Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 13 21553890 21553890 + Silent SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr13:21553890G>A c.2712C>T c.(2710-2712)ttC>ttT p.F904F BLCA 13 21555655 21555655 + Nonsense_Mutation SNP G G C TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr13:21555655G>C c.2615C>G c.(2614-2616)tCa>tGa p.S872* BLCA 13 21557738 21557738 + Missense_Mutation SNP C C T TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr13:21557738C>T c.2107G>A c.(2107-2109)Gat>Aat p.D703N BLCA 13 21557868 21557868 + Missense_Mutation SNP C C G TCGA-ZF-A9RD-01A-11D-A42E-08 TCGA-ZF-A9RD-10A-01D-A42H-08 g.chr13:21557868C>G c.1977G>C c.(1975-1977)aaG>aaC p.K659N BLCA 13 21562107 21562107 + Silent SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr13:21562107G>A c.1812C>T c.(1810-1812)ttC>ttT p.F604F BLCA 13 21562346 21562346 + Missense_Mutation SNP G G A TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr13:21562346G>A c.1573C>T c.(1573-1575)Cgc>Tgc p.R525C BLCA 13 21562482 21562483 + In_Frame_Ins INS - - GGGGCG TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr13:21562482_21562483insGGGGCG c.1436_1437insCGCCCC c.(1435-1437)ccg>ccCGCCCCg p.479_479P>PAP BLCA 13 21619974 21619974 + Missense_Mutation SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr13:21619974C>T c.192G>A c.(190-192)atG>atA p.M64I BLCA 13 21620025 21620025 + Silent SNP C C T TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr13:21620025C>T c.141G>A c.(139-141)ctG>ctA p.L47L BRCA 13 21549155 21549155 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr13:21549155T>G c.3121A>C c.(3121-3123)Acc>Ccc p.T1041P BRCA 13 21557447 21557447 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:21557447C>A c.2398G>T c.(2398-2400)Gat>Tat p.D800Y BRCA 13 21557891 21557891 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:21557891C>A c.1954G>T c.(1954-1956)Gag>Tag p.E652* BRCA 13 21563383 21563383 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr13:21563383G>A c.536C>T c.(535-537)tCg>tTg p.S179L BRCA 13 21563388 21563388 + Silent SNP G G T TCGA-A2-A3XZ-01A-42D-A23C-09 TCGA-A2-A3XZ-10A-01D-A23C-09 g.chr13:21563388G>T c.531C>A c.(529-531)ggC>ggA p.G177G CESC 13 21549039 21549039 + Silent SNP C C T TCGA-MU-A51Y-01A-11D-A26G-09 TCGA-MU-A51Y-10A-01D-A26G-09 g.chr13:21549039C>T c.3237G>A c.(3235-3237)caG>caA p.Q1079Q CESC 13 21562747 21562747 + Missense_Mutation SNP C C T TCGA-C5-A1BF-01B-11D-A13W-08 TCGA-C5-A1BF-10A-01D-A13W-08 g.chr13:21562747C>T c.1172G>A c.(1171-1173)cGc>cAc p.R391H CESC 13 21619910 21619910 + Missense_Mutation SNP G G A TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr13:21619910G>A c.256C>T c.(256-258)Cct>Tct p.P86S COAD 13 21549228 21549228 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr13:21549228T>C c.3048A>G c.(3046-3048)gaA>gaG p.E1016E COAD 13 21549231 21549231 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:21549231G>A c.3045C>T c.(3043-3045)agC>agT p.S1015S COAD 13 21549283 21549283 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:21549283T>C c.2993A>G c.(2992-2994)gAc>gGc p.D998G COAD 13 21549309 21549309 + Silent SNP G G A TCGA-AA-3930-01A-01W-0995-10 TCGA-AA-3930-10A-01W-0995-10 g.chr13:21549309G>A c.2967C>T c.(2965-2967)taC>taT p.Y989Y COAD 13 21549342 21549342 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:21549342G>T c.2934C>A c.(2932-2934)ttC>ttA p.F978L COAD 13 21549418 21549418 + Missense_Mutation SNP C C A TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr13:21549418C>A c.2858G>T c.(2857-2859)tGc>tTc p.C953F COAD 13 21549419 21549419 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:21549419A>C c.2857T>G c.(2857-2859)Tgc>Ggc p.C953G COAD 13 21553890 21553890 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:21553890G>A c.2712C>T c.(2710-2712)ttC>ttT p.F904F COAD 13 21553895 21553895 + Missense_Mutation SNP G G T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr13:21553895G>T c.2707C>A c.(2707-2709)Ctc>Atc p.L903I COAD 13 21555628 21555628 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:21555628G>A c.2642C>T c.(2641-2643)gCa>gTa p.A881V COAD 13 21557537 21557537 + Missense_Mutation SNP A A G TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr13:21557537A>G c.2308T>C c.(2308-2310)Ttc>Ctc p.F770L COAD 13 21557817 21557817 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:21557817G>A c.2028C>T c.(2026-2028)atC>atT p.I676I COAD 13 21557822 21557822 + Missense_Mutation SNP C C A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr13:21557822C>A c.2023G>T c.(2023-2025)Ggg>Tgg p.G675W COAD 13 21562245 21562245 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr13:21562245G>A c.1674C>T c.(1672-1674)cgC>cgT p.R558R COAD 13 21562246 21562246 + Missense_Mutation SNP C C A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr13:21562246C>A c.1673G>T c.(1672-1674)cGc>cTc p.R558L COAD 13 21563345 21563345 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr13:21563345C>T c.574G>A c.(574-576)Gag>Aag p.E192K COAD 13 21620046 21620046 + Silent SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr13:21620046T>C c.120A>G c.(118-120)ggA>ggG p.G40G COAD 13 21620046 21620046 + Silent SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr13:21620046T>C c.120A>G c.(118-120)ggA>ggG p.G40G COAD 13 21620047 21620047 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr13:21620047C>A c.119G>T c.(118-120)gGa>gTa p.G40V COAD 13 21620119 21620119 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr13:21620119C>T c.47G>A c.(46-48)cGg>cAg p.R16Q COADREAD 13 21549228 21549228 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr13:21549228T>C c.3048A>G c.(3046-3048)gaA>gaG p.E1016E COADREAD 13 21549228 21549228 + Silent SNP T T C TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr13:21549228T>C c.3048A>G c.(3046-3048)gaA>gaG p.E1016E COADREAD 13 21549231 21549231 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr13:21549231G>A c.3045C>T c.(3043-3045)agC>agT p.S1015S COADREAD 13 21549283 21549283 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:21549283T>C c.2993A>G c.(2992-2994)gAc>gGc p.D998G COADREAD 13 21549309 21549309 + Silent SNP G G A TCGA-AA-3930-01A-01W-0995-10 TCGA-AA-3930-10A-01W-0995-10 g.chr13:21549309G>A c.2967C>T c.(2965-2967)taC>taT p.Y989Y COADREAD 13 21549342 21549342 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:21549342G>T c.2934C>A c.(2932-2934)ttC>ttA p.F978L COADREAD 13 21549418 21549418 + Missense_Mutation SNP C C A TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr13:21549418C>A c.2858G>T c.(2857-2859)tGc>tTc p.C953F COADREAD 13 21549419 21549419 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr13:21549419A>C c.2857T>G c.(2857-2859)Tgc>Ggc p.C953G COADREAD 13 21553890 21553890 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:21553890G>A c.2712C>T c.(2710-2712)ttC>ttT p.F904F COADREAD 13 21553895 21553895 + Missense_Mutation SNP G G T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr13:21553895G>T c.2707C>A c.(2707-2709)Ctc>Atc p.L903I COADREAD 13 21555628 21555628 + Missense_Mutation SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr13:21555628G>A c.2642C>T c.(2641-2643)gCa>gTa p.A881V COADREAD 13 21557537 21557537 + Missense_Mutation SNP A A G TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr13:21557537A>G c.2308T>C c.(2308-2310)Ttc>Ctc p.F770L COADREAD 13 21557817 21557817 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:21557817G>A c.2028C>T c.(2026-2028)atC>atT p.I676I COADREAD 13 21557822 21557822 + Missense_Mutation SNP C C A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr13:21557822C>A c.2023G>T c.(2023-2025)Ggg>Tgg p.G675W COADREAD 13 21562238 21562238 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:21562238C>T c.1681G>A c.(1681-1683)Gcc>Acc p.A561T COADREAD 13 21562245 21562245 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr13:21562245G>A c.1674C>T c.(1672-1674)cgC>cgT p.R558R COADREAD 13 21562246 21562246 + Missense_Mutation SNP C C A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr13:21562246C>A c.1673G>T c.(1672-1674)cGc>cTc p.R558L COADREAD 13 21563345 21563345 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr13:21563345C>T c.574G>A c.(574-576)Gag>Aag p.E192K COADREAD 13 21620046 21620046 + Silent SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr13:21620046T>C c.120A>G c.(118-120)ggA>ggG p.G40G COADREAD 13 21620046 21620046 + Silent SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr13:21620046T>C c.120A>G c.(118-120)ggA>ggG p.G40G COADREAD 13 21620047 21620047 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr13:21620047C>A c.119G>T c.(118-120)gGa>gTa p.G40V COADREAD 13 21620068 21620068 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:21620068G>A c.98C>T c.(97-99)tCg>tTg p.S33L COADREAD 13 21620119 21620119 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr13:21620119C>T c.47G>A c.(46-48)cGg>cAg p.R16Q DLBC 13 21562181 21562181 + Missense_Mutation SNP C C T TCGA-FA-A82F-01A-11D-A382-10 TCGA-FA-A82F-10A-01D-A385-10 g.chr13:21562181C>T c.1738G>A c.(1738-1740)Gtc>Atc p.V580I DLBC 13 21563311 21563311 + Missense_Mutation SNP G G A TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr13:21563311G>A c.608C>T c.(607-609)gCg>gTg p.A203V ESCA 13 21555733 21555733 + Missense_Mutation SNP G G A TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr13:21555733G>A c.2537C>T c.(2536-2538)tCt>tTt p.S846F ESCA 13 21557918 21557918 + Missense_Mutation SNP G G T TCGA-Z6-A8JE-01A-11D-A37C-09 TCGA-Z6-A8JE-10A-01D-A37F-09 g.chr13:21557918G>T c.1927C>A c.(1927-1929)Cag>Aag p.Q643K ESCA 13 21562128 21562128 + Nonsense_Mutation SNP G G T TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr13:21562128G>T c.1791C>A c.(1789-1791)taC>taA p.Y597* ESCA 13 21562178 21562178 + Missense_Mutation SNP G G A TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr13:21562178G>A c.1741C>T c.(1741-1743)Cgc>Tgc p.R581C ESCA 13 21562256 21562256 + Missense_Mutation SNP C C A TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chr13:21562256C>A c.1663G>T c.(1663-1665)Gac>Tac p.D555Y GBMLGG 13 21549235 21549235 + Missense_Mutation SNP G G A TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr13:21549235G>A c.3041C>T c.(3040-3042)gCc>gTc p.A1014V GBMLGG 13 21549240 21549240 + Silent SNP G G A TCGA-HT-7480-01A-11D-2086-08 TCGA-HT-7480-10A-01D-2086-08 g.chr13:21549240G>A c.3036C>T c.(3034-3036)aaC>aaT p.N1012N GBMLGG 13 21549263 21549263 + Missense_Mutation SNP C C T TCGA-CS-6670-01A-11D-1893-08 TCGA-CS-6670-10A-01D-1893-08 g.chr13:21549263C>T c.3013G>A c.(3013-3015)Gta>Ata p.V1005I GBMLGG 13 21557518 21557518 + Missense_Mutation SNP G G A TCGA-TM-A7C5-01A-11D-A32B-08 TCGA-TM-A7C5-10A-01D-A329-08 g.chr13:21557518G>A c.2327C>T c.(2326-2328)aCt>aTt p.T776I GBMLGG 13 21557659 21557659 + Missense_Mutation SNP A A T TCGA-HT-8113-01A-11D-2395-08 TCGA-HT-8113-10A-01D-2396-08 g.chr13:21557659A>T c.2186T>A c.(2185-2187)gTc>gAc p.V729D GBMLGG 13 21562142 21562142 + Missense_Mutation SNP G G A TCGA-FG-A60J-01A-11D-A289-08 TCGA-FG-A60J-10A-01D-A289-08 g.chr13:21562142G>A c.1777C>T c.(1777-1779)Cgc>Tgc p.R593C GBMLGG 13 21562426 21562426 + Missense_Mutation SNP C C A TCGA-DU-7300-01A-21D-2086-08 TCGA-DU-7300-10A-01D-2086-08 g.chr13:21562426C>A c.1493G>T c.(1492-1494)gGc>gTc p.G498V GBMLGG 13 21563346 21563346 + Silent SNP G G A TCGA-DB-A4XH-01A-11D-A27K-08 TCGA-DB-A4XH-10A-01D-A27N-08 g.chr13:21563346G>A c.573C>T c.(571-573)taC>taT p.Y191Y HNSC 13 21549414 21549414 + Silent SNP G G A TCGA-CQ-5333-01A-01D-2394-08 TCGA-CQ-5333-10A-01D-2394-08 g.chr13:21549414G>A c.2862C>T c.(2860-2862)tcC>tcT p.S954S HNSC 13 21555623 21555623 + Missense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr13:21555623C>T c.2647G>A c.(2647-2649)Gag>Aag p.E883K HNSC 13 21557591 21557591 + Missense_Mutation SNP C C A TCGA-D6-8569-01A-11D-2394-08 TCGA-D6-8569-10A-01D-2394-08 g.chr13:21557591C>A c.2254G>T c.(2254-2256)Gac>Tac p.D752Y HNSC 13 21562740 21562740 + Silent SNP G G A TCGA-CN-6019-01A-11D-1683-08 TCGA-CN-6019-10A-01D-1683-08 g.chr13:21562740G>A c.1179C>T c.(1177-1179)caC>caT p.H393H HNSC 13 21562921 21562921 + Missense_Mutation SNP G G C TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr13:21562921G>C c.998C>G c.(997-999)tCc>tGc p.S333C HNSC 13 21563351 21563351 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr13:21563351G>A c.568C>T c.(568-570)Ccc>Tcc p.P190S HNSC 13 21565462 21565462 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr13:21565462G>A c.424C>T c.(424-426)Ctg>Ttg p.L142L HNSC 13 21565463 21565463 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr13:21565463G>A c.423C>T c.(421-423)taC>taT p.Y141Y HNSC 13 21565493 21565493 + Silent SNP G G A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr13:21565493G>A c.393C>T c.(391-393)gcC>gcT p.A131A HNSC 13 21565494 21565494 + Missense_Mutation SNP G G A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr13:21565494G>A c.392C>T c.(391-393)gCc>gTc p.A131V HNSC 13 21565498 21565498 + Missense_Mutation SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr13:21565498C>T c.388G>A c.(388-390)Gag>Aag p.E130K KICH 13 21557476 21557476 + Missense_Mutation SNP C C T TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr13:21557476C>T c.2369G>A c.(2368-2370)cGa>cAa p.R790Q KIPAN 13 21557476 21557476 + Missense_Mutation SNP C C T TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr13:21557476C>T c.2369G>A c.(2368-2370)cGa>cAa p.R790Q KIPAN 13 21557669 21557669 + Missense_Mutation SNP C C T TCGA-BP-4326-01A-01D-1366-10 TCGA-BP-4326-11A-01D-1366-10 g.chr13:21557669C>T c.2176G>A c.(2176-2178)Gag>Aag p.E726K KIPAN 13 21557681 21557681 + Nonsense_Mutation SNP C C A TCGA-B0-5711-01A-11D-1669-08 TCGA-B0-5711-11A-01D-1669-08 g.chr13:21557681C>A c.2164G>T c.(2164-2166)Gag>Tag p.E722* KIPAN 13 21557772 21557773 + Frame_Shift_Ins INS - - T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr13:21557772_21557773insT c.2072_2073insA c.(2071-2073)cacfs p.H691fs KIPAN 13 21562131 21562131 + Missense_Mutation SNP G G C TCGA-CW-5589-01A-01D-1534-10 TCGA-CW-5589-11A-01D-1535-10 g.chr13:21562131G>C c.1788C>G c.(1786-1788)agC>agG p.S596R KIRC 13 21557669 21557669 + Missense_Mutation SNP C C T TCGA-BP-4326-01A-01D-1366-10 TCGA-BP-4326-11A-01D-1366-10 g.chr13:21557669C>T c.2176G>A c.(2176-2178)Gag>Aag p.E726K KIRC 13 21557681 21557681 + Nonsense_Mutation SNP C C A TCGA-B0-5711-01A-11D-1669-08 TCGA-B0-5711-11A-01D-1669-08 g.chr13:21557681C>A c.2164G>T c.(2164-2166)Gag>Tag p.E722* KIRC 13 21557772 21557773 + Frame_Shift_Ins INS - - T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr13:21557772_21557773insT c.2072_2073insA c.(2071-2073)cacfs p.H691fs KIRC 13 21562131 21562131 + Missense_Mutation SNP G G C TCGA-CW-5589-01A-01D-1534-10 TCGA-CW-5589-11A-01D-1535-10 g.chr13:21562131G>C c.1788C>G c.(1786-1788)agC>agG p.S596R LGG 13 21549235 21549235 + Missense_Mutation SNP G G A TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr13:21549235G>A c.3041C>T c.(3040-3042)gCc>gTc p.A1014V LGG 13 21549240 21549240 + Silent SNP G G A TCGA-HT-7480-01A-11D-2086-08 TCGA-HT-7480-10A-01D-2086-08 g.chr13:21549240G>A c.3036C>T c.(3034-3036)aaC>aaT p.N1012N LGG 13 21549263 21549263 + Missense_Mutation SNP C C T TCGA-CS-6670-01A-11D-1893-08 TCGA-CS-6670-10A-01D-1893-08 g.chr13:21549263C>T c.3013G>A c.(3013-3015)Gta>Ata p.V1005I LGG 13 21557518 21557518 + Missense_Mutation SNP G G A TCGA-TM-A7C5-01A-11D-A32B-08 TCGA-TM-A7C5-10A-01D-A329-08 g.chr13:21557518G>A c.2327C>T c.(2326-2328)aCt>aTt p.T776I LGG 13 21557659 21557659 + Missense_Mutation SNP A A T TCGA-HT-8113-01A-11D-2395-08 TCGA-HT-8113-10A-01D-2396-08 g.chr13:21557659A>T c.2186T>A c.(2185-2187)gTc>gAc p.V729D LGG 13 21562142 21562142 + Missense_Mutation SNP G G A TCGA-FG-A60J-01A-11D-A289-08 TCGA-FG-A60J-10A-01D-A289-08 g.chr13:21562142G>A c.1777C>T c.(1777-1779)Cgc>Tgc p.R593C LGG 13 21562426 21562426 + Missense_Mutation SNP C C A TCGA-DU-7300-01A-21D-2086-08 TCGA-DU-7300-10A-01D-2086-08 g.chr13:21562426C>A c.1493G>T c.(1492-1494)gGc>gTc p.G498V LGG 13 21563346 21563346 + Silent SNP G G A TCGA-DB-A4XH-01A-11D-A27K-08 TCGA-DB-A4XH-10A-01D-A27N-08 g.chr13:21563346G>A c.573C>T c.(571-573)taC>taT p.Y191Y LIHC 13 21549409 21549409 + Missense_Mutation SNP T T A TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr13:21549409T>A c.2867A>T c.(2866-2868)gAc>gTc p.D956V LIHC 13 21555755 21555755 + Missense_Mutation SNP T T C TCGA-FV-A2QR-01A-11D-A20W-10 TCGA-FV-A2QR-11A-11D-A20W-10 g.chr13:21555755T>C c.2515A>G c.(2515-2517)Agc>Ggc p.S839G LIHC 13 21555762 21555762 + Missense_Mutation SNP C C A TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr13:21555762C>A c.2508G>T c.(2506-2508)atG>atT p.M836I LUAD 13 21549028 21549028 + Missense_Mutation SNP C C T TCGA-50-5044-01A-21D-1855-08 TCGA-50-5044-10A-01D-1855-08 g.chr13:21549028C>T c.3248G>A c.(3247-3249)tGc>tAc p.C1083Y LUAD 13 21549230 21549230 + Missense_Mutation SNP C C T TCGA-17-Z036-01A-01W-0746-08 TCGA-17-Z036-11A-01W-0746-08 g.chr13:21549230C>T c.3046G>A c.(3046-3048)Gaa>Aaa p.E1016K LUAD 13 21549289 21549289 + Missense_Mutation SNP G G A TCGA-64-5775-01A-01D-1625-08 TCGA-64-5775-10A-01D-1625-08 g.chr13:21549289G>A c.2987C>T c.(2986-2988)cCc>cTc p.P996L LUAD 13 21549420 21549420 + Silent SNP G G A TCGA-62-A46P-01A-11D-A24D-08 TCGA-62-A46P-10A-01D-A24F-08 g.chr13:21549420G>A c.2856C>T c.(2854-2856)tgC>tgT p.C952C LUAD 13 21557438 21557438 + Missense_Mutation SNP C C A TCGA-44-6774-01A-21D-1855-08 TCGA-44-6774-10A-01D-1855-08 g.chr13:21557438C>A c.2407G>T c.(2407-2409)Ggt>Tgt p.G803C LUAD 13 21557766 21557766 + Silent SNP C C A TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr13:21557766C>A c.2079G>T c.(2077-2079)ctG>ctT p.L693L LUAD 13 21557801 21557801 + Missense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr13:21557801C>A c.2044G>T c.(2044-2046)Gtg>Ttg p.V682L LUAD 13 21557821 21557821 + Missense_Mutation SNP C C A TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr13:21557821C>A c.2024G>T c.(2023-2025)gGg>gTg p.G675V LUAD 13 21562482 21562483 + In_Frame_Ins INS - - GGGGCG TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr13:21562482_21562483insGGGGCG c.1436_1437insCGCCCC c.(1435-1437)ccg>ccCGCCCCg p.479_479P>PAP LUAD 13 21562678 21562678 + Missense_Mutation SNP G G A TCGA-38-4630-01A-01D-1265-08 TCGA-38-4630-11A-01D-1265-08 g.chr13:21562678G>A c.1241C>T c.(1240-1242)cCg>cTg p.P414L LUAD 13 21563266 21563266 + Missense_Mutation SNP C C A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr13:21563266C>A c.653G>T c.(652-654)gGa>gTa p.G218V LUAD 13 21565414 21565414 + Missense_Mutation SNP G G A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr13:21565414G>A c.472C>T c.(472-474)Cca>Tca p.P158S LUAD 13 21565415 21565415 + Silent SNP G G A TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chr13:21565415G>A c.471C>T c.(469-471)tcC>tcT p.S157S LUAD 13 21565435 21565435 + Missense_Mutation SNP G G A TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr13:21565435G>A c.451C>T c.(451-453)Cgg>Tgg p.R151W LUAD 13 21620119 21620119 + Missense_Mutation SNP C C A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr13:21620119C>A c.47G>T c.(46-48)cGg>cTg p.R16L LUSC 13 21562336 21562336 + Missense_Mutation SNP G G A TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr13:21562336G>A c.1583C>T c.(1582-1584)tCg>tTg p.S528L LUSC 13 21562372 21562372 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr13:21562372G>A c.1547C>T c.(1546-1548)cCg>cTg p.P516L LUSC 13 21563271 21563271 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr13:21563271G>A c.648C>T c.(646-648)ttC>ttT p.F216F OV 13 21553914 21553914 + Nonsense_Mutation SNP C C T TCGA-59-2372-01A-01D-1526-09 TCGA-59-2372-10A-01D-1526-09 g.chr13:21553914C>T c.2688G>A c.(2686-2688)tgG>tgA p.W896* OV 13 21619951 21619951 + Missense_Mutation SNP G G A TCGA-36-1568-01A-01W-0615-10 TCGA-36-1568-10A-01W-0615-10 g.chr13:21619951G>A c.215C>T c.(214-216)cCt>cTt p.P72L PAAD 13 21549149 21549149 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:21549149G>A c.3127C>T c.(3127-3129)Cga>Tga p.R1043* PAAD 13 21562295 21562295 + Missense_Mutation SNP G G T TCGA-2J-AAB8-01A-12D-A40W-08 TCGA-2J-AAB8-10A-01D-A40W-08 g.chr13:21562295G>T c.1624C>A c.(1624-1626)Cag>Aag p.Q542K PAAD 13 21562296 21562296 + Silent SNP C C T TCGA-2J-AAB8-01A-12D-A40W-08 TCGA-2J-AAB8-10A-01D-A40W-08 g.chr13:21562296C>T c.1623G>A c.(1621-1623)gaG>gaA p.E541E PAAD 13 21562824 21562824 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:21562824G>T c.1095C>A c.(1093-1095)acC>acA p.T365T PCPG 13 21555612 21555612 + Silent SNP G G T TCGA-QR-A6GW-01A-11D-A35D-08 TCGA-QR-A6GW-10A-01D-A35B-08 g.chr13:21555612G>T c.2658C>A c.(2656-2658)ctC>ctA p.L886L PRAD 13 21557700 21557700 + Silent SNP G G A TCGA-CH-5750-01A-11D-1576-08 TCGA-CH-5750-10A-01D-1576-08 g.chr13:21557700G>A c.2145C>T c.(2143-2145)gcC>gcT p.A715A PRAD 13 21562221 21562221 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr13:21562221G>A c.1698C>T c.(1696-1698)ggC>ggT p.G566G PRAD 13 21562482 21562483 + In_Frame_Ins INS - - GGGGCG TCGA-EJ-7784-01A-11D-2114-08 TCGA-EJ-7784-10A-01D-2114-08 g.chr13:21562482_21562483insGGGGCG c.1436_1437insCGCCCC c.(1435-1437)ccg>ccCGCCCCg p.479_479P>PAP READ 13 21549228 21549228 + Silent SNP T T C TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr13:21549228T>C c.3048A>G c.(3046-3048)gaA>gaG p.E1016E READ 13 21562238 21562238 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:21562238C>T c.1681G>A c.(1681-1683)Gcc>Acc p.A561T READ 13 21620068 21620068 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:21620068G>A c.98C>T c.(97-99)tCg>tTg p.S33L SARC 13 21563156 21563156 + Missense_Mutation SNP G G A TCGA-DX-AB32-01A-11D-A417-09 TCGA-DX-AB32-10A-01D-A41A-09 g.chr13:21563156G>A c.763C>T c.(763-765)Cgg>Tgg p.R255W SARC 13 21563188 21563188 + Missense_Mutation SNP G G A TCGA-IE-A4EH-01A-11D-A24N-09 TCGA-IE-A4EH-10A-01D-A24N-09 g.chr13:21563188G>A c.731C>T c.(730-732)gCa>gTa p.A244V SKCM 13 21549192 21549192 + Silent SNP G G T TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr13:21549192G>T c.3084C>A c.(3082-3084)ccC>ccA p.P1028P SKCM 13 21549220 21549220 + Missense_Mutation SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr13:21549220G>A c.3056C>T c.(3055-3057)aCc>aTc p.T1019I SKCM 13 21555718 21555718 + Missense_Mutation SNP C C T TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr13:21555718C>T c.2552G>A c.(2551-2553)gGg>gAg p.G851E SKCM 13 21557379 21557379 + Silent SNP G G A TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr13:21557379G>A c.2466C>T c.(2464-2466)tcC>tcT p.S822S SKCM 13 21557732 21557732 + Silent SNP G G A TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr13:21557732G>A c.2113C>T c.(2113-2115)Ctg>Ttg p.L705L SKCM 13 21557827 21557827 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:21557827G>A c.2018C>T c.(2017-2019)aCc>aTc p.T673I SKCM 13 21562052 21562052 + Missense_Mutation SNP G G A TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr13:21562052G>A c.1867C>T c.(1867-1869)Cgg>Tgg p.R623W SKCM 13 21562053 21562053 + Silent SNP G G A TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr13:21562053G>A c.1866C>T c.(1864-1866)aaC>aaT p.N622N SKCM 13 21562189 21562189 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr13:21562189G>A c.1730C>T c.(1729-1731)cCc>cTc p.P577L SKCM 13 21562821 21562821 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr13:21562821G>A c.1098C>T c.(1096-1098)tcC>tcT p.S366S SKCM 13 21562821 21562821 + Silent SNP G G A TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chr13:21562821G>A c.1098C>T c.(1096-1098)tcC>tcT p.S366S SKCM 13 21563271 21563271 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr13:21563271G>A c.648C>T c.(646-648)ttC>ttT p.F216F SKCM 13 21563423 21563423 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr13:21563423G>A c.496C>T c.(496-498)Cca>Tca p.P166S SKCM 13 21565530 21565530 + Missense_Mutation SNP C C T TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr13:21565530C>T c.356G>A c.(355-357)cGa>cAa p.R119Q

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 13 21548995 21548995 single base substitution T G 3_prime_UTR_variant BLCA-CN 13 21548995 21548995 single base substitution T G downstream_gene_variant BLCA-US 13 21562346 21562346 single base substitution G A downstream_gene_variant BLCA-US 13 21562346 21562346 single base substitution G A missense_variant R525C 1573C>T BOCA-FR 13 21571175 21571175 single base substitution G T intron_variant BRCA-EU 13 21542734 21542734 single base substitution G C downstream_gene_variant BRCA-EU 13 21543151 21543151 single base substitution G A downstream_gene_variant BRCA-EU 13 21543471 21543471 single base substitution T C downstream_gene_variant BRCA-EU 13 21547001 21547001 single base substitution C G downstream_gene_variant BRCA-EU 13 21547831 21547831 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 13 21547831 21547831 deletion of <=200bp A - downstream_gene_variant BRCA-EU 13 21547945 21547945 insertion of <=200bp - T 3_prime_UTR_variant BRCA-EU 13 21547945 21547945 insertion of <=200bp - T downstream_gene_variant BRCA-EU 13 21550066 21550066 single base substitution G A intron_variant BRCA-EU 13 21550701 21550701 single base substitution G C intron_variant BRCA-EU 13 21551525 21551525 single base substitution A C intron_variant BRCA-EU 13 21552023 21552023 single base substitution G A intron_variant BRCA-EU 13 21553962 21553962 single base substitution C G intron_variant BRCA-EU 13 21554103 21554103 single base substitution G A intron_variant BRCA-EU 13 21554172 21554172 single base substitution T C intron_variant BRCA-EU 13 21554585 21554585 single base substitution T C intron_variant BRCA-EU 13 21556553 21556553 single base substitution C T intron_variant BRCA-EU 13 21558730 21558730 deletion of <=200bp A - downstream_gene_variant BRCA-EU 13 21558730 21558730 deletion of <=200bp A - intron_variant BRCA-EU 13 21559872 21559872 single base substitution G A downstream_gene_variant BRCA-EU 13 21559872 21559872 single base substitution G A intron_variant BRCA-EU 13 21560529 21560529 single base substitution C T downstream_gene_variant BRCA-EU 13 21560529 21560529 single base substitution C T intron_variant BRCA-EU 13 21561692 21561692 single base substitution C G downstream_gene_variant BRCA-EU 13 21561692 21561692 single base substitution C G intron_variant BRCA-EU 13 21562426 21562426 single base substitution C T downstream_gene_variant BRCA-EU 13 21562426 21562426 single base substitution C T missense_variant G498D 1493G>A BRCA-EU 13 21565913 21565913 single base substitution A T intron_variant BRCA-EU 13 21566085 21566085 single base substitution C T intron_variant BRCA-EU 13 21566212 21566212 single base substitution G C intron_variant BRCA-EU 13 21568580 21568580 single base substitution C T intron_variant BRCA-EU 13 21569835 21569835 insertion of <=200bp - A intron_variant BRCA-EU 13 21571087 21571087 single base substitution G A intron_variant BRCA-EU 13 21571853 21571853 single base substitution C A intron_variant BRCA-EU 13 21572498 21572498 single base substitution A T intron_variant BRCA-EU 13 21572863 21572863 single base substitution C T intron_variant BRCA-EU 13 21574793 21574793 single base substitution G A intron_variant BRCA-EU 13 21576062 21576062 deletion of <=200bp T - intron_variant BRCA-EU 13 21578513 21578513 single base substitution C T intron_variant BRCA-EU 13 21579468 21579468 single base substitution T C intron_variant BRCA-EU 13 21580037 21580037 single base substitution G A intron_variant BRCA-EU 13 21580290 21580290 single base substitution G C intron_variant BRCA-EU 13 21580397 21580397 single base substitution A T intron_variant BRCA-EU 13 21580734 21580734 single base substitution G A intron_variant BRCA-EU 13 21581449 21581449 single base substitution C G intron_variant BRCA-EU 13 21582109 21582109 single base substitution G T intron_variant BRCA-EU 13 21586897 21586897 single base substitution G C intron_variant BRCA-EU 13 21587218 21587218 single base substitution G C intron_variant BRCA-EU 13 21587455 21587455 single base substitution T G intron_variant BRCA-EU 13 21591949 21591949 single base substitution G C intron_variant BRCA-EU 13 21596150 21596150 single base substitution A C intron_variant BRCA-EU 13 21596644 21596644 single base substitution C T intron_variant BRCA-EU 13 21597021 21597021 single base substitution G A intron_variant BRCA-EU 13 21597087 21597087 single base substitution T A intron_variant BRCA-EU 13 21597275 21597275 single base substitution C T intron_variant BRCA-EU 13 21597275 21597275 single base substitution C T upstream_gene_variant BRCA-EU 13 21600179 21600179 single base substitution G A intron_variant BRCA-EU 13 21600179 21600179 single base substitution G A upstream_gene_variant BRCA-EU 13 21601106 21601106 single base substitution G T intron_variant BRCA-EU 13 21601106 21601106 single base substitution G T upstream_gene_variant BRCA-EU 13 21601452 21601452 single base substitution G T intron_variant BRCA-EU 13 21601452 21601452 single base substitution G T upstream_gene_variant BRCA-EU 13 21602694 21602694 single base substitution A T intron_variant BRCA-EU 13 21603458 21603458 single base substitution T C intron_variant BRCA-EU 13 21603916 21603916 single base substitution C T intron_variant BRCA-EU 13 21603995 21603995 single base substitution G A intron_variant BRCA-EU 13 21604084 21604084 single base substitution G A intron_variant BRCA-EU 13 21607494 21607494 single base substitution G T intron_variant BRCA-EU 13 21608110 21608110 single base substitution G A intron_variant BRCA-EU 13 21610010 21610010 single base substitution G A intron_variant BRCA-EU 13 21611518 21611518 single base substitution G A intron_variant BRCA-EU 13 21612944 21612944 single base substitution C A intron_variant BRCA-EU 13 21613284 21613284 deletion of <=200bp A - intron_variant BRCA-EU 13 21613575 21613575 single base substitution G C intron_variant BRCA-EU 13 21614231 21614231 single base substitution G T intron_variant BRCA-EU 13 21616086 21616086 single base substitution G C intron_variant BRCA-EU 13 21616326 21616326 single base substitution G T intron_variant BRCA-EU 13 21617198 21617198 single base substitution C T intron_variant BRCA-EU 13 21620801 21620801 single base substitution C T intron_variant BRCA-EU 13 21622175 21622175 single base substitution G C intron_variant BRCA-EU 13 21622736 21622736 single base substitution C G intron_variant BRCA-EU 13 21622747 21622747 single base substitution G A intron_variant BRCA-EU 13 21624218 21624218 single base substitution C G intron_variant BRCA-EU 13 21625247 21625247 single base substitution G A intron_variant BRCA-EU 13 21625313 21625313 single base substitution T C intron_variant BRCA-EU 13 21625319 21625319 single base substitution C T intron_variant BRCA-EU 13 21625936 21625936 single base substitution A C intron_variant BRCA-EU 13 21628281 21628283 deletion of <=200bp TGG - intron_variant BRCA-EU 13 21629015 21629015 single base substitution G A intron_variant BRCA-EU 13 21629138 21629138 single base substitution C T intron_variant BRCA-EU 13 21629262 21629262 single base substitution A C intron_variant BRCA-EU 13 21630334 21630334 single base substitution G C intron_variant BRCA-EU 13 21631298 21631298 single base substitution G C intron_variant BRCA-EU 13 21631709 21631709 single base substitution G A intron_variant BRCA-EU 13 21631776 21631776 single base substitution A T intron_variant BRCA-EU 13 21633435 21633435 single base substitution A G intron_variant BRCA-EU 13 21633556 21633556 single base substitution G A intron_variant BRCA-EU 13 21633593 21633593 single base substitution G A intron_variant BRCA-EU 13 21634355 21634355 single base substitution A G 5_prime_UTR_variant BRCA-EU 13 21634355 21634355 single base substitution A G intron_variant BRCA-EU 13 21635250 21635250 single base substitution C T intron_variant BRCA-EU 13 21635250 21635250 single base substitution C T upstream_gene_variant BRCA-EU 13 21635305 21635305 single base substitution G A intron_variant BRCA-EU 13 21635305 21635305 single base substitution G A upstream_gene_variant BRCA-EU 13 21635658 21635658 single base substitution C G 5_prime_UTR_variant BRCA-EU 13 21635658 21635658 single base substitution C G upstream_gene_variant BRCA-EU 13 21636378 21636378 single base substitution C T upstream_gene_variant BRCA-EU 13 21637104 21637104 single base substitution T C upstream_gene_variant BRCA-EU 13 21637777 21637777 single base substitution G C upstream_gene_variant BRCA-EU 13 21638663 21638663 single base substitution T C upstream_gene_variant BRCA-EU 13 21638955 21638955 single base substitution G C upstream_gene_variant BRCA-EU 13 21638997 21638997 single base substitution A G upstream_gene_variant BRCA-EU 13 21639218 21639218 single base substitution C T upstream_gene_variant BRCA-EU 13 21640401 21640401 single base substitution G C upstream_gene_variant BRCA-FR 13 21542596 21542596 single base substitution G T downstream_gene_variant BRCA-FR 13 21543471 21543471 single base substitution T C downstream_gene_variant BRCA-FR 13 21550701 21550701 single base substitution G C intron_variant BRCA-FR 13 21553962 21553962 single base substitution C G intron_variant BRCA-FR 13 21579468 21579468 single base substitution T C intron_variant BRCA-FR 13 21580037 21580037 single base substitution G A intron_variant BRCA-FR 13 21580290 21580290 single base substitution G C intron_variant BRCA-FR 13 21581449 21581449 single base substitution C G intron_variant BRCA-FR 13 21612650 21612650 single base substitution C A intron_variant BRCA-FR 13 21616086 21616086 single base substitution G C intron_variant BRCA-FR 13 21631709 21631709 single base substitution G A intron_variant BRCA-FR 13 21635658 21635658 single base substitution C G 5_prime_UTR_variant BRCA-FR 13 21635658 21635658 single base substitution C G upstream_gene_variant BRCA-KR 13 21562373 21562373 single base substitution G A downstream_gene_variant BRCA-KR 13 21562373 21562373 single base substitution G A missense_variant P516S 1546C>T BRCA-UK 13 21555716 21555716 single base substitution C T missense_variant D852N 2554G>A BRCA-UK 13 21568580 21568580 single base substitution C T intron_variant BRCA-UK 13 21608110 21608110 single base substitution G A intron_variant BRCA-UK 13 21626450 21626450 single base substitution G T intron_variant BRCA-UK 13 21637777 21637777 single base substitution G C upstream_gene_variant BRCA-US 13 21549155 21549155 single base substitution T G missense_variant T1041P 3121A>C BRCA-US 13 21557447 21557447 single base substitution C A missense_variant D800Y 2398G>T BRCA-US 13 21557891 21557891 single base substitution C A stop_gained E652* 1954G>T BRCA-US 13 21563383 21563383 single base substitution G A exon_variant BRCA-US 13 21563383 21563383 single base substitution G A missense_variant S179L 536C>T BRCA-US 13 21563388 21563388 single base substitution G T exon_variant BRCA-US 13 21563388 21563388 single base substitution G T synonymous_variant G177G 531C>A BTCA-JP 13 21557805 21557805 single base substitution T A synonymous_variant G680G 2040A>T BTCA-JP 13 21561954 21561954 single base substitution C T downstream_gene_variant BTCA-JP 13 21561954 21561954 single base substitution C T intron_variant BTCA-JP 13 21562335 21562335 single base substitution C T downstream_gene_variant BTCA-JP 13 21562335 21562335 single base substitution C T synonymous_variant S528S 1584G>A BTCA-JP 13 21563108 21563108 single base substitution G A downstream_gene_variant BTCA-JP 13 21563108 21563108 single base substitution G A missense_variant R271C 811C>T CESC-US 13 21549039 21549039 single base substitution C T synonymous_variant Q1079Q 3237G>A CESC-US 13 21562747 21562747 single base substitution C T downstream_gene_variant CESC-US 13 21562747 21562747 single base substitution C T missense_variant R391H 1172G>A CESC-US 13 21619910 21619910 single base substitution G A missense_variant P86S 256C>T CLLE-ES 13 21579042 21579042 single base substitution G C intron_variant CLLE-ES 13 21589859 21589859 single base substitution G A intron_variant CLLE-ES 13 21598813 21598813 single base substitution G T intron_variant CLLE-ES 13 21598813 21598813 single base substitution G T upstream_gene_variant CLLE-ES 13 21616226 21616226 single base substitution T A intron_variant CLLE-ES 13 21634887 21634887 single base substitution G C intron_variant CLLE-ES 13 21634887 21634887 single base substitution G C upstream_gene_variant COAD-US 13 21549283 21549283 single base substitution T C missense_variant D998G 2993A>G COAD-US 13 21549342 21549342 single base substitution G T missense_variant F978L 2934C>A COAD-US 13 21553890 21553890 single base substitution G A synonymous_variant F904F 2712C>T COAD-US 13 21555625 21555625 single base substitution G A missense_variant P882L 2645C>T COAD-US 13 21557537 21557537 single base substitution A G missense_variant F770L 2308T>C COAD-US 13 21557822 21557822 single base substitution C A missense_variant G675W 2023G>T COAD-US 13 21562371 21562371 single base substitution C T downstream_gene_variant COAD-US 13 21562371 21562371 single base substitution C T synonymous_variant P516P 1548G>A COAD-US 13 21562832 21562832 single base substitution C T downstream_gene_variant COAD-US 13 21562832 21562832 single base substitution C T missense_variant G363S 1087G>A COAD-US 13 21562948 21562948 single base substitution G A downstream_gene_variant COAD-US 13 21562948 21562948 single base substitution G A missense_variant A324V 971C>T COAD-US 13 21563345 21563345 single base substitution C T exon_variant COAD-US 13 21563345 21563345 single base substitution C T missense_variant E192K 574G>A COAD-US 13 21620085 21620085 single base substitution T C synonymous_variant K27K 81A>G COAD-US 13 21620119 21620119 single base substitution C T missense_variant R16Q 47G>A COCA-CN 13 21549404 21549404 single base substitution G A missense_variant R958C 2872C>T COCA-CN 13 21557528 21557528 single base substitution C T missense_variant A773T 2317G>A COCA-CN 13 21557605 21557605 single base substitution T C missense_variant Y747C 2240A>G COCA-CN 13 21562308 21562308 single base substitution G A downstream_gene_variant COCA-CN 13 21562308 21562308 single base substitution G A synonymous_variant C537C 1611C>T COCA-CN 13 21562768 21562768 single base substitution G A downstream_gene_variant COCA-CN 13 21562768 21562768 single base substitution G A missense_variant P384L 1151C>T COCA-CN 13 21562820 21562820 single base substitution C T downstream_gene_variant COCA-CN 13 21562820 21562820 single base substitution C T missense_variant V367I 1099G>A COCA-CN 13 21562864 21562864 single base substitution C T downstream_gene_variant COCA-CN 13 21562864 21562864 single base substitution C T missense_variant R352Q 1055G>A COCA-CN 13 21562982 21562982 single base substitution C T downstream_gene_variant COCA-CN 13 21562982 21562982 single base substitution C T missense_variant V313M 937G>A COCA-CN 13 21562983 21562983 single base substitution G A downstream_gene_variant COCA-CN 13 21562983 21562983 single base substitution G A synonymous_variant Y312Y 936C>T COCA-CN 13 21563311 21563311 single base substitution G A exon_variant COCA-CN 13 21563311 21563311 single base substitution G A missense_variant A203V 608C>T COCA-CN 13 21563314 21563314 single base substitution G A exon_variant COCA-CN 13 21563314 21563314 single base substitution G A missense_variant T202M 605C>T COCA-CN 13 21565404 21565404 single base substitution G A splice_region_variant COCA-CN 13 21579946 21579946 single base substitution A T intron_variant COCA-CN 13 21579947 21579947 single base substitution A T intron_variant COCA-CN 13 21604747 21604747 single base substitution A G intron_variant EOPC-DE 13 21569460 21569460 single base substitution C A intron_variant ESAD-UK 13 21542278 21542278 single base substitution C T downstream_gene_variant ESAD-UK 13 21542711 21542711 single base substitution G A downstream_gene_variant ESAD-UK 13 21545687 21545687 single base substitution A C downstream_gene_variant ESAD-UK 13 21545765 21545765 insertion of <=200bp - T downstream_gene_variant ESAD-UK 13 21546356 21546356 single base substitution A T downstream_gene_variant ESAD-UK 13 21546575 21546575 single base substitution A G downstream_gene_variant ESAD-UK 13 21546687 21546687 single base substitution G A downstream_gene_variant ESAD-UK 13 21547680 21547680 single base substitution C G 3_prime_UTR_variant ESAD-UK 13 21547680 21547680 single base substitution C G downstream_gene_variant ESAD-UK 13 21550234 21550234 single base substitution C G intron_variant ESAD-UK 13 21551267 21551267 single base substitution G A intron_variant ESAD-UK 13 21556346 21556346 single base substitution G A intron_variant ESAD-UK 13 21556759 21556759 single base substitution A G intron_variant ESAD-UK 13 21557820 21557820 single base substitution C A synonymous_variant G675G 2025G>T ESAD-UK 13 21558227 21558227 single base substitution G A downstream_gene_variant ESAD-UK 13 21558227 21558227 single base substitution G A intron_variant ESAD-UK 13 21559555 21559555 deletion of <=200bp A - downstream_gene_variant ESAD-UK 13 21559555 21559555 deletion of <=200bp A - intron_variant ESAD-UK 13 21559653 21559653 single base substitution G A downstream_gene_variant ESAD-UK 13 21559653 21559653 single base substitution G A intron_variant ESAD-UK 13 21562831 21562831 single base substitution C G downstream_gene_variant ESAD-UK 13 21562831 21562831 single base substitution C G missense_variant G363A 1088G>C ESAD-UK 13 21565212 21565212 single base substitution C T intron_variant ESAD-UK 13 21569345 21569345 single base substitution A G intron_variant ESAD-UK 13 21572576 21572576 single base substitution T A intron_variant ESAD-UK 13 21572747 21572747 single base substitution C T intron_variant ESAD-UK 13 21574242 21574242 single base substitution C T intron_variant ESAD-UK 13 21576838 21576838 single base substitution A T intron_variant ESAD-UK 13 21583209 21583209 single base substitution C T intron_variant ESAD-UK 13 21584246 21584246 single base substitution C G intron_variant ESAD-UK 13 21586870 21586870 single base substitution C T intron_variant ESAD-UK 13 21590289 21590289 single base substitution C T intron_variant ESAD-UK 13 21591759 21591759 single base substitution T C intron_variant ESAD-UK 13 21592415 21592415 single base substitution T G intron_variant ESAD-UK 13 21592997 21592997 single base substitution C T intron_variant ESAD-UK 13 21594827 21594827 single base substitution C A intron_variant ESAD-UK 13 21596377 21596377 single base substitution A T intron_variant ESAD-UK 13 21597724 21597724 single base substitution T C intron_variant ESAD-UK 13 21597724 21597724 single base substitution T C upstream_gene_variant ESAD-UK 13 21598764 21598764 single base substitution G A intron_variant ESAD-UK 13 21598764 21598764 single base substitution G A upstream_gene_variant ESAD-UK 13 21604522 21604522 single base substitution A G intron_variant ESAD-UK 13 21606775 21606775 single base substitution C G intron_variant ESAD-UK 13 21614471 21614471 single base substitution G A intron_variant ESAD-UK 13 21615787 21615787 single base substitution A T intron_variant ESAD-UK 13 21616140 21616140 single base substitution C G intron_variant ESAD-UK 13 21617210 21617210 single base substitution C T intron_variant ESAD-UK 13 21619210 21619210 single base substitution T C intron_variant ESAD-UK 13 21620223 21620223 single base substitution A T 5_prime_UTR_variant ESAD-UK 13 21620491 21620491 single base substitution G A intron_variant ESAD-UK 13 21620701 21620701 single base substitution G T intron_variant ESAD-UK 13 21621588 21621588 single base substitution C T intron_variant ESAD-UK 13 21621607 21621607 single base substitution C A intron_variant ESAD-UK 13 21621784 21621784 single base substitution G A intron_variant ESAD-UK 13 21621976 21621976 single base substitution C G intron_variant ESAD-UK 13 21622411 21622411 single base substitution T A intron_variant ESAD-UK 13 21622924 21622924 single base substitution C T intron_variant ESAD-UK 13 21623273 21623273 single base substitution C T intron_variant ESAD-UK 13 21623602 21623602 single base substitution C T intron_variant ESAD-UK 13 21624046 21624046 single base substitution G T intron_variant ESAD-UK 13 21625081 21625081 single base substitution A G intron_variant ESAD-UK 13 21625890 21625890 single base substitution G A intron_variant ESAD-UK 13 21626333 21626333 single base substitution C A intron_variant ESAD-UK 13 21626651 21626651 single base substitution G A intron_variant ESAD-UK 13 21627861 21627861 single base substitution G A intron_variant ESAD-UK 13 21630059 21630059 single base substitution A C intron_variant ESAD-UK 13 21631395 21631395 single base substitution C A intron_variant ESAD-UK 13 21632044 21632044 single base substitution C A intron_variant ESAD-UK 13 21635880 21635880 single base substitution G C upstream_gene_variant ESAD-UK 13 21636702 21636702 single base substitution G A upstream_gene_variant ESAD-UK 13 21639131 21639131 single base substitution G T upstream_gene_variant ESAD-UK 13 21640209 21640209 single base substitution C A upstream_gene_variant ESAD-UK 13 21640515 21640515 single base substitution G A upstream_gene_variant ESCA-CN 13 21563322 21563322 single base substitution G A exon_variant ESCA-CN 13 21563322 21563322 single base substitution G A synonymous_variant D199D 597C>T KIRC-US 13 21557521 21557521 single base substitution A G missense_variant L775P 2324T>C KIRC-US 13 21557669 21557669 single base substitution C T missense_variant E726K 2176G>A KIRC-US 13 21557681 21557681 single base substitution C A stop_gained E722* 2164G>T KIRC-US 13 21557772 21557772 insertion of <=200bp - T frameshift_variant H691H? KIRC-US 13 21562131 21562131 single base substitution G C downstream_gene_variant KIRC-US 13 21562131 21562131 single base substitution G C missense_variant S596R 1788C>G KIRP-US 13 21562482 21562482 insertion of <=200bp - GGGGCG downstream_gene_variant KIRP-US 13 21562482 21562482 insertion of <=200bp - GGGGCG inframe_insertion P479PRP LAML-KR 13 21590314 21590314 single base substitution C T intron_variant LAML-KR 13 21590333 21590333 single base substitution C T intron_variant LAML-KR 13 21598255 21598255 single base substitution G A intron_variant LAML-KR 13 21598255 21598255 single base substitution G A upstream_gene_variant LGG-US 13 21549240 21549240 single base substitution G A synonymous_variant N1012N 3036C>T LGG-US 13 21557659 21557659 single base substitution A T missense_variant V729D 2186T>A LGG-US 13 21562142 21562142 single base substitution G A downstream_gene_variant LGG-US 13 21562142 21562142 single base substitution G A missense_variant R593C 1777C>T LGG-US 13 21562426 21562426 single base substitution C A downstream_gene_variant LGG-US 13 21562426 21562426 single base substitution C A missense_variant G498V 1493G>T LGG-US 13 21563346 21563346 single base substitution G A exon_variant LGG-US 13 21563346 21563346 single base substitution G A synonymous_variant Y191Y 573C>T LICA-FR 13 21549364 21549364 single base substitution G A missense_variant P971L 2912C>T LICA-FR 13 21557497 21557497 single base substitution T C missense_variant H783R 2348A>G LICA-FR 13 21561810 21561810 single base substitution T C downstream_gene_variant LICA-FR 13 21561810 21561810 single base substitution T C intron_variant LICA-FR 13 21562383 21562383 single base substitution C A downstream_gene_variant LICA-FR 13 21562383 21562383 single base substitution C A missense_variant R512S 1536G>T LICA-FR 13 21562820 21562820 single base substitution C A downstream_gene_variant LICA-FR 13 21562820 21562820 single base substitution C A missense_variant V367F 1099G>T LICA-FR 13 21563429 21563429 single base substitution G A exon_variant LICA-FR 13 21563429 21563429 single base substitution G A missense_variant P164S 490C>T LICA-FR 13 21570517 21570517 deletion of <=200bp T - intron_variant LICA-FR 13 21572580 21572580 single base substitution C G intron_variant LICA-FR 13 21574792 21574792 single base substitution G T intron_variant LICA-FR 13 21597859 21597859 single base substitution T G intron_variant LICA-FR 13 21597859 21597859 single base substitution T G upstream_gene_variant LICA-FR 13 21624259 21624259 insertion of <=200bp - ATAGACAGACAG intron_variant LICA-FR 13 21636448 21636448 deletion of <=200bp A - upstream_gene_variant LIHC-US 13 21549409 21549409 single base substitution T A missense_variant D956V 2867A>T LINC-JP 13 21549388 21549388 single base substitution C T missense_variant G963E 2888G>A LINC-JP 13 21551103 21551103 single base substitution C A intron_variant LINC-JP 13 21553981 21553981 single base substitution C T intron_variant LINC-JP 13 21554018 21554018 single base substitution G C intron_variant LINC-JP 13 21575448 21575448 single base substitution T C intron_variant LINC-JP 13 21577336 21577336 single base substitution G T intron_variant LINC-JP 13 21579248 21579248 single base substitution T G intron_variant LINC-JP 13 21585876 21585876 single base substitution T A intron_variant LINC-JP 13 21596532 21596532 single base substitution C A intron_variant LINC-JP 13 21607962 21607962 single base substitution T C intron_variant LINC-JP 13 21611534 21611534 single base substitution T C intron_variant LINC-JP 13 21619825 21619825 single base substitution T C missense_variant Q114R 341A>G LINC-JP 13 21619938 21619938 single base substitution G A synonymous_variant A76A 228C>T LINC-JP 13 21620102 21620102 single base substitution T C missense_variant I22V 64A>G LINC-JP 13 21621867 21621867 single base substitution T C intron_variant LINC-JP 13 21633770 21633770 single base substitution T C intron_variant LINC-JP 13 21635743 21635743 single base substitution G A upstream_gene_variant LIRI-JP 13 21546119 21546119 single base substitution C A downstream_gene_variant LIRI-JP 13 21548174 21548175 deletion of <=200bp TC - 3_prime_UTR_variant LIRI-JP 13 21548174 21548175 deletion of <=200bp TC - downstream_gene_variant LIRI-JP 13 21548306 21548306 single base substitution T A 3_prime_UTR_variant LIRI-JP 13 21548306 21548306 single base substitution T A downstream_gene_variant LIRI-JP 13 21549394 21549394 single base substitution C T missense_variant R961Q 2882G>A LIRI-JP 13 21549642 21549642 single base substitution T C intron_variant LIRI-JP 13 21550384 21550384 single base substitution T C intron_variant LIRI-JP 13 21550601 21550601 single base substitution T C intron_variant LIRI-JP 13 21552535 21552535 single base substitution T C intron_variant LIRI-JP 13 21552538 21552538 single base substitution T C intron_variant LIRI-JP 13 21552622 21552622 single base substitution T C intron_variant LIRI-JP 13 21554054 21554054 single base substitution G A intron_variant LIRI-JP 13 21554155 21554155 single base substitution T C intron_variant LIRI-JP 13 21554278 21554278 single base substitution A C intron_variant LIRI-JP 13 21554303 21554303 single base substitution G T intron_variant LIRI-JP 13 21554773 21554773 single base substitution C T intron_variant LIRI-JP 13 21555910 21555910 single base substitution T C intron_variant LIRI-JP 13 21559329 21559329 single base substitution A G downstream_gene_variant LIRI-JP 13 21559329 21559329 single base substitution A G intron_variant LIRI-JP 13 21561120 21561120 single base substitution T C downstream_gene_variant LIRI-JP 13 21561120 21561120 single base substitution T C intron_variant LIRI-JP 13 21565569 21565569 single base substitution A C intron_variant LIRI-JP 13 21567152 21567152 single base substitution C A intron_variant LIRI-JP 13 21569997 21569997 single base substitution T C intron_variant LIRI-JP 13 21571343 21571343 single base substitution T C intron_variant LIRI-JP 13 21573811 21573811 single base substitution G A intron_variant LIRI-JP 13 21576947 21576947 single base substitution C A intron_variant LIRI-JP 13 21576948 21576948 single base substitution C G intron_variant LIRI-JP 13 21578415 21578415 single base substitution C T intron_variant LIRI-JP 13 21579383 21579383 single base substitution C A intron_variant LIRI-JP 13 21583435 21583435 single base substitution G C intron_variant LIRI-JP 13 21587695 21587695 single base substitution G T intron_variant LIRI-JP 13 21589125 21589125 single base substitution G C intron_variant LIRI-JP 13 21590713 21590713 single base substitution T A intron_variant LIRI-JP 13 21593757 21593757 single base substitution T C intron_variant LIRI-JP 13 21594363 21594363 single base substitution T A intron_variant LIRI-JP 13 21596332 21596332 single base substitution T C intron_variant LIRI-JP 13 21597293 21597293 insertion of <=200bp - GA intron_variant LIRI-JP 13 21597293 21597293 insertion of <=200bp - GA upstream_gene_variant LIRI-JP 13 21599033 21599033 single base substitution C T intron_variant LIRI-JP 13 21599033 21599033 single base substitution C T upstream_gene_variant LIRI-JP 13 21603111 21603111 single base substitution T A intron_variant LIRI-JP 13 21605125 21605125 single base substitution T C intron_variant LIRI-JP 13 21611681 21611681 single base substitution C T intron_variant LIRI-JP 13 21614207 21614207 single base substitution C T intron_variant LIRI-JP 13 21614398 21614398 single base substitution C T intron_variant LIRI-JP 13 21614406 21614406 single base substitution G A intron_variant LIRI-JP 13 21618947 21618947 single base substitution A C intron_variant LIRI-JP 13 21619317 21619317 insertion of <=200bp - T intron_variant LIRI-JP 13 21621149 21621149 single base substitution T A intron_variant LIRI-JP 13 21623096 21623096 single base substitution G C intron_variant LIRI-JP 13 21623363 21623363 single base substitution A G intron_variant LIRI-JP 13 21626973 21626973 single base substitution A C intron_variant LIRI-JP 13 21628402 21628402 single base substitution A T intron_variant LIRI-JP 13 21631583 21631583 single base substitution T C intron_variant LIRI-JP 13 21632796 21632796 single base substitution A G intron_variant LIRI-JP 13 21632898 21632898 single base substitution C A intron_variant LIRI-JP 13 21637277 21637277 single base substitution C T upstream_gene_variant LIRI-JP 13 21638222 21638222 single base substitution G T upstream_gene_variant LUSC-KR 13 21542720 21542720 single base substitution G C downstream_gene_variant LUSC-KR 13 21543398 21543398 single base substitution G C downstream_gene_variant LUSC-KR 13 21549585 21549585 single base substitution C T intron_variant LUSC-KR 13 21550510 21550510 single base substitution C A intron_variant LUSC-KR 13 21566792 21566792 single base substitution C A intron_variant LUSC-KR 13 21579746 21579746 single base substitution G T intron_variant LUSC-KR 13 21589963 21589963 single base substitution C T intron_variant LUSC-KR 13 21591991 21591991 single base substitution C G intron_variant LUSC-KR 13 21594017 21594017 single base substitution G T intron_variant LUSC-KR 13 21599811 21599811 single base substitution C A intron_variant LUSC-KR 13 21599811 21599811 single base substitution C A upstream_gene_variant LUSC-KR 13 21602314 21602314 single base substitution C T intron_variant LUSC-KR 13 21602370 21602370 single base substitution C A intron_variant LUSC-KR 13 21603013 21603013 single base substitution C T intron_variant LUSC-KR 13 21603170 21603170 single base substitution C G intron_variant LUSC-KR 13 21603228 21603228 single base substitution C T intron_variant LUSC-KR 13 21603482 21603482 single base substitution C T intron_variant LUSC-KR 13 21604052 21604052 single base substitution C T intron_variant LUSC-KR 13 21604425 21604425 single base substitution A G intron_variant LUSC-KR 13 21604476 21604476 single base substitution C G intron_variant LUSC-KR 13 21628368 21628368 single base substitution C T intron_variant LUSC-KR 13 21635246 21635246 single base substitution C A intron_variant LUSC-KR 13 21635246 21635246 single base substitution C A upstream_gene_variant LUSC-KR 13 21636339 21636339 single base substitution C A upstream_gene_variant LUSC-KR 13 21636582 21636582 single base substitution A T upstream_gene_variant LUSC-KR 13 21640209 21640209 single base substitution C G upstream_gene_variant LUSC-US 13 21562336 21562336 single base substitution G A downstream_gene_variant LUSC-US 13 21562336 21562336 single base substitution G A missense_variant S528L 1583C>T LUSC-US 13 21562372 21562372 single base substitution G A downstream_gene_variant LUSC-US 13 21562372 21562372 single base substitution G A missense_variant P516L 1547C>T LUSC-US 13 21563271 21563271 single base substitution G A exon_variant LUSC-US 13 21563271 21563271 single base substitution G A synonymous_variant F216F 648C>T MALY-DE 13 21542330 21542330 single base substitution C A downstream_gene_variant MALY-DE 13 21543108 21543108 single base substitution T G downstream_gene_variant MALY-DE 13 21546848 21546848 single base substitution T C downstream_gene_variant MALY-DE 13 21551537 21551537 single base substitution A T intron_variant MALY-DE 13 21555290 21555290 single base substitution C T intron_variant MALY-DE 13 21564545 21564545 single base substitution T G intron_variant MALY-DE 13 21568942 21568942 single base substitution G C intron_variant MALY-DE 13 21569345 21569345 insertion of <=200bp - A intron_variant MALY-DE 13 21574384 21574384 single base substitution G A intron_variant MALY-DE 13 21576438 21576438 single base substitution C A intron_variant MALY-DE 13 21579648 21579648 single base substitution T A intron_variant MALY-DE 13 21580865 21580865 single base substitution G A intron_variant MALY-DE 13 21583656 21583656 deletion of <=200bp T - intron_variant MALY-DE 13 21585718 21585718 single base substitution T C intron_variant MALY-DE 13 21594364 21594364 single base substitution T C intron_variant MALY-DE 13 21594389 21594389 single base substitution C G intron_variant MALY-DE 13 21595058 21595058 single base substitution T G intron_variant MALY-DE 13 21596197 21596197 single base substitution G T intron_variant MALY-DE 13 21597016 21597018 deletion of <=200bp ATC - intron_variant MALY-DE 13 21597724 21597724 single base substitution T G intron_variant MALY-DE 13 21597724 21597724 single base substitution T G upstream_gene_variant MALY-DE 13 21619506 21619506 single base substitution A C intron_variant MALY-DE 13 21622814 21622814 single base substitution T C intron_variant MALY-DE 13 21629309 21629309 single base substitution G A intron_variant MALY-DE 13 21631292 21631292 single base substitution T G intron_variant MALY-DE 13 21632861 21632861 single base substitution G C intron_variant MALY-DE 13 21634054 21634054 single base substitution A G intron_variant MELA-AU 13 21542202 21542202 single base substitution G A downstream_gene_variant MELA-AU 13 21542301 21542301 single base substitution C T downstream_gene_variant MELA-AU 13 21542781 21542781 single base substitution A C downstream_gene_variant MELA-AU 13 21543054 21543054 single base substitution G A downstream_gene_variant MELA-AU 13 21544279 21544279 single base substitution C T downstream_gene_variant MELA-AU 13 21544458 21544458 single base substitution T G downstream_gene_variant MELA-AU 13 21545508 21545508 single base substitution G A downstream_gene_variant MELA-AU 13 21546504 21546504 single base substitution G A downstream_gene_variant MELA-AU 13 21546760 21546760 single base substitution G A downstream_gene_variant MELA-AU 13 21547231 21547231 single base substitution G A 3_prime_UTR_variant MELA-AU 13 21547231 21547231 single base substitution G A downstream_gene_variant MELA-AU 13 21547276 21547276 single base substitution C T 3_prime_UTR_variant MELA-AU 13 21547276 21547276 single base substitution C T downstream_gene_variant MELA-AU 13 21547289 21547289 single base substitution G A 3_prime_UTR_variant MELA-AU 13 21547289 21547289 single base substitution G A downstream_gene_variant MELA-AU 13 21547748 21547748 single base substitution A G 3_prime_UTR_variant MELA-AU 13 21547748 21547748 single base substitution A G downstream_gene_variant MELA-AU 13 21549473 21549473 single base substitution G A missense_variant P935S 2803C>T MELA-AU 13 21549957 21549958 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 21550492 21550492 single base substitution G A intron_variant MELA-AU 13 21550850 21550850 single base substitution G A intron_variant MELA-AU 13 21551201 21551201 single base substitution A C intron_variant MELA-AU 13 21551419 21551419 single base substitution A G intron_variant MELA-AU 13 21552023 21552023 single base substitution G A intron_variant MELA-AU 13 21553005 21553005 single base substitution G A intron_variant MELA-AU 13 21553991 21553991 single base substitution G A intron_variant MELA-AU 13 21554442 21554442 single base substitution G A intron_variant MELA-AU 13 21555025 21555025 single base substitution G A intron_variant MELA-AU 13 21555152 21555152 single base substitution G A intron_variant MELA-AU 13 21556432 21556432 single base substitution G A intron_variant MELA-AU 13 21556670 21556670 single base substitution G A intron_variant MELA-AU 13 21557379 21557379 single base substitution G A synonymous_variant S822S 2466C>T MELA-AU 13 21557639 21557639 single base substitution G A stop_gained Q736* 2206C>T MELA-AU 13 21558368 21558368 single base substitution C A downstream_gene_variant MELA-AU 13 21558368 21558368 single base substitution C A intron_variant MELA-AU 13 21558478 21558478 single base substitution G A downstream_gene_variant MELA-AU 13 21558478 21558478 single base substitution G A intron_variant MELA-AU 13 21559410 21559410 single base substitution C T downstream_gene_variant MELA-AU 13 21559410 21559410 single base substitution C T intron_variant MELA-AU 13 21559903 21559904 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 21559903 21559904 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 21559969 21559969 single base substitution G A downstream_gene_variant MELA-AU 13 21559969 21559969 single base substitution G A intron_variant MELA-AU 13 21560352 21560352 single base substitution G A downstream_gene_variant MELA-AU 13 21560352 21560352 single base substitution G A intron_variant MELA-AU 13 21562100 21562100 single base substitution C T downstream_gene_variant MELA-AU 13 21562100 21562100 single base substitution C T missense_variant E607K 1819G>A MELA-AU 13 21562189 21562189 single base substitution G A downstream_gene_variant MELA-AU 13 21562189 21562189 single base substitution G A missense_variant P577L 1730C>T MELA-AU 13 21562503 21562503 single base substitution G A downstream_gene_variant MELA-AU 13 21562503 21562503 single base substitution G A synonymous_variant A472A 1416C>T MELA-AU 13 21562821 21562821 single base substitution G A downstream_gene_variant MELA-AU 13 21562821 21562821 single base substitution G A synonymous_variant S366S 1098C>T MELA-AU 13 21563271 21563271 single base substitution G A exon_variant MELA-AU 13 21563271 21563271 single base substitution G A synonymous_variant F216F 648C>T MELA-AU 13 21563773 21563773 single base substitution G A intron_variant MELA-AU 13 21564280 21564280 single base substitution A T intron_variant MELA-AU 13 21564394 21564394 single base substitution A G intron_variant MELA-AU 13 21564536 21564536 single base substitution C T intron_variant MELA-AU 13 21564598 21564598 single base substitution G A intron_variant MELA-AU 13 21564670 21564670 single base substitution A G intron_variant MELA-AU 13 21565176 21565176 single base substitution G A intron_variant MELA-AU 13 21565813 21565813 single base substitution G A intron_variant MELA-AU 13 21565816 21565816 single base substitution A G intron_variant MELA-AU 13 21566096 21566096 single base substitution G A intron_variant MELA-AU 13 21566404 21566404 single base substitution G A intron_variant MELA-AU 13 21566849 21566849 single base substitution G A intron_variant MELA-AU 13 21567938 21567938 single base substitution G A intron_variant MELA-AU 13 21568210 21568210 single base substitution G A intron_variant MELA-AU 13 21570326 21570326 single base substitution A G intron_variant MELA-AU 13 21570651 21570651 single base substitution G A intron_variant MELA-AU 13 21571074 21571074 single base substitution G A intron_variant MELA-AU 13 21572338 21572338 single base substitution A G intron_variant MELA-AU 13 21572708 21572708 single base substitution G A intron_variant MELA-AU 13 21572949 21572949 single base substitution G A intron_variant MELA-AU 13 21574224 21574224 single base substitution A T intron_variant MELA-AU 13 21574663 21574663 single base substitution G A intron_variant MELA-AU 13 21575994 21575994 single base substitution G A intron_variant MELA-AU 13 21577027 21577027 single base substitution G A intron_variant MELA-AU 13 21577033 21577033 single base substitution G T intron_variant MELA-AU 13 21578738 21578738 single base substitution G A intron_variant MELA-AU 13 21579215 21579215 single base substitution A C intron_variant MELA-AU 13 21580110 21580110 single base substitution G A intron_variant MELA-AU 13 21580134 21580134 single base substitution C T intron_variant MELA-AU 13 21580704 21580704 single base substitution C T intron_variant MELA-AU 13 21581672 21581672 single base substitution T G intron_variant MELA-AU 13 21584042 21584042 single base substitution G A intron_variant MELA-AU 13 21584110 21584110 single base substitution G A intron_variant MELA-AU 13 21584368 21584369 multiple base substitution (>=2bp and <=200bp) CC AA intron_variant MELA-AU 13 21584643 21584643 single base substitution G A intron_variant MELA-AU 13 21585406 21585406 single base substitution G A intron_variant MELA-AU 13 21585591 21585591 single base substitution A T intron_variant MELA-AU 13 21585894 21585894 single base substitution G A intron_variant MELA-AU 13 21585965 21585965 single base substitution A C intron_variant MELA-AU 13 21586032 21586032 deletion of <=200bp C - intron_variant MELA-AU 13 21587218 21587218 single base substitution G A intron_variant MELA-AU 13 21589154 21589154 single base substitution C T intron_variant MELA-AU 13 21592049 21592050 deletion of <=200bp AC - intron_variant MELA-AU 13 21593235 21593235 single base substitution C T intron_variant MELA-AU 13 21594307 21594307 single base substitution C T intron_variant MELA-AU 13 21594731 21594731 single base substitution T C intron_variant MELA-AU 13 21595971 21595971 single base substitution C T intron_variant MELA-AU 13 21596979 21596980 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 21597094 21597094 single base substitution G A intron_variant MELA-AU 13 21597172 21597172 insertion of <=200bp - AGTCC intron_variant MELA-AU 13 21597316 21597317 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 21597316 21597317 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 13 21597318 21597319 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 21597318 21597319 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 13 21597633 21597633 single base substitution G A intron_variant MELA-AU 13 21597633 21597633 single base substitution G A upstream_gene_variant MELA-AU 13 21597727 21597727 single base substitution G A intron_variant MELA-AU 13 21597727 21597727 single base substitution G A upstream_gene_variant MELA-AU 13 21598088 21598088 single base substitution G A intron_variant MELA-AU 13 21598088 21598088 single base substitution G A upstream_gene_variant MELA-AU 13 21598349 21598349 single base substitution G A intron_variant MELA-AU 13 21598349 21598349 single base substitution G A upstream_gene_variant MELA-AU 13 21599046 21599046 single base substitution G A intron_variant MELA-AU 13 21599046 21599046 single base substitution G A upstream_gene_variant MELA-AU 13 21599188 21599188 single base substitution T C intron_variant MELA-AU 13 21599188 21599188 single base substitution T C upstream_gene_variant MELA-AU 13 21599198 21599198 single base substitution T C intron_variant MELA-AU 13 21599198 21599198 single base substitution T C upstream_gene_variant MELA-AU 13 21599460 21599460 single base substitution G A intron_variant MELA-AU 13 21599460 21599460 single base substitution G A upstream_gene_variant MELA-AU 13 21599639 21599639 single base substitution G A intron_variant MELA-AU 13 21599639 21599639 single base substitution G A upstream_gene_variant MELA-AU 13 21599642 21599642 single base substitution G A intron_variant MELA-AU 13 21599642 21599642 single base substitution G A upstream_gene_variant MELA-AU 13 21599991 21599992 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 13 21599991 21599992 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 13 21600277 21600277 single base substitution G A intron_variant MELA-AU 13 21600277 21600277 single base substitution G A upstream_gene_variant MELA-AU 13 21600871 21600871 single base substitution G A intron_variant MELA-AU 13 21600871 21600871 single base substitution G A upstream_gene_variant MELA-AU 13 21603344 21603344 single base substitution G A intron_variant MELA-AU 13 21603917 21603917 single base substitution G A intron_variant MELA-AU 13 21604102 21604102 single base substitution A G intron_variant MELA-AU 13 21604437 21604437 single base substitution G A intron_variant MELA-AU 13 21606070 21606070 single base substitution G A intron_variant MELA-AU 13 21606131 21606131 single base substitution A C intron_variant MELA-AU 13 21606714 21606714 single base substitution C T intron_variant MELA-AU 13 21606801 21606801 single base substitution G A intron_variant MELA-AU 13 21608622 21608622 single base substitution G A intron_variant MELA-AU 13 21608674 21608674 single base substitution G A intron_variant MELA-AU 13 21608806 21608806 single base substitution A C intron_variant MELA-AU 13 21608931 21608931 single base substitution C T intron_variant MELA-AU 13 21609923 21609923 single base substitution G A intron_variant MELA-AU 13 21609974 21609974 single base substitution G A intron_variant MELA-AU 13 21610629 21610629 single base substitution G T intron_variant MELA-AU 13 21610931 21610931 single base substitution C A intron_variant MELA-AU 13 21610935 21610935 single base substitution A C intron_variant MELA-AU 13 21611730 21611730 single base substitution G A intron_variant MELA-AU 13 21612872 21612872 single base substitution C T intron_variant MELA-AU 13 21612895 21612895 single base substitution C T intron_variant MELA-AU 13 21613799 21613799 single base substitution G A intron_variant MELA-AU 13 21614857 21614857 single base substitution G A intron_variant MELA-AU 13 21619610 21619610 single base substitution G A intron_variant MELA-AU 13 21620223 21620223 single base substitution A T 5_prime_UTR_variant MELA-AU 13 21620312 21620312 single base substitution T A 5_prime_UTR_variant MELA-AU 13 21620476 21620476 single base substitution A G intron_variant MELA-AU 13 21621069 21621069 single base substitution G T intron_variant MELA-AU 13 21621305 21621305 deletion of <=200bp G - intron_variant MELA-AU 13 21621782 21621783 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 21622349 21622350 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 13 21622964 21622964 single base substitution G A intron_variant MELA-AU 13 21623967 21623967 single base substitution G A intron_variant MELA-AU 13 21625607 21625607 single base substitution G A intron_variant MELA-AU 13 21625699 21625699 single base substitution G A intron_variant MELA-AU 13 21626364 21626364 single base substitution C G intron_variant MELA-AU 13 21626733 21626733 single base substitution C T intron_variant MELA-AU 13 21627277 21627277 single base substitution G A intron_variant MELA-AU 13 21628366 21628366 single base substitution G A intron_variant MELA-AU 13 21628872 21628872 single base substitution C T intron_variant MELA-AU 13 21629336 21629336 single base substitution G A intron_variant MELA-AU 13 21629701 21629701 single base substitution C T intron_variant MELA-AU 13 21630081 21630081 single base substitution G A intron_variant MELA-AU 13 21630567 21630567 single base substitution G A intron_variant MELA-AU 13 21631776 21631776 single base substitution A T intron_variant MELA-AU 13 21632903 21632903 single base substitution G A intron_variant MELA-AU 13 21633556 21633556 single base substitution G A intron_variant MELA-AU 13 21634431 21634431 single base substitution A G intron_variant MELA-AU 13 21634431 21634431 single base substitution A G upstream_gene_variant MELA-AU 13 21634713 21634713 single base substitution G A intron_variant MELA-AU 13 21634713 21634713 single base substitution G A upstream_gene_variant MELA-AU 13 21635979 21635980 multiple base substitution (>=2bp and <=200bp) GT AG upstream_gene_variant MELA-AU 13 21636062 21636062 single base substitution A T upstream_gene_variant MELA-AU 13 21637119 21637119 single base substitution G A upstream_gene_variant MELA-AU 13 21637700 21637700 single base substitution G A upstream_gene_variant MELA-AU 13 21637883 21637883 single base substitution C T upstream_gene_variant MELA-AU 13 21638954 21638954 single base substitution G A upstream_gene_variant MELA-AU 13 21639100 21639100 single base substitution G A upstream_gene_variant MELA-AU 13 21639605 21639605 single base substitution T A upstream_gene_variant MELA-AU 13 21639864 21639864 single base substitution G A upstream_gene_variant MELA-AU 13 21639895 21639895 single base substitution G A upstream_gene_variant MELA-AU 13 21640284 21640284 single base substitution C T upstream_gene_variant MELA-AU 13 21640450 21640450 single base substitution C T upstream_gene_variant MELA-AU 13 21640556 21640556 single base substitution G A upstream_gene_variant MELA-AU 13 21640602 21640602 single base substitution C T upstream_gene_variant ORCA-IN 13 21544630 21544630 single base substitution C A downstream_gene_variant ORCA-IN 13 21547357 21547357 single base substitution C T 3_prime_UTR_variant ORCA-IN 13 21547357 21547357 single base substitution C T downstream_gene_variant ORCA-IN 13 21549567 21549567 single base substitution G A intron_variant ORCA-IN 13 21557607 21557607 single base substitution G T missense_variant D746E 2238C>A ORCA-IN 13 21557669 21557669 single base substitution C G missense_variant E726Q 2176G>C ORCA-IN 13 21562740 21562740 single base substitution G A downstream_gene_variant ORCA-IN 13 21562740 21562740 single base substitution G A synonymous_variant H393H 1179C>T ORCA-IN 13 21615309 21615309 single base substitution C T intron_variant ORCA-IN 13 21618836 21618836 single base substitution T G intron_variant ORCA-IN 13 21618867 21618867 single base substitution G T intron_variant ORCA-IN 13 21628374 21628374 single base substitution G A intron_variant ORCA-IN 13 21636263 21636263 single base substitution T A upstream_gene_variant OV-AU 13 21544353 21544353 single base substitution A G downstream_gene_variant OV-AU 13 21551819 21551819 single base substitution G C intron_variant OV-AU 13 21553403 21553403 single base substitution C T intron_variant OV-AU 13 21554529 21554529 single base substitution T C intron_variant OV-AU 13 21555504 21555504 single base substitution C A intron_variant OV-AU 13 21557529 21557529 single base substitution G C missense_variant I772M 2316C>G OV-AU 13 21572630 21572630 single base substitution G A intron_variant OV-AU 13 21576941 21576941 single base substitution C T intron_variant OV-AU 13 21583293 21583293 single base substitution G A intron_variant OV-AU 13 21583892 21583892 single base substitution C G intron_variant OV-AU 13 21588769 21588769 single base substitution G C intron_variant OV-AU 13 21593401 21593401 single base substitution T C intron_variant OV-AU 13 21597625 21597625 single base substitution C T intron_variant OV-AU 13 21597625 21597625 single base substitution C T upstream_gene_variant OV-AU 13 21608830 21608830 single base substitution G T intron_variant OV-AU 13 21620222 21620222 single base substitution T A 5_prime_UTR_variant OV-AU 13 21621908 21621908 single base substitution A T intron_variant OV-AU 13 21635805 21635805 single base substitution C G upstream_gene_variant PACA-AU 13 21547601 21547601 single base substitution C A 3_prime_UTR_variant PACA-AU 13 21547601 21547601 single base substitution C A downstream_gene_variant PACA-AU 13 21550668 21550668 single base substitution C G intron_variant PACA-AU 13 21555728 21555731 deletion of <=200bp AGTT - frameshift_variant NC847 PACA-AU 13 21557034 21557034 single base substitution G A intron_variant PACA-AU 13 21560557 21560557 single base substitution C T downstream_gene_variant PACA-AU 13 21560557 21560557 single base substitution C T intron_variant PACA-AU 13 21563178 21563178 single base substitution C A exon_variant PACA-AU 13 21563178 21563178 single base substitution C A synonymous_variant P247P 741G>T PACA-AU 13 21579097 21579097 single base substitution C T intron_variant PACA-AU 13 21580144 21580144 single base substitution C T intron_variant PACA-AU 13 21582544 21582544 single base substitution G T intron_variant PACA-AU 13 21590579 21590579 single base substitution T A intron_variant PACA-AU 13 21594434 21594434 single base substitution A C intron_variant PACA-AU 13 21615358 21615358 single base substitution G A intron_variant PACA-AU 13 21622604 21622604 single base substitution C G intron_variant PACA-AU 13 21626005 21626005 deletion of <=200bp A - intron_variant PACA-AU 13 21631774 21631774 insertion of <=200bp - T intron_variant PACA-AU 13 21635266 21635266 single base substitution C T intron_variant PACA-AU 13 21635266 21635266 single base substitution C T upstream_gene_variant PACA-AU 13 21638679 21638679 single base substitution A G upstream_gene_variant PACA-AU 13 21639924 21639924 single base substitution A G upstream_gene_variant PACA-CA 13 21549195 21549195 single base substitution C T synonymous_variant S1027S 3081G>A PACA-CA 13 21549208 21549208 single base substitution T C missense_variant D1023G 3068A>G PACA-CA 13 21550266 21550266 single base substitution T G intron_variant PACA-CA 13 21552755 21552755 single base substitution A G intron_variant PACA-CA 13 21554267 21554267 single base substitution T C intron_variant PACA-CA 13 21563297 21563297 single base substitution G A exon_variant PACA-CA 13 21563297 21563297 single base substitution G A missense_variant P208S 622C>T PACA-CA 13 21563330 21563330 single base substitution C T exon_variant PACA-CA 13 21563330 21563330 single base substitution C T missense_variant G197S 589G>A PACA-CA 13 21565454 21565454 single base substitution C T exon_variant PACA-CA 13 21565454 21565454 single base substitution C T synonymous_variant P144P 432G>A PACA-CA 13 21566484 21566484 single base substitution A T intron_variant PACA-CA 13 21567651 21567651 single base substitution C T intron_variant PACA-CA 13 21567677 21567677 single base substitution G A intron_variant PACA-CA 13 21568411 21568411 single base substitution T A intron_variant PACA-CA 13 21570402 21570402 single base substitution T C intron_variant PACA-CA 13 21571410 21571410 single base substitution A G intron_variant PACA-CA 13 21572238 21572238 single base substitution G A intron_variant PACA-CA 13 21572830 21572830 single base substitution C T intron_variant PACA-CA 13 21575585 21575585 single base substitution T G intron_variant PACA-CA 13 21578616 21578616 single base substitution A T intron_variant PACA-CA 13 21581263 21581263 single base substitution A G intron_variant PACA-CA 13 21583814 21583814 single base substitution T C intron_variant PACA-CA 13 21584010 21584010 single base substitution C G intron_variant PACA-CA 13 21584551 21584551 single base substitution C T intron_variant PACA-CA 13 21585530 21585530 single base substitution T C intron_variant PACA-CA 13 21586284 21586284 single base substitution A G intron_variant PACA-CA 13 21597692 21597692 single base substitution C T intron_variant PACA-CA 13 21597692 21597692 single base substitution C T upstream_gene_variant PACA-CA 13 21598502 21598502 single base substitution G A intron_variant PACA-CA 13 21598502 21598502 single base substitution G A upstream_gene_variant PACA-CA 13 21599400 21599400 single base substitution A T intron_variant PACA-CA 13 21599400 21599400 single base substitution A T upstream_gene_variant PACA-CA 13 21601209 21601209 single base substitution C T intron_variant PACA-CA 13 21601209 21601209 single base substitution C T upstream_gene_variant PACA-CA 13 21602772 21602772 single base substitution C T intron_variant PACA-CA 13 21603823 21603823 single base substitution G A intron_variant PACA-CA 13 21610100 21610100 single base substitution C A intron_variant PACA-CA 13 21617581 21617581 single base substitution C G intron_variant PACA-CA 13 21625514 21625514 deletion of <=200bp T - intron_variant PACA-CA 13 21627817 21627817 single base substitution C T intron_variant PACA-CA 13 21632094 21632094 single base substitution T G intron_variant PACA-CA 13 21634083 21634083 single base substitution G A intron_variant PACA-CA 13 21637253 21637253 single base substitution G A upstream_gene_variant PAEN-AU 13 21572915 21572915 single base substitution C T intron_variant PAEN-AU 13 21631682 21631682 single base substitution G A intron_variant PAEN-AU 13 21634607 21634607 single base substitution G A intron_variant PAEN-AU 13 21634607 21634607 single base substitution G A upstream_gene_variant PAEN-AU 13 21636889 21636889 single base substitution C T upstream_gene_variant PAEN-IT 13 21544389 21544389 single base substitution G C downstream_gene_variant PAEN-IT 13 21556554 21556554 single base substitution G T intron_variant PAEN-IT 13 21578589 21578589 single base substitution A G intron_variant PAEN-IT 13 21595483 21595483 single base substitution G A intron_variant PBCA-DE 13 21542516 21542516 single base substitution A G downstream_gene_variant PBCA-DE 13 21547127 21547127 single base substitution G A downstream_gene_variant PBCA-DE 13 21549230 21549230 single base substitution C T missense_variant E1016K 3046G>A PBCA-DE 13 21551104 21551104 single base substitution C T intron_variant PBCA-DE 13 21552701 21552701 single base substitution T C intron_variant PBCA-DE 13 21562362 21562362 single base substitution C T downstream_gene_variant PBCA-DE 13 21562362 21562362 single base substitution C T synonymous_variant P519P 1557G>A PBCA-DE 13 21562759 21562759 single base substitution T C downstream_gene_variant PBCA-DE 13 21562759 21562759 single base substitution T C missense_variant E387G 1160A>G PBCA-DE 13 21573671 21573671 single base substitution G A intron_variant PBCA-DE 13 21576062 21576062 deletion of <=200bp T - intron_variant PBCA-DE 13 21576683 21576698 deletion of <=200bp TTTCTGTATTTTTTAG - intron_variant PBCA-DE 13 21592815 21592815 single base substitution C T intron_variant PBCA-DE 13 21597387 21597387 single base substitution C G intron_variant PBCA-DE 13 21597387 21597387 single base substitution C G upstream_gene_variant PBCA-DE 13 21601928 21601928 insertion of <=200bp - A intron_variant PBCA-DE 13 21601928 21601928 insertion of <=200bp - A upstream_gene_variant PBCA-DE 13 21607753 21607753 single base substitution T G intron_variant PBCA-DE 13 21607873 21607873 insertion of <=200bp - AG intron_variant PBCA-DE 13 21625015 21625015 single base substitution T C intron_variant PRAD-CA 13 21603642 21603642 single base substitution T C intron_variant PRAD-CA 13 21632068 21632068 single base substitution A T intron_variant PRAD-CA 13 21639531 21639531 single base substitution A T upstream_gene_variant PRAD-UK 13 21545461 21545461 single base substitution A T downstream_gene_variant PRAD-UK 13 21560628 21560630 deletion of <=200bp GTC - downstream_gene_variant PRAD-UK 13 21560628 21560630 deletion of <=200bp GTC - intron_variant PRAD-UK 13 21561452 21561452 single base substitution G C downstream_gene_variant PRAD-UK 13 21561452 21561452 single base substitution G C intron_variant PRAD-UK 13 21563045 21563045 single base substitution T C downstream_gene_variant PRAD-UK 13 21563045 21563045 single base substitution T C missense_variant K292E 874A>G PRAD-UK 13 21567833 21567833 single base substitution G A intron_variant PRAD-UK 13 21567842 21567842 single base substitution G C intron_variant PRAD-UK 13 21573628 21573628 insertion of <=200bp - T intron_variant PRAD-UK 13 21582469 21582469 single base substitution G C intron_variant PRAD-UK 13 21591069 21591069 single base substitution G C intron_variant PRAD-UK 13 21619054 21619054 single base substitution G A intron_variant PRAD-UK 13 21626073 21626073 single base substitution G C intron_variant PRAD-UK 13 21632146 21632146 single base substitution G C intron_variant PRAD-UK 13 21633167 21633167 single base substitution T A intron_variant PRAD-UK 13 21634527 21634527 single base substitution A G intron_variant PRAD-UK 13 21634527 21634527 single base substitution A G upstream_gene_variant PRAD-US 13 21557700 21557700 single base substitution G A synonymous_variant A715A 2145C>T PRAD-US 13 21562482 21562482 insertion of <=200bp - GGGGCG downstream_gene_variant PRAD-US 13 21562482 21562482 insertion of <=200bp - GGGGCG inframe_insertion P479PRP READ-US 13 21553889 21553889 single base substitution C T missense_variant E905K 2713G>A READ-US 13 21562832 21562832 single base substitution C T downstream_gene_variant READ-US 13 21562832 21562832 single base substitution C T missense_variant G363S 1087G>A READ-US 13 21562948 21562948 single base substitution G A downstream_gene_variant READ-US 13 21562948 21562948 single base substitution G A missense_variant A324V 971C>T RECA-EU 13 21548025 21548025 single base substitution C T 3_prime_UTR_variant RECA-EU 13 21548025 21548025 single base substitution C T downstream_gene_variant RECA-EU 13 21557719 21557719 single base substitution T C missense_variant Q709R 2126A>G RECA-EU 13 21560012 21560012 single base substitution C A downstream_gene_variant RECA-EU 13 21560012 21560012 single base substitution C A intron_variant RECA-EU 13 21563651 21563651 single base substitution G T intron_variant RECA-EU 13 21566245 21566245 single base substitution C A intron_variant RECA-EU 13 21568655 21568655 single base substitution G A intron_variant RECA-EU 13 21568656 21568656 single base substitution C A intron_variant RECA-EU 13 21591336 21591336 single base substitution C T intron_variant RECA-EU 13 21592335 21592335 single base substitution T C intron_variant RECA-EU 13 21593105 21593105 single base substitution A T intron_variant RECA-EU 13 21598250 21598250 single base substitution A G intron_variant RECA-EU 13 21598250 21598250 single base substitution A G upstream_gene_variant RECA-EU 13 21599552 21599552 single base substitution A C intron_variant RECA-EU 13 21599552 21599552 single base substitution A C upstream_gene_variant RECA-EU 13 21613380 21613380 single base substitution C G intron_variant RECA-EU 13 21618078 21618078 single base substitution T C intron_variant RECA-EU 13 21622139 21622139 single base substitution A G intron_variant RECA-EU 13 21623922 21623922 single base substitution G C intron_variant RECA-EU 13 21624264 21624264 single base substitution C T intron_variant RECA-EU 13 21624272 21624272 single base substitution T C intron_variant RECA-EU 13 21624274 21624274 single base substitution G C intron_variant RECA-EU 13 21624278 21624278 single base substitution G C intron_variant RECA-EU 13 21624290 21624290 single base substitution C G intron_variant RECA-EU 13 21626978 21626978 single base substitution G A intron_variant RECA-EU 13 21638451 21638451 single base substitution C A upstream_gene_variant RECA-EU 13 21638779 21638779 single base substitution T G upstream_gene_variant SKCA-BR 13 21544037 21544043 deletion of <=200bp CAAAAAA - downstream_gene_variant SKCA-BR 13 21544657 21544657 single base substitution G A downstream_gene_variant SKCA-BR 13 21546410 21546410 single base substitution G A downstream_gene_variant SKCA-BR 13 21546606 21546606 single base substitution C G downstream_gene_variant SKCA-BR 13 21551782 21551783 deletion of <=200bp TA - intron_variant SKCA-BR 13 21553422 21553422 single base substitution G A intron_variant SKCA-BR 13 21554442 21554442 single base substitution G A intron_variant SKCA-BR 13 21560056 21560056 single base substitution G C downstream_gene_variant SKCA-BR 13 21560056 21560056 single base substitution G C intron_variant SKCA-BR 13 21562482 21562482 insertion of <=200bp - CGGGGCG downstream_gene_variant SKCA-BR 13 21562482 21562482 insertion of <=200bp - CGGGGCG frameshift_variant P479PRP? SKCA-BR 13 21562642 21562642 single base substitution A G downstream_gene_variant SKCA-BR 13 21562642 21562642 single base substitution A G missense_variant L426P 1277T>C SKCA-BR 13 21562646 21562646 single base substitution A G downstream_gene_variant SKCA-BR 13 21562646 21562646 single base substitution A G missense_variant S425P 1273T>C SKCA-BR 13 21563038 21563038 single base substitution T C downstream_gene_variant SKCA-BR 13 21563038 21563038 single base substitution T C missense_variant Q294R 881A>G SKCA-BR 13 21563290 21563290 single base substitution G A exon_variant SKCA-BR 13 21563290 21563290 single base substitution G A missense_variant P210L 629C>T SKCA-BR 13 21564108 21564108 single base substitution G A intron_variant SKCA-BR 13 21565126 21565126 single base substitution C A intron_variant SKCA-BR 13 21568996 21568996 insertion of <=200bp - AAT intron_variant SKCA-BR 13 21570516 21570519 deletion of <=200bp ATTT - intron_variant SKCA-BR 13 21570565 21570565 single base substitution T G intron_variant SKCA-BR 13 21571587 21571587 single base substitution A C intron_variant SKCA-BR 13 21572735 21572735 single base substitution A C intron_variant SKCA-BR 13 21572749 21572749 single base substitution G A intron_variant SKCA-BR 13 21573266 21573266 single base substitution G A intron_variant SKCA-BR 13 21576513 21576514 deletion of <=200bp CT - intron_variant SKCA-BR 13 21579946 21579946 single base substitution A T intron_variant SKCA-BR 13 21579947 21579947 single base substitution A T intron_variant SKCA-BR 13 21581650 21581650 single base substitution G A intron_variant SKCA-BR 13 21581702 21581702 insertion of <=200bp - AC intron_variant SKCA-BR 13 21581706 21581706 insertion of <=200bp - AG intron_variant SKCA-BR 13 21581716 21581716 insertion of <=200bp - AC intron_variant SKCA-BR 13 21584335 21584335 insertion of <=200bp - TCAAACAAA intron_variant SKCA-BR 13 21584340 21584340 insertion of <=200bp - AAAACAAACAAAC intron_variant SKCA-BR 13 21584341 21584341 single base substitution A T intron_variant SKCA-BR 13 21586044 21586044 single base substitution T G intron_variant SKCA-BR 13 21587229 21587229 single base substitution G A intron_variant SKCA-BR 13 21587540 21587540 single base substitution A T intron_variant SKCA-BR 13 21588095 21588095 single base substitution G A intron_variant SKCA-BR 13 21588116 21588119 deletion of <=200bp CAAA - intron_variant SKCA-BR 13 21589114 21589114 single base substitution C G intron_variant SKCA-BR 13 21592277 21592277 single base substitution A G intron_variant SKCA-BR 13 21592326 21592326 single base substitution G T intron_variant SKCA-BR 13 21592327 21592327 single base substitution G T intron_variant SKCA-BR 13 21593119 21593119 single base substitution C G intron_variant SKCA-BR 13 21594112 21594112 insertion of <=200bp - TA intron_variant SKCA-BR 13 21597806 21597823 deletion of <=200bp AAAAAAAAAAAAAAAAAC - intron_variant SKCA-BR 13 21597806 21597823 deletion of <=200bp AAAAAAAAAAAAAAAAAC - upstream_gene_variant SKCA-BR 13 21597807 21597823 deletion of <=200bp AAAAAAAAAAAAAAAAC - intron_variant SKCA-BR 13 21597807 21597823 deletion of <=200bp AAAAAAAAAAAAAAAAC - upstream_gene_variant SKCA-BR 13 21597814 21597823 deletion of <=200bp AAAAAAAAAC - intron_variant SKCA-BR 13 21597814 21597823 deletion of <=200bp AAAAAAAAAC - upstream_gene_variant SKCA-BR 13 21597816 21597823 deletion of <=200bp AAAAAAAC - intron_variant SKCA-BR 13 21597816 21597823 deletion of <=200bp AAAAAAAC - upstream_gene_variant SKCA-BR 13 21597821 21597823 deletion of <=200bp AAC - intron_variant SKCA-BR 13 21597821 21597823 deletion of <=200bp AAC - upstream_gene_variant SKCA-BR 13 21598232 21598234 deletion of <=200bp CAA - intron_variant SKCA-BR 13 21598232 21598234 deletion of <=200bp CAA - upstream_gene_variant SKCA-BR 13 21598250 21598250 single base substitution A G intron_variant SKCA-BR 13 21598250 21598250 single base substitution A G upstream_gene_variant SKCA-BR 13 21599410 21599410 single base substitution A G intron_variant SKCA-BR 13 21599410 21599410 single base substitution A G upstream_gene_variant SKCA-BR 13 21599552 21599552 insertion of <=200bp - AC intron_variant SKCA-BR 13 21599552 21599552 insertion of <=200bp - AC upstream_gene_variant SKCA-BR 13 21604751 21604752 deletion of <=200bp GA - intron_variant SKCA-BR 13 21605924 21605924 single base substitution G A intron_variant SKCA-BR 13 21606220 21606220 single base substitution G A intron_variant SKCA-BR 13 21608026 21608026 single base substitution A C intron_variant SKCA-BR 13 21608858 21608858 single base substitution T G intron_variant SKCA-BR 13 21610077 21610077 single base substitution G A intron_variant SKCA-BR 13 21615724 21615724 single base substitution C T intron_variant SKCA-BR 13 21617412 21617412 single base substitution G A intron_variant SKCA-BR 13 21624264 21624264 insertion of <=200bp - CAGACAGACAGATAGATAGATAGAT intron_variant SKCA-BR 13 21624264 21624264 insertion of <=200bp - CAGACAGATAGATAGAT intron_variant SKCA-BR 13 21624268 21624268 single base substitution T C intron_variant SKCA-BR 13 21624274 21624274 single base substitution G C intron_variant SKCA-BR 13 21624278 21624278 insertion of <=200bp - GATACATAC intron_variant SKCA-BR 13 21624278 21624278 single base substitution G C intron_variant SKCA-BR 13 21624282 21624282 insertion of <=200bp - GATACATACATAC intron_variant SKCA-BR 13 21624282 21624282 single base substitution G C intron_variant SKCA-BR 13 21624286 21624286 single base substitution G C intron_variant SKCA-BR 13 21624310 21624310 insertion of <=200bp - CATACATACATACATAC intron_variant SKCA-BR 13 21634824 21634824 single base substitution A G intron_variant SKCA-BR 13 21634824 21634824 single base substitution A G upstream_gene_variant SKCA-BR 13 21638554 21638554 single base substitution G A upstream_gene_variant SKCA-BR 13 21640043 21640043 single base substitution G A upstream_gene_variant SKCM-US 13 21549192 21549192 single base substitution G T synonymous_variant P1028P 3084C>A SKCM-US 13 21549220 21549220 single base substitution G A missense_variant T1019I 3056C>T SKCM-US 13 21555718 21555718 single base substitution C T missense_variant G851E 2552G>A SKCM-US 13 21557379 21557379 single base substitution G A synonymous_variant S822S 2466C>T SKCM-US 13 21557732 21557732 single base substitution G A synonymous_variant L705L 2113C>T SKCM-US 13 21557827 21557827 single base substitution G A missense_variant T673I 2018C>T SKCM-US 13 21562189 21562189 single base substitution G A downstream_gene_variant SKCM-US 13 21562189 21562189 single base substitution G A missense_variant P577L 1730C>T SKCM-US 13 21562821 21562821 single base substitution G A downstream_gene_variant SKCM-US 13 21562821 21562821 single base substitution G A synonymous_variant S366S 1098C>T SKCM-US 13 21563271 21563271 single base substitution G A exon_variant SKCM-US 13 21563271 21563271 single base substitution G A synonymous_variant F216F 648C>T SKCM-US 13 21563423 21563423 single base substitution G A exon_variant SKCM-US 13 21563423 21563423 single base substitution G A missense_variant P166S 496C>T STAD-US 13 21549231 21549231 single base substitution G A synonymous_variant S1015S 3045C>T STAD-US 13 21555688 21555688 single base substitution G A missense_variant A861V 2582C>T STAD-US 13 21555776 21555776 single base substitution T C missense_variant R832G 2494A>G STAD-US 13 21557370 21557370 single base substitution G A synonymous_variant Y825Y 2475C>T STAD-US 13 21557416 21557416 single base substitution A G missense_variant F810S 2429T>C STAD-US 13 21557671 21557671 single base substitution T C missense_variant N725S 2174A>G STAD-US 13 21557772 21557772 single base substitution G A synonymous_variant H691H 2073C>T STAD-US 13 21562282 21562282 single base substitution G A downstream_gene_variant STAD-US 13 21562282 21562282 single base substitution G A missense_variant A546V 1637C>T STAD-US 13 21562308 21562308 single base substitution G A downstream_gene_variant STAD-US 13 21562308 21562308 single base substitution G A synonymous_variant C537C 1611C>T STAD-US 13 21562745 21562745 single base substitution C T downstream_gene_variant STAD-US 13 21562745 21562745 single base substitution C T missense_variant A392T 1174G>A STAD-US 13 21562755 21562755 single base substitution C T downstream_gene_variant STAD-US 13 21562755 21562755 single base substitution C T synonymous_variant A388A 1164G>A STAD-US 13 21562886 21562886 single base substitution G A downstream_gene_variant STAD-US 13 21562886 21562886 single base substitution G A stop_gained Q345* 1033C>T STAD-US 13 21562928 21562928 single base substitution G T downstream_gene_variant STAD-US 13 21562928 21562928 single base substitution G T missense_variant L331M 991C>A STAD-US 13 21562970 21562970 single base substitution G A downstream_gene_variant STAD-US 13 21562970 21562970 single base substitution G A missense_variant H317Y 949C>T STAD-US 13 21562993 21562993 single base substitution G A downstream_gene_variant STAD-US 13 21562993 21562993 single base substitution G A missense_variant A309V 926C>T STAD-US 13 21563168 21563168 single base substitution C T exon_variant STAD-US 13 21563168 21563168 single base substitution C T missense_variant A251T 751G>A STAD-US 13 21563291 21563291 single base substitution G A exon_variant STAD-US 13 21563291 21563291 single base substitution G A missense_variant P210S 628C>T STAD-US 13 21563349 21563349 deletion of <=200bp G - exon_variant STAD-US 13 21563349 21563349 deletion of <=200bp G - frameshift_variant P190 STAD-US 13 21563416 21563416 single base substitution G A exon_variant STAD-US 13 21563416 21563416 single base substitution G A missense_variant T168M 503C>T THCA-SA 13 21547984 21547984 single base substitution C T 3_prime_UTR_variant THCA-SA 13 21547984 21547984 single base substitution C T downstream_gene_variant THCA-SA 13 21563350 21563350 single base substitution G C exon_variant THCA-SA 13 21563350 21563350 single base substitution G C missense_variant P190R 569C>G THCA-US 13 21562776 21562776 single base substitution C A downstream_gene_variant THCA-US 13 21562776 21562776 single base substitution C A synonymous_variant L381L 1143G>T UCEC-US 13 21549116 21549116 single base substitution G A stop_gained R1054* 3160C>T UCEC-US 13 21549161 21549161 single base substitution C T missense_variant E1039K 3115G>A UCEC-US 13 21549231 21549231 single base substitution G A synonymous_variant S1015S 3045C>T UCEC-US 13 21549354 21549354 single base substitution G A synonymous_variant S974S 2922C>T UCEC-US 13 21549368 21549368 single base substitution G T missense_variant H970N 2908C>A UCEC-US 13 21549377 21549377 single base substitution G T missense_variant L967M 2899C>A UCEC-US 13 21555630 21555630 single base substitution G A synonymous_variant I880I 2640C>T UCEC-US 13 21555749 21555749 single base substitution G A missense_variant L841F 2521C>T UCEC-US 13 21557528 21557528 single base substitution C T missense_variant A773T 2317G>A UCEC-US 13 21557768 21557768 single base substitution G T missense_variant L693M 2077C>A UCEC-US 13 21562178 21562178 single base substitution G A downstream_gene_variant UCEC-US 13 21562178 21562178 single base substitution G A missense_variant R581C 1741C>T UCEC-US 13 21562246 21562246 single base substitution C T downstream_gene_variant UCEC-US 13 21562246 21562246 single base substitution C T missense_variant R558H 1673G>A UCEC-US 13 21562430 21562430 single base substitution C T downstream_gene_variant UCEC-US 13 21562430 21562430 single base substitution C T missense_variant A497T 1489G>A UCEC-US 13 21562636 21562636 single base substitution G A downstream_gene_variant UCEC-US 13 21562636 21562636 single base substitution G A missense_variant A428V 1283C>T UCEC-US 13 21562742 21562743 deletion of <=200bp GC - downstream_gene_variant UCEC-US 13 21562742 21562743 deletion of <=200bp GC - frameshift_variant AH392 UCEC-US 13 21563416 21563416 single base substitution G A exon_variant UCEC-US 13 21563416 21563416 single base substitution G A missense_variant T168M 503C>T UCEC-US 13 21565499 21565499 single base substitution G A exon_variant UCEC-US 13 21565499 21565499 single base substitution G A synonymous_variant I129I 387C>T UCEC-US 13 21619838 21619838 single base substitution C T missense_variant A110T 328G>A UCEC-US 13 21619894 21619894 single base substitution G A missense_variant S91L 272C>T UCEC-US 13 21619928 21619928 deletion of <=200bp T - frameshift_variant I80 UCEC-US 13 21620000 21620000 single base substitution C A missense_variant D56Y 166G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Gp2D COSM2265643 c.2705T>A p.I902N Substitution - Missense 13:20979758-20979758 - sysucc-1163T COSM2265719 c.1151C>T p.P384L Substitution - Missense 13:20988629-20988629 - TCGA-59-2372-01 COSM1322940 c.2688G>A p.W896* Substitution - Nonsense 13:20979775-20979775 - CRC-19T COSM5481117 c.608C>T p.A203V Substitution - Missense 13:20989172-20989172 - KPOPBR-07-T COSM5964130 c.1546C>T p.P516S Substitution - Missense 13:20988234-20988234 - TCGA-CI-6620-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - HCT-15 COSM1677515 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - TCGA-EK-A2RJ-01 COSM4832005 c.256C>T p.P86S Substitution - Missense 13:21045771-21045771 - TCGA-AF-6655-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-D9-A6EC-06 COSM4402155 c.1098C>T p.S366S Substitution - coding silent 13:20988682-20988682 - TCGA-B5-A11J-01 COSM945937 c.1489G>A p.A497T Substitution - Missense 13:20988291-20988291 - NCI-H2126 COSM12866 c.119G>A p.G40E Substitution - Missense 13:21045908-21045908 - Gp5D COSM2265643 c.2705T>A p.I902N Substitution - Missense 13:20979758-20979758 - S02284 COSM5684053 c.3037G>T p.D1013Y Substitution - Missense 13:20975100-20975100 - PTC-77C COSM5446052 c.1413_1414insGCCCCC p.A480_A481insPA Insertion - In frame 13:20988366-20988367 - TCGA-G4-6311-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AN-A046-01 COSM3813549 c.1954G>T p.E652* Substitution - Nonsense 13:20983752-20983752 - CSCC-19-T COSM4567200 c.602_603CC>TT p.P201L Substitution - Missense 13:20989177-20989178 - BZ12 COSM5701081 c.1436_1437insCGCCCC p.A480_A481insPA Insertion - In frame 13:20988343-20988344 - RKO COSM2265695 c.1706A>G p.D569G Substitution - Missense 13:20988074-20988074 - OSCC-GB_00160111 COSM3711042 c.1179C>T p.H393H Substitution - coding silent 13:20988601-20988601 - T1760 COSM4697512 c.3161G>A p.R1054Q Substitution - Missense 13:20974976-20974976 - 61 COSM5739902 c.1531C>T p.R511W Substitution - Missense 13:20988249-20988249 - TCGA-EE-A2M6-06 COSM2265656 c.2466C>T p.S822S Substitution - coding silent 13:20983240-20983240 - DLD1 COSM1677512 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - TCGA-EE-A2MR-06 COSM1147170 c.648C>T p.F216F Substitution - coding silent 13:20989132-20989132 - CSCC-38-T COSM1586986 c.272C>T p.S91L Substitution - Missense 13:21045755-21045755 - HCC132T COSM1606909 c.228C>T p.A76A Substitution - coding silent 13:21045799-21045799 - TCGA-DM-A1DA-01 COSM1365813 c.2023G>T p.G675W Substitution - Missense 13:20983683-20983683 - TCGA-C5-A1BF-01 COSM1213133 c.1172G>A p.R391H Substitution - Missense 13:20988608-20988608 - T2418 COSM4697521 c.1615G>C p.G539R Substitution - Missense 13:20988165-20988165 - CSCC-7-T COSM4475533 c.1997C>T p.S666F Substitution - Missense 13:20983709-20983709 - YUKAT COSM5376501 c.2772+1G>A p.? Unknown 13:20979690-20979690 - TCGA-AP-A056-01 COSM1586986 c.272C>T p.S91L Substitution - Missense 13:21045755-21045755 - BZ12 COSM5701080 c.1436_1437insCGCCCC p.A480_A481insPA Insertion - In frame 13:20988343-20988344 - TCGA-59-2372-01 COSM1322939 c.2688G>A p.W896* Substitution - Nonsense 13:20979775-20979775 - TCGA-AG-3592-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-D5-5541-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-EK-A2RJ-01 COSM4832006 c.256C>T p.P86S Substitution - Missense 13:21045771-21045771 - QC2-39-T2 COSM5655721 c.1972T>G p.L658V Substitution - Missense 13:20983734-20983734 - Gp5D COSM2265627 c.3257T>C p.V1086A Substitution - Missense 13:20974880-20974880 - TCGA-18-3409-01 COSM1147170 c.648C>T p.F216F Substitution - coding silent 13:20989132-20989132 - BN44T COSM3704485 c.2888G>A p.G963E Substitution - Missense 13:20975249-20975249 - BN44 COSM3704485 c.2888G>A p.G963E Substitution - Missense 13:20975249-20975249 - TCGA-EE-A29L-06 COSM3467656 c.1730C>T p.P577L Substitution - Missense 13:20988050-20988050 - TCGA-AH-6644-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-D1-A103-01 COSM1586990 c.1176_1177delGC p.H393fs*6 Deletion - Frameshift 13:20988603-20988604 - TCGA-BR-6452-01 COSM4046442 c.1164G>A p.A388A Substitution - coding silent 13:20988616-20988616 - LIM2405 COSM2265697 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - 16T COSM3711042 c.1179C>T p.H393H Substitution - coding silent 13:20988601-20988601 - pfg122T COSM4751035 c.284C>T p.A95V Substitution - Missense 13:21045743-21045743 - QC2-39-T2 COSM5655722 c.1972T>G p.L658V Substitution - Missense 13:20983734-20983734 - CSCC-19-T COSM4567201 c.602_603CC>TT p.P201L Substitution - Missense 13:20989177-20989178 - TARGET-30-PATHVK COSM1285885 c.1650G>T p.E550D Substitution - Missense 13:20988130-20988130 - ICGC_MB61 COSM3764461 c.3046G>A p.E1016K Substitution - Missense 13:20975091-20975091 - HCC71 COSM3704487 c.64A>G p.I22V Substitution - Missense 13:21045963-21045963 - U2940 COSM5621146 c.1445A>G p.E482G Substitution - Missense 13:20988335-20988335 - CSCC-11-T COSM4504965 c.67C>T p.R23C Substitution - Missense 13:21045960-21045960 - BCM723T COSM4956237 c.490C>T p.P164S Substitution - Missense 13:20989290-20989290 - TCGA-G4-6293-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - PD11368a COSM5786314 c.1493G>A p.G498D Substitution - Missense 13:20988287-20988287 - TCGA-AX-A0J0-01 COSM945941 c.387C>T p.I129I Substitution - coding silent 13:20991360-20991360 - HCC132 COSM1606910 c.228C>T p.A76A Substitution - coding silent 13:21045799-21045799 - CHC1148T COSM4954577 c.2912C>T p.P971L Substitution - Missense 13:20975225-20975225 - TCGA-B5-A11E-01 COSM42744 c.1673G>A p.R558H Substitution - Missense 13:20988107-20988107 - TCGA-BP-4762-01 COSM3360015 c.2324T>C p.L775P Substitution - Missense 13:20983382-20983382 - TCGA-FP-A4BE-01 COSM1586999 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - ESO-0013 COSM1256341 c.1994A>G p.K665R Substitution - Missense 13:20983712-20983712 - HCC71 COSM3704486 c.64A>G p.I22V Substitution - Missense 13:21045963-21045963 - T1760 COSM4697511 c.3161G>A p.R1054Q Substitution - Missense 13:20974976-20974976 - TCGA-46-3769-01 COSM1147168 c.1583C>T p.S528L Substitution - Missense 13:20988197-20988197 - SC_9037 COSM5565313 c.812G>A p.R271H Substitution - Missense 13:20988968-20988968 - Gp5D COSM2265628 c.3257T>C p.V1086A Substitution - Missense 13:20974880-20974880 - SJHGG118_A COSM4972025 c.529_530delGG p.G177fs*22 Deletion - Frameshift 13:20989250-20989251 - TCGA-AN-A046-01 COSM3813548 c.2398G>T p.D800Y Substitution - Missense 13:20983308-20983308 - CHC884T COSM4958457 c.1099G>T p.V367F Substitution - Missense 13:20988681-20988681 - 1_RESISTANT COSM1719348 c.2512C>T p.P838S Substitution - Missense 13:20981619-20981619 - TCGA-B5-A11E-01 COSM945933 c.2521C>T p.L841F Substitution - Missense 13:20981610-20981610 - TCGA-AP-A059-01 COSM1586997 c.2899C>A p.L967M Substitution - Missense 13:20975238-20975238 - S00022 COSM5656455 c.666C>A p.H222Q Substitution - Missense 13:20989114-20989114 - CCK81 COSM2265662 c.2449A>G p.R817G Substitution - Missense 13:20983257-20983257 - CSCC-32-T COSM4482970 c.2659C>T p.R887C Substitution - Missense 13:20981472-20981472 - sysucc-783T COSM4046439 c.1611C>T p.C537C Substitution - coding silent 13:20988169-20988169 - CAL33 COSM4594349 c.1340T>A p.V447E Substitution - Missense 13:20988440-20988440 - TCGA-G4-6315-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-AA-3662-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - ICGC_MB102 COSM3764463 c.1557G>A p.P519P Substitution - coding silent 13:20988223-20988223 - S00827 COSM5701081 c.1436_1437insCGCCCC p.A480_A481insPA Insertion - In frame 13:20988343-20988344 - 3006_T COSM3955435 c.2441C>G p.T814S Substitution - Missense 13:20983265-20983265 - SW948 COSM2265690 c.1872G>A p.R624R Substitution - coding silent 13:20987908-20987908 - TCGA-G4-6320-01 COSM3688639 c.2645C>T p.P882L Substitution - Missense 13:20981486-20981486 - CHC1040T COSM4799507 c.1536G>T p.R512S Substitution - Missense 13:20988244-20988244 - 1_RESISTANT COSM1721269 c.1424C>T p.P475L Substitution - Missense 13:20988356-20988356 - C086 COSM5533679 c.2747C>T p.P916L Substitution - Missense 13:20979716-20979716 - PT23_2 COSM5903846 c.581C>T p.P194L Substitution - Missense 13:20989199-20989199 - TCGA-A6-5656-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - U2940 COSM5621149 c.1424C>G p.P475R Substitution - Missense 13:20988356-20988356 - ICGC_MB102 COSM3764462 c.1557G>A p.P519P Substitution - coding silent 13:20988223-20988223 - CSCC-41-T COSM4478053 c.2206C>T p.Q736* Substitution - Nonsense 13:20983500-20983500 - TCGA-BT-A0YX-01 COSM1133414 c.1673G>A p.R558H Substitution - Missense 13:20988107-20988107 - TCGA-EE-A20H-06 COSM3467653 c.2552G>A p.G851E Substitution - Missense 13:20981579-20981579 - TCGA-AF-6655-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AF-2687-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - Gp2D COSM2265697 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - TCGA-B5-A11E-01 COSM1586995 c.2521C>T p.L841F Substitution - Missense 13:20981610-20981610 - U2940 COSM5621148 c.1424C>G p.P475R Substitution - Missense 13:20988356-20988356 - TCGA-EE-A2M6-06 COSM2265657 c.2466C>T p.S822S Substitution - coding silent 13:20983240-20983240 - TCGA-18-3409-01 COSM695816 c.1547C>T p.P516L Substitution - Missense 13:20988233-20988233 - C008 COSM5523000 c.3080C>T p.S1027L Substitution - Missense 13:20975057-20975057 - YUKAT COSM5376500 c.2772+1G>A p.? Unknown 13:20979690-20979690 - Gp2D COSM2265627 c.3257T>C p.V1086A Substitution - Missense 13:20974880-20974880 - S00938 COSM5663265 c.2948G>A p.R983Q Substitution - Missense 13:20975189-20975189 - EV001-R1 COSM1161920 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-FW-A3R5-06 COSM3885084 c.2018C>T p.T673I Substitution - Missense 13:20983688-20983688 - CHEWS021 COSM4575867 c.2030G>T p.G677V Substitution - Missense 13:20983676-20983676 - HCT8 COSM4633791 c.978C>T p.H326H Substitution - coding silent 13:20988802-20988802 - CHC1040T COSM4799506 c.1536G>T p.R512S Substitution - Missense 13:20988244-20988244 - CCK81 COSM2265663 c.2449A>G p.R817G Substitution - Missense 13:20983257-20983257 - KPOPBR-07-T COSM5964129 c.1546C>T p.P516S Substitution - Missense 13:20988234-20988234 - PTC-88C COSM5446052 c.1413_1414insGCCCCC p.A480_A481insPA Insertion - In frame 13:20988366-20988367 - TCGA-DU-7300-01 COSM3968567 c.1493G>T p.G498V Substitution - Missense 13:20988287-20988287 - ESCC_47 COSM1192377 c.2276G>A p.R759Q Substitution - Missense 13:20983430-20983430 - LS513 COSM2265631 c.3036C>T p.N1012N Substitution - coding silent 13:20975101-20975101 - T2769 COSM4697514 c.3127C>T p.R1043* Substitution - Nonsense 13:20975010-20975010 - MO_1012 COSM5547119 c.664delC p.H222fs*18 Deletion - Frameshift 13:20989116-20989116 - BCM723T COSM4956238 c.490C>T p.P164S Substitution - Missense 13:20989290-20989290 - TCGA-EE-A2MR-06 COSM695815 c.648C>T p.F216F Substitution - coding silent 13:20989132-20989132 - TCGA-AA-3663-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - CSCC-38-T COSM945943 c.272C>T p.S91L Substitution - Missense 13:21045755-21045755 - Gp2D COSM2265642 c.2705T>A p.I902N Substitution - Missense 13:20979758-20979758 - CRC-19T COSM5481118 c.608C>T p.A203V Substitution - Missense 13:20989172-20989172 - ICGC_MB61 COSM48481 c.3046G>A p.E1016K Substitution - Missense 13:20975091-20975091 - TCGA-A2-A3XZ-01 COSM3813553 c.531C>A p.G177G Substitution - coding silent 13:20989249-20989249 - TCGA-BR-6452-01 COSM4046437 c.1637C>T p.A546V Substitution - Missense 13:20988143-20988143 - SNU-175 COSM2265757 c.52C>T p.R18* Substitution - Nonsense 13:21045975-21045975 - BK0057 COSM4188247 c.2003_2006delTTGT p.F668fs*28 Deletion - Frameshift 13:20983700-20983703 - TCGA-BR-7851-01 COSM4046429 c.2475C>T p.Y825Y Substitution - coding silent 13:20983231-20983231 - TARGET-30-PAPUWY COSM1285889 c.3144C>T p.D1048D Substitution - coding silent 13:20974993-20974993 - PD4120a COSM162123 c.2554G>A p.D852N Substitution - Missense 13:20981577-20981577 - TCGA-F4-6463-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - 001 COSM1161919 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - LC_S12 COSM1188679 c.1361C>T p.P454L Substitution - Missense 13:20988419-20988419 - PT37 COSM5920602 c.343-8C>T p.? Unknown 13:20991412-20991412 - 4 COSM5732134 c.1732G>A p.V578I Substitution - Missense 13:20988048-20988048 - Pat_66_A COSM4046454 c.628C>T p.P210S Substitution - Missense 13:20989152-20989152 - TCGA-AN-A046-01 COSM3813550 c.1954G>T p.E652* Substitution - Nonsense 13:20983752-20983752 - TCGA-EE-A184-06 COSM3467650 c.3084C>A p.P1028P Substitution - coding silent 13:20975053-20975053 - PT42 COSM4697520 c.1759G>A p.E587K Substitution - Missense 13:20988021-20988021 - Br27P COSM40255 c.2725G>A p.G909R Substitution - Missense 13:20979738-20979738 - PT46 COSM5929482 c.2281G>A p.E761K Substitution - Missense 13:20983425-20983425 - TCGA-CI-6619-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - OSCC-GB_00540111 COSM4889451 c.2176G>C p.E726Q Substitution - Missense 13:20983530-20983530 - pfg034T COSM4751026 c.1861G>C p.V621L Substitution - Missense 13:20987919-20987919 - LUAD-YINHD COSM348809 c.548A>G p.Y183C Substitution - Missense 13:20989232-20989232 - KM12 COSM2265640 c.2741delT p.L914fs*10 Deletion - Frameshift 13:20979722-20979722 - PTC-7C COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-BR-6452-01 COSM4046436 c.1637C>T p.A546V Substitution - Missense 13:20988143-20988143 - CHC884T COSM4958458 c.1099G>T p.V367F Substitution - Missense 13:20988681-20988681 - TCGA-RP-A695-06 COSM4897137 c.3056C>T p.T1019I Substitution - Missense 13:20975081-20975081 - TCGA-AY-6196-01 COSM3753613 c.1548G>A p.P516P Substitution - coding silent 13:20988232-20988232 - TCGA-B5-A11E-01 COSM945935 c.2077C>A p.L693M Substitution - Missense 13:20983629-20983629 - TCGA-AG-A002-01 COSM261742 c.1681G>A p.A561T Substitution - Missense 13:20988099-20988099 - RMS105_ COSM4986200 c.475+1G>A p.? Unknown 13:20991271-20991271 - TCGA-F5-6702-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-46-3769-01 COSM695817 c.1583C>T p.S528L Substitution - Missense 13:20988197-20988197 - T3091 COSM4697524 c.1479G>A p.A493A Substitution - coding silent 13:20988301-20988301 - sysucc-1397T COSM5473451 c.937G>A p.V313M Substitution - Missense 13:20988843-20988843 - 001 COSM1161920 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-AN-A046-01 COSM94599 c.536C>T p.S179L Substitution - Missense 13:20989244-20989244 - CSCC-42-T COSM4486104 c.3011C>T p.P1004L Substitution - Missense 13:20975126-20975126 - C008 COSM5523002 c.1140C>T p.S380S Substitution - coding silent 13:20988640-20988640 - TCGA-BR-4368-01 COSM4046454 c.628C>T p.P210S Substitution - Missense 13:20989152-20989152 - TCGA-D5-5541-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AY-6196-01 COSM3753612 c.1548G>A p.P516P Substitution - coding silent 13:20988232-20988232 - CHEWS031 COSM4575869 c.327C>T p.N109N Substitution - coding silent 13:21045700-21045700 - TCGA-CA-6718-01 COSM1365801 c.2993A>G p.D998G Substitution - Missense 13:20975144-20975144 - SW948 COSM2265689 c.1872G>A p.R624R Substitution - coding silent 13:20987908-20987908 - LS513 COSM2265632 c.3036C>T p.N1012N Substitution - coding silent 13:20975101-20975101 - T3174 COSM4697519 c.1759G>A p.E587K Substitution - Missense 13:20988021-20988021 - HCT15 COSM1677512 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - S00934 COSM4147630 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - TCGA-BR-8363-01 COSM4046440 c.1174G>A p.A392T Substitution - Missense 13:20988606-20988606 - RKO COSM4647687 c.2114T>C p.L705P Substitution - Missense 13:20983592-20983592 - TCGA-18-3409-01 COSM695815 c.648C>T p.F216F Substitution - coding silent 13:20989132-20989132 - TCGA-D1-A103-01 COSM945938 c.1283C>T p.A428V Substitution - Missense 13:20988497-20988497 - TCGA-BR-4361-01 COSM4046432 c.2174A>G p.N725S Substitution - Missense 13:20983532-20983532 - C008 COSM5522997 c.1139C>T p.S380F Substitution - Missense 13:20988641-20988641 - TCGA-FG-A60J-01 COSM3968566 c.1777C>T p.R593C Substitution - Missense 13:20988003-20988003 - RKO COSM4647686 c.2114T>C p.L705P Substitution - Missense 13:20983592-20983592 - TARGET-30-PATHVK COSM1285884 c.1650G>T p.E550D Substitution - Missense 13:20988130-20988130 - TCGA-D1-A103-01 COSM945939 c.1176_1177delGC p.H393fs*6 Deletion - Frameshift 13:20988603-20988604 - TCGA-BP-4326-01 COSM3360017 c.2176G>A p.E726K Substitution - Missense 13:20983530-20983530 - Pat_01_A COSM5842268 c.1097C>T p.S366F Substitution - Missense 13:20988683-20988683 - sysucc-1397T COSM5473449 c.1099G>A p.V367I Substitution - Missense 13:20988681-20988681 - T3091 COSM4697523 c.1479G>A p.A493A Substitution - coding silent 13:20988301-20988301 - CRC-02T COSM5454210 c.2872C>T p.R958C Substitution - Missense 13:20975265-20975265 - CSCC-7-T COSM4475532 c.1997C>T p.S666F Substitution - Missense 13:20983709-20983709 - PTC-73C COSM4147630 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - CSCC-41-T COSM4478052 c.2206C>T p.Q736* Substitution - Nonsense 13:20983500-20983500 - NCI-H2126 COSM12866 c.119G>A p.G40E Substitution - Missense 13:21045908-21045908 - ccRCC-47 COSM1662566 c.3128G>T p.R1043L Substitution - Missense 13:20975009-20975009 - S02209 COSM4147631 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - 3N44-VS-3T44 COSM4982190 c.806T>C p.V269A Substitution - Missense 13:20988974-20988974 - NCI-H2009 COSM12865 c.2775G>A p.V925V Substitution - coding silent 13:20975362-20975362 - TCGA-EE-A29L-06 COSM3467657 c.1730C>T p.P577L Substitution - Missense 13:20988050-20988050 - TCGA-BR-8487-01 COSM4046453 c.751G>A p.A251T Substitution - Missense 13:20989029-20989029 - C709 COSM4443844 c.1920G>T p.E640D Substitution - Missense 13:20983786-20983786 - S01578 COSM4147631 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - BCM723T COSM4956237 c.490C>T p.P164S Substitution - Missense 13:20989290-20989290 - SC_9037 COSM5565314 c.812G>A p.R271H Substitution - Missense 13:20988968-20988968 - HCT-15 COSM1677517 c.2295G>T p.E765D Substitution - Missense 13:20983411-20983411 - TCGA-CG-5721-01 COSM4046444 c.1033C>T p.Q345* Substitution - Nonsense 13:20988747-20988747 - S02065 COSM5672586 c.1404G>C p.A468A Substitution - coding silent 13:20988376-20988376 - SNU-175 COSM2265756 c.52C>T p.R18* Substitution - Nonsense 13:21045975-21045975 - pfg122T COSM4751034 c.284C>T p.A95V Substitution - Missense 13:21045743-21045743 - QC2-34-T2 COSM5654918 c.562G>A p.G188S Substitution - Missense 13:20989218-20989218 - TCGA-BR-4184-01 COSM4046425 c.2582C>T p.A861V Substitution - Missense 13:20981549-20981549 - 587284 COSM1213132 c.623C>T p.P208L Substitution - Missense 13:20989157-20989157 - Pat_01_B COSM5842267 c.1097C>T p.S366F Substitution - Missense 13:20988683-20988683 - TCGA-AP-A0LM-01 COSM945932 c.2640C>T p.I880I Substitution - coding silent 13:20981491-20981491 - 3006_T COSM3955436 c.2441C>G p.T814S Substitution - Missense 13:20983265-20983265 - CRC-16T COSM945934 c.2317G>A p.A773T Substitution - Missense 13:20983389-20983389 - TCGA-CH-5750-01 COSM4879493 c.2145C>T p.A715A Substitution - coding silent 13:20983561-20983561 - PT46 COSM5929483 c.2281G>A p.E761K Substitution - Missense 13:20983425-20983425 - HCC37 COSM1606907 c.341A>G p.Q114R Substitution - Missense 13:21045686-21045686 - TCGA-BP-4762-01 COSM3360016 c.2324T>C p.L775P Substitution - Missense 13:20983382-20983382 - TCGA-BR-6452-01 COSM4046443 c.1164G>A p.A388A Substitution - coding silent 13:20988616-20988616 - CAL33 COSM4594350 c.1340T>A p.V447E Substitution - Missense 13:20988440-20988440 - A9 COSM5349882 c.2769G>A p.L923L Substitution - coding silent 13:20979694-20979694 - TCGA-CC-A7IK-01 COSM4924785 c.2867A>T p.D956V Substitution - Missense 13:20975270-20975270 - CRC-19T COSM5481116 c.2240A>G p.Y747C Substitution - Missense 13:20983466-20983466 - C086 COSM5533680 c.2747C>T p.P916L Substitution - Missense 13:20979716-20979716 - pfg034T COSM4751025 c.1861G>C p.V621L Substitution - Missense 13:20987919-20987919 - TCGA-CA-6718-01 COSM1365800 c.2993A>G p.D998G Substitution - Missense 13:20975144-20975144 - TCGA-AH-6644-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-F5-6702-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AG-3725-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-BR-4362-01 COSM1586989 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - TCGA-EE-A20H-06 COSM3467652 c.2552G>A p.G851E Substitution - Missense 13:20981579-20981579 - PTC-77C COSM5446053 c.1413_1414insGCCCCC p.A480_A481insPA Insertion - In frame 13:20988366-20988367 - HCT-15 COSM1677512 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - TCGA-F5-6571-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-AA-3662-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AY-6196-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - T3024 COSM4697526 c.532G>A p.D178N Substitution - Missense 13:20989248-20989248 - U2940 COSM5621147 c.1445A>G p.E482G Substitution - Missense 13:20988335-20988335 - T2418 COSM4697522 c.1615G>C p.G539R Substitution - Missense 13:20988165-20988165 - TCGA-B5-A11E-01 COSM1586993 c.2077C>A p.L693M Substitution - Missense 13:20983629-20983629 - PCSI_0588_Pa_P_526 COSM4647688 c.589G>A p.G197S Substitution - Missense 13:20989191-20989191 - TCGA-AP-A059-01 COSM945931 c.2899C>A p.L967M Substitution - Missense 13:20975238-20975238 - TCGA-BG-A0MU-01 COSM1586985 c.238delA p.I80fs*20 Deletion - Frameshift 13:21045789-21045789 - TCGA-B0-5711-01 COSM469237 c.2164G>T p.E722* Substitution - Nonsense 13:20983542-20983542 - 417 COSM4431606 c.2478G>C p.Q826H Substitution - Missense 13:20983228-20983228 - TCGA-CC-A7IK-01 COSM4924786 c.2867A>T p.D956V Substitution - Missense 13:20975270-20975270 - DLD1 COSM1677513 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - TCGA-AA-3930-01 COSM296596 c.2967C>T p.Y989Y Substitution - coding silent 13:20975170-20975170 - TCGA-EE-A2A0-06 COSM3467655 c.2113C>T p.L705L Substitution - coding silent 13:20983593-20983593 - HCT-15 COSM1677514 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - C0041T COSM4152727 c.2126A>G p.Q709R Substitution - Missense 13:20983580-20983580 - PT42 COSM4697519 c.1759G>A p.E587K Substitution - Missense 13:20988021-20988021 - PT37 COSM5920601 c.343-8C>T p.? Unknown 13:20991412-20991412 - TCGA-A2-A0T5-01 COSM3813546 c.3121A>C p.T1041P Substitution - Missense 13:20975016-20975016 - TCGA-EE-A184-06 COSM3467651 c.3084C>A p.P1028P Substitution - coding silent 13:20975053-20975053 - CSCC-31-T COSM4566143 c.3155_3156CC>TT p.P1052L Substitution - Missense 13:20974981-20974982 - 16T COSM3711041 c.1179C>T p.H393H Substitution - coding silent 13:20988601-20988601 - Pat_66_A COSM4046455 c.628C>T p.P210S Substitution - Missense 13:20989152-20989152 - T3262 COSM4697518 c.1800C>T p.Y600Y Substitution - coding silent 13:20987980-20987980 - 9121_T COSM5038676 c.247_255delTCCTTGTTG p.S83_L85delSLL Deletion - In frame 13:21045772-21045780 - ESCC-158T COSM3936257 c.597C>T p.D199D Substitution - coding silent 13:20989183-20989183 - 1_PRE-TREATMENT COSM1719349 c.2512C>T p.P838S Substitution - Missense 13:20981619-20981619 - CHC1040T COSM4799506 c.1536G>T p.R512S Substitution - Missense 13:20988244-20988244 - 16929 COSM48481 c.3046G>A p.E1016K Substitution - Missense 13:20975091-20975091 - TCGA-BR-7851-01 COSM4046434 c.2073C>T p.H691H Substitution - coding silent 13:20983633-20983633 - 4 COSM5732133 c.1732G>A p.V578I Substitution - Missense 13:20988048-20988048 - PT13 COSM5896205 c.3232G>A p.D1078N Substitution - Missense 13:20974905-20974905 - TCGA-BR-4368-01 COSM4046455 c.628C>T p.P210S Substitution - Missense 13:20989152-20989152 - CSCC-11-T COSM4516163 c.1638_1639GG>AA p.G547S Substitution - Missense 13:20988141-20988142 - TCGA-CM-5868-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - CRC-06T COSM5456377 c.475+7C>T p.? Unknown 13:20991265-20991265 - TCGA-AA-3712-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-A2-A3XZ-01 COSM3813552 c.531C>A p.G177G Substitution - coding silent 13:20989249-20989249 - CHC884T COSM4958457 c.1099G>T p.V367F Substitution - Missense 13:20988681-20988681 - TCGA-G4-6311-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-CG-5721-01 COSM4046445 c.1033C>T p.Q345* Substitution - Nonsense 13:20988747-20988747 - TCGA-D9-A6EC-06 COSM4402154 c.1098C>T p.S366S Substitution - coding silent 13:20988682-20988682 - ccRCC-47 COSM1662567 c.3128G>T p.R1043L Substitution - Missense 13:20975009-20975009 - HCT-15 COSM1677516 c.2295G>T p.E765D Substitution - Missense 13:20983411-20983411 - CSCC-27-T COSM4494371 c.431C>T p.P144L Substitution - Missense 13:20991316-20991316 - SA214 COSM212218 c.3200A>C p.E1067A Substitution - Missense 13:20974937-20974937 - TCGA-HT-8113-01 COSM3968563 c.2186T>A p.V729D Substitution - Missense 13:20983520-20983520 - TCGA-BR-6852-01 COSM4046439 c.1611C>T p.C537C Substitution - coding silent 13:20988169-20988169 - CSCC-42-T COSM4486103 c.3011C>T p.P1004L Substitution - Missense 13:20975126-20975126 - 1_PRE-TREATMENT COSM1719348 c.2512C>T p.P838S Substitution - Missense 13:20981619-20981619 - CHEWS018 COSM4575865 c.2792C>T p.T931M Substitution - Missense 13:20975345-20975345 - Gp2D COSM2265628 c.3257T>C p.V1086A Substitution - Missense 13:20974880-20974880 - CRC-02T COSM5454209 c.2872C>T p.R958C Substitution - Missense 13:20975265-20975265 - TCGA-A5-A0VQ-01 COSM1152607 c.1741C>T p.R581C Substitution - Missense 13:20988039-20988039 - 2 COSM4172098 c.424C>A p.L142M Substitution - Missense 13:20991323-20991323 - sysucc-1370T COSM5470141 c.936C>T p.Y312Y Substitution - coding silent 13:20988844-20988844 - TCGA-FW-A3R5-06 COSM3885085 c.496C>T p.P166S Substitution - Missense 13:20989284-20989284 - HCT15 COSM1677514 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - EV001-R3 COSM1161920 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-F4-6703-01 COSM1365811 c.2308T>C p.F770L Substitution - Missense 13:20983398-20983398 - TCGA-F4-6570-01 COSM1365823 c.47G>A p.R16Q Substitution - Missense 13:21045980-21045980 - TCGA-EE-A2MF-06 COSM4402155 c.1098C>T p.S366S Substitution - coding silent 13:20988682-20988682 - ESO-0013 COSM1256342 c.1994A>G p.K665R Substitution - Missense 13:20983712-20983712 - BK0057 COSM4188245 c.2063T>G p.V688G Substitution - Missense 13:20983643-20983643 - HCC132 COSM1606909 c.228C>T p.A76A Substitution - coding silent 13:21045799-21045799 - S01578 COSM5670301 c.1440T>C p.A480A Substitution - coding silent 13:20988340-20988340 - TCGA-EE-A2A0-06 COSM3467654 c.2113C>T p.L705L Substitution - coding silent 13:20983593-20983593 - sysucc-1163T COSM2265720 c.1151C>T p.P384L Substitution - Missense 13:20988629-20988629 - NOKSI COSM4595936 c.1681G>A p.A561T Substitution - Missense 13:20988099-20988099 - TCGA-36-1568-01 COSM77997 c.215C>T p.P72L Substitution - Missense 13:21045812-21045812 - HCT15 COSM1677515 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - TCGA-EE-A2MF-06 COSM4402154 c.1098C>T p.S366S Substitution - coding silent 13:20988682-20988682 - MO_1012 COSM5547120 c.664delC p.H222fs*18 Deletion - Frameshift 13:20989116-20989116 - TCGA-BR-8372-01 COSM1586989 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - TCGA-FW-A3R5-06 COSM3885086 c.496C>T p.P166S Substitution - Missense 13:20989284-20989284 - 61 COSM5739904 c.289G>A p.A97T Substitution - Missense 13:21045738-21045738 - 587342 COSM1213133 c.1172G>A p.R391H Substitution - Missense 13:20988608-20988608 - TCGA-BS-A0UV-01 COSM1586999 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - DLD1 COSM1677515 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - T3262 COSM4697517 c.1800C>T p.Y600Y Substitution - coding silent 13:20987980-20987980 - 107430 COSM94599 c.536C>T p.S179L Substitution - Missense 13:20989244-20989244 - EV001-R3 COSM1161919 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - H1703 COSM1196658 c.3232G>T p.D1078Y Substitution - Missense 13:20974905-20974905 - TCGA-FP-7735-01 COSM4046426 c.2494A>G p.R832G Substitution - Missense 13:20981637-20981637 - TCGA-D1-A17Q-01 COSM1587001 c.3160C>T p.R1054* Substitution - Nonsense 13:20974977-20974977 - TCGA-BR-8680-01 COSM4046430 c.2429T>C p.F810S Substitution - Missense 13:20983277-20983277 - OSCC-GB_00990111 COSM4885820 c.2238C>A p.D746E Substitution - Missense 13:20983468-20983468 - LOVO COSM1147169 c.1547C>T p.P516L Substitution - Missense 13:20988233-20988233 - TCGA-AA-A00N-01 COSM275827 c.2028C>T p.I676I Substitution - coding silent 13:20983678-20983678 - CHC1148T COSM4954576 c.2912C>T p.P971L Substitution - Missense 13:20975225-20975225 - 587342 COSM1213134 c.1172G>A p.R391H Substitution - Missense 13:20988608-20988608 - PTC-28C COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - HCT-15 COSM1677513 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - 587284 COSM1213131 c.623C>T p.P208L Substitution - Missense 13:20989157-20989157 - RKO COSM2265696 c.1706A>G p.D569G Substitution - Missense 13:20988074-20988074 - LUAD-5V8LT COSM401407 c.314A>C p.Q105P Substitution - Missense 13:21045713-21045713 - sysucc-834T COSM5485653 c.605C>T p.T202M Substitution - Missense 13:20989175-20989175 - TCGA-EL-A3T3-01 COSM3369041 c.1143G>T p.L381L Substitution - coding silent 13:20988637-20988637 - C008 COSM5522998 c.1139C>T p.S380F Substitution - Missense 13:20988641-20988641 - TCGA-AA-3713-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - HCT8 COSM1677515 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - TCGA-BR-8487-01 COSM4046447 c.991C>A p.L331M Substitution - Missense 13:20988789-20988789 - C086 COSM5533682 c.2746C>T p.P916S Substitution - Missense 13:20979717-20979717 - ESCC-158T COSM3936256 c.597C>T p.D199D Substitution - coding silent 13:20989183-20989183 - PTC-73C COSM4147631 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - T2269 COSM4697509 c.3261C>T p.Y1087Y Substitution - coding silent 13:20974876-20974876 - TCGA-B5-A0JY-01 COSM1586984 c.166G>T p.D56Y Substitution - Missense 13:21045861-21045861 - TCGA-BT-A20J-01 COSM416417 c.1573C>T p.R525C Substitution - Missense 13:20988207-20988207 - RMS105_ COSM4986199 c.475+1G>A p.? Unknown 13:20991271-20991271 - CSCC-32-T COSM4482969 c.2659C>T p.R887C Substitution - Missense 13:20981472-20981472 - RK308_C01 COSM3744084 c.2882G>A p.R961Q Substitution - Missense 13:20975255-20975255 - CSCC-10-T COSM4509927 c.821C>T p.S274F Substitution - Missense 13:20988959-20988959 - CSCC-27-T COSM4494370 c.431C>T p.P144L Substitution - Missense 13:20991316-20991316 - AOCS-095-3-1 COSM3981954 c.2316C>G p.I772M Substitution - Missense 13:20983390-20983390 - ESO-717 COSM1242455 c.2587A>G p.K863E Substitution - Missense 13:20981544-20981544 - TCGA-B5-A11E-01 COSM1586994 c.2317G>A p.A773T Substitution - Missense 13:20983389-20983389 - CHC1040T COSM4799507 c.1536G>T p.R512S Substitution - Missense 13:20988244-20988244 - TCGA-CG-5721-01 COSM4046449 c.949C>T p.H317Y Substitution - Missense 13:20988831-20988831 - TCGA-D5-6931-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - 587278 COSM1213129 c.1243C>T p.R415W Substitution - Missense 13:20988537-20988537 - TCGA-BR-7851-01 COSM4046428 c.2475C>T p.Y825Y Substitution - coding silent 13:20983231-20983231 - AOCS-095-3-1 COSM3981955 c.2316C>G p.I772M Substitution - Missense 13:20983390-20983390 - S02248 COSM5679459 c.1407T>G p.P469P Substitution - coding silent 13:20988373-20988373 - PTC-28C COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - SJOS001118_D1 COSM5023221 c.2373C>A p.D791E Substitution - Missense 13:20983333-20983333 - ESO-717 COSM1242456 c.2587A>G p.K863E Substitution - Missense 13:20981544-20981544 - TCGA-F5-6864-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-CI-6624-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - S00934 COSM4147631 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - TCGA-D1-A103-01 COSM1586991 c.1283C>T p.A428V Substitution - Missense 13:20988497-20988497 - HCC37 COSM1606908 c.341A>G p.Q114R Substitution - Missense 13:21045686-21045686 - PD0880a COSM20656 c.2859C>A p.C953* Substitution - Nonsense 13:20975278-20975278 - S02209 COSM4147630 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - CRC-16T COSM1586994 c.2317G>A p.A773T Substitution - Missense 13:20983389-20983389 - TCGA-CW-5589-01 COSM469238 c.1788C>G p.S596R Substitution - Missense 13:20987992-20987992 - EV001-R8 COSM1161919 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-HT-7480-01 COSM2265632 c.3036C>T p.N1012N Substitution - coding silent 13:20975101-20975101 - Gp5D COSM2265697 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - TCGA-AA-3713-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-MU-A51Y-01 COSM4836451 c.3237G>A p.Q1079Q Substitution - coding silent 13:20974900-20974900 - HCC71T COSM3704486 c.64A>G p.I22V Substitution - Missense 13:21045963-21045963 - 8044180 COSM3384761 c.741G>T p.P247P Substitution - coding silent 13:20989039-20989039 - Pat_01_A COSM5842267 c.1097C>T p.S366F Substitution - Missense 13:20988683-20988683 - NB-0419 COSM1285886 c.2679C>A p.L893L Substitution - coding silent 13:20979784-20979784 - A9 COSM5349883 c.2769G>A p.L923L Substitution - coding silent 13:20979694-20979694 - CSCC-31-T COSM4566142 c.3155_3156CC>TT p.P1052L Substitution - Missense 13:20974981-20974982 - TCGA-B5-A11J-01 COSM1586992 c.1489G>A p.A497T Substitution - Missense 13:20988291-20988291 - TCGA-AX-A0J1-01 COSM1586987 c.328G>A p.A110T Substitution - Missense 13:21045699-21045699 - CSCC-42-T COSM1586999 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - TCGA-DB-A4XH-01 COSM3968569 c.573C>T p.Y191Y Substitution - coding silent 13:20989207-20989207 - CSCC-10-T COSM4509926 c.821C>T p.S274F Substitution - Missense 13:20988959-20988959 - ESO-114 COSM1256343 c.359C>G p.A120G Substitution - Missense 13:20991388-20991388 - PD0880a COSM20656 c.2859C>A p.C953* Substitution - Nonsense 13:20975278-20975278 - S00827 COSM5701080 c.1436_1437insCGCCCC p.A480_A481insPA Insertion - In frame 13:20988343-20988344 - H1703 COSM1196657 c.3232G>T p.D1078Y Substitution - Missense 13:20974905-20974905 - TCGA-C5-A1BF-01 COSM1213134 c.1172G>A p.R391H Substitution - Missense 13:20988608-20988608 - TCGA-CM-5868-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - Gp5D COSM2265698 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - HCC132T COSM1606910 c.228C>T p.A76A Substitution - coding silent 13:21045799-21045799 - TCGA-AY-6197-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-AX-A0J1-01 COSM945942 c.328G>A p.A110T Substitution - Missense 13:21045699-21045699 - 537 COSM3722347 c.2562G>A p.L854L Substitution - coding silent 13:20981569-20981569 - PCSI_0588_Pa_P_526 COSM4647689 c.589G>A p.G197S Substitution - Missense 13:20989191-20989191 - CHEWS031 COSM4575868 c.327C>T p.N109N Substitution - coding silent 13:21045700-21045700 - TCGA-DU-7300-01 COSM3968568 c.1493G>T p.G498V Substitution - Missense 13:20988287-20988287 - HCC37T COSM1606908 c.341A>G p.Q114R Substitution - Missense 13:21045686-21045686 - TCGA-AH-6644-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-G4-6293-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AZ-6601-01 COSM1365818 c.574G>A p.E192K Substitution - Missense 13:20989206-20989206 - TCGA-AF-2687-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - T2269 COSM4697510 c.3261C>T p.Y1087Y Substitution - coding silent 13:20974876-20974876 - 9121_T COSM5038677 c.247_255delTCCTTGTTG p.S83_L85delSLL Deletion - In frame 13:21045772-21045780 - PCSI_0216_Pa_P_526 COSM5762240 c.622C>T p.P208S Substitution - Missense 13:20989158-20989158 - sysucc-1397T COSM5473452 c.937G>A p.V313M Substitution - Missense 13:20988843-20988843 - HCT8 COSM4633790 c.978C>T p.H326H Substitution - coding silent 13:20988802-20988802 - TCGA-D1-A17Q-01 COSM945927 c.3160C>T p.R1054* Substitution - Nonsense 13:20974977-20974977 - HCT15 COSM1677513 c.3122C>T p.T1041I Substitution - Missense 13:20975015-20975015 - TCGA-CG-5721-01 COSM4046448 c.949C>T p.H317Y Substitution - Missense 13:20988831-20988831 - C086 COSM5533681 c.2746C>T p.P916S Substitution - Missense 13:20979717-20979717 - PT23_2 COSM5903845 c.581C>T p.P194L Substitution - Missense 13:20989199-20989199 - HCC71T COSM3704487 c.64A>G p.I22V Substitution - Missense 13:21045963-21045963 - TCGA-FP-7735-01 COSM4046427 c.2494A>G p.R832G Substitution - Missense 13:20981637-20981637 - C0041T COSM4152728 c.2126A>G p.Q709R Substitution - Missense 13:20983580-20983580 - RK308_C01 COSM3744085 c.2882G>A p.R961Q Substitution - Missense 13:20975255-20975255 - C008 COSM5522999 c.3080C>T p.S1027L Substitution - Missense 13:20975057-20975057 - 417 COSM4431607 c.2478G>C p.Q826H Substitution - Missense 13:20983228-20983228 - CHC1148T COSM4954576 c.2912C>T p.P971L Substitution - Missense 13:20975225-20975225 - TCGA-13-1409-01 COSM118128 c.2964C>A p.P988P Substitution - coding silent 13:20975173-20975173 - TCGA-EL-A3T3-01 COSM3369042 c.1143G>T p.L381L Substitution - coding silent 13:20988637-20988637 - CSCC-11-T COSM4516162 c.1638_1639GG>AA p.G547S Substitution - Missense 13:20988141-20988142 - SM-4B295 COSM5032725 c.2025G>T p.G675G Substitution - coding silent 13:20983681-20983681 - TCGA-BR-7851-01 COSM4046435 c.2073C>T p.H691H Substitution - coding silent 13:20983633-20983633 - TCGA-AP-A0LM-01 COSM945940 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - RKO COSM4647688 c.589G>A p.G197S Substitution - Missense 13:20989191-20989191 - PCSI_0216_Pa_P_526 COSM5762241 c.622C>T p.P208S Substitution - Missense 13:20989158-20989158 - TCGA-BR-8680-01 COSM4046431 c.2429T>C p.F810S Substitution - Missense 13:20983277-20983277 - TCGA-B5-A0JZ-01 COSM1152606 c.2908C>A p.H970N Substitution - Missense 13:20975229-20975229 - TCGA-BG-A0MU-01 COSM945944 c.238delA p.I80fs*20 Deletion - Frameshift 13:21045789-21045789 - TCGA-B5-A11E-01 COSM945934 c.2317G>A p.A773T Substitution - Missense 13:20983389-20983389 - TCGA-MU-A51Y-01 COSM4836452 c.3237G>A p.Q1079Q Substitution - coding silent 13:20974900-20974900 - TCGA-BM-6198-01 COSM3417420 c.2713G>A p.E905K Substitution - Missense 13:20979750-20979750 - KM12 COSM2265739 c.486C>T p.L162L Substitution - coding silent 13:20989294-20989294 - TCGA-AA-A010-01 COSM282373 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - TCGA-CA-6717-01 COSM1365803 c.2934C>A p.F978L Substitution - Missense 13:20975203-20975203 - KM12 COSM2265641 c.2741delT p.L914fs*10 Deletion - Frameshift 13:20979722-20979722 - HCT8 COSM1677514 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - TCGA-F5-6864-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-CW-5589-01 COSM1135466 c.1788C>G p.S596R Substitution - Missense 13:20987992-20987992 - NB-0419 COSM1285887 c.2679C>A p.L893L Substitution - coding silent 13:20979784-20979784 - sysucc-1370T COSM5470142 c.936C>T p.Y312Y Substitution - coding silent 13:20988844-20988844 - TCGA-BR-4362-01 COSM945940 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - HCC37T COSM1606907 c.341A>G p.Q114R Substitution - Missense 13:21045686-21045686 - TCGA-AZ-6601-01 COSM1365819 c.574G>A p.E192K Substitution - Missense 13:20989206-20989206 - ESO-114 COSM1256344 c.359C>G p.A120G Substitution - Missense 13:20991388-20991388 - TCGA-B5-A0JZ-01 COSM945930 c.2908C>A p.H970N Substitution - Missense 13:20975229-20975229 - TCGA-AA-3662-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AG-3725-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - SJHGG118_A COSM4972024 c.529_530delGG p.G177fs*22 Deletion - Frameshift 13:20989250-20989251 - 1_RESISTANT COSM1721268 c.1424C>T p.P475L Substitution - Missense 13:20988356-20988356 - NOKSI COSM261742 c.1681G>A p.A561T Substitution - Missense 13:20988099-20988099 - LUAD_E00623 COSM353836 c.2568C>T p.T856T Substitution - coding silent 13:20981563-20981563 - 3N44-VS-3T44 COSM4982189 c.806T>C p.V269A Substitution - Missense 13:20988974-20988974 - sysucc-1397T COSM5473450 c.1099G>A p.V367I Substitution - Missense 13:20988681-20988681 - BD165T COSM5506432 c.2040A>T p.G680G Substitution - coding silent 13:20983666-20983666 - BN44 COSM3704484 c.2888G>A p.G963E Substitution - Missense 13:20975249-20975249 - 61 COSM5739905 c.289G>A p.A97T Substitution - Missense 13:21045738-21045738 - TCGA-AP-A0LM-01 COSM1586996 c.2640C>T p.I880I Substitution - coding silent 13:20981491-20981491 - TCGA-F4-6703-01 COSM1365810 c.2308T>C p.F770L Substitution - Missense 13:20983398-20983398 - TARGET-30-PAPUWY COSM1285888 c.3144C>T p.D1048D Substitution - coding silent 13:20974993-20974993 - PCSI_0193_Pa_P COSM3376501 c.432G>A p.P144P Substitution - coding silent 13:20991315-20991315 - C008 COSM5523001 c.1140C>T p.S380S Substitution - coding silent 13:20988640-20988640 - TCGA-F5-6864-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-BR-4184-01 COSM4046424 c.2582C>T p.A861V Substitution - Missense 13:20981549-20981549 - T2769 COSM4697513 c.3127C>T p.R1043* Substitution - Nonsense 13:20975010-20975010 - TCGA-D1-A103-01 COSM945929 c.2922C>T p.S974S Substitution - coding silent 13:20975215-20975215 - SM-4B295 COSM5032726 c.2025G>T p.G675G Substitution - coding silent 13:20983681-20983681 - TCGA-BM-6198-01 COSM3417421 c.2713G>A p.E905K Substitution - Missense 13:20979750-20979750 - TCGA-CL-4957-01 COSM432207 c.1087G>A p.G363S Substitution - Missense 13:20988693-20988693 - TCGA-BR-6452-01 COSM4046450 c.926C>T p.A309V Substitution - Missense 13:20988854-20988854 - 1238_T COSM3955438 c.1846A>G p.T616A Substitution - Missense 13:20987934-20987934 - TCGA-HT-7480-01 COSM2265631 c.3036C>T p.N1012N Substitution - coding silent 13:20975101-20975101 - SJOS001118_D1 COSM5023220 c.2373C>A p.D791E Substitution - Missense 13:20983333-20983333 - CSCC-42-T COSM282373 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - EV001-R2 COSM1161920 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-DM-A1DA-01 COSM1365812 c.2023G>T p.G675W Substitution - Missense 13:20983683-20983683 - TCGA-D1-A103-01 COSM1586998 c.2922C>T p.S974S Substitution - coding silent 13:20975215-20975215 - BK0057 COSM4188246 c.2003_2006delTTGT p.F668fs*28 Deletion - Frameshift 13:20983700-20983703 - PD11368a COSM5786315 c.1493G>A p.G498D Substitution - Missense 13:20988287-20988287 - TCGA-AM-5821-01 COSM3753615 c.81A>G p.K27K Substitution - coding silent 13:21045946-21045946 - TCGA-BR-8487-01 COSM4046452 c.751G>A p.A251T Substitution - Missense 13:20989029-20989029 - TCGA-BS-A0UV-01 COSM945928 c.3115G>A p.E1039K Substitution - Missense 13:20975022-20975022 - KM12 COSM2265740 c.486C>T p.L162L Substitution - coding silent 13:20989294-20989294 - TCGA-AP-A056-01 COSM945943 c.272C>T p.S91L Substitution - Missense 13:21045755-21045755 - TCGA-CI-6619-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-BR-8363-01 COSM4046441 c.1174G>A p.A392T Substitution - Missense 13:20988606-20988606 - CHC884T COSM4958458 c.1099G>T p.V367F Substitution - Missense 13:20988681-20988681 - PTC-88C COSM5446053 c.1413_1414insGCCCCC p.A480_A481insPA Insertion - In frame 13:20988366-20988367 - T28 COSM5342296 c.714C>T p.S238S Substitution - coding silent 13:20989066-20989066 - S01578 COSM5670302 c.1440T>C p.A480A Substitution - coding silent 13:20988340-20988340 - TCGA-AN-A046-01 COSM3813551 c.536C>T p.S179L Substitution - Missense 13:20989244-20989244 - BD167T COSM5501058 c.1584G>A p.S528S Substitution - coding silent 13:20988196-20988196 - BD167T COSM5501059 c.1584G>A p.S528S Substitution - coding silent 13:20988196-20988196 - YUKAT COSM5376502 c.95C>T p.S32F Substitution - Missense 13:21045932-21045932 - PT08_1 COSM5893738 c.98C>T p.S33L Substitution - Missense 13:21045929-21045929 - T3174 COSM4697520 c.1759G>A p.E587K Substitution - Missense 13:20988021-20988021 - PT13 COSM5896206 c.3232G>A p.D1078N Substitution - Missense 13:20974905-20974905 - TCGA-FW-A3R5-06 COSM3885083 c.2018C>T p.T673I Substitution - Missense 13:20983688-20983688 - 1_RESISTANT COSM1719349 c.2512C>T p.P838S Substitution - Missense 13:20981619-20981619 - S00938 COSM5663264 c.2948G>A p.R983Q Substitution - Missense 13:20975189-20975189 - TCGA-A2-A0T5-01 COSM3813545 c.3121A>C p.T1041P Substitution - Missense 13:20975016-20975016 - OSCC-GB_00160111 COSM3711041 c.1179C>T p.H393H Substitution - coding silent 13:20988601-20988601 - QC2-34-T2 COSM5654917 c.562G>A p.G188S Substitution - Missense 13:20989218-20989218 - TCGA-BR-6852-01 COSM4046438 c.1611C>T p.C537C Substitution - coding silent 13:20988169-20988169 - TCGA-DB-A4XH-01 COSM3968570 c.573C>T p.Y191Y Substitution - coding silent 13:20989207-20989207 - CHEWS018 COSM4575864 c.2792C>T p.T931M Substitution - Missense 13:20975345-20975345 - PT08_2 COSM5893738 c.98C>T p.S33L Substitution - Missense 13:21045929-21045929 - CSCC-11-T COSM4504966 c.67C>T p.R23C Substitution - Missense 13:21045960-21045960 - TCGA-F4-6570-01 COSM1365822 c.47G>A p.R16Q Substitution - Missense 13:21045980-21045980 - TCGA-CA-6717-01 COSM1365809 c.2712C>T p.F904F Substitution - coding silent 13:20979751-20979751 - TCGA-B0-5711-01 COSM1135465 c.2164G>T p.E722* Substitution - Nonsense 13:20983542-20983542 - EV001-R8 COSM1161920 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - Pat_01_B COSM5842268 c.1097C>T p.S366F Substitution - Missense 13:20988683-20988683 - T368 COSM4697515 c.2964delC p.Y989fs*17 Deletion - Frameshift 13:20975173-20975173 - 537 COSM3722346 c.2562G>A p.L854L Substitution - coding silent 13:20981569-20981569 - TCGA-CA-6717-01 COSM1365808 c.2712C>T p.F904F Substitution - coding silent 13:20979751-20979751 - CHC1148T COSM4954577 c.2912C>T p.P971L Substitution - Missense 13:20975225-20975225 - sysucc-783T COSM4046438 c.1611C>T p.C537C Substitution - coding silent 13:20988169-20988169 - sysucc-834T COSM5485652 c.605C>T p.T202M Substitution - Missense 13:20989175-20989175 - TCGA-AA-3713-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - BK0057 COSM4188244 c.2063T>G p.V688G Substitution - Missense 13:20983643-20983643 - BN44T COSM3704484 c.2888G>A p.G963E Substitution - Missense 13:20975249-20975249 - S02248 COSM5679458 c.1407T>G p.P469P Substitution - coding silent 13:20988373-20988373 - TCGA-BS-A0UV-01 COSM282373 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - BD165T COSM5506433 c.2040A>T p.G680G Substitution - coding silent 13:20983666-20983666 - TCGA-AA-3663-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-AX-A0J0-01 COSM1586988 c.387C>T p.I129I Substitution - coding silent 13:20991360-20991360 - T8 COSM5342293 c.3105C>T p.H1035H Substitution - coding silent 13:20975032-20975032 - ESCC_47 COSM1192376 c.2276G>A p.R759Q Substitution - Missense 13:20983430-20983430 - DLD1 COSM1677514 c.2305C>T p.R769W Substitution - Missense 13:20983401-20983401 - TCGA-CH-5750-01 COSM1128397 c.2145C>T p.A715A Substitution - coding silent 13:20983561-20983561 - NCI-H2009 COSM12865 c.2775G>A p.V925V Substitution - coding silent 13:20975362-20975362 - CHEWS021 COSM4575866 c.2030G>T p.G677V Substitution - Missense 13:20983676-20983676 - TCGA-BP-4326-01 COSM3360018 c.2176G>A p.E726K Substitution - Missense 13:20983530-20983530 - P05-3852 COSM245406 c.1696G>T p.G566C Substitution - Missense 13:20988084-20988084 - S02284 COSM5684052 c.3037G>T p.D1013Y Substitution - Missense 13:20975100-20975100 - OSCC-GB_00540111 COSM4889450 c.2176G>C p.E726Q Substitution - Missense 13:20983530-20983530 - Gp2D COSM2265698 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - TCGA-FP-A4BE-01 COSM282373 c.3045C>T p.S1015S Substitution - coding silent 13:20975092-20975092 - S01578 COSM4147630 c.1437G>C p.P479P Substitution - coding silent 13:20988343-20988343 - HCC2998 COSM2265653 c.2583G>A p.A861A Substitution - coding silent 13:20981548-20981548 - CRC-06T COSM5456376 c.475+7C>T p.? Unknown 13:20991265-20991265 - 2 COSM4172097 c.424C>A p.L142M Substitution - Missense 13:20991323-20991323 - PCSI_0193_Pa_P COSM3376502 c.432G>A p.P144P Substitution - coding silent 13:20991315-20991315 - S02065 COSM5672587 c.1404G>C p.A468A Substitution - coding silent 13:20988376-20988376 - TCGA-BR-4361-01 COSM4046433 c.2174A>G p.N725S Substitution - Missense 13:20983532-20983532 - TCGA-BT-A20J-01 COSM1133415 c.1573C>T p.R525C Substitution - Missense 13:20988207-20988207 - T8 COSM5342294 c.3105C>T p.H1035H Substitution - coding silent 13:20975032-20975032 - YUKAT COSM5376503 c.95C>T p.S32F Substitution - Missense 13:21045932-21045932 - PT08_1 COSM169171 c.98C>T p.S33L Substitution - Missense 13:21045929-21045929 - EV001-R1 COSM1161919 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - CRC-19T COSM5481115 c.2240A>G p.Y747C Substitution - Missense 13:20983466-20983466 - T368 COSM4697516 c.2964delC p.Y989fs*17 Deletion - Frameshift 13:20975173-20975173 - OSCC-GB_00990111 COSM4885819 c.2238C>A p.D746E Substitution - Missense 13:20983468-20983468 - C709 COSM4443843 c.1920G>T p.E640D Substitution - Missense 13:20983786-20983786 - LOVO COSM695816 c.1547C>T p.P516L Substitution - Missense 13:20988233-20988233 - 61 COSM5739903 c.1531C>T p.R511W Substitution - Missense 13:20988249-20988249 - BCM723T COSM4956238 c.490C>T p.P164S Substitution - Missense 13:20989290-20989290 - PT08_2 COSM169171 c.98C>T p.S33L Substitution - Missense 13:21045929-21045929 - TCGA-AP-A0LM-01 COSM1586989 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - HCC2998 COSM2265652 c.2583G>A p.A861A Substitution - coding silent 13:20981548-20981548 - 10 COSM87704 c.1436_1437insGGGGCG p.P479_A480insGR Insertion - In frame 13:20988343-20988344 - 1238_T COSM3955437 c.1846A>G p.T616A Substitution - Missense 13:20987934-20987934 - TCGA-CA-6717-01 COSM1365802 c.2934C>A p.F978L Substitution - Missense 13:20975203-20975203 - TCGA-B5-A11E-01 COSM1133414 c.1673G>A p.R558H Substitution - Missense 13:20988107-20988107 - TCGA-AN-A046-01 COSM3813547 c.2398G>T p.D800Y Substitution - Missense 13:20983308-20983308 - LIM2405 COSM2265698 c.1659C>T p.G553G Substitution - coding silent 13:20988121-20988121 - TCGA-AM-5821-01 COSM3753614 c.81A>G p.K27K Substitution - coding silent 13:21045946-21045946 - TCGA-18-3409-01 COSM1147169 c.1547C>T p.P516L Substitution - Missense 13:20988233-20988233 - LC_S12 COSM1188678 c.1361C>T p.P454L Substitution - Missense 13:20988419-20988419 - T3024 COSM4697525 c.532G>A p.D178N Substitution - Missense 13:20989248-20989248 - TCGA-A5-A0VQ-01 COSM945936 c.1741C>T p.R581C Substitution - Missense 13:20988039-20988039 - Gp5D COSM2265642 c.2705T>A p.I902N Substitution - Missense 13:20979758-20979758 - TCGA-BS-A0UV-01 COSM1587000 c.3115G>A p.E1039K Substitution - Missense 13:20975022-20975022 - TCGA-BR-8372-01 COSM945940 c.503C>T p.T168M Substitution - Missense 13:20989277-20989277 - EV001-R2 COSM1161919 c.1771G>T p.E591* Substitution - Nonsense 13:20988009-20988009 - TCGA-AY-6196-01 COSM1477132 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - TCGA-FG-A60J-01 COSM3968565 c.1777C>T p.R593C Substitution - Missense 13:20988003-20988003 - T28 COSM5342295 c.714C>T p.S238S Substitution - coding silent 13:20989066-20989066 - S00022 COSM5656454 c.666C>A p.H222Q Substitution - Missense 13:20989114-20989114 - 8044180 COSM3384760 c.741G>T p.P247P Substitution - coding silent 13:20989039-20989039 - TCGA-BR-6452-01 COSM4046451 c.926C>T p.A309V Substitution - Missense 13:20988854-20988854 - TCGA-A6-5656-01 COSM432208 c.971C>T p.A324V Substitution - Missense 13:20988809-20988809 - 587278 COSM1213130 c.1243C>T p.R415W Substitution - Missense 13:20988537-20988537 - RKO COSM4647689 c.589G>A p.G197S Substitution - Missense 13:20989191-20989191 - TCGA-B5-A0JY-01 COSM945945 c.166G>T p.D56Y Substitution - Missense 13:21045861-21045861 - TCGA-G4-6320-01 COSM3688640 c.2645C>T p.P882L Substitution - Missense 13:20981486-20981486 - TCGA-HT-8113-01 COSM3968564 c.2186T>A p.V729D Substitution - Missense 13:20983520-20983520 - TCGA-RP-A695-06 COSM4897136 c.3056C>T p.T1019I Substitution - Missense 13:20975081-20975081 - TCGA-BR-8487-01 COSM4046446 c.991C>A p.L331M Substitution - Missense 13:20988789-20988789 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.78960 13q11-q12 604861

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L775P c.2324T>C 13 21557521 RCCC C A Missense p.E550D c.1650G>T 13 21562269 NB C A Missense p.G218V c.653G>T 13 21563266 LUAD C A Missense p.G498V c.1493G>T 13 21562426 LGG C A Missense p.G803C c.2407G>T 13 21557438 LUAD C A Missense p.R16L c.47G>T 13 21620119 LUAD C A Nonsense p.E722* c.2164G>T 13 21557681 RCCC C T Missense p.A497T c.1489G>A 13 21562430 UCEC C T Missense p.C1083Y c.3248G>A 13 21549028 LUAD C T Missense p.D852N c.2554G>A 13 21555716 BRCA C T Missense p.E1016K c.3046G>A 13 21549230 LUAD C T Missense p.E1016K c.3046G>A 13 21549230 MB C T Missense p.E726K c.2176G>A 13 21557669 RCCC C T Missense p.G851E c.2552G>A 13 21555718 CM C T Missense p.G92S c.274G>A 13 21619892 CM C T Missense p.R558H c.1673G>A 13 21562246 BLCA C T Missense p.V1005I c.3013G>A 13 21549263 LGG G A Missense p.A861V c.2582C>T 13 21555688 BRCA G A Missense p.G909R c.2725G>A 13 21553877 GBM G A Missense p.P210S c.628C>T 13 21563291 STAD G A Missense p.P414L c.1241C>T 13 21562678 LUAD G A Missense p.P577L c.1730C>T 13 21562189 CM G A Missense p.P72L c.215C>T 13 21619951 OV G A Missense p.P996L c.2987C>T 13 21549289 LUAD G A Missense p.R525C c.1573C>T 13 21562346 BLCA G A Missense p.R581C c.1741C>T 13 21562178 UCEC G A Missense p.S366F c.1097C>T 13 21562822 CM G A Missense p.S528L c.1583C>T 13 21562336 LUSC G A Synonymous p.A715A c.2145C>T 13 21557700 PRAD G A Synonymous p.C537C c.1611C>T 13 21562308 STAD G A Synonymous p.D1048D c.3144C>T 13 21549132 NB G A Synonymous p.F216F c.648C>T 13 21563271 CM G A Synonymous p.H393H c.1179C>T 13 21562740 HNSC G A Synonymous p.L705L c.2113C>T 13 21557732 CM G A Synonymous p.L841L c.2523C>T 13 21555747 CM G A Synonymous p.N1012N c.3036C>T 13 21549240 LGG G A Synonymous p.P217P c.651C>T 13 21563268 CM G A Synonymous p.S366S c.1098C>T 13 21562821 CM G A Synonymous p.S822S c.2466C>T 13 21557379 CM G A Synonymous p.Y989Y c.2967C>T 13 21549309 COREAD GCCGGGGCGGGGGCGGGGGCGGGG - InFrameDeletion p.P473_A480delPAPAPAPA c.1416_1439delCCCCGCCCCCGCCCCCGCCCCGGC 13 21562480 BRCA G C Missense p.A120G c.359C>G 13 21565527 ESCA G C Missense p.P190R c.569C>G 13 21563350 BRCA G C Missense p.Q643E c.1927C>G 13 21557918 LUAD G C Missense p.S596R c.1788C>G 13 21562131 RCCC GG AA Missense p.P305L c.913_914delinsTT 13 21563005 CM GG AA Missense p.R623W c.1866_1867delinsTT 13 21562052 CM - GGGGCG InFrameInsertion p.P479_A480insPP c.1437_1438insCCCCCG 13 21562483 PRAD - GGGGCG InFrameInsertion p.P479_A480insPP c.1437_1438insCCCCCG 13 21562483 THCA G T Missense p.H970N c.2908C>A 13 21549368 UCEC G T Missense p.P38H c.113C>A 13 21620053 STAD G T Synonymous p.L893L c.2679C>A 13 21553923 NB G T Synonymous p.P1028P c.3084C>A 13 21549192 CM G T Synonymous p.P988P c.2964C>A 13 21549312 OV T C Missense p.K665R c.1994A>G 13 21557851 ESCA - T Frameshift p.H691Qfs*36 c.2072dupA 13 21557773 RCCC T - Frameshift p.I80Sfs*20 c.238delA 13 21619928 UCEC T G Missense p.E1067A c.3200A>C 13 21549076 BRCA