G T TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr11:36594961G>T c.107G>T c.(106-108)aGa>aTa p.R36I LUAD 11 36594979 36594979 + Missense_Mutation SNP C C A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr11:36594979C>A c.125C>A c.(124-126)cCt>cAt p.P42H LUAD 11 36594998 36594998 + Missense_Mutation SNP A A T TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr11:36594998A>T c.144A>T c.(142-144)gaA>gaT p.E48D LUAD 11 36595046 36595046 + Silent SNP A A T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr11:36595046A>T c.192A>T c.(190-192)gcA>gcT p.A64A LUAD 11 36595131 36595131 + Missense_Mutation SNP G G C TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr11:36595131G>C c.277G>C c.(277-279)Gac>Cac p.D93H LUAD 11 36595368 36595368 + Missense_Mutation SNP C C A TCGA-86-8054-01A-11D-2238-08 TCGA-86-8054-10A-01D-2238-08 g.chr11:36595368C>A c.514C>A c.(514-516)Ccc>Acc p.P172T LUAD 11 36595447 36595447 + Missense_Mutation SNP G G A TCGA-17-Z054-01A-01W-0747-08 TCGA-17-Z054-11A-01W-0747-08 g.chr11:36595447G>A c.593G>A c.(592-594)aGg>aAg p.R198K LUAD 11 36595593 36595593 + Missense_Mutation SNP C C T TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr11:36595593C>T c.739C>T c.(739-741)Cgt>Tgt p.R247C LUAD 11 36595703 36595703 + Missense_Mutation SNP C C A TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chr11:36595703C>A c.849C>A c.(847-849)ttC>ttA p.F283L LUAD 11 36595843 36595843 + Missense_Mutation SNP C C A TCGA-62-A46R-01A-11D-A24D-08 TCGA-62-A46R-10A-01D-A24F-08 g.chr11:36595843C>A c.989C>A c.(988-990)tCt>tAt p.S330Y LUAD 11 36595901 36595901 + Missense_Mutation SNP C C A TCGA-NJ-A55R-01A-11D-A25L-08 TCGA-NJ-A55R-10A-01D-A25L-08 g.chr11:36595901C>A c.1047C>A c.(1045-1047)agC>agA p.S349R LUAD 11 36595915 36595915 + Missense_Mutation SNP T T A TCGA-75-7031-01A-11D-1945-08 TCGA-75-7031-10A-01D-1946-08 g.chr11:36595915T>A c.1061T>A c.(1060-1062)cTg>cAg p.L354Q LUAD 11 36595976 36595976 + Missense_Mutation SNP C C G TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr11:36595976C>G c.1122C>G c.(1120-1122)caC>caG p.H374Q LUAD 11 36596039 36596039 + Silent SNP C C A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr11:36596039C>A c.1185C>A c.(1183-1185)ccC>ccA p.P395P LUAD 11 36596221 36596221 + Missense_Mutation SNP C C T TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr11:36596221C>T c.1367C>T c.(1366-1368)gCc>gTc p.A456V LUAD 11 36596315 36596315 + Missense_Mutation SNP G G A TCGA-55-8514-01A-11D-2393-08 TCGA-55-8514-10A-01D-2393-08 g.chr11:36596315G>A c.1461G>A c.(1459-1461)atG>atA p.M487I LUAD 11 36596358 36596358 + Missense_Mutation SNP C C T TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr11:36596358C>T c.1504C>T c.(1504-1506)Cct>Tct p.P502S LUAD 11 36596365 36596365 + Missense_Mutation SNP A A C TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr11:36596365A>C c.1511A>C c.(1510-1512)cAt>cCt p.H504P LUAD 11 36596398 36596398 + Missense_Mutation SNP C C A TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr11:36596398C>A c.1544C>A c.(1543-1545)cCa>cAa p.P515Q LUAD 11 36596428 36596428 + Missense_Mutation SNP C C A TCGA-93-7348-01A-21D-2036-08 TCGA-93-7348-10A-01D-2036-08 g.chr11:36596428C>A c.1574C>A c.(1573-1575)cCt>cAt p.P525H LUAD 11 36596535 36596535 + Missense_Mutation SNP C C T TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr11:36596535C>T c.1681C>T c.(1681-1683)Cgc>Tgc p.R561C LUAD 11 36596541 36596541 + Missense_Mutation SNP G G T TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-10A-01D-2036-08 g.chr11:36596541G>T c.1687G>T c.(1687-1689)Gat>Tat p.D563Y LUAD 11 36596655 36596655 + Missense_Mutation SNP T T C TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr11:36596655T>C c.1801T>C c.(1801-1803)Tct>Cct p.S601P LUAD 11 36596881 36596881 + Missense_Mutation SNP G G C TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr11:36596881G>C c.2027G>C c.(2026-2028)aGt>aCt p.S676T LUAD 11 36596940 36596940 + Missense_Mutation SNP G G T TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr11:36596940G>T c.2086G>T c.(2086-2088)Ggc>Tgc p.G696C LUAD 11 36597068 36597068 + Silent SNP G G C TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr11:36597068G>C c.2214G>C c.(2212-2214)ctG>ctC p.L738L LUAD 11 36597072 36597072 + Missense_Mutation SNP G G T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:36597072G>T c.2218G>T c.(2218-2220)Gcc>Tcc p.A740S LUAD 11 36597145 36597145 + Missense_Mutation SNP G G T TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr11:36597145G>T c.2291G>T c.(2290-2292)cGt>cTt p.R764L LUAD 11 36597180 36597180 + Silent SNP C C A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr11:36597180C>A c.2326C>A c.(2326-2328)Cgg>Agg p.R776R LUAD 11 36597194 36597194 + Missense_Mutation SNP A A T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr11:36597194A>T c.2340A>T c.(2338-2340)aaA>aaT p.K780N LUAD 11 36597288 36597288 + Missense_Mutation SNP C C G TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr11:36597288C>G c.2434C>G c.(2434-2436)Cag>Gag p.Q812E LUAD 11 36597395 36597395 + Silent SNP A A G TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr11:36597395A>G c.2541A>G c.(2539-2541)aaA>aaG p.K847K LUAD 11 36597424 36597424 + Missense_Mutation SNP C C T TCGA-50-6595-01A-12D-1855-08 TCGA-50-6595-11A-01D-1855-08 g.chr11:36597424C>T c.2570C>T c.(2569-2571)gCc>gTc p.A857V LUAD 11 36597479 36597479 + Silent SNP C C T TCGA-38-4627-01A-01D-1553-08 TCGA-38-4627-11A-01D-1553-08 g.chr11:36597479C>T c.2625C>T c.(2623-2625)tcC>tcT p.S875S LUAD 11 36597537 36597537 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr11:36597537G>T c.2683G>T c.(2683-2685)Gta>Tta p.V895L LUAD 11 36597635 36597635 + Missense_Mutation SNP C C G TCGA-69-8253-01A-11D-2284-08 TCGA-69-8253-10A-01D-2284-08 g.chr11:36597635C>G c.2781C>G c.(2779-2781)ttC>ttG p.F927L LUAD 11 36597777 36597777 + Silent SNP C C A TCGA-49-6761-01A-31D-1945-08 TCGA-49-6761-11A-01D-1945-08 g.chr11:36597777C>A c.2923C>A c.(2923-2925)Cgg>Agg p.R975R LUAD 11 36597979 36597979 + Missense_Mutation SNP A A G TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:36597979A>G c.3125A>G c.(3124-3126)gAa>gGa p.E1042G LUSC 11 36595189 36595189 + Missense_Mutation SNP G G T TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chr11:36595189G>T c.335G>T c.(334-336)cGc>cTc p.R112L LUSC 11 36595199 36595199 + Silent SNP G G T TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr11:36595199G>T c.345G>T c.(343-345)ggG>ggT p.G115G LUSC 11 36595604 36595604 + Missense_Mutation SNP G G T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr11:36595604G>T c.750G>T c.(748-750)aaG>aaT p.K250N LUSC 11 36595984 36595984 + Nonsense_Mutation SNP C C G TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr11:36595984C>G c.1130C>G c.(1129-1131)tCa>tGa p.S377* LUSC 11 36596185 36596185 + Missense_Mutation SNP C C T TCGA-63-6202-01A-11D-1817-08 TCGA-63-6202-10A-01D-1817-08 g.chr11:36596185C>T c.1331C>T c.(1330-1332)gCg>gTg p.A444V LUSC 11 36596776 36596776 + Missense_Mutation SNP T T G TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr11:36596776T>G c.1922T>G c.(1921-1923)gTg>gGg p.V641G LUSC 11 36597771 36597771 + Missense_Mutation SNP C C A TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr11:36597771C>A c.2917C>A c.(2917-2919)Cgc>Agc p.R973S LUSC 11 36597797 36597797 + Missense_Mutation SNP G G T TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr11:36597797G>T c.2943G>T c.(2941-2943)caG>caT p.Q981H OV 11 36597760 36597760 + Missense_Mutation SNP A A C TCGA-09-2050-01A-01W-0799-08 TCGA-09-2050-10A-01W-0799-08 g.chr11:36597760A>C c.2906A>C c.(2905-2907)aAa>aCa p.K969T PAAD 11 36595176 36595176 + Nonsense_Mutation SNP C C T TCGA-HZ-A9TJ-01A-11D-A40W-08 TCGA-HZ-A9TJ-10A-01D-A40W-08 g.chr11:36595176C>T c.322C>T c.(322-324)Cga>Tga p.R108* PAAD 11 36595189 36595189 + Missense_Mutation SNP G G A TCGA-2J-AAB8-01A-12D-A40W-08 TCGA-2J-AAB8-10A-01D-A40W-08 g.chr11:36595189G>A c.335G>A c.(334-336)cGc>cAc p.R112H PAAD 11 36596004 36596004 + Nonsense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:36596004G>T c.1150G>T c.(1150-1152)Gag>Tag p.E384* PAAD 11 36597180 36597180 + Missense_Mutation SNP C C T TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr11:36597180C>T c.2326C>T c.(2326-2328)Cgg>Tgg p.R776W PRAD 11 36594954 36594954 + Missense_Mutation SNP C C T TCGA-HC-A8D1-01A-11D-A364-08 TCGA-HC-A8D1-10A-01D-A362-08 g.chr11:36594954C>T c.100C>T c.(100-102)Cgg>Tgg p.R34W PRAD 11 36595189 36595189 + Missense_Mutation SNP G G A TCGA-CH-5768-01A-11D-1576-08 TCGA-CH-5768-11A-01D-1576-08 g.chr11:36595189G>A c.335G>A c.(334-336)cGc>cAc p.R112H PRAD 11 36595189 36595189 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:36595189G>A c.335G>A c.(334-336)cGc>cAc p.R112H PRAD 11 36595191 36595191 + Missense_Mutation SNP A A G TCGA-YL-A8S8-01A-11D-A377-08 TCGA-YL-A8S8-10A-01D-A37A-08 g.chr11:36595191A>G c.337A>G c.(337-339)Atc>Gtc p.I113V PRAD 11 36595849 36595849 + Missense_Mutation SNP G G A TCGA-HC-7742-01A-11D-2114-08 TCGA-HC-7742-10A-01D-2115-08 g.chr11:36595849G>A c.995G>A c.(994-996)cGa>cAa p.R332Q PRAD 11 36595998 36595998 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:36595998T>C c.1144T>C c.(1144-1146)Tca>Cca p.S382P PRAD 11 36596041 36596041 + Missense_Mutation SNP G G A TCGA-HC-7820-01A-11D-2114-08 TCGA-HC-7820-10A-01D-2115-08 g.chr11:36596041G>A c.1187G>A c.(1186-1188)cGc>cAc p.R396H PRAD 11 36597054 36597054 + Missense_Mutation SNP G G C TCGA-KK-A8I6-01A-11D-A364-08 TCGA-KK-A8I6-11A-12D-A362-08 g.chr11:36597054G>C c.2200G>C c.(2200-2202)Gat>Cat p.D734H PRAD 11 36597064 36597064 + Missense_Mutation SNP G G A TCGA-J4-8198-01A-11D-2260-08 TCGA-J4-8198-10A-01D-2260-08 g.chr11:36597064G>A c.2210G>A c.(2209-2211)cGt>cAt p.R737H PRAD 11 36597450 36597450 + Missense_Mutation SNP G G A TCGA-EJ-5502-01A-01D-1576-08 TCGA-EJ-5502-10A-01D-1577-08 g.chr11:36597450G>A c.2596G>A c.(2596-2598)Gtg>Atg p.V866M PRAD 11 36597480 36597480 + Missense_Mutation SNP G G A TCGA-HC-7230-01A-11D-2114-08 TCGA-HC-7230-10A-01D-2115-08 g.chr11:36597480G>A c.2626G>A c.(2626-2628)Gag>Aag p.E876K READ 11 36595001 36595001 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:36595001G>T c.147G>T c.(145-147)aaG>aaT p.K49N READ 11 36595361 36595361 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:36595361G>A c.507G>A c.(505-507)tcG>tcA p.S169S READ 11 36596514 36596514 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:36596514G>A c.1660G>A c.(1660-1662)Gac>Aac p.D554N READ 11 36596672 36596672 + Silent SNP A A G TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr11:36596672A>G c.1818A>G c.(1816-1818)ggA>ggG p.G606G READ 11 36596949 36596949 + Missense_Mutation SNP C C T TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr11:36596949C>T c.2095C>T c.(2095-2097)Cgg>Tgg p.R699W READ 11 36597747 36597747 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:36597747G>T c.2893G>T c.(2893-2895)Gag>Tag p.E965* SKCM 11 36594953 36594953 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:36594953C>T c.99C>T c.(97-99)ttC>ttT p.F33F SKCM 11 36594964 36594964 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr11:36594964C>T c.110C>T c.(109-111)tCc>tTc p.S37F SKCM 11 36595095 36595095 + Missense_Mutation SNP T T G TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr11:36595095T>G c.241T>G c.(241-243)Tta>Gta p.L81V SKCM 11 36595117 36595117 + Missense_Mutation SNP C C T TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr11:36595117C>T c.263C>T c.(262-264)tCa>tTa p.S88L SKCM 11 36595229 36595229 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:36595229G>A c.375G>A c.(373-375)agG>agA p.R125R SKCM 11 36595249 36595249 + Missense_Mutation SNP C C T TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr11:36595249C>T c.395C>T c.(394-396)cCt>cTt p.P132L SKCM 11 36595296 36595296 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:36595296G>A c.442G>A c.(442-444)Gct>Act p.A148T SKCM 11 36595303 36595303 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr11:36595303C>T c.449C>T c.(448-450)tCc>tTc p.S150F SKCM 11 36595461 36595461 + Missense_Mutation SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr11:36595461G>A c.607G>A c.(607-609)Gag>Aag p.E203K SKCM 11 36595523 36595523 + Silent SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr11:36595523G>A c.669G>A c.(667-669)agG>agA p.R223R SKCM 11 36595792 36595792 + Missense_Mutation SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr11:36595792G>A c.938G>A c.(937-939)tGc>tAc p.C313Y SKCM 11 36595854 36595854 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr11:36595854C>T c.1000C>T c.(1000-1002)Cca>Tca p.P334S SKCM 11 36596150 36596150 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:36596150C>T c.1296C>T c.(1294-1296)tcC>tcT p.S432S SKCM 11 36596185 36596185 + Missense_Mutation SNP C C T TCGA-FS-A1ZJ-06A-12D-A197-08 TCGA-FS-A1ZJ-10A-01D-A199-08 g.chr11:36596185C>T c.1331C>T c.(1330-1332)gCg>gTg p.A444V SKCM 11 36596233 36596233 + Missense_Mutation SNP G G A TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr11:36596233G>A c.1379G>A c.(1378-1380)gGa>gAa p.G460E SKCM 11 36596355 36596355 + Nonsense_Mutation SNP C C T TCGA-DA-A3F3-06A-11D-A20D-08 TCGA-DA-A3F3-10A-01D-A20D-08 g.chr11:36596355C>T c.1501C>T c.(1501-1503)Cag>Tag p.Q501* SKCM 11 36596622 36596622 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:36596622C>T c.1768C>T c.(1768-1770)Ctg>Ttg p.L590L SKCM 11 36596675 36596675 + Silent SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr11:36596675C>T c.1821C>T c.(1819-1821)gaC>gaT p.D607D SKCM 11 36596731 36596731 + Missense_Mutation SNP C C T TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chr11:36596731C>T c.1877C>T c.(1876-1878)tCa>tTa p.S626L SKCM 11 36596800 36596800 + Missense_Mutation SNP C C T TCGA-EE-A2MQ-06A-11D-A197-08 TCGA-EE-A2MQ-10A-01D-A199-08 g.chr11:36596800C>T c.1946C>T c.(1945-1947)cCt>cTt p.P649L SKCM 11 36596859 36596859 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr11:36596859G>A c.2005G>A c.(2005-2007)Gag>Aag p.E669K SKCM 11 36597025 36597025 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr11:36597025C>T c.2171C>T c.(2170-2172)tCt>tTt p.S724F SKCM 11 36597162 36597162 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr11:36597162G>A c.2308G>A c.(2308-2310)Gag>Aag p.E770K SKCM 11 36597233 36597233 + Silent SNP C C T TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr11:36597233C>T c.2379C>T c.(2377-2379)tcC>tcT p.S793S SKCM 11 36597316 36597316 + Missense_Mutation SNP A A G TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr11:36597316A>G c.2462A>G c.(2461-2463)aAt>aGt p.N821S SKCM 11 36597596 36597596 + Silent SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr11:36597596C>T c.2742C>T c.(2740-2742)ttC>ttT p.F914F SKCM 11 36597709 36597709 + Missense_Mutation SNP G G T TCGA-GF-A4EO-06A-12D-A24R-08 TCGA-GF-A4EO-10A-01D-A24R-08 g.chr11:36597709G>T c.2855G>T c.(2854-2856)aGg>aTg p.R952M SKCM 11 36597719 36597719 + Silent SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr11:36597719C>T c.2865C>T c.(2863-2865)tcC>tcT p.S955S SKCM 11 36597825 36597825 + Silent SNP C C T TCGA-EE-A2MQ-06A-11D-A197-08 TCGA-EE-A2MQ-10A-01D-A199-08 g.chr11:36597825C>T c.2971C>T c.(2971-2973)Ctg>Ttg p.L991L SKCM 11 36597850 36597850 + Missense_Mutation SNP C C T TCGA-FS-A4F0-06A-11D-A24R-08 TCGA-FS-A4F0-10A-01D-A24R-08 g.chr11:36597850C>T c.2996C>T c.(2995-2997)tCc>tTc p.S999F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 36595204 36595204 single base substitution C T exon_variant BLCA-CN 11 36595204 36595204 single base substitution C T missense_variant S117F 350C>T BLCA-CN 11 36615210 36615210 single base substitution T G downstream_gene_variant BLCA-US 11 36595001 36595001 single base substitution G A exon_variant BLCA-US 11 36595001 36595001 single base substitution G A synonymous_variant K49K 147G>A BLCA-US 11 36614207 36614207 single base substitution G T intron_variant BLCA-US 11 36614675 36614675 single base substitution C G 3_prime_UTR_variant BLCA-US 11 36615460 36615460 single base substitution C G downstream_gene_variant BOCA-FR 11 36542343 36542343 single base substitution G T intron_variant BRCA-EU 11 36527396 36527399 multiple base substitution (>=2bp and <=200bp) CTGA CCT upstream_gene_variant BRCA-EU 11 36530782 36530785 deletion of <=200bp AATT - upstream_gene_variant BRCA-EU 11 36530800 36530800 single base substitution G A upstream_gene_variant BRCA-EU 11 36530988 36530988 single base substitution T A upstream_gene_variant BRCA-EU 11 36531079 36531079 single base substitution A G upstream_gene_variant BRCA-EU 11 36532296 36532296 single base substitution C A exon_variant BRCA-EU 11 36532296 36532296 single base substitution C A upstream_gene_variant BRCA-EU 11 36533015 36533015 single base substitution G A intron_variant BRCA-EU 11 36533015 36533015 single base substitution G A upstream_gene_variant BRCA-EU 11 36535393 36535393 single base substitution C G intron_variant BRCA-EU 11 36535393 36535393 single base substitution C G upstream_gene_variant BRCA-EU 11 36535489 36535489 single base substitution A C intron_variant BRCA-EU 11 36535489 36535489 single base substitution A C upstream_gene_variant BRCA-EU 11 36536214 36536214 single base substitution C T intron_variant BRCA-EU 11 36536214 36536214 single base substitution C T upstream_gene_variant BRCA-EU 11 36538031 36538031 single base substitution C T intron_variant BRCA-EU 11 36539226 36539226 single base substitution A C intron_variant BRCA-EU 11 36539635 36539635 single base substitution A G intron_variant BRCA-EU 11 36540167 36540167 single base substitution C T intron_variant BRCA-EU 11 36540265 36540265 single base substitution G T intron_variant BRCA-EU 11 36542073 36542073 single base substitution C T intron_variant BRCA-EU 11 36543971 36543971 single base substitution C G intron_variant BRCA-EU 11 36545035 36545035 single base substitution C G intron_variant BRCA-EU 11 36545154 36545154 single base substitution T C intron_variant BRCA-EU 11 36545850 36545850 single base substitution C G intron_variant BRCA-EU 11 36545990 36545990 single base substitution T C intron_variant BRCA-EU 11 36547167 36547167 single base substitution C T intron_variant BRCA-EU 11 36547390 36547390 single base substitution A C intron_variant BRCA-EU 11 36547698 36547698 single base substitution A C intron_variant BRCA-EU 11 36548656 36548656 single base substitution G T intron_variant BRCA-EU 11 36548983 36548983 single base substitution A T intron_variant BRCA-EU 11 36549449 36549449 single base substitution T C intron_variant BRCA-EU 11 36549451 36549451 single base substitution G A intron_variant BRCA-EU 11 36549613 36549613 single base substitution C A intron_variant BRCA-EU 11 36549746 36549746 single base substitution C G intron_variant BRCA-EU 11 36549781 36549781 single base substitution A C intron_variant BRCA-EU 11 36549883 36549883 single base substitution A G intron_variant BRCA-EU 11 36550582 36550582 single base substitution G T intron_variant BRCA-EU 11 36552066 36552066 single base substitution G T intron_variant BRCA-EU 11 36552487 36552487 single base substitution C G intron_variant BRCA-EU 11 36553383 36553383 single base substitution C T intron_variant BRCA-EU 11 36554236 36554236 single base substitution C G intron_variant BRCA-EU 11 36554582 36554582 single base substitution T C intron_variant BRCA-EU 11 36554933 36554933 single base substitution T A intron_variant BRCA-EU 11 36555355 36555355 deletion of <=200bp T - intron_variant BRCA-EU 11 36556271 36556271 single base substitution C T intron_variant BRCA-EU 11 36556331 36556331 single base substitution A C intron_variant BRCA-EU 11 36558466 36558466 single base substitution G A downstream_gene_variant BRCA-EU 11 36558466 36558466 single base substitution G A intron_variant BRCA-EU 11 36558764 36558764 single base substitution G T downstream_gene_variant BRCA-EU 11 36558764 36558764 single base substitution G T intron_variant BRCA-EU 11 36558959 36558959 single base substitution C T downstream_gene_variant BRCA-EU 11 36558959 36558959 single base substitution C T intron_variant BRCA-EU 11 36559151 36559151 single base substitution C G downstream_gene_variant BRCA-EU 11 36559151 36559151 single base substitution C G intron_variant BRCA-EU 11 36559207 36559207 single base substitution G C downstream_gene_variant BRCA-EU 11 36559207 36559207 single base substitution G C intron_variant BRCA-EU 11 36559217 36559217 single base substitution C G downstream_gene_variant BRCA-EU 11 36559217 36559217 single base substitution C G intron_variant BRCA-EU 11 36559615 36559615 single base substitution G T downstream_gene_variant BRCA-EU 11 36559615 36559615 single base substitution G T intron_variant BRCA-EU 11 36560874 36560874 single base substitution C T downstream_gene_variant BRCA-EU 11 36560874 36560874 single base substitution C T intron_variant BRCA-EU 11 36562361 36562361 single base substitution T C downstream_gene_variant BRCA-EU 11 36562361 36562361 single base substitution T C intron_variant BRCA-EU 11 36562873 36562873 single base substitution C A intron_variant BRCA-EU 11 36563433 36563433 deletion of <=200bp A - intron_variant BRCA-EU 11 36563748 36563748 single base substitution C T intron_variant BRCA-EU 11 36564200 36564200 single base substitution G A intron_variant BRCA-EU 11 36565051 36565051 single base substitution G A intron_variant BRCA-EU 11 36565683 36565683 single base substitution C T intron_variant BRCA-EU 11 36566600 36566600 single base substitution G A intron_variant BRCA-EU 11 36566622 36566622 single base substitution T C intron_variant BRCA-EU 11 36567958 36567958 single base substitution C A intron_variant BRCA-EU 11 36568033 36568033 single base substitution G A intron_variant BRCA-EU 11 36568092 36568092 single base substitution C G intron_variant BRCA-EU 11 36568473 36568473 single base substitution C G intron_variant BRCA-EU 11 36569727 36569727 single base substitution G T intron_variant BRCA-EU 11 36578834 36578834 single base substitution C G intron_variant BRCA-EU 11 36579186 36579186 single base substitution C G intron_variant BRCA-EU 11 36579591 36579591 single base substitution C G intron_variant BRCA-EU 11 36580681 36580681 deletion of <=200bp T - intron_variant BRCA-EU 11 36582660 36582660 single base substitution A G intron_variant BRCA-EU 11 36583736 36583736 single base substitution C T intron_variant BRCA-EU 11 36584218 36584218 single base substitution A T intron_variant BRCA-EU 11 36585867 36585867 single base substitution C A intron_variant BRCA-EU 11 36585867 36585867 single base substitution C A upstream_gene_variant BRCA-EU 11 36586358 36586358 single base substitution C T intron_variant BRCA-EU 11 36586358 36586358 single base substitution C T upstream_gene_variant BRCA-EU 11 36586456 36586456 insertion of <=200bp - C intron_variant BRCA-EU 11 36586456 36586456 insertion of <=200bp - C upstream_gene_variant BRCA-EU 11 36588076 36588076 insertion of <=200bp - G 5_prime_UTR_variant BRCA-EU 11 36588076 36588076 insertion of <=200bp - G upstream_gene_variant BRCA-EU 11 36589138 36589138 single base substitution T C intron_variant BRCA-EU 11 36589138 36589138 single base substitution T C upstream_gene_variant BRCA-EU 11 36591270 36591270 single base substitution A T intron_variant BRCA-EU 11 36591515 36591551 deletion of <=200bp CATATGCATCAGTGCATACAGAAAATTAAATTTTCTG - intron_variant BRCA-EU 11 36592002 36592002 single base substitution T C intron_variant BRCA-EU 11 36592795 36592795 single base substitution A C intron_variant BRCA-EU 11 36593694 36593694 single base substitution A G intron_variant BRCA-EU 11 36594089 36594089 single base substitution A T intron_variant BRCA-EU 11 36594223 36594223 single base substitution T C intron_variant BRCA-EU 11 36594436 36594436 single base substitution G A intron_variant BRCA-EU 11 36594497 36594497 single base substitution A C intron_variant BRCA-EU 11 36595506 36595506 single base substitution C T exon_variant BRCA-EU 11 36595506 36595506 single base substitution C T missense_variant R218C 652C>T BRCA-EU 11 36595626 36595626 single base substitution A C exon_variant BRCA-EU 11 36595626 36595626 single base substitution A C missense_variant S258R 772A>C BRCA-EU 11 36595688 36595688 single base substitution C G exon_variant BRCA-EU 11 36595688 36595688 single base substitution C G synonymous_variant L278L 834C>G BRCA-EU 11 36597064 36597064 single base substitution G A exon_variant BRCA-EU 11 36597064 36597064 single base substitution G A missense_variant R737H 2210G>A BRCA-EU 11 36597358 36597358 single base substitution C G exon_variant BRCA-EU 11 36597358 36597358 single base substitution C G missense_variant T835R 2504C>G BRCA-EU 11 36597479 36597479 single base substitution C T exon_variant BRCA-EU 11 36597479 36597479 single base substitution C T synonymous_variant S875S 2625C>T BRCA-EU 11 36598644 36598644 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 36598644 36598644 single base substitution C G intron_variant BRCA-EU 11 36598818 36598818 single base substitution T G 3_prime_UTR_variant BRCA-EU 11 36598818 36598818 single base substitution T G intron_variant BRCA-EU 11 36599931 36599931 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 11 36599931 36599931 deletion of <=200bp T - intron_variant BRCA-EU 11 36601655 36601655 single base substitution C T downstream_gene_variant BRCA-EU 11 36601655 36601655 single base substitution C T intron_variant BRCA-EU 11 36601876 36601876 single base substitution C T downstream_gene_variant BRCA-EU 11 36601876 36601876 single base substitution C T intron_variant BRCA-EU 11 36601904 36601904 single base substitution C T downstream_gene_variant BRCA-EU 11 36601904 36601904 single base substitution C T intron_variant BRCA-EU 11 36601926 36601926 single base substitution A C downstream_gene_variant BRCA-EU 11 36601926 36601926 single base substitution A C intron_variant BRCA-EU 11 36604865 36604865 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 36604865 36604865 deletion of <=200bp T - intron_variant BRCA-EU 11 36604866 36604866 single base substitution T C downstream_gene_variant BRCA-EU 11 36604866 36604866 single base substitution T C intron_variant BRCA-EU 11 36606745 36606745 deletion of <=200bp A - intron_variant BRCA-EU 11 36608140 36608140 single base substitution G A intron_variant BRCA-EU 11 36609266 36609266 single base substitution A G intron_variant BRCA-EU 11 36610047 36610047 single base substitution G T intron_variant BRCA-EU 11 36610119 36610119 single base substitution G A intron_variant BRCA-EU 11 36613753 36613753 single base substitution C A intron_variant BRCA-EU 11 36614341 36614341 single base substitution C T intron_variant BRCA-EU 11 36614952 36614952 single base substitution A T downstream_gene_variant BRCA-EU 11 36615827 36615827 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 36616440 36616440 single base substitution A G downstream_gene_variant BRCA-EU 11 36617089 36617089 single base substitution C T downstream_gene_variant BRCA-EU 11 36617615 36617615 single base substitution C T downstream_gene_variant BRCA-EU 11 36618723 36618723 single base substitution C G downstream_gene_variant BRCA-EU 11 36619524 36619524 single base substitution C T downstream_gene_variant BRCA-FR 11 36537796 36537796 single base substitution C G intron_variant BRCA-FR 11 36545850 36545850 single base substitution C G intron_variant BRCA-FR 11 36550582 36550582 single base substitution G T intron_variant BRCA-FR 11 36559151 36559151 single base substitution C G downstream_gene_variant BRCA-FR 11 36559151 36559151 single base substitution C G intron_variant BRCA-FR 11 36559615 36559615 single base substitution G T downstream_gene_variant BRCA-FR 11 36559615 36559615 single base substitution G T intron_variant BRCA-FR 11 36562873 36562873 single base substitution C A intron_variant BRCA-FR 11 36573410 36573410 single base substitution T G intron_variant BRCA-FR 11 36579186 36579186 single base substitution C G intron_variant BRCA-FR 11 36583736 36583736 single base substitution C T intron_variant BRCA-FR 11 36590674 36590674 single base substitution G A intron_variant BRCA-FR 11 36597479 36597479 single base substitution C T exon_variant BRCA-FR 11 36597479 36597479 single base substitution C T synonymous_variant S875S 2625C>T BRCA-FR 11 36601876 36601876 single base substitution C T downstream_gene_variant BRCA-FR 11 36601876 36601876 single base substitution C T intron_variant BRCA-FR 11 36608173 36608173 single base substitution G T intron_variant BRCA-FR 11 36608437 36608437 single base substitution G T intron_variant BRCA-FR 11 36609266 36609266 single base substitution A G intron_variant BRCA-FR 11 36610205 36610205 single base substitution A G intron_variant BRCA-FR 11 36614341 36614341 single base substitution C T intron_variant BRCA-UK 11 36530800 36530800 single base substitution G A upstream_gene_variant BRCA-UK 11 36536214 36536214 single base substitution C T intron_variant BRCA-UK 11 36536214 36536214 single base substitution C T upstream_gene_variant BRCA-UK 11 36565683 36565683 single base substitution C T intron_variant BRCA-UK 11 36592002 36592002 single base substitution T C intron_variant BRCA-UK 11 36594436 36594436 single base substitution G A intron_variant BRCA-UK 11 36596597 36596597 single base substitution G C exon_variant BRCA-UK 11 36596597 36596597 single base substitution G C missense_variant M581I 1743G>C BRCA-US 11 36595236 36595236 single base substitution C G exon_variant BRCA-US 11 36595236 36595236 single base substitution C G missense_variant P128A 382C>G BRCA-US 11 36595756 36595756 single base substitution C A exon_variant BRCA-US 11 36595756 36595756 single base substitution C A missense_variant A301D 902C>A BRCA-US 11 36595870 36595870 single base substitution A T exon_variant BRCA-US 11 36595870 36595870 single base substitution A T missense_variant D339V 1016A>T BRCA-US 11 36596585 36596585 single base substitution C T exon_variant BRCA-US 11 36596585 36596585 single base substitution C T synonymous_variant I577I 1731C>T BRCA-US 11 36597190 36597190 single base substitution T G exon_variant BRCA-US 11 36597190 36597190 single base substitution T G missense_variant V779G 2336T>G BRCA-US 11 36597333 36597333 single base substitution G C exon_variant BRCA-US 11 36597333 36597333 single base substitution G C missense_variant E827Q 2479G>C BRCA-US 11 36597340 36597340 single base substitution G T exon_variant BRCA-US 11 36597340 36597340 single base substitution G T missense_variant R829M 2486G>T BRCA-US 11 36597453 36597453 single base substitution G A exon_variant BRCA-US 11 36597453 36597453 single base substitution G A missense_variant D867N 2599G>A BRCA-US 11 36614637 36614637 single base substitution G A 3_prime_UTR_variant BRCA-US 11 36615502 36615502 single base substitution G A downstream_gene_variant BTCA-JP 11 36595134 36595134 single base substitution A T exon_variant BTCA-JP 11 36595134 36595134 single base substitution A T missense_variant N94Y 280A>T BTCA-JP 11 36611931 36611931 single base substitution C T splice_region_variant BTCA-JP 11 36612028 36612028 single base substitution G T splice_region_variant BTCA-JP 11 36612136 36612136 single base substitution G A intron_variant BTCA-JP 11 36614796 36614796 single base substitution G T downstream_gene_variant BTCA-JP 11 36615788 36615788 single base substitution A G downstream_gene_variant CESC-US 11 36595309 36595309 single base substitution C T exon_variant CESC-US 11 36595309 36595309 single base substitution C T missense_variant P152L 455C>T CESC-US 11 36596661 36596661 single base substitution G C exon_variant CESC-US 11 36596661 36596661 single base substitution G C missense_variant D603H 1807G>C CESC-US 11 36614675 36614675 single base substitution C G 3_prime_UTR_variant CLLE-ES 11 36544520 36544520 single base substitution T C intron_variant CLLE-ES 11 36551033 36551033 single base substitution G T intron_variant CLLE-ES 11 36563643 36563643 single base substitution A G intron_variant CLLE-ES 11 36589337 36589337 single base substitution T C intron_variant CLLE-ES 11 36589337 36589337 single base substitution T C upstream_gene_variant CLLE-ES 11 36597129 36597129 single base substitution C T exon_variant CLLE-ES 11 36597129 36597129 single base substitution C T missense_variant R759C 2275C>T CLLE-ES 11 36602112 36602112 single base substitution C T downstream_gene_variant CLLE-ES 11 36602112 36602112 single base substitution C T intron_variant CLLE-ES 11 36617337 36617337 single base substitution A G downstream_gene_variant CLLE-ES 11 36618901 36618901 single base substitution C A downstream_gene_variant COAD-US 11 36594954 36594954 single base substitution C T exon_variant COAD-US 11 36594954 36594954 single base substitution C T missense_variant R34W 100C>T COAD-US 11 36595136 36595136 single base substitution C T exon_variant COAD-US 11 36595136 36595136 single base substitution C T synonymous_variant N94N 282C>T COAD-US 11 36595417 36595417 single base substitution G A exon_variant COAD-US 11 36595417 36595417 single base substitution G A missense_variant S188N 563G>A COAD-US 11 36595451 36595451 single base substitution C T exon_variant COAD-US 11 36595451 36595451 single base substitution C T synonymous_variant N199N 597C>T COAD-US 11 36596059 36596059 single base substitution T C exon_variant COAD-US 11 36596059 36596059 single base substitution T C missense_variant L402P 1205T>C COAD-US 11 36596344 36596344 single base substitution G A exon_variant COAD-US 11 36596344 36596344 single base substitution G A missense_variant R497K 1490G>A COAD-US 11 36596790 36596790 single base substitution G T exon_variant COAD-US 11 36596790 36596790 single base substitution G T stop_gained E646* 1936G>T COAD-US 11 36596837 36596837 single base substitution G A exon_variant COAD-US 11 36596837 36596837 single base substitution G A missense_variant M661I 1983G>A COAD-US 11 36596949 36596949 single base substitution C T exon_variant COAD-US 11 36596949 36596949 single base substitution C T missense_variant R699W 2095C>T COAD-US 11 36597030 36597030 single base substitution T C exon_variant COAD-US 11 36597030 36597030 single base substitution T C missense_variant S726P 2176T>C COAD-US 11 36597734 36597734 single base substitution A G intron_variant COAD-US 11 36597734 36597734 single base substitution A G synonymous_variant A960A 2880A>G COAD-US 11 36600718 36600718 insertion of <=200bp - T 3_prime_UTR_variant COAD-US 11 36600718 36600718 insertion of <=200bp - T intron_variant COAD-US 11 36614690 36614690 single base substitution G T 3_prime_UTR_variant COAD-US 11 36615130 36615130 single base substitution G A downstream_gene_variant COCA-CN 11 36537896 36537896 single base substitution G A intron_variant COCA-CN 11 36545292 36545292 single base substitution A T intron_variant COCA-CN 11 36566009 36566009 single base substitution T G intron_variant COCA-CN 11 36569067 36569067 single base substitution A G intron_variant COCA-CN 11 36570894 36570894 single base substitution G A intron_variant COCA-CN 11 36574882 36574882 single base substitution T C intron_variant COCA-CN 11 36585091 36585091 single base substitution A T intron_variant COCA-CN 11 36585091 36585091 single base substitution A T upstream_gene_variant COCA-CN 11 36595606 36595606 single base substitution G T exon_variant COCA-CN 11 36595606 36595606 single base substitution G T missense_variant R251I 752G>T COCA-CN 11 36595848 36595848 single base substitution C T exon_variant COCA-CN 11 36595848 36595848 single base substitution C T stop_gained R332* 994C>T COCA-CN 11 36597064 36597064 single base substitution G A exon_variant COCA-CN 11 36597064 36597064 single base substitution G A missense_variant R737H 2210G>A COCA-CN 11 36597607 36597607 single base substitution G A exon_variant COCA-CN 11 36597607 36597607 single base substitution G A missense_variant R918H 2753G>A COCA-CN 11 36607871 36607871 single base substitution C A intron_variant COCA-CN 11 36614462 36614462 single base substitution G A intron_variant COCA-CN 11 36614690 36614690 single base substitution G T 3_prime_UTR_variant COCA-CN 11 36614963 36614963 single base substitution C G downstream_gene_variant COCA-CN 11 36615440 36615440 single base substitution G T downstream_gene_variant COCA-CN 11 36615573 36615573 single base substitution T G downstream_gene_variant COCA-CN 11 36615777 36615777 single base substitution G T downstream_gene_variant EOPC-DE 11 36613448 36613448 single base substitution C A intron_variant ESAD-UK 11 36530659 36530659 single base substitution G C upstream_gene_variant ESAD-UK 11 36531922 36531922 single base substitution G T upstream_gene_variant ESAD-UK 11 36531923 36531923 single base substitution G T upstream_gene_variant ESAD-UK 11 36532368 36532368 single base substitution A G exon_variant ESAD-UK 11 36532368 36532368 single base substitution A G upstream_gene_variant ESAD-UK 11 36534470 36534470 single base substitution C T intron_variant ESAD-UK 11 36534470 36534470 single base substitution C T upstream_gene_variant ESAD-UK 11 36534713 36534713 single base substitution G A intron_variant ESAD-UK 11 36534713 36534713 single base substitution G A upstream_gene_variant ESAD-UK 11 36534835 36534835 single base substitution C G intron_variant ESAD-UK 11 36534835 36534835 single base substitution C G upstream_gene_variant ESAD-UK 11 36535006 36535006 single base substitution T C intron_variant ESAD-UK 11 36535006 36535006 single base substitution T C upstream_gene_variant ESAD-UK 11 36536176 36536176 single base substitution G A intron_variant ESAD-UK 11 36536176 36536176 single base substitution G A upstream_gene_variant ESAD-UK 11 36536699 36536699 single base substitution C G intron_variant ESAD-UK 11 36536699 36536699 single base substitution C G upstream_gene_variant ESAD-UK 11 36537330 36537330 single base substitution A T intron_variant ESAD-UK 11 36537774 36537774 single base substitution G A intron_variant ESAD-UK 11 36538788 36538788 single base substitution G T intron_variant ESAD-UK 11 36538843 36538843 single base substitution G C intron_variant ESAD-UK 11 36539322 36539322 single base substitution C A intron_variant ESAD-UK 11 36540866 36540866 single base substitution C T intron_variant ESAD-UK 11 36542293 36542293 single base substitution T A intron_variant ESAD-UK 11 36544363 36544363 single base substitution T A intron_variant ESAD-UK 11 36544402 36544402 single base substitution A G intron_variant ESAD-UK 11 36544456 36544465 deletion of <=200bp TTTTGGCCAA - intron_variant ESAD-UK 11 36544953 36544953 single base substitution C A intron_variant ESAD-UK 11 36545285 36545285 insertion of <=200bp - T intron_variant ESAD-UK 11 36545291 36545291 single base substitution T A intron_variant ESAD-UK 11 36547168 36547168 single base substitution G A intron_variant ESAD-UK 11 36548047 36548047 single base substitution T G intron_variant ESAD-UK 11 36549761 36549761 single base substitution C A intron_variant ESAD-UK 11 36549983 36549983 single base substitution C A intron_variant ESAD-UK 11 36550131 36550131 single base substitution A C intron_variant ESAD-UK 11 36550263 36550263 insertion of <=200bp - T intron_variant ESAD-UK 11 36550336 36550336 single base substitution G C intron_variant ESAD-UK 11 36550684 36550684 single base substitution T G intron_variant ESAD-UK 11 36550933 36550933 single base substitution C T intron_variant ESAD-UK 11 36551425 36551425 single base substitution G A intron_variant ESAD-UK 11 36551824 36551824 single base substitution T C intron_variant ESAD-UK 11 36552234 36552234 single base substitution A C intron_variant ESAD-UK 11 36552444 36552444 single base substitution C G intron_variant ESAD-UK 11 36553197 36553197 single base substitution G T intron_variant ESAD-UK 11 36554525 36554525 single base substitution G A intron_variant ESAD-UK 11 36555179 36555179 single base substitution C A intron_variant ESAD-UK 11 36555583 36555583 single base substitution A T intron_variant ESAD-UK 11 36556896 36556896 single base substitution A G intron_variant ESAD-UK 11 36557773 36557773 single base substitution A C downstream_gene_variant ESAD-UK 11 36557773 36557773 single base substitution A C intron_variant ESAD-UK 11 36560977 36560977 single base substitution C T downstream_gene_variant ESAD-UK 11 36560977 36560977 single base substitution C T intron_variant ESAD-UK 11 36561004 36561004 single base substitution C T downstream_gene_variant ESAD-UK 11 36561004 36561004 single base substitution C T intron_variant ESAD-UK 11 36561030 36561030 deletion of <=200bp T - downstream_gene_variant ESAD-UK 11 36561030 36561030 deletion of <=200bp T - intron_variant ESAD-UK 11 36561300 36561300 single base substitution T C downstream_gene_variant ESAD-UK 11 36561300 36561300 single base substitution T C intron_variant ESAD-UK 11 36562206 36562206 single base substitution T G downstream_gene_variant ESAD-UK 11 36562206 36562206 single base substitution T G intron_variant ESAD-UK 11 36562756 36562756 single base substitution C G intron_variant ESAD-UK 11 36564346 36564346 single base substitution A T intron_variant ESAD-UK 11 36565329 36565329 single base substitution T G intron_variant ESAD-UK 11 36565391 36565391 single base substitution A C intron_variant ESAD-UK 11 36565645 36565645 deletion of <=200bp T - intron_variant ESAD-UK 11 36565756 36565756 single base substitution T G intron_variant ESAD-UK 11 36565813 36565813 single base substitution G A intron_variant ESAD-UK 11 36565827 36565827 single base substitution A C intron_variant ESAD-UK 11 36565935 36565935 single base substitution G C intron_variant ESAD-UK 11 36566444 36566444 single base substitution C A intron_variant ESAD-UK 11 36566880 36566880 single base substitution G T intron_variant ESAD-UK 11 36567683 36567683 single base substitution C A intron_variant ESAD-UK 11 36567760 36567760 single base substitution C T intron_variant ESAD-UK 11 36569928 36569928 single base substitution G A intron_variant ESAD-UK 11 36569987 36569987 single base substitution A C intron_variant ESAD-UK 11 36570434 36570434 single base substitution T C intron_variant ESAD-UK 11 36571191 36571191 single base substitution T C intron_variant ESAD-UK 11 36579177 36579177 single base substitution G A intron_variant ESAD-UK 11 36581517 36581517 single base substitution T A intron_variant ESAD-UK 11 36582759 36582759 single base substitution T G intron_variant ESAD-UK 11 36582917 36582917 single base substitution T G intron_variant ESAD-UK 11 36583809 36583809 single base substitution A C intron_variant ESAD-UK 11 36584195 36584195 single base substitution T G intron_variant ESAD-UK 11 36584265 36584265 single base substitution T G intron_variant ESAD-UK 11 36584345 36584345 single base substitution A C intron_variant ESAD-UK 11 36584478 36584478 single base substitution T C intron_variant ESAD-UK 11 36584690 36584690 single base substitution T A intron_variant ESAD-UK 11 36584690 36584690 single base substitution T A upstream_gene_variant ESAD-UK 11 36585097 36585097 single base substitution T G intron_variant ESAD-UK 11 36585097 36585097 single base substitution T G upstream_gene_variant ESAD-UK 11 36586330 36586330 single base substitution T G intron_variant ESAD-UK 11 36586330 36586330 single base substitution T G upstream_gene_variant ESAD-UK 11 36588076 36588076 insertion of <=200bp - G 5_prime_UTR_variant ESAD-UK 11 36588076 36588076 insertion of <=200bp - G upstream_gene_variant ESAD-UK 11 36588967 36588967 single base substitution G A 5_prime_UTR_variant ESAD-UK 11 36588967 36588967 single base substitution G A upstream_gene_variant ESAD-UK 11 36589083 36589083 single base substitution G T intron_variant ESAD-UK 11 36589083 36589083 single base substitution G T upstream_gene_variant ESAD-UK 11 36589783 36589783 single base substitution A G intron_variant ESAD-UK 11 36589841 36589841 single base substitution A C intron_variant ESAD-UK 11 36590594 36590594 single base substitution A C intron_variant ESAD-UK 11 36592454 36592454 single base substitution T G intron_variant ESAD-UK 11 36592982 36592982 single base substitution T C intron_variant ESAD-UK 11 36594479 36594479 single base substitution A C intron_variant ESAD-UK 11 36594879 36594879 single base substitution T G exon_variant ESAD-UK 11 36594879 36594879 single base substitution T G missense_variant L9V 25T>G ESAD-UK 11 36595720 36595720 single base substitution A C exon_variant ESAD-UK 11 36595720 36595720 single base substitution A C missense_variant K289T 866A>C ESAD-UK 11 36596534 36596534 single base substitution C A exon_variant ESAD-UK 11 36596534 36596534 single base substitution C A missense_variant F560L 1680C>A ESAD-UK 11 36596577 36596577 single base substitution G A exon_variant ESAD-UK 11 36596577 36596577 single base substitution G A missense_variant E575K 1723G>A ESAD-UK 11 36596676 36596676 single base substitution G A exon_variant ESAD-UK 11 36596676 36596676 single base substitution G A missense_variant V608M 1822G>A ESAD-UK 11 36596959 36596959 single base substitution A G exon_variant ESAD-UK 11 36596959 36596959 single base substitution A G missense_variant K702R 2105A>G ESAD-UK 11 36597092 36597092 single base substitution C A exon_variant ESAD-UK 11 36597092 36597092 single base substitution C A missense_variant F746L 2238C>A ESAD-UK 11 36597108 36597108 single base substitution A C exon_variant ESAD-UK 11 36597108 36597108 single base substitution A C missense_variant S752R 2254A>C ESAD-UK 11 36597638 36597638 single base substitution G A exon_variant ESAD-UK 11 36597638 36597638 single base substitution G A synonymous_variant K928K 2784G>A ESAD-UK 11 36599666 36599666 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 36599666 36599666 single base substitution T C intron_variant ESAD-UK 11 36599712 36599712 single base substitution A G 3_prime_UTR_variant ESAD-UK 11 36599712 36599712 single base substitution A G intron_variant ESAD-UK 11 36599784 36599784 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 36599784 36599784 single base substitution T C intron_variant ESAD-UK 11 36599973 36599973 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 36599973 36599973 single base substitution C T intron_variant ESAD-UK 11 36600651 36600651 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 36600651 36600651 single base substitution T G intron_variant ESAD-UK 11 36600670 36600670 single base substitution T A 3_prime_UTR_variant ESAD-UK 11 36600670 36600670 single base substitution T A intron_variant ESAD-UK 11 36600822 36600822 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 36600822 36600822 single base substitution T G intron_variant ESAD-UK 11 36601019 36601019 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 36601019 36601019 single base substitution T G intron_variant ESAD-UK 11 36601350 36601350 single base substitution A C downstream_gene_variant ESAD-UK 11 36601350 36601350 single base substitution A C intron_variant ESAD-UK 11 36603938 36603938 single base substitution G A downstream_gene_variant ESAD-UK 11 36603938 36603938 single base substitution G A intron_variant ESAD-UK 11 36604155 36604155 single base substitution T G downstream_gene_variant ESAD-UK 11 36604155 36604155 single base substitution T G intron_variant ESAD-UK 11 36604607 36604607 single base substitution C T downstream_gene_variant ESAD-UK 11 36604607 36604607 single base substitution C T intron_variant ESAD-UK 11 36604699 36604699 single base substitution A T downstream_gene_variant ESAD-UK 11 36604699 36604699 single base substitution A T intron_variant ESAD-UK 11 36605055 36605055 single base substitution A G downstream_gene_variant ESAD-UK 11 36605055 36605055 single base substitution A G intron_variant ESAD-UK 11 36605101 36605101 single base substitution T G downstream_gene_variant ESAD-UK 11 36605101 36605101 single base substitution T G intron_variant ESAD-UK 11 36605263 36605263 single base substitution T G downstream_gene_variant ESAD-UK 11 36605263 36605263 single base substitution T G intron_variant ESAD-UK 11 36605377 36605377 single base substitution G T downstream_gene_variant ESAD-UK 11 36605377 36605377 single base substitution G T intron_variant ESAD-UK 11 36606047 36606047 single base substitution A G downstream_gene_variant ESAD-UK 11 36606047 36606047 single base substitution A G intron_variant ESAD-UK 11 36606628 36606628 single base substitution G T intron_variant ESAD-UK 11 36607184 36607184 single base substitution C T intron_variant ESAD-UK 11 36607875 36607875 single base substitution G A intron_variant ESAD-UK 11 36607981 36607981 single base substitution T G intron_variant ESAD-UK 11 36608602 36608602 single base substitution C G intron_variant ESAD-UK 11 36609485 36609485 single base substitution G T intron_variant ESAD-UK 11 36609506 36609506 single base substitution C A intron_variant ESAD-UK 11 36610074 36610074 single base substitution C A intron_variant ESAD-UK 11 36611417 36611417 single base substitution T G intron_variant ESAD-UK 11 36611453 36611453 single base substitution T A intron_variant ESAD-UK 11 36611470 36611470 single base substitution C A intron_variant ESAD-UK 11 36611605 36611605 single base substitution A C intron_variant ESAD-UK 11 36612722 36612722 single base substitution G A intron_variant ESAD-UK 11 36612957 36612957 single base substitution A T intron_variant ESAD-UK 11 36613468 36613468 single base substitution A G intron_variant ESAD-UK 11 36613737 36613737 deletion of <=200bp T - intron_variant ESAD-UK 11 36613831 36613831 single base substitution C T intron_variant ESAD-UK 11 36613848 36613848 single base substitution T C intron_variant ESAD-UK 11 36613851 36613851 single base substitution G C intron_variant ESAD-UK 11 36613970 36613970 single base substitution T C intron_variant ESAD-UK 11 36614535 36614535 single base substitution C A 3_prime_UTR_variant ESAD-UK 11 36614837 36614837 single base substitution G T downstream_gene_variant ESAD-UK 11 36615268 36615268 single base substitution T C downstream_gene_variant ESAD-UK 11 36615719 36615719 single base substitution A T downstream_gene_variant ESAD-UK 11 36615978 36615978 single base substitution T C downstream_gene_variant ESAD-UK 11 36616008 36616008 single base substitution C T downstream_gene_variant ESAD-UK 11 36617968 36617968 single base substitution A C downstream_gene_variant ESAD-UK 11 36619250 36619250 single base substitution T G downstream_gene_variant ESCA-CN 11 36594890 36594890 single base substitution T G exon_variant ESCA-CN 11 36594890 36594890 single base substitution T G missense_variant S12R 36T>G ESCA-CN 11 36595999 36595999 single base substitution C G exon_variant ESCA-CN 11 36595999 36595999 single base substitution C G stop_gained S382* 1145C>G ESCA-CN 11 36596877 36596877 single base substitution C T exon_variant ESCA-CN 11 36596877 36596877 single base substitution C T synonymous_variant L675L 2023C>T ESCA-CN 11 36599287 36599287 single base substitution A T 3_prime_UTR_variant ESCA-CN 11 36599287 36599287 single base substitution A T intron_variant GBM-US 11 36595309 36595309 single base substitution C T exon_variant GBM-US 11 36595309 36595309 single base substitution C T missense_variant P152L 455C>T GBM-US 11 36596029 36596029 single base substitution G T exon_variant GBM-US 11 36596029 36596029 single base substitution G T missense_variant G392V 1175G>T GBM-US 11 36596275 36596275 single base substitution G A exon_variant GBM-US 11 36596275 36596275 single base substitution G A missense_variant R474H 1421G>A GBM-US 11 36596452 36596452 single base substitution C T exon_variant GBM-US 11 36596452 36596452 single base substitution C T missense_variant T533I 1598C>T GBM-US 11 36596877 36596877 single base substitution C T exon_variant GBM-US 11 36596877 36596877 single base substitution C T synonymous_variant L675L 2023C>T GBM-US 11 36597064 36597064 single base substitution G A exon_variant GBM-US 11 36597064 36597064 single base substitution G A missense_variant R737H 2210G>A GBM-US 11 36614338 36614338 single base substitution G T intron_variant GBM-US 11 36614899 36614899 single base substitution C A downstream_gene_variant KIRC-US 11 36614395 36614395 insertion of <=200bp - G intron_variant KIRC-US 11 36614945 36614945 single base substitution G A downstream_gene_variant KIRP-US 11 36614896 36614896 single base substitution C T downstream_gene_variant LAML-KR 11 36556710 36556710 single base substitution G A intron_variant LAML-KR 11 36574682 36574682 single base substitution C A intron_variant LAML-KR 11 36608794 36608794 single base substitution A G intron_variant LGG-US 11 36596675 36596675 single base substitution C T exon_variant LGG-US 11 36596675 36596675 single base substitution C T synonymous_variant D607D 1821C>T LGG-US 11 36614246 36614246 single base substitution G A intron_variant LICA-CN 11 36595148 36595148 single base substitution A G exon_variant LICA-CN 11 36595148 36595148 single base substitution A G synonymous_variant R98R 294A>G LICA-CN 11 36614718 36614718 single base substitution T A downstream_gene_variant LICA-CN 11 36614719 36614719 single base substitution C T downstream_gene_variant LICA-CN 11 36615041 36615041 single base substitution A T downstream_gene_variant LICA-CN 11 36615044 36615044 single base substitution G A downstream_gene_variant LICA-CN 11 36615705 36615705 single base substitution A C downstream_gene_variant LICA-FR 11 36541238 36541238 single base substitution G T intron_variant LICA-FR 11 36581966 36581966 single base substitution A G intron_variant LICA-FR 11 36596903 36596903 single base substitution G A exon_variant LICA-FR 11 36596903 36596903 single base substitution G A synonymous_variant E683E 2049G>A LICA-FR 11 36596960 36596960 single base substitution G T exon_variant LICA-FR 11 36596960 36596960 single base substitution G T missense_variant K702N 2106G>T LICA-FR 11 36597353 36597353 single base substitution G A exon_variant LICA-FR 11 36597353 36597353 single base substitution G A synonymous_variant Q833Q 2499G>A LICA-FR 11 36605263 36605263 single base substitution T G downstream_gene_variant LICA-FR 11 36605263 36605263 single base substitution T G intron_variant LICA-FR 11 36610722 36610722 single base substitution C G intron_variant LICA-FR 11 36613149 36613150 deletion of <=200bp AC - intron_variant LICA-FR 11 36614388 36614388 single base substitution A T intron_variant LICA-FR 11 36614818 36614818 single base substitution C T downstream_gene_variant LICA-FR 11 36615212 36615212 single base substitution T A downstream_gene_variant LICA-FR 11 36615318 36615318 single base substitution G A downstream_gene_variant LICA-FR 11 36615620 36615620 single base substitution T C downstream_gene_variant LIHC-US 11 36595488 36595488 single base substitution G T exon_variant LIHC-US 11 36595488 36595488 single base substitution G T missense_variant D212Y 634G>T LIHC-US 11 36596385 36596385 single base substitution A T exon_variant LIHC-US 11 36596385 36596385 single base substitution A T stop_gained K511* 1531A>T LIHC-US 11 36596559 36596559 single base substitution G T exon_variant LIHC-US 11 36596559 36596559 single base substitution G T missense_variant A569S 1705G>T LIHC-US 11 36596843 36596843 single base substitution A C exon_variant LIHC-US 11 36596843 36596843 single base substitution A C synonymous_variant A663A 1989A>C LIHC-US 11 36597509 36597509 single base substitution G A exon_variant LIHC-US 11 36597509 36597509 single base substitution G A synonymous_variant L885L 2655G>A LIHC-US 11 36597714 36597714 single base substitution G T intron_variant LIHC-US 11 36597714 36597714 single base substitution G T missense_variant G954C 2860G>T LIHC-US 11 36614459 36614459 single base substitution G T intron_variant LIHC-US 11 36614915 36614915 single base substitution A G downstream_gene_variant LINC-JP 11 36550281 36550281 single base substitution A G intron_variant LINC-JP 11 36558916 36558916 single base substitution G A downstream_gene_variant LINC-JP 11 36558916 36558916 single base substitution G A intron_variant LINC-JP 11 36561228 36561228 single base substitution A G downstream_gene_variant LINC-JP 11 36561228 36561228 single base substitution A G intron_variant LINC-JP 11 36571445 36571445 single base substitution G C intron_variant LINC-JP 11 36588222 36588222 single base substitution T A intron_variant LINC-JP 11 36588222 36588222 single base substitution T A upstream_gene_variant LINC-JP 11 36595123 36595123 single base substitution A C exon_variant LINC-JP 11 36595123 36595123 single base substitution A C missense_variant K90T 269A>C LINC-JP 11 36596738 36596738 deletion of <=200bp A - exon_variant LINC-JP 11 36596738 36596738 deletion of <=200bp A - frameshift_variant T628 LINC-JP 11 36603532 36603532 single base substitution G T downstream_gene_variant LINC-JP 11 36603532 36603532 single base substitution G T intron_variant LINC-JP 11 36609376 36609376 single base substitution G A intron_variant LINC-JP 11 36609499 36609499 single base substitution T C intron_variant LINC-JP 11 36610912 36610912 single base substitution G A intron_variant LIRI-JP 11 36527639 36527639 single base substitution G A upstream_gene_variant LIRI-JP 11 36528004 36528004 single base substitution T C upstream_gene_variant LIRI-JP 11 36528647 36528647 single base substitution A G upstream_gene_variant LIRI-JP 11 36530677 36530677 single base substitution T G upstream_gene_variant LIRI-JP 11 36535216 36535216 single base substitution G A intron_variant LIRI-JP 11 36535216 36535216 single base substitution G A upstream_gene_variant LIRI-JP 11 36536694 36536694 single base substitution G A intron_variant LIRI-JP 11 36536694 36536694 single base substitution G A upstream_gene_variant LIRI-JP 11 36537459 36537459 single base substitution A G intron_variant LIRI-JP 11 36540772 36540772 single base substitution G T intron_variant LIRI-JP 11 36541136 36541136 single base substitution A G intron_variant LIRI-JP 11 36543049 36543049 single base substitution C A intron_variant LIRI-JP 11 36543373 36543373 single base substitution G A intron_variant LIRI-JP 11 36543418 36543418 single base substitution A G intron_variant LIRI-JP 11 36544791 36544791 single base substitution G C intron_variant LIRI-JP 11 36546873 36546873 single base substitution C G intron_variant LIRI-JP 11 36547531 36547531 single base substitution G A intron_variant LIRI-JP 11 36547575 36547575 single base substitution T G intron_variant LIRI-JP 11 36549826 36549826 single base substitution A G intron_variant LIRI-JP 11 36550056 36550056 single base substitution A G intron_variant LIRI-JP 11 36552026 36552026 single base substitution C T intron_variant LIRI-JP 11 36552510 36552510 single base substitution A G intron_variant LIRI-JP 11 36553958 36553958 single base substitution G T intron_variant LIRI-JP 11 36557782 36557782 single base substitution A G downstream_gene_variant LIRI-JP 11 36557782 36557782 single base substitution A G intron_variant LIRI-JP 11 36557868 36557868 single base substitution A G downstream_gene_variant LIRI-JP 11 36557868 36557868 single base substitution A G intron_variant LIRI-JP 11 36558039 36558039 single base substitution A G downstream_gene_variant LIRI-JP 11 36558039 36558039 single base substitution A G intron_variant LIRI-JP 11 36558334 36558334 single base substitution A G downstream_gene_variant LIRI-JP 11 36558334 36558334 single base substitution A G intron_variant LIRI-JP 11 36558830 36558830 single base substitution C T downstream_gene_variant LIRI-JP 11 36558830 36558830 single base substitution C T intron_variant LIRI-JP 11 36559591 36559591 single base substitution C T downstream_gene_variant LIRI-JP 11 36559591 36559591 single base substitution C T intron_variant LIRI-JP 11 36560331 36560331 single base substitution G T downstream_gene_variant LIRI-JP 11 36560331 36560331 single base substitution G T intron_variant LIRI-JP 11 36561860 36561860 single base substitution T A downstream_gene_variant LIRI-JP 11 36561860 36561860 single base substitution T A intron_variant LIRI-JP 11 36562155 36562155 single base substitution A G downstream_gene_variant LIRI-JP 11 36562155 36562155 single base substitution A G intron_variant LIRI-JP 11 36564456 36564456 single base substitution C T intron_variant LIRI-JP 11 36565752 36565752 single base substitution G A intron_variant LIRI-JP 11 36566019 36566019 single base substitution C T intron_variant LIRI-JP 11 36566264 36566264 single base substitution C G intron_variant LIRI-JP 11 36566820 36566820 single base substitution T C intron_variant LIRI-JP 11 36566900 36566900 single base substitution G T intron_variant LIRI-JP 11 36567775 36567775 single base substitution G T intron_variant LIRI-JP 11 36572907 36572907 single base substitution A G intron_variant LIRI-JP 11 36581171 36581171 single base substitution C A intron_variant LIRI-JP 11 36581683 36581683 single base substitution A G intron_variant LIRI-JP 11 36583489 36583489 single base substitution G T intron_variant LIRI-JP 11 36584057 36584057 single base substitution C T intron_variant LIRI-JP 11 36584641 36584641 single base substitution G A intron_variant LIRI-JP 11 36584641 36584641 single base substitution G A upstream_gene_variant LIRI-JP 11 36591565 36591565 single base substitution T C intron_variant LIRI-JP 11 36594132 36594132 single base substitution G A intron_variant LIRI-JP 11 36596064 36596064 single base substitution C A exon_variant LIRI-JP 11 36596064 36596064 single base substitution C A synonymous_variant R404R 1210C>A LIRI-JP 11 36599149 36599149 single base substitution T C 3_prime_UTR_variant LIRI-JP 11 36599149 36599149 single base substitution T C intron_variant LIRI-JP 11 36599646 36599646 single base substitution G T 3_prime_UTR_variant LIRI-JP 11 36599646 36599646 single base substitution G T intron_variant LIRI-JP 11 36600471 36600471 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 36600471 36600471 single base substitution G A intron_variant LIRI-JP 11 36600758 36600758 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 36600758 36600758 single base substitution C T intron_variant LIRI-JP 11 36601450 36601450 single base substitution A G downstream_gene_variant LIRI-JP 11 36601450 36601450 single base substitution A G intron_variant LIRI-JP 11 36602727 36602727 single base substitution A G downstream_gene_variant LIRI-JP 11 36602727 36602727 single base substitution A G intron_variant LIRI-JP 11 36603344 36603344 single base substitution C T downstream_gene_variant LIRI-JP 11 36603344 36603344 single base substitution C T intron_variant LIRI-JP 11 36606647 36606647 single base substitution A C intron_variant LIRI-JP 11 36607136 36607136 single base substitution T C intron_variant LIRI-JP 11 36610776 36610776 single base substitution G A intron_variant LIRI-JP 11 36611055 36611055 single base substitution A G intron_variant LIRI-JP 11 36611169 36611169 single base substitution A G intron_variant LIRI-JP 11 36612280 36612280 single base substitution C T intron_variant LIRI-JP 11 36612864 36612864 single base substitution A G intron_variant LIRI-JP 11 36613539 36613539 single base substitution A G intron_variant LIRI-JP 11 36613737 36613737 deletion of <=200bp T - intron_variant LIRI-JP 11 36614614 36614614 single base substitution T C 3_prime_UTR_variant LIRI-JP 11 36614831 36614831 single base substitution C A downstream_gene_variant LIRI-JP 11 36617309 36617309 single base substitution G A downstream_gene_variant LIRI-JP 11 36619641 36619641 single base substitution A G downstream_gene_variant LUSC-KR 11 36528236 36528236 single base substitution C T upstream_gene_variant LUSC-KR 11 36531790 36531790 single base substitution G T upstream_gene_variant LUSC-KR 11 36533665 36533665 single base substitution G T intron_variant LUSC-KR 11 36533665 36533665 single base substitution G T upstream_gene_variant LUSC-KR 11 36534707 36534707 single base substitution T A intron_variant LUSC-KR 11 36534707 36534707 single base substitution T A upstream_gene_variant LUSC-KR 11 36536289 36536289 single base substitution C T intron_variant LUSC-KR 11 36536289 36536289 single base substitution C T upstream_gene_variant LUSC-KR 11 36551402 36551402 single base substitution G T intron_variant LUSC-KR 11 36551621 36551621 single base substitution G T intron_variant LUSC-KR 11 36553761 36553761 single base substitution G C intron_variant LUSC-KR 11 36555289 36555289 single base substitution A G intron_variant LUSC-KR 11 36556033 36556033 single base substitution G T intron_variant LUSC-KR 11 36556250 36556250 single base substitution A G intron_variant LUSC-KR 11 36559413 36559413 single base substitution C A downstream_gene_variant LUSC-KR 11 36559413 36559413 single base substitution C A intron_variant LUSC-KR 11 36560024 36560024 single base substitution G T downstream_gene_variant LUSC-KR 11 36560024 36560024 single base substitution G T intron_variant LUSC-KR 11 36562117 36562117 single base substitution G T downstream_gene_variant LUSC-KR 11 36562117 36562117 single base substitution G T intron_variant LUSC-KR 11 36563215 36563215 single base substitution C T intron_variant LUSC-KR 11 36564876 36564876 single base substitution C G intron_variant LUSC-KR 11 36566021 36566021 single base substitution C A intron_variant LUSC-KR 11 36569710 36569710 single base substitution C A intron_variant LUSC-KR 11 36575795 36575795 single base substitution C G intron_variant LUSC-KR 11 36581024 36581024 single base substitution T G intron_variant LUSC-KR 11 36581857 36581857 single base substitution C T intron_variant LUSC-KR 11 36582814 36582814 single base substitution G T intron_variant LUSC-KR 11 36583590 36583590 single base substitution A G intron_variant LUSC-KR 11 36587986 36587986 single base substitution T C intron_variant LUSC-KR 11 36587986 36587986 single base substitution T C upstream_gene_variant LUSC-KR 11 36590003 36590003 single base substitution C T intron_variant LUSC-KR 11 36590285 36590285 single base substitution G T intron_variant LUSC-KR 11 36593063 36593063 single base substitution G A intron_variant LUSC-KR 11 36593290 36593290 single base substitution G T intron_variant LUSC-KR 11 36599548 36599548 single base substitution A G 3_prime_UTR_variant LUSC-KR 11 36599548 36599548 single base substitution A G intron_variant LUSC-KR 11 36601636 36601636 single base substitution C T downstream_gene_variant LUSC-KR 11 36601636 36601636 single base substitution C T intron_variant LUSC-KR 11 36601643 36601643 single base substitution G T downstream_gene_variant LUSC-KR 11 36601643 36601643 single base substitution G T intron_variant LUSC-KR 11 36602073 36602073 single base substitution C G downstream_gene_variant LUSC-KR 11 36602073 36602073 single base substitution C G intron_variant LUSC-KR 11 36605135 36605135 single base substitution G T downstream_gene_variant LUSC-KR 11 36605135 36605135 single base substitution G T intron_variant LUSC-KR 11 36609102 36609102 single base substitution C A intron_variant LUSC-KR 11 36611594 36611594 single base substitution C T intron_variant LUSC-KR 11 36612882 36612882 single base substitution G A intron_variant LUSC-KR 11 36615620 36615620 single base substitution T A downstream_gene_variant LUSC-KR 11 36615671 36615671 single base substitution C A downstream_gene_variant LUSC-KR 11 36615844 36615844 single base substitution A T downstream_gene_variant LUSC-US 11 36595189 36595189 single base substitution G T exon_variant LUSC-US 11 36595189 36595189 single base substitution G T missense_variant R112L 335G>T LUSC-US 11 36595199 36595199 single base substitution G T exon_variant LUSC-US 11 36595199 36595199 single base substitution G T synonymous_variant G115G 345G>T LUSC-US 11 36595604 36595604 single base substitution G T exon_variant LUSC-US 11 36595604 36595604 single base substitution G T missense_variant K250N 750G>T LUSC-US 11 36595984 36595984 single base substitution C G exon_variant LUSC-US 11 36595984 36595984 single base substitution C G stop_gained S377* 1130C>G LUSC-US 11 36596185 36596185 single base substitution C T exon_variant LUSC-US 11 36596185 36596185 single base substitution C T missense_variant A444V 1331C>T LUSC-US 11 36596776 36596776 single base substitution T G exon_variant LUSC-US 11 36596776 36596776 single base substitution T G missense_variant V641G 1922T>G LUSC-US 11 36597771 36597771 single base substitution C A intron_variant LUSC-US 11 36597771 36597771 single base substitution C A missense_variant R973S 2917C>A LUSC-US 11 36597797 36597797 single base substitution G T intron_variant LUSC-US 11 36597797 36597797 single base substitution G T missense_variant Q981H 2943G>T LUSC-US 11 36614281 36614281 single base substitution C G intron_variant LUSC-US 11 36614556 36614556 single base substitution G C 3_prime_UTR_variant LUSC-US 11 36615433 36615433 single base substitution C A downstream_gene_variant LUSC-US 11 36615574 36615574 single base substitution C G downstream_gene_variant MALY-DE 11 36530419 36530419 single base substitution T C upstream_gene_variant MALY-DE 11 36540902 36540902 single base substitution T G intron_variant MALY-DE 11 36543658 36543658 single base substitution T G intron_variant MALY-DE 11 36556843 36556843 single base substitution A G intron_variant MALY-DE 11 36557401 36557401 insertion of <=200bp - T intron_variant MALY-DE 11 36557616 36557616 single base substitution T C downstream_gene_variant MALY-DE 11 36557616 36557616 single base substitution T C intron_variant MALY-DE 11 36559486 36559486 single base substitution C T downstream_gene_variant MALY-DE 11 36559486 36559486 single base substitution C T intron_variant MALY-DE 11 36566705 36566705 insertion of <=200bp - T intron_variant MALY-DE 11 36567434 36567434 single base substitution C T intron_variant MALY-DE 11 36570080 36570080 deletion of <=200bp A - intron_variant MALY-DE 11 36580144 36580144 single base substitution C G intron_variant MALY-DE 11 36582860 36582860 single base substitution C A intron_variant MALY-DE 11 36587632 36587633 deletion of <=200bp AG - intron_variant MALY-DE 11 36587632 36587633 deletion of <=200bp AG - upstream_gene_variant MALY-DE 11 36589024 36589024 single base substitution T G intron_variant MALY-DE 11 36589024 36589024 single base substitution T G upstream_gene_variant MALY-DE 11 36591099 36591099 single base substitution C A intron_variant MALY-DE 11 36591465 36591465 single base substitution C A intron_variant MALY-DE 11 36600210 36600210 single base substitution A G 3_prime_UTR_variant MALY-DE 11 36600210 36600210 single base substitution A G intron_variant MALY-DE 11 36601097 36601097 deletion of <=200bp T - 3_prime_UTR_variant MALY-DE 11 36601097 36601097 deletion of <=200bp T - intron_variant MALY-DE 11 36603178 36603178 single base substitution C T downstream_gene_variant MALY-DE 11 36603178 36603178 single base substitution C T intron_variant MALY-DE 11 36606043 36606043 single base substitution C G downstream_gene_variant MALY-DE 11 36606043 36606043 single base substitution C G intron_variant MALY-DE 11 36608776 36608776 single base substitution G C intron_variant MALY-DE 11 36612241 36612242 deletion of <=200bp AC - intron_variant MALY-DE 11 36613149 36613150 deletion of <=200bp AC - intron_variant MALY-DE 11 36614848 36614848 single base substitution A T downstream_gene_variant MALY-DE 11 36615091 36615091 single base substitution T C downstream_gene_variant MALY-DE 11 36619456 36619456 single base substitution A G downstream_gene_variant MELA-AU 11 36527300 36527300 single base substitution T A upstream_gene_variant MELA-AU 11 36528004 36528004 single base substitution T A upstream_gene_variant MELA-AU 11 36529762 36529762 single base substitution G A upstream_gene_variant MELA-AU 11 36530030 36530030 single base substitution G A upstream_gene_variant MELA-AU 11 36531216 36531216 single base substitution G C upstream_gene_variant MELA-AU 11 36531449 36531449 single base substitution G A upstream_gene_variant MELA-AU 11 36531906 36531907 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 36531964 36531964 single base substitution C T upstream_gene_variant MELA-AU 11 36533344 36533344 single base substitution G A intron_variant MELA-AU 11 36533344 36533344 single base substitution G A upstream_gene_variant MELA-AU 11 36533598 36533599 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 36533598 36533599 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 36534607 36534607 single base substitution C T intron_variant MELA-AU 11 36534607 36534607 single base substitution C T upstream_gene_variant MELA-AU 11 36534954 36534954 single base substitution C T intron_variant MELA-AU 11 36534954 36534954 single base substitution C T upstream_gene_variant MELA-AU 11 36534967 36534967 single base substitution G A intron_variant MELA-AU 11 36534967 36534967 single base substitution G A upstream_gene_variant MELA-AU 11 36535740 36535740 single base substitution C T intron_variant MELA-AU 11 36535740 36535740 single base substitution C T upstream_gene_variant MELA-AU 11 36535915 36535915 single base substitution C T intron_variant MELA-AU 11 36535915 36535915 single base substitution C T upstream_gene_variant MELA-AU 11 36536373 36536373 single base substitution C T intron_variant MELA-AU 11 36536373 36536373 single base substitution C T upstream_gene_variant MELA-AU 11 36536521 36536521 single base substitution C T intron_variant MELA-AU 11 36536521 36536521 single base substitution C T upstream_gene_variant MELA-AU 11 36536843 36536843 single base substitution C T intron_variant MELA-AU 11 36536843 36536843 single base substitution C T upstream_gene_variant MELA-AU 11 36537119 36537119 single base substitution C T intron_variant MELA-AU 11 36537541 36537541 single base substitution C T intron_variant MELA-AU 11 36537614 36537614 single base substitution C T intron_variant MELA-AU 11 36537644 36537644 single base substitution T G intron_variant MELA-AU 11 36537945 36537945 single base substitution C T intron_variant MELA-AU 11 36538245 36538245 single base substitution T C intron_variant MELA-AU 11 36538256 36538256 single base substitution C T intron_variant MELA-AU 11 36539691 36539691 single base substitution C T intron_variant MELA-AU 11 36540203 36540203 single base substitution C T intron_variant MELA-AU 11 36540460 36540460 single base substitution C T intron_variant MELA-AU 11 36540826 36540826 single base substitution C T intron_variant MELA-AU 11 36540827 36540827 single base substitution C T intron_variant MELA-AU 11 36540859 36540859 single base substitution C T intron_variant MELA-AU 11 36541627 36541627 single base substitution G A intron_variant MELA-AU 11 36542277 36542277 single base substitution C T intron_variant MELA-AU 11 36542374 36542374 single base substitution C T intron_variant MELA-AU 11 36542850 36542850 single base substitution G A intron_variant MELA-AU 11 36543805 36543805 single base substitution C T intron_variant MELA-AU 11 36544140 36544140 single base substitution C T intron_variant MELA-AU 11 36544795 36544795 single base substitution G A intron_variant MELA-AU 11 36545482 36545482 single base substitution C T intron_variant MELA-AU 11 36545540 36545540 single base substitution C T intron_variant MELA-AU 11 36546078 36546078 single base substitution C T intron_variant MELA-AU 11 36546161 36546161 single base substitution C T intron_variant MELA-AU 11 36546451 36546451 single base substitution C T intron_variant MELA-AU 11 36546605 36546605 single base substitution C T intron_variant MELA-AU 11 36546631 36546631 single base substitution C T intron_variant MELA-AU 11 36547039 36547039 single base substitution C T intron_variant MELA-AU 11 36547118 36547118 single base substitution C T intron_variant MELA-AU 11 36547150 36547150 single base substitution C T intron_variant MELA-AU 11 36547163 36547163 single base substitution C T intron_variant MELA-AU 11 36547242 36547242 single base substitution C T intron_variant MELA-AU 11 36547574 36547574 single base substitution C G intron_variant MELA-AU 11 36547788 36547788 single base substitution C T intron_variant MELA-AU 11 36547821 36547821 single base substitution C T intron_variant MELA-AU 11 36547914 36547914 single base substitution G A intron_variant MELA-AU 11 36548130 36548130 single base substitution C T intron_variant MELA-AU 11 36548534 36548534 single base substitution C T intron_variant MELA-AU 11 36548789 36548789 single base substitution C T intron_variant MELA-AU 11 36549131 36549131 single base substitution C T intron_variant MELA-AU 11 36549189 36549189 single base substitution T C intron_variant MELA-AU 11 36549450 36549450 single base substitution C T intron_variant MELA-AU 11 36549662 36549662 single base substitution G A intron_variant MELA-AU 11 36550011 36550011 single base substitution A G intron_variant MELA-AU 11 36550232 36550232 single base substitution C T intron_variant MELA-AU 11 36550461 36550461 single base substitution C T intron_variant MELA-AU 11 36550509 36550509 single base substitution C T intron_variant MELA-AU 11 36551300 36551300 single base substitution C T intron_variant MELA-AU 11 36551402 36551402 single base substitution G T intron_variant MELA-AU 11 36551578 36551578 single base substitution C T intron_variant MELA-AU 11 36551678 36551678 single base substitution C T intron_variant MELA-AU 11 36552302 36552302 single base substitution C T intron_variant MELA-AU 11 36552710 36552710 single base substitution T C intron_variant MELA-AU 11 36552740 36552740 single base substitution C T intron_variant MELA-AU 11 36552940 36552940 single base substitution C T intron_variant MELA-AU 11 36553966 36553966 single base substitution C G intron_variant MELA-AU 11 36553971 36553971 single base substitution C T intron_variant MELA-AU 11 36554050 36554050 single base substitution C T intron_variant MELA-AU 11 36554320 36554320 single base substitution G A intron_variant MELA-AU 11 36554474 36554474 single base substitution C T intron_variant MELA-AU 11 36554585 36554585 single base substitution C T intron_variant MELA-AU 11 36554828 36554828 single base substitution C T intron_variant MELA-AU 11 36554915 36554915 single base substitution A T intron_variant MELA-AU 11 36555239 36555239 single base substitution C T intron_variant MELA-AU 11 36555916 36555916 single base substitution A T intron_variant MELA-AU 11 36556098 36556098 single base substitution C T intron_variant MELA-AU 11 36556364 36556364 single base substitution C T intron_variant MELA-AU 11 36556510 36556510 single base substitution C T intron_variant MELA-AU 11 36557569 36557569 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 36557569 36557569 single base substitution C T downstream_gene_variant MELA-AU 11 36558005 36558005 single base substitution A G downstream_gene_variant MELA-AU 11 36558005 36558005 single base substitution A G intron_variant MELA-AU 11 36558768 36558768 single base substitution C G downstream_gene_variant MELA-AU 11 36558768 36558768 single base substitution C G intron_variant MELA-AU 11 36559065 36559065 single base substitution A T downstream_gene_variant MELA-AU 11 36559065 36559065 single base substitution A T intron_variant MELA-AU 11 36559235 36559235 single base substitution A G downstream_gene_variant MELA-AU 11 36559235 36559235 single base substitution A G intron_variant MELA-AU 11 36559596 36559596 single base substitution C T downstream_gene_variant MELA-AU 11 36559596 36559596 single base substitution C T intron_variant MELA-AU 11 36560737 36560737 single base substitution C T downstream_gene_variant MELA-AU 11 36560737 36560737 single base substitution C T intron_variant MELA-AU 11 36561125 36561126 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 36561125 36561126 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 36561283 36561283 single base substitution C T downstream_gene_variant MELA-AU 11 36561283 36561283 single base substitution C T intron_variant MELA-AU 11 36561737 36561737 single base substitution C T downstream_gene_variant MELA-AU 11 36561737 36561737 single base substitution C T intron_variant MELA-AU 11 36561993 36561993 single base substitution C T downstream_gene_variant MELA-AU 11 36561993 36561993 single base substitution C T intron_variant MELA-AU 11 36562131 36562131 single base substitution G A downstream_gene_variant MELA-AU 11 36562131 36562131 single base substitution G A intron_variant MELA-AU 11 36562624 36562624 single base substitution C T intron_variant MELA-AU 11 36562629 36562629 single base substitution G A intron_variant MELA-AU 11 36563179 36563179 single base substitution C T intron_variant MELA-AU 11 36563865 36563865 single base substitution G A intron_variant MELA-AU 11 36564120 36564120 single base substitution G A intron_variant MELA-AU 11 36564171 36564171 single base substitution T A intron_variant MELA-AU 11 36564286 36564286 single base substitution G C intron_variant MELA-AU 11 36564495 36564495 single base substitution C T intron_variant MELA-AU 11 36564624 36564624 single base substitution C T intron_variant MELA-AU 11 36564734 36564734 single base substitution G A intron_variant MELA-AU 11 36564817 36564817 single base substitution C T intron_variant MELA-AU 11 36564856 36564857 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 36564889 36564889 single base substitution G A intron_variant MELA-AU 11 36564923 36564923 single base substitution C T intron_variant MELA-AU 11 36564971 36564971 single base substitution C T intron_variant MELA-AU 11 36565031 36565032 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 36565321 36565321 single base substitution G A intron_variant MELA-AU 11 36565387 36565387 single base substitution G A intron_variant MELA-AU 11 36565500 36565500 single base substitution A G intron_variant MELA-AU 11 36565947 36565947 single base substitution G A intron_variant MELA-AU 11 36565975 36565975 single base substitution G A intron_variant MELA-AU 11 36566115 36566115 single base substitution C T intron_variant MELA-AU 11 36566152 36566152 single base substitution C T intron_variant MELA-AU 11 36566219 36566219 single base substitution C T intron_variant MELA-AU 11 36566324 36566324 single base substitution C T intron_variant MELA-AU 11 36566344 36566344 single base substitution T A intron_variant MELA-AU 11 36566473 36566473 single base substitution C T intron_variant MELA-AU 11 36566704 36566704 single base substitution C T intron_variant MELA-AU 11 36566795 36566795 single base substitution T A intron_variant MELA-AU 11 36567047 36567047 single base substitution C T intron_variant MELA-AU 11 36567475 36567475 single base substitution T C intron_variant MELA-AU 11 36567623 36567623 single base substitution G A intron_variant MELA-AU 11 36567947 36567947 single base substitution A G intron_variant MELA-AU 11 36568297 36568297 single base substitution C T intron_variant MELA-AU 11 36569030 36569030 single base substitution G A intron_variant MELA-AU 11 36569118 36569118 single base substitution A T intron_variant MELA-AU 11 36569213 36569213 single base substitution C T intron_variant MELA-AU 11 36569308 36569308 single base substitution C T intron_variant MELA-AU 11 36569385 36569385 single base substitution C T intron_variant MELA-AU 11 36569717 36569717 single base substitution C T intron_variant MELA-AU 11 36570104 36570104 single base substitution C T intron_variant MELA-AU 11 36570199 36570199 single base substitution C T intron_variant MELA-AU 11 36570277 36570277 single base substitution C T intron_variant MELA-AU 11 36570679 36570679 single base substitution G A intron_variant MELA-AU 11 36570690 36570690 single base substitution T C intron_variant MELA-AU 11 36571261 36571261 single base substitution C T intron_variant MELA-AU 11 36571957 36571957 single base substitution C T intron_variant MELA-AU 11 36571996 36571996 single base substitution C T intron_variant MELA-AU 11 36571997 36571997 single base substitution C T intron_variant MELA-AU 11 36572005 36572005 single base substitution G T intron_variant MELA-AU 11 36572401 36572401 single base substitution C T intron_variant MELA-AU 11 36572469 36572469 single base substitution G A intron_variant MELA-AU 11 36572794 36572794 single base substitution C T intron_variant MELA-AU 11 36573405 36573405 single base substitution G A intron_variant MELA-AU 11 36579334 36579334 single base substitution C T intron_variant MELA-AU 11 36579371 36579371 single base substitution G T intron_variant MELA-AU 11 36579372 36579372 single base substitution G A intron_variant MELA-AU 11 36579598 36579598 single base substitution C T intron_variant MELA-AU 11 36579960 36579960 single base substitution C T intron_variant MELA-AU 11 36580271 36580271 single base substitution C T intron_variant MELA-AU 11 36580597 36580597 single base substitution C T intron_variant MELA-AU 11 36580963 36580963 single base substitution C T intron_variant MELA-AU 11 36581017 36581017 single base substitution C T intron_variant MELA-AU 11 36581018 36581018 single base substitution C T intron_variant MELA-AU 11 36581165 36581165 single base substitution C T intron_variant MELA-AU 11 36581281 36581281 single base substitution C T intron_variant MELA-AU 11 36581399 36581399 single base substitution C T intron_variant MELA-AU 11 36581570 36581570 single base substitution G A intron_variant MELA-AU 11 36581578 36581578 single base substitution C T intron_variant MELA-AU 11 36581714 36581714 single base substitution C T intron_variant MELA-AU 11 36581802 36581802 single base substitution T C intron_variant MELA-AU 11 36581897 36581897 single base substitution C T intron_variant MELA-AU 11 36582329 36582329 single base substitution C T intron_variant MELA-AU 11 36582351 36582351 single base substitution C T intron_variant MELA-AU 11 36582422 36582422 single base substitution T G intron_variant MELA-AU 11 36582576 36582576 single base substitution C T intron_variant MELA-AU 11 36582756 36582756 single base substitution T A intron_variant MELA-AU 11 36582878 36582878 single base substitution G A intron_variant MELA-AU 11 36583190 36583190 single base substitution G A intron_variant MELA-AU 11 36583334 36583334 single base substitution C T intron_variant MELA-AU 11 36583596 36583596 single base substitution C T intron_variant MELA-AU 11 36583774 36583774 single base substitution C T intron_variant MELA-AU 11 36584005 36584005 single base substitution C T intron_variant MELA-AU 11 36584116 36584116 single base substitution G A intron_variant MELA-AU 11 36584249 36584249 single base substitution C T intron_variant MELA-AU 11 36584723 36584723 single base substitution C T intron_variant MELA-AU 11 36584723 36584723 single base substitution C T upstream_gene_variant MELA-AU 11 36584988 36584988 single base substitution G A 5_prime_UTR_variant MELA-AU 11 36584988 36584988 single base substitution G A upstream_gene_variant MELA-AU 11 36585063 36585063 single base substitution C T intron_variant MELA-AU 11 36585063 36585063 single base substitution C T upstream_gene_variant MELA-AU 11 36585073 36585073 single base substitution C T intron_variant MELA-AU 11 36585073 36585073 single base substitution C T upstream_gene_variant MELA-AU 11 36585125 36585125 single base substitution C T intron_variant MELA-AU 11 36585125 36585125 single base substitution C T upstream_gene_variant MELA-AU 11 36585621 36585621 single base substitution C T intron_variant MELA-AU 11 36585621 36585621 single base substitution C T upstream_gene_variant MELA-AU 11 36586796 36586796 single base substitution G A intron_variant MELA-AU 11 36586796 36586796 single base substitution G A upstream_gene_variant MELA-AU 11 36587625 36587625 single base substitution G A intron_variant MELA-AU 11 36587625 36587625 single base substitution G A upstream_gene_variant MELA-AU 11 36587662 36587662 single base substitution C T intron_variant MELA-AU 11 36587662 36587662 single base substitution C T upstream_gene_variant MELA-AU 11 36587663 36587663 single base substitution C T intron_variant MELA-AU 11 36587663 36587663 single base substitution C T upstream_gene_variant MELA-AU 11 36588031 36588031 single base substitution C T 5_prime_UTR_variant MELA-AU 11 36588031 36588031 single base substitution C T upstream_gene_variant MELA-AU 11 36588521 36588523 multiple base substitution (>=2bp and <=200bp) TTA CCT intron_variant MELA-AU 11 36588521 36588523 multiple base substitution (>=2bp and <=200bp) TTA CCT upstream_gene_variant MELA-AU 11 36588616 36588616 single base substitution C T intron_variant MELA-AU 11 36588616 36588616 single base substitution C T upstream_gene_variant MELA-AU 11 36589098 36589098 single base substitution C T intron_variant MELA-AU 11 36589098 36589098 single base substitution C T upstream_gene_variant MELA-AU 11 36589454 36589454 single base substitution C T intron_variant MELA-AU 11 36589454 36589454 single base substitution C T upstream_gene_variant MELA-AU 11 36589505 36589505 single base substitution G T intron_variant MELA-AU 11 36589505 36589505 single base substitution G T upstream_gene_variant MELA-AU 11 36589834 36589834 single base substitution G A intron_variant MELA-AU 11 36590265 36590265 single base substitution T A intron_variant MELA-AU 11 36591135 36591136 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 36591369 36591369 single base substitution C T intron_variant MELA-AU 11 36591627 36591627 single base substitution C T intron_variant MELA-AU 11 36591777 36591777 single base substitution A T intron_variant MELA-AU 11 36591851 36591851 single base substitution C T intron_variant MELA-AU 11 36592373 36592373 single base substitution T A intron_variant MELA-AU 11 36592385 36592385 single base substitution T C intron_variant MELA-AU 11 36592444 36592444 single base substitution T G intron_variant MELA-AU 11 36593300 36593300 single base substitution G A intron_variant MELA-AU 11 36593425 36593425 single base substitution C T intron_variant MELA-AU 11 36593594 36593594 single base substitution C T intron_variant MELA-AU 11 36593796 36593796 single base substitution C T intron_variant MELA-AU 11 36594065 36594065 single base substitution G A intron_variant MELA-AU 11 36594146 36594146 single base substitution C T intron_variant MELA-AU 11 36594177 36594177 single base substitution C T intron_variant MELA-AU 11 36594453 36594453 single base substitution T A intron_variant MELA-AU 11 36594686 36594686 single base substitution C T intron_variant MELA-AU 11 36594869 36594869 single base substitution C T exon_variant MELA-AU 11 36594869 36594869 single base substitution C T synonymous_variant F5F 15C>T MELA-AU 11 36595042 36595042 single base substitution C T exon_variant MELA-AU 11 36595042 36595042 single base substitution C T missense_variant P63L 188C>T MELA-AU 11 36595157 36595157 single base substitution G A exon_variant MELA-AU 11 36595157 36595157 single base substitution G A synonymous_variant A101A 303G>A MELA-AU 11 36595176 36595176 single base substitution C T exon_variant MELA-AU 11 36595176 36595176 single base substitution C T stop_gained R108* 322C>T MELA-AU 11 36595231 36595231 single base substitution G A exon_variant MELA-AU 11 36595231 36595231 single base substitution G A missense_variant R126K 377G>A MELA-AU 11 36595272 36595272 single base substitution C T exon_variant MELA-AU 11 36595272 36595272 single base substitution C T missense_variant L140F 418C>T MELA-AU 11 36595448 36595448 single base substitution G A exon_variant MELA-AU 11 36595448 36595448 single base substitution G A synonymous_variant R198R 594G>A MELA-AU 11 36595614 36595614 single base substitution C T exon_variant MELA-AU 11 36595614 36595614 single base substitution C T stop_gained Q254* 760C>T MELA-AU 11 36595703 36595703 single base substitution C T exon_variant MELA-AU 11 36595703 36595703 single base substitution C T synonymous_variant F283F 849C>T MELA-AU 11 36595872 36595872 single base substitution C T exon_variant MELA-AU 11 36595872 36595872 single base substitution C T synonymous_variant L340L 1018C>T MELA-AU 11 36595892 36595892 single base substitution C T exon_variant MELA-AU 11 36595892 36595892 single base substitution C T synonymous_variant S346S 1038C>T MELA-AU 11 36596056 36596056 single base substitution C T exon_variant MELA-AU 11 36596056 36596056 single base substitution C T missense_variant S401L 1202C>T MELA-AU 11 36596232 36596232 single base substitution G A exon_variant MELA-AU 11 36596232 36596232 single base substitution G A missense_variant G460R 1378G>A MELA-AU 11 36596233 36596233 single base substitution G A exon_variant MELA-AU 11 36596233 36596233 single base substitution G A missense_variant G460E 1379G>A MELA-AU 11 36596306 36596306 single base substitution C T exon_variant MELA-AU 11 36596306 36596306 single base substitution C T synonymous_variant Y484Y 1452C>T MELA-AU 11 36596435 36596435 single base substitution G A exon_variant MELA-AU 11 36596435 36596435 single base substitution G A synonymous_variant K527K 1581G>A MELA-AU 11 36596585 36596585 single base substitution C T exon_variant MELA-AU 11 36596585 36596585 single base substitution C T synonymous_variant I577I 1731C>T MELA-AU 11 36596963 36596963 single base substitution C T exon_variant MELA-AU 11 36596963 36596963 single base substitution C T synonymous_variant F703F 2109C>T MELA-AU 11 36597043 36597043 single base substitution G T exon_variant MELA-AU 11 36597043 36597043 single base substitution G T missense_variant C730F 2189G>T MELA-AU 11 36597245 36597245 single base substitution C T exon_variant MELA-AU 11 36597245 36597245 single base substitution C T synonymous_variant L797L 2391C>T MELA-AU 11 36597341 36597341 single base substitution G A exon_variant MELA-AU 11 36597341 36597341 single base substitution G A synonymous_variant R829R 2487G>A MELA-AU 11 36597659 36597659 single base substitution C T intron_variant MELA-AU 11 36597659 36597659 single base substitution C T synonymous_variant I935I 2805C>T MELA-AU 11 36597776 36597776 single base substitution C T intron_variant MELA-AU 11 36597776 36597776 single base substitution C T synonymous_variant F974F 2922C>T MELA-AU 11 36598008 36598008 single base substitution T C 3_prime_UTR_variant MELA-AU 11 36598008 36598008 single base substitution T C intron_variant MELA-AU 11 36598574 36598574 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36598574 36598574 single base substitution C T intron_variant MELA-AU 11 36598911 36598911 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36598911 36598911 single base substitution C T intron_variant MELA-AU 11 36599182 36599182 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36599182 36599182 single base substitution C T intron_variant MELA-AU 11 36599262 36599263 multiple base substitution (>=2bp and <=200bp) GG CA 3_prime_UTR_variant MELA-AU 11 36599262 36599263 multiple base substitution (>=2bp and <=200bp) GG CA intron_variant MELA-AU 11 36599550 36599550 single base substitution G A 3_prime_UTR_variant MELA-AU 11 36599550 36599550 single base substitution G A intron_variant MELA-AU 11 36599831 36599831 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36599831 36599831 single base substitution C T intron_variant MELA-AU 11 36600207 36600207 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36600207 36600207 single base substitution C T intron_variant MELA-AU 11 36600598 36600598 single base substitution G A 3_prime_UTR_variant MELA-AU 11 36600598 36600598 single base substitution G A intron_variant MELA-AU 11 36600644 36600644 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36600644 36600644 single base substitution C T intron_variant MELA-AU 11 36600654 36600654 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36600654 36600654 single base substitution C T intron_variant MELA-AU 11 36600692 36600692 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36600692 36600692 single base substitution C T intron_variant MELA-AU 11 36600772 36600772 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36600772 36600772 single base substitution C T intron_variant MELA-AU 11 36600794 36600794 single base substitution T C 3_prime_UTR_variant MELA-AU 11 36600794 36600794 single base substitution T C intron_variant MELA-AU 11 36600816 36600816 single base substitution G A 3_prime_UTR_variant MELA-AU 11 36600816 36600816 single base substitution G A intron_variant MELA-AU 11 36601003 36601003 single base substitution C T 3_prime_UTR_variant MELA-AU 11 36601003 36601003 single base substitution C T intron_variant MELA-AU 11 36601491 36601491 single base substitution C T downstream_gene_variant MELA-AU 11 36601491 36601491 single base substitution C T intron_variant MELA-AU 11 36601811 36601811 single base substitution G A downstream_gene_variant MELA-AU 11 36601811 36601811 single base substitution G A intron_variant MELA-AU 11 36602077 36602077 single base substitution G A downstream_gene_variant MELA-AU 11 36602077 36602077 single base substitution G A intron_variant MELA-AU 11 36602266 36602266 single base substitution C T downstream_gene_variant MELA-AU 11 36602266 36602266 single base substitution C T intron_variant MELA-AU 11 36602300 36602300 single base substitution G A downstream_gene_variant MELA-AU 11 36602300 36602300 single base substitution G A intron_variant MELA-AU 11 36602322 36602322 single base substitution C T downstream_gene_variant MELA-AU 11 36602322 36602322 single base substitution C T intron_variant MELA-AU 11 36602454 36602454 single base substitution C T downstream_gene_variant MELA-AU 11 36602454 36602454 single base substitution C T intron_variant MELA-AU 11 36602499 36602499 single base substitution C T downstream_gene_variant MELA-AU 11 36602499 36602499 single base substitution C T intron_variant MELA-AU 11 36602629 36602629 single base substitution C A downstream_gene_variant MELA-AU 11 36602629 36602629 single base substitution C A intron_variant MELA-AU 11 36602651 36602651 single base substitution C T downstream_gene_variant MELA-AU 11 36602651 36602651 single base substitution C T intron_variant MELA-AU 11 36602790 36602790 single base substitution G A downstream_gene_variant MELA-AU 11 36602790 36602790 single base substitution G A intron_variant MELA-AU 11 36602794 36602794 single base substitution G A downstream_gene_variant MELA-AU 11 36602794 36602794 single base substitution G A intron_variant MELA-AU 11 36602936 36602936 single base substitution C T downstream_gene_variant MELA-AU 11 36602936 36602936 single base substitution C T intron_variant MELA-AU 11 36603103 36603103 single base substitution C T downstream_gene_variant MELA-AU 11 36603103 36603103 single base substitution C T intron_variant MELA-AU 11 36603109 36603109 single base substitution G A downstream_gene_variant MELA-AU 11 36603109 36603109 single base substitution G A intron_variant MELA-AU 11 36603135 36603135 single base substitution C T downstream_gene_variant MELA-AU 11 36603135 36603135 single base substitution C T intron_variant MELA-AU 11 36603141 36603141 single base substitution G A downstream_gene_variant MELA-AU 11 36603141 36603141 single base substitution G A intron_variant MELA-AU 11 36603269 36603269 single base substitution C T downstream_gene_variant MELA-AU 11 36603269 36603269 single base substitution C T intron_variant MELA-AU 11 36603712 36603712 single base substitution C T downstream_gene_variant MELA-AU 11 36603712 36603712 single base substitution C T intron_variant MELA-AU 11 36604257 36604257 single base substitution A G downstream_gene_variant MELA-AU 11 36604257 36604257 single base substitution A G intron_variant MELA-AU 11 36604641 36604641 single base substitution C T downstream_gene_variant MELA-AU 11 36604641 36604641 single base substitution C T intron_variant MELA-AU 11 36604655 36604655 single base substitution C T downstream_gene_variant MELA-AU 11 36604655 36604655 single base substitution C T intron_variant MELA-AU 11 36605236 36605236 single base substitution C T downstream_gene_variant MELA-AU 11 36605236 36605236 single base substitution C T intron_variant MELA-AU 11 36605351 36605351 single base substitution G A downstream_gene_variant MELA-AU 11 36605351 36605351 single base substitution G A intron_variant MELA-AU 11 36605426 36605426 single base substitution G T downstream_gene_variant MELA-AU 11 36605426 36605426 single base substitution G T intron_variant MELA-AU 11 36605690 36605690 single base substitution G A downstream_gene_variant MELA-AU 11 36605690 36605690 single base substitution G A intron_variant MELA-AU 11 36605702 36605702 single base substitution C T downstream_gene_variant MELA-AU 11 36605702 36605702 single base substitution C T intron_variant MELA-AU 11 36605834 36605834 single base substitution C T downstream_gene_variant MELA-AU 11 36605834 36605834 single base substitution C T intron_variant MELA-AU 11 36605847 36605847 single base substitution G A downstream_gene_variant MELA-AU 11 36605847 36605847 single base substitution G A intron_variant MELA-AU 11 36605865 36605865 single base substitution C T downstream_gene_variant MELA-AU 11 36605865 36605865 single base substitution C T intron_variant MELA-AU 11 36605872 36605872 single base substitution G A downstream_gene_variant MELA-AU 11 36605872 36605872 single base substitution G A intron_variant MELA-AU 11 36605953 36605953 single base substitution G A downstream_gene_variant MELA-AU 11 36605953 36605953 single base substitution G A intron_variant MELA-AU 11 36605991 36605991 single base substitution C T downstream_gene_variant MELA-AU 11 36605991 36605991 single base substitution C T intron_variant MELA-AU 11 36606040 36606040 single base substitution C T downstream_gene_variant MELA-AU 11 36606040 36606040 single base substitution C T intron_variant MELA-AU 11 36606281 36606281 single base substitution G A downstream_gene_variant MELA-AU 11 36606281 36606281 single base substitution G A intron_variant MELA-AU 11 36606563 36606563 single base substitution G A intron_variant MELA-AU 11 36606831 36606831 single base substitution G A intron_variant MELA-AU 11 36606911 36606911 single base substitution C T intron_variant MELA-AU 11 36607083 36607083 single base substitution A G intron_variant MELA-AU 11 36607363 36607363 single base substitution G A intron_variant MELA-AU 11 36607488 36607488 single base substitution G A intron_variant MELA-AU 11 36607818 36607818 single base substitution G A intron_variant MELA-AU 11 36608110 36608110 single base substitution C T intron_variant MELA-AU 11 36608679 36608679 single base substitution C T intron_variant MELA-AU 11 36608748 36608749 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 11 36608776 36608776 single base substitution G C intron_variant MELA-AU 11 36608799 36608799 single base substitution T C intron_variant MELA-AU 11 36609143 36609143 single base substitution A G intron_variant MELA-AU 11 36609289 36609289 single base substitution G A intron_variant MELA-AU 11 36609295 36609295 single base substitution G A intron_variant MELA-AU 11 36609344 36609344 single base substitution C T intron_variant MELA-AU 11 36609369 36609369 single base substitution G T intron_variant MELA-AU 11 36610027 36610027 single base substitution G A intron_variant MELA-AU 11 36610097 36610097 single base substitution G A intron_variant MELA-AU 11 36610111 36610111 single base substitution C T intron_variant MELA-AU 11 36610112 36610112 single base substitution C T intron_variant MELA-AU 11 36610238 36610238 single base substitution G A intron_variant MELA-AU 11 36610429 36610429 single base substitution G A intron_variant MELA-AU 11 36610582 36610582 single base substitution C T intron_variant MELA-AU 11 36610682 36610682 single base substitution G A intron_variant MELA-AU 11 36610799 36610799 single base substitution G A intron_variant MELA-AU 11 36610839 36610839 single base substitution C T intron_variant MELA-AU 11 36610916 36610916 single base substitution G A intron_variant MELA-AU 11 36611127 36611127 single base substitution C T intron_variant MELA-AU 11 36611129 36611129 single base substitution T G intron_variant MELA-AU 11 36611154 36611154 single base substitution C T intron_variant MELA-AU 11 36611988 36611989 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 11 36612034 36612034 single base substitution C T intron_variant MELA-AU 11 36612456 36612456 single base substitution T G intron_variant MELA-AU 11 36612768 36612768 single base substitution T G intron_variant MELA-AU 11 36612851 36612851 single base substitution C T intron_variant MELA-AU 11 36612969 36612969 single base substitution G A intron_variant MELA-AU 11 36612980 36612980 single base substitution C T intron_variant MELA-AU 11 36612986 36612986 single base substitution G A intron_variant MELA-AU 11 36613241 36613241 single base substitution A G intron_variant MELA-AU 11 36613387 36613387 single base substitution A T intron_variant MELA-AU 11 36613448 36613448 single base substitution C T intron_variant MELA-AU 11 36613662 36613662 single base substitution G A intron_variant MELA-AU 11 36614213 36614213 single base substitution C T intron_variant MELA-AU 11 36614235 36614235 single base substitution A G intron_variant MELA-AU 11 36614273 36614273 single base substitution C T intron_variant MELA-AU 11 36614397 36614397 single base substitution G A intron_variant MELA-AU 11 36614448 36614448 single base substitution T A intron_variant MELA-AU 11 36614751 36614751 single base substitution C T downstream_gene_variant MELA-AU 11 36614763 36614763 single base substitution C T downstream_gene_variant MELA-AU 11 36614764 36614764 single base substitution C T downstream_gene_variant MELA-AU 11 36614827 36614827 single base substitution C T downstream_gene_variant MELA-AU 11 36615058 36615058 single base substitution C T downstream_gene_variant MELA-AU 11 36615098 36615098 single base substitution A C downstream_gene_variant MELA-AU 11 36615263 36615263 single base substitution C T downstream_gene_variant MELA-AU 11 36615431 36615431 single base substitution C T downstream_gene_variant MELA-AU 11 36615432 36615432 single base substitution C T downstream_gene_variant MELA-AU 11 36615890 36615890 single base substitution C T downstream_gene_variant MELA-AU 11 36615972 36615972 single base substitution G A downstream_gene_variant MELA-AU 11 36616187 36616187 single base substitution G C downstream_gene_variant MELA-AU 11 36617432 36617432 single base substitution G A downstream_gene_variant MELA-AU 11 36618531 36618531 single base substitution C T downstream_gene_variant MELA-AU 11 36618906 36618906 single base substitution C T downstream_gene_variant MELA-AU 11 36619396 36619396 single base substitution C T downstream_gene_variant ORCA-IN 11 36537781 36537781 single base substitution T G intron_variant ORCA-IN 11 36549380 36549380 single base substitution G A intron_variant ORCA-IN 11 36562438 36562438 single base substitution C T downstream_gene_variant ORCA-IN 11 36562438 36562438 single base substitution C T intron_variant ORCA-IN 11 36573035 36573035 single base substitution T A intron_variant ORCA-IN 11 36591924 36591924 single base substitution A T intron_variant ORCA-IN 11 36595614 36595614 single base substitution C G exon_variant ORCA-IN 11 36595614 36595614 single base substitution C G missense_variant Q254E 760C>G ORCA-IN 11 36600917 36600917 single base substitution G C 3_prime_UTR_variant ORCA-IN 11 36600917 36600917 single base substitution G C intron_variant ORCA-IN 11 36613173 36613173 single base substitution A T intron_variant ORCA-IN 11 36615352 36615352 single base substitution G A downstream_gene_variant OV-AU 11 36529427 36529427 single base substitution T C upstream_gene_variant OV-AU 11 36529634 36529634 single base substitution C T upstream_gene_variant OV-AU 11 36532941 36532941 single base substitution C T intron_variant OV-AU 11 36532941 36532941 single base substitution C T upstream_gene_variant OV-AU 11 36534297 36534297 single base substitution C T intron_variant OV-AU 11 36534297 36534297 single base substitution C T upstream_gene_variant OV-AU 11 36541775 36541775 single base substitution G T 5_prime_UTR_variant OV-AU 11 36541775 36541775 single base substitution G T exon_variant OV-AU 11 36545914 36545914 single base substitution A G intron_variant OV-AU 11 36551694 36551694 single base substitution A C intron_variant OV-AU 11 36553595 36553595 single base substitution T C intron_variant OV-AU 11 36566186 36566186 single base substitution T C intron_variant OV-AU 11 36571620 36571620 single base substitution C G intron_variant OV-AU 11 36583408 36583408 single base substitution A G intron_variant OV-AU 11 36587314 36587314 single base substitution T C intron_variant OV-AU 11 36587314 36587314 single base substitution T C upstream_gene_variant OV-AU 11 36589271 36589271 single base substitution G C intron_variant OV-AU 11 36589271 36589271 single base substitution G C upstream_gene_variant OV-AU 11 36592776 36592776 single base substitution A T intron_variant OV-AU 11 36598676 36598676 single base substitution T G 3_prime_UTR_variant OV-AU 11 36598676 36598676 single base substitution T G intron_variant OV-AU 11 36598823 36598823 single base substitution G A 3_prime_UTR_variant OV-AU 11 36598823 36598823 single base substitution G A intron_variant OV-AU 11 36601606 36601606 single base substitution T A downstream_gene_variant OV-AU 11 36601606 36601606 single base substitution T A intron_variant OV-AU 11 36608776 36608776 single base substitution G C intron_variant OV-AU 11 36611572 36611572 single base substitution C G intron_variant OV-AU 11 36616999 36616999 single base substitution C G downstream_gene_variant PACA-AU 11 36533113 36533137 deletion of <=200bp ATGCTTCTCTTTTTAAGAAGAATTT - intron_variant PACA-AU 11 36533113 36533137 deletion of <=200bp ATGCTTCTCTTTTTAAGAAGAATTT - upstream_gene_variant PACA-AU 11 36541100 36541100 single base substitution C G intron_variant PACA-AU 11 36541125 36541125 single base substitution A T intron_variant PACA-AU 11 36545840 36545840 single base substitution T C intron_variant PACA-AU 11 36546607 36546607 single base substitution C T intron_variant PACA-AU 11 36549634 36549634 single base substitution C G intron_variant PACA-AU 11 36556518 36556518 single base substitution G C intron_variant PACA-AU 11 36556795 36556795 single base substitution G A intron_variant PACA-AU 11 36557352 36557352 single base substitution A G intron_variant PACA-AU 11 36558144 36558144 single base substitution T G downstream_gene_variant PACA-AU 11 36558144 36558144 single base substitution T G intron_variant PACA-AU 11 36560710 36560710 single base substitution G T downstream_gene_variant PACA-AU 11 36560710 36560710 single base substitution G T intron_variant PACA-AU 11 36561696 36561696 single base substitution A C downstream_gene_variant PACA-AU 11 36561696 36561696 single base substitution A C intron_variant PACA-AU 11 36561704 36561704 single base substitution G A downstream_gene_variant PACA-AU 11 36561704 36561704 single base substitution G A intron_variant PACA-AU 11 36562648 36562648 single base substitution G C intron_variant PACA-AU 11 36562664 36562664 single base substitution G A intron_variant PACA-AU 11 36562665 36562665 single base substitution G A intron_variant PACA-AU 11 36562808 36562808 single base substitution G C intron_variant PACA-AU 11 36562940 36562940 single base substitution G A intron_variant PACA-AU 11 36563154 36563154 single base substitution G A intron_variant PACA-AU 11 36563721 36563721 single base substitution G C intron_variant PACA-AU 11 36563847 36563847 single base substitution C T intron_variant PACA-AU 11 36563872 36563872 single base substitution G A intron_variant PACA-AU 11 36563908 36563908 single base substitution G C intron_variant PACA-AU 11 36564051 36564051 single base substitution G A intron_variant PACA-AU 11 36564096 36564096 single base substitution G A intron_variant PACA-AU 11 36564415 36564415 single base substitution G C intron_variant PACA-AU 11 36564910 36564910 single base substitution G A intron_variant PACA-AU 11 36565260 36565260 single base substitution T A intron_variant PACA-AU 11 36567775 36567775 single base substitution G T intron_variant PACA-AU 11 36572552 36572552 single base substitution G T intron_variant PACA-AU 11 36579124 36579124 single base substitution C T intron_variant PACA-AU 11 36579436 36579436 single base substitution C G intron_variant PACA-AU 11 36580507 36580507 single base substitution T G intron_variant PACA-AU 11 36581393 36581393 single base substitution G C intron_variant PACA-AU 11 36588727 36588727 single base substitution C T intron_variant PACA-AU 11 36588727 36588727 single base substitution C T upstream_gene_variant PACA-AU 11 36591851 36591851 single base substitution C T intron_variant PACA-AU 11 36594863 36594863 single base substitution C T exon_variant PACA-AU 11 36594863 36594863 single base substitution C T synonymous_variant A3A 9C>T PACA-AU 11 36596608 36596608 single base substitution A G exon_variant PACA-AU 11 36596608 36596608 single base substitution A G missense_variant D585G 1754A>G PACA-AU 11 36596723 36596723 single base substitution C T exon_variant PACA-AU 11 36596723 36596723 single base substitution C T synonymous_variant V623V 1869C>T PACA-AU 11 36596949 36596949 single base substitution C T exon_variant PACA-AU 11 36596949 36596949 single base substitution C T missense_variant R699W 2095C>T PACA-AU 11 36597187 36597187 single base substitution G A exon_variant PACA-AU 11 36597187 36597187 single base substitution G A missense_variant R778Q 2333G>A PACA-AU 11 36598372 36598372 single base substitution T C 3_prime_UTR_variant PACA-AU 11 36598372 36598372 single base substitution T C intron_variant PACA-AU 11 36600832 36600832 single base substitution T G 3_prime_UTR_variant PACA-AU 11 36600832 36600832 single base substitution T G intron_variant PACA-AU 11 36603945 36603945 single base substitution C T downstream_gene_variant PACA-AU 11 36603945 36603945 single base substitution C T intron_variant PACA-AU 11 36606122 36606122 single base substitution G A downstream_gene_variant PACA-AU 11 36606122 36606122 single base substitution G A intron_variant PACA-AU 11 36607314 36607314 insertion of <=200bp - A intron_variant PACA-AU 11 36607346 36607346 single base substitution T A intron_variant PACA-AU 11 36608774 36608774 single base substitution C G intron_variant PACA-AU 11 36608776 36608776 single base substitution G C intron_variant PACA-AU 11 36608782 36608782 single base substitution G A intron_variant PACA-AU 11 36609742 36609742 single base substitution T C intron_variant PACA-AU 11 36613575 36613575 single base substitution C T intron_variant PACA-AU 11 36614183 36614183 single base substitution T G intron_variant PACA-AU 11 36614905 36614905 single base substitution C A downstream_gene_variant PACA-CA 11 36530481 36530482 deletion of <=200bp TT - upstream_gene_variant PACA-CA 11 36535140 36535140 single base substitution T A intron_variant PACA-CA 11 36535140 36535140 single base substitution T A upstream_gene_variant PACA-CA 11 36537578 36537578 single base substitution T C intron_variant PACA-CA 11 36538778 36538778 single base substitution T A intron_variant PACA-CA 11 36539190 36539190 single base substitution C G intron_variant PACA-CA 11 36539287 36539287 single base substitution T A intron_variant PACA-CA 11 36539405 36539405 single base substitution T A intron_variant PACA-CA 11 36543662 36543662 single base substitution G T intron_variant PACA-CA 11 36543680 36543680 single base substitution G T intron_variant PACA-CA 11 36547510 36547514 deletion of <=200bp CTTTT - intron_variant PACA-CA 11 36547933 36547933 single base substitution T G intron_variant PACA-CA 11 36548093 36548093 single base substitution C T intron_variant PACA-CA 11 36550393 36550393 single base substitution G A intron_variant PACA-CA 11 36550584 36550584 single base substitution C T intron_variant PACA-CA 11 36551128 36551128 single base substitution C T intron_variant PACA-CA 11 36551591 36551591 single base substitution C T intron_variant PACA-CA 11 36553516 36553516 single base substitution T G intron_variant PACA-CA 11 36556344 36556344 single base substitution T G intron_variant PACA-CA 11 36556582 36556582 insertion of <=200bp - T intron_variant PACA-CA 11 36557401 36557401 deletion of <=200bp T - intron_variant PACA-CA 11 36558896 36558896 single base substitution G A downstream_gene_variant PACA-CA 11 36558896 36558896 single base substitution G A intron_variant PACA-CA 11 36559416 36559416 deletion of <=200bp T - downstream_gene_variant PACA-CA 11 36559416 36559416 deletion of <=200bp T - intron_variant PACA-CA 11 36561498 36561498 single base substitution A C downstream_gene_variant PACA-CA 11 36561498 36561498 single base substitution A C intron_variant PACA-CA 11 36564405 36564405 deletion of <=200bp A - intron_variant PACA-CA 11 36564415 36564415 insertion of <=200bp - A intron_variant PACA-CA 11 36566267 36566267 single base substitution G A intron_variant PACA-CA 11 36568243 36568243 single base substitution A T intron_variant PACA-CA 11 36570409 36570409 single base substitution C A intron_variant PACA-CA 11 36579127 36579127 single base substitution C T intron_variant PACA-CA 11 36580680 36580680 insertion of <=200bp - T intron_variant PACA-CA 11 36581690 36581690 single base substitution G T intron_variant PACA-CA 11 36583625 36583625 single base substitution T C intron_variant PACA-CA 11 36585071 36585071 insertion of <=200bp - TC intron_variant PACA-CA 11 36585071 36585071 insertion of <=200bp - TC upstream_gene_variant PACA-CA 11 36586724 36586724 single base substitution C T intron_variant PACA-CA 11 36586724 36586724 single base substitution C T upstream_gene_variant PACA-CA 11 36590633 36590633 single base substitution C T intron_variant PACA-CA 11 36596151 36596151 single base substitution G C exon_variant PACA-CA 11 36596151 36596151 single base substitution G C missense_variant V433L 1297G>C PACA-CA 11 36597326 36597326 single base substitution T G exon_variant PACA-CA 11 36597326 36597326 single base substitution T G synonymous_variant A824A 2472T>G PACA-CA 11 36602578 36602578 single base substitution C T downstream_gene_variant PACA-CA 11 36602578 36602578 single base substitution C T intron_variant PACA-CA 11 36603532 36603532 single base substitution G A downstream_gene_variant PACA-CA 11 36603532 36603532 single base substitution G A intron_variant PACA-CA 11 36605630 36605630 single base substitution G A downstream_gene_variant PACA-CA 11 36605630 36605630 single base substitution G A intron_variant PACA-CA 11 36607997 36607997 single base substitution G A intron_variant PACA-CA 11 36608776 36608776 single base substitution G C intron_variant PACA-CA 11 36613468 36613468 single base substitution A C intron_variant PACA-CA 11 36615031 36615031 single base substitution G C downstream_gene_variant PACA-CA 11 36617013 36617013 deletion of <=200bp A - downstream_gene_variant PACA-CA 11 36617037 36617037 single base substitution T G downstream_gene_variant PACA-CA 11 36617211 36617211 single base substitution T C downstream_gene_variant PACA-CA 11 36617712 36617712 single base substitution G T downstream_gene_variant PACA-CA 11 36618261 36618261 single base substitution T C downstream_gene_variant PAEN-AU 11 36566967 36566967 single base substitution T A intron_variant PAEN-AU 11 36566968 36566968 single base substitution C A intron_variant PAEN-AU 11 36572617 36572617 single base substitution C A intron_variant PAEN-AU 11 36600052 36600052 single base substitution G T 3_prime_UTR_variant PAEN-AU 11 36600052 36600052 single base substitution G T intron_variant PAEN-AU 11 36607341 36607341 single base substitution G A intron_variant PAEN-AU 11 36610155 36610155 single base substitution C T intron_variant PAEN-IT 11 36591099 36591099 single base substitution C T intron_variant PAEN-IT 11 36597742 36597742 single base substitution G A intron_variant PAEN-IT 11 36597742 36597742 single base substitution G A missense_variant G963E 2888G>A PBCA-DE 11 36530707 36530707 single base substitution A G upstream_gene_variant PBCA-DE 11 36536028 36536028 single base substitution T C intron_variant PBCA-DE 11 36536028 36536028 single base substitution T C upstream_gene_variant PBCA-DE 11 36548393 36548393 single base substitution C A intron_variant PBCA-DE 11 36548868 36548868 single base substitution C A intron_variant PBCA-DE 11 36553927 36553927 single base substitution A G intron_variant PBCA-DE 11 36557163 36557163 single base substitution G A intron_variant PBCA-DE 11 36564405 36564405 insertion of <=200bp - A intron_variant PBCA-DE 11 36569927 36569927 single base substitution C T intron_variant PBCA-DE 11 36587632 36587632 insertion of <=200bp - AGAG intron_variant PBCA-DE 11 36587632 36587632 insertion of <=200bp - AGAG upstream_gene_variant PBCA-DE 11 36587632 36587633 deletion of <=200bp AG - intron_variant PBCA-DE 11 36587632 36587633 deletion of <=200bp AG - upstream_gene_variant PBCA-DE 11 36596950 36596950 single base substitution G A exon_variant PBCA-DE 11 36596950 36596950 single base substitution G A missense_variant R699Q 2096G>A PBCA-DE 11 36597732 36597732 single base substitution G A intron_variant PBCA-DE 11 36597732 36597732 single base substitution G A missense_variant A960T 2878G>A PBCA-DE 11 36598357 36598357 single base substitution T A 3_prime_UTR_variant PBCA-DE 11 36598357 36598357 single base substitution T A intron_variant PBCA-DE 11 36598724 36598727 deletion of <=200bp ACAG - 3_prime_UTR_variant PBCA-DE 11 36598724 36598727 deletion of <=200bp ACAG - intron_variant PBCA-DE 11 36598740 36598740 insertion of <=200bp - T 3_prime_UTR_variant PBCA-DE 11 36598740 36598740 insertion of <=200bp - T intron_variant PBCA-DE 11 36606386 36606386 single base substitution G T intron_variant PBCA-DE 11 36608795 36608796 deletion of <=200bp TG - intron_variant PBCA-DE 11 36612241 36612242 deletion of <=200bp AC - intron_variant PBCA-DE 11 36612958 36612958 insertion of <=200bp - T intron_variant PBCA-DE 11 36613149 36613150 deletion of <=200bp AC - intron_variant PBCA-DE 11 36613807 36613807 single base substitution T C intron_variant PRAD-CA 11 36528424 36528424 single base substitution T G upstream_gene_variant PRAD-CA 11 36551402 36551402 single base substitution G T intron_variant PRAD-CA 11 36589119 36589119 single base substitution C A intron_variant PRAD-CA 11 36589119 36589119 single base substitution C A upstream_gene_variant PRAD-CA 11 36608796 36608796 single base substitution G A intron_variant PRAD-CA 11 36617772 36617772 single base substitution G T downstream_gene_variant PRAD-UK 11 36527477 36527477 single base substitution T C upstream_gene_variant PRAD-UK 11 36535095 36535095 single base substitution C T intron_variant PRAD-UK 11 36535095 36535095 single base substitution C T upstream_gene_variant PRAD-UK 11 36538029 36538029 single base substitution G A intron_variant PRAD-UK 11 36543198 36543198 single base substitution G T intron_variant PRAD-UK 11 36547681 36547681 single base substitution A G intron_variant PRAD-UK 11 36553372 36553372 single base substitution C A intron_variant PRAD-UK 11 36558448 36558448 single base substitution A G downstream_gene_variant PRAD-UK 11 36558448 36558448 single base substitution A G intron_variant PRAD-UK 11 36561539 36561539 single base substitution T C downstream_gene_variant PRAD-UK 11 36561539 36561539 single base substitution T C intron_variant PRAD-UK 11 36566351 36566351 single base substitution T G intron_variant PRAD-UK 11 36580392 36580392 single base substitution G C intron_variant PRAD-UK 11 36595391 36595391 single base substitution C A exon_variant PRAD-UK 11 36595391 36595391 single base substitution C A stop_gained C179* 537C>A PRAD-UK 11 36598859 36598859 single base substitution G T 3_prime_UTR_variant PRAD-UK 11 36598859 36598859 single base substitution G T intron_variant PRAD-UK 11 36605673 36605673 insertion of <=200bp - T downstream_gene_variant PRAD-UK 11 36605673 36605673 insertion of <=200bp - T intron_variant PRAD-UK 11 36605834 36605834 single base substitution C T downstream_gene_variant PRAD-UK 11 36605834 36605834 single base substitution C T intron_variant PRAD-UK 11 36607359 36607359 single base substitution A G intron_variant PRAD-UK 11 36607495 36607495 single base substitution G A intron_variant PRAD-UK 11 36616117 36616117 insertion of <=200bp - T downstream_gene_variant PRAD-US 11 36595189 36595189 single base substitution G A exon_variant PRAD-US 11 36595189 36595189 single base substitution G A missense_variant R112H 335G>A PRAD-US 11 36595849 36595849 single base substitution G A exon_variant PRAD-US 11 36595849 36595849 single base substitution G A missense_variant R332Q 995G>A PRAD-US 11 36596041 36596041 single base substitution G A exon_variant PRAD-US 11 36596041 36596041 single base substitution G A missense_variant R396H 1187G>A PRAD-US 11 36597064 36597064 single base substitution G A exon_variant PRAD-US 11 36597064 36597064 single base substitution G A missense_variant R737H 2210G>A PRAD-US 11 36597450 36597450 single base substitution G A exon_variant PRAD-US 11 36597450 36597450 single base substitution G A missense_variant V866M 2596G>A PRAD-US 11 36597480 36597480 single base substitution G A exon_variant PRAD-US 11 36597480 36597480 single base substitution G A missense_variant E876K 2626G>A PRAD-US 11 36615227 36615227 single base substitution A G downstream_gene_variant READ-US 11 36595177 36595177 single base substitution G A exon_variant READ-US 11 36595177 36595177 single base substitution G A missense_variant R108Q 323G>A READ-US 11 36595510 36595510 single base substitution G A exon_variant READ-US 11 36595510 36595510 single base substitution G A missense_variant R219Q 656G>A READ-US 11 36615301 36615301 single base substitution G T downstream_gene_variant RECA-EU 11 36533651 36533651 single base substitution T A intron_variant RECA-EU 11 36533651 36533651 single base substitution T A upstream_gene_variant RECA-EU 11 36567698 36567698 single base substitution G C intron_variant RECA-EU 11 36567823 36567823 single base substitution A T intron_variant RECA-EU 11 36592414 36592414 single base substitution G A intron_variant RECA-EU 11 36609638 36609638 single base substitution C A intron_variant RECA-EU 11 36611206 36611206 single base substitution A T intron_variant SKCA-BR 11 36528068 36528068 single base substitution A C upstream_gene_variant SKCA-BR 11 36528515 36528515 single base substitution T A upstream_gene_variant SKCA-BR 11 36528734 36528734 single base substitution T C upstream_gene_variant SKCA-BR 11 36528996 36528996 single base substitution A G upstream_gene_variant SKCA-BR 11 36531505 36531505 single base substitution A C upstream_gene_variant SKCA-BR 11 36533753 36533753 single base substitution G A intron_variant SKCA-BR 11 36533753 36533753 single base substitution G A upstream_gene_variant SKCA-BR 11 36534798 36534798 single base substitution C T intron_variant SKCA-BR 11 36534798 36534798 single base substitution C T upstream_gene_variant SKCA-BR 11 36537331 36537331 single base substitution G A intron_variant SKCA-BR 11 36537592 36537592 single base substitution G A intron_variant SKCA-BR 11 36537882 36537882 insertion of <=200bp - GT intron_variant SKCA-BR 11 36540348 36540348 single base substitution T C intron_variant SKCA-BR 11 36540707 36540707 insertion of <=200bp - AT intron_variant SKCA-BR 11 36540859 36540859 single base substitution C T intron_variant SKCA-BR 11 36543456 36543456 single base substitution G A intron_variant SKCA-BR 11 36543944 36543944 single base substitution C T intron_variant SKCA-BR 11 36546182 36546182 single base substitution G T intron_variant SKCA-BR 11 36547785 36547785 single base substitution T C intron_variant SKCA-BR 11 36547792 36547792 single base substitution A C intron_variant SKCA-BR 11 36548131 36548131 single base substitution C T intron_variant SKCA-BR 11 36548536 36548536 single base substitution C T intron_variant SKCA-BR 11 36550815 36550815 single base substitution C T intron_variant SKCA-BR 11 36551561 36551561 single base substitution A T intron_variant SKCA-BR 11 36554128 36554128 single base substitution C T intron_variant SKCA-BR 11 36557962 36557962 single base substitution C T downstream_gene_variant SKCA-BR 11 36557962 36557962 single base substitution C T intron_variant SKCA-BR 11 36559770 36559770 single base substitution C T downstream_gene_variant SKCA-BR 11 36559770 36559770 single base substitution C T intron_variant SKCA-BR 11 36559922 36559922 single base substitution C T downstream_gene_variant SKCA-BR 11 36559922 36559922 single base substitution C T intron_variant SKCA-BR 11 36560237 36560237 single base substitution T C downstream_gene_variant SKCA-BR 11 36560237 36560237 single base substitution T C intron_variant SKCA-BR 11 36563952 36563952 single base substitution C G intron_variant SKCA-BR 11 36564161 36564161 single base substitution C T intron_variant SKCA-BR 11 36567864 36567864 single base substitution C T intron_variant SKCA-BR 11 36568262 36568262 single base substitution T G intron_variant SKCA-BR 11 36570174 36570174 single base substitution G A intron_variant SKCA-BR 11 36572156 36572156 single base substitution C T intron_variant SKCA-BR 11 36573282 36573282 single base substitution T C intron_variant SKCA-BR 11 36574939 36574939 single base substitution C T intron_variant SKCA-BR 11 36580511 36580511 single base substitution C T intron_variant SKCA-BR 11 36581578 36581578 single base substitution C T intron_variant SKCA-BR 11 36582167 36582167 single base substitution C T intron_variant SKCA-BR 11 36584528 36584528 single base substitution T A intron_variant SKCA-BR 11 36588930 36588930 single base substitution C T 5_prime_UTR_variant SKCA-BR 11 36588930 36588930 single base substitution C T upstream_gene_variant SKCA-BR 11 36596724 36596724 single base substitution C T exon_variant SKCA-BR 11 36596724 36596724 single base substitution C T missense_variant R624C 1870C>T SKCA-BR 11 36596941 36596941 single base substitution G A exon_variant SKCA-BR 11 36596941 36596941 single base substitution G A missense_variant G696D 2087G>A SKCA-BR 11 36599256 36599256 single base substitution C T 3_prime_UTR_variant SKCA-BR 11 36599256 36599256 single base substitution C T intron_variant SKCA-BR 11 36601649 36601649 single base substitution G A downstream_gene_variant SKCA-BR 11 36601649 36601649 single base substitution G A intron_variant SKCA-BR 11 36601712 36601712 single base substitution C T downstream_gene_variant SKCA-BR 11 36601712 36601712 single base substitution C T intron_variant SKCA-BR 11 36605027 36605027 single base substitution G A downstream_gene_variant SKCA-BR 11 36605027 36605027 single base substitution G A intron_variant SKCA-BR 11 36608792 36608792 insertion of <=200bp - ATG intron_variant SKCA-BR 11 36610097 36610097 single base substitution G A intron_variant SKCA-BR 11 36611514 36611514 single base substitution C T intron_variant SKCA-BR 11 36611731 36611731 single base substitution G A intron_variant SKCA-BR 11 36614147 36614147 single base substitution C T intron_variant SKCA-BR 11 36619046 36619046 single base substitution C T downstream_gene_variant SKCM-US 11 36594863 36594863 single base substitution C T exon_variant SKCM-US 11 36594863 36594863 single base substitution C T synonymous_variant A3A 9C>T SKCM-US 11 36594953 36594953 single base substitution C T exon_variant SKCM-US 11 36594953 36594953 single base substitution C T synonymous_variant F33F 99C>T SKCM-US 11 36594964 36594964 single base substitution C T exon_variant SKCM-US 11 36594964 36594964 single base substitution C T missense_variant S37F 110C>T SKCM-US 11 36594965 36594965 single base substitution C T exon_variant SKCM-US 11 36594965 36594965 single base substitution C T synonymous_variant S37S 111C>T SKCM-US 11 36595095 36595095 single base substitution T G exon_variant SKCM-US 11 36595095 36595095 single base substitution T G missense_variant L81V 241T>G SKCM-US 11 36595117 36595117 single base substitution C T exon_variant SKCM-US 11 36595117 36595117 single base substitution C T missense_variant S88L 263C>T SKCM-US 11 36595128 36595128 single base substitution C T exon_variant SKCM-US 11 36595128 36595128 single base substitution C T missense_variant H92Y 274C>T SKCM-US 11 36595229 36595229 single base substitution G A exon_variant SKCM-US 11 36595229 36595229 single base substitution G A synonymous_variant R125R 375G>A SKCM-US 11 36595249 36595249 single base substitution C T exon_variant SKCM-US 11 36595249 36595249 single base substitution C T missense_variant P132L 395C>T SKCM-US 11 36595296 36595296 single base substitution G A exon_variant SKCM-US 11 36595296 36595296 single base substitution G A missense_variant A148T 442G>A SKCM-US 11 36595303 36595303 single base substitution C T exon_variant SKCM-US 11 36595303 36595303 single base substitution C T missense_variant S150F 449C>T SKCM-US 11 36595523 36595523 single base substitution G A exon_variant SKCM-US 11 36595523 36595523 single base substitution G A synonymous_variant R223R 669G>A SKCM-US 11 36595652 36595652 single base substitution C T exon_variant SKCM-US 11 36595652 36595652 single base substitution C T synonymous_variant I266I 798C>T SKCM-US 11 36595792 36595792 single base substitution G A exon_variant SKCM-US 11 36595792 36595792 single base substitution G A missense_variant C313Y 938G>A SKCM-US 11 36595854 36595854 single base substitution C T exon_variant SKCM-US 11 36595854 36595854 single base substitution C T missense_variant P334S 1000C>T SKCM-US 11 36596150 36596150 single base substitution C T exon_variant SKCM-US 11 36596150 36596150 single base substitution C T synonymous_variant S432S 1296C>T SKCM-US 11 36596185 36596185 single base substitution C T exon_variant SKCM-US 11 36596185 36596185 single base substitution C T missense_variant A444V 1331C>T SKCM-US 11 36596355 36596355 single base substitution C T exon_variant SKCM-US 11 36596355 36596355 single base substitution C T stop_gained Q501* 1501C>T SKCM-US 11 36596519 36596519 single base substitution C T exon_variant SKCM-US 11 36596519 36596519 single base substitution C T synonymous_variant T555T 1665C>T SKCM-US 11 36596622 36596622 single base substitution C T exon_variant SKCM-US 11 36596622 36596622 single base substitution C T synonymous_variant L590L 1768C>T SKCM-US 11 36596675 36596675 single base substitution C T exon_variant SKCM-US 11 36596675 36596675 single base substitution C T synonymous_variant D607D 1821C>T SKCM-US 11 36596731 36596731 single base substitution C T exon_variant SKCM-US 11 36596731 36596731 single base substitution C T missense_variant S626L 1877C>T SKCM-US 11 36596800 36596800 single base substitution C T exon_variant SKCM-US 11 36596800 36596800 single base substitution C T missense_variant P649L 1946C>T SKCM-US 11 36596859 36596859 single base substitution G A exon_variant SKCM-US 11 36596859 36596859 single base substitution G A missense_variant E669K 2005G>A SKCM-US 11 36597001 36597001 single base substitution G A exon_variant SKCM-US 11 36597001 36597001 single base substitution G A missense_variant R716Q 2147G>A SKCM-US 11 36597009 36597009 single base substitution G A exon_variant SKCM-US 11 36597009 36597009 single base substitution G A missense_variant E719K 2155G>A SKCM-US 11 36597025 36597025 single base substitution C T exon_variant SKCM-US 11 36597025 36597025 single base substitution C T missense_variant S724F 2171C>T SKCM-US 11 36597162 36597162 single base substitution G A exon_variant SKCM-US 11 36597162 36597162 single base substitution G A missense_variant E770K 2308G>A SKCM-US 11 36597229 36597229 single base substitution C T exon_variant SKCM-US 11 36597229 36597229 single base substitution C T missense_variant P792L 2375C>T SKCM-US 11 36597233 36597233 single base substitution C T exon_variant SKCM-US 11 36597233 36597233 single base substitution C T synonymous_variant S793S 2379C>T SKCM-US 11 36597316 36597316 single base substitution A G exon_variant SKCM-US 11 36597316 36597316 single base substitution A G missense_variant N821S 2462A>G SKCM-US 11 36597596 36597596 single base substitution C T exon_variant SKCM-US 11 36597596 36597596 single base substitution C T synonymous_variant F914F 2742C>T SKCM-US 11 36597709 36597709 single base substitution G T intron_variant SKCM-US 11 36597709 36597709 single base substitution G T missense_variant R952M 2855G>T SKCM-US 11 36597719 36597719 single base substitution C T intron_variant SKCM-US 11 36597719 36597719 single base substitution C T synonymous_variant S955S 2865C>T SKCM-US 11 36597825 36597825 single base substitution C T intron_variant SKCM-US 11 36597825 36597825 single base substitution C T synonymous_variant L991L 2971C>T SKCM-US 11 36597850 36597850 single base substitution C T intron_variant SKCM-US 11 36597850 36597850 single base substitution C T missense_variant S999F 2996C>T SKCM-US 11 36614165 36614165 single base substitution C T intron_variant SKCM-US 11 36614213 36614213 single base substitution C T intron_variant SKCM-US 11 36614241 36614241 single base substitution C T intron_variant SKCM-US 11 36614248 36614248 single base substitution G A intron_variant SKCM-US 11 36614256 36614256 single base substitution A G intron_variant SKCM-US 11 36614379 36614379 single base substitution G A intron_variant SKCM-US 11 36614441 36614441 single base substitution A G intron_variant SKCM-US 11 36614448 36614448 single base substitution T A intron_variant SKCM-US 11 36614459 36614459 single base substitution G A intron_variant SKCM-US 11 36614599 36614599 single base substitution C T 3_prime_UTR_variant SKCM-US 11 36614751 36614751 single base substitution C T downstream_gene_variant SKCM-US 11 36614757 36614757 single base substitution T C downstream_gene_variant SKCM-US 11 36614827 36614827 single base substitution C T downstream_gene_variant SKCM-US 11 36614842 36614842 single base substitution C T downstream_gene_variant SKCM-US 11 36615058 36615058 single base substitution C T downstream_gene_variant SKCM-US 11 36615100 36615100 single base substitution G A downstream_gene_variant SKCM-US 11 36615118 36615118 single base substitution G A downstream_gene_variant SKCM-US 11 36615272 36615272 single base substitution C T downstream_gene_variant SKCM-US 11 36615273 36615273 single base substitution C T downstream_gene_variant SKCM-US 11 36615431 36615431 single base substitution C T downstream_gene_variant SKCM-US 11 36615435 36615435 single base substitution C T downstream_gene_variant SKCM-US 11 36615566 36615566 single base substitution C A downstream_gene_variant STAD-US 11 36594879 36594879 single base substitution T G exon_variant STAD-US 11 36594879 36594879 single base substitution T G missense_variant L9V 25T>G STAD-US 11 36595009 36595009 single base substitution C A exon_variant STAD-US 11 36595009 36595009 single base substitution C A missense_variant S52Y 155C>A STAD-US 11 36595248 36595248 single base substitution C T exon_variant STAD-US 11 36595248 36595248 single base substitution C T missense_variant P132S 394C>T STAD-US 11 36595270 36595270 single base substitution G A exon_variant STAD-US 11 36595270 36595270 single base substitution G A missense_variant G139D 416G>A STAD-US 11 36595301 36595301 single base substitution T G exon_variant STAD-US 11 36595301 36595301 single base substitution T G synonymous_variant T149T 447T>G STAD-US 11 36595310 36595310 single base substitution G A exon_variant STAD-US 11 36595310 36595310 single base substitution G A synonymous_variant P152P 456G>A STAD-US 11 36595554 36595554 deletion of <=200bp A - exon_variant STAD-US 11 36595554 36595554 deletion of <=200bp A - frameshift_variant K234 STAD-US 11 36595732 36595732 single base substitution G A exon_variant STAD-US 11 36595732 36595732 single base substitution G A missense_variant C293Y 878G>A STAD-US 11 36595836 36595836 single base substitution T C exon_variant STAD-US 11 36595836 36595836 single base substitution T C missense_variant C328R 982T>C STAD-US 11 36596057 36596057 single base substitution G A exon_variant STAD-US 11 36596057 36596057 single base substitution G A synonymous_variant S401S 1203G>A STAD-US 11 36596082 36596082 single base substitution C T exon_variant STAD-US 11 36596082 36596082 single base substitution C T missense_variant R410W 1228C>T STAD-US 11 36597271 36597271 single base substitution A G exon_variant STAD-US 11 36597271 36597271 single base substitution A G missense_variant E806G 2417A>G STAD-US 11 36597479 36597479 single base substitution C T exon_variant STAD-US 11 36597479 36597479 single base substitution C T synonymous_variant S875S 2625C>T STAD-US 11 36597722 36597722 insertion of <=200bp - G frameshift_variant I956M? STAD-US 11 36597722 36597722 insertion of <=200bp - G intron_variant STAD-US 11 36597723 36597723 insertion of <=200bp - G frameshift_variant G957G? STAD-US 11 36597723 36597723 insertion of <=200bp - G intron_variant STAD-US 11 36597806 36597806 single base substitution C G intron_variant STAD-US 11 36597806 36597806 single base substitution C G missense_variant C984W 2952C>G STAD-US 11 36597940 36597940 single base substitution T C intron_variant STAD-US 11 36597940 36597940 single base substitution T C missense_variant L1029S 3086T>C STAD-US 11 36614195 36614195 deletion of <=200bp T - intron_variant STAD-US 11 36614223 36614223 deletion of <=200bp T - intron_variant STAD-US 11 36614484 36614484 single base substitution T C intron_variant STAD-US 11 36614733 36614733 single base substitution A C downstream_gene_variant STAD-US 11 36614878 36614878 single base substitution T G downstream_gene_variant STAD-US 11 36615184 36615184 single base substitution G T downstream_gene_variant STAD-US 11 36615566 36615566 single base substitution C T downstream_gene_variant THCA-SA 11 36595600 36595600 single base substitution A G exon_variant THCA-SA 11 36595600 36595600 single base substitution A G missense_variant H249R 746A>G THCA-SA 11 36597313 36597313 single base substitution A G exon_variant THCA-SA 11 36597313 36597313 single base substitution A G missense_variant K820R 2459A>G THCA-SA 11 36601170 36601170 single base substitution G A 3_prime_UTR_variant THCA-SA 11 36601170 36601170 single base substitution G A intron_variant THCA-SA 11 36613807 36613807 single base substitution T C intron_variant THCA-US 11 36597776 36597776 single base substitution C T intron_variant THCA-US 11 36597776 36597776 single base substitution C T synonymous_variant F974F 2922C>T UCEC-US 11 36595105 36595105 single base substitution A C exon_variant UCEC-US 11 36595105 36595105 single base substitution A C missense_variant H84P 251A>C UCEC-US 11 36595177 36595177 single base substitution G A exon_variant UCEC-US 11 36595177 36595177 single base substitution G A missense_variant R108Q 323G>A UCEC-US 11 36595938 36595938 single base substitution G T exon_variant UCEC-US 11 36595938 36595938 single base substitution G T stop_gained E362* 1084G>T UCEC-US 11 36595982 36595982 single base substitution C A exon_variant UCEC-US 11 36595982 36595982 single base substitution C A synonymous_variant I376I 1128C>A UCEC-US 11 36596004 36596004 single base substitution G T exon_variant UCEC-US 11 36596004 36596004 single base substitution G T stop_gained E384* 1150G>T UCEC-US 11 36596127 36596127 single base substitution G T exon_variant UCEC-US 11 36596127 36596127 single base substitution G T stop_gained E425* 1273G>T UCEC-US 11 36596348 36596348 single base substitution G T exon_variant UCEC-US 11 36596348 36596348 single base substitution G T missense_variant Q498H 1494G>T UCEC-US 11 36596826 36596826 single base substitution T G exon_variant UCEC-US 11 36596826 36596826 single base substitution T G missense_variant L658V 1972T>G UCEC-US 11 36596928 36596928 single base substitution C T exon_variant UCEC-US 11 36596928 36596928 single base substitution C T missense_variant L692F 2074C>T UCEC-US 11 36597014 36597014 single base substitution C T exon_variant UCEC-US 11 36597014 36597014 single base substitution C T synonymous_variant G720G 2160C>T UCEC-US 11 36597072 36597072 single base substitution G T exon_variant UCEC-US 11 36597072 36597072 single base substitution G T missense_variant A740S 2218G>T UCEC-US 11 36597145 36597145 single base substitution G A exon_variant UCEC-US 11 36597145 36597145 single base substitution G A missense_variant R764H 2291G>A UCEC-US 11 36597502 36597502 single base substitution G T exon_variant UCEC-US 11 36597502 36597502 single base substitution G T missense_variant R883M 2648G>T UCEC-US 11 36597530 36597530 single base substitution G T exon_variant UCEC-US 11 36597530 36597530 single base substitution G T missense_variant M892I 2676G>T UCEC-US 11 36597629 36597629 single base substitution G A exon_variant UCEC-US 11 36597629 36597629 single base substitution G A synonymous_variant T925T 2775G>A UCEC-US 11 36597696 36597696 single base substitution G T intron_variant UCEC-US 11 36597696 36597696 single base substitution G T stop_gained E948* 2842G>T UCEC-US 11 36597771 36597771 single base substitution C T intron_variant UCEC-US 11 36597771 36597771 single base substitution C T missense_variant R973C 2917C>T UCEC-US 11 36614195 36614195 single base substitution T C intron_variant UCEC-US 11 36614412 36614412 single base substitution G C intron_variant UCEC-US 11 36614483 36614483 single base substitution C A intron_variant UCEC-US 11 36614523 36614523 single base substitution A C 3_prime_UTR_variant UCEC-US 11 36614556 36614556 single base substitution G A 3_prime_UTR_variant UCEC-US 11 36614556 36614556 single base substitution G T 3_prime_UTR_variant UCEC-US 11 36614670 36614670 single base substitution C T 3_prime_UTR_variant UCEC-US 11 36614684 36614684 single base substitution G T 3_prime_UTR_variant UCEC-US 11 36614849 36614849 single base substitution G A downstream_gene_variant UCEC-US 11 36614907 36614907 single base substitution A C downstream_gene_variant UCEC-US 11 36615130 36615130 single base substitution G T downstream_gene_variant UCEC-US 11 36615244 36615244 single base substitution G A downstream_gene_variant UCEC-US 11 36615256 36615256 single base substitution G T downstream_gene_variant UCEC-US 11 36615270 36615270 single base substitution T C downstream_gene_variant UCEC-US 11 36615357 36615357 single base substitution G T downstream_gene_variant UCEC-US 11 36615380 36615380 single base substitution A G downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESO-1096 COSM1263747 c.1544C>T p.P515L Substitution - Missense 11:36574848-36574848 + TCGA-EE-A29M-06 COSM1978224 c.110C>T p.S37F Substitution - Missense 11:36573414-36573414 + BK0023 COSM4186392 c.1566G>A p.W522* Substitution - Nonsense 11:36574870-36574870 + LUAD-F00089 COSM339567 c.77C>A p.S26* Substitution - Nonsense 11:36573381-36573381 + TCGA-51-4079-01 COSM687411 c.1922T>G p.V641G Substitution - Missense 11:36575226-36575226 + ESCC_BICR_023T COSM5436294 c.1145C>G p.S382* Substitution - Nonsense 11:36574449-36574449 + P116 COSM1736538 c.455C>T p.P152L Substitution - Missense 11:36573759-36573759 + TCGA-19-2631-01 COSM1736538 c.455C>T p.P152L Substitution - Missense 11:36573759-36573759 + TCGA-FW-A3R5-06 COSM3869119 c.1296C>T p.S432S Substitution - coding silent 11:36574600-36574600 + C70 COSM4619388 c.1210C>T p.R404W Substitution - Missense 11:36574514-36574514 + CSCC-42-T COSM4451410 c.1207A>T p.T403S Substitution - Missense 11:36574511-36574511 + T3431 COSM3670758 c.995G>A p.R332Q Substitution - Missense 11:36574299-36574299 + SS6003149 COSM4032612 c.25T>G p.L9V Substitution - Missense 11:36573329-36573329 + SMS-CTR COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + TCGA-B5-A11Y-01 COSM926740 c.2291G>A p.R764H Substitution - Missense 11:36575595-36575595 + HCC2998 COSM1978226 c.180G>A p.E60E Substitution - coding silent 11:36573484-36573484 + TCGA-B5-A0K9-01 COSM926728 c.251A>C p.H84P Substitution - Missense 11:36573555-36573555 + pfg181T COSM4752831 c.2146C>T p.R716W Substitution - Missense 11:36575450-36575450 + DN1201B COSM542379 c.2625C>T p.S875S Substitution - coding silent 11:36575929-36575929 + ACINAR03 COSM1734379 c.226C>A p.P76T Substitution - Missense 11:36573530-36573530 + CSCC-62-T COSM4461293 c.11C>T p.S4F Substitution - Missense 11:36573315-36573315 + TCGA-AP-A051-01 COSM926737 c.2074C>T p.L692F Substitution - Missense 11:36575378-36575378 + TCGA-EE-A3JA-06 COSM3869120 c.2171C>T p.S724F Substitution - Missense 11:36575475-36575475 + 2334201 COSM322973 c.2143G>T p.V715L Substitution - Missense 11:36575447-36575447 + TCGA-09-2050-01 COSM72375 c.2906A>C p.K969T Substitution - Missense 11:36576210-36576210 + TCGA-FU-A2QG-01 COSM1736538 c.455C>T p.P152L Substitution - Missense 11:36573759-36573759 + CSCC-19-T COSM4474902 c.1950C>T p.N650N Substitution - coding silent 11:36575254-36575254 + 8062308 COSM84060 c.1754A>G p.D585G Substitution - Missense 11:36575058-36575058 + TCGA-19-4068-01 COSM1470480 c.2210G>A p.R737H Substitution - Missense 11:36575514-36575514 + SKCO-1 COSM1978290 c.3130T>G p.*1044E Nonstop extension 11:36576434-36576434 + TCGA-EE-A29D-06 COSM3447053 c.449C>T p.S150F Substitution - Missense 11:36573753-36573753 + TCGA-G4-6302-01 COSM3752352 c.2176T>C p.S726P Substitution - Missense 11:36575480-36575480 + TCGA-EI-6917-01 COSM926730 c.323G>A p.R108Q Substitution - Missense 11:36573627-36573627 + YUKAT COSM5372419 c.2475C>T p.S825S Substitution - coding silent 11:36575779-36575779 + TCGA-BH-A0HF-01 COSM3809165 c.902C>A p.A301D Substitution - Missense 11:36574206-36574206 + PD13302a COSM1470480 c.2210G>A p.R737H Substitution - Missense 11:36575514-36575514 + S13_post COSM5574917 c.1076C>T p.P359L Substitution - Missense 11:36574380-36574380 + S13_pre COSM5574917 c.1076C>T p.P359L Substitution - Missense 11:36574380-36574380 + RMS80_ COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + SS6003113 COSM5032923 c.1680C>A p.F560L Substitution - Missense 11:36574984-36574984 + LUAD-B01970 COSM355977 c.2326C>T p.R776W Substitution - Missense 11:36575630-36575630 + TCGA-EE-A3J7-06 COSM3869118 c.938G>A p.C313Y Substitution - Missense 11:36574242-36574242 + sysucc-1370T COSM1470480 c.2210G>A p.R737H Substitution - Missense 11:36575514-36575514 + TCGA-EE-A2MQ-06 COSM3447061 c.1946C>T p.P649L Substitution - Missense 11:36575250-36575250 + HCC92T COSM1604519 c.269A>C p.K90T Substitution - Missense 11:36573573-36573573 + TCGA-BR-6452-01 COSM4032623 c.3086T>C p.L1029S Substitution - Missense 11:36576390-36576390 + 8068033 COSM3383449 c.9C>T p.A3A Substitution - coding silent 11:36573313-36573313 + LUAD-B02515 COSM335997 c.2894A>T p.E965V Substitution - Missense 11:36576198-36576198 + TCGA-AG-3892-01 COSM257852 c.2893G>T p.E965* Substitution - Nonsense 11:36576197-36576197 + YUSWI COSM1703818 c.589_590CC>TT p.P197L Substitution - Missense 11:36573893-36573894 + TCGA-AP-A0LM-01 COSM687410 c.2648G>T p.R883M Substitution - Missense 11:36575952-36575952 + TCGA-63-6202-01 COSM687412 c.1331C>T p.A444V Substitution - Missense 11:36574635-36574635 + 12T COSM108879 c.629C>T p.S210F Substitution - Missense 11:36573933-36573933 + CSCC-60-T COSM167756 c.1660G>A p.D554N Substitution - Missense 11:36574964-36574964 + 2492700 COSM5600337 c.797T>A p.I266N Substitution - Missense 11:36574101-36574101 + TCGA-27-1830-01 COSM3397658 c.2023C>T p.L675L Substitution - coding silent 11:36575327-36575327 + LP6005935-DNA_C03 COSM5035954 c.1723G>A p.E575K Substitution - Missense 11:36575027-36575027 + TCGA-EE-A2GM-06 COSM3447067 c.2379C>T p.S793S Substitution - coding silent 11:36575683-36575683 + PET128T COSM5825030 c.2888G>A p.G963E Substitution - Missense 11:36576192-36576192 + CHC892T COSM4797810 c.2499G>A p.Q833Q Substitution - coding silent 11:36575803-36575803 + TCGA-D3-A3C8-06 COSM3447051 c.395C>T p.P132L Substitution - Missense 11:36573699-36573699 + TCGA-BR-A4J8-01 COSM4032622 c.2952C>G p.C984W Substitution - Missense 11:36576256-36576256 + ESO-0149 COSM1263746 c.708C>A p.L236L Substitution - coding silent 11:36574012-36574012 + YUKAT COSM5372415 c.1654C>T p.P552S Substitution - Missense 11:36574958-36574958 + TCGA-AX-A0J0-01 COSM926742 c.2775G>A p.T925T Substitution - coding silent 11:36576079-36576079 + RMS77_ COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + LUAD-E00443 COSM363644 c.2097G>T p.R699R Substitution - coding silent 11:36575401-36575401 + TCGA-EE-A180-06 COSM3447060 c.1877C>T p.S626L Substitution - Missense 11:36575181-36575181 + TCGA-06-0122-01 COSM2149249 c.1598C>T p.T533I Substitution - Missense 11:36574902-36574902 + 173-01-3TD COSM145840 c.2275C>T p.R759C Substitution - Missense 11:36575579-36575579 + S00943 COSM314666 c.2735A>T p.Y912F Substitution - Missense 11:36576039-36576039 + 2492702 COSM5600337 c.797T>A p.I266N Substitution - Missense 11:36574101-36574101 + S02328 COSM5691775 c.1248G>T p.L416L Substitution - coding silent 11:36574552-36574552 + PD24304a COSM5787423 c.2504C>G p.T835R Substitution - Missense 11:36575808-36575808 + TCGA-FI-A2F8-01 COSM926744 c.2917C>T p.R973C Substitution - Missense 11:36576221-36576221 + LUAD-S01357 COSM386382 c.2327G>T p.R776L Substitution - Missense 11:36575631-36575631 + 10-P8045 COSM4574350 c.2279A>G p.Y760C Substitution - Missense 11:36575583-36575583 + TCGA-D9-A3Z4-01 COSM3447063 c.2147G>A p.R716Q Substitution - Missense 11:36575451-36575451 + C086 COSM1978288 c.3083C>T p.P1028L Substitution - Missense 11:36576387-36576387 + 19 COSM5747237 c.523T>C p.F175L Substitution - Missense 11:36573827-36573827 + LB2241-RCC COSM13951 c.1818A>T p.G606G Substitution - coding silent 11:36575122-36575122 + TCGA-BR-8687-01 COSM4032616 c.447T>G p.T149T Substitution - coding silent 11:36573751-36573751 + TCGA-DU-5855-01 COSM3447059 c.1821C>T p.D607D Substitution - coding silent 11:36575125-36575125 + HT115 COSM1978229 c.283G>A p.E95K Substitution - Missense 11:36573587-36573587 + S01873 COSM5672028 c.2867T>C p.I956T Substitution - Missense 11:36576171-36576171 + S00944 COSM314667 c.1486G>T p.G496W Substitution - Missense 11:36574790-36574790 + T2950 COSM1353713 c.100C>T p.R34W Substitution - Missense 11:36573404-36573404 + TCGA-19-2631 COSM1736538 c.455C>T p.P152L Substitution - Missense 11:36573759-36573759 + TCGA-BR-8361-01 COSM542379 c.2625C>T p.S875S Substitution - coding silent 11:36575929-36575929 + TCGA-EE-A181-06 COSM3447058 c.1768C>T p.L590L Substitution - coding silent 11:36575072-36575072 + T3094 COSM4720037 c.1182G>A p.R394R Substitution - coding silent 11:36574486-36574486 + TCGA-CH-5768-01 COSM3782618 c.335G>A p.R112H Substitution - Missense 11:36573639-36573639 + CSCC-31-T COSM4457256 c.1038C>T p.S346S Substitution - coding silent 11:36574342-36574342 + TCGA-J4-8198-01 COSM1470480 c.2210G>A p.R737H Substitution - Missense 11:36575514-36575514 + TCGA-66-2780-01 COSM687416 c.335G>T p.R112L Substitution - Missense 11:36573639-36573639 + C058 COSM5525488 c.2970C>T p.V990V Substitution - coding silent 11:36576274-36576274 + TCGA-EE-A2GO-06 COSM3447065 c.2308G>A p.E770K Substitution - Missense 11:36575612-36575612 + KM12 COSM1675946 c.1525G>A p.A509T Substitution - Missense 11:36574829-36574829 + T263 COSM4720039 c.1786G>A p.V596M Substitution - Missense 11:36575090-36575090 + T1154 COSM3869121 c.2742C>T p.F914F Substitution - coding silent 11:36576046-36576046 + Gp5D COSM1978222 c.69T>C p.I23I Substitution - coding silent 11:36573373-36573373 + TCGA-EE-A3AC-06 COSM3447048 c.241T>G p.L81V Substitution - Missense 11:36573545-36573545 + TCGA-BR-7851-01 COSM1978251 c.1203G>A p.S401S Substitution - coding silent 11:36574507-36574507 + TCGA-A6-6653-01 COSM1353715 c.597C>T p.N199N Substitution - coding silent 11:36573901-36573901 + 2_RESISTANT COSM1722592 c.2464C>T p.P822S Substitution - Missense 11:36575768-36575768 + CSCC-49-T COSM4543817 c.344G>A p.G115E Substitution - Missense 11:36573648-36573648 + pfg035T COSM4752832 c.2686T>G p.W896G Substitution - Missense 11:36575990-36575990 + P48 COSM328851 c.1949A>C p.N650T Substitution - Missense 11:36575253-36575253 + PT38 COSM5922926 c.38C>T p.S13F Substitution - Missense 11:36573342-36573342 + 19M COSM5579448 c.546C>T p.I182I Substitution - coding silent 11:36573850-36573850 + TCGA-AA-A00N-01 COSM276989 c.2690G>A p.R897Q Substitution - Missense 11:36575994-36575994 + SJHGG118_A COSM1470479 c.2626G>A p.E876K Substitution - Missense 11:36575930-36575930 + 169 COSM3728654 c.1377G>A p.Q459Q Substitution - coding silent 11:36574681-36574681 + TCGA-AA-A010-01 COSM284453 c.2777A>C p.K926T Substitution - Missense 11:36576081-36576081 + YULONE COSM5372417 c.2030C>T p.P677L Substitution - Missense 11:36575334-36575334 + TCGA-AZ-4315-01 COSM1353717 c.1490G>A p.R497K Substitution - Missense 11:36574794-36574794 + SS6003309 COSM3716763 c.2238C>A p.F746L Substitution - Missense 11:36575542-36575542 + TCGA-D1-A177-01 COSM926732 c.1128C>A p.I376I Substitution - coding silent 11:36574432-36574432 + PDA_055 COSM5000864 c.655C>T p.R219W Substitution - Missense 11:36573959-36573959 + PD13603a COSM542379 c.2625C>T p.S875S Substitution - coding silent 11:36575929-36575929 + S00944 COSM314667 c.1486G>T p.G496W Substitution - Missense 11:36574790-36574790 + TCGA-AB-2855-03 COSM1317316 c.1061T>G p.L354R Substitution - Missense 11:36574365-36574365 + ZZUFHECRKL-G027T COSM5445340 c.36T>G p.S12R Substitution - Missense 11:36573340-36573340 + CT-TC COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + LUAD-NYU739 COSM376240 c.451T>C p.W151R Substitution - Missense 11:36573755-36573755 + TCGA-HC-7230-01 COSM1470479 c.2626G>A p.E876K Substitution - Missense 11:36575930-36575930 + NCI-H1437 COSM13915 c.1863G>T p.K621N Substitution - Missense 11:36575167-36575167 + HCT8 COSM4633303 c.982T>G p.C328G Substitution - Missense 11:36574286-36574286 + CSCC-18-T COSM4542049 c.3115G>T p.D1039Y Substitution - Missense 11:36576419-36576419 + T368 COSM4720038 c.1321G>A p.A441T Substitution - Missense 11:36574625-36574625 + TCGA-GF-A4EO-06 COSM3447069 c.2855G>T p.R952M Substitution - Missense 11:36576159-36576159 + TARGET-30-PATHVK COSM1287527 c.240G>T p.L80F Substitution - Missense 11:36573544-36573544 + 2492703 COSM5600337 c.797T>A p.I266N Substitution - Missense 11:36574101-36574101 + TCGA-E2-A10C-01 COSM428955 c.2479G>C p.E827Q Substitution - Missense 11:36575783-36575783 + 1115154 COSM5550396 c.206C>A p.A69D Substitution - Missense 11:36573510-36573510 + ESCC_13 COSM5625077 c.2124C>T p.T708T Substitution - coding silent 11:36575428-36575428 + ESO-1145 COSM1263748 c.1574C>T p.P525L Substitution - Missense 11:36574878-36574878 + 2_PRE-TREATMENT COSM1722592 c.2464C>T p.P822S Substitution - Missense 11:36575768-36575768 + TCGA-06-2569-01 COSM3397656 c.1175G>T p.G392V Substitution - Missense 11:36574479-36574479 + TCGA-66-2793-01 COSM687415 c.345G>T p.G115G Substitution - coding silent 11:36573649-36573649 + TCGA-D9-A4Z3-01 COSM3447047 c.111C>T p.S37S Substitution - coding silent 11:36573415-36573415 + TCGA-B5-A0JY-01 COSM926743 c.2842G>T p.E948* Substitution - Nonsense 11:36576146-36576146 + TCGA-AA-3715-01 COSM269995 c.1569G>A p.Q523Q Substitution - coding silent 11:36574873-36574873 + SM-4B295 COSM5032791 c.2105A>G p.K702R Substitution - Missense 11:36575409-36575409 + CHC892T COSM4795552 c.2049G>A p.E683E Substitution - coding silent 11:36575353-36575353 + TCGA-D3-A2JF-06 COSM3447055 c.1000C>T p.P334S Substitution - Missense 11:36574304-36574304 + TCGA-AP-A051-01 COSM926738 c.2160C>T p.G720G Substitution - coding silent 11:36575464-36575464 + TCGA-B6-A0RG-01 COSM428954 c.1016A>T p.D339V Substitution - Missense 11:36574320-36574320 + TCGA-AP-A059-01 COSM926736 c.1972T>G p.L658V Substitution - Missense 11:36575276-36575276 + TCGA-AR-A1AI-01 COSM428956 c.2599G>A p.D867N Substitution - Missense 11:36575903-36575903 + EGC15 COSM5050790 c.2290C>T p.R764C Substitution - Missense 11:36575594-36575594 + 227_T COSM3979602 c.2693C>G p.S898* Substitution - Nonsense 11:36575997-36575997 + TCGA-AX-A05Z-01 COSM926730 c.323G>A p.R108Q Substitution - Missense 11:36573627-36573627 + YUWIA COSM5372413 c.1536A>T p.V512V Substitution - coding silent 11:36574840-36574840 + cSCCP4 COSM138808 c.1910G>A p.S637N Substitution - Missense 11:36575214-36575214 + OSCC-GB_00070111 COSM3710072 c.760C>G p.Q254E Substitution - Missense 11:36574064-36574064 + ME009T COSM223454 c.727G>A p.A243T Substitution - Missense 11:36574031-36574031 + TCGA-19-4068 COSM1470480 c.2210G>A p.R737H Substitution - Missense 11:36575514-36575514 + CSCC-54-T COSM1722592 c.2464C>T p.P822S Substitution - Missense 11:36575768-36575768 + TCGA-HC-7820-01 COSM304336 c.1187G>A p.R396H Substitution - Missense 11:36574491-36574491 + KM12 COSM1675946 c.1525G>A p.A509T Substitution - Missense 11:36574829-36574829 + TCGA-HC-7742-01 COSM3670758 c.995G>A p.R332Q Substitution - Missense 11:36574299-36574299 + SCC-9 COSM1978263 c.1802C>G p.S601C Substitution - Missense 11:36575106-36575106 + PD22357a COSM5784037 c.772A>C p.S258R Substitution - Missense 11:36574076-36574076 + LUAD-F00018 COSM338957 c.1814T>C p.M605T Substitution - Missense 11:36575118-36575118 + RD COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + Pat_76_B COSM5838489 c.985C>T p.P329S Substitution - Missense 11:36574289-36574289 + cSCCP6 COSM136829 c.334C>T p.R112C Substitution - Missense 11:36573638-36573638 + TCGA-BR-8369-01 COSM4032621 c.2417A>G p.E806G Substitution - Missense 11:36575721-36575721 + B80 COSM1746222 c.350C>T p.S117F Substitution - Missense 11:36573654-36573654 + T2269 COSM4720034 c.417C>T p.G139G Substitution - coding silent 11:36573721-36573721 + CHC892T COSM4797810 c.2499G>A p.Q833Q Substitution - coding silent 11:36575803-36575803 + TCGA-UB-A7MB-01 COSM4931758 c.1989A>C p.A663A Substitution - coding silent 11:36575293-36575293 + TCGA-KR-A7K0-01 COSM4918177 c.2655G>A p.L885L Substitution - coding silent 11:36575959-36575959 + Au1 COSM1978269 c.2109C>T p.F703F Substitution - coding silent 11:36575413-36575413 + S00050 COSM317943 c.366G>C p.E122D Substitution - Missense 11:36573670-36573670 + TCGA-D9-A4Z3-01 COSM3447064 c.2155G>A p.E719K Substitution - Missense 11:36575459-36575459 + CHC892T COSM4795552 c.2049G>A p.E683E Substitution - coding silent 11:36575353-36575353 + CSCC-60-T COSM4480144 c.2392C>T p.H798Y Substitution - Missense 11:36575696-36575696 + HCC1T COSM1604520 c.1884delA p.I629fs*2 Deletion - Frameshift 11:36575188-36575188 + YUKAT COSM5372418 c.2168C>T p.A723V Substitution - Missense 11:36575472-36575472 + 61 COSM5739215 c.145A>C p.K49Q Substitution - Missense 11:36573449-36573449 + TCGA-A6-5661-01 COSM287899 c.2095C>T p.R699W Substitution - Missense 11:36575399-36575399 + PT25 COSM5904970 c.2084G>A p.G695E Substitution - Missense 11:36575388-36575388 + HCT-15 COSM1675945 c.395C>A p.P132H Substitution - Missense 11:36573699-36573699 + EGC3 COSM5050788 c.1872delT p.S626fs*5 Deletion - Frameshift 11:36575176-36575176 + 8031867 COSM287899 c.2095C>T p.R699W Substitution - Missense 11:36575399-36575399 + SCMC_RM2_ COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + 8013142 COSM3383449 c.9C>T p.A3A Substitution - coding silent 11:36573313-36573313 + S00050 COSM317943 c.366G>C p.E122D Substitution - Missense 11:36573670-36573670 + LUAD-RT-S01487 COSM377837 c.2633_2634GG>TC p.R878I Substitution - Missense 11:36575937-36575938 + RMS110_ COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + TCGA-BR-4257-01 COSM4032618 c.878G>A p.C293Y Substitution - Missense 11:36574182-36574182 + TCGA-06-0122 COSM2149249 c.1598C>T p.T533I Substitution - Missense 11:36574902-36574902 + TCGA-EE-A2GR-06 COSM3447059 c.1821C>T p.D607D Substitution - coding silent 11:36575125-36575125 + TCGA-EE-A3J7-06 COSM3869117 c.669G>A p.R223R Substitution - coding silent 11:36573973-36573973 + TCGA-ER-A19K-01 COSM3447066 c.2375C>T p.P792L Substitution - Missense 11:36575679-36575679 + HCT15 COSM1675945 c.395C>A p.P132H Substitution - Missense 11:36573699-36573699 + Pa14C COSM84060 c.1754A>G p.D585G Substitution - Missense 11:36575058-36575058 + T3499 COSM4720036 c.851C>A p.P284Q Substitution - Missense 11:36574155-36574155 + TCGA-CF-A1HR-01 COSM415610 c.1681C>A p.R561S Substitution - Missense 11:36574985-36574985 + TCGA-AP-A0LM-01 COSM926731 c.1084G>T p.E362* Substitution - Nonsense 11:36574388-36574388 + LP6007504-DNA_A01 COSM4408663 c.866A>C p.K289T Substitution - Missense 11:36574170-36574170 + TCGA-GN-A26A-06 COSM3447049 c.263C>T p.S88L Substitution - Missense 11:36573567-36573567 + TCGA-18-4083-01 COSM687409 c.2917C>A p.R973S Substitution - Missense 11:36576221-36576221 + pfg151T COSM4752830 c.1216G>T p.A406S Substitution - Missense 11:36574520-36574520 + SA235 COSM212763 c.3124G>T p.E1042* Substitution - Nonsense 11:36576428-36576428 + TCGA-EE-A2MS-06 COSM3447046 c.99C>T p.F33F Substitution - coding silent 11:36573403-36573403 + TCGA-A6-5661-01 COSM1353713 c.100C>T p.R34W Substitution - Missense 11:36573404-36573404 + CSCC-62-T COSM4471111 c.16C>T p.P6S Substitution - Missense 11:36573320-36573320 + TCGA-06-0237-01 COSM3397657 c.1421G>A p.R474H Substitution - Missense 11:36574725-36574725 + 12924 COSM5613356 c.552C>A p.H184Q Substitution - Missense 11:36573856-36573856 + TCGA-K7-A6G5-01 COSM4939306 c.1705G>T p.A569S Substitution - Missense 11:36575009-36575009 + TCGA-B0-5098-01 COSM1492530 c.2125G>T p.G709C Substitution - Missense 11:36575429-36575429 + 587342 COSM1223038 c.3062C>A p.P1021H Substitution - Missense 11:36576366-36576366 + TCGA-EE-A29D-06 COSM3447068 c.2462A>G p.N821S Substitution - Missense 11:36575766-36575766 + D-07 COSM1353713 c.100C>T p.R34W Substitution - Missense 11:36573404-36573404 + C547 COSM4442334 c.1718T>C p.M573T Substitution - Missense 11:36575022-36575022 + TCGA-BS-A0U8-01 COSM926729 c.282C>T p.N94N Substitution - coding silent 11:36573586-36573586 + YUGURT COSM5372420 c.2521C>T p.R841W Substitution - Missense 11:36575825-36575825 + LUAD-S01331 COSM396370 c.657G>A p.R219R Substitution - coding silent 11:36573961-36573961 + S0029 COSM5882067 c.142G>A p.E48K Substitution - Missense 11:36573446-36573446 + I2L-P7-Tumor-Organoid COSM5361004 c.1017C>T p.D339D Substitution - coding silent 11:36574321-36574321 + 8015299 COSM1168721 c.2333G>A p.R778Q Substitution - Missense 11:36575637-36575637 + CSCC-60-T COSM4467921 c.1515C>T p.A505A Substitution - coding silent 11:36574819-36574819 + Au3 COSM5602177 c.322C>T p.R108* Substitution - Nonsense 11:36573626-36573626 + TCGA-AP-A056-01 COSM926734 c.1273G>T p.E425* Substitution - Nonsense 11:36574577-36574577 + 585223 COSM322972 c.3121A>T p.M1041L Substitution - Missense 11:36576425-36576425 + C086 COSM171937 c.507G>A p.S169S Substitution - coding silent 11:36573811-36573811 + PT33 COSM5372420 c.2521C>T p.R841W Substitution - Missense 11:36575825-36575825 + TCGA-AR-A24Q-01 COSM1475405 c.1731C>T p.I577I Substitution - coding silent 11:36575035-36575035 + TCGA-AD-6889-01 COSM1353716 c.1205T>C p.L402P Substitution - Missense 11:36574509-36574509 + CSCC-54-T COSM4485926 c.2993C>T p.T998I Substitution - Missense 11:36576297-36576297 + TCGA-EJ-5502-01 COSM1127793 c.2596G>A p.V866M Substitution - Missense 11:36575900-36575900 + ME100L COSM231244 c.67A>T p.I23F Substitution - Missense 11:36573371-36573371 + SC_9081 COSM5050790 c.2290C>T p.R764C Substitution - Missense 11:36575594-36575594 + TCGA-AG-3583-01 COSM287899 c.2095C>T p.R699W Substitution - Missense 11:36575399-36575399 + YUKSI COSM5372416 c.1748C>T p.S583F Substitution - Missense 11:36575052-36575052 + ESO-003 COSM1263745 c.2976A>G p.K992K Substitution - coding silent 11:36576280-36576280 + Pat_41_B COSM5838488 c.418C>T p.L140F Substitution - Missense 11:36573722-36573722 + LB2241-RCC COSM13951 c.1818A>T p.G606G Substitution - coding silent 11:36575122-36575122 + STC246 COSM5050789 c.2126G>A p.G709D Substitution - Missense 11:36575430-36575430 + TCGA-AM-5821-01 COSM3752353 c.2880A>G p.A960A Substitution - coding silent 11:36576184-36576184 + CSCC-56-T COSM4498198 c.514C>T p.P172S Substitution - Missense 11:36573818-36573818 + CSCC-55-T COSM4480596 c.2434C>T p.Q812* Substitution - Nonsense 11:36575738-36575738 + 12 COSM687412 c.1331C>T p.A444V Substitution - Missense 11:36574635-36574635 + CSCC-55-T COSM4485933 c.2994C>T p.T998T Substitution - coding silent 11:36576298-36576298 + TCGA-DD-A3A9-01 COSM4920589 c.1531A>T p.K511* Substitution - Nonsense 11:36574835-36574835 + PTC-7C COSM3752353 c.2880A>G p.A960A Substitution - coding silent 11:36576184-36576184 + LUAD-NYU1051S COSM368513 c.101G>T p.R34L Substitution - Missense 11:36573405-36573405 + HCA7 COSM4629720 c.2918G>A p.R973H Substitution - Missense 11:36576222-36576222 + CLL093 COSM1289550 c.3072C>T p.S1024S Substitution - coding silent 11:36576376-36576376 + TCGA-DA-A3F3-06 COSM3447056 c.1501C>T p.Q501* Substitution - Nonsense 11:36574805-36574805 + DLD1 COSM1675945 c.395C>A p.P132H Substitution - Missense 11:36573699-36573699 + TCGA-D3-A51G-06 COSM3447070 c.2865C>T p.S955S Substitution - coding silent 11:36576169-36576169 + TCGA-AA-3510-01 COSM1353720 c.1936G>T p.E646* Substitution - Nonsense 11:36575240-36575240 + 9113_T COSM5039098 c.1834C>A p.H612N Substitution - Missense 11:36575138-36575138 + TCGA-EE-A2MR-06 COSM3447052 c.442G>A p.A148T Substitution - Missense 11:36573746-36573746 + 173 COSM145840 c.2275C>T p.R759C Substitution - Missense 11:36575579-36575579 + ATL002 COSM5703988 c.3112C>T p.Q1038* Substitution - Nonsense 11:36576416-36576416 + TCGA-DD-A113-01 COSM4925222 c.2860G>T p.G954C Substitution - Missense 11:36576164-36576164 + TCGA-A8-A0A6-01 COSM3809166 c.2336T>G p.V779G Substitution - Missense 11:36575640-36575640 + B80-Tumor COSM1746222 c.350C>T p.S117F Substitution - Missense 11:36573654-36573654 + TCGA-GF-A2C7-01 COSM3447054 c.798C>T p.I266I Substitution - coding silent 11:36574102-36574102 + TCGA-AN-A046-01 COSM3809167 c.2486G>T p.R829M Substitution - Missense 11:36575790-36575790 + LUAD-B02594 COSM336373 c.787A>T p.M263L Substitution - Missense 11:36574091-36574091 + RMS10_ COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + LUAD-NYU1219 COSM369807 c.2544A>T p.P848P Substitution - coding silent 11:36575848-36575848 + LIM2551 COSM4643536 c.425G>A p.R142Q Substitution - Missense 11:36573729-36573729 + pfg181T COSM4765170 c.802_803insA p.N268fs*4 Insertion - Frameshift 11:36574106-36574107 + TCGA-BH-A0B6-01 COSM3809164 c.382C>G p.P128A Substitution - Missense 11:36573686-36573686 + TCGA-QB-A6FS-06 COSM3869121 c.2742C>T p.F914F Substitution - coding silent 11:36576046-36576046 + TCGA-AZ-4315-01 COSM1353714 c.563G>A p.S188N Substitution - Missense 11:36573867-36573867 + EGC8 COSM5050787 c.994C>T p.R332* Substitution - Nonsense 11:36574298-36574298 + LUAD-S01315 COSM343989 c.507G>C p.S169S Substitution - coding silent 11:36573811-36573811 + 63 COSM5012319 c.571C>T p.P191S Substitution - Missense 11:36573875-36573875 + TCGA-EE-A29D-06 COSM3447057 c.1665C>T p.T555T Substitution - coding silent 11:36574969-36574969 + TCGA-A6-6781-01 COSM1353721 c.1983G>A p.M661I Substitution - Missense 11:36575287-36575287 + C086 COSM5537973 c.2481G>A p.E827E Substitution - coding silent 11:36575785-36575785 + S02375 COSM4032623 c.3086T>C p.L1029S Substitution - Missense 11:36576390-36576390 + 2492701 COSM5600337 c.797T>A p.I266N Substitution - Missense 11:36574101-36574101 + SW620 COSM1978223 c.101G>A p.R34Q Substitution - Missense 11:36573405-36573405 + TCGA-EE-A2MQ-06 COSM3447071 c.2971C>T p.L991L Substitution - coding silent 11:36576275-36576275 + LUAD-S00488 COSM394912 c.1839G>T p.G613G Substitution - coding silent 11:36575143-36575143 + TCGA-DO-A2HM-01 COSM3368357 c.2922C>T p.F974F Substitution - coding silent 11:36576226-36576226 + pfg122T COSM4746985 c.615delC p.H207fs*57 Deletion - Frameshift 11:36573919-36573919 + 40 COSM5012318 c.35G>T p.S12I Substitution - Missense 11:36573339-36573339 + PCSI_0090_Pa_X COSM3375788 c.2472T>G p.A824A Substitution - coding silent 11:36575776-36575776 + BCM501T COSM4951969 c.2106G>T p.K702N Substitution - Missense 11:36575410-36575410 + TCGA-AP-A051-01 COSM926739 c.2218G>T p.A740S Substitution - Missense 11:36575522-36575522 + PD4203a COSM163910 c.1743G>C p.M581I Substitution - Missense 11:36575047-36575047 + TCGA-AA-3662-01 COSM926729 c.282C>T p.N94N Substitution - coding silent 11:36573586-36573586 + XHDG35 COSM4769573 c.1745G>A p.R582K Substitution - Missense 11:36575049-36575049 + TCGA-FS-A1ZJ-06 COSM687412 c.1331C>T p.A444V Substitution - Missense 11:36574635-36574635 + SW48 COSM1978256 c.1362G>A p.L454L Substitution - coding silent 11:36574666-36574666 + TCGA-AG-3892-01 COSM257851 c.147G>T p.K49N Substitution - Missense 11:36573451-36573451 + TCGA-BR-4256-01 COSM4032617 c.456G>A p.P152P Substitution - coding silent 11:36573760-36573760 + CSCC-41-T COSM4483911 c.274C>G p.H92D Substitution - Missense 11:36573578-36573578 + TCGA-EI-6917-01 COSM3415831 c.656G>A p.R219Q Substitution - Missense 11:36573960-36573960 + TCGA-AX-A0J0-01 COSM926733 c.1150G>T p.E384* Substitution - Nonsense 11:36574454-36574454 + YUWIA COSM5372414 c.1537C>T p.L513F Substitution - Missense 11:36574841-36574841 + XHDG17 COSM4768687 c.3023C>A p.A1008D Substitution - Missense 11:36576327-36576327 + PD24202a COSM5774278 c.834C>G p.L278L Substitution - coding silent 11:36574138-36574138 + 587376 COSM276989 c.2690G>A p.R897Q Substitution - Missense 11:36575994-36575994 + BCM501T COSM4951969 c.2106G>T p.K702N Substitution - Missense 11:36575410-36575410 + TCGA-BF-A1PZ-01 COSM1978228 c.274C>T p.H92Y Substitution - Missense 11:36573578-36573578 + CRC-3 COSM304336 c.1187G>A p.R396H Substitution - Missense 11:36574491-36574491 + TCGA-BG-A2AE-01 COSM926745 c.3070A>G p.S1024G Substitution - Missense 11:36576374-36576374 + TCGA-33-6737-01 COSM687413 c.1130C>G p.S377* Substitution - Nonsense 11:36574434-36574434 + ZZUFHECRKL-G063T COSM3397658 c.2023C>T p.L675L Substitution - coding silent 11:36575327-36575327 + HCC92 COSM1604519 c.269A>C p.K90T Substitution - Missense 11:36573573-36573573 + TCGA-D7-6525-01 COSM4032612 c.25T>G p.L9V Substitution - Missense 11:36573329-36573329 + BD227T COSM5517995 c.280A>T p.N94Y Substitution - Missense 11:36573584-36573584 + 2217530 COSM4421890 c.1198C>G p.L400V Substitution - Missense 11:36574502-36574502 + RK122_C01 COSM3739041 c.1210C>A p.R404R Substitution - coding silent 11:36574514-36574514 + 3101B7_041_T COSM5040573 c.1985T>A p.L662Q Substitution - Missense 11:36575289-36575289 + TCGA-33-4566-01 COSM687408 c.2943G>T p.Q981H Substitution - Missense 11:36576247-36576247 + Pat_76_A COSM5838489 c.985C>T p.P329S Substitution - Missense 11:36574289-36574289 + 8016470 COSM3383450 c.1869C>T p.V623V Substitution - coding silent 11:36575173-36575173 + SN12C COSM1675947 c.1546G>C p.G516R Substitution - Missense 11:36574850-36574850 + CSCC-49-T COSM4482579 c.2621C>T p.P874L Substitution - Missense 11:36575925-36575925 + TCGA-JW-A5VL-01 COSM4846939 c.1807G>C p.D603H Substitution - Missense 11:36575111-36575111 + TCGA-BF-A3DJ-01 COSM3383449 c.9C>T p.A3A Substitution - coding silent 11:36573313-36573313 + TCGA-CD-A48A-01 COSM4032614 c.394C>T p.P132S Substitution - Missense 11:36573698-36573698 + HRA19 COSM4637622 c.2166G>C p.E722D Substitution - Missense 11:36575470-36575470 + CSB22 COSM5027380 c.1564T>A p.W522R Substitution - Missense 11:36574868-36574868 + 7T COSM3710072 c.760C>G p.Q254E Substitution - Missense 11:36574064-36574064 + Pat_41_B COSM5838490 c.2710G>A p.E904K Substitution - Missense 11:36576014-36576014 + ATL016 COSM5703987 c.314C>T p.A105V Substitution - Missense 11:36573618-36573618 + TCGA-EE-A29E-06 COSM3447062 c.2005G>A p.E669K Substitution - Missense 11:36575309-36575309 + CHOL35 COSM1744232 c.2931G>A p.M977I Substitution - Missense 11:36576235-36576235 + TCGA-BR-4184-01 COSM4032615 c.416G>A p.G139D Substitution - Missense 11:36573720-36573720 + TCGA-CC-A5UE-01 COSM4933879 c.634G>T p.D212Y Substitution - Missense 11:36573938-36573938 + LUAD_E00522 COSM352369 c.1642G>T p.V548L Substitution - Missense 11:36574946-36574946 + TCGA-BR-7707-01 COSM4032619 c.982T>C p.C328R Substitution - Missense 11:36574286-36574286 + T1180 COSM4720035 c.771C>T p.I257I Substitution - coding silent 11:36574075-36574075 + CSCC-19-T COSM4522029 c.1141G>A p.E381K Substitution - Missense 11:36574445-36574445 + TCGA-46-3769-01 COSM687414 c.750G>T p.K250N Substitution - Missense 11:36574054-36574054 + TCGA-BR-8683-01 COSM4032613 c.155C>A p.S52Y Substitution - Missense 11:36573459-36573459 + TCGA-BR-4370-01 COSM4032620 c.1228C>T p.R410W Substitution - Missense 11:36574532-36574532 + TCGA-D1-A16X-01 COSM926741 c.2676G>T p.M892I Substitution - Missense 11:36575980-36575980 + T3090 COSM4720040 c.3106G>A p.E1036K Substitution - Missense 11:36576410-36576410 + HCC030T COSM5815990 c.294A>G p.R98R Substitution - coding silent 11:36573598-36573598 + TCGA-AP-A051-01 COSM926735 c.1494G>T p.Q498H Substitution - Missense 11:36574798-36574798 + TCGA-ER-A193-06 COSM3447050 c.375G>A p.R125R Substitution - coding silent 11:36573679-36573679 + TCGA-BL-A3JM-01 COSM1298010 c.147G>A p.K49K Substitution - coding silent 11:36573451-36573451 + NCI-H1437 COSM13915 c.1863G>T p.K621N Substitution - Missense 11:36575167-36575167 + QC2-32-T2 COSM4985912 c.2459A>G p.K820R Substitution - Missense 11:36575763-36575763 + TCGA-FS-A4F0-06 COSM1978285 c.2996C>T p.S999F Substitution - Missense 11:36576300-36576300 + Au2 COSM5600337 c.797T>A p.I266N Substitution - Missense 11:36574101-36574101 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.73958 11p13 179615 2421437|dbSNP|BC037344|C/T|coding|Ala156Val|1103|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.3129+132A>C 11 36598115 ESCA A C Missense p.H504P c.1511A>C 11 36596365 LUAD A C Missense p.H84P c.251A>C 11 36595105 UCEC A C Missense p.K969T c.2906A>C 11 36597760 OV A C Missense p.S12R c.34A>C 11 36594888 LUAD A C Synonymous p.A804A c.2412A>C 11 36597266 BRCA A G Missense p.D585G c.1754A>G 11 36596608 PAAD A G Synonymous p.K992K c.2976A>G 11 36597830 ESCA A T Missense p.D339V c.1016A>T 11 36595870 BRCA A T Missense p.I23F c.67A>T 11 36594921 CM A T Missense p.M1041L c.3121A>T 11 36597975 SCLC A T Missense p.Q911L c.2732A>T 11 36597586 HNSC A T Missense p.Y912F c.2735A>T 11 36597589 SCLC C A 3-UTRSNV . c.3129+393C>A 11 36598376 MB C A Missense p.H184Q c.552C>A 11 36595406 NSCLC C A Missense p.P21Q c.62C>A 11 36594916 LUAD C A Missense p.P515Q c.1544C>A 11 36596398 LUAD C A Missense p.R737S c.2209C>A 11 36597063 CM C A Missense p.R973S c.2917C>A 11 36597771 LUSC C A Synonymous p.I376I c.1128C>A 11 36595982 UCEC C A Synonymous p.L236L c.708C>A 11 36595562 ESCA C A Synonymous p.P395P c.1185C>A 11 36596039 LUAD C A Synonymous p.R776R c.2326C>A 11 36597180 LUAD C A Synonymous p.R778R c.2332C>A 11 36597186 CM C G Missense p.H374Q c.1122C>G 11 36595976 LUAD C G Missense p.S999C c.2996C>G 11 36597850 HNSC C G Nonsense p.S377* c.1130C>G 11 36595984 LUSC C T Missense p.A444V c.1331C>T 11 36596185 CM C T Missense p.A444V c.1331C>T 11 36596185 LUSC C T Missense p.A456V c.1367C>T 11 36596221 LUAD C T Missense p.A857V c.2570C>T 11 36597424 LUAD C T Missense p.H92Y c.274C>T 11 36595128 CM C T Missense p.P132L c.395C>T 11 36595249 CM C T Missense p.P152L c.455C>T 11 36595309 GBM C T Missense p.P15L c.44C>T 11 36594898 LUAD C T Missense p.P334S c.1000C>T 11 36595854 CM C T Missense p.P337L c.1010C>T 11 36595864 HNSC C T Missense p.P502S c.1504C>T 11 36596358 LUAD C T Missense p.P515L c.1544C>T 11 36596398 ESCA C T Missense p.P525L c.1574C>T 11 36596428 ESCA C T Missense p.P649L c.1946C>T 11 36596800 CM C T Missense p.P792L c.2375C>T 11 36597229 CM C T Missense p.R396C c.1186C>T 11 36596040 HNSC C T Missense p.R410W c.1228C>T 11 36596082 STAD C T Missense p.R561C c.1681C>T 11 36596535 LUAD C T Missense p.R699W c.2095C>T 11 36596949 COREAD C T Missense p.R759C c.2275C>T 11 36597129 CLL C T Missense p.R973C c.2917C>T 11 36597771 UCEC C T Missense p.S37F c.110C>T 11 36594964 CM C T Missense p.S626L c.1877C>T 11 36596731 CM C T Missense p.S724F c.2171C>T 11 36597025 CM C T Missense p.S88L c.263C>T 11 36595117 CM C T Missense p.S908F c.2723C>T 11 36597577 CM C T Missense p.T533I c.1598C>T 11 36596452 GBM C T Missense p.T670M c.2009C>T 11 36596863 COREAD C T Nonsense p.Q501* c.1501C>T 11 36596355 CM C T Synonymous p.A3A c.9C>T 11 36594863 CM C T Synonymous p.D607D c.1821C>T 11 36596675 CM C T Synonymous p.D607D c.1821C>T 11 36596675 LGG C T Synonymous p.F33F c.99C>T 11 36594953 CM C T Synonymous p.F787F c.2361C>T 11 36597215 CM C T Synonymous p.F974F c.2922C>T 11 36597776 THCA C T Synonymous p.I266I c.798C>T 11 36595652 CM C T Synonymous p.I577I c.1731C>T 11 36596585 BRCA C T Synonymous p.L590L c.1768C>T 11 36596622 CM C T Synonymous p.L675L c.2023C>T 11 36596877 GBM C T Synonymous p.L698L c.2094C>T 11 36596948 CM C T Synonymous p.L991L c.2971C>T 11 36597825 CM C T Synonymous p.S1024S c.3072C>T 11 36597926 CLL C T Synonymous p.S793S c.2379C>T 11 36597233 CM C T Synonymous p.S875S c.2625C>T 11 36597479 LUAD G A 3-UTRSNV . c.3129+2488G>A 11 36600471 HC G A Missense p.A1023T c.3067G>A 11 36597921 BRCA G A Missense p.A243T c.727G>A 11 36595581 CM G A Missense p.C293Y c.878G>A 11 36595732 STAD G A Missense p.C313Y c.938G>A 11 36595792 CM G A Missense p.D867N c.2599G>A 11 36597453 BRCA G A Missense p.E770K c.2308G>A 11 36597162 CM G A Missense p.E876K c.2626G>A 11 36597480 PRAD G A Missense p.G604R c.1810G>A 11 36596664 CM G A Missense p.R198K c.593G>A 11 36595447 LUAD G A Missense p.R332Q c.995G>A 11 36595849 PRAD G A Missense p.R396H c.1187G>A 11 36596041 PRAD G A Missense p.R474H c.1421G>A 11 36596275 GBM G A Missense p.R737H c.2210G>A 11 36597064 GBM G A Missense p.R737H c.2210G>A 11 36597064 PRAD G A Missense p.R764H c.2291G>A 11 36597145 UCEC G A Missense p.V866M c.2596G>A 11 36597450 PRAD G A Synonymous p.E384E c.1152G>A 11 36596006 CM G A Synonymous p.K49K c.147G>A 11 36595001 BLCA G A Synonymous p.P152P c.456G>A 11 36595310 STAD G A Synonymous p.R125R c.375G>A 11 36595229 CM G A Synonymous p.R223R c.669G>A 11 36595523 CM G A Synonymous p.V288V c.864G>A 11 36595718 CM G C Missense p.E122D c.366G>C 11 36595220 SCLC G C Missense p.L80F c.240G>C 11 36595094 HNSC G C Missense p.M581I c.1743G>C 11 36596597 BRCA G C Missense p.S676T c.2027G>C 11 36596881 LUAD G C Synonymous p.L738L c.2214G>C 11 36597068 LUAD G T Missense p.C316F c.947G>T 11 36595801 HNSC G T Missense p.G392V c.1175G>T 11 36596029 GBM G T Missense p.G496W c.1486G>T 11 36596340 SCLC G T Missense p.G696C c.2086G>T 11 36596940 LUAD G T Missense p.K250N c.750G>T 11 36595604 LUSC G T Missense p.L80F c.240G>T 11 36595094 NB G T Missense p.R112L c.335G>T 11 36595189 LUSC G T Missense p.R764L c.2291G>T 11 36597145 LUAD G T Missense p.V715L c.2143G>T 11 36596997 SCLC G T Missense p.V895L c.2683G>T 11 36597537 LUAD G T Nonsense p.E1042* c.3124G>T 11 36597978 BRCA G T Synonymous p.G115G c.345G>T 11 36595199 LUSC T A Missense p.W522R c.1564T>A 11 36596418 BRCA T C 3-UTRSNV . c.3129+1166T>C 11 36599149 HC T G 3-UTRSNV . c.3129+28T>G 11 36598011 ESCA T G Missense p.L81V c.241T>G 11 36595095 CM T G Missense p.L9V c.25T>G 11 36594879 STAD T G Missense p.V641G c.1922T>G 11 36596776 LUSC