Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 3 108407467 108407467 + Missense_Mutation SNP A A G TCGA-OR-A5LL-01A-11D-A29I-10 TCGA-OR-A5LL-10A-01D-A29L-10 g.chr3:108407467A>G c.3298A>G c.(3298-3300)Aat>Gat p.N1100D BLCA 3 108343354 108343354 + Missense_Mutation SNP G G A TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr3:108343354G>A c.439G>A c.(439-441)Gaa>Aaa p.E147K BLCA 3 108348003 108348003 + Missense_Mutation SNP G G A TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr3:108348003G>A c.676G>A c.(676-678)Gat>Aat p.D226N BLCA 3 108355502 108355502 + Missense_Mutation SNP G G A TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chr3:108355502G>A c.958G>A c.(958-960)Ggt>Agt p.G320S BLCA 3 108355512 108355512 + Missense_Mutation SNP T T C TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr3:108355512T>C c.968T>C c.(967-969)gTa>gCa p.V323A BLCA 3 108355537 108355537 + Silent SNP T T G TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr3:108355537T>G c.993T>G c.(991-993)ccT>ccG p.P331P BLCA 3 108363112 108363112 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr3:108363112G>A c.1243G>A c.(1243-1245)Gct>Act p.A415T BLCA 3 108363414 108363414 + Missense_Mutation SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr3:108363414G>T c.1545G>T c.(1543-1545)gaG>gaT p.E515D BLCA 3 108363559 108363559 + Nonsense_Mutation SNP C C T TCGA-ZF-A9RN-01A-11D-A42E-08 TCGA-ZF-A9RN-10A-01D-A42H-08 g.chr3:108363559C>T c.1690C>T c.(1690-1692)Cag>Tag p.Q564* BLCA 3 108380728 108380728 + Missense_Mutation SNP C C T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr3:108380728C>T c.2204C>T c.(2203-2205)tCa>tTa p.S735L BLCA 3 108403160 108403160 + Missense_Mutation SNP C C T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr3:108403160C>T c.2981C>T c.(2980-2982)tCt>tTt p.S994F BLCA 3 108407451 108407451 + Silent SNP A A G TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr3:108407451A>G c.3282A>G c.(3280-3282)aaA>aaG p.K1094K BRCA 3 108335487 108335487 + Missense_Mutation SNP C C G TCGA-AR-A1AP-01A-11D-A12Q-09 TCGA-AR-A1AP-10A-01D-A12Q-09 g.chr3:108335487C>G c.358C>G c.(358-360)Caa>Gaa p.Q120E BRCA 3 108344740 108344740 + Nonsense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr3:108344740C>T c.505C>T c.(505-507)Caa>Taa p.Q169* BRCA 3 108355480 108355480 + Missense_Mutation SNP A A T TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr3:108355480A>T c.936A>T c.(934-936)aaA>aaT p.K312N BRCA 3 108361332 108361332 + Missense_Mutation SNP C C T TCGA-AN-A0FW-01A-11W-A050-09 TCGA-AN-A0FW-10A-01W-A055-09 g.chr3:108361332C>T c.1112C>T c.(1111-1113)cCg>cTg p.P371L BRCA 3 108367765 108367765 + Splice_Site SNP G G C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr3:108367765G>C c.1963G>C c.(1963-1965)Gtt>Ctt p.V655L BRCA 3 108388553 108388553 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr3:108388553G>T c.2449G>T c.(2449-2451)Gat>Tat p.D817Y BRCA 3 108388567 108388567 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr3:108388567G>T c.2463G>T c.(2461-2463)aaG>aaT p.K821N BRCA 3 108403129 108403129 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr3:108403129C>G c.2950C>G c.(2950-2952)Caa>Gaa p.Q984E BRCA 3 108407718 108407718 + Silent SNP C C T TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr3:108407718C>T c.3463C>T c.(3463-3465)Ctg>Ttg p.L1155L BRCA 3 108409716 108409716 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr3:108409716A>C c.3599A>C c.(3598-3600)cAc>cCc p.H1200P CESC 3 108351882 108351882 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr3:108351882C>T c.779C>T c.(778-780)tCt>tTt p.S260F CESC 3 108355553 108355553 + Missense_Mutation SNP T T G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr3:108355553T>G c.1009T>G c.(1009-1011)Ttg>Gtg p.L337V CESC 3 108361302 108361302 + Missense_Mutation SNP C C G TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr3:108361302C>G c.1082C>G c.(1081-1083)tCt>tGt p.S361C CESC 3 108366903 108366903 + Missense_Mutation SNP G G T TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chr3:108366903G>T c.1906G>T c.(1906-1908)Gat>Tat p.D636Y CESC 3 108392964 108392964 + Missense_Mutation SNP C C A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr3:108392964C>A c.2629C>A c.(2629-2631)Cat>Aat p.H877N CESC 3 108403096 108403096 + Nonsense_Mutation SNP G G T TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr3:108403096G>T c.2917G>T c.(2917-2919)Gaa>Taa p.E973* CESC 3 108407541 108407541 + Silent SNP C C T TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr3:108407541C>T c.3372C>T c.(3370-3372)ctC>ctT p.L1124L CHOL 3 108344792 108344792 + Missense_Mutation SNP G G T TCGA-WD-A7RX-01A-12D-A417-09 TCGA-WD-A7RX-10A-01D-A41A-09 g.chr3:108344792G>T c.557G>T c.(556-558)gGt>gTt p.G186V CHOL 3 108361320 108361320 + Missense_Mutation SNP C C G TCGA-ZU-A8S4-01A-11D-A417-09 TCGA-ZU-A8S4-10A-01D-A41A-09 g.chr3:108361320C>G c.1100C>G c.(1099-1101)aCt>aGt p.T367S COAD 3 108330025 108330025 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108330025A>C c.107A>C c.(106-108)aAa>aCa p.K36T COAD 3 108353778 108353778 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:108353778delA c.877delA c.(877-879)aaafs p.K294fs COAD 3 108363077 108363077 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:108363077C>T c.1208C>T c.(1207-1209)tCt>tTt p.S403F COAD 3 108363156 108363156 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:108363156G>T c.1287G>T c.(1285-1287)aaG>aaT p.K429N COAD 3 108363176 108363176 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr3:108363176A>G c.1307A>G c.(1306-1308)tAc>tGc p.Y436C COAD 3 108363318 108363319 + Frame_Shift_Ins INS - - A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:108363318_108363319insA c.1449_1450insA c.(1450-1452)aaafs p.K484fs COAD 3 108363342 108363342 + Silent SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr3:108363342G>A c.1473G>A c.(1471-1473)ccG>ccA p.P491P COAD 3 108363417 108363417 + Silent SNP T T A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108363417T>A c.1548T>A c.(1546-1548)atT>atA p.I516I COAD 3 108373053 108373053 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr3:108373053A>G c.2095A>G c.(2095-2097)Agt>Ggt p.S699G COAD 3 108373068 108373068 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108373068G>T c.2110G>T c.(2110-2112)Gat>Tat p.D704Y COAD 3 108380750 108380750 + Silent SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr3:108380750C>T c.2226C>T c.(2224-2226)gaC>gaT p.D742D COAD 3 108391418 108391418 + Missense_Mutation SNP A A G TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr3:108391418A>G c.2504A>G c.(2503-2505)gAa>gGa p.E835G COAD 3 108394662 108394662 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr3:108394662C>T c.2723C>T c.(2722-2724)gCg>gTg p.A908V COAD 3 108406841 108406841 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr3:108406841C>A c.3168C>A c.(3166-3168)ttC>ttA p.F1056L COAD 3 108406861 108406861 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:108406861C>T c.3188C>T c.(3187-3189)gCt>gTt p.A1063V COAD 3 108406945 108406945 + Splice_Site SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:108406945T>C c.e29+2 COADREAD 3 108324275 108324275 + Frame_Shift_Del DEL T T - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:108324275delT c.22delT c.(22-24)tttfs p.F9fs COADREAD 3 108330025 108330025 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108330025A>C c.107A>C c.(106-108)aAa>aCa p.K36T COADREAD 3 108330154 108330154 + Missense_Mutation SNP A A G TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr3:108330154A>G c.236A>G c.(235-237)gAt>gGt p.D79G COADREAD 3 108353778 108353778 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:108353778delA c.877delA c.(877-879)aaafs p.K294fs COADREAD 3 108363077 108363077 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:108363077C>T c.1208C>T c.(1207-1209)tCt>tTt p.S403F COADREAD 3 108363156 108363156 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr3:108363156G>T c.1287G>T c.(1285-1287)aaG>aaT p.K429N COADREAD 3 108363176 108363176 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr3:108363176A>G c.1307A>G c.(1306-1308)tAc>tGc p.Y436C COADREAD 3 108363318 108363319 + Frame_Shift_Ins INS - - A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:108363318_108363319insA c.1449_1450insA c.(1450-1452)aaafs p.K484fs COADREAD 3 108363342 108363342 + Silent SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr3:108363342G>A c.1473G>A c.(1471-1473)ccG>ccA p.P491P COADREAD 3 108363417 108363417 + Silent SNP T T A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108363417T>A c.1548T>A c.(1546-1548)atT>atA p.I516I COADREAD 3 108373053 108373053 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr3:108373053A>G c.2095A>G c.(2095-2097)Agt>Ggt p.S699G COADREAD 3 108373068 108373068 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:108373068G>T c.2110G>T c.(2110-2112)Gat>Tat p.D704Y COADREAD 3 108380750 108380750 + Silent SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr3:108380750C>T c.2226C>T c.(2224-2226)gaC>gaT p.D742D COADREAD 3 108381086 108381086 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:108381086G>A c.2405G>A c.(2404-2406)gGa>gAa p.G802E COADREAD 3 108391418 108391418 + Missense_Mutation SNP A A G TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr3:108391418A>G c.2504A>G c.(2503-2505)gAa>gGa p.E835G COADREAD 3 108391419 108391419 + Silent SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr3:108391419A>G c.2505A>G c.(2503-2505)gaA>gaG p.E835E COADREAD 3 108394662 108394662 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr3:108394662C>T c.2723C>T c.(2722-2724)gCg>gTg p.A908V COADREAD 3 108406841 108406841 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr3:108406841C>A c.3168C>A c.(3166-3168)ttC>ttA p.F1056L COADREAD 3 108406861 108406861 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:108406861C>T c.3188C>T c.(3187-3189)gCt>gTt p.A1063V COADREAD 3 108406945 108406945 + Splice_Site SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:108406945T>C c.e29+2 ESCA 3 108353773 108353773 + Missense_Mutation SNP G G T TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr3:108353773G>T c.872G>T c.(871-873)tGc>tTc p.C291F ESCA 3 108363103 108363103 + Missense_Mutation SNP T T C TCGA-V5-A7RC-01B-11D-A403-09 TCGA-V5-A7RC-10A-01D-A403-09 g.chr3:108363103T>C c.1234T>C c.(1234-1236)Ttt>Ctt p.F412L ESCA 3 108394694 108394694 + Missense_Mutation SNP G G T TCGA-JY-A938-01A-11D-A37C-09 TCGA-JY-A938-10A-01D-A37F-09 g.chr3:108394694G>T c.2755G>T c.(2755-2757)Gtt>Ttt p.V919F GBM 3 108353719 108353719 + Splice_Site SNP G G T TCGA-06-0216-01B-01D-1492-08 TCGA-06-0216-10A-01D-1492-08 g.chr3:108353719G>T c.818G>T c.(817-819)gGa>gTa p.G273V GBMLGG 3 108335404 108335404 + Missense_Mutation SNP A A G TCGA-E1-A7YU-01A-11D-A34J-08 TCGA-E1-A7YU-10A-01D-A34M-08 g.chr3:108335404A>G c.275A>G c.(274-276)aAc>aGc p.N92S GBMLGG 3 108351853 108351853 + Silent SNP G G A TCGA-TQ-A7RM-01A-11D-A33T-08 TCGA-TQ-A7RM-10A-01D-A33W-08 g.chr3:108351853G>A c.750G>A c.(748-750)acG>acA p.T250T GBMLGG 3 108353719 108353719 + Splice_Site SNP G G T TCGA-06-0216-01B-01D-1492-08 TCGA-06-0216-10A-01D-1492-08 g.chr3:108353719G>T c.818G>T c.(817-819)gGa>gTa p.G273V GBMLGG 3 108353774 108353774 + Silent SNP C C T TCGA-DU-A76R-01A-11D-A32B-08 TCGA-DU-A76R-10A-01D-A329-08 g.chr3:108353774C>T c.873C>T c.(871-873)tgC>tgT p.C291C GBMLGG 3 108363603 108363603 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:108363603G>T c.1734G>T c.(1732-1734)caG>caT p.Q578H GBMLGG 3 108366851 108366851 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:108366851C>T c.1854C>T c.(1852-1854)taC>taT p.Y618Y HNSC 3 108324266 108324266 + Missense_Mutation SNP C C G TCGA-QK-A6VC-01A-23D-A34J-08 TCGA-QK-A6VC-10B-01D-A34M-08 g.chr3:108324266C>G c.13C>G c.(13-15)Cca>Gca p.P5A HNSC 3 108326985 108326985 + Missense_Mutation SNP G G C TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr3:108326985G>C c.82G>C c.(82-84)Gaa>Caa p.E28Q HNSC 3 108335438 108335438 + Silent SNP G G A TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr3:108335438G>A c.309G>A c.(307-309)ttG>ttA p.L103L HNSC 3 108344785 108344785 + Nonsense_Mutation SNP G G T TCGA-CN-6012-01A-11D-1683-08 TCGA-CN-6012-10A-01D-1683-08 g.chr3:108344785G>T c.550G>T c.(550-552)Gga>Tga p.G184* HNSC 3 108353773 108353773 + Missense_Mutation SNP G G T TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr3:108353773G>T c.872G>T c.(871-873)tGc>tTc p.C291F HNSC 3 108355484 108355484 + Missense_Mutation SNP T T A TCGA-CV-7421-01A-11D-2078-08 TCGA-CV-7421-10A-01D-2078-08 g.chr3:108355484T>A c.940T>A c.(940-942)Ttg>Atg p.L314M HNSC 3 108355486 108355486 + Missense_Mutation SNP G G C TCGA-BB-8596-01A-11D-2394-08 TCGA-BB-8596-10A-01D-2394-08 g.chr3:108355486G>C c.942G>C c.(940-942)ttG>ttC p.L314F HNSC 3 108363276 108363276 + Silent SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr3:108363276C>T c.1407C>T c.(1405-1407)ctC>ctT p.L469L HNSC 3 108366924 108366924 + Missense_Mutation SNP G G A TCGA-BA-A8YP-01A-11D-A391-08 TCGA-BA-A8YP-10A-01D-A394-08 g.chr3:108366924G>A c.1927G>A c.(1927-1929)Gaa>Aaa p.E643K HNSC 3 108373010 108373010 + Missense_Mutation SNP G G T TCGA-CR-7399-01A-11D-2012-08 TCGA-CR-7399-10A-01D-2013-08 g.chr3:108373010G>T c.2052G>T c.(2050-2052)aaG>aaT p.K684N HNSC 3 108373044 108373044 + Missense_Mutation SNP C C T TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr3:108373044C>T c.2086C>T c.(2086-2088)Cac>Tac p.H696Y HNSC 3 108373054 108373054 + Missense_Mutation SNP G G A TCGA-QK-A8Z7-01A-11D-A391-08 TCGA-QK-A8Z7-10A-01D-A394-08 g.chr3:108373054G>A c.2096G>A c.(2095-2097)aGt>aAt p.S699N HNSC 3 108380811 108380811 + Nonsense_Mutation SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr3:108380811C>T c.2287C>T c.(2287-2289)Cag>Tag p.Q763* HNSC 3 108391474 108391474 + Missense_Mutation SNP G G A TCGA-CV-A6JD-01A-11D-A31L-08 TCGA-CV-A6JD-10A-01D-A31J-08 g.chr3:108391474G>A c.2560G>A c.(2560-2562)Gca>Aca p.A854T HNSC 3 108393015 108393015 + Missense_Mutation SNP C C G TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr3:108393015C>G c.2680C>G c.(2680-2682)Cac>Gac p.H894D HNSC 3 108394684 108394685 + Frame_Shift_Del DEL TG TG - TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr3:108394684_108394685delTG c.2745_2746delTG c.(2743-2748)attgtgfs p.V916fs HNSC 3 108396445 108396445 + Splice_Site SNP G G A TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chr3:108396445G>A c.2883G>A c.(2881-2883)ctG>ctA p.L961L HNSC 3 108403092 108403092 + Silent SNP G G C TCGA-CN-5363-01A-01D-1434-08 TCGA-CN-5363-10A-01D-1434-08 g.chr3:108403092G>C c.2913G>C c.(2911-2913)gtG>gtC p.V971V KIPAN 3 108324275 108324275 + Frame_Shift_Del DEL T T - TCGA-HE-7128-01A-11D-1961-08 TCGA-HE-7128-10A-01D-1962-08 g.chr3:108324275delT c.22delT c.(22-24)tttfs p.F9fs KIRP 3 108324275 108324275 + Frame_Shift_Del DEL T T - TCGA-HE-7128-01A-11D-1961-08 TCGA-HE-7128-10A-01D-1962-08 g.chr3:108324275delT c.22delT c.(22-24)tttfs p.F9fs LGG 3 108335404 108335404 + Missense_Mutation SNP A A G TCGA-E1-A7YU-01A-11D-A34J-08 TCGA-E1-A7YU-10A-01D-A34M-08 g.chr3:108335404A>G c.275A>G c.(274-276)aAc>aGc p.N92S LGG 3 108351853 108351853 + Silent SNP G G A TCGA-TQ-A7RM-01A-11D-A33T-08 TCGA-TQ-A7RM-10A-01D-A33W-08 g.chr3:108351853G>A c.750G>A c.(748-750)acG>acA p.T250T LGG 3 108353774 108353774 + Silent SNP C C T TCGA-DU-A76R-01A-11D-A32B-08 TCGA-DU-A76R-10A-01D-A329-08 g.chr3:108353774C>T c.873C>T c.(871-873)tgC>tgT p.C291C LGG 3 108363603 108363603 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:108363603G>T c.1734G>T c.(1732-1734)caG>caT p.Q578H LGG 3 108366851 108366851 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:108366851C>T c.1854C>T c.(1852-1854)taC>taT p.Y618Y LIHC 3 108347953 108347953 + Missense_Mutation SNP T T C TCGA-RC-A7SK-01A-11D-A34Z-10 TCGA-RC-A7SK-10A-01D-A34Z-10 g.chr3:108347953T>C c.626T>C c.(625-627)aTt>aCt p.I209T LIHC 3 108366815 108366815 + Missense_Mutation SNP T T A TCGA-DD-AAEG-01A-11D-A38X-10 TCGA-DD-AAEG-10A-01D-A38X-10 g.chr3:108366815T>A c.1818T>A c.(1816-1818)aaT>aaA p.N606K LIHC 3 108367792 108367792 + Missense_Mutation SNP A A G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr3:108367792A>G c.1990A>G c.(1990-1992)Aag>Gag p.K664E LIHC 3 108373044 108373044 + Missense_Mutation SNP C C T TCGA-DD-A4NO-01A-11D-A28X-10 TCGA-DD-A4NO-10A-01D-A28X-10 g.chr3:108373044C>T c.2086C>T c.(2086-2088)Cac>Tac p.H696Y LIHC 3 108373111 108373111 + Missense_Mutation SNP A A G TCGA-DD-AACC-01A-11D-A40R-10 TCGA-DD-AACC-10A-01D-A40U-10 g.chr3:108373111A>G c.2153A>G c.(2152-2154)aAg>aGg p.K718R LIHC 3 108380762 108380762 + Silent SNP T T A TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr3:108380762T>A c.2238T>A c.(2236-2238)acT>acA p.T746T LIHC 3 108396342 108396342 + Splice_Site SNP A A T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr3:108396342A>T c.e26-1 LIHC 3 108396438 108396438 + Missense_Mutation SNP A A T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr3:108396438A>T c.2876A>T c.(2875-2877)gAg>gTg p.E959V LIHC 3 108407715 108407715 + Missense_Mutation SNP A A T TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr3:108407715A>T c.3460A>T c.(3460-3462)Aat>Tat p.N1154Y LUAD 3 108327004 108327004 + Splice_Site SNP T T A TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr3:108327004T>A c.101T>A c.(100-102)cTg>cAg p.L34Q LUAD 3 108343296 108343296 + Missense_Mutation SNP C C G TCGA-17-Z023-01A-01W-0746-08 TCGA-17-Z023-11A-01W-0746-08 g.chr3:108343296C>G c.381C>G c.(379-381)caC>caG p.H127Q LUAD 3 108343371 108343371 + Splice_Site SNP G G T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr3:108343371G>T c.456G>T c.(454-456)gaG>gaT p.E152D LUAD 3 108344739 108344739 + Silent SNP C C A TCGA-17-Z017-01A-01W-0746-08 TCGA-17-Z017-11A-01W-0746-08 g.chr3:108344739C>A c.504C>A c.(502-504)atC>atA p.I168I LUAD 3 108353773 108353773 + Missense_Mutation SNP G G T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr3:108353773G>T c.872G>T c.(871-873)tGc>tTc p.C291F LUAD 3 108353817 108353817 + Nonsense_Mutation SNP C C T TCGA-38-4629-01A-02D-1265-08 TCGA-38-4629-11A-01D-1265-08 g.chr3:108353817C>T c.916C>T c.(916-918)Cag>Tag p.Q306* LUAD 3 108355508 108355508 + Missense_Mutation SNP A A C TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr3:108355508A>C c.964A>C c.(964-966)Atg>Ctg p.M322L LUAD 3 108355516 108355516 + Missense_Mutation SNP G G T TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr3:108355516G>T c.972G>T c.(970-972)agG>agT p.R324S LUAD 3 108363053 108363053 + Missense_Mutation SNP A A G TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chr3:108363053A>G c.1184A>G c.(1183-1185)cAt>cGt p.H395R LUAD 3 108363053 108363053 + Missense_Mutation SNP A A T TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr3:108363053A>T c.1184A>T c.(1183-1185)cAt>cTt p.H395L LUAD 3 108363233 108363233 + Missense_Mutation SNP C C A TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr3:108363233C>A c.1364C>A c.(1363-1365)cCt>cAt p.P455H LUAD 3 108363265 108363265 + Missense_Mutation SNP G G C TCGA-99-8033-01A-11D-2238-08 TCGA-99-8033-10A-01D-2238-08 g.chr3:108363265G>C c.1396G>C c.(1396-1398)Gac>Cac p.D466H LUAD 3 108363427 108363427 + Missense_Mutation SNP G G T TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr3:108363427G>T c.1558G>T c.(1558-1560)Ggt>Tgt p.G520C LUAD 3 108363525 108363525 + Missense_Mutation SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr3:108363525G>T c.1656G>T c.(1654-1656)gaG>gaT p.E552D LUAD 3 108366847 108366847 + Frame_Shift_Del DEL A A - TCGA-78-7153-01A-11D-2036-08 TCGA-78-7153-10A-01D-2036-08 g.chr3:108366847delA c.1850delA c.(1849-1851)gagfs p.E617fs LUAD 3 108366907 108366907 + Missense_Mutation SNP G G T TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr3:108366907G>T c.1910G>T c.(1909-1911)gGg>gTg p.G637V LUAD 3 108380804 108380804 + Missense_Mutation SNP G G C TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr3:108380804G>C c.2280G>C c.(2278-2280)ttG>ttC p.L760F LUAD 3 108388547 108388547 + Missense_Mutation SNP G G C TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr3:108388547G>C c.2443G>C c.(2443-2445)Gct>Cct p.A815P LUAD 3 108391450 108391450 + Missense_Mutation SNP A A G TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr3:108391450A>G c.2536A>G c.(2536-2538)Aaa>Gaa p.K846E LUAD 3 108392970 108392970 + Nonsense_Mutation SNP G G T TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr3:108392970G>T c.2635G>T c.(2635-2637)Gag>Tag p.E879* LUAD 3 108394644 108394644 + Nonsense_Mutation SNP C C G TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr3:108394644C>G c.2705C>G c.(2704-2706)tCa>tGa p.S902* LUAD 3 108396394 108396394 + Missense_Mutation SNP T T A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr3:108396394T>A c.2832T>A c.(2830-2832)agT>agA p.S944R LUAD 3 108403079 108403079 + Missense_Mutation SNP G G T TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr3:108403079G>T c.2900G>T c.(2899-2901)gGa>gTa p.G967V LUAD 3 108403121 108403121 + Missense_Mutation SNP C C T TCGA-75-5125-01A-01D-1753-08 TCGA-75-5125-10A-01D-1753-08 g.chr3:108403121C>T c.2942C>T c.(2941-2943)aCt>aTt p.T981I LUAD 3 108403123 108403123 + Missense_Mutation SNP G G C TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr3:108403123G>C c.2944G>C c.(2944-2946)Gtt>Ctt p.V982L LUAD 3 108403130 108403130 + Frame_Shift_Del DEL A A - TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr3:108403130delA c.2951delA c.(2950-2952)caafs p.Q984fs LUAD 3 108403180 108403181 + Frame_Shift_Ins INS - - C TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr3:108403180_108403181insC c.3001_3002insC c.(3001-3003)gccfs p.A1001fs LUAD 3 108405387 108405387 + Missense_Mutation SNP G G T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr3:108405387G>T c.3105G>T c.(3103-3105)gaG>gaT p.E1035D LUAD 3 108406848 108406848 + Missense_Mutation SNP A A G TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr3:108406848A>G c.3175A>G c.(3175-3177)Aaa>Gaa p.K1059E LUAD 3 108407534 108407534 + Missense_Mutation SNP G G A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr3:108407534G>A c.3365G>A c.(3364-3366)aGg>aAg p.R1122K LUAD 3 108407548 108407548 + Missense_Mutation SNP C C A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr3:108407548C>A c.3379C>A c.(3379-3381)Cag>Aag p.Q1127K LUSC 3 108363257 108363257 + Missense_Mutation SNP A A T TCGA-43-3920-01A-01D-0983-08 TCGA-43-3920-10A-01D-0983-08 g.chr3:108363257A>T c.1388A>T c.(1387-1389)aAa>aTa p.K463I LUSC 3 108363259 108363259 + Nonsense_Mutation SNP C C T TCGA-22-1002-01A-01D-1521-08 TCGA-22-1002-11A-01D-1521-08 g.chr3:108363259C>T c.1390C>T c.(1390-1392)Cag>Tag p.Q464* LUSC 3 108373066 108373066 + Missense_Mutation SNP A A T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr3:108373066A>T c.2108A>T c.(2107-2109)aAa>aTa p.K703I LUSC 3 108391468 108391468 + Missense_Mutation SNP C C A TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chr3:108391468C>A c.2554C>A c.(2554-2556)Ctg>Atg p.L852M LUSC 3 108394691 108394691 + Missense_Mutation SNP G G A TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr3:108394691G>A c.2752G>A c.(2752-2754)Gat>Aat p.D918N LUSC 3 108403065 108403065 + Missense_Mutation SNP G G T TCGA-60-2723-01A-01D-1522-08 TCGA-60-2723-11A-01D-1522-08 g.chr3:108403065G>T c.2886G>T c.(2884-2886)atG>atT p.M962I LUSC 3 108403129 108403129 + Missense_Mutation SNP C C G TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr3:108403129C>G c.2950C>G c.(2950-2952)Caa>Gaa p.Q984E LUSC 3 108406926 108406926 + Missense_Mutation SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr3:108406926G>A c.3253G>A c.(3253-3255)Gac>Aac p.D1085N LUSC 3 108409675 108409675 + Silent SNP G G A TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr3:108409675G>A c.3558G>A c.(3556-3558)acG>acA p.T1186T OV 3 108363568 108363568 + Missense_Mutation SNP G G C TCGA-13-0762-01A-01W-0370-10 TCGA-13-0762-10A-01W-0370-10 g.chr3:108363568G>C c.1699G>C c.(1699-1701)Gtc>Ctc p.V567L PAAD 3 108335411 108335411 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:108335411G>A c.282G>A c.(280-282)caG>caA p.Q94Q PAAD 3 108353719 108353719 + Splice_Site SNP G G C TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr3:108353719G>C c.818G>C c.(817-819)gGa>gCa p.G273A PAAD 3 108363319 108363319 + Frame_Shift_Del DEL A A - TCGA-RB-AA9M-01A-11D-A397-08 TCGA-RB-AA9M-10A-01D-A39A-08 g.chr3:108363319delA c.1450delA c.(1450-1452)aaafs p.K485fs PAAD 3 108363319 108363319 + Frame_Shift_Del DEL A A - TCGA-US-A776-01A-13D-A33T-08 TCGA-US-A776-11A-11D-A33W-08 g.chr3:108363319delA c.1450delA c.(1450-1452)aaafs p.K485fs PAAD 3 108363438 108363438 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:108363438G>A c.1569G>A c.(1567-1569)gaG>gaA p.E523E PAAD 3 108366893 108366893 + Missense_Mutation SNP A A C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:108366893A>C c.1896A>C c.(1894-1896)gaA>gaC p.E632D PAAD 3 108381086 108381086 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:108381086G>A c.2405G>A c.(2404-2406)gGa>gAa p.G802E PAAD 3 108394663 108394663 + Silent SNP G G A TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr3:108394663G>A c.2724G>A c.(2722-2724)gcG>gcA p.A908A PRAD 3 108347996 108347996 + Silent SNP A A G TCGA-EJ-5504-01A-01D-1576-08 TCGA-EJ-5504-10A-01D-1577-08 g.chr3:108347996A>G c.669A>G c.(667-669)gaA>gaG p.E223E PRAD 3 108363248 108363248 + Missense_Mutation SNP C C T TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr3:108363248C>T c.1379C>T c.(1378-1380)cCg>cTg p.P460L PRAD 3 108363630 108363630 + Splice_Site SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:108363630T>C c.e14+2 PRAD 3 108391473 108391473 + Silent SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr3:108391473C>T c.2559C>T c.(2557-2559)aaC>aaT p.N853N READ 3 108324275 108324275 + Frame_Shift_Del DEL T T - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:108324275delT c.22delT c.(22-24)tttfs p.F9fs READ 3 108330154 108330154 + Missense_Mutation SNP A A G TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr3:108330154A>G c.236A>G c.(235-237)gAt>gGt p.D79G READ 3 108381086 108381086 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:108381086G>A c.2405G>A c.(2404-2406)gGa>gAa p.G802E READ 3 108391419 108391419 + Silent SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr3:108391419A>G c.2505A>G c.(2503-2505)gaA>gaG p.E835E SARC 3 108361310 108361310 + Missense_Mutation SNP A A G TCGA-DX-AB2J-01A-11D-A387-09 TCGA-DX-AB2J-10A-01D-A38A-09 g.chr3:108361310A>G c.1090A>G c.(1090-1092)Ata>Gta p.I364V SARC 3 108406846 108406846 + Missense_Mutation SNP G G A TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr3:108406846G>A c.3173G>A c.(3172-3174)cGg>cAg p.R1058Q SKCM 3 108330161 108330161 + Silent SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr3:108330161C>T c.243C>T c.(241-243)tcC>tcT p.S81S SKCM 3 108363029 108363029 + Missense_Mutation SNP A A T TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr3:108363029A>T c.1160A>T c.(1159-1161)aAg>aTg p.K387M SKCM 3 108363052 108363052 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:108363052C>T c.1183C>T c.(1183-1185)Cat>Tat p.H395Y SKCM 3 108363184 108363184 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:108363184C>T c.1315C>T c.(1315-1317)Ctt>Ttt p.L439F SKCM 3 108363192 108363192 + Silent SNP C C T TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr3:108363192C>T c.1323C>T c.(1321-1323)acC>acT p.T441T SKCM 3 108363472 108363472 + Missense_Mutation SNP G G A TCGA-EE-A29N-06A-12D-A197-08 TCGA-EE-A29N-10A-01D-A199-08 g.chr3:108363472G>A c.1603G>A c.(1603-1605)Gat>Aat p.D535N SKCM 3 108363492 108363492 + Silent SNP G G A TCGA-ER-A19T-06A-11D-A19A-08 TCGA-ER-A19T-10A-01D-A19A-08 g.chr3:108363492G>A c.1623G>A c.(1621-1623)ggG>ggA p.G541G SKCM 3 108363531 108363531 + Silent SNP C C A TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr3:108363531C>A c.1662C>A c.(1660-1662)ccC>ccA p.P554P SKCM 3 108363543 108363543 + Silent SNP C C T TCGA-EE-A29T-06A-11D-A197-08 TCGA-EE-A29T-10A-01D-A199-08 g.chr3:108363543C>T c.1674C>T c.(1672-1674)atC>atT p.I558I SKCM 3 108367771 108367771 + Missense_Mutation SNP A A T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:108367771A>T c.1969A>T c.(1969-1971)Agt>Tgt p.S657C SKCM 3 108380784 108380784 + Nonsense_Mutation SNP C C T TCGA-D3-A51N-06A-11D-A25O-08 TCGA-D3-A51N-10A-01D-A25O-08 g.chr3:108380784C>T c.2260C>T c.(2260-2262)Caa>Taa p.Q754* SKCM 3 108396404 108396404 + Missense_Mutation SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr3:108396404C>T c.2842C>T c.(2842-2844)Cca>Tca p.P948S SKCM 3 108405367 108405367 + Missense_Mutation SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr3:108405367C>T c.3085C>T c.(3085-3087)Ccc>Tcc p.P1029S SKCM 3 108406916 108406916 + Silent SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr3:108406916C>T c.3243C>T c.(3241-3243)tcC>tcT p.S1081S SKCM 3 108407695 108407695 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr3:108407695C>T c.3440C>T c.(3439-3441)cCt>cTt p.P1147L SKCM 3 108409671 108409671 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr3:108409671C>T c.3554C>T c.(3553-3555)cCa>cTa p.P1185L

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 3 108326960 108326960 single base substitution G A 5_prime_UTR_variant BLCA-CN 3 108326960 108326960 single base substitution G A exon_variant BLCA-CN 3 108326960 108326960 single base substitution G A synonymous_variant R19R 57G>A BLCA-CN 3 108326992 108326992 single base substitution C T 5_prime_UTR_variant BLCA-CN 3 108326992 108326992 single base substitution C T exon_variant BLCA-CN 3 108326992 108326992 single base substitution C T missense_variant S30L 89C>T BLCA-CN 3 108347909 108347909 single base substitution A T missense_variant R110S 330A>T BLCA-CN 3 108347909 108347909 single base substitution A T missense_variant R194S 582A>T BLCA-CN 3 108347909 108347909 single base substitution A T splice_region_variant BLCA-US 3 108343354 108343354 single base substitution G A exon_variant BLCA-US 3 108343354 108343354 single base substitution G A missense_variant E147K 439G>A BLCA-US 3 108343354 108343354 single base substitution G A missense_variant E63K 187G>A BLCA-US 3 108355537 108355537 single base substitution T G 3_prime_UTR_variant BLCA-US 3 108355537 108355537 single base substitution T G synonymous_variant P331P 993T>G BLCA-US 3 108380728 108380728 single base substitution C T 3_prime_UTR_variant BLCA-US 3 108380728 108380728 single base substitution C T missense_variant S735L 2204C>T BLCA-US 3 108403160 108403160 single base substitution C T 3_prime_UTR_variant BLCA-US 3 108403160 108403160 single base substitution C T missense_variant S994F 2981C>T BLCA-US 3 108407451 108407451 single base substitution A G 3_prime_UTR_variant BLCA-US 3 108407451 108407451 single base substitution A G synonymous_variant K1094K 3282A>G BOCA-FR 3 108352784 108352784 single base substitution T C downstream_gene_variant BOCA-FR 3 108352784 108352784 single base substitution T C intron_variant BRCA-EU 3 108303992 108303992 single base substitution C G upstream_gene_variant BRCA-EU 3 108304285 108304285 single base substitution C T upstream_gene_variant BRCA-EU 3 108306025 108306025 single base substitution C T upstream_gene_variant BRCA-EU 3 108306571 108306571 single base substitution C T upstream_gene_variant BRCA-EU 3 108306628 108306628 deletion of <=200bp T - upstream_gene_variant BRCA-EU 3 108306628 108306628 insertion of <=200bp - T upstream_gene_variant BRCA-EU 3 108306731 108306731 single base substitution C T upstream_gene_variant BRCA-EU 3 108307526 108307526 single base substitution C A upstream_gene_variant BRCA-EU 3 108308413 108308413 single base substitution C G upstream_gene_variant BRCA-EU 3 108308939 108308939 insertion of <=200bp - T 5_prime_UTR_variant BRCA-EU 3 108308939 108308939 insertion of <=200bp - T intron_variant BRCA-EU 3 108311123 108311123 single base substitution T C intron_variant BRCA-EU 3 108311136 108311136 single base substitution G T intron_variant BRCA-EU 3 108311811 108311811 deletion of <=200bp T - intron_variant BRCA-EU 3 108311947 108311947 single base substitution C G intron_variant BRCA-EU 3 108313003 108313003 single base substitution A G intron_variant BRCA-EU 3 108313123 108313123 single base substitution T C intron_variant BRCA-EU 3 108313172 108313172 single base substitution C G intron_variant BRCA-EU 3 108314052 108314054 deletion of <=200bp TTG - intron_variant BRCA-EU 3 108315704 108315704 single base substitution C T intron_variant BRCA-EU 3 108317006 108317006 single base substitution C G intron_variant BRCA-EU 3 108317006 108317006 single base substitution C G upstream_gene_variant BRCA-EU 3 108318190 108318190 single base substitution T G intron_variant BRCA-EU 3 108318190 108318190 single base substitution T G upstream_gene_variant BRCA-EU 3 108318381 108318381 single base substitution C T intron_variant BRCA-EU 3 108318381 108318381 single base substitution C T upstream_gene_variant BRCA-EU 3 108319889 108319889 single base substitution G A intron_variant BRCA-EU 3 108319889 108319889 single base substitution G A upstream_gene_variant BRCA-EU 3 108321621 108321621 single base substitution C T intron_variant BRCA-EU 3 108321621 108321621 single base substitution C T upstream_gene_variant BRCA-EU 3 108321628 108321628 single base substitution T A intron_variant BRCA-EU 3 108321628 108321628 single base substitution T A upstream_gene_variant BRCA-EU 3 108321937 108321937 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 3 108321937 108321937 single base substitution C G intron_variant BRCA-EU 3 108326762 108326762 single base substitution C T intron_variant BRCA-EU 3 108327236 108327236 deletion of <=200bp A - intron_variant BRCA-EU 3 108327925 108327925 single base substitution C A intron_variant BRCA-EU 3 108328397 108328397 single base substitution G T intron_variant BRCA-EU 3 108328676 108328676 single base substitution A G intron_variant BRCA-EU 3 108329407 108329407 single base substitution C T intron_variant BRCA-EU 3 108330358 108330358 single base substitution A G downstream_gene_variant BRCA-EU 3 108330358 108330358 single base substitution A G intron_variant BRCA-EU 3 108330411 108330411 single base substitution T C downstream_gene_variant BRCA-EU 3 108330411 108330411 single base substitution T C intron_variant BRCA-EU 3 108331030 108331030 single base substitution T C downstream_gene_variant BRCA-EU 3 108331030 108331030 single base substitution T C intron_variant BRCA-EU 3 108331654 108331654 single base substitution C G downstream_gene_variant BRCA-EU 3 108331654 108331654 single base substitution C G intron_variant BRCA-EU 3 108332021 108332021 single base substitution A G downstream_gene_variant BRCA-EU 3 108332021 108332021 single base substitution A G intron_variant BRCA-EU 3 108332411 108332411 single base substitution G T downstream_gene_variant BRCA-EU 3 108332411 108332411 single base substitution G T intron_variant BRCA-EU 3 108333068 108333068 single base substitution G A downstream_gene_variant BRCA-EU 3 108333068 108333068 single base substitution G A intron_variant BRCA-EU 3 108333354 108333354 single base substitution C G downstream_gene_variant BRCA-EU 3 108333354 108333354 single base substitution C G intron_variant BRCA-EU 3 108333891 108333891 single base substitution C A downstream_gene_variant BRCA-EU 3 108333891 108333891 single base substitution C A intron_variant BRCA-EU 3 108334482 108334482 single base substitution C T downstream_gene_variant BRCA-EU 3 108334482 108334482 single base substitution C T intron_variant BRCA-EU 3 108334894 108334894 single base substitution G A downstream_gene_variant BRCA-EU 3 108334894 108334894 single base substitution G A intron_variant BRCA-EU 3 108335473 108335473 single base substitution C T exon_variant BRCA-EU 3 108335473 108335473 single base substitution C T missense_variant A115V 344C>T BRCA-EU 3 108335473 108335473 single base substitution C T missense_variant A31V 92C>T BRCA-EU 3 108335751 108335751 single base substitution C G intron_variant BRCA-EU 3 108336409 108336409 deletion of <=200bp A - intron_variant BRCA-EU 3 108336889 108336889 single base substitution A G intron_variant BRCA-EU 3 108336892 108336892 single base substitution A G intron_variant BRCA-EU 3 108337459 108337459 single base substitution A G intron_variant BRCA-EU 3 108338965 108338965 single base substitution C A intron_variant BRCA-EU 3 108339133 108339133 single base substitution G A intron_variant BRCA-EU 3 108339279 108339279 single base substitution C G intron_variant BRCA-EU 3 108339802 108339802 single base substitution G A intron_variant BRCA-EU 3 108342370 108342370 single base substitution A G intron_variant BRCA-EU 3 108343105 108343105 single base substitution C G intron_variant BRCA-EU 3 108343108 108343108 single base substitution C G intron_variant BRCA-EU 3 108343111 108343111 single base substitution G T intron_variant BRCA-EU 3 108343112 108343112 single base substitution G T intron_variant BRCA-EU 3 108343368 108343368 single base substitution A G exon_variant BRCA-EU 3 108343368 108343368 single base substitution A G synonymous_variant K151K 453A>G BRCA-EU 3 108343368 108343368 single base substitution A G synonymous_variant K67K 201A>G BRCA-EU 3 108344002 108344002 insertion of <=200bp - T intron_variant BRCA-EU 3 108344989 108344989 deletion of <=200bp T - intron_variant BRCA-EU 3 108345691 108345691 single base substitution C A intron_variant BRCA-EU 3 108346056 108346056 single base substitution G C intron_variant BRCA-EU 3 108348847 108348847 single base substitution C G downstream_gene_variant BRCA-EU 3 108348847 108348847 single base substitution C G intron_variant BRCA-EU 3 108349302 108349302 single base substitution C T downstream_gene_variant BRCA-EU 3 108349302 108349302 single base substitution C T intron_variant BRCA-EU 3 108349306 108349306 single base substitution A C downstream_gene_variant BRCA-EU 3 108349306 108349306 single base substitution A C intron_variant BRCA-EU 3 108349711 108349711 single base substitution T C downstream_gene_variant BRCA-EU 3 108349711 108349711 single base substitution T C intron_variant BRCA-EU 3 108350252 108350252 single base substitution C G downstream_gene_variant BRCA-EU 3 108350252 108350252 single base substitution C G intron_variant BRCA-EU 3 108350497 108350497 single base substitution C A downstream_gene_variant BRCA-EU 3 108350497 108350497 single base substitution C A intron_variant BRCA-EU 3 108350528 108350528 single base substitution C G downstream_gene_variant BRCA-EU 3 108350528 108350528 single base substitution C G intron_variant BRCA-EU 3 108351453 108351453 single base substitution T C downstream_gene_variant BRCA-EU 3 108351453 108351453 single base substitution T C intron_variant BRCA-EU 3 108352362 108352362 single base substitution G A downstream_gene_variant BRCA-EU 3 108352362 108352362 single base substitution G A intron_variant BRCA-EU 3 108356320 108356320 deletion of <=200bp T - intron_variant BRCA-EU 3 108357362 108357362 single base substitution C T intron_variant BRCA-EU 3 108358874 108358874 single base substitution G T intron_variant BRCA-EU 3 108359035 108359035 single base substitution C G intron_variant BRCA-EU 3 108360003 108360003 single base substitution A C intron_variant BRCA-EU 3 108360108 108360108 single base substitution T C intron_variant BRCA-EU 3 108361006 108361006 deletion of <=200bp T - intron_variant BRCA-EU 3 108361099 108361099 single base substitution C G intron_variant BRCA-EU 3 108361268 108361268 insertion of <=200bp - T intron_variant BRCA-EU 3 108361473 108361473 single base substitution T G intron_variant BRCA-EU 3 108361520 108361520 single base substitution T G intron_variant BRCA-EU 3 108362409 108362409 single base substitution G A intron_variant BRCA-EU 3 108362443 108362443 single base substitution C A intron_variant BRCA-EU 3 108362642 108362642 single base substitution G A intron_variant BRCA-EU 3 108363276 108363276 single base substitution C T 3_prime_UTR_variant BRCA-EU 3 108363276 108363276 single base substitution C T synonymous_variant L469L 1407C>T BRCA-EU 3 108363979 108363979 single base substitution C G intron_variant BRCA-EU 3 108364090 108364091 deletion of <=200bp AC - intron_variant BRCA-EU 3 108364560 108364560 single base substitution G C intron_variant BRCA-EU 3 108364989 108364989 deletion of <=200bp T - intron_variant BRCA-EU 3 108365217 108365217 single base substitution T C intron_variant BRCA-EU 3 108365251 108365251 deletion of <=200bp T - intron_variant BRCA-EU 3 108365588 108365588 single base substitution C A intron_variant BRCA-EU 3 108365888 108365888 deletion of <=200bp A - intron_variant BRCA-EU 3 108365888 108365888 insertion of <=200bp - A intron_variant BRCA-EU 3 108366218 108366218 deletion of <=200bp A - intron_variant BRCA-EU 3 108366308 108366308 single base substitution C T intron_variant BRCA-EU 3 108366394 108366394 single base substitution A C intron_variant BRCA-EU 3 108366842 108366842 single base substitution C T 3_prime_UTR_variant BRCA-EU 3 108366842 108366842 single base substitution C T synonymous_variant L615L 1845C>T BRCA-EU 3 108368525 108368525 single base substitution A T downstream_gene_variant BRCA-EU 3 108368525 108368525 single base substitution A T intron_variant BRCA-EU 3 108369109 108369109 single base substitution G A downstream_gene_variant BRCA-EU 3 108369109 108369109 single base substitution G A intron_variant BRCA-EU 3 108369403 108369403 single base substitution A G downstream_gene_variant BRCA-EU 3 108369403 108369403 single base substitution A G intron_variant BRCA-EU 3 108369728 108369728 single base substitution A C downstream_gene_variant BRCA-EU 3 108369728 108369728 single base substitution A C intron_variant BRCA-EU 3 108370665 108370665 single base substitution C A downstream_gene_variant BRCA-EU 3 108370665 108370665 single base substitution C A intron_variant BRCA-EU 3 108371973 108371973 single base substitution G T intron_variant BRCA-EU 3 108372638 108372638 single base substitution G C intron_variant BRCA-EU 3 108373079 108373079 single base substitution T C 3_prime_UTR_variant BRCA-EU 3 108373079 108373079 single base substitution T C synonymous_variant S707S 2121T>C BRCA-EU 3 108373244 108373244 single base substitution A T intron_variant BRCA-EU 3 108373328 108373328 deletion of <=200bp A - intron_variant BRCA-EU 3 108373592 108373592 deletion of <=200bp T - intron_variant BRCA-EU 3 108374024 108374024 deletion of <=200bp A - intron_variant BRCA-EU 3 108375045 108375045 single base substitution C G intron_variant BRCA-EU 3 108375487 108375487 single base substitution C T intron_variant BRCA-EU 3 108375799 108375799 single base substitution A G intron_variant BRCA-EU 3 108376484 108376484 single base substitution C T intron_variant BRCA-EU 3 108378593 108378593 single base substitution C G intron_variant BRCA-EU 3 108379090 108379090 single base substitution A T intron_variant BRCA-EU 3 108379168 108379168 single base substitution C G intron_variant BRCA-EU 3 108379884 108379884 single base substitution G T intron_variant BRCA-EU 3 108380013 108380013 single base substitution C T intron_variant BRCA-EU 3 108380495 108380495 single base substitution A G intron_variant BRCA-EU 3 108381174 108381174 single base substitution T C intron_variant BRCA-EU 3 108382476 108382476 single base substitution C G intron_variant BRCA-EU 3 108382662 108382662 single base substitution G T intron_variant BRCA-EU 3 108383811 108383811 single base substitution C T intron_variant BRCA-EU 3 108384060 108384060 single base substitution C A intron_variant BRCA-EU 3 108384598 108384598 single base substitution A G intron_variant BRCA-EU 3 108384975 108384975 single base substitution C G intron_variant BRCA-EU 3 108385085 108385085 deletion of <=200bp A - intron_variant BRCA-EU 3 108386825 108386825 single base substitution C T intron_variant BRCA-EU 3 108386834 108386834 single base substitution A T intron_variant BRCA-EU 3 108387114 108387114 single base substitution A G intron_variant BRCA-EU 3 108390988 108390988 single base substitution T C intron_variant BRCA-EU 3 108391112 108391112 single base substitution G T intron_variant BRCA-EU 3 108391516 108391516 single base substitution C T intron_variant BRCA-EU 3 108392420 108392420 single base substitution A C intron_variant BRCA-EU 3 108392728 108392728 single base substitution A G intron_variant BRCA-EU 3 108395480 108395480 single base substitution C T intron_variant BRCA-EU 3 108397082 108397082 single base substitution C T intron_variant BRCA-EU 3 108397295 108397295 single base substitution C G intron_variant BRCA-EU 3 108398456 108398456 single base substitution A T intron_variant BRCA-EU 3 108398713 108398713 single base substitution G T intron_variant BRCA-EU 3 108399568 108399568 single base substitution C G intron_variant BRCA-EU 3 108399747 108399747 single base substitution T C intron_variant BRCA-EU 3 108400101 108400101 single base substitution C T intron_variant BRCA-EU 3 108400238 108400238 single base substitution C A intron_variant BRCA-EU 3 108400497 108400497 single base substitution G C intron_variant BRCA-EU 3 108400626 108400626 single base substitution A T intron_variant BRCA-EU 3 108400777 108400777 single base substitution G C intron_variant BRCA-EU 3 108400787 108400787 single base substitution G T intron_variant BRCA-EU 3 108400811 108400811 single base substitution A T intron_variant BRCA-EU 3 108401336 108401340 deletion of <=200bp GTTAT - intron_variant BRCA-EU 3 108401664 108401664 single base substitution T C intron_variant BRCA-EU 3 108401824 108401824 deletion of <=200bp T - intron_variant BRCA-EU 3 108401931 108401931 single base substitution C T intron_variant BRCA-EU 3 108403021 108403021 single base substitution G T intron_variant BRCA-EU 3 108403725 108403725 single base substitution T A intron_variant BRCA-EU 3 108405508 108405508 single base substitution A G intron_variant BRCA-EU 3 108405859 108405859 single base substitution G A intron_variant BRCA-EU 3 108406214 108406214 single base substitution A C intron_variant BRCA-EU 3 108406612 108406612 single base substitution C G intron_variant BRCA-EU 3 108407185 108407185 single base substitution G A intron_variant BRCA-EU 3 108408534 108408534 insertion of <=200bp - A intron_variant BRCA-EU 3 108409506 108409506 single base substitution C T intron_variant BRCA-EU 3 108410430 108410430 single base substitution C G downstream_gene_variant BRCA-EU 3 108410430 108410430 single base substitution C G intron_variant BRCA-EU 3 108411067 108411067 deletion of <=200bp T - downstream_gene_variant BRCA-EU 3 108411067 108411067 deletion of <=200bp T - intron_variant BRCA-EU 3 108411954 108411954 deletion of <=200bp T - downstream_gene_variant BRCA-EU 3 108411954 108411954 deletion of <=200bp T - intron_variant BRCA-EU 3 108412148 108412148 single base substitution A C downstream_gene_variant BRCA-EU 3 108412148 108412148 single base substitution A C intron_variant BRCA-EU 3 108412359 108412359 single base substitution T C 3_prime_UTR_variant BRCA-EU 3 108412359 108412359 single base substitution T C downstream_gene_variant BRCA-EU 3 108412682 108412682 single base substitution G A 3_prime_UTR_variant BRCA-EU 3 108412682 108412682 single base substitution G A downstream_gene_variant BRCA-EU 3 108414428 108414428 single base substitution C G downstream_gene_variant BRCA-EU 3 108414828 108414828 single base substitution T G downstream_gene_variant BRCA-EU 3 108415239 108415239 single base substitution G A downstream_gene_variant BRCA-EU 3 108416696 108416696 single base substitution C A downstream_gene_variant BRCA-EU 3 108417197 108417197 single base substitution G A downstream_gene_variant BRCA-EU 3 108417207 108417207 single base substitution C G downstream_gene_variant BRCA-FR 3 108307526 108307526 single base substitution C A upstream_gene_variant BRCA-FR 3 108308996 108308996 single base substitution C G intron_variant BRCA-FR 3 108318381 108318381 single base substitution C T intron_variant BRCA-FR 3 108318381 108318381 single base substitution C T upstream_gene_variant BRCA-FR 3 108329407 108329407 single base substitution C T intron_variant BRCA-FR 3 108331654 108331654 single base substitution C G downstream_gene_variant BRCA-FR 3 108331654 108331654 single base substitution C G intron_variant BRCA-FR 3 108333354 108333354 single base substitution C G downstream_gene_variant BRCA-FR 3 108333354 108333354 single base substitution C G intron_variant BRCA-FR 3 108334482 108334482 single base substitution C T downstream_gene_variant BRCA-FR 3 108334482 108334482 single base substitution C T intron_variant BRCA-FR 3 108335751 108335751 single base substitution C G intron_variant BRCA-FR 3 108350252 108350252 single base substitution C G downstream_gene_variant BRCA-FR 3 108350252 108350252 single base substitution C G intron_variant BRCA-FR 3 108361473 108361473 single base substitution T G intron_variant BRCA-FR 3 108366887 108366887 single base substitution T A 3_prime_UTR_variant BRCA-FR 3 108366887 108366887 single base substitution T A missense_variant F630L 1890T>A BRCA-FR 3 108375045 108375045 single base substitution C G intron_variant BRCA-FR 3 108379168 108379168 single base substitution C G intron_variant BRCA-FR 3 108382662 108382662 single base substitution G T intron_variant BRCA-FR 3 108383811 108383811 single base substitution C T intron_variant BRCA-FR 3 108384060 108384060 single base substitution C A intron_variant BRCA-FR 3 108384975 108384975 single base substitution C G intron_variant BRCA-FR 3 108384978 108384978 single base substitution G A intron_variant BRCA-FR 3 108386825 108386825 single base substitution C T intron_variant BRCA-FR 3 108395271 108395271 single base substitution T C intron_variant BRCA-FR 3 108397295 108397295 single base substitution C G intron_variant BRCA-FR 3 108398456 108398456 single base substitution A T intron_variant BRCA-FR 3 108399568 108399568 single base substitution C G intron_variant BRCA-FR 3 108400101 108400101 single base substitution C T intron_variant BRCA-FR 3 108401664 108401664 single base substitution T C intron_variant BRCA-FR 3 108409506 108409506 single base substitution C T intron_variant BRCA-FR 3 108411458 108411458 single base substitution A C downstream_gene_variant BRCA-FR 3 108411458 108411458 single base substitution A C intron_variant BRCA-UK 3 108315704 108315704 single base substitution C T intron_variant BRCA-UK 3 108321937 108321937 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-UK 3 108321937 108321937 single base substitution C G intron_variant BRCA-UK 3 108332021 108332021 single base substitution A G downstream_gene_variant BRCA-UK 3 108332021 108332021 single base substitution A G intron_variant BRCA-UK 3 108363434 108363434 single base substitution C G 3_prime_UTR_variant BRCA-UK 3 108363434 108363434 single base substitution C G missense_variant T522S 1565C>G BRCA-UK 3 108363540 108363540 single base substitution T A 3_prime_UTR_variant BRCA-UK 3 108363540 108363540 single base substitution T A missense_variant N557K 1671T>A BRCA-UK 3 108366903 108366903 single base substitution G C 3_prime_UTR_variant BRCA-UK 3 108366903 108366903 single base substitution G C missense_variant D636H 1906G>C BRCA-UK 3 108413980 108413980 single base substitution G A downstream_gene_variant BRCA-US 3 108335487 108335487 single base substitution C G exon_variant BRCA-US 3 108335487 108335487 single base substitution C G missense_variant Q120E 358C>G BRCA-US 3 108335487 108335487 single base substitution C G missense_variant Q36E 106C>G BRCA-US 3 108344740 108344740 single base substitution C T exon_variant BRCA-US 3 108344740 108344740 single base substitution C T stop_gained Q169* 505C>T BRCA-US 3 108344740 108344740 single base substitution C T stop_gained Q85* 253C>T BRCA-US 3 108355480 108355480 single base substitution A T 3_prime_UTR_variant BRCA-US 3 108355480 108355480 single base substitution A T missense_variant K312N 936A>T BRCA-US 3 108361332 108361332 single base substitution C T 3_prime_UTR_variant BRCA-US 3 108361332 108361332 single base substitution C T missense_variant P371L 1112C>T BRCA-US 3 108367765 108367765 single base substitution G C 3_prime_UTR_variant BRCA-US 3 108367765 108367765 single base substitution G C downstream_gene_variant BRCA-US 3 108367765 108367765 single base substitution G C missense_variant V655L 1963G>C BRCA-US 3 108388553 108388553 single base substitution G T 3_prime_UTR_variant BRCA-US 3 108388553 108388553 single base substitution G T missense_variant D817Y 2449G>T BRCA-US 3 108388567 108388567 single base substitution G T 3_prime_UTR_variant BRCA-US 3 108388567 108388567 single base substitution G T missense_variant K821N 2463G>T BRCA-US 3 108403129 108403129 single base substitution C G 3_prime_UTR_variant BRCA-US 3 108403129 108403129 single base substitution C G missense_variant Q984E 2950C>G BRCA-US 3 108407718 108407718 single base substitution C T 3_prime_UTR_variant BRCA-US 3 108407718 108407718 single base substitution C T synonymous_variant L1155L 3463C>T BRCA-US 3 108409716 108409716 single base substitution A C 3_prime_UTR_variant BRCA-US 3 108409716 108409716 single base substitution A C missense_variant H1200P 3599A>C BTCA-JP 3 108308054 108308054 single base substitution C T upstream_gene_variant BTCA-JP 3 108324361 108324361 single base substitution G A intron_variant BTCA-JP 3 108330124 108330124 single base substitution T C 5_prime_UTR_variant BTCA-JP 3 108330124 108330124 single base substitution T C exon_variant BTCA-JP 3 108330124 108330124 single base substitution T C missense_variant V69A 206T>C BTCA-JP 3 108335357 108335357 single base substitution T C intron_variant BTCA-JP 3 108353767 108353767 single base substitution A C exon_variant BTCA-JP 3 108353767 108353767 single base substitution A C missense_variant K289T 866A>C BTCA-JP 3 108355587 108355587 single base substitution T C intron_variant BTCA-JP 3 108355588 108355588 single base substitution C T intron_variant BTCA-JP 3 108361276 108361276 single base substitution C G intron_variant BTCA-JP 3 108361321 108361321 single base substitution T A 3_prime_UTR_variant BTCA-JP 3 108361321 108361321 single base substitution T A synonymous_variant T367T 1101T>A BTCA-JP 3 108372991 108372991 single base substitution G A splice_acceptor_variant BTCA-JP 3 108373253 108373253 single base substitution G T intron_variant BTCA-JP 3 108380816 108380816 single base substitution T C 3_prime_UTR_variant BTCA-JP 3 108380816 108380816 single base substitution T C synonymous_variant C764C 2292T>C BTCA-JP 3 108381125 108381125 single base substitution A G intron_variant BTCA-JP 3 108393047 108393047 insertion of <=200bp - T intron_variant BTCA-JP 3 108403020 108403020 deletion of <=200bp G - intron_variant BTCA-JP 3 108405321 108405321 single base substitution G A intron_variant BTCA-JP 3 108405321 108405321 single base substitution G A synonymous_variant A1013A 3039G>A BTCA-JP 3 108407421 108407421 single base substitution A T intron_variant BTCA-JP 3 108407693 108407693 single base substitution G A 3_prime_UTR_variant BTCA-JP 3 108407693 108407693 single base substitution G A synonymous_variant E1146E 3438G>A CESC-US 3 108351882 108351882 single base substitution C T downstream_gene_variant CESC-US 3 108351882 108351882 single base substitution C T exon_variant CESC-US 3 108351882 108351882 single base substitution C T missense_variant S260F 779C>T CESC-US 3 108355553 108355553 single base substitution T G missense_variant L337V 1009T>G CESC-US 3 108355553 108355553 single base substitution T G splice_region_variant CESC-US 3 108361302 108361302 single base substitution C G 3_prime_UTR_variant CESC-US 3 108361302 108361302 single base substitution C G missense_variant S361C 1082C>G CESC-US 3 108366903 108366903 single base substitution G T 3_prime_UTR_variant CESC-US 3 108366903 108366903 single base substitution G T missense_variant D636Y 1906G>T CESC-US 3 108392964 108392964 single base substitution C A 3_prime_UTR_variant CESC-US 3 108392964 108392964 single base substitution C A missense_variant H877N 2629C>A CESC-US 3 108403096 108403096 single base substitution G T 3_prime_UTR_variant CESC-US 3 108403096 108403096 single base substitution G T stop_gained E973* 2917G>T CESC-US 3 108407541 108407541 single base substitution C T 3_prime_UTR_variant CESC-US 3 108407541 108407541 single base substitution C T synonymous_variant L1124L 3372C>T CLLE-ES 3 108303548 108303548 single base substitution T G upstream_gene_variant CLLE-ES 3 108312295 108312295 single base substitution A T intron_variant CLLE-ES 3 108405281 108405281 single base substitution G A intron_variant CLLE-ES 3 108409425 108409425 single base substitution G A intron_variant CLLE-ES 3 108412285 108412285 single base substitution T C 3_prime_UTR_variant CLLE-ES 3 108412285 108412285 single base substitution T C downstream_gene_variant COAD-US 3 108303930 108303930 single base substitution C T upstream_gene_variant COAD-US 3 108303933 108303933 single base substitution T A upstream_gene_variant COAD-US 3 108330025 108330025 single base substitution A C 5_prime_UTR_variant COAD-US 3 108330025 108330025 single base substitution A C exon_variant COAD-US 3 108330025 108330025 single base substitution A C missense_variant K36T 107A>C COAD-US 3 108353778 108353778 deletion of <=200bp A - exon_variant COAD-US 3 108353778 108353778 deletion of <=200bp A - frameshift_variant K293 COAD-US 3 108363156 108363156 single base substitution G T 3_prime_UTR_variant COAD-US 3 108363156 108363156 single base substitution G T missense_variant K429N 1287G>T COAD-US 3 108363318 108363318 insertion of <=200bp - A 3_prime_UTR_variant COAD-US 3 108363318 108363318 insertion of <=200bp - A frameshift_variant P483P? COAD-US 3 108363417 108363417 single base substitution T A 3_prime_UTR_variant COAD-US 3 108363417 108363417 single base substitution T A synonymous_variant I516I 1548T>A COAD-US 3 108373022 108373022 single base substitution G A 3_prime_UTR_variant COAD-US 3 108373022 108373022 single base substitution G A synonymous_variant L688L 2064G>A COAD-US 3 108373068 108373068 single base substitution G T 3_prime_UTR_variant COAD-US 3 108373068 108373068 single base substitution G T missense_variant D704Y 2110G>T COAD-US 3 108406841 108406841 single base substitution C A 3_prime_UTR_variant COAD-US 3 108406841 108406841 single base substitution C A missense_variant F1056L 3168C>A COAD-US 3 108406945 108406945 single base substitution T C splice_donor_variant COCA-CN 3 108304575 108304575 single base substitution C A upstream_gene_variant COCA-CN 3 108308106 108308106 single base substitution C G upstream_gene_variant COCA-CN 3 108330187 108330187 single base substitution A G downstream_gene_variant COCA-CN 3 108330187 108330187 single base substitution A G intron_variant COCA-CN 3 108347898 108347898 single base substitution A C intron_variant COCA-CN 3 108354086 108354086 single base substitution C A intron_variant COCA-CN 3 108365488 108365488 single base substitution G A 3_prime_UTR_variant COCA-CN 3 108365488 108365488 single base substitution G A missense_variant G595D 1784G>A COCA-CN 3 108372984 108372984 single base substitution G A splice_region_variant COCA-CN 3 108388489 108388489 single base substitution A C intron_variant COCA-CN 3 108394807 108394807 single base substitution G A intron_variant COCA-CN 3 108403021 108403021 single base substitution G T intron_variant COCA-CN 3 108407472 108407472 single base substitution T C 3_prime_UTR_variant COCA-CN 3 108407472 108407472 single base substitution T C synonymous_variant C1101C 3303T>C EOPC-DE 3 108345943 108345943 single base substitution G A intron_variant ESAD-UK 3 108304623 108304623 single base substitution A G upstream_gene_variant ESAD-UK 3 108305906 108305906 single base substitution A C upstream_gene_variant ESAD-UK 3 108307040 108307040 single base substitution G A upstream_gene_variant ESAD-UK 3 108307371 108307371 single base substitution C T upstream_gene_variant ESAD-UK 3 108309165 108309165 single base substitution A T intron_variant ESAD-UK 3 108311078 108311078 single base substitution G T intron_variant ESAD-UK 3 108312945 108312945 single base substitution A T intron_variant ESAD-UK 3 108313978 108313978 deletion of <=200bp T - intron_variant ESAD-UK 3 108315021 108315021 single base substitution G A intron_variant ESAD-UK 3 108315717 108315717 single base substitution C A intron_variant ESAD-UK 3 108316354 108316354 single base substitution A G intron_variant ESAD-UK 3 108317309 108317309 single base substitution C T intron_variant ESAD-UK 3 108317309 108317309 single base substitution C T upstream_gene_variant ESAD-UK 3 108319073 108319073 single base substitution C T intron_variant ESAD-UK 3 108319073 108319073 single base substitution C T upstream_gene_variant ESAD-UK 3 108319828 108319828 single base substitution C A intron_variant ESAD-UK 3 108319828 108319828 single base substitution C A upstream_gene_variant ESAD-UK 3 108320571 108320571 single base substitution A G intron_variant ESAD-UK 3 108320571 108320571 single base substitution A G upstream_gene_variant ESAD-UK 3 108322815 108322815 single base substitution G A intron_variant ESAD-UK 3 108323190 108323190 single base substitution C G intron_variant ESAD-UK 3 108324862 108324862 single base substitution C A intron_variant ESAD-UK 3 108325518 108325518 single base substitution A G intron_variant ESAD-UK 3 108326413 108326413 single base substitution G T intron_variant ESAD-UK 3 108327889 108327889 single base substitution C T intron_variant ESAD-UK 3 108328108 108328108 single base substitution G A intron_variant ESAD-UK 3 108329764 108329764 single base substitution G A intron_variant ESAD-UK 3 108329904 108329904 single base substitution T A intron_variant ESAD-UK 3 108330865 108330865 single base substitution C G downstream_gene_variant ESAD-UK 3 108330865 108330865 single base substitution C G intron_variant ESAD-UK 3 108333801 108333801 single base substitution C A downstream_gene_variant ESAD-UK 3 108333801 108333801 single base substitution C A intron_variant ESAD-UK 3 108337083 108337083 single base substitution T C intron_variant ESAD-UK 3 108339363 108339363 single base substitution T A intron_variant ESAD-UK 3 108339909 108339909 single base substitution C T intron_variant ESAD-UK 3 108340702 108340702 single base substitution C G intron_variant ESAD-UK 3 108341404 108341414 deletion of <=200bp TTAGGTATTCA - intron_variant ESAD-UK 3 108342282 108342282 single base substitution C G intron_variant ESAD-UK 3 108342318 108342318 single base substitution C A intron_variant ESAD-UK 3 108343356 108343356 single base substitution A G exon_variant ESAD-UK 3 108343356 108343356 single base substitution A G synonymous_variant E147E 441A>G ESAD-UK 3 108343356 108343356 single base substitution A G synonymous_variant E63E 189A>G ESAD-UK 3 108343428 108343428 single base substitution C G intron_variant ESAD-UK 3 108344651 108344651 deletion of <=200bp T - intron_variant ESAD-UK 3 108347443 108347443 single base substitution C A intron_variant ESAD-UK 3 108350090 108350090 single base substitution G T downstream_gene_variant ESAD-UK 3 108350090 108350090 single base substitution G T intron_variant ESAD-UK 3 108354824 108354824 single base substitution C T intron_variant ESAD-UK 3 108355442 108355442 single base substitution T C intron_variant ESAD-UK 3 108356447 108356447 single base substitution T A intron_variant ESAD-UK 3 108356661 108356661 single base substitution C A intron_variant ESAD-UK 3 108358812 108358812 single base substitution A C intron_variant ESAD-UK 3 108359929 108359929 deletion of <=200bp T - intron_variant ESAD-UK 3 108361428 108361428 single base substitution T C intron_variant ESAD-UK 3 108361891 108361891 single base substitution A C intron_variant ESAD-UK 3 108361966 108361966 single base substitution C T intron_variant ESAD-UK 3 108363249 108363249 single base substitution G A 3_prime_UTR_variant ESAD-UK 3 108363249 108363249 single base substitution G A synonymous_variant P460P 1380G>A ESAD-UK 3 108363665 108363665 single base substitution C A intron_variant ESAD-UK 3 108364210 108364210 single base substitution C T intron_variant ESAD-UK 3 108364552 108364552 single base substitution C T intron_variant ESAD-UK 3 108366174 108366174 deletion of <=200bp T - intron_variant ESAD-UK 3 108368266 108368266 single base substitution C A downstream_gene_variant ESAD-UK 3 108368266 108368266 single base substitution C A intron_variant ESAD-UK 3 108368395 108368395 single base substitution A C downstream_gene_variant ESAD-UK 3 108368395 108368395 single base substitution A C intron_variant ESAD-UK 3 108369303 108369303 single base substitution G A downstream_gene_variant ESAD-UK 3 108369303 108369303 single base substitution G A intron_variant ESAD-UK 3 108370906 108370906 deletion of <=200bp T - downstream_gene_variant ESAD-UK 3 108370906 108370906 deletion of <=200bp T - intron_variant ESAD-UK 3 108371115 108371115 single base substitution G T downstream_gene_variant ESAD-UK 3 108371115 108371115 single base substitution G T intron_variant ESAD-UK 3 108371517 108371517 single base substitution C T downstream_gene_variant ESAD-UK 3 108371517 108371517 single base substitution C T intron_variant ESAD-UK 3 108372934 108372934 single base substitution T G intron_variant ESAD-UK 3 108373646 108373646 single base substitution A G intron_variant ESAD-UK 3 108375129 108375129 single base substitution C T intron_variant ESAD-UK 3 108378018 108378018 single base substitution C T intron_variant ESAD-UK 3 108380949 108380949 single base substitution A T intron_variant ESAD-UK 3 108381178 108381178 single base substitution T G intron_variant ESAD-UK 3 108381180 108381180 single base substitution A C intron_variant ESAD-UK 3 108383051 108383051 single base substitution A C intron_variant ESAD-UK 3 108384871 108384871 single base substitution A G intron_variant ESAD-UK 3 108387558 108387558 single base substitution T G intron_variant ESAD-UK 3 108387967 108387967 single base substitution T G intron_variant ESAD-UK 3 108391121 108391121 single base substitution T C intron_variant ESAD-UK 3 108391215 108391215 single base substitution T G intron_variant ESAD-UK 3 108392283 108392283 single base substitution A T intron_variant ESAD-UK 3 108392490 108392490 single base substitution C A intron_variant ESAD-UK 3 108393297 108393297 single base substitution G A intron_variant ESAD-UK 3 108394133 108394133 single base substitution G A intron_variant ESAD-UK 3 108395688 108395688 single base substitution T G intron_variant ESAD-UK 3 108397016 108397016 single base substitution A T intron_variant ESAD-UK 3 108398954 108398954 single base substitution A C intron_variant ESAD-UK 3 108399967 108399967 single base substitution C T intron_variant ESAD-UK 3 108400171 108400171 deletion of <=200bp A - intron_variant ESAD-UK 3 108401919 108401919 single base substitution A G intron_variant ESAD-UK 3 108403021 108403021 insertion of <=200bp - T intron_variant ESAD-UK 3 108409464 108409464 single base substitution C A intron_variant ESAD-UK 3 108411067 108411067 insertion of <=200bp - T downstream_gene_variant ESAD-UK 3 108411067 108411067 insertion of <=200bp - T intron_variant ESAD-UK 3 108411742 108411742 single base substitution A G downstream_gene_variant ESAD-UK 3 108411742 108411742 single base substitution A G intron_variant ESAD-UK 3 108411749 108411749 single base substitution A G downstream_gene_variant ESAD-UK 3 108411749 108411749 single base substitution A G intron_variant ESAD-UK 3 108413805 108413805 single base substitution G A downstream_gene_variant ESAD-UK 3 108416224 108416224 single base substitution G A downstream_gene_variant ESAD-UK 3 108417503 108417503 single base substitution A G downstream_gene_variant ESAD-UK 3 108418173 108418173 single base substitution T G downstream_gene_variant ESAD-UK 3 108418485 108418485 insertion of <=200bp - T downstream_gene_variant ESCA-CN 3 108326995 108326995 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN 3 108326995 108326995 single base substitution C G exon_variant ESCA-CN 3 108326995 108326995 single base substitution C G missense_variant S31C 92C>G ESCA-CN 3 108335253 108335253 insertion of <=200bp - T intron_variant ESCA-CN 3 108351893 108351893 single base substitution G A downstream_gene_variant ESCA-CN 3 108351893 108351893 single base substitution G A exon_variant ESCA-CN 3 108351893 108351893 single base substitution G A missense_variant D264N 790G>A ESCA-CN 3 108353706 108353706 insertion of <=200bp - T intron_variant GBM-US 3 108353719 108353719 single base substitution G T missense_variant G273V 818G>T GBM-US 3 108353719 108353719 single base substitution G T splice_region_variant KIRP-US 3 108324275 108324275 deletion of <=200bp T - exon_variant KIRP-US 3 108324275 108324275 deletion of <=200bp T - frameshift_variant F8 KIRP-US 3 108324275 108324275 deletion of <=200bp T - intron_variant LAML-KR 3 108359284 108359284 single base substitution A T intron_variant LAML-KR 3 108379601 108379601 single base substitution A C intron_variant LAML-KR 3 108396656 108396656 single base substitution T G intron_variant LGG-US 3 108308132 108308132 single base substitution G A upstream_gene_variant LICA-CN 3 108330108 108330108 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 3 108330108 108330108 single base substitution C G exon_variant LICA-CN 3 108330108 108330108 single base substitution C G missense_variant L64V 190C>G LICA-FR 3 108304695 108304695 insertion of <=200bp - T upstream_gene_variant LICA-FR 3 108308673 108308673 single base substitution C T 5_prime_UTR_variant LICA-FR 3 108308673 108308673 single base substitution C T upstream_gene_variant LICA-FR 3 108309330 108309330 single base substitution G A intron_variant LICA-FR 3 108316393 108316393 single base substitution G A intron_variant LICA-FR 3 108333164 108333164 single base substitution A G downstream_gene_variant LICA-FR 3 108333164 108333164 single base substitution A G intron_variant LICA-FR 3 108345649 108345649 single base substitution A G intron_variant LICA-FR 3 108349855 108349855 single base substitution T C downstream_gene_variant LICA-FR 3 108349855 108349855 single base substitution T C intron_variant LICA-FR 3 108357165 108357165 insertion of <=200bp - TTTG intron_variant LICA-FR 3 108357988 108357988 single base substitution A T intron_variant LICA-FR 3 108379002 108379002 single base substitution A G intron_variant LIHC-US 3 108347953 108347953 single base substitution T C exon_variant LIHC-US 3 108347953 108347953 single base substitution T C missense_variant I125T 374T>C LIHC-US 3 108347953 108347953 single base substitution T C missense_variant I209T 626T>C LIHC-US 3 108363329 108363329 single base substitution G A 3_prime_UTR_variant LIHC-US 3 108363329 108363329 single base substitution G A stop_gained W487* 1460G>A LIHC-US 3 108367792 108367792 single base substitution A G 3_prime_UTR_variant LIHC-US 3 108367792 108367792 single base substitution A G downstream_gene_variant LIHC-US 3 108367792 108367792 single base substitution A G missense_variant K664E 1990A>G LIHC-US 3 108373044 108373044 single base substitution C T 3_prime_UTR_variant LIHC-US 3 108373044 108373044 single base substitution C T missense_variant H696Y 2086C>T LIHC-US 3 108396342 108396342 single base substitution A T splice_acceptor_variant LIHC-US 3 108396438 108396438 single base substitution A T 3_prime_UTR_variant LIHC-US 3 108396438 108396438 single base substitution A T missense_variant E959V 2876A>T LIHC-US 3 108407750 108407750 single base substitution C T 3_prime_UTR_variant LIHC-US 3 108407750 108407750 single base substitution C T synonymous_variant C1165C 3495C>T LINC-JP 3 108303869 108303869 single base substitution A G upstream_gene_variant LINC-JP 3 108319205 108319205 single base substitution T A intron_variant LINC-JP 3 108319205 108319205 single base substitution T A upstream_gene_variant LINC-JP 3 108335266 108335266 single base substitution A T intron_variant LINC-JP 3 108337965 108337965 single base substitution C T intron_variant LINC-JP 3 108338173 108338173 single base substitution T G intron_variant LINC-JP 3 108345081 108345081 single base substitution C T intron_variant LINC-JP 3 108353863 108353863 single base substitution A T intron_variant LINC-JP 3 108356310 108356310 single base substitution T C intron_variant LINC-JP 3 108363594 108363594 single base substitution A G 3_prime_UTR_variant LINC-JP 3 108363594 108363594 single base substitution A G synonymous_variant E575E 1725A>G LINC-JP 3 108372833 108372833 single base substitution A G intron_variant LINC-JP 3 108373348 108373348 single base substitution G A intron_variant LINC-JP 3 108379877 108379877 single base substitution G A intron_variant LINC-JP 3 108398066 108398066 single base substitution A T intron_variant LINC-JP 3 108403165 108403165 single base substitution A G 3_prime_UTR_variant LINC-JP 3 108403165 108403165 single base substitution A G missense_variant T996A 2986A>G LINC-JP 3 108404617 108404617 single base substitution C T intron_variant LIRI-JP 3 108304105 108304105 single base substitution T C upstream_gene_variant LIRI-JP 3 108304883 108304883 single base substitution T C upstream_gene_variant LIRI-JP 3 108305520 108305520 single base substitution G T upstream_gene_variant LIRI-JP 3 108306185 108306185 single base substitution C G upstream_gene_variant LIRI-JP 3 108308800 108308800 single base substitution C A intron_variant LIRI-JP 3 108308800 108308800 single base substitution C A upstream_gene_variant LIRI-JP 3 108312647 108312647 single base substitution G T intron_variant LIRI-JP 3 108312719 108312719 single base substitution G A intron_variant LIRI-JP 3 108313449 108313449 single base substitution G A intron_variant LIRI-JP 3 108313972 108313972 single base substitution A G intron_variant LIRI-JP 3 108314913 108314913 single base substitution A T intron_variant LIRI-JP 3 108315081 108315081 single base substitution G T intron_variant LIRI-JP 3 108316455 108316455 single base substitution A G intron_variant LIRI-JP 3 108317776 108317776 single base substitution A G intron_variant LIRI-JP 3 108317776 108317776 single base substitution A G upstream_gene_variant LIRI-JP 3 108318811 108318811 single base substitution C A intron_variant LIRI-JP 3 108318811 108318811 single base substitution C A upstream_gene_variant LIRI-JP 3 108319045 108319045 single base substitution A G intron_variant LIRI-JP 3 108319045 108319045 single base substitution A G upstream_gene_variant LIRI-JP 3 108320544 108320544 single base substitution A C intron_variant LIRI-JP 3 108320544 108320544 single base substitution A C upstream_gene_variant LIRI-JP 3 108321350 108321350 single base substitution A G intron_variant LIRI-JP 3 108321350 108321350 single base substitution A G upstream_gene_variant LIRI-JP 3 108321492 108321492 single base substitution G T intron_variant LIRI-JP 3 108321492 108321492 single base substitution G T upstream_gene_variant LIRI-JP 3 108325169 108325169 single base substitution C G intron_variant LIRI-JP 3 108327097 108327097 single base substitution G A intron_variant LIRI-JP 3 108328484 108328484 single base substitution T A intron_variant LIRI-JP 3 108328522 108328522 single base substitution T C intron_variant LIRI-JP 3 108328893 108328893 single base substitution T G intron_variant LIRI-JP 3 108329151 108329151 single base substitution A G intron_variant LIRI-JP 3 108330112 108330112 insertion of <=200bp - CAAAAGGTT 5_prime_UTR_variant LIRI-JP 3 108330112 108330112 insertion of <=200bp - CAAAAGGTT exon_variant LIRI-JP 3 108330112 108330112 insertion of <=200bp - CAAAAGGTT inframe_insertion P65PKGS LIRI-JP 3 108330827 108330827 single base substitution G A downstream_gene_variant LIRI-JP 3 108330827 108330827 single base substitution G A intron_variant LIRI-JP 3 108332187 108332187 single base substitution A G downstream_gene_variant LIRI-JP 3 108332187 108332187 single base substitution A G intron_variant LIRI-JP 3 108337451 108337451 single base substitution T G intron_variant LIRI-JP 3 108337630 108337630 single base substitution C T intron_variant LIRI-JP 3 108338225 108338225 single base substitution C T intron_variant LIRI-JP 3 108339170 108339170 single base substitution T C intron_variant LIRI-JP 3 108340786 108340786 single base substitution A G intron_variant LIRI-JP 3 108342819 108342819 single base substitution A G intron_variant LIRI-JP 3 108346540 108346540 single base substitution A C intron_variant LIRI-JP 3 108347300 108347300 single base substitution G A intron_variant LIRI-JP 3 108349295 108349295 single base substitution T C downstream_gene_variant LIRI-JP 3 108349295 108349295 single base substitution T C intron_variant LIRI-JP 3 108351056 108351056 single base substitution C T downstream_gene_variant LIRI-JP 3 108351056 108351056 single base substitution C T intron_variant LIRI-JP 3 108352880 108352880 single base substitution G A downstream_gene_variant LIRI-JP 3 108352880 108352880 single base substitution G A intron_variant LIRI-JP 3 108353256 108353256 single base substitution A G intron_variant LIRI-JP 3 108353648 108353648 single base substitution A T intron_variant LIRI-JP 3 108357483 108357483 single base substitution A G intron_variant LIRI-JP 3 108359078 108359078 single base substitution G T intron_variant LIRI-JP 3 108359318 108359318 single base substitution A T intron_variant LIRI-JP 3 108361756 108361756 single base substitution A T intron_variant LIRI-JP 3 108362678 108362678 single base substitution G T intron_variant LIRI-JP 3 108363290 108363290 insertion of <=200bp - T 3_prime_UTR_variant LIRI-JP 3 108363290 108363290 insertion of <=200bp - T frameshift_variant I474I? LIRI-JP 3 108364245 108364245 single base substitution A G intron_variant LIRI-JP 3 108366599 108366599 single base substitution A C intron_variant LIRI-JP 3 108367721 108367721 single base substitution G A 3_prime_UTR_variant LIRI-JP 3 108367721 108367721 single base substitution G A downstream_gene_variant LIRI-JP 3 108367721 108367721 single base substitution G A intron_variant LIRI-JP 3 108368504 108368504 single base substitution G A downstream_gene_variant LIRI-JP 3 108368504 108368504 single base substitution G A intron_variant LIRI-JP 3 108368796 108368796 single base substitution A T downstream_gene_variant LIRI-JP 3 108368796 108368796 single base substitution A T intron_variant LIRI-JP 3 108369948 108369948 single base substitution T G downstream_gene_variant LIRI-JP 3 108369948 108369948 single base substitution T G intron_variant LIRI-JP 3 108371924 108371924 single base substitution A G downstream_gene_variant LIRI-JP 3 108371924 108371924 single base substitution A G intron_variant LIRI-JP 3 108371953 108371953 single base substitution G T downstream_gene_variant LIRI-JP 3 108371953 108371953 single base substitution G T intron_variant LIRI-JP 3 108372024 108372024 single base substitution A G intron_variant LIRI-JP 3 108372429 108372429 single base substitution T C intron_variant LIRI-JP 3 108372978 108372978 single base substitution T C intron_variant LIRI-JP 3 108373426 108373426 single base substitution G T intron_variant LIRI-JP 3 108374292 108374292 single base substitution G T intron_variant LIRI-JP 3 108374654 108374654 single base substitution G A intron_variant LIRI-JP 3 108375468 108375468 single base substitution G A intron_variant LIRI-JP 3 108381296 108381301 deletion of <=200bp CACTAT - intron_variant LIRI-JP 3 108381826 108381826 single base substitution A G intron_variant LIRI-JP 3 108382585 108382585 single base substitution C G intron_variant LIRI-JP 3 108386937 108386937 single base substitution A G intron_variant LIRI-JP 3 108387142 108387142 single base substitution G A intron_variant LIRI-JP 3 108387565 108387565 deletion of <=200bp A - intron_variant LIRI-JP 3 108388237 108388237 single base substitution C T intron_variant LIRI-JP 3 108390496 108390496 deletion of <=200bp G - intron_variant LIRI-JP 3 108391324 108391324 single base substitution A G intron_variant LIRI-JP 3 108391870 108391870 single base substitution A G intron_variant LIRI-JP 3 108392277 108392277 single base substitution T C intron_variant LIRI-JP 3 108393374 108393374 single base substitution A G intron_variant LIRI-JP 3 108395766 108395766 single base substitution G A intron_variant LIRI-JP 3 108396239 108396239 single base substitution A G intron_variant LIRI-JP 3 108397748 108397748 single base substitution G A intron_variant LIRI-JP 3 108400500 108400500 single base substitution C A intron_variant LIRI-JP 3 108400946 108400946 single base substitution C T intron_variant LIRI-JP 3 108402187 108402187 single base substitution A T intron_variant LIRI-JP 3 108406272 108406272 single base substitution A G intron_variant LIRI-JP 3 108407690 108407690 single base substitution A G 3_prime_UTR_variant LIRI-JP 3 108407690 108407690 single base substitution A G synonymous_variant E1145E 3435A>G LIRI-JP 3 108408381 108408381 single base substitution A G intron_variant LIRI-JP 3 108409390 108409390 single base substitution G T intron_variant LIRI-JP 3 108411261 108411261 single base substitution C T downstream_gene_variant LIRI-JP 3 108411261 108411261 single base substitution C T intron_variant LIRI-JP 3 108411669 108411669 single base substitution A T downstream_gene_variant LIRI-JP 3 108411669 108411669 single base substitution A T intron_variant LIRI-JP 3 108412753 108412753 single base substitution A T 3_prime_UTR_variant LIRI-JP 3 108412753 108412753 single base substitution A T downstream_gene_variant LIRI-JP 3 108412776 108412776 single base substitution A G 3_prime_UTR_variant LIRI-JP 3 108412776 108412776 single base substitution A G downstream_gene_variant LIRI-JP 3 108414669 108414669 single base substitution C T downstream_gene_variant LIRI-JP 3 108414968 108414968 single base substitution G T downstream_gene_variant LUSC-KR 3 108308603 108308603 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 3 108308603 108308603 single base substitution C T upstream_gene_variant LUSC-KR 3 108308786 108308786 single base substitution G A intron_variant LUSC-KR 3 108308786 108308786 single base substitution G A upstream_gene_variant LUSC-KR 3 108311267 108311267 single base substitution G A intron_variant LUSC-KR 3 108314262 108314262 single base substitution G T intron_variant LUSC-KR 3 108314279 108314279 single base substitution G T intron_variant LUSC-KR 3 108314280 108314280 single base substitution G T intron_variant LUSC-KR 3 108320071 108320071 single base substitution C T intron_variant LUSC-KR 3 108320071 108320071 single base substitution C T upstream_gene_variant LUSC-KR 3 108328770 108328770 single base substitution C A intron_variant LUSC-KR 3 108333303 108333303 single base substitution G T downstream_gene_variant LUSC-KR 3 108333303 108333303 single base substitution G T intron_variant LUSC-KR 3 108333858 108333858 single base substitution G A downstream_gene_variant LUSC-KR 3 108333858 108333858 single base substitution G A intron_variant LUSC-KR 3 108338137 108338137 single base substitution G T intron_variant LUSC-KR 3 108341076 108341076 single base substitution G A intron_variant LUSC-KR 3 108346248 108346248 single base substitution T C intron_variant LUSC-KR 3 108347265 108347265 single base substitution G T intron_variant LUSC-KR 3 108348932 108348932 single base substitution A C downstream_gene_variant LUSC-KR 3 108348932 108348932 single base substitution A C intron_variant LUSC-KR 3 108349110 108349110 single base substitution G T downstream_gene_variant LUSC-KR 3 108349110 108349110 single base substitution G T intron_variant LUSC-KR 3 108350047 108350047 single base substitution C G downstream_gene_variant LUSC-KR 3 108350047 108350047 single base substitution C G intron_variant LUSC-KR 3 108350235 108350235 single base substitution C G downstream_gene_variant LUSC-KR 3 108350235 108350235 single base substitution C G intron_variant LUSC-KR 3 108352833 108352833 single base substitution A C downstream_gene_variant LUSC-KR 3 108352833 108352833 single base substitution A C intron_variant LUSC-KR 3 108352978 108352978 single base substitution A C intron_variant LUSC-KR 3 108353309 108353309 single base substitution A G intron_variant LUSC-KR 3 108357330 108357330 single base substitution T C intron_variant LUSC-KR 3 108357459 108357459 single base substitution C A intron_variant LUSC-KR 3 108359269 108359269 single base substitution G T intron_variant LUSC-KR 3 108366756 108366756 single base substitution T G intron_variant LUSC-KR 3 108368430 108368430 single base substitution G C downstream_gene_variant LUSC-KR 3 108368430 108368430 single base substitution G C intron_variant LUSC-KR 3 108368500 108368500 single base substitution G C downstream_gene_variant LUSC-KR 3 108368500 108368500 single base substitution G C intron_variant LUSC-KR 3 108371307 108371307 single base substitution A G downstream_gene_variant LUSC-KR 3 108371307 108371307 single base substitution A G intron_variant LUSC-KR 3 108373657 108373657 single base substitution G C intron_variant LUSC-KR 3 108376596 108376596 single base substitution C G intron_variant LUSC-KR 3 108377914 108377914 single base substitution G C intron_variant LUSC-KR 3 108379601 108379601 single base substitution A C intron_variant LUSC-KR 3 108380196 108380196 single base substitution G T intron_variant LUSC-KR 3 108382886 108382886 single base substitution G T intron_variant LUSC-KR 3 108383799 108383799 single base substitution T A intron_variant LUSC-KR 3 108386507 108386507 single base substitution G T intron_variant LUSC-KR 3 108389485 108389485 single base substitution C T intron_variant LUSC-KR 3 108390854 108390854 single base substitution G T intron_variant LUSC-KR 3 108392112 108392112 single base substitution C A intron_variant LUSC-KR 3 108392254 108392254 single base substitution A G intron_variant LUSC-KR 3 108395469 108395469 single base substitution G A intron_variant LUSC-KR 3 108395762 108395762 single base substitution A T intron_variant LUSC-KR 3 108396199 108396199 single base substitution G T intron_variant LUSC-KR 3 108396551 108396551 single base substitution A T intron_variant LUSC-KR 3 108398484 108398484 single base substitution G T intron_variant LUSC-KR 3 108400897 108400897 single base substitution A T intron_variant LUSC-KR 3 108401482 108401482 single base substitution G A intron_variant LUSC-KR 3 108401655 108401655 single base substitution C G intron_variant LUSC-KR 3 108402159 108402159 single base substitution C T intron_variant LUSC-KR 3 108403198 108403198 single base substitution T C intron_variant LUSC-KR 3 108404927 108404927 single base substitution G C intron_variant LUSC-KR 3 108408490 108408490 single base substitution G T intron_variant LUSC-KR 3 108410344 108410344 single base substitution C T downstream_gene_variant LUSC-KR 3 108410344 108410344 single base substitution C T intron_variant LUSC-KR 3 108412059 108412059 single base substitution T A downstream_gene_variant LUSC-KR 3 108412059 108412059 single base substitution T A intron_variant LUSC-KR 3 108414689 108414689 single base substitution G A downstream_gene_variant LUSC-KR 3 108416036 108416036 single base substitution A G downstream_gene_variant LUSC-KR 3 108416277 108416277 single base substitution A G downstream_gene_variant LUSC-KR 3 108418384 108418384 single base substitution C T downstream_gene_variant LUSC-US 3 108363257 108363257 single base substitution A T 3_prime_UTR_variant LUSC-US 3 108363257 108363257 single base substitution A T missense_variant K463I 1388A>T LUSC-US 3 108363259 108363259 single base substitution C T 3_prime_UTR_variant LUSC-US 3 108363259 108363259 single base substitution C T stop_gained Q464* 1390C>T LUSC-US 3 108373066 108373066 single base substitution A T 3_prime_UTR_variant LUSC-US 3 108373066 108373066 single base substitution A T missense_variant K703I 2108A>T LUSC-US 3 108391468 108391468 single base substitution C A 3_prime_UTR_variant LUSC-US 3 108391468 108391468 single base substitution C A missense_variant L852M 2554C>A LUSC-US 3 108394691 108394691 single base substitution G A 3_prime_UTR_variant LUSC-US 3 108394691 108394691 single base substitution G A missense_variant D918N 2752G>A LUSC-US 3 108403065 108403065 single base substitution G T missense_variant M962I 2886G>T LUSC-US 3 108403065 108403065 single base substitution G T splice_region_variant LUSC-US 3 108403129 108403129 single base substitution C G 3_prime_UTR_variant LUSC-US 3 108403129 108403129 single base substitution C G missense_variant Q984E 2950C>G LUSC-US 3 108406926 108406926 single base substitution G A 3_prime_UTR_variant LUSC-US 3 108406926 108406926 single base substitution G A missense_variant D1085N 3253G>A LUSC-US 3 108409675 108409675 single base substitution G A 3_prime_UTR_variant LUSC-US 3 108409675 108409675 single base substitution G A synonymous_variant T1186T 3558G>A MALY-DE 3 108311367 108311367 single base substitution C T intron_variant MALY-DE 3 108311669 108311669 single base substitution C T intron_variant MALY-DE 3 108321472 108321472 single base substitution C A intron_variant MALY-DE 3 108321472 108321472 single base substitution C A upstream_gene_variant MALY-DE 3 108348467 108348468 deletion of <=200bp AC - downstream_gene_variant MALY-DE 3 108348467 108348468 deletion of <=200bp AC - intron_variant MALY-DE 3 108357109 108357109 single base substitution C A intron_variant MALY-DE 3 108359278 108359278 single base substitution A T intron_variant MALY-DE 3 108366245 108366245 deletion of <=200bp G - intron_variant MALY-DE 3 108372403 108372403 single base substitution T G intron_variant MALY-DE 3 108377637 108377637 insertion of <=200bp - A intron_variant MALY-DE 3 108380264 108380264 single base substitution T A intron_variant MALY-DE 3 108384580 108384597 deletion of <=200bp ATGAGAACAGTAATTTGA - intron_variant MALY-DE 3 108388868 108388868 single base substitution G A intron_variant MALY-DE 3 108393110 108393110 single base substitution T A intron_variant MALY-DE 3 108395907 108395907 single base substitution T G intron_variant MALY-DE 3 108397908 108397908 single base substitution A T intron_variant MALY-DE 3 108403021 108403021 single base substitution G T intron_variant MALY-DE 3 108417629 108417629 deletion of <=200bp T - downstream_gene_variant MELA-AU 3 108303659 108303659 single base substitution G A upstream_gene_variant MELA-AU 3 108303964 108303964 deletion of <=200bp G - upstream_gene_variant MELA-AU 3 108304227 108304227 single base substitution A C upstream_gene_variant MELA-AU 3 108304242 108304242 single base substitution C T upstream_gene_variant MELA-AU 3 108304611 108304611 single base substitution G A upstream_gene_variant MELA-AU 3 108304864 108304864 single base substitution T C upstream_gene_variant MELA-AU 3 108305989 108305989 single base substitution G A upstream_gene_variant MELA-AU 3 108306097 108306097 single base substitution C T upstream_gene_variant MELA-AU 3 108306620 108306620 single base substitution A G upstream_gene_variant MELA-AU 3 108308315 108308315 single base substitution C T upstream_gene_variant MELA-AU 3 108308355 108308355 single base substitution G A upstream_gene_variant MELA-AU 3 108308508 108308508 single base substitution G A upstream_gene_variant MELA-AU 3 108310336 108310336 single base substitution G A intron_variant MELA-AU 3 108310618 108310618 single base substitution G A intron_variant MELA-AU 3 108310860 108310860 single base substitution C T intron_variant MELA-AU 3 108310861 108310861 single base substitution C T intron_variant MELA-AU 3 108310939 108310939 single base substitution A T intron_variant MELA-AU 3 108311100 108311100 single base substitution C A intron_variant MELA-AU 3 108311100 108311100 single base substitution C T intron_variant MELA-AU 3 108311446 108311446 single base substitution C T intron_variant MELA-AU 3 108312527 108312527 single base substitution T C intron_variant MELA-AU 3 108312842 108312842 single base substitution C T intron_variant MELA-AU 3 108313023 108313023 single base substitution C T intron_variant MELA-AU 3 108313836 108313836 single base substitution T A intron_variant MELA-AU 3 108313887 108313887 single base substitution C A intron_variant MELA-AU 3 108314219 108314219 single base substitution C T intron_variant MELA-AU 3 108314530 108314530 single base substitution C G intron_variant MELA-AU 3 108315190 108315190 single base substitution A G intron_variant MELA-AU 3 108316119 108316119 single base substitution C T intron_variant MELA-AU 3 108316447 108316447 single base substitution C T intron_variant MELA-AU 3 108316632 108316632 single base substitution C T intron_variant MELA-AU 3 108316772 108316772 single base substitution C T intron_variant MELA-AU 3 108316772 108316772 single base substitution C T upstream_gene_variant MELA-AU 3 108317228 108317228 single base substitution C T intron_variant MELA-AU 3 108317228 108317228 single base substitution C T upstream_gene_variant MELA-AU 3 108317872 108317873 multiple base substitution (>=2bp and <=200bp) GA AT intron_variant MELA-AU 3 108317872 108317873 multiple base substitution (>=2bp and <=200bp) GA AT upstream_gene_variant MELA-AU 3 108318347 108318347 single base substitution A G intron_variant MELA-AU 3 108318347 108318347 single base substitution A G upstream_gene_variant MELA-AU 3 108318451 108318451 single base substitution G A intron_variant MELA-AU 3 108318451 108318451 single base substitution G A upstream_gene_variant MELA-AU 3 108318841 108318841 single base substitution C T intron_variant MELA-AU 3 108318841 108318841 single base substitution C T upstream_gene_variant MELA-AU 3 108319112 108319112 single base substitution C T intron_variant MELA-AU 3 108319112 108319112 single base substitution C T upstream_gene_variant MELA-AU 3 108319167 108319167 single base substitution G A intron_variant MELA-AU 3 108319167 108319167 single base substitution G A upstream_gene_variant MELA-AU 3 108319400 108319400 single base substitution T A intron_variant MELA-AU 3 108319400 108319400 single base substitution T A upstream_gene_variant MELA-AU 3 108319454 108319454 single base substitution C T intron_variant MELA-AU 3 108319454 108319454 single base substitution C T upstream_gene_variant MELA-AU 3 108319540 108319540 single base substitution G A intron_variant MELA-AU 3 108319540 108319540 single base substitution G A upstream_gene_variant MELA-AU 3 108319685 108319685 single base substitution G A intron_variant MELA-AU 3 108319685 108319685 single base substitution G A upstream_gene_variant MELA-AU 3 108319800 108319800 single base substitution T C intron_variant MELA-AU 3 108319800 108319800 single base substitution T C upstream_gene_variant MELA-AU 3 108319880 108319880 single base substitution C T intron_variant MELA-AU 3 108319880 108319880 single base substitution C T upstream_gene_variant MELA-AU 3 108319946 108319946 single base substitution C T intron_variant MELA-AU 3 108319946 108319946 single base substitution C T upstream_gene_variant MELA-AU 3 108320532 108320532 insertion of <=200bp - C intron_variant MELA-AU 3 108320532 108320532 insertion of <=200bp - C upstream_gene_variant MELA-AU 3 108320639 108320639 single base substitution G A intron_variant MELA-AU 3 108320639 108320639 single base substitution G A upstream_gene_variant MELA-AU 3 108320696 108320696 single base substitution C T intron_variant MELA-AU 3 108320696 108320696 single base substitution C T upstream_gene_variant MELA-AU 3 108320929 108320929 deletion of <=200bp T - intron_variant MELA-AU 3 108320929 108320929 deletion of <=200bp T - upstream_gene_variant MELA-AU 3 108321429 108321429 single base substitution G A intron_variant MELA-AU 3 108321429 108321429 single base substitution G A upstream_gene_variant MELA-AU 3 108321485 108321485 single base substitution C T intron_variant MELA-AU 3 108321485 108321485 single base substitution C T upstream_gene_variant MELA-AU 3 108321942 108321942 single base substitution C T 5_prime_UTR_variant MELA-AU 3 108321942 108321942 single base substitution C T intron_variant MELA-AU 3 108323406 108323406 single base substitution C T intron_variant MELA-AU 3 108323632 108323633 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 108323777 108323777 single base substitution C T intron_variant MELA-AU 3 108324115 108324115 single base substitution C T intron_variant MELA-AU 3 108324174 108324174 single base substitution C T intron_variant MELA-AU 3 108324174 108324174 single base substitution C T splice_region_variant MELA-AU 3 108324393 108324393 single base substitution C T intron_variant MELA-AU 3 108326213 108326213 single base substitution C T intron_variant MELA-AU 3 108327470 108327470 single base substitution G A intron_variant MELA-AU 3 108328314 108328314 single base substitution C T intron_variant MELA-AU 3 108328432 108328432 single base substitution C T intron_variant MELA-AU 3 108329067 108329067 single base substitution T C intron_variant MELA-AU 3 108329844 108329844 single base substitution C T intron_variant MELA-AU 3 108329845 108329845 single base substitution C T intron_variant MELA-AU 3 108329956 108329956 single base substitution C A intron_variant MELA-AU 3 108330126 108330126 single base substitution C T 5_prime_UTR_variant MELA-AU 3 108330126 108330126 single base substitution C T exon_variant MELA-AU 3 108330126 108330126 single base substitution C T missense_variant P70S 208C>T MELA-AU 3 108330924 108330925 multiple base substitution (>=2bp and <=200bp) CT TA downstream_gene_variant MELA-AU 3 108330924 108330925 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 3 108331079 108331079 single base substitution G A downstream_gene_variant MELA-AU 3 108331079 108331079 single base substitution G A intron_variant MELA-AU 3 108331411 108331411 single base substitution C T downstream_gene_variant MELA-AU 3 108331411 108331411 single base substitution C T intron_variant MELA-AU 3 108331644 108331644 single base substitution C T downstream_gene_variant MELA-AU 3 108331644 108331644 single base substitution C T intron_variant MELA-AU 3 108332085 108332085 single base substitution C T downstream_gene_variant MELA-AU 3 108332085 108332085 single base substitution C T intron_variant MELA-AU 3 108332444 108332444 single base substitution A T downstream_gene_variant MELA-AU 3 108332444 108332444 single base substitution A T intron_variant MELA-AU 3 108332941 108332941 single base substitution A G downstream_gene_variant MELA-AU 3 108332941 108332941 single base substitution A G intron_variant MELA-AU 3 108333081 108333081 single base substitution C T downstream_gene_variant MELA-AU 3 108333081 108333081 single base substitution C T intron_variant MELA-AU 3 108333082 108333082 single base substitution C T downstream_gene_variant MELA-AU 3 108333082 108333082 single base substitution C T intron_variant MELA-AU 3 108333389 108333389 single base substitution C T downstream_gene_variant MELA-AU 3 108333389 108333389 single base substitution C T intron_variant MELA-AU 3 108333662 108333662 single base substitution C T downstream_gene_variant MELA-AU 3 108333662 108333662 single base substitution C T intron_variant MELA-AU 3 108333738 108333738 single base substitution C T downstream_gene_variant MELA-AU 3 108333738 108333738 single base substitution C T intron_variant MELA-AU 3 108334092 108334092 single base substitution T C downstream_gene_variant MELA-AU 3 108334092 108334092 single base substitution T C intron_variant MELA-AU 3 108334349 108334349 single base substitution C T downstream_gene_variant MELA-AU 3 108334349 108334349 single base substitution C T intron_variant MELA-AU 3 108334709 108334709 single base substitution T C downstream_gene_variant MELA-AU 3 108334709 108334709 single base substitution T C intron_variant MELA-AU 3 108335387 108335387 single base substitution G A splice_acceptor_variant MELA-AU 3 108335564 108335564 single base substitution A G intron_variant MELA-AU 3 108335653 108335653 single base substitution C T intron_variant MELA-AU 3 108335813 108335813 single base substitution C T intron_variant MELA-AU 3 108336379 108336379 single base substitution G A intron_variant MELA-AU 3 108336457 108336457 single base substitution C T intron_variant MELA-AU 3 108336459 108336459 single base substitution C T intron_variant MELA-AU 3 108336781 108336781 single base substitution T A intron_variant MELA-AU 3 108337160 108337160 single base substitution G T intron_variant MELA-AU 3 108338586 108338586 single base substitution C A intron_variant MELA-AU 3 108338979 108338979 single base substitution C T intron_variant MELA-AU 3 108339156 108339156 single base substitution A G intron_variant MELA-AU 3 108339488 108339488 single base substitution A C intron_variant MELA-AU 3 108339823 108339823 single base substitution C T intron_variant MELA-AU 3 108339866 108339866 single base substitution C T intron_variant MELA-AU 3 108339990 108339991 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 108340710 108340710 single base substitution C T intron_variant MELA-AU 3 108341183 108341183 single base substitution C T intron_variant MELA-AU 3 108342374 108342374 single base substitution C T intron_variant MELA-AU 3 108342876 108342876 single base substitution C T intron_variant MELA-AU 3 108342959 108342959 single base substitution G A intron_variant MELA-AU 3 108343202 108343202 single base substitution T A intron_variant MELA-AU 3 108343691 108343691 single base substitution G A intron_variant MELA-AU 3 108343708 108343708 single base substitution T C intron_variant MELA-AU 3 108344358 108344358 single base substitution C T intron_variant MELA-AU 3 108345488 108345488 single base substitution G A intron_variant MELA-AU 3 108345690 108345690 single base substitution C T intron_variant MELA-AU 3 108345783 108345783 single base substitution C T intron_variant MELA-AU 3 108345984 108345984 single base substitution C T intron_variant MELA-AU 3 108346350 108346350 single base substitution C T intron_variant MELA-AU 3 108346474 108346474 single base substitution C T intron_variant MELA-AU 3 108346515 108346515 single base substitution C T intron_variant MELA-AU 3 108346532 108346532 single base substitution C T intron_variant MELA-AU 3 108346533 108346533 single base substitution C T intron_variant MELA-AU 3 108346588 108346588 single base substitution C T intron_variant MELA-AU 3 108346665 108346665 single base substitution C T intron_variant MELA-AU 3 108346813 108346813 single base substitution A G intron_variant MELA-AU 3 108346959 108346959 single base substitution C T intron_variant MELA-AU 3 108346965 108346965 single base substitution C T intron_variant MELA-AU 3 108347160 108347160 single base substitution C A intron_variant MELA-AU 3 108347309 108347309 single base substitution C T intron_variant MELA-AU 3 108347313 108347313 single base substitution C T intron_variant MELA-AU 3 108347352 108347352 single base substitution T C intron_variant MELA-AU 3 108347673 108347673 single base substitution C T intron_variant MELA-AU 3 108348067 108348067 single base substitution G A downstream_gene_variant MELA-AU 3 108348067 108348067 single base substitution G A intron_variant MELA-AU 3 108348093 108348093 single base substitution C T downstream_gene_variant MELA-AU 3 108348093 108348093 single base substitution C T intron_variant MELA-AU 3 108348311 108348311 single base substitution C T downstream_gene_variant MELA-AU 3 108348311 108348311 single base substitution C T intron_variant MELA-AU 3 108348383 108348384 multiple base substitution (>=2bp and <=200bp) GC CT downstream_gene_variant MELA-AU 3 108348383 108348384 multiple base substitution (>=2bp and <=200bp) GC CT intron_variant MELA-AU 3 108348467 108348467 insertion of <=200bp - AC downstream_gene_variant MELA-AU 3 108348467 108348467 insertion of <=200bp - AC intron_variant MELA-AU 3 108348627 108348627 single base substitution G A downstream_gene_variant MELA-AU 3 108348627 108348627 single base substitution G A intron_variant MELA-AU 3 108348769 108348769 single base substitution C T downstream_gene_variant MELA-AU 3 108348769 108348769 single base substitution C T intron_variant MELA-AU 3 108348977 108348977 single base substitution C T downstream_gene_variant MELA-AU 3 108348977 108348977 single base substitution C T intron_variant MELA-AU 3 108349019 108349019 single base substitution T A downstream_gene_variant MELA-AU 3 108349019 108349019 single base substitution T A intron_variant MELA-AU 3 108349156 108349156 single base substitution C A downstream_gene_variant MELA-AU 3 108349156 108349156 single base substitution C A intron_variant MELA-AU 3 108349512 108349512 single base substitution C T downstream_gene_variant MELA-AU 3 108349512 108349512 single base substitution C T intron_variant MELA-AU 3 108349704 108349704 single base substitution C T downstream_gene_variant MELA-AU 3 108349704 108349704 single base substitution C T intron_variant MELA-AU 3 108349791 108349792 multiple base substitution (>=2bp and <=200bp) CC TG downstream_gene_variant MELA-AU 3 108349791 108349792 multiple base substitution (>=2bp and <=200bp) CC TG intron_variant MELA-AU 3 108350045 108350045 single base substitution T C downstream_gene_variant MELA-AU 3 108350045 108350045 single base substitution T C intron_variant MELA-AU 3 108350200 108350200 single base substitution C T downstream_gene_variant MELA-AU 3 108350200 108350200 single base substitution C T intron_variant MELA-AU 3 108350312 108350312 single base substitution C T downstream_gene_variant MELA-AU 3 108350312 108350312 single base substitution C T intron_variant MELA-AU 3 108350477 108350478 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 3 108350477 108350478 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 108350872 108350872 single base substitution C T downstream_gene_variant MELA-AU 3 108350872 108350872 single base substitution C T intron_variant MELA-AU 3 108351943 108351943 single base substitution T C downstream_gene_variant MELA-AU 3 108351943 108351943 single base substitution T C intron_variant MELA-AU 3 108352498 108352498 single base substitution C T downstream_gene_variant MELA-AU 3 108352498 108352498 single base substitution C T intron_variant MELA-AU 3 108352689 108352689 single base substitution C T downstream_gene_variant MELA-AU 3 108352689 108352689 single base substitution C T intron_variant MELA-AU 3 108353332 108353332 single base substitution C T intron_variant MELA-AU 3 108353338 108353338 single base substitution G A intron_variant MELA-AU 3 108353629 108353629 single base substitution G A intron_variant MELA-AU 3 108353830 108353830 single base substitution C T intron_variant MELA-AU 3 108353959 108353959 single base substitution C T intron_variant MELA-AU 3 108354436 108354436 single base substitution C T intron_variant MELA-AU 3 108355516 108355516 single base substitution G A 3_prime_UTR_variant MELA-AU 3 108355516 108355516 single base substitution G A synonymous_variant R324R 972G>A MELA-AU 3 108355879 108355879 single base substitution T A intron_variant MELA-AU 3 108356325 108356325 single base substitution T A intron_variant MELA-AU 3 108356374 108356374 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108356374 108356374 single base substitution C T missense_variant T348I 1043C>T MELA-AU 3 108356521 108356521 single base substitution C T intron_variant MELA-AU 3 108356622 108356622 single base substitution A T intron_variant MELA-AU 3 108356883 108356883 single base substitution C T intron_variant MELA-AU 3 108357008 108357008 single base substitution C T intron_variant MELA-AU 3 108357550 108357550 single base substitution C T intron_variant MELA-AU 3 108357701 108357701 single base substitution C T intron_variant MELA-AU 3 108357986 108357986 single base substitution T G intron_variant MELA-AU 3 108357997 108357997 single base substitution C T intron_variant MELA-AU 3 108358198 108358198 single base substitution T C intron_variant MELA-AU 3 108358255 108358255 single base substitution C T intron_variant MELA-AU 3 108358402 108358402 single base substitution G A intron_variant MELA-AU 3 108358500 108358500 single base substitution C T intron_variant MELA-AU 3 108358655 108358655 single base substitution C T intron_variant MELA-AU 3 108358739 108358739 single base substitution C T intron_variant MELA-AU 3 108359526 108359526 single base substitution C T intron_variant MELA-AU 3 108359879 108359879 single base substitution C T intron_variant MELA-AU 3 108359945 108359945 single base substitution T C intron_variant MELA-AU 3 108360273 108360273 single base substitution C T intron_variant MELA-AU 3 108360916 108360916 single base substitution T G intron_variant MELA-AU 3 108361229 108361229 single base substitution G T intron_variant MELA-AU 3 108361231 108361231 single base substitution C A intron_variant MELA-AU 3 108361333 108361333 single base substitution G A 3_prime_UTR_variant MELA-AU 3 108361333 108361333 single base substitution G A synonymous_variant P371P 1113G>A MELA-AU 3 108361732 108361732 single base substitution T C intron_variant MELA-AU 3 108361748 108361748 single base substitution G A intron_variant MELA-AU 3 108361913 108361913 single base substitution C T intron_variant MELA-AU 3 108362471 108362471 single base substitution C T intron_variant MELA-AU 3 108362525 108362525 single base substitution C T intron_variant MELA-AU 3 108362614 108362614 single base substitution C T intron_variant MELA-AU 3 108362627 108362627 single base substitution A G intron_variant MELA-AU 3 108362818 108362818 single base substitution T G intron_variant MELA-AU 3 108362830 108362830 single base substitution G A intron_variant MELA-AU 3 108363029 108363029 single base substitution A T 3_prime_UTR_variant MELA-AU 3 108363029 108363029 single base substitution A T missense_variant K387M 1160A>T MELA-AU 3 108363124 108363124 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108363124 108363124 single base substitution C T missense_variant P419S 1255C>T MELA-AU 3 108363432 108363432 single base substitution C A 3_prime_UTR_variant MELA-AU 3 108363432 108363432 single base substitution C A synonymous_variant L521L 1563C>A MELA-AU 3 108363453 108363453 single base substitution A C 3_prime_UTR_variant MELA-AU 3 108363453 108363453 single base substitution A C synonymous_variant S528S 1584A>C MELA-AU 3 108363531 108363531 single base substitution C A 3_prime_UTR_variant MELA-AU 3 108363531 108363531 single base substitution C A synonymous_variant P554P 1662C>A MELA-AU 3 108363982 108363982 single base substitution C T intron_variant MELA-AU 3 108364024 108364024 single base substitution G A intron_variant MELA-AU 3 108364430 108364430 single base substitution C T intron_variant MELA-AU 3 108364864 108364864 single base substitution C T intron_variant MELA-AU 3 108364903 108364903 single base substitution C T intron_variant MELA-AU 3 108365014 108365014 single base substitution C T intron_variant MELA-AU 3 108365392 108365392 single base substitution C T intron_variant MELA-AU 3 108365449 108365449 single base substitution C T intron_variant MELA-AU 3 108366059 108366059 single base substitution T A intron_variant MELA-AU 3 108366063 108366063 single base substitution C T intron_variant MELA-AU 3 108366558 108366558 single base substitution C T intron_variant MELA-AU 3 108366644 108366644 single base substitution C T intron_variant MELA-AU 3 108367087 108367087 single base substitution A G 3_prime_UTR_variant MELA-AU 3 108367087 108367087 single base substitution A G downstream_gene_variant MELA-AU 3 108367087 108367087 single base substitution A G intron_variant MELA-AU 3 108367106 108367106 single base substitution T A 3_prime_UTR_variant MELA-AU 3 108367106 108367106 single base substitution T A downstream_gene_variant MELA-AU 3 108367106 108367106 single base substitution T A intron_variant MELA-AU 3 108367349 108367349 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108367349 108367349 single base substitution C T downstream_gene_variant MELA-AU 3 108367349 108367349 single base substitution C T intron_variant MELA-AU 3 108368643 108368643 single base substitution C T downstream_gene_variant MELA-AU 3 108368643 108368643 single base substitution C T intron_variant MELA-AU 3 108369085 108369085 single base substitution C T downstream_gene_variant MELA-AU 3 108369085 108369085 single base substitution C T intron_variant MELA-AU 3 108369526 108369527 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 3 108369526 108369527 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 108369638 108369638 single base substitution A T downstream_gene_variant MELA-AU 3 108369638 108369638 single base substitution A T intron_variant MELA-AU 3 108370004 108370004 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108370004 108370004 single base substitution C T downstream_gene_variant MELA-AU 3 108370004 108370004 single base substitution C T synonymous_variant D676D 2028C>T MELA-AU 3 108370025 108370025 single base substitution T C downstream_gene_variant MELA-AU 3 108370025 108370025 single base substitution T C intron_variant MELA-AU 3 108370107 108370107 single base substitution C T downstream_gene_variant MELA-AU 3 108370107 108370107 single base substitution C T intron_variant MELA-AU 3 108371020 108371020 single base substitution C T downstream_gene_variant MELA-AU 3 108371020 108371020 single base substitution C T intron_variant MELA-AU 3 108371119 108371119 single base substitution C T downstream_gene_variant MELA-AU 3 108371119 108371119 single base substitution C T intron_variant MELA-AU 3 108371381 108371381 single base substitution T A downstream_gene_variant MELA-AU 3 108371381 108371381 single base substitution T A intron_variant MELA-AU 3 108371619 108371619 single base substitution C T downstream_gene_variant MELA-AU 3 108371619 108371619 single base substitution C T intron_variant MELA-AU 3 108371815 108371815 single base substitution C T downstream_gene_variant MELA-AU 3 108371815 108371815 single base substitution C T intron_variant MELA-AU 3 108372022 108372022 single base substitution T C intron_variant MELA-AU 3 108372078 108372078 single base substitution C T intron_variant MELA-AU 3 108372237 108372237 single base substitution G A intron_variant MELA-AU 3 108372551 108372551 single base substitution G A intron_variant MELA-AU 3 108373235 108373235 single base substitution C T intron_variant MELA-AU 3 108373382 108373382 single base substitution C T intron_variant MELA-AU 3 108373432 108373432 single base substitution G A intron_variant MELA-AU 3 108373438 108373438 single base substitution C T intron_variant MELA-AU 3 108374004 108374004 single base substitution T G intron_variant MELA-AU 3 108374412 108374412 single base substitution C T intron_variant MELA-AU 3 108374584 108374584 single base substitution C T intron_variant MELA-AU 3 108374585 108374585 single base substitution C T intron_variant MELA-AU 3 108374886 108374886 single base substitution C T intron_variant MELA-AU 3 108374894 108374894 single base substitution C T intron_variant MELA-AU 3 108374966 108374966 single base substitution C T intron_variant MELA-AU 3 108375089 108375089 single base substitution C T intron_variant MELA-AU 3 108375441 108375441 single base substitution C T intron_variant MELA-AU 3 108375460 108375460 single base substitution C T intron_variant MELA-AU 3 108375585 108375585 single base substitution C T intron_variant MELA-AU 3 108377063 108377063 single base substitution C T intron_variant MELA-AU 3 108378004 108378004 single base substitution C T intron_variant MELA-AU 3 108378043 108378043 single base substitution G A intron_variant MELA-AU 3 108378195 108378195 single base substitution C T intron_variant MELA-AU 3 108378609 108378609 single base substitution C A intron_variant MELA-AU 3 108379065 108379065 single base substitution A T intron_variant MELA-AU 3 108379742 108379742 single base substitution C T intron_variant MELA-AU 3 108379917 108379917 single base substitution C T intron_variant MELA-AU 3 108379925 108379925 single base substitution G A intron_variant MELA-AU 3 108380633 108380633 single base substitution A G intron_variant MELA-AU 3 108381566 108381566 single base substitution C T intron_variant MELA-AU 3 108381903 108381903 single base substitution T C intron_variant MELA-AU 3 108382125 108382125 single base substitution C T intron_variant MELA-AU 3 108382151 108382151 single base substitution C T intron_variant MELA-AU 3 108382160 108382160 single base substitution T G intron_variant MELA-AU 3 108382317 108382317 single base substitution C T intron_variant MELA-AU 3 108382349 108382349 single base substitution G A intron_variant MELA-AU 3 108382560 108382560 single base substitution C T intron_variant MELA-AU 3 108382849 108382850 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 108382927 108382927 single base substitution G A intron_variant MELA-AU 3 108382991 108382991 single base substitution T A intron_variant MELA-AU 3 108383437 108383437 single base substitution C T intron_variant MELA-AU 3 108383492 108383492 single base substitution C T intron_variant MELA-AU 3 108383735 108383735 single base substitution C T intron_variant MELA-AU 3 108384182 108384182 single base substitution G A intron_variant MELA-AU 3 108384614 108384614 single base substitution C T intron_variant MELA-AU 3 108384939 108384939 single base substitution C T intron_variant MELA-AU 3 108385413 108385413 single base substitution C G intron_variant MELA-AU 3 108385417 108385417 single base substitution C T intron_variant MELA-AU 3 108385884 108385884 single base substitution G A intron_variant MELA-AU 3 108386059 108386059 single base substitution C T intron_variant MELA-AU 3 108386318 108386318 single base substitution C T intron_variant MELA-AU 3 108386625 108386625 single base substitution G T intron_variant MELA-AU 3 108386638 108386638 single base substitution G C intron_variant MELA-AU 3 108386828 108386828 single base substitution C T intron_variant MELA-AU 3 108386913 108386913 single base substitution G A intron_variant MELA-AU 3 108387215 108387215 single base substitution G A intron_variant MELA-AU 3 108387542 108387542 single base substitution T G intron_variant MELA-AU 3 108387679 108387679 single base substitution C T intron_variant MELA-AU 3 108387728 108387728 single base substitution C T intron_variant MELA-AU 3 108387772 108387772 single base substitution C G intron_variant MELA-AU 3 108388256 108388256 single base substitution A T intron_variant MELA-AU 3 108388385 108388385 single base substitution G A intron_variant MELA-AU 3 108388952 108388952 single base substitution C T intron_variant MELA-AU 3 108388997 108388997 single base substitution C T intron_variant MELA-AU 3 108389153 108389153 single base substitution C T intron_variant MELA-AU 3 108389289 108389289 single base substitution C T intron_variant MELA-AU 3 108389375 108389375 single base substitution C T intron_variant MELA-AU 3 108389386 108389386 single base substitution G A intron_variant MELA-AU 3 108389551 108389551 single base substitution G A intron_variant MELA-AU 3 108389717 108389717 single base substitution C T intron_variant MELA-AU 3 108389747 108389747 single base substitution C T intron_variant MELA-AU 3 108389773 108389773 single base substitution C T intron_variant MELA-AU 3 108389799 108389799 single base substitution C T intron_variant MELA-AU 3 108389860 108389860 single base substitution C T intron_variant MELA-AU 3 108390038 108390038 single base substitution C T intron_variant MELA-AU 3 108390039 108390039 single base substitution C T intron_variant MELA-AU 3 108390075 108390075 single base substitution T C intron_variant MELA-AU 3 108390212 108390213 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 3 108390485 108390485 single base substitution C T intron_variant MELA-AU 3 108390603 108390603 single base substitution G A intron_variant MELA-AU 3 108391156 108391156 single base substitution C T intron_variant MELA-AU 3 108391562 108391562 single base substitution A T intron_variant MELA-AU 3 108391637 108391637 single base substitution T C intron_variant MELA-AU 3 108392009 108392009 single base substitution A G intron_variant MELA-AU 3 108392467 108392467 single base substitution C T intron_variant MELA-AU 3 108392506 108392506 single base substitution C T intron_variant MELA-AU 3 108392666 108392666 single base substitution G A intron_variant MELA-AU 3 108392745 108392745 single base substitution G A intron_variant MELA-AU 3 108392984 108392984 single base substitution G A 3_prime_UTR_variant MELA-AU 3 108392984 108392984 single base substitution G A synonymous_variant K883K 2649G>A MELA-AU 3 108393173 108393173 single base substitution C T intron_variant MELA-AU 3 108393182 108393182 single base substitution C T intron_variant MELA-AU 3 108393461 108393461 single base substitution C T intron_variant MELA-AU 3 108393702 108393702 single base substitution T A intron_variant MELA-AU 3 108394007 108394007 single base substitution C T intron_variant MELA-AU 3 108394144 108394144 single base substitution G A intron_variant MELA-AU 3 108394316 108394316 single base substitution C T intron_variant MELA-AU 3 108394377 108394377 single base substitution C T intron_variant MELA-AU 3 108394510 108394510 single base substitution T C intron_variant MELA-AU 3 108394607 108394607 single base substitution C T intron_variant MELA-AU 3 108394619 108394619 single base substitution C T intron_variant MELA-AU 3 108394807 108394807 single base substitution G A intron_variant MELA-AU 3 108394821 108394821 single base substitution C T intron_variant MELA-AU 3 108395153 108395153 single base substitution C T intron_variant MELA-AU 3 108395253 108395253 single base substitution T C intron_variant MELA-AU 3 108395282 108395282 single base substitution T C intron_variant MELA-AU 3 108395523 108395523 single base substitution C T intron_variant MELA-AU 3 108395888 108395888 single base substitution C T intron_variant MELA-AU 3 108396015 108396015 single base substitution T A intron_variant MELA-AU 3 108396024 108396024 single base substitution T A intron_variant MELA-AU 3 108396619 108396619 single base substitution G A intron_variant MELA-AU 3 108397350 108397350 single base substitution C T intron_variant MELA-AU 3 108397933 108397933 single base substitution C T intron_variant MELA-AU 3 108397943 108397943 single base substitution C T intron_variant MELA-AU 3 108398571 108398571 single base substitution T G intron_variant MELA-AU 3 108398590 108398590 single base substitution C T intron_variant MELA-AU 3 108398891 108398891 single base substitution C T intron_variant MELA-AU 3 108398910 108398910 single base substitution A T intron_variant MELA-AU 3 108399447 108399447 single base substitution C T intron_variant MELA-AU 3 108399538 108399538 single base substitution T A intron_variant MELA-AU 3 108399724 108399724 single base substitution G C intron_variant MELA-AU 3 108399771 108399771 single base substitution C T intron_variant MELA-AU 3 108399814 108399814 single base substitution T C intron_variant MELA-AU 3 108400006 108400006 single base substitution G A intron_variant MELA-AU 3 108400553 108400553 single base substitution T C intron_variant MELA-AU 3 108401387 108401387 single base substitution C T intron_variant MELA-AU 3 108401577 108401577 single base substitution T C intron_variant MELA-AU 3 108402361 108402361 single base substitution T C intron_variant MELA-AU 3 108402458 108402458 single base substitution C T intron_variant MELA-AU 3 108402540 108402540 single base substitution C T intron_variant MELA-AU 3 108402652 108402652 single base substitution C T intron_variant MELA-AU 3 108403107 108403107 single base substitution T A 3_prime_UTR_variant MELA-AU 3 108403107 108403107 single base substitution T A missense_variant F976L 2928T>A MELA-AU 3 108404530 108404530 single base substitution C T intron_variant MELA-AU 3 108404719 108404719 single base substitution C T intron_variant MELA-AU 3 108405247 108405247 single base substitution C T intron_variant MELA-AU 3 108406350 108406350 single base substitution C T intron_variant MELA-AU 3 108406638 108406638 single base substitution C T intron_variant MELA-AU 3 108406807 108406807 single base substitution C T intron_variant MELA-AU 3 108407018 108407018 single base substitution C T intron_variant MELA-AU 3 108407018 108407019 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 108407259 108407259 single base substitution A T intron_variant MELA-AU 3 108407551 108407551 single base substitution G A 3_prime_UTR_variant MELA-AU 3 108407551 108407551 single base substitution G A missense_variant G1128S 3382G>A MELA-AU 3 108407695 108407695 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108407695 108407695 single base substitution C T missense_variant P1147L 3440C>T MELA-AU 3 108407718 108407718 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108407718 108407718 single base substitution C T synonymous_variant L1155L 3463C>T MELA-AU 3 108407789 108407789 single base substitution C T intron_variant MELA-AU 3 108407820 108407820 single base substitution C T intron_variant MELA-AU 3 108407878 108407878 single base substitution G T intron_variant MELA-AU 3 108408563 108408563 single base substitution G A intron_variant MELA-AU 3 108408877 108408877 single base substitution C T intron_variant MELA-AU 3 108408949 108408949 single base substitution T C intron_variant MELA-AU 3 108408994 108408994 single base substitution C T intron_variant MELA-AU 3 108409178 108409178 single base substitution C T intron_variant MELA-AU 3 108409354 108409354 single base substitution C T intron_variant MELA-AU 3 108409510 108409510 single base substitution C T intron_variant MELA-AU 3 108410321 108410321 single base substitution G A downstream_gene_variant MELA-AU 3 108410321 108410321 single base substitution G A intron_variant MELA-AU 3 108410389 108410389 single base substitution G A downstream_gene_variant MELA-AU 3 108410389 108410389 single base substitution G A intron_variant MELA-AU 3 108410520 108410520 single base substitution G A downstream_gene_variant MELA-AU 3 108410520 108410520 single base substitution G A intron_variant MELA-AU 3 108411042 108411042 single base substitution A T downstream_gene_variant MELA-AU 3 108411042 108411042 single base substitution A T intron_variant MELA-AU 3 108411196 108411196 single base substitution G A downstream_gene_variant MELA-AU 3 108411196 108411196 single base substitution G A intron_variant MELA-AU 3 108412444 108412444 single base substitution A G 3_prime_UTR_variant MELA-AU 3 108412444 108412444 single base substitution A G downstream_gene_variant MELA-AU 3 108412990 108412990 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108412990 108412990 single base substitution C T downstream_gene_variant MELA-AU 3 108413111 108413111 single base substitution T C 3_prime_UTR_variant MELA-AU 3 108413111 108413111 single base substitution T C downstream_gene_variant MELA-AU 3 108413230 108413230 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108413230 108413230 single base substitution C T downstream_gene_variant MELA-AU 3 108413282 108413282 single base substitution G A 3_prime_UTR_variant MELA-AU 3 108413282 108413282 single base substitution G A downstream_gene_variant MELA-AU 3 108413302 108413302 single base substitution C T 3_prime_UTR_variant MELA-AU 3 108413302 108413302 single base substitution C T downstream_gene_variant MELA-AU 3 108414150 108414150 single base substitution A T downstream_gene_variant MELA-AU 3 108414348 108414348 single base substitution G A downstream_gene_variant MELA-AU 3 108414688 108414688 single base substitution C T downstream_gene_variant MELA-AU 3 108414755 108414755 single base substitution T A downstream_gene_variant MELA-AU 3 108414892 108414892 single base substitution C T downstream_gene_variant MELA-AU 3 108415041 108415041 single base substitution C T downstream_gene_variant MELA-AU 3 108415219 108415219 single base substitution C T downstream_gene_variant MELA-AU 3 108415314 108415314 single base substitution C T downstream_gene_variant MELA-AU 3 108415911 108415911 single base substitution G A downstream_gene_variant MELA-AU 3 108416356 108416356 single base substitution G A downstream_gene_variant MELA-AU 3 108416818 108416818 single base substitution C T downstream_gene_variant MELA-AU 3 108416940 108416940 single base substitution C T downstream_gene_variant MELA-AU 3 108416996 108416996 single base substitution T A downstream_gene_variant MELA-AU 3 108417269 108417269 single base substitution C T downstream_gene_variant MELA-AU 3 108417489 108417489 single base substitution G A downstream_gene_variant MELA-AU 3 108417568 108417568 single base substitution T C downstream_gene_variant MELA-AU 3 108417953 108417953 single base substitution A C downstream_gene_variant MELA-AU 3 108417965 108417965 single base substitution C T downstream_gene_variant MELA-AU 3 108418126 108418126 single base substitution C T downstream_gene_variant MELA-AU 3 108418408 108418408 single base substitution C T downstream_gene_variant MELA-AU 3 108418412 108418412 single base substitution G A downstream_gene_variant MELA-AU 3 108418605 108418605 single base substitution C T downstream_gene_variant MELA-AU 3 108418643 108418643 single base substitution C T downstream_gene_variant ORCA-IN 3 108325745 108325745 single base substitution G T intron_variant ORCA-IN 3 108331440 108331440 single base substitution G A downstream_gene_variant ORCA-IN 3 108331440 108331440 single base substitution G A intron_variant ORCA-IN 3 108362288 108362288 single base substitution C T intron_variant ORCA-IN 3 108373788 108373788 single base substitution G A intron_variant ORCA-IN 3 108381784 108381784 single base substitution T G intron_variant ORCA-IN 3 108386526 108386526 single base substitution C G intron_variant OV-AU 3 108306858 108306858 single base substitution C T upstream_gene_variant OV-AU 3 108309541 108309541 single base substitution C A intron_variant OV-AU 3 108318439 108318439 single base substitution G T intron_variant OV-AU 3 108318439 108318439 single base substitution G T upstream_gene_variant OV-AU 3 108327774 108327774 single base substitution G T intron_variant OV-AU 3 108331079 108331079 single base substitution G C downstream_gene_variant OV-AU 3 108331079 108331079 single base substitution G C intron_variant OV-AU 3 108331179 108331179 single base substitution C T downstream_gene_variant OV-AU 3 108331179 108331179 single base substitution C T intron_variant OV-AU 3 108337301 108337301 single base substitution C A intron_variant OV-AU 3 108339793 108339793 single base substitution C T intron_variant OV-AU 3 108339816 108339816 single base substitution G A intron_variant OV-AU 3 108342125 108342125 single base substitution G A intron_variant OV-AU 3 108342154 108342154 single base substitution G T intron_variant OV-AU 3 108346560 108346560 single base substitution T G intron_variant OV-AU 3 108351929 108351929 single base substitution T C downstream_gene_variant OV-AU 3 108351929 108351929 single base substitution T C intron_variant OV-AU 3 108354545 108354545 single base substitution T C intron_variant OV-AU 3 108357443 108357443 single base substitution C T intron_variant OV-AU 3 108358457 108358457 single base substitution G C intron_variant OV-AU 3 108358458 108358458 single base substitution C A intron_variant OV-AU 3 108360004 108360004 single base substitution C G intron_variant OV-AU 3 108366225 108366225 single base substitution A T intron_variant OV-AU 3 108368699 108368699 single base substitution G A downstream_gene_variant OV-AU 3 108368699 108368699 single base substitution G A intron_variant OV-AU 3 108370344 108370344 single base substitution C G downstream_gene_variant OV-AU 3 108370344 108370344 single base substitution C G intron_variant OV-AU 3 108370827 108370827 single base substitution T C downstream_gene_variant OV-AU 3 108370827 108370827 single base substitution T C intron_variant OV-AU 3 108372593 108372593 single base substitution A G intron_variant OV-AU 3 108382363 108382363 single base substitution G T intron_variant OV-AU 3 108390949 108390949 single base substitution T A intron_variant OV-AU 3 108398378 108398378 single base substitution A T intron_variant OV-AU 3 108399242 108399242 single base substitution G A intron_variant OV-AU 3 108404522 108404522 single base substitution G A intron_variant OV-AU 3 108412869 108412869 single base substitution A C 3_prime_UTR_variant OV-AU 3 108412869 108412869 single base substitution A C downstream_gene_variant OV-AU 3 108415811 108415811 single base substitution T C downstream_gene_variant OV-AU 3 108416050 108416050 single base substitution A T downstream_gene_variant OV-AU 3 108416677 108416677 single base substitution G C downstream_gene_variant PACA-AU 3 108310035 108310035 single base substitution G A intron_variant PACA-AU 3 108311263 108311263 single base substitution A T intron_variant PACA-AU 3 108312253 108312253 single base substitution G C intron_variant PACA-AU 3 108312254 108312254 single base substitution G T intron_variant PACA-AU 3 108312527 108312527 single base substitution T C intron_variant PACA-AU 3 108312531 108312531 single base substitution T C intron_variant PACA-AU 3 108314902 108314902 single base substitution G A intron_variant PACA-AU 3 108314923 108314923 single base substitution G A intron_variant PACA-AU 3 108315557 108315557 single base substitution G T intron_variant PACA-AU 3 108315678 108315678 single base substitution G A intron_variant PACA-AU 3 108327051 108327051 insertion of <=200bp - AAC intron_variant PACA-AU 3 108329422 108329422 single base substitution C A intron_variant PACA-AU 3 108334623 108334623 single base substitution A T downstream_gene_variant PACA-AU 3 108334623 108334623 single base substitution A T intron_variant PACA-AU 3 108340147 108340147 single base substitution A C intron_variant PACA-AU 3 108351305 108351305 single base substitution A G downstream_gene_variant PACA-AU 3 108351305 108351305 single base substitution A G intron_variant PACA-AU 3 108351661 108351661 deletion of <=200bp A - downstream_gene_variant PACA-AU 3 108351661 108351661 deletion of <=200bp A - intron_variant PACA-AU 3 108352709 108352709 single base substitution G A downstream_gene_variant PACA-AU 3 108352709 108352709 single base substitution G A intron_variant PACA-AU 3 108353351 108353351 single base substitution A C intron_variant PACA-AU 3 108355542 108355542 single base substitution T C 3_prime_UTR_variant PACA-AU 3 108355542 108355542 single base substitution T C missense_variant I333T 998T>C PACA-AU 3 108356675 108356675 single base substitution G T intron_variant PACA-AU 3 108357937 108357937 single base substitution C T intron_variant PACA-AU 3 108360139 108360139 insertion of <=200bp - T intron_variant PACA-AU 3 108363449 108363449 single base substitution A G 3_prime_UTR_variant PACA-AU 3 108363449 108363449 single base substitution A G missense_variant N527S 1580A>G PACA-AU 3 108368727 108368727 single base substitution A G downstream_gene_variant PACA-AU 3 108368727 108368727 single base substitution A G intron_variant PACA-AU 3 108370687 108370687 single base substitution G T downstream_gene_variant PACA-AU 3 108370687 108370687 single base substitution G T intron_variant PACA-AU 3 108371115 108371115 single base substitution G C downstream_gene_variant PACA-AU 3 108371115 108371115 single base substitution G C intron_variant PACA-AU 3 108372374 108372374 single base substitution A G intron_variant PACA-AU 3 108372438 108372438 single base substitution T A intron_variant PACA-AU 3 108372728 108372728 single base substitution T C intron_variant PACA-AU 3 108373213 108373213 single base substitution G A intron_variant PACA-AU 3 108376343 108376343 single base substitution A T intron_variant PACA-AU 3 108390685 108390685 insertion of <=200bp - T intron_variant PACA-AU 3 108393729 108393729 single base substitution T G intron_variant PACA-AU 3 108399007 108399007 single base substitution C T intron_variant PACA-AU 3 108402289 108402289 deletion of <=200bp T - intron_variant PACA-AU 3 108404901 108404901 insertion of <=200bp - T intron_variant PACA-AU 3 108406732 108406732 single base substitution C T intron_variant PACA-AU 3 108413103 108413103 insertion of <=200bp - A 3_prime_UTR_variant PACA-AU 3 108413103 108413103 insertion of <=200bp - A downstream_gene_variant PACA-CA 3 108308373 108308373 single base substitution A G upstream_gene_variant PACA-CA 3 108308591 108308591 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 3 108308591 108308591 single base substitution C G upstream_gene_variant PACA-CA 3 108313327 108313327 single base substitution G A intron_variant PACA-CA 3 108314239 108314239 insertion of <=200bp - T intron_variant PACA-CA 3 108315283 108315283 single base substitution C G intron_variant PACA-CA 3 108317235 108317235 single base substitution C G intron_variant PACA-CA 3 108317235 108317235 single base substitution C G upstream_gene_variant PACA-CA 3 108319206 108319206 single base substitution A T intron_variant PACA-CA 3 108319206 108319206 single base substitution A T upstream_gene_variant PACA-CA 3 108320419 108320419 single base substitution A G intron_variant PACA-CA 3 108320419 108320419 single base substitution A G upstream_gene_variant PACA-CA 3 108322711 108322711 single base substitution C A intron_variant PACA-CA 3 108335235 108335235 single base substitution T C intron_variant PACA-CA 3 108336202 108336202 single base substitution C T intron_variant PACA-CA 3 108339806 108339806 single base substitution C A intron_variant PACA-CA 3 108341192 108341192 single base substitution A G intron_variant PACA-CA 3 108341782 108341782 single base substitution C T intron_variant PACA-CA 3 108342074 108342074 single base substitution T G intron_variant PACA-CA 3 108346195 108346195 single base substitution C T intron_variant PACA-CA 3 108346392 108346392 insertion of <=200bp - C intron_variant PACA-CA 3 108349416 108349416 single base substitution C G downstream_gene_variant PACA-CA 3 108349416 108349416 single base substitution C G intron_variant PACA-CA 3 108349901 108349901 single base substitution C T downstream_gene_variant PACA-CA 3 108349901 108349901 single base substitution C T intron_variant PACA-CA 3 108352442 108352442 single base substitution A G downstream_gene_variant PACA-CA 3 108352442 108352442 single base substitution A G intron_variant PACA-CA 3 108352779 108352779 single base substitution A G downstream_gene_variant PACA-CA 3 108352779 108352779 single base substitution A G intron_variant PACA-CA 3 108352784 108352784 single base substitution T C downstream_gene_variant PACA-CA 3 108352784 108352784 single base substitution T C intron_variant PACA-CA 3 108352833 108352833 single base substitution A C downstream_gene_variant PACA-CA 3 108352833 108352833 single base substitution A C intron_variant PACA-CA 3 108355654 108355654 single base substitution T C intron_variant PACA-CA 3 108362323 108362323 single base substitution A G intron_variant PACA-CA 3 108362423 108362423 single base substitution T C intron_variant PACA-CA 3 108362652 108362652 single base substitution G T intron_variant PACA-CA 3 108364675 108364675 single base substitution G C intron_variant PACA-CA 3 108366472 108366472 single base substitution G C intron_variant PACA-CA 3 108369509 108369509 single base substitution G A downstream_gene_variant PACA-CA 3 108369509 108369509 single base substitution G A intron_variant PACA-CA 3 108373153 108373153 single base substitution A C 3_prime_UTR_variant PACA-CA 3 108373153 108373153 single base substitution A C missense_variant E732A 2195A>C PACA-CA 3 108374174 108374174 single base substitution A C intron_variant PACA-CA 3 108375602 108375602 single base substitution G A intron_variant PACA-CA 3 108379826 108379826 single base substitution G T intron_variant PACA-CA 3 108381015 108381015 single base substitution G A 3_prime_UTR_variant PACA-CA 3 108381015 108381015 single base substitution G A stop_gained W778* 2334G>A PACA-CA 3 108381060 108381060 single base substitution A T 3_prime_UTR_variant PACA-CA 3 108381060 108381060 single base substitution A T synonymous_variant A793A 2379A>T PACA-CA 3 108383324 108383324 single base substitution C A intron_variant PACA-CA 3 108385580 108385580 single base substitution C T intron_variant PACA-CA 3 108386223 108386223 insertion of <=200bp - A intron_variant PACA-CA 3 108390302 108390302 single base substitution A G intron_variant PACA-CA 3 108391307 108391307 single base substitution T C intron_variant PACA-CA 3 108393164 108393164 insertion of <=200bp - T intron_variant PACA-CA 3 108399568 108399568 single base substitution C G intron_variant PACA-CA 3 108399900 108399900 single base substitution G T intron_variant PACA-CA 3 108400528 108400528 single base substitution A G intron_variant PACA-CA 3 108401270 108401270 single base substitution T G intron_variant PACA-CA 3 108405509 108405509 single base substitution T C intron_variant PACA-CA 3 108406895 108406895 single base substitution T G 3_prime_UTR_variant PACA-CA 3 108406895 108406895 single base substitution T G missense_variant D1074E 3222T>G PACA-CA 3 108409675 108409675 single base substitution G T 3_prime_UTR_variant PACA-CA 3 108409675 108409675 single base substitution G T synonymous_variant T1186T 3558G>T PACA-CA 3 108411068 108411068 single base substitution T A downstream_gene_variant PACA-CA 3 108411068 108411068 single base substitution T A intron_variant PACA-CA 3 108411742 108411742 single base substitution A G downstream_gene_variant PACA-CA 3 108411742 108411742 single base substitution A G intron_variant PACA-CA 3 108418688 108418688 single base substitution C T downstream_gene_variant PAEN-AU 3 108335160 108335160 single base substitution A G intron_variant PAEN-AU 3 108343224 108343224 single base substitution A T intron_variant PAEN-AU 3 108360699 108360702 deletion of <=200bp TTTG - intron_variant PAEN-AU 3 108375778 108375778 single base substitution G A intron_variant PAEN-AU 3 108406187 108406187 single base substitution A G intron_variant PAEN-IT 3 108346024 108346024 single base substitution G A intron_variant PBCA-DE 3 108308400 108308400 single base substitution G T upstream_gene_variant PBCA-DE 3 108313235 108313236 deletion of <=200bp TC - intron_variant PBCA-DE 3 108321889 108321889 single base substitution A T 5_prime_UTR_variant PBCA-DE 3 108321889 108321889 single base substitution A T intron_variant PBCA-DE 3 108323726 108323726 single base substitution T C intron_variant PBCA-DE 3 108338150 108338151 deletion of <=200bp TG - intron_variant PBCA-DE 3 108339738 108339738 single base substitution G A intron_variant PBCA-DE 3 108348350 108348350 single base substitution G A downstream_gene_variant PBCA-DE 3 108348350 108348350 single base substitution G A intron_variant PBCA-DE 3 108348467 108348468 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 3 108348467 108348468 deletion of <=200bp AC - intron_variant PBCA-DE 3 108352756 108352759 deletion of <=200bp TCTC - downstream_gene_variant PBCA-DE 3 108352756 108352759 deletion of <=200bp TCTC - intron_variant PBCA-DE 3 108366218 108366218 deletion of <=200bp A - intron_variant PBCA-DE 3 108374515 108374515 single base substitution C T intron_variant PBCA-DE 3 108378197 108378197 single base substitution A G intron_variant PBCA-DE 3 108383875 108383875 single base substitution A G intron_variant PBCA-DE 3 108386001 108386001 insertion of <=200bp - A intron_variant PBCA-DE 3 108399109 108399109 single base substitution T A intron_variant PBCA-DE 3 108417378 108417378 single base substitution C A downstream_gene_variant PRAD-CA 3 108309323 108309323 single base substitution C T intron_variant PRAD-CA 3 108322597 108322597 single base substitution T C intron_variant PRAD-CA 3 108326689 108326689 single base substitution G A intron_variant PRAD-CA 3 108328257 108328257 single base substitution G T intron_variant PRAD-CA 3 108329149 108329149 single base substitution A G intron_variant PRAD-CA 3 108338802 108338802 single base substitution T G intron_variant PRAD-CA 3 108340442 108340442 single base substitution A G intron_variant PRAD-CA 3 108341727 108341727 single base substitution C G intron_variant PRAD-CA 3 108349904 108349904 single base substitution T A downstream_gene_variant PRAD-CA 3 108349904 108349904 single base substitution T A intron_variant PRAD-CA 3 108352482 108352482 single base substitution C G downstream_gene_variant PRAD-CA 3 108352482 108352482 single base substitution C G intron_variant PRAD-CA 3 108352709 108352709 single base substitution G A downstream_gene_variant PRAD-CA 3 108352709 108352709 single base substitution G A intron_variant PRAD-CA 3 108359880 108359880 single base substitution C T intron_variant PRAD-CA 3 108368271 108368271 single base substitution G A downstream_gene_variant PRAD-CA 3 108368271 108368271 single base substitution G A intron_variant PRAD-CA 3 108371683 108371683 single base substitution C T downstream_gene_variant PRAD-CA 3 108371683 108371683 single base substitution C T intron_variant PRAD-CA 3 108384346 108384346 single base substitution T G intron_variant PRAD-CA 3 108389295 108389295 single base substitution T A intron_variant PRAD-CA 3 108389363 108389363 single base substitution T A intron_variant PRAD-CA 3 108394814 108394814 single base substitution A G intron_variant PRAD-CA 3 108395035 108395035 single base substitution G T intron_variant PRAD-CA 3 108401109 108401109 single base substitution C A intron_variant PRAD-CA 3 108404322 108404322 single base substitution C G intron_variant PRAD-CA 3 108409155 108409155 single base substitution T G intron_variant PRAD-UK 3 108310946 108310946 single base substitution C G intron_variant PRAD-UK 3 108316580 108316580 single base substitution T G intron_variant PRAD-UK 3 108332087 108332087 single base substitution C G downstream_gene_variant PRAD-UK 3 108332087 108332087 single base substitution C G intron_variant PRAD-UK 3 108341451 108341451 single base substitution T C intron_variant PRAD-UK 3 108355588 108355588 deletion of <=200bp C - intron_variant PRAD-UK 3 108366123 108366123 single base substitution T C intron_variant PRAD-UK 3 108385178 108385178 single base substitution T A intron_variant PRAD-UK 3 108388722 108388722 single base substitution A C intron_variant PRAD-UK 3 108405695 108405695 single base substitution C T intron_variant PRAD-UK 3 108416153 108416153 single base substitution C T downstream_gene_variant PRAD-UK 3 108418109 108418109 single base substitution A T downstream_gene_variant PRAD-US 3 108347996 108347996 single base substitution A G downstream_gene_variant PRAD-US 3 108347996 108347996 single base substitution A G exon_variant PRAD-US 3 108347996 108347996 single base substitution A G synonymous_variant E223E 669A>G PRAD-US 3 108363248 108363248 single base substitution C T 3_prime_UTR_variant PRAD-US 3 108363248 108363248 single base substitution C T missense_variant P460L 1379C>T PRAD-US 3 108391473 108391473 single base substitution C T 3_prime_UTR_variant PRAD-US 3 108391473 108391473 single base substitution C T synonymous_variant N853N 2559C>T READ-US 3 108324275 108324275 deletion of <=200bp T - exon_variant READ-US 3 108324275 108324275 deletion of <=200bp T - frameshift_variant F8 READ-US 3 108324275 108324275 deletion of <=200bp T - intron_variant READ-US 3 108330091 108330091 single base substitution T C 5_prime_UTR_variant READ-US 3 108330091 108330091 single base substitution T C exon_variant READ-US 3 108330091 108330091 single base substitution T C missense_variant L58S 173T>C READ-US 3 108330154 108330154 single base substitution A G 5_prime_UTR_variant READ-US 3 108330154 108330154 single base substitution A G downstream_gene_variant READ-US 3 108330154 108330154 single base substitution A G exon_variant READ-US 3 108330154 108330154 single base substitution A G missense_variant D79G 236A>G READ-US 3 108335391 108335391 single base substitution G T exon_variant READ-US 3 108335391 108335391 single base substitution G T stop_gained E4* 10G>T READ-US 3 108335391 108335391 single base substitution G T stop_gained E88* 262G>T READ-US 3 108353748 108353748 single base substitution T C exon_variant READ-US 3 108353748 108353748 single base substitution T C missense_variant C283R 847T>C RECA-EU 3 108326164 108326164 single base substitution A C intron_variant RECA-EU 3 108327685 108327685 single base substitution C T intron_variant RECA-EU 3 108328341 108328341 single base substitution T G intron_variant RECA-EU 3 108329190 108329190 single base substitution C A intron_variant RECA-EU 3 108329447 108329447 single base substitution A G intron_variant RECA-EU 3 108338208 108338208 single base substitution A T intron_variant RECA-EU 3 108343421 108343421 single base substitution A T intron_variant RECA-EU 3 108352784 108352784 single base substitution T C downstream_gene_variant RECA-EU 3 108352784 108352784 single base substitution T C intron_variant RECA-EU 3 108384714 108384714 single base substitution A G intron_variant RECA-EU 3 108386529 108386529 single base substitution A T intron_variant RECA-EU 3 108388965 108388965 single base substitution G T intron_variant RECA-EU 3 108401344 108401344 single base substitution A C intron_variant SKCA-BR 3 108304990 108304990 single base substitution T C upstream_gene_variant SKCA-BR 3 108307962 108307962 single base substitution A C upstream_gene_variant SKCA-BR 3 108315419 108315419 single base substitution C A intron_variant SKCA-BR 3 108315455 108315455 single base substitution A G intron_variant SKCA-BR 3 108315471 108315471 single base substitution T C intron_variant SKCA-BR 3 108315675 108315675 single base substitution G A intron_variant SKCA-BR 3 108317563 108317563 single base substitution C T intron_variant SKCA-BR 3 108317563 108317563 single base substitution C T upstream_gene_variant SKCA-BR 3 108319107 108319107 single base substitution G A intron_variant SKCA-BR 3 108319107 108319107 single base substitution G A upstream_gene_variant SKCA-BR 3 108322263 108322263 single base substitution C T intron_variant SKCA-BR 3 108322658 108322658 single base substitution A T intron_variant SKCA-BR 3 108327292 108327292 single base substitution C T intron_variant SKCA-BR 3 108330500 108330500 single base substitution T C downstream_gene_variant SKCA-BR 3 108330500 108330500 single base substitution T C intron_variant SKCA-BR 3 108332087 108332087 single base substitution C T downstream_gene_variant SKCA-BR 3 108332087 108332087 single base substitution C T intron_variant SKCA-BR 3 108338149 108338149 insertion of <=200bp - ATG intron_variant SKCA-BR 3 108342003 108342003 single base substitution C T intron_variant SKCA-BR 3 108346817 108346817 single base substitution C T intron_variant SKCA-BR 3 108346849 108346849 single base substitution C T intron_variant SKCA-BR 3 108350636 108350636 single base substitution C T downstream_gene_variant SKCA-BR 3 108350636 108350636 single base substitution C T intron_variant SKCA-BR 3 108352442 108352442 single base substitution A G downstream_gene_variant SKCA-BR 3 108352442 108352442 single base substitution A G intron_variant SKCA-BR 3 108352566 108352568 deletion of <=200bp ATC - downstream_gene_variant SKCA-BR 3 108352566 108352568 deletion of <=200bp ATC - intron_variant SKCA-BR 3 108352683 108352689 deletion of <=200bp ATCTCTC - downstream_gene_variant SKCA-BR 3 108352683 108352689 deletion of <=200bp ATCTCTC - intron_variant SKCA-BR 3 108352747 108352747 single base substitution T C downstream_gene_variant SKCA-BR 3 108352747 108352747 single base substitution T C intron_variant SKCA-BR 3 108358251 108358251 single base substitution C T intron_variant SKCA-BR 3 108358432 108358432 single base substitution C T intron_variant SKCA-BR 3 108359278 108359278 single base substitution A T intron_variant SKCA-BR 3 108363052 108363052 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 108363052 108363052 single base substitution C T missense_variant H395Y 1183C>T SKCA-BR 3 108364322 108364322 single base substitution C T intron_variant SKCA-BR 3 108364392 108364392 single base substitution T C intron_variant SKCA-BR 3 108365073 108365073 single base substitution G A intron_variant SKCA-BR 3 108365760 108365760 single base substitution T G intron_variant SKCA-BR 3 108371370 108371370 single base substitution A G downstream_gene_variant SKCA-BR 3 108371370 108371370 single base substitution A G intron_variant SKCA-BR 3 108372354 108372354 insertion of <=200bp - GTGTATATA intron_variant SKCA-BR 3 108372356 108372356 single base substitution A G intron_variant SKCA-BR 3 108372444 108372444 single base substitution C T intron_variant SKCA-BR 3 108373336 108373336 single base substitution G A intron_variant SKCA-BR 3 108373897 108373897 single base substitution T C intron_variant SKCA-BR 3 108375247 108375247 single base substitution C T intron_variant SKCA-BR 3 108375438 108375438 single base substitution C T intron_variant SKCA-BR 3 108377974 108377974 single base substitution C T intron_variant SKCA-BR 3 108377975 108377975 single base substitution C T intron_variant SKCA-BR 3 108378017 108378017 single base substitution C T intron_variant SKCA-BR 3 108382420 108382420 single base substitution G A intron_variant SKCA-BR 3 108383014 108383014 single base substitution G A intron_variant SKCA-BR 3 108388086 108388086 single base substitution C T intron_variant SKCA-BR 3 108391804 108391804 single base substitution C T intron_variant SKCA-BR 3 108393194 108393194 single base substitution C T intron_variant SKCA-BR 3 108393884 108393884 single base substitution C G intron_variant SKCA-BR 3 108396904 108396904 single base substitution C T intron_variant SKCA-BR 3 108398590 108398590 single base substitution C T intron_variant SKCA-BR 3 108399738 108399738 single base substitution G T intron_variant SKCA-BR 3 108400238 108400238 single base substitution C T intron_variant SKCA-BR 3 108404196 108404196 single base substitution C T intron_variant SKCA-BR 3 108404883 108404883 single base substitution T A intron_variant SKCA-BR 3 108406705 108406705 single base substitution C T intron_variant SKCA-BR 3 108407253 108407253 single base substitution A G intron_variant SKCA-BR 3 108409634 108409634 single base substitution T G missense_variant C1173G 3517T>G SKCA-BR 3 108409634 108409634 single base substitution T G splice_region_variant SKCA-BR 3 108414229 108414229 single base substitution T C downstream_gene_variant SKCA-BR 3 108414336 108414337 deletion of <=200bp GC - downstream_gene_variant SKCA-BR 3 108414750 108414750 single base substitution T C downstream_gene_variant SKCA-BR 3 108415595 108415595 single base substitution T A downstream_gene_variant SKCA-BR 3 108417084 108417084 single base substitution C T downstream_gene_variant SKCM-US 3 108330161 108330161 single base substitution C T 5_prime_UTR_variant SKCM-US 3 108330161 108330161 single base substitution C T downstream_gene_variant SKCM-US 3 108330161 108330161 single base substitution C T exon_variant SKCM-US 3 108330161 108330161 single base substitution C T synonymous_variant S81S 243C>T SKCM-US 3 108351803 108351803 single base substitution C T downstream_gene_variant SKCM-US 3 108351803 108351803 single base substitution C T exon_variant SKCM-US 3 108351803 108351803 single base substitution C T missense_variant L234F 700C>T SKCM-US 3 108363029 108363029 single base substitution A T 3_prime_UTR_variant SKCM-US 3 108363029 108363029 single base substitution A T missense_variant K387M 1160A>T SKCM-US 3 108363052 108363052 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108363052 108363052 single base substitution C T missense_variant H395Y 1183C>T SKCM-US 3 108363184 108363184 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108363184 108363184 single base substitution C T missense_variant L439F 1315C>T SKCM-US 3 108363192 108363192 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108363192 108363192 single base substitution C T synonymous_variant T441T 1323C>T SKCM-US 3 108363309 108363309 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108363309 108363309 single base substitution C T synonymous_variant F480F 1440C>T SKCM-US 3 108363472 108363472 single base substitution G A 3_prime_UTR_variant SKCM-US 3 108363472 108363472 single base substitution G A missense_variant D535N 1603G>A SKCM-US 3 108363492 108363492 single base substitution G A 3_prime_UTR_variant SKCM-US 3 108363492 108363492 single base substitution G A synonymous_variant G541G 1623G>A SKCM-US 3 108363531 108363531 single base substitution C A 3_prime_UTR_variant SKCM-US 3 108363531 108363531 single base substitution C A synonymous_variant P554P 1662C>A SKCM-US 3 108367771 108367771 single base substitution A T 3_prime_UTR_variant SKCM-US 3 108367771 108367771 single base substitution A T downstream_gene_variant SKCM-US 3 108367771 108367771 single base substitution A T missense_variant S657C 1969A>T SKCM-US 3 108380723 108380723 single base substitution G A splice_acceptor_variant SKCM-US 3 108380784 108380784 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108380784 108380784 single base substitution C T stop_gained Q754* 2260C>T SKCM-US 3 108396404 108396404 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108396404 108396404 single base substitution C T missense_variant P948S 2842C>T SKCM-US 3 108405367 108405367 single base substitution C T intron_variant SKCM-US 3 108405367 108405367 single base substitution C T missense_variant P1029S 3085C>T SKCM-US 3 108406916 108406916 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108406916 108406916 single base substitution C T synonymous_variant S1081S 3243C>T SKCM-US 3 108407695 108407695 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108407695 108407695 single base substitution C T missense_variant P1147L 3440C>T SKCM-US 3 108409671 108409671 single base substitution C T 3_prime_UTR_variant SKCM-US 3 108409671 108409671 single base substitution C T missense_variant P1185L 3554C>T STAD-US 3 108363261 108363261 single base substitution G A 3_prime_UTR_variant STAD-US 3 108363261 108363261 single base substitution G A synonymous_variant Q464Q 1392G>A STAD-US 3 108363342 108363342 single base substitution G A 3_prime_UTR_variant STAD-US 3 108363342 108363342 single base substitution G A synonymous_variant P491P 1473G>A STAD-US 3 108363512 108363512 single base substitution A G 3_prime_UTR_variant STAD-US 3 108363512 108363512 single base substitution A G missense_variant D548G 1643A>G STAD-US 3 108363596 108363596 single base substitution T C 3_prime_UTR_variant STAD-US 3 108363596 108363596 single base substitution T C missense_variant I576T 1727T>C STAD-US 3 108366943 108366943 single base substitution T C 3_prime_UTR_variant STAD-US 3 108366943 108366943 single base substitution T C missense_variant L649P 1946T>C STAD-US 3 108373083 108373083 single base substitution G C 3_prime_UTR_variant STAD-US 3 108373083 108373083 single base substitution G C missense_variant V709L 2125G>C STAD-US 3 108380769 108380769 single base substitution G A 3_prime_UTR_variant STAD-US 3 108380769 108380769 single base substitution G A missense_variant E749K 2245G>A STAD-US 3 108380774 108380774 single base substitution G A 3_prime_UTR_variant STAD-US 3 108380774 108380774 single base substitution G A synonymous_variant R750R 2250G>A STAD-US 3 108388536 108388536 single base substitution G A 3_prime_UTR_variant STAD-US 3 108388536 108388536 single base substitution G A missense_variant R811H 2432G>A STAD-US 3 108392929 108392929 single base substitution A T 3_prime_UTR_variant STAD-US 3 108392929 108392929 single base substitution A T missense_variant Y865F 2594A>T STAD-US 3 108405322 108405322 single base substitution C T intron_variant STAD-US 3 108405322 108405322 single base substitution C T missense_variant P1014S 3040C>T STAD-US 3 108405333 108405333 single base substitution C T intron_variant STAD-US 3 108405333 108405333 single base substitution C T synonymous_variant D1017D 3051C>T STAD-US 3 108409687 108409687 single base substitution C T 3_prime_UTR_variant STAD-US 3 108409687 108409687 single base substitution C T synonymous_variant H1190H 3570C>T STAD-US 3 108409725 108409725 single base substitution G A 3_prime_UTR_variant STAD-US 3 108409725 108409725 single base substitution G A missense_variant R1203Q 3608G>A THCA-SA 3 108373022 108373022 single base substitution G A 3_prime_UTR_variant THCA-SA 3 108373022 108373022 single base substitution G A synonymous_variant L688L 2064G>A THCA-US 3 108391411 108391411 single base substitution C A 3_prime_UTR_variant THCA-US 3 108391411 108391411 single base substitution C A missense_variant Q833K 2497C>A THCA-US 3 108405390 108405390 single base substitution A G intron_variant THCA-US 3 108405390 108405390 single base substitution A G synonymous_variant R1036R 3108A>G UCEC-US 3 108308220 108308220 single base substitution C A upstream_gene_variant UCEC-US 3 108326951 108326951 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 108326951 108326951 single base substitution G T exon_variant UCEC-US 3 108326951 108326951 single base substitution G T missense_variant E16D 48G>T UCEC-US 3 108353782 108353782 single base substitution A G exon_variant UCEC-US 3 108353782 108353782 single base substitution A G missense_variant K294R 881A>G UCEC-US 3 108353789 108353789 single base substitution G T exon_variant UCEC-US 3 108353789 108353789 single base substitution G T missense_variant K296N 888G>T UCEC-US 3 108361346 108361346 single base substitution A C 3_prime_UTR_variant UCEC-US 3 108361346 108361346 single base substitution A C missense_variant K376Q 1126A>C UCEC-US 3 108363063 108363063 single base substitution T C 3_prime_UTR_variant UCEC-US 3 108363063 108363063 single base substitution T C synonymous_variant H398H 1194T>C UCEC-US 3 108363341 108363341 single base substitution C T 3_prime_UTR_variant UCEC-US 3 108363341 108363341 single base substitution C T missense_variant P491L 1472C>T UCEC-US 3 108365482 108365482 single base substitution T C 3_prime_UTR_variant UCEC-US 3 108365482 108365482 single base substitution T C missense_variant I593T 1778T>C UCEC-US 3 108365497 108365497 single base substitution G A splice_donor_variant UCEC-US 3 108367791 108367791 single base substitution G A 3_prime_UTR_variant UCEC-US 3 108367791 108367791 single base substitution G A downstream_gene_variant UCEC-US 3 108367791 108367791 single base substitution G A synonymous_variant K663K 1989G>A UCEC-US 3 108373065 108373065 single base substitution A C 3_prime_UTR_variant UCEC-US 3 108373065 108373065 single base substitution A C missense_variant K703Q 2107A>C UCEC-US 3 108380779 108380779 single base substitution C T 3_prime_UTR_variant UCEC-US 3 108380779 108380779 single base substitution C T missense_variant A752V 2255C>T UCEC-US 3 108381042 108381042 single base substitution G T 3_prime_UTR_variant UCEC-US 3 108381042 108381042 single base substitution G T missense_variant K787N 2361G>T UCEC-US 3 108388540 108388540 single base substitution A C 3_prime_UTR_variant UCEC-US 3 108388540 108388540 single base substitution A C missense_variant Q812H 2436A>C UCEC-US 3 108388553 108388553 single base substitution G T 3_prime_UTR_variant UCEC-US 3 108388553 108388553 single base substitution G T missense_variant D817Y 2449G>T UCEC-US 3 108393004 108393004 single base substitution C T 3_prime_UTR_variant UCEC-US 3 108393004 108393004 single base substitution C T missense_variant A890V 2669C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-EE-A2MS-06 COSM3585023 c.3554C>T p.P1185L Substitution - Missense 3:108690824-108690824 + PD14439a COSM5786948 c.344C>T p.A115V Substitution - Missense 3:108616626-108616626 + TCGA-AA-3821-01 COSM294337 c.2723C>T p.A908V Substitution - Missense 3:108675815-108675815 + S00842 COSM5701655 c.2747_2748TG>GT p.V916G Substitution - Missense 3:108675839-108675840 + TCGA-HU-A4H4-01 COSM4112083 c.1727T>C p.I576T Substitution - Missense 3:108644749-108644749 + BD223T COSM5496475 c.1065-9C>G p.? Unknown 3:108642429-108642429 + TCGA-D8-A1XK-01 COSM3845763 c.1963G>C p.V655L Substitution - Missense 3:108648918-108648918 + CSCC-18-T COSM3585020 c.3085C>T p.P1029S Substitution - Missense 3:108686520-108686520 + TCGA-UC-A7PF-01 COSM4829965 c.1082C>G p.S361C Substitution - Missense 3:108642455-108642455 + RK136_C01 COSM3767157 c.3435A>G p.E1145E Substitution - coding silent 3:108688843-108688843 + TCGA-AG-3731-01 COSM1566357 c.236A>G p.D79G Substitution - Missense 3:108611307-108611307 + TCGA-EI-6507-01 COSM1566358 c.22delT p.F9fs*2 Deletion - Frameshift 3:108605428-108605428 + TCGA-D3-A2JH-06 COSM3585021 c.3243C>T p.S1081S Substitution - coding silent 3:108688069-108688069 + TCGA-EK-A3GK-01 COSM4854384 c.779C>T p.S260F Substitution - Missense 3:108633035-108633035 + C086 COSM5530293 c.776G>A p.R259Q Substitution - Missense 3:108633032-108633032 + TCGA-HU-A4H8-01 COSM4112092 c.3608G>A p.R1203Q Substitution - Missense 3:108690878-108690878 + S00837 COSM310782 c.2888A>T p.Q963L Substitution - Missense 3:108684220-108684220 + T38 COSM5344292 c.837C>A p.C279* Substitution - Nonsense 3:108634891-108634891 + 445 COSM4434893 c.2007G>T p.K669N Substitution - Missense 3:108648962-108648962 + ESCC_140 COSM5643407 c.553C>T p.R185C Substitution - Missense 3:108625941-108625941 + B65-Tumor COSM1752782 c.582A>T p.R194S Substitution - Missense 3:108629062-108629062 + LUAD-YINHD COSM350699 c.1948A>G p.K650E Substitution - Missense 3:108648098-108648098 + TCGA-BS-A0UJ-01 COSM1036086 c.881A>G p.K294R Substitution - Missense 3:108634935-108634935 + LUAD-S01354 COSM385931 c.521G>T p.C174F Substitution - Missense 3:108625909-108625909 + S02293 COSM1536029 c.872G>T p.C291F Substitution - Missense 3:108634926-108634926 + TCGA-EQ-8122-01 COSM1036097 c.2432G>A p.R811H Substitution - Missense 3:108669689-108669689 + TCGA-33-4586-01 COSM727382 c.2554C>A p.L852M Substitution - Missense 3:108672621-108672621 + pfg122T COSM4747742 c.237delT p.S81fs*23 Deletion - Frameshift 3:108611308-108611308 + LP6007548-DNA_A01 COSM3729821 c.1380G>A p.P460P Substitution - coding silent 3:108644402-108644402 + TCGA-D1-A16D-01 COSM1036090 c.1472C>T p.P491L Substitution - Missense 3:108644494-108644494 + TCGA-AN-A046-01 COSM3845764 c.2463G>T p.K821N Substitution - Missense 3:108669720-108669720 + 10-P1058 COSM4583772 c.92C>A p.S31Y Substitution - Missense 3:108608148-108608148 + 7285 COSM5615153 c.1435G>A p.V479M Substitution - Missense 3:108644457-108644457 + TCGA-60-2723-01 COSM727380 c.2886G>T p.M962I Substitution - Missense 3:108684218-108684218 + 53M COSM2917013 c.242C>T p.S81F Substitution - Missense 3:108611313-108611313 + TCGA-EJ-7782-01 COSM3783641 c.1379C>T p.P460L Substitution - Missense 3:108644401-108644401 + CSCC-27-T COSM4467433 c.148C>T p.L50L Substitution - coding silent 3:108611219-108611219 + CSCC-35-T COSM4467548 c.1496C>T p.S499F Substitution - Missense 3:108644518-108644518 + 31 COSM4945160 c.3047_3049GAG>AAA p.G1016_D1017>EN Complex - compound substitution 3:108686482-108686484 + PD6730b COSM5791746 c.453A>G p.K151K Substitution - coding silent 3:108624521-108624521 + TCGA-RC-A7SK-01 COSM4918515 c.626T>C p.I209T Substitution - Missense 3:108629106-108629106 + BD49T COSM5497720 c.3438G>A p.E1146E Substitution - coding silent 3:108688846-108688846 + TCGA-AP-A0LM-01 COSM1036092 c.1792+1G>A p.? Unknown 3:108646650-108646650 + CLL095 COSM1291571 c.512A>G p.N171S Substitution - Missense 3:108625900-108625900 + CSCC-47-T COSM4450391 c.582-1G>A p.? Unknown 3:108629061-108629061 + ESCC-237T COSM3940185 c.92C>G p.S31C Substitution - Missense 3:108608148-108608148 + CSCC-15-T COSM4480907 c.2467C>T p.L823F Substitution - Missense 3:108669724-108669724 + TCGA-QA-A7B7-01 COSM4909940 c.3495C>T p.C1165C Substitution - coding silent 3:108688903-108688903 + B89-10 COSM1752780 c.57G>A p.R19R Substitution - coding silent 3:108608113-108608113 + TCGA-HF-7132-01 COSM4112081 c.1392G>A p.Q464Q Substitution - coding silent 3:108644414-108644414 + HCC41 COSM1616688 c.2986A>G p.T996A Substitution - Missense 3:108684318-108684318 + CSCC-20-T COSM4487892 c.3242C>T p.S1081F Substitution - Missense 3:108688068-108688068 + PT27 COSM2917013 c.242C>T p.S81F Substitution - Missense 3:108611313-108611313 + PCSI_0090_Pa_X COSM3380324 c.2195A>C p.E732A Substitution - Missense 3:108654306-108654306 + T207 COSM4679956 c.990A>G p.V330V Substitution - coding silent 3:108636687-108636687 + LUAD-RT-S01721 COSM380555 c.2864C>T p.P955L Substitution - Missense 3:108677579-108677579 + YULAN COSM1693124 c.1361C>T p.P454L Substitution - Missense 3:108644383-108644383 + CSCC-62-T COSM4470675 c.1676C>T p.S559F Substitution - Missense 3:108644698-108644698 + HCC27 COSM3660072 c.1725A>G p.E575E Substitution - coding silent 3:108644747-108644747 + HF-23896 COSM1193018 c.3415-7_3415-6insT p.? Unknown 3:108688816-108688817 + YULAN COSM1693125 c.2854C>T p.P952S Substitution - Missense 3:108677569-108677569 + TCGA-UB-A7MB-01 COSM4930739 c.2782-2A>T p.? Unknown 3:108677495-108677495 + SJHGG003_A COSM4968829 c.3488delT p.L1163fs*16 Deletion - Frameshift 3:108688896-108688896 + TCGA-B5-A11G-01 COSM1036091 c.1778T>C p.I593T Substitution - Missense 3:108646635-108646635 + 49M COSM5590708 c.1386C>T p.S462S Substitution - coding silent 3:108644408-108644408 + TCGA-66-2734-01 COSM727383 c.2108A>T p.K703I Substitution - Missense 3:108654219-108654219 + PD9847a COSM5792732 c.1845C>T p.L615L Substitution - coding silent 3:108647995-108647995 + TCGA-KK-A59V-01 COSM2917061 c.2559C>T p.N853N Substitution - coding silent 3:108672626-108672626 + TCGA-BR-8591-01 COSM4112087 c.2250G>A p.R750R Substitution - coding silent 3:108661927-108661927 + TCGA-DD-A39Z-01 COSM4915925 c.1990A>G p.K664E Substitution - Missense 3:108648945-108648945 + 585208 COSM325223 c.2199G>C p.Q733H Substitution - Missense 3:108654310-108654310 + TCGA-AP-A056-01 COSM1036100 c.2669C>T p.A890V Substitution - Missense 3:108674157-108674157 + S00941 COSM5663772 c.2321T>A p.V774E Substitution - Missense 3:108662155-108662155 + TARGET-30-PASWVY COSM1284675 c.2343C>T p.N781N Substitution - coding silent 3:108662177-108662177 + TCGA-33-6737-01 COSM727377 c.3558G>A p.T1186T Substitution - coding silent 3:108690828-108690828 + 587278 COSM1204846 c.1213A>G p.T405A Substitution - Missense 3:108644235-108644235 + TCGA-FS-A4F5-06 COSM3585020 c.3085C>T p.P1029S Substitution - Missense 3:108686520-108686520 + TCGA-FR-A3YO-06 COSM3585019 c.2842C>T p.P948S Substitution - Missense 3:108677557-108677557 + TCGA-AA-A00N-01 COSM274923 c.1208C>T p.S403F Substitution - Missense 3:108644230-108644230 + TCGA-BS-A0UV-01 COSM1036094 c.2107A>C p.K703Q Substitution - Missense 3:108654218-108654218 + TCGA-F5-6814-01 COSM3426857 c.173T>C p.L58S Substitution - Missense 3:108611244-108611244 + EGC8 COSM5059189 c.343G>A p.A115T Substitution - Missense 3:108616625-108616625 + B65 COSM1752782 c.582A>T p.R194S Substitution - Missense 3:108629062-108629062 + TCGA-FW-A3R5-06 COSM3914489 c.1969A>T p.S657C Substitution - Missense 3:108648924-108648924 + YUSCA COSM5397742 c.1165G>T p.D389Y Substitution - Missense 3:108644187-108644187 + TCGA-E2-A10C-01 COSM445273 c.3463C>T p.L1155L Substitution - coding silent 3:108688871-108688871 + TCGA-AX-A05Z-01 COSM1036087 c.888G>T p.K296N Substitution - Missense 3:108634942-108634942 + LUAD-B00915 COSM332910 c.964A>T p.M322L Substitution - Missense 3:108636661-108636661 + TCGA-06-0216 COSM2150885 c.818G>T p.G273V Substitution - Missense 3:108634872-108634872 + 8035735 COSM3391951 c.1580A>G p.N527S Substitution - Missense 3:108644602-108644602 + S00539 COSM310781 c.2099G>T p.R700I Substitution - Missense 3:108654210-108654210 + TCGA-AP-A059-01 COSM1036089 c.1194T>C p.H398H Substitution - coding silent 3:108644216-108644216 + CSCC-11-T COSM4482217 c.2586C>A p.A862A Substitution - coding silent 3:108672653-108672653 + PR-3035 COSM244176 c.377C>T p.A126V Substitution - Missense 3:108624445-108624445 + ESCC-141T COSM3940186 c.790G>A p.D264N Substitution - Missense 3:108633046-108633046 + DN14010 COSM5962384 c.1890T>A p.F630L Substitution - Missense 3:108648040-108648040 + TCGA-43-3920-01 COSM727385 c.1388A>T p.K463I Substitution - Missense 3:108644410-108644410 + EGC28 COSM5059188 c.102G>T p.L34L Substitution - coding silent 3:108608158-108608158 + HT115 COSM2917026 c.750G>A p.T250T Substitution - coding silent 3:108633006-108633006 + TCGA-18-5595-01 COSM727379 c.2950C>G p.Q984E Substitution - Missense 3:108684282-108684282 + CSCC-29-T COSM4484886 c.2867C>T p.P956L Substitution - Missense 3:108677582-108677582 + ESCC_156 COSM5646049 c.1563C>G p.L521L Substitution - coding silent 3:108644585-108644585 + SW1222 COSM4654854 c.3019A>T p.I1007L Substitution - Missense 3:108686454-108686454 + MEL-Ma-Mel-108 COSM1167672 c.3427_3429delGAA p.E1146delE Deletion - In frame 3:108688835-108688837 + S00539 COSM310781 c.2099G>T p.R700I Substitution - Missense 3:108654210-108654210 + HT115 COSM2917065 c.2917G>T p.E973* Substitution - Nonsense 3:108684249-108684249 + TCGA-AZ-6601-01 COSM1417652 c.3270+2T>C p.? Unknown 3:108688098-108688098 + TCGA-AM-5820-01 COSM3759597 c.2064G>A p.L688L Substitution - coding silent 3:108654175-108654175 + 1N34-VS-1T34 COSM4974752 c.707A>G p.N236S Substitution - Missense 3:108632963-108632963 + S02376 COSM5697120 c.3315T>C p.S1105S Substitution - coding silent 3:108688637-108688637 + 49M COSM5590709 c.1677C>T p.S559S Substitution - coding silent 3:108644699-108644699 + TCGA-EE-A29N-06 COSM3585015 c.1603G>A p.D535N Substitution - Missense 3:108644625-108644625 + ESO-081 COSM1243218 c.3052G>A p.A1018T Substitution - Missense 3:108686487-108686487 + ME009T COSM222827 c.3396G>A p.W1132* Substitution - Nonsense 3:108688718-108688718 + TCGA-BS-A0UF-01 COSM1036099 c.2449G>T p.D817Y Substitution - Missense 3:108669706-108669706 + TCGA-BS-A0UF-01 COSM1036093 c.1989G>A p.K663K Substitution - coding silent 3:108648944-108648944 + TCGA-EE-A3AA-06 COSM3585022 c.3440C>T p.P1147L Substitution - Missense 3:108688848-108688848 + PDA_089 COSM5002950 c.1461G>A p.W487* Substitution - Nonsense 3:108644483-108644483 + TCGA-CA-6717-01 COSM1417644 c.107A>C p.K36T Substitution - Missense 3:108611178-108611178 + 8030353 COSM218737 c.998T>C p.I333T Substitution - Missense 3:108636695-108636695 + TCGA-BR-8487-01 COSM4112082 c.1643A>G p.D548G Substitution - Missense 3:108644665-108644665 + PT36 COSM4487552 c.3200C>T p.S1067F Substitution - Missense 3:108688026-108688026 + TCGA-AR-A1AP-01 COSM445270 c.358C>G p.Q120E Substitution - Missense 3:108616640-108616640 + WA40 COSM236731 c.1721C>A p.P574Q Substitution - Missense 3:108644743-108644743 + TCGA-CA-6717-01 COSM1417649 c.2110G>T p.D704Y Substitution - Missense 3:108654221-108654221 + 18195 COSM1308366 c.3282A>G p.K1094K Substitution - coding silent 3:108688604-108688604 + TCGA-AD-6889-01 COSM1417647 c.1449_1450insA p.G486fs*10 Insertion - Frameshift 3:108644471-108644472 + CSCC-16-T COSM4480581 c.2431C>T p.R811C Substitution - Missense 3:108669688-108669688 + HCC2998 COSM1670407 c.1226G>A p.R409Q Substitution - Missense 3:108644248-108644248 + 49M COSM5590707 c.676G>A p.D226N Substitution - Missense 3:108629156-108629156 + PCSI_0090_Pa_X COSM3380325 c.2334G>A p.W778* Substitution - Nonsense 3:108662168-108662168 + PT38 COSM2917013 c.242C>T p.S81F Substitution - Missense 3:108611313-108611313 + ESCC_29 COSM5627532 c.95G>T p.G32V Substitution - Missense 3:108608151-108608151 + 35M COSM5580931 c.2315G>A p.R772K Substitution - Missense 3:108662149-108662149 + TCGA-BG-A18B-01 COSM1036096 c.2361G>T p.K787N Substitution - Missense 3:108662195-108662195 + TCGA-22-5473-01 COSM727378 c.3253G>A p.D1085N Substitution - Missense 3:108688079-108688079 + TCGA-06-0216-01 COSM2150885 c.818G>T p.G273V Substitution - Missense 3:108634872-108634872 + TCGA-AC-A23H-01 COSM727379 c.2950C>G p.Q984E Substitution - Missense 3:108684282-108684282 + TCGA-EM-A3FQ-06 COSM3372945 c.2497C>A p.Q833K Substitution - Missense 3:108672564-108672564 + Br27P COSM40046 c.2503G>A p.E835K Substitution - Missense 3:108672570-108672570 + TCGA-CA-6717-01 COSM1417648 c.1548T>A p.I516I Substitution - coding silent 3:108644570-108644570 + HT115 COSM2917052 c.2157C>A p.F719L Substitution - Missense 3:108654268-108654268 + TCGA-AC-A23H-01 COSM3845762 c.505C>T p.Q169* Substitution - Nonsense 3:108625893-108625893 + EGC15 COSM5059190 c.2588A>G p.E863G Substitution - Missense 3:108672655-108672655 + CSCC-27-T COSM2917013 c.242C>T p.S81F Substitution - Missense 3:108611313-108611313 + 3N49-VS-3T49 COSM4982873 c.1697C>A p.S566Y Substitution - Missense 3:108644719-108644719 + TCGA-HU-A4GU-01 COSM4112089 c.3040C>T p.P1014S Substitution - Missense 3:108686475-108686475 + TCGA-DK-A2I6-01 COSM1308365 c.439G>A p.E147K Substitution - Missense 3:108624507-108624507 + LUAD-S01345 COSM397219 c.2497C>G p.Q833E Substitution - Missense 3:108672564-108672564 + LOVO COSM2917069 c.3041C>A p.P1014H Substitution - Missense 3:108686476-108686476 + MO_1012 COSM5563988 c.2604G>A p.Q868Q Substitution - coding silent 3:108674092-108674092 + T2269 COSM4679958 c.2376C>T p.I792I Substitution - coding silent 3:108662210-108662210 + T155 COSM1177203 c.19G>T p.E7* Substitution - Nonsense 3:108605425-108605425 + TCGA-FU-A3HZ-01 COSM4839359 c.1009T>G p.L337V Substitution - Missense 3:108636706-108636706 + PD4132a COSM160625 c.1906G>C p.D636H Substitution - Missense 3:108648056-108648056 + S01563 COSM310783 c.1210_1211GG>TT p.G404>? Complex 3:108644232-108644233 + HCC2998 COSM1670409 c.2473G>T p.E825* Substitution - Nonsense 3:108669730-108669730 + SH-0622 COSM5018128 c.3137_3138delCA p.Q1047fs*23 Deletion - Frameshift 3:108686572-108686573 + WSU-HN8 COSM4602575 c.1181A>G p.Y394C Substitution - Missense 3:108644203-108644203 + pfg064T COSM4759966 c.3580C>T p.P1194S Substitution - Missense 3:108690850-108690850 + TCGA-22-1002-01 COSM727384 c.1390C>T p.Q464* Substitution - Nonsense 3:108644412-108644412 + CSCC-10-T COSM4487552 c.3200C>T p.S1067F Substitution - Missense 3:108688026-108688026 + TCGA-46-3767-01 COSM727381 c.2752G>A p.D918N Substitution - Missense 3:108675844-108675844 + HCC2998 COSM4317601 c.1008T>G p.I336M Substitution - Missense 3:108636705-108636705 + S02347 COSM5694253 c.49G>C p.D17H Substitution - Missense 3:108608105-108608105 + 403 COSM4429930 c.3557C>T p.T1186M Substitution - Missense 3:108690827-108690827 + TCGA-13-0762-01 COSM77624 c.1699G>C p.V567L Substitution - Missense 3:108644721-108644721 + TCGA-AZ-4315-01 COSM1417651 c.3168C>A p.F1056L Substitution - Missense 3:108687994-108687994 + 35M COSM5580932 c.1419T>C p.L473L Substitution - coding silent 3:108644441-108644441 + TCGA-BR-6452-01 COSM4112088 c.2594A>T p.Y865F Substitution - Missense 3:108674082-108674082 + pfg130T COSM4747743 c.2221_2222delAC p.T741fs*6 Deletion - Frameshift 3:108661898-108661899 + TCGA-EE-A2MC-06 COSM3585016 c.1662C>A p.P554P Substitution - coding silent 3:108644684-108644684 + 587284 COSM1204847 c.2349G>C p.M783I Substitution - Missense 3:108662183-108662183 + B104-0 COSM1752781 c.89C>T p.S30L Substitution - Missense 3:108608145-108608145 + TCGA-AP-A051-01 COSM1036095 c.2255C>T p.A752V Substitution - Missense 3:108661932-108661932 + SNUH_G76_S1 COSM4419592 c.3009+10T>C p.? Unknown 3:108684351-108684351 + TCGA-F5-6814-01 COSM3426858 c.262G>T p.E88* Substitution - Nonsense 3:108616544-108616544 + XHDG37 COSM4679959 c.3172C>T p.R1058W Substitution - Missense 3:108687998-108687998 + TCGA-BS-A0UF-01 COSM1036088 c.1126A>C p.K376Q Substitution - Missense 3:108642499-108642499 + ESO-137 COSM1250879 c.1616G>T p.R539L Substitution - Missense 3:108644638-108644638 + S01023 COSM5666636 c.2957C>T p.P986L Substitution - Missense 3:108684289-108684289 + T2269 COSM4679957 c.1828G>T p.E610* Substitution - Nonsense 3:108647978-108647978 + T3668 COSM4679959 c.3172C>T p.R1058W Substitution - Missense 3:108687998-108687998 + BD72T COSM5511922 c.206T>C p.V69A Substitution - Missense 3:108611277-108611277 + BD124T COSM5491697 c.2292T>C p.C764C Substitution - coding silent 3:108661969-108661969 + TCGA-Q1-A5R2-01 COSM4850466 c.1906G>T p.D636Y Substitution - Missense 3:108648056-108648056 + PD4100a COSM160623 c.1565C>G p.T522S Substitution - Missense 3:108644587-108644587 + HCC27T COSM3660072 c.1725A>G p.E575E Substitution - coding silent 3:108644747-108644747 + pfg222T COSM2917060 c.2545G>A p.V849I Substitution - Missense 3:108672612-108672612 + ESO-043 COSM1250878 c.116A>G p.N39S Substitution - Missense 3:108611187-108611187 + PR-04-3222 COSM244177 c.3220G>A p.D1074N Substitution - Missense 3:108688046-108688046 + S01563 COSM310783 c.1210_1211GG>TT p.G404>? Complex 3:108644232-108644233 + TCGA-DK-A3WW-01 COSM3800859 c.2981C>T p.S994F Substitution - Missense 3:108684313-108684313 + PCSI_0529_Pa_P_526 COSM5761247 c.2379A>T p.A793A Substitution - coding silent 3:108662213-108662213 + TCGA-D9-A6EC-06 COSM4406143 c.1315C>T p.L439F Substitution - Missense 3:108644337-108644337 + NCI-ADR-RES COSM1670408 c.1583C>G p.S528* Substitution - Nonsense 3:108644605-108644605 + pfg008T COSM1642044 c.1842T>A p.P614P Substitution - coding silent 3:108647992-108647992 + TCGA-UB-A7MB-01 COSM4930668 c.2876A>T p.E959V Substitution - Missense 3:108677591-108677591 + TCGA-EB-A4IS-01 COSM3585017 c.2200-1G>A p.? Unknown 3:108661876-108661876 + B89-10-Tumor COSM1752780 c.57G>A p.R19R Substitution - coding silent 3:108608113-108608113 + HX33T COSM3660072 c.1725A>G p.E575E Substitution - coding silent 3:108644747-108644747 + HCC2998 COSM1670407 c.1226G>A p.R409Q Substitution - Missense 3:108644248-108644248 + RKO COSM4648638 c.2025A>G p.E675E Substitution - coding silent 3:108651154-108651154 + PCSI_0226_Pa_P_526 COSM4809056 c.3222T>G p.D1074E Substitution - Missense 3:108688048-108688048 + TCGA-E5-A2PC-01 COSM1308366 c.3282A>G p.K1094K Substitution - coding silent 3:108688604-108688604 + TCGA-BR-8078-01 COSM200961 c.1473G>A p.P491P Substitution - coding silent 3:108644495-108644495 + TCGA-EB-A430-01 COSM3585014 c.1440C>T p.F480F Substitution - coding silent 3:108644462-108644462 + 145 COSM3735242 c.3412C>T p.P1138S Substitution - Missense 3:108688734-108688734 + TCGA-BR-6452-01 COSM4112084 c.1946T>C p.L649P Substitution - Missense 3:108648096-108648096 + TCGA-CM-6171-01 COSM1417645 c.877delA p.K294fs*5 Deletion - Frameshift 3:108634931-108634931 + CRC-5 COSM304776 c.2254G>C p.A752P Substitution - Missense 3:108661931-108661931 + TCGA-B7-5816-01 COSM4112085 c.2125G>C p.V709L Substitution - Missense 3:108654236-108654236 + TCGA-A8-A0A6-01 COSM3845765 c.3599A>C p.H1200P Substitution - Missense 3:108690869-108690869 + YUKAT COSM2917013 c.242C>T p.S81F Substitution - Missense 3:108611313-108611313 + TCGA-AP-A059-01 COSM1036085 c.48G>T p.E16D Substitution - Missense 3:108608104-108608104 + T578 COSM4679955 c.508G>T p.E170* Substitution - Nonsense 3:108625896-108625896 + TCGA-A7-A0DA-01 COSM445271 c.936A>T p.K312N Substitution - Missense 3:108636633-108636633 + TCGA-EE-A2GB-06 COSM3585012 c.1160A>T p.K387M Substitution - Missense 3:108644182-108644182 + CSCC-27-T COSM4543859 c.3459G>T p.E1153D Substitution - Missense 3:108688867-108688867 + sysucc-311T COSM5465669 c.2034-8G>A p.? Unknown 3:108654137-108654137 + TCGA-AA-3966-01 COSM272621 c.2095A>G p.S699G Substitution - Missense 3:108654206-108654206 + CSCC-32-T COSM4528653 c.1554G>A p.M518I Substitution - Missense 3:108644576-108644576 + AOCS-119-3-9 COSM4136467 c.816+10T>C p.? Unknown 3:108633082-108633082 + S01873 COSM5672243 c.2175G>T p.L725F Substitution - Missense 3:108654286-108654286 + 07-P8041 COSM4583773 c.2216_2219delTAAC p.T740fs*31 Deletion - Frameshift 3:108661893-108661896 + B104-0-Tumor COSM1752781 c.89C>T p.S30L Substitution - Missense 3:108608145-108608145 + PD4100a COSM160624 c.1671T>A p.N557K Substitution - Missense 3:108644693-108644693 + TCGA-AX-A0J0-01 COSM1036098 c.2436A>C p.Q812H Substitution - Missense 3:108669693-108669693 + TCGA-CA-6718-01 COSM1417646 c.1287G>T p.K429N Substitution - Missense 3:108644309-108644309 + LP6005500-DNA_B03 COSM4408548 c.441A>G p.E147E Substitution - coding silent 3:108624509-108624509 + 169 COSM3729821 c.1380G>A p.P460P Substitution - coding silent 3:108644402-108644402 + TCGA-IM-A3U3-01 COSM3372946 c.3108A>G p.R1036R Substitution - coding silent 3:108686543-108686543 + CSCC-60-T COSM4467770 c.1507C>T p.L503L Substitution - coding silent 3:108644529-108644529 + PT35 COSM5911880 c.208C>T p.P70S Substitution - Missense 3:108611279-108611279 + TCGA-FU-A3HZ-01 COSM2917065 c.2917G>T p.E973* Substitution - Nonsense 3:108684249-108684249 + TCGA-ER-A19T-06 COSM4897742 c.1623G>A p.G541G Substitution - coding silent 3:108644645-108644645 + TCGA-BR-8368-01 COSM4112091 c.3570C>T p.H1190H Substitution - coding silent 3:108690840-108690840 + TCGA-F5-6814-01 COSM3426859 c.847T>C p.C283R Substitution - Missense 3:108634901-108634901 + TCGA-D1-A17H-01 COSM1036097 c.2432G>A p.R811H Substitution - Missense 3:108669689-108669689 + TCGA-FP-A4BE-01 COSM4112090 c.3051C>T p.D1017D Substitution - coding silent 3:108686486-108686486 + CSCC-27-T COSM4570901 c.3456T>A p.H1152Q Substitution - Missense 3:108688864-108688864 + TCGA-D3-A2JA-06 COSM3585013 c.1323C>T p.T441T Substitution - coding silent 3:108644345-108644345 + CSCC-60-T COSM4488651 c.3360C>T p.A1120A Substitution - coding silent 3:108688682-108688682 + BD124T COSM5491698 c.3039G>A p.A1013A Substitution - coding silent 3:108686474-108686474 + TCGA-FW-A3R5-06 COSM3914488 c.1183C>T p.H395Y Substitution - Missense 3:108644205-108644205 + HCC003T COSM5819624 c.190C>G p.L64V Substitution - Missense 3:108611261-108611261 + QC2-30-T2 COSM5653629 c.979C>A p.Q327K Substitution - Missense 3:108636676-108636676 + P130 COSM1736891 c.275A>G p.N92S Substitution - Missense 3:108616557-108616557 + TCGA-BF-A1Q0-01 COSM3585011 c.700C>T p.L234F Substitution - Missense 3:108632956-108632956 + TCGA-EJ-5503-01 COSM1130380 c.578A>G p.K193R Substitution - Missense 3:108625966-108625966 + TCGA-EJ-5504-01 COSM1130379 c.669A>G p.E223E Substitution - coding silent 3:108629149-108629149 + CSCC-20-T COSM4533411 c.1979G>A p.R660K Substitution - Missense 3:108648934-108648934 + TCGA-D3-A51N-06 COSM3585018 c.2260C>T p.Q754* Substitution - Nonsense 3:108661937-108661937 + CSCC-4-T COSM4554491 c.622G>A p.E208K Substitution - Missense 3:108629102-108629102 + TCGA-BR-4366-01 COSM4112086 c.2245G>A p.E749K Substitution - Missense 3:108661922-108661922 + TCGA-AN-A046-01 COSM1036099 c.2449G>T p.D817Y Substitution - Missense 3:108669706-108669706 + CSCC-49-T COSM4536688 c.2331G>A p.R777R Substitution - coding silent 3:108662165-108662165 + LUAD-S01304 COSM385478 c.1255C>T p.P419S Substitution - Missense 3:108644277-108644277 + TCGA-AN-A0FW-01 COSM445272 c.1112C>T p.P371L Substitution - Missense 3:108642485-108642485 + TCGA-DD-A4NO-01 COSM4912914 c.2086C>T p.H696Y Substitution - Missense 3:108654197-108654197 + ICGC_0063 COSM218737 c.998T>C p.I333T Substitution - Missense 3:108636695-108636695 + PCSI_0090_Pa_P COSM3380325 c.2334G>A p.W778* Substitution - Nonsense 3:108662168-108662168 + HCC41T COSM1616688 c.2986A>G p.T996A Substitution - Missense 3:108684318-108684318 + TCGA-DK-A3WW-01 COSM3800858 c.2204C>T p.S735L Substitution - Missense 3:108661881-108661881 + CSCC-57-T COSM4466562 c.1441C>T p.P481S Substitution - Missense 3:108644463-108644463 + OVCAR-8 COSM1670408 c.1583C>G p.S528* Substitution - Nonsense 3:108644605-108644605 + 2521260 COSM5891345 c.3514C>T p.Q1172* Substitution - Nonsense 3:108688922-108688922 + 61 COSM5736702 c.2890C>T p.Q964* Substitution - Nonsense 3:108684222-108684222 + 2881_T COSM3944639 c.363T>C p.A121A Substitution - coding silent 3:108616645-108616645 + TCGA-D3-A3MR-06 COSM3585010 c.243C>T p.S81S Substitution - coding silent 3:108611314-108611314 + S00837 COSM310782 c.2888A>T p.Q963L Substitution - Missense 3:108684220-108684220 + TCGA-BT-A3PK-01 COSM3800857 c.993T>G p.P331P Substitution - coding silent 3:108636690-108636690 + TCGA-CC-A5UC-01 COSM4911925 c.1460G>A p.W487* Substitution - Nonsense 3:108644482-108644482 + LOXIMVI COSM1670410 c.2687C>T p.A896V Substitution - Missense 3:108674175-108674175 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.409210 3q13.13 608672

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.M322L c.964A>C 3 108355508 LUAD A G Missense p.K1059E c.3175A>G 3 108406848 LUAD A G Missense p.K294R c.881A>G 3 108353782 CM A G Missense p.N171S c.512A>G 3 108344747 CLL A G Missense p.N39S c.116A>G 3 108330034 ESCA A G Synonymous p.E223E c.669A>G 3 108347996 PRAD A G Synonymous p.K1094K c.3282A>G 3 108407451 BLCA A G Synonymous p.R1036R c.3108A>G 3 108405390 THCA A T IntronicSNV . c.1-2365A>T 3 108321889 MB A T Missense p.K312N c.936A>T 3 108355480 BRCA A T Missense p.K387M c.1160A>T 3 108363029 CM A T Missense p.K463I c.1388A>T 3 108363257 LUSC A T Missense p.K703I c.2108A>T 3 108373066 LUSC A T Missense p.Q963L c.2888A>T 3 108403067 SCLC A T Nonsense p.K922* c.2764A>T 3 108394703 BRCA C A Missense p.L852M c.2554C>A 3 108391468 LUSC C A Missense p.P455H c.1364C>A 3 108363233 LUAD C A Missense p.Q1127K c.3379C>A 3 108407548 LUAD C A Nonsense p.C1165* c.3495C>A 3 108407750 STAD C A Synonymous p.I168I c.504C>A 3 108344739 LUAD C A Synonymous p.P554P c.1662C>A 3 108363531 CM C G Missense p.H127Q c.381C>G 3 108343296 LUAD C G Missense p.Q120E c.358C>G 3 108335487 BRCA C G Missense p.Q984E c.2950C>G 3 108403129 LUSC C G Missense p.T522S c.1565C>G 3 108363434 BRCA C T Missense p.L234F c.700C>T 3 108351803 CM C T Missense p.P1147L c.3440C>T 3 108407695 CM C T Missense p.P1185L c.3554C>T 3 108409671 CM C T Missense p.P371L c.1112C>T 3 108361332 BRCA C T Missense p.P491L c.1472C>T 3 108363341 UCEC C T Missense p.R1026W c.3076C>T 3 108405358 STAD C T Missense p.S1095L c.3284C>T 3 108407453 CM C T Missense p.S1103L c.3308C>T 3 108407477 CM C T Missense p.S81F c.242C>T 3 108330160 CM C T Missense p.T981I c.2942C>T 3 108403121 LUAD C T Nonsense p.Q306* c.916C>T 3 108353817 LUAD C T Nonsense p.Q464* c.1390C>T 3 108363259 LUSC C T Nonsense p.Q763* c.2287C>T 3 108380811 HNSC C T Synonymous p.I558I c.1674C>T 3 108363543 CM C T Synonymous p.I576I c.1728C>T 3 108363597 MM C T Synonymous p.L611L c.1831C>T 3 108366828 CM C T Synonymous p.N781N c.2343C>T 3 108381024 NB C T Synonymous p.S1081S c.3243C>T 3 108406916 CM C T Synonymous p.S81S c.243C>T 3 108330161 CM C T Synonymous p.T441T c.1323C>T 3 108363192 CM C T Synonymous p.Y568Y c.1704C>T 3 108363573 STAD GAA - InFrameDeletion p.E1146delE c.3435_3437delAGA 3 108407682 CM G A Missense p.D1085N c.3253G>A 3 108406926 LUSC G A Missense p.D535N c.1603G>A 3 108363472 CM G A Missense p.D918N c.2752G>A 3 108394691 LUSC G A Missense p.E147K c.439G>A 3 108343354 BLCA G A Missense p.E749K c.2245G>A 3 108380769 STAD G A Missense p.E835K c.2503G>A 3 108391417 GBM G A Missense p.V479M c.1435G>A 3 108363304 NSCLC G A Nonsense p.W1132* c.3396G>A 3 108407565 CM G A Synonymous p.L103L c.309G>A 3 108335438 HNSC G A Synonymous p.T1186T c.3558G>A 3 108409675 LUSC G C Missense p.D211H c.631G>C 3 108347958 CM G C Missense p.D636H c.1906G>C 3 108366903 BRCA G C Missense p.Q733H c.2199G>C 3 108373157 SCLC G C Missense p.V567L c.1699G>C 3 108363568 OV G C Missense p.V709L c.2125G>C 3 108373083 STAD G C Missense p.V982L c.2944G>C 3 108403123 LUAD G C Synonymous p.V971V c.2913G>C 3 108403092 HNSC GG TT Missense p.G404F c.1210_1211delinsTT 3 108363079 SCLC G T Missense p.C291F c.872G>T 3 108353773 HNSC G T Missense p.G273V c.818G>T 3 108353719 GBM G T Missense p.G520C c.1558G>T 3 108363427 LUAD G T Missense p.K684N c.2052G>T 3 108373010 HNSC G T Missense p.K787N c.2361G>T 3 108381042 UCEC G T Missense p.M962I c.2886G>T 3 108403065 LUSC G T Missense p.R1026L c.3077G>T 3 108405359 CM G T Missense p.R539L c.1616G>T 3 108363485 ESCA G T Missense p.R700I c.2099G>T 3 108373057 SCLC G T Nonsense p.G184* c.550G>T 3 108344785 HNSC G T SpliceDonorSNV . c.3624+10G>T 3 108409751 LUAD T A Missense p.L314M c.940T>A 3 108355484 HNSC T A Missense p.L34Q c.101T>A 3 108327004 LUAD T A Missense p.N557K c.1671T>A 3 108363540 BRCA T A Synonymous p.P614P c.1842T>A 3 108366839 STAD T C Missense p.I333T c.998T>C 3 108355542 PAAD T C Missense p.I593T c.1778T>C 3 108365482 UCEC T C Synonymous p.D712D c.2136T>C 3 108373094 CM T G Synonymous p.A815A c.2445T>G 3 108388549 BRCA T G Synonymous p.P331P c.993T>G 3 108355537 BLCA