Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 4 40103906 40103906 + Silent SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:40103906G>A c.441G>A c.(439-441)caG>caA p.Q147Q BLCA 4 40104102 40104102 + Missense_Mutation SNP A A C TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr4:40104102A>C c.637A>C c.(637-639)Aac>Cac p.N213H BLCA 4 40104297 40104297 + Missense_Mutation SNP C C G TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr4:40104297C>G c.832C>G c.(832-834)Caa>Gaa p.Q278E BLCA 4 40104376 40104376 + Missense_Mutation SNP G G A TCGA-GC-A3I6-01A-11D-A20D-08 TCGA-GC-A3I6-10A-01D-A20D-08 g.chr4:40104376G>A c.911G>A c.(910-912)gGt>gAt p.G304D BLCA 4 40104488 40104488 + Silent SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr4:40104488G>A c.1023G>A c.(1021-1023)gtG>gtA p.V341V BLCA 4 40121623 40121627 + Frame_Shift_Del DEL AGTTC AGTTC - TCGA-GU-A764-01A-11D-A34U-08 TCGA-GU-A764-10B-01D-A34X-08 g.chr4:40121623_40121627delAGTTC c.1892_1896delAGTTC c.(1891-1896)gagttcfs p.EF631fs BLCA 4 40122276 40122276 + Missense_Mutation SNP G G C TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr4:40122276G>C c.2545G>C c.(2545-2547)Gag>Cag p.E849Q BLCA 4 40122320 40122320 + Silent SNP C C A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr4:40122320C>A c.2589C>A c.(2587-2589)ctC>ctA p.L863L BLCA 4 40122364 40122364 + Nonsense_Mutation SNP C C A TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr4:40122364C>A c.2633C>A c.(2632-2634)tCa>tAa p.S878* BLCA 4 40122579 40122579 + Missense_Mutation SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr4:40122579G>A c.2848G>A c.(2848-2850)Gaa>Aaa p.E950K BLCA 4 40123217 40123217 + Silent SNP T T C TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr4:40123217T>C c.3486T>C c.(3484-3486)atT>atC p.I1162I BLCA 4 40123254 40123254 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:40123254C>T c.3523C>T c.(3523-3525)Cct>Tct p.P1175S BLCA 4 40123292 40123292 + Silent SNP C C T TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr4:40123292C>T c.3561C>T c.(3559-3561)aaC>aaT p.N1187N BLCA 4 40123713 40123713 + Missense_Mutation SNP G G A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr4:40123713G>A c.3982G>A c.(3982-3984)Gaa>Aaa p.E1328K BLCA 4 40123716 40123716 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr4:40123716G>A c.3985G>A c.(3985-3987)Gaa>Aaa p.E1329K BLCA 4 40133519 40133519 + Silent SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr4:40133519G>A c.4626G>A c.(4624-4626)gtG>gtA p.V1542V BLCA 4 40144375 40144375 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:40144375G>A c.4868G>A c.(4867-4869)aGa>aAa p.R1623K BLCA 4 40146258 40146258 + Missense_Mutation SNP C C G TCGA-FD-A3NA-01A-11D-A21A-08 TCGA-FD-A3NA-10A-01D-A21A-08 g.chr4:40146258C>G c.4981C>G c.(4981-4983)Ctt>Gtt p.L1661V BLCA 4 40146341 40146341 + Missense_Mutation SNP G G C TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr4:40146341G>C c.5064G>C c.(5062-5064)caG>caC p.Q1688H BLCA 4 40146392 40146392 + Missense_Mutation SNP G G C TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr4:40146392G>C c.5115G>C c.(5113-5115)ttG>ttC p.L1705F BRCA 4 40104198 40104198 + Missense_Mutation SNP C C A TCGA-B6-A0IP-01A-11D-A045-09 TCGA-B6-A0IP-10A-01W-A055-09 g.chr4:40104198C>A c.733C>A c.(733-735)Ctc>Atc p.L245I BRCA 4 40104400 40104400 + Missense_Mutation SNP C C T TCGA-AN-A0FZ-01A-11W-A050-09 TCGA-AN-A0FZ-10A-01W-A055-09 g.chr4:40104400C>T c.935C>T c.(934-936)aCt>aTt p.T312I BRCA 4 40104561 40104561 + Missense_Mutation SNP A A G TCGA-AN-A0FV-01A-11W-A019-09 TCGA-AN-A0FV-10A-01W-A021-09 g.chr4:40104561A>G c.1096A>G c.(1096-1098)Atg>Gtg p.M366V BRCA 4 40121887 40121887 + Missense_Mutation SNP C C A TCGA-D8-A1JG-01B-11D-A13L-09 TCGA-D8-A1JG-10A-01D-A13O-09 g.chr4:40121887C>A c.2156C>A c.(2155-2157)tCt>tAt p.S719Y BRCA 4 40121932 40121934 + In_Frame_Del DEL AAG AAG - TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-10A-01D-A29N-09 g.chr4:40121932_40121934delAAG c.2201_2203delAAG c.(2200-2205)caagaa>caa p.E735del BRCA 4 40122051 40122051 + Missense_Mutation SNP T T C TCGA-C8-A1HK-01A-21D-A13L-09 TCGA-C8-A1HK-10A-01D-A13O-09 g.chr4:40122051T>C c.2320T>C c.(2320-2322)Tcg>Ccg p.S774P BRCA 4 40124825 40124825 + Missense_Mutation SNP C C T TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chr4:40124825C>T c.4277C>T c.(4276-4278)tCt>tTt p.S1426F BRCA 4 40127807 40127807 + Missense_Mutation SNP C C G TCGA-A2-A0EY-01A-11W-A050-09 TCGA-A2-A0EY-10A-01W-A055-09 g.chr4:40127807C>G c.4384C>G c.(4384-4386)Cag>Gag p.Q1462E BRCA 4 40144366 40144366 + Missense_Mutation SNP A A T TCGA-BH-A203-01A-12D-A167-09 TCGA-BH-A203-11A-42D-A167-09 g.chr4:40144366A>T c.4859A>T c.(4858-4860)gAt>gTt p.D1620V CESC 4 40103779 40103779 + Missense_Mutation SNP C C G TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr4:40103779C>G c.314C>G c.(313-315)tCt>tGt p.S105C CESC 4 40103848 40103848 + Missense_Mutation SNP C C T TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr4:40103848C>T c.383C>T c.(382-384)tCa>tTa p.S128L CESC 4 40122816 40122816 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr4:40122816G>C c.3085G>C c.(3085-3087)Gaa>Caa p.E1029Q CHOL 4 40122733 40122733 + Missense_Mutation SNP A A G TCGA-3X-AAV9-01A-72D-A417-09 TCGA-3X-AAV9-10A-01D-A41A-09 g.chr4:40122733A>G c.3002A>G c.(3001-3003)cAa>cGa p.Q1001R CHOL 4 40133497 40133497 + Missense_Mutation SNP C C T TCGA-W5-AA2Z-01A-11D-A417-09 TCGA-W5-AA2Z-11A-11D-A41A-09 g.chr4:40133497C>T c.4604C>T c.(4603-4605)gCc>gTc p.A1535V CHOL 4 40154490 40154490 + Missense_Mutation SNP C C T TCGA-3X-AAVA-01A-11D-A417-09 TCGA-3X-AAVA-10A-01D-A41A-09 g.chr4:40154490C>T c.5234C>T c.(5233-5235)gCt>gTt p.A1745V COAD 4 40103771 40103771 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr4:40103771C>T c.306C>T c.(304-306)ttC>ttT p.F102F COAD 4 40103824 40103824 + Missense_Mutation SNP G G A TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr4:40103824G>A c.359G>A c.(358-360)cGt>cAt p.R120H COAD 4 40103897 40103897 + Silent SNP C C A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:40103897C>A c.432C>A c.(430-432)tcC>tcA p.S144S COAD 4 40103911 40103911 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:40103911C>T c.446C>T c.(445-447)gCt>gTt p.A149V COAD 4 40104016 40104016 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:40104016C>T c.551C>T c.(550-552)tCa>tTa p.S184L COAD 4 40104739 40104739 + Frame_Shift_Del DEL C C - TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr4:40104739delC c.1274delC c.(1273-1275)accfs p.T425fs COAD 4 40113761 40113761 + Missense_Mutation SNP A A G TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr4:40113761A>G c.1556A>G c.(1555-1557)cAg>cGg p.Q519R COAD 4 40121581 40121581 + Frame_Shift_Del DEL A A - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:40121581delA c.1850delA c.(1849-1851)gaafs p.E617fs COAD 4 40122539 40122539 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr4:40122539A>C c.2808A>C c.(2806-2808)caA>caC p.Q936H COAD 4 40122652 40122652 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:40122652C>T c.2921C>T c.(2920-2922)tCg>tTg p.S974L COAD 4 40122829 40122829 + Missense_Mutation SNP T T C TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr4:40122829T>C c.3098T>C c.(3097-3099)aTt>aCt p.I1033T COAD 4 40123098 40123098 + Missense_Mutation SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr4:40123098A>G c.3367A>G c.(3367-3369)Agc>Ggc p.S1123G COAD 4 40123185 40123185 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40123185C>T c.3454C>T c.(3454-3456)Cct>Tct p.P1152S COAD 4 40123356 40123356 + Missense_Mutation SNP G G A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr4:40123356G>A c.3625G>A c.(3625-3627)Gtc>Atc p.V1209I COAD 4 40123641 40123641 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40123641T>C c.3910T>C c.(3910-3912)Tat>Cat p.Y1304H COAD 4 40123770 40123770 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:40123770A>C c.4039A>C c.(4039-4041)Agt>Cgt p.S1347R COAD 4 40124774 40124774 + Missense_Mutation SNP T T C TCGA-F4-6704-01A-11D-1835-10 TCGA-F4-6704-11A-01D-1835-10 g.chr4:40124774T>C c.4226T>C c.(4225-4227)gTt>gCt p.V1409A COAD 4 40127790 40127790 + Missense_Mutation SNP C C A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:40127790C>A c.4367C>A c.(4366-4368)cCt>cAt p.P1456H COAD 4 40127795 40127796 + Frame_Shift_Ins INS - - A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr4:40127795_40127796insA c.4372_4373insA c.(4372-4374)caafs p.Q1458fs COAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COAD 4 40138608 40138609 + Missense_Mutation DNP AA AA GG TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr4:40138608_40138609AA>GG c.4691_4692AA>GG c.(4690-4692)gAA>gGG p.E1564G COAD 4 40138609 40138609 + Silent SNP A A G TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr4:40138609A>G c.4692A>G c.(4690-4692)gaA>gaG p.E1564E COAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs COAD 4 40146318 40146318 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40146318G>A c.5041G>A c.(5041-5043)Gtc>Atc p.V1681I COAD 4 40146341 40146341 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:40146341G>T c.5064G>T c.(5062-5064)caG>caT p.Q1688H COAD 4 40155844 40155844 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:40155844T>C c.5300T>C c.(5299-5301)gTc>gCc p.V1767A COADREAD 4 40103771 40103771 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr4:40103771C>T c.306C>T c.(304-306)ttC>ttT p.F102F COADREAD 4 40103824 40103824 + Missense_Mutation SNP G G A TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr4:40103824G>A c.359G>A c.(358-360)cGt>cAt p.R120H COADREAD 4 40103897 40103897 + Silent SNP C C A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:40103897C>A c.432C>A c.(430-432)tcC>tcA p.S144S COADREAD 4 40103911 40103911 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:40103911C>T c.446C>T c.(445-447)gCt>gTt p.A149V COADREAD 4 40104016 40104016 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:40104016C>T c.551C>T c.(550-552)tCa>tTa p.S184L COADREAD 4 40104123 40104123 + Missense_Mutation SNP G G A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr4:40104123G>A c.658G>A c.(658-660)Gtt>Att p.V220I COADREAD 4 40104571 40104571 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:40104571C>T c.1106C>T c.(1105-1107)gCt>gTt p.A369V COADREAD 4 40104739 40104739 + Frame_Shift_Del DEL C C - TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr4:40104739delC c.1274delC c.(1273-1275)accfs p.T425fs COADREAD 4 40113761 40113761 + Missense_Mutation SNP A A G TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr4:40113761A>G c.1556A>G c.(1555-1557)cAg>cGg p.Q519R COADREAD 4 40121581 40121581 + Frame_Shift_Del DEL A A - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:40121581delA c.1850delA c.(1849-1851)gaafs p.E617fs COADREAD 4 40122539 40122539 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr4:40122539A>C c.2808A>C c.(2806-2808)caA>caC p.Q936H COADREAD 4 40122652 40122652 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:40122652C>T c.2921C>T c.(2920-2922)tCg>tTg p.S974L COADREAD 4 40122829 40122829 + Missense_Mutation SNP T T C TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr4:40122829T>C c.3098T>C c.(3097-3099)aTt>aCt p.I1033T COADREAD 4 40122870 40122870 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:40122870G>T c.3139G>T c.(3139-3141)Gat>Tat p.D1047Y COADREAD 4 40123067 40123067 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:40123067G>T c.3336G>T c.(3334-3336)gaG>gaT p.E1112D COADREAD 4 40123098 40123098 + Missense_Mutation SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr4:40123098A>G c.3367A>G c.(3367-3369)Agc>Ggc p.S1123G COADREAD 4 40123185 40123185 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40123185C>T c.3454C>T c.(3454-3456)Cct>Tct p.P1152S COADREAD 4 40123356 40123356 + Missense_Mutation SNP G G A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr4:40123356G>A c.3625G>A c.(3625-3627)Gtc>Atc p.V1209I COADREAD 4 40123641 40123641 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40123641T>C c.3910T>C c.(3910-3912)Tat>Cat p.Y1304H COADREAD 4 40123770 40123770 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:40123770A>C c.4039A>C c.(4039-4041)Agt>Cgt p.S1347R COADREAD 4 40124774 40124774 + Missense_Mutation SNP T T C TCGA-F4-6704-01A-11D-1835-10 TCGA-F4-6704-11A-01D-1835-10 g.chr4:40124774T>C c.4226T>C c.(4225-4227)gTt>gCt p.V1409A COADREAD 4 40127790 40127790 + Missense_Mutation SNP C C A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:40127790C>A c.4367C>A c.(4366-4368)cCt>cAt p.P1456H COADREAD 4 40127795 40127796 + Frame_Shift_Ins INS - - A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr4:40127795_40127796insA c.4372_4373insA c.(4372-4374)caafs p.Q1458fs COADREAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COADREAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COADREAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COADREAD 4 40138608 40138608 + Missense_Mutation SNP A A G TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr4:40138608A>G c.4691A>G c.(4690-4692)gAa>gGa p.E1564G COADREAD 4 40138608 40138609 + Missense_Mutation DNP AA AA GG TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr4:40138608_40138609AA>GG c.4691_4692AA>GG c.(4690-4692)gAA>gGG p.E1564G COADREAD 4 40138609 40138609 + Silent SNP A A G TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr4:40138609A>G c.4692A>G c.(4690-4692)gaA>gaG p.E1564E COADREAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs COADREAD 4 40146318 40146318 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:40146318G>A c.5041G>A c.(5041-5043)Gtc>Atc p.V1681I COADREAD 4 40146341 40146341 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:40146341G>T c.5064G>T c.(5062-5064)caG>caT p.Q1688H COADREAD 4 40155844 40155844 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:40155844T>C c.5300T>C c.(5299-5301)gTc>gCc p.V1767A DLBC 4 40122377 40122377 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr4:40122377G>A c.2646G>A c.(2644-2646)atG>atA p.M882I DLBC 4 40122453 40122453 + Missense_Mutation SNP C C T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr4:40122453C>T c.2722C>T c.(2722-2724)Ccc>Tcc p.P908S ESCA 4 40098975 40098975 + Missense_Mutation SNP G G T TCGA-VR-A8EZ-01A-11D-A36J-09 TCGA-VR-A8EZ-10A-01D-A36M-09 g.chr4:40098975G>T c.15G>T c.(13-15)agG>agT p.R5S ESCA 4 40103753 40103755 + In_Frame_Del DEL ATC ATC - TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chr4:40103753_40103755delATC c.288_290delATC c.(286-291)gaatca>gaa p.S99del ESCA 4 40104792 40104792 + Missense_Mutation SNP G G T TCGA-JY-A6FE-01A-11D-A33E-09 TCGA-JY-A6FE-10A-01D-A33H-09 g.chr4:40104792G>T c.1327G>T c.(1327-1329)Gtt>Ttt p.V443F ESCA 4 40124821 40124821 + Nonsense_Mutation SNP G G T TCGA-L5-A8NR-01A-11D-A37C-09 TCGA-L5-A8NR-11A-11D-A37F-09 g.chr4:40124821G>T c.4273G>T c.(4273-4275)Gaa>Taa p.E1425* ESCA 4 40144359 40144359 + Missense_Mutation SNP G G A TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr4:40144359G>A c.4852G>A c.(4852-4854)Gac>Aac p.D1618N GBM 4 40119548 40119548 + Missense_Mutation SNP G G A TCGA-27-2523-01A-01D-1494-08 TCGA-27-2523-10A-01D-1494-08 g.chr4:40119548G>A c.1724G>A c.(1723-1725)cGt>cAt p.R575H GBM 4 40122570 40122570 + Nonsense_Mutation SNP G G T TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chr4:40122570G>T c.2839G>T c.(2839-2841)Gga>Tga p.G947* GBM 4 40127847 40127847 + Missense_Mutation SNP C C T TCGA-76-6193-01A-11D-1696-08 TCGA-76-6193-10A-01D-1696-08 g.chr4:40127847C>T c.4424C>T c.(4423-4425)tCt>tTt p.S1475F GBMLGG 4 40104251 40104252 + Frame_Shift_Ins INS - - A TCGA-HT-8113-01A-11D-2395-08 TCGA-HT-8113-10A-01D-2396-08 g.chr4:40104251_40104252insA c.786_787insA c.(787-789)aatfs p.N263fs GBMLGG 4 40108548 40108548 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40108548G>A c.1402G>A c.(1402-1404)Gtc>Atc p.V468I GBMLGG 4 40119548 40119548 + Missense_Mutation SNP G G A TCGA-27-2523-01A-01D-1494-08 TCGA-27-2523-10A-01D-1494-08 g.chr4:40119548G>A c.1724G>A c.(1723-1725)cGt>cAt p.R575H GBMLGG 4 40121734 40121734 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40121734T>C c.2003T>C c.(2002-2004)aTg>aCg p.M668T GBMLGG 4 40122570 40122570 + Nonsense_Mutation SNP G G T TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chr4:40122570G>T c.2839G>T c.(2839-2841)Gga>Tga p.G947* GBMLGG 4 40127847 40127847 + Missense_Mutation SNP C C T TCGA-76-6193-01A-11D-1696-08 TCGA-76-6193-10A-01D-1696-08 g.chr4:40127847C>T c.4424C>T c.(4423-4425)tCt>tTt p.S1475F GBMLGG 4 40133443 40133443 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40133443A>G c.4550A>G c.(4549-4551)gAa>gGa p.E1517G HNSC 4 40104316 40104316 + Missense_Mutation SNP T T C TCGA-CV-5432-01A-02D-1683-08 TCGA-CV-5432-10A-01D-1870-08 g.chr4:40104316T>C c.851T>C c.(850-852)gTa>gCa p.V284A HNSC 4 40115063 40115063 + Missense_Mutation SNP C C A TCGA-CR-7399-01A-11D-2012-08 TCGA-CR-7399-10A-01D-2013-08 g.chr4:40115063C>A c.1599C>A c.(1597-1599)caC>caA p.H533Q HNSC 4 40122006 40122006 + Missense_Mutation SNP A A G TCGA-CQ-A4C7-01A-11D-A25D-08 TCGA-CQ-A4C7-10A-01D-A25E-08 g.chr4:40122006A>G c.2275A>G c.(2275-2277)Aga>Gga p.R759G HNSC 4 40122465 40122465 + Missense_Mutation SNP A A G TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr4:40122465A>G c.2734A>G c.(2734-2736)Att>Gtt p.I912V HNSC 4 40122594 40122594 + Missense_Mutation SNP G G A TCGA-CV-7437-01A-21D-2129-08 TCGA-CV-7437-10A-01D-2129-08 g.chr4:40122594G>A c.2863G>A c.(2863-2865)Gaa>Aaa p.E955K HNSC 4 40123657 40123657 + Missense_Mutation SNP T T C TCGA-CN-4729-01A-01D-1434-08 TCGA-CN-4729-10A-01D-1434-08 g.chr4:40123657T>C c.3926T>C c.(3925-3927)cTt>cCt p.L1309P KIPAN 4 40103811 40103811 + Missense_Mutation SNP A A G TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chr4:40103811A>G c.346A>G c.(346-348)Ata>Gta p.I116V KIPAN 4 40121601 40121601 + Missense_Mutation SNP T T C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr4:40121601T>C c.1870T>C c.(1870-1872)Tct>Cct p.S624P KIPAN 4 40121716 40121716 + Frame_Shift_Del DEL G G - TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chr4:40121716delG c.1985delG c.(1984-1986)agafs p.R662fs KIPAN 4 40122134 40122134 + Frame_Shift_Del DEL A A - TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr4:40122134delA c.2403delA c.(2401-2403)acafs p.T801fs KIPAN 4 40122527 40122527 + Silent SNP C C T TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr4:40122527C>T c.2796C>T c.(2794-2796)ggC>ggT p.G932G KIPAN 4 40122682 40122682 + Missense_Mutation SNP C C G TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr4:40122682C>G c.2951C>G c.(2950-2952)cCa>cGa p.P984R KIPAN 4 40122970 40122970 + Frame_Shift_Del DEL A A - TCGA-G7-7502-01A-11D-2201-08 TCGA-G7-7502-10A-01D-2201-08 g.chr4:40122970delA c.3239delA c.(3238-3240)gaafs p.E1080fs KIRC 4 40121716 40121716 + Frame_Shift_Del DEL G G - TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chr4:40121716delG c.1985delG c.(1984-1986)agafs p.R662fs KIRC 4 40122527 40122527 + Silent SNP C C T TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr4:40122527C>T c.2796C>T c.(2794-2796)ggC>ggT p.G932G KIRP 4 40103811 40103811 + Missense_Mutation SNP A A G TCGA-G7-6793-01A-11D-1961-08 TCGA-G7-6793-10A-01D-1962-08 g.chr4:40103811A>G c.346A>G c.(346-348)Ata>Gta p.I116V KIRP 4 40121601 40121601 + Missense_Mutation SNP T T C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr4:40121601T>C c.1870T>C c.(1870-1872)Tct>Cct p.S624P KIRP 4 40122134 40122134 + Frame_Shift_Del DEL A A - TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr4:40122134delA c.2403delA c.(2401-2403)acafs p.T801fs KIRP 4 40122682 40122682 + Missense_Mutation SNP C C G TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr4:40122682C>G c.2951C>G c.(2950-2952)cCa>cGa p.P984R KIRP 4 40122970 40122970 + Frame_Shift_Del DEL A A - TCGA-G7-7502-01A-11D-2201-08 TCGA-G7-7502-10A-01D-2201-08 g.chr4:40122970delA c.3239delA c.(3238-3240)gaafs p.E1080fs LGG 4 40104251 40104252 + Frame_Shift_Ins INS - - A TCGA-HT-8113-01A-11D-2395-08 TCGA-HT-8113-10A-01D-2396-08 g.chr4:40104251_40104252insA c.786_787insA c.(787-789)aatfs p.N263fs LGG 4 40108548 40108548 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40108548G>A c.1402G>A c.(1402-1404)Gtc>Atc p.V468I LGG 4 40121734 40121734 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40121734T>C c.2003T>C c.(2002-2004)aTg>aCg p.M668T LGG 4 40133443 40133443 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:40133443A>G c.4550A>G c.(4549-4551)gAa>gGa p.E1517G LIHC 4 40098980 40098980 + Missense_Mutation SNP A A G TCGA-MR-A8JO-01A-12D-A35Z-10 TCGA-MR-A8JO-10A-01D-A35Z-10 g.chr4:40098980A>G c.20A>G c.(19-21)aAt>aGt p.N7S LIHC 4 40103840 40103840 + Missense_Mutation SNP T T G TCGA-G3-A5SM-01A-12D-A28X-10 TCGA-G3-A5SM-10A-01D-A28X-10 g.chr4:40103840T>G c.375T>G c.(373-375)agT>agG p.S125R LIHC 4 40121838 40121838 + Missense_Mutation SNP A A G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr4:40121838A>G c.2107A>G c.(2107-2109)Ata>Gta p.I703V LIHC 4 40122514 40122514 + Missense_Mutation SNP A A T TCGA-DD-AAE9-01A-11D-A40R-10 TCGA-DD-AAE9-10A-01D-A40U-10 g.chr4:40122514A>T c.2783A>T c.(2782-2784)gAg>gTg p.E928V LIHC 4 40122641 40122641 + Silent SNP G G A TCGA-5C-A9VG-01A-11D-A36X-10 TCGA-5C-A9VG-10A-01D-A370-10 g.chr4:40122641G>A c.2910G>A c.(2908-2910)ggG>ggA p.G970G LIHC 4 40123848 40123848 + Missense_Mutation SNP A A G TCGA-ZP-A9D1-01A-11D-A382-10 TCGA-ZP-A9D1-10B-01D-A385-10 g.chr4:40123848A>G c.4117A>G c.(4117-4119)Ata>Gta p.I1373V LIHC 4 40123872 40123872 + Frame_Shift_Del DEL C C - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr4:40123872delC c.4141delC c.(4141-4143)cccfs p.P1382fs LIHC 4 40154482 40154482 + Missense_Mutation SNP C C G TCGA-DD-AACG-01A-11D-A40R-10 TCGA-DD-AACG-10A-01D-A40U-10 g.chr4:40154482C>G c.5226C>G c.(5224-5226)atC>atG p.I1742M LUAD 4 40099000 40099000 + Missense_Mutation SNP C C T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr4:40099000C>T c.40C>T c.(40-42)Cgg>Tgg p.R14W LUAD 4 40104082 40104082 + Missense_Mutation SNP C C G TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr4:40104082C>G c.617C>G c.(616-618)tCt>tGt p.S206C LUAD 4 40104131 40104131 + Silent SNP C C T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr4:40104131C>T c.666C>T c.(664-666)aaC>aaT p.N222N LUAD 4 40104284 40104284 + Missense_Mutation SNP G G T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr4:40104284G>T c.819G>T c.(817-819)gaG>gaT p.E273D LUAD 4 40104287 40104287 + Silent SNP C C T TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr4:40104287C>T c.822C>T c.(820-822)tgC>tgT p.C274C LUAD 4 40104480 40104480 + Nonsense_Mutation SNP A A T TCGA-78-7147-01A-11D-2036-08 TCGA-78-7147-10A-01D-2036-08 g.chr4:40104480A>T c.1015A>T c.(1015-1017)Aag>Tag p.K339* LUAD 4 40104598 40104598 + Missense_Mutation SNP G G T TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr4:40104598G>T c.1133G>T c.(1132-1134)gGc>gTc p.G378V LUAD 4 40113714 40113714 + Silent SNP A A T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr4:40113714A>T c.1509A>T c.(1507-1509)gcA>gcT p.A503A LUAD 4 40115055 40115055 + Nonsense_Mutation SNP C C T TCGA-J2-8192-01A-11D-2238-08 TCGA-J2-8192-10A-01D-2238-08 g.chr4:40115055C>T c.1591C>T c.(1591-1593)Cag>Tag p.Q531* LUAD 4 40115128 40115128 + Splice_Site SNP G G T TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr4:40115128G>T c.1664G>T c.(1663-1665)aGg>aTg p.R555M LUAD 4 40121580 40121580 + Missense_Mutation SNP G G C TCGA-95-7948-01A-11D-2184-08 TCGA-95-7948-10A-01D-2184-08 g.chr4:40121580G>C c.1849G>C c.(1849-1851)Gaa>Caa p.E617Q LUAD 4 40122226 40122226 + Missense_Mutation SNP C C G TCGA-50-6673-01A-11D-1945-08 TCGA-50-6673-11A-02D-1945-08 g.chr4:40122226C>G c.2495C>G c.(2494-2496)tCt>tGt p.S832C LUAD 4 40122548 40122548 + Missense_Mutation SNP G G C TCGA-95-7948-01A-11D-2184-08 TCGA-95-7948-10A-01D-2184-08 g.chr4:40122548G>C c.2817G>C c.(2815-2817)aaG>aaC p.K939N LUAD 4 40122701 40122701 + Silent SNP A A G TCGA-75-7027-01A-11D-1945-08 TCGA-75-7027-10A-01D-1946-08 g.chr4:40122701A>G c.2970A>G c.(2968-2970)gtA>gtG p.V990V LUAD 4 40122932 40122932 + Silent SNP A A G TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr4:40122932A>G c.3201A>G c.(3199-3201)ccA>ccG p.P1067P LUAD 4 40127837 40127837 + Missense_Mutation SNP T T G TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr4:40127837T>G c.4414T>G c.(4414-4416)Tta>Gta p.L1472V LUAD 4 40146365 40146365 + Silent SNP G G C TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr4:40146365G>C c.5088G>C c.(5086-5088)ctG>ctC p.L1696L LUSC 4 40099026 40099026 + Silent SNP T T G TCGA-66-2755-01A-01D-1522-08 TCGA-66-2755-11A-01D-1522-08 g.chr4:40099026T>G c.66T>G c.(64-66)gtT>gtG p.V22V LUSC 4 40121557 40121558 + Missense_Mutation DNP GA GA TT TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr4:40121557_40121558GA>TT c.1826_1827GA>TT c.(1825-1827)aGA>aTT p.R609I LUSC 4 40121773 40121773 + Missense_Mutation SNP C C A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr4:40121773C>A c.2042C>A c.(2041-2043)cCa>cAa p.P681Q LUSC 4 40122763 40122763 + Missense_Mutation SNP T T C TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chr4:40122763T>C c.3032T>C c.(3031-3033)gTa>gCa p.V1011A LUSC 4 40123254 40123254 + Missense_Mutation SNP C C A TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr4:40123254C>A c.3523C>A c.(3523-3525)Cct>Act p.P1175T LUSC 4 40123482 40123482 + Missense_Mutation SNP C C T TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr4:40123482C>T c.3751C>T c.(3751-3753)Cca>Tca p.P1251S LUSC 4 40123493 40123493 + Silent SNP A A G TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr4:40123493A>G c.3762A>G c.(3760-3762)ctA>ctG p.L1254L OV 4 40104288 40104288 + Missense_Mutation SNP G G A TCGA-61-1738-01A-01W-0639-09 TCGA-61-1738-11A-01W-0639-09 g.chr4:40104288G>A c.823G>A c.(823-825)Gtt>Att p.V275I OV 4 40124773 40124773 + Missense_Mutation SNP G G A TCGA-24-0966-01A-01W-0977-09 TCGA-24-0966-10A-01W-0421-09 g.chr4:40124773G>A c.4225G>A c.(4225-4227)Gtt>Att p.V1409I OV 4 40144436 40144436 + Silent SNP T T A TCGA-36-2542-01A-01D-1526-09 TCGA-36-2542-10A-01D-1526-09 g.chr4:40144436T>A c.4929T>A c.(4927-4929)gcT>gcA p.A1643A PAAD 4 40103869 40103869 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40103869A>G c.404A>G c.(403-405)gAc>gGc p.D135G PAAD 4 40104536 40104536 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40104536G>A c.1071G>A c.(1069-1071)ccG>ccA p.P357P PAAD 4 40122325 40122325 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40122325G>T c.2594G>T c.(2593-2595)aGc>aTc p.S865I PAAD 4 40122738 40122738 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40122738C>T c.3007C>T c.(3007-3009)Cct>Tct p.P1003S PAAD 4 40138628 40138628 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40138628G>A c.4711G>A c.(4711-4713)Gtt>Att p.V1571I PAAD 4 40144448 40144449 + Frame_Shift_Ins INS - - A TCGA-FB-AAPQ-01A-11D-A40W-08 TCGA-FB-AAPQ-11A-11D-A40W-08 g.chr4:40144448_40144449insA c.4941_4942insA c.(4942-4944)aaafs p.K1648fs PAAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-2L-AAQI-01A-12D-A397-08 TCGA-2L-AAQI-11A-11D-A39A-08 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs PAAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-HZ-8637-01A-11D-2396-08 TCGA-HZ-8637-10A-01D-2396-08 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs PAAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-HZ-A9TJ-01A-11D-A40W-08 TCGA-HZ-A9TJ-10A-01D-A40W-08 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs PAAD 4 40144449 40144449 + Frame_Shift_Del DEL A A - TCGA-IB-A5SP-01A-11D-A32N-08 TCGA-IB-A5SP-10A-01D-A32N-08 g.chr4:40144449delA c.4942delA c.(4942-4944)aaafs p.K1649fs PAAD 4 40154517 40154517 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:40154517G>T c.5261G>T c.(5260-5262)aGc>aTc p.S1754I PRAD 4 40108585 40108585 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:40108585G>A c.1439G>A c.(1438-1440)gGa>gAa p.G480E PRAD 4 40119567 40119567 + Missense_Mutation SNP A A G TCGA-EJ-7123-01A-11D-1961-08 TCGA-EJ-7123-10A-01D-1961-08 g.chr4:40119567A>G c.1743A>G c.(1741-1743)atA>atG p.I581M PRAD 4 40123039 40123039 + Nonsense_Mutation SNP C C A TCGA-EJ-A8FS-01A-11D-A34U-08 TCGA-EJ-A8FS-10A-01D-A34X-08 g.chr4:40123039C>A c.3308C>A c.(3307-3309)tCa>tAa p.S1103* PRAD 4 40123912 40123912 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:40123912C>A c.4181C>A c.(4180-4182)cCt>cAt p.P1394H READ 4 40104123 40104123 + Missense_Mutation SNP G G A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr4:40104123G>A c.658G>A c.(658-660)Gtt>Att p.V220I READ 4 40104571 40104571 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:40104571C>T c.1106C>T c.(1105-1107)gCt>gTt p.A369V READ 4 40122870 40122870 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:40122870G>T c.3139G>T c.(3139-3141)Gat>Tat p.D1047Y READ 4 40123067 40123067 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:40123067G>T c.3336G>T c.(3334-3336)gaG>gaT p.E1112D SARC 4 40099030 40099030 + Missense_Mutation SNP G G A TCGA-DX-A23U-01A-11D-A26G-09 TCGA-DX-A23U-10A-01D-A26G-09 g.chr4:40099030G>A c.70G>A c.(70-72)Gta>Ata p.V24I SARC 4 40108621 40108621 + Missense_Mutation SNP C C T TCGA-N1-A6IA-01A-12D-A32I-09 TCGA-N1-A6IA-11A-11D-A32I-09 g.chr4:40108621C>T c.1475C>T c.(1474-1476)gCa>gTa p.A492V SKCM 4 40098995 40098995 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr4:40098995C>T c.35C>T c.(34-36)cCt>cTt p.P12L SKCM 4 40104513 40104513 + Missense_Mutation SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr4:40104513C>T c.1048C>T c.(1048-1050)Ctc>Ttc p.L350F SKCM 4 40104546 40104546 + Missense_Mutation SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr4:40104546C>T c.1081C>T c.(1081-1083)Ccg>Tcg p.P361S SKCM 4 40104609 40104609 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr4:40104609C>T c.1144C>T c.(1144-1146)Cct>Tct p.P382S SKCM 4 40104657 40104657 + Missense_Mutation SNP C C T TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr4:40104657C>T c.1192C>T c.(1192-1194)Cca>Tca p.P398S SKCM 4 40104726 40104726 + Nonsense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr4:40104726C>T c.1261C>T c.(1261-1263)Caa>Taa p.Q421* SKCM 4 40104811 40104811 + Missense_Mutation SNP C C G TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr4:40104811C>G c.1346C>G c.(1345-1347)cCg>cGg p.P449R SKCM 4 40104813 40104813 + Nonsense_Mutation SNP G G T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr4:40104813G>T c.1348G>T c.(1348-1350)Gga>Tga p.G450* SKCM 4 40108641 40108641 + Missense_Mutation SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr4:40108641C>T c.1495C>T c.(1495-1497)Cgt>Tgt p.R499C SKCM 4 40108641 40108641 + Missense_Mutation SNP C C T TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr4:40108641C>T c.1495C>T c.(1495-1497)Cgt>Tgt p.R499C SKCM 4 40119499 40119499 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr4:40119499C>T c.1675C>T c.(1675-1677)Cat>Tat p.H559Y SKCM 4 40121902 40121902 + Missense_Mutation SNP C C T TCGA-DA-A3F3-06A-11D-A20D-08 TCGA-DA-A3F3-10A-01D-A20D-08 g.chr4:40121902C>T c.2171C>T c.(2170-2172)tCa>tTa p.S724L SKCM 4 40121980 40121980 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr4:40121980C>T c.2249C>T c.(2248-2250)tCc>tTc p.S750F SKCM 4 40123006 40123006 + Missense_Mutation SNP T T C TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr4:40123006T>C c.3275T>C c.(3274-3276)cTt>cCt p.L1092P SKCM 4 40123361 40123361 + Silent SNP T T A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr4:40123361T>A c.3630T>A c.(3628-3630)acT>acA p.T1210T SKCM 4 40123586 40123586 + Silent SNP T T A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr4:40123586T>A c.3855T>A c.(3853-3855)tcT>tcA p.S1285S SKCM 4 40123874 40123874 + Silent SNP C C T TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr4:40123874C>T c.4143C>T c.(4141-4143)ccC>ccT p.P1381P SKCM 4 40127760 40127760 + Missense_Mutation SNP C C T TCGA-GN-A4U3-06A-11D-A32N-08 TCGA-GN-A4U3-10F-01D-A32N-08 g.chr4:40127760C>T c.4337C>T c.(4336-4338)tCc>tTc p.S1446F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 4 40103906 40103906 single base substitution G A 3_prime_UTR_variant BLCA-US 4 40103906 40103906 single base substitution G A synonymous_variant Q147Q 441G>A BLCA-US 4 40103906 40103906 single base substitution G A synonymous_variant Q67Q 201G>A BLCA-US 4 40103906 40103906 single base substitution G A upstream_gene_variant BLCA-US 4 40104102 40104102 single base substitution A C 3_prime_UTR_variant BLCA-US 4 40104102 40104102 single base substitution A C missense_variant N133H 397A>C BLCA-US 4 40104102 40104102 single base substitution A C missense_variant N213H 637A>C BLCA-US 4 40104102 40104102 single base substitution A C upstream_gene_variant BLCA-US 4 40104376 40104376 single base substitution G A 3_prime_UTR_variant BLCA-US 4 40104376 40104376 single base substitution G A downstream_gene_variant BLCA-US 4 40104376 40104376 single base substitution G A missense_variant G304D 911G>A BLCA-US 4 40104376 40104376 single base substitution G A upstream_gene_variant BLCA-US 4 40104488 40104488 single base substitution G A 3_prime_UTR_variant BLCA-US 4 40104488 40104488 single base substitution G A downstream_gene_variant BLCA-US 4 40104488 40104488 single base substitution G A synonymous_variant V341V 1023G>A BLCA-US 4 40104488 40104488 single base substitution G A upstream_gene_variant BLCA-US 4 40122276 40122276 single base substitution G C 3_prime_UTR_variant BLCA-US 4 40122276 40122276 single base substitution G C missense_variant E495Q 1483G>C BLCA-US 4 40122276 40122276 single base substitution G C missense_variant E849Q 2545G>C BLCA-US 4 40123217 40123217 single base substitution T C 3_prime_UTR_variant BLCA-US 4 40123217 40123217 single base substitution T C synonymous_variant I1162I 3486T>C BLCA-US 4 40123217 40123217 single base substitution T C synonymous_variant I808I 2424T>C BLCA-US 4 40123254 40123254 single base substitution C T 3_prime_UTR_variant BLCA-US 4 40123254 40123254 single base substitution C T missense_variant P1175S 3523C>T BLCA-US 4 40123254 40123254 single base substitution C T missense_variant P821S 2461C>T BLCA-US 4 40123292 40123292 single base substitution C T 3_prime_UTR_variant BLCA-US 4 40123292 40123292 single base substitution C T synonymous_variant N1187N 3561C>T BLCA-US 4 40123292 40123292 single base substitution C T synonymous_variant N833N 2499C>T BLCA-US 4 40123716 40123716 single base substitution G A 3_prime_UTR_variant BLCA-US 4 40123716 40123716 single base substitution G A missense_variant E1329K 3985G>A BLCA-US 4 40123716 40123716 single base substitution G A missense_variant E975K 2923G>A BLCA-US 4 40144375 40144375 single base substitution G A 3_prime_UTR_variant BLCA-US 4 40144375 40144375 single base substitution G A missense_variant R1252K 3755G>A BLCA-US 4 40144375 40144375 single base substitution G A missense_variant R1623K 4868G>A BLCA-US 4 40146258 40146258 single base substitution C G 3_prime_UTR_variant BLCA-US 4 40146258 40146258 single base substitution C G missense_variant L1290V 3868C>G BLCA-US 4 40146258 40146258 single base substitution C G missense_variant L1661V 4981C>G BLCA-US 4 40146392 40146392 single base substitution G C 3_prime_UTR_variant BLCA-US 4 40146392 40146392 single base substitution G C missense_variant L1334F 4002G>C BLCA-US 4 40146392 40146392 single base substitution G C missense_variant L1705F 5115G>C BOCA-FR 4 40056849 40056849 single base substitution G C upstream_gene_variant BOCA-FR 4 40064771 40064771 single base substitution C A intron_variant BRCA-EU 4 40053911 40053911 single base substitution T C upstream_gene_variant BRCA-EU 4 40054535 40054535 single base substitution G A upstream_gene_variant BRCA-EU 4 40055535 40055535 single base substitution G T upstream_gene_variant BRCA-EU 4 40057496 40057496 single base substitution T A upstream_gene_variant BRCA-EU 4 40058185 40058185 single base substitution G A upstream_gene_variant BRCA-EU 4 40058325 40058325 deletion of <=200bp G - upstream_gene_variant BRCA-EU 4 40059548 40059548 single base substitution T C intron_variant BRCA-EU 4 40059759 40059763 deletion of <=200bp AAAAA - intron_variant BRCA-EU 4 40060889 40060889 single base substitution C T intron_variant BRCA-EU 4 40060903 40060903 single base substitution A G intron_variant BRCA-EU 4 40061589 40061589 single base substitution G C intron_variant BRCA-EU 4 40063321 40063321 single base substitution G A intron_variant BRCA-EU 4 40065972 40065972 single base substitution G A intron_variant BRCA-EU 4 40066029 40066029 single base substitution G A intron_variant BRCA-EU 4 40069417 40069417 single base substitution C T intron_variant BRCA-EU 4 40071033 40071033 deletion of <=200bp A - intron_variant BRCA-EU 4 40072078 40072078 deletion of <=200bp T - intron_variant BRCA-EU 4 40073695 40073695 single base substitution A T intron_variant BRCA-EU 4 40075953 40075953 single base substitution C T intron_variant BRCA-EU 4 40078963 40079010 multiple base substitution (>=2bp and <=200bp) TTACCATGTTGCCCAGGTTGATCTTGAACTCCCAACCTCAAGTGATCT TCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGGTCC intron_variant BRCA-EU 4 40079364 40079364 single base substitution G A intron_variant BRCA-EU 4 40079964 40079964 single base substitution G T intron_variant BRCA-EU 4 40080231 40080231 single base substitution G A intron_variant BRCA-EU 4 40080591 40080591 single base substitution G A intron_variant BRCA-EU 4 40081391 40081391 single base substitution C T intron_variant BRCA-EU 4 40084586 40084586 single base substitution C G intron_variant BRCA-EU 4 40084660 40084660 single base substitution G C intron_variant BRCA-EU 4 40085904 40085906 deletion of <=200bp ATG - intron_variant BRCA-EU 4 40087976 40087976 single base substitution G C intron_variant BRCA-EU 4 40091867 40091867 single base substitution T C intron_variant BRCA-EU 4 40092497 40092497 single base substitution G A intron_variant BRCA-EU 4 40094109 40094109 single base substitution C G intron_variant BRCA-EU 4 40095036 40095036 deletion of <=200bp T - intron_variant BRCA-EU 4 40096159 40096159 single base substitution T C intron_variant BRCA-EU 4 40097163 40097163 single base substitution G C intron_variant BRCA-EU 4 40097304 40097304 single base substitution G T intron_variant BRCA-EU 4 40097845 40097845 single base substitution G A intron_variant BRCA-EU 4 40100730 40100730 single base substitution A G intron_variant BRCA-EU 4 40100730 40100730 single base substitution A G upstream_gene_variant BRCA-EU 4 40102966 40102966 single base substitution G C intron_variant BRCA-EU 4 40102966 40102966 single base substitution G C upstream_gene_variant BRCA-EU 4 40103040 40103040 insertion of <=200bp - A intron_variant BRCA-EU 4 40103040 40103040 insertion of <=200bp - A upstream_gene_variant BRCA-EU 4 40103755 40103755 single base substitution C A 3_prime_UTR_variant BRCA-EU 4 40103755 40103755 single base substitution C A stop_gained S17* 50C>A BRCA-EU 4 40103755 40103755 single base substitution C A stop_gained S97* 290C>A BRCA-EU 4 40103755 40103755 single base substitution C A upstream_gene_variant BRCA-EU 4 40103790 40103790 single base substitution G C 3_prime_UTR_variant BRCA-EU 4 40103790 40103790 single base substitution G C missense_variant V109L 325G>C BRCA-EU 4 40103790 40103790 single base substitution G C missense_variant V29L 85G>C BRCA-EU 4 40103790 40103790 single base substitution G C upstream_gene_variant BRCA-EU 4 40103827 40103827 single base substitution C G 3_prime_UTR_variant BRCA-EU 4 40103827 40103827 single base substitution C G missense_variant P121R 362C>G BRCA-EU 4 40103827 40103827 single base substitution C G missense_variant P41R 122C>G BRCA-EU 4 40103827 40103827 single base substitution C G upstream_gene_variant BRCA-EU 4 40107948 40107948 insertion of <=200bp - T downstream_gene_variant BRCA-EU 4 40107948 40107948 insertion of <=200bp - T intron_variant BRCA-EU 4 40108127 40108127 single base substitution G T downstream_gene_variant BRCA-EU 4 40108127 40108127 single base substitution G T intron_variant BRCA-EU 4 40110621 40110621 single base substitution G T intron_variant BRCA-EU 4 40111171 40111171 single base substitution C G intron_variant BRCA-EU 4 40113054 40113054 single base substitution T C intron_variant BRCA-EU 4 40114944 40114944 single base substitution A G intron_variant BRCA-EU 4 40115096 40115096 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 40115096 40115096 single base substitution A G synonymous_variant T190T 570A>G BRCA-EU 4 40115096 40115096 single base substitution A G synonymous_variant T544T 1632A>G BRCA-EU 4 40117241 40117241 single base substitution C G intron_variant BRCA-EU 4 40121646 40121646 single base substitution G C 3_prime_UTR_variant BRCA-EU 4 40121646 40121646 single base substitution G C missense_variant D285H 853G>C BRCA-EU 4 40121646 40121646 single base substitution G C missense_variant D639H 1915G>C BRCA-EU 4 40122627 40122627 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 4 40122627 40122627 insertion of <=200bp - A frameshift_variant K612K? BRCA-EU 4 40122627 40122627 insertion of <=200bp - A frameshift_variant K966K? BRCA-EU 4 40123935 40123935 single base substitution G A splice_region_variant BRCA-EU 4 40129447 40129447 single base substitution A T intron_variant BRCA-EU 4 40135176 40135176 single base substitution G A intron_variant BRCA-EU 4 40136273 40136283 multiple base substitution (>=2bp and <=200bp) AATTGTTGGTA ATTAG intron_variant BRCA-EU 4 40137786 40137786 single base substitution T G intron_variant BRCA-EU 4 40138400 40138400 insertion of <=200bp - T intron_variant BRCA-EU 4 40138686 40138686 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 40138686 40138686 single base substitution A G missense_variant K1236R 3707A>G BRCA-EU 4 40138686 40138686 single base substitution A G missense_variant K1590R 4769A>G BRCA-EU 4 40140781 40140781 single base substitution C G intron_variant BRCA-EU 4 40142115 40142115 single base substitution C T intron_variant BRCA-EU 4 40142438 40142438 single base substitution C T intron_variant BRCA-EU 4 40143356 40143356 single base substitution C A intron_variant BRCA-EU 4 40143535 40143535 single base substitution G A intron_variant BRCA-EU 4 40144681 40144681 single base substitution T G intron_variant BRCA-EU 4 40146842 40146842 deletion of <=200bp G - intron_variant BRCA-EU 4 40149228 40149228 single base substitution G A intron_variant BRCA-EU 4 40151358 40151358 single base substitution C A intron_variant BRCA-EU 4 40151709 40151709 single base substitution G A intron_variant BRCA-EU 4 40152342 40152342 single base substitution C T intron_variant BRCA-EU 4 40152685 40152685 single base substitution T G intron_variant BRCA-EU 4 40152814 40152814 insertion of <=200bp - ATGACTG intron_variant BRCA-EU 4 40153475 40153475 single base substitution G C intron_variant BRCA-EU 4 40154277 40154277 single base substitution G C intron_variant BRCA-EU 4 40154640 40154640 single base substitution T A intron_variant BRCA-EU 4 40154665 40154665 single base substitution G C intron_variant BRCA-EU 4 40155371 40155371 single base substitution G A intron_variant BRCA-EU 4 40155689 40155689 single base substitution A C intron_variant BRCA-EU 4 40155939 40155939 single base substitution T A 3_prime_UTR_variant BRCA-EU 4 40157362 40157362 single base substitution G C 3_prime_UTR_variant BRCA-EU 4 40157362 40157362 single base substitution G C downstream_gene_variant BRCA-EU 4 40158813 40158813 single base substitution G A 3_prime_UTR_variant BRCA-EU 4 40158813 40158813 single base substitution G A downstream_gene_variant BRCA-EU 4 40160018 40160018 single base substitution G A downstream_gene_variant BRCA-EU 4 40160351 40160351 single base substitution C T downstream_gene_variant BRCA-EU 4 40163055 40163055 single base substitution G A downstream_gene_variant BRCA-EU 4 40163803 40163803 single base substitution T A downstream_gene_variant BRCA-FR 4 40057496 40057496 single base substitution T A upstream_gene_variant BRCA-FR 4 40058676 40058676 single base substitution G C intron_variant BRCA-FR 4 40071114 40071114 single base substitution C T intron_variant BRCA-FR 4 40081391 40081391 single base substitution C T intron_variant BRCA-FR 4 40084660 40084660 single base substitution G C intron_variant BRCA-FR 4 40085592 40085592 single base substitution T G intron_variant BRCA-FR 4 40087976 40087976 single base substitution G C intron_variant BRCA-FR 4 40094983 40094983 single base substitution G A intron_variant BRCA-FR 4 40097163 40097163 single base substitution G C intron_variant BRCA-FR 4 40114944 40114944 single base substitution A G intron_variant BRCA-FR 4 40118274 40118274 single base substitution T A intron_variant BRCA-FR 4 40133614 40133614 single base substitution T C intron_variant BRCA-FR 4 40144405 40144405 single base substitution G C 3_prime_UTR_variant BRCA-FR 4 40144405 40144405 single base substitution G C missense_variant R1262T 3785G>C BRCA-FR 4 40144405 40144405 single base substitution G C missense_variant R1633T 4898G>C BRCA-FR 4 40151709 40151709 single base substitution G A intron_variant BRCA-FR 4 40152342 40152342 single base substitution C T intron_variant BRCA-FR 4 40155359 40155359 single base substitution G A intron_variant BRCA-FR 4 40162427 40162427 single base substitution G C downstream_gene_variant BRCA-FR 4 40163055 40163055 single base substitution G A downstream_gene_variant BRCA-UK 4 40070641 40070641 single base substitution G A intron_variant BRCA-UK 4 40079964 40079964 single base substitution G T intron_variant BRCA-UK 4 40094680 40094680 single base substitution C T intron_variant BRCA-UK 4 40117233 40117233 single base substitution C T intron_variant BRCA-UK 4 40127783 40127783 single base substitution G C 3_prime_UTR_variant BRCA-UK 4 40127783 40127783 single base substitution G C missense_variant D1100H 3298G>C BRCA-UK 4 40127783 40127783 single base substitution G C missense_variant D1454H 4360G>C BRCA-US 4 40104198 40104198 single base substitution C A 3_prime_UTR_variant BRCA-US 4 40104198 40104198 single base substitution C A missense_variant L165I 493C>A BRCA-US 4 40104198 40104198 single base substitution C A missense_variant L245I 733C>A BRCA-US 4 40104198 40104198 single base substitution C A upstream_gene_variant BRCA-US 4 40104400 40104400 single base substitution C T 3_prime_UTR_variant BRCA-US 4 40104400 40104400 single base substitution C T downstream_gene_variant BRCA-US 4 40104400 40104400 single base substitution C T missense_variant T312I 935C>T BRCA-US 4 40104400 40104400 single base substitution C T upstream_gene_variant BRCA-US 4 40104561 40104561 single base substitution A G 3_prime_UTR_variant BRCA-US 4 40104561 40104561 single base substitution A G downstream_gene_variant BRCA-US 4 40104561 40104561 single base substitution A G missense_variant M12V 34A>G BRCA-US 4 40104561 40104561 single base substitution A G missense_variant M366V 1096A>G BRCA-US 4 40121887 40121887 single base substitution C A 3_prime_UTR_variant BRCA-US 4 40121887 40121887 single base substitution C A missense_variant S365Y 1094C>A BRCA-US 4 40121887 40121887 single base substitution C A missense_variant S719Y 2156C>A BRCA-US 4 40121932 40121934 deletion of <=200bp AAG - 3_prime_UTR_variant BRCA-US 4 40121932 40121934 deletion of <=200bp AAG - inframe_deletion QE380Q BRCA-US 4 40121932 40121934 deletion of <=200bp AAG - inframe_deletion QE734Q BRCA-US 4 40122051 40122051 single base substitution T C 3_prime_UTR_variant BRCA-US 4 40122051 40122051 single base substitution T C missense_variant S420P 1258T>C BRCA-US 4 40122051 40122051 single base substitution T C missense_variant S774P 2320T>C BRCA-US 4 40123795 40123795 single base substitution A G 3_prime_UTR_variant BRCA-US 4 40123795 40123795 single base substitution A G missense_variant E1001G 3002A>G BRCA-US 4 40123795 40123795 single base substitution A G missense_variant E1355G 4064A>G BRCA-US 4 40124825 40124825 single base substitution C T 3_prime_UTR_variant BRCA-US 4 40124825 40124825 single base substitution C T missense_variant S1072F 3215C>T BRCA-US 4 40124825 40124825 single base substitution C T missense_variant S1426F 4277C>T BRCA-US 4 40127807 40127807 single base substitution C G 3_prime_UTR_variant BRCA-US 4 40127807 40127807 single base substitution C G missense_variant Q1108E 3322C>G BRCA-US 4 40127807 40127807 single base substitution C G missense_variant Q1462E 4384C>G BRCA-US 4 40144366 40144366 single base substitution A T 3_prime_UTR_variant BRCA-US 4 40144366 40144366 single base substitution A T missense_variant D1249V 3746A>T BRCA-US 4 40144366 40144366 single base substitution A T missense_variant D1620V 4859A>T BTCA-JP 4 40101544 40101544 deletion of <=200bp T - intron_variant BTCA-JP 4 40101544 40101544 deletion of <=200bp T - upstream_gene_variant BTCA-JP 4 40121754 40121754 single base substitution G T 3_prime_UTR_variant BTCA-JP 4 40121754 40121754 single base substitution G T missense_variant A321S 961G>T BTCA-JP 4 40121754 40121754 single base substitution G T missense_variant A675S 2023G>T CESC-US 4 40103779 40103779 single base substitution C G 3_prime_UTR_variant CESC-US 4 40103779 40103779 single base substitution C G missense_variant S105C 314C>G CESC-US 4 40103779 40103779 single base substitution C G missense_variant S25C 74C>G CESC-US 4 40103779 40103779 single base substitution C G upstream_gene_variant CESC-US 4 40103848 40103848 single base substitution C T 3_prime_UTR_variant CESC-US 4 40103848 40103848 single base substitution C T missense_variant S128L 383C>T CESC-US 4 40103848 40103848 single base substitution C T missense_variant S48L 143C>T CESC-US 4 40103848 40103848 single base substitution C T upstream_gene_variant CESC-US 4 40122816 40122816 single base substitution G C 3_prime_UTR_variant CESC-US 4 40122816 40122816 single base substitution G C missense_variant E1029Q 3085G>C CESC-US 4 40122816 40122816 single base substitution G C missense_variant E675Q 2023G>C CLLE-ES 4 40126994 40126994 single base substitution A G intron_variant CLLE-ES 4 40129014 40129014 single base substitution T C intron_variant CLLE-ES 4 40155344 40155344 single base substitution G A intron_variant CLLE-ES 4 40163006 40163006 single base substitution A G downstream_gene_variant COAD-US 4 40103771 40103771 single base substitution C T 3_prime_UTR_variant COAD-US 4 40103771 40103771 single base substitution C T synonymous_variant F102F 306C>T COAD-US 4 40103771 40103771 single base substitution C T synonymous_variant F22F 66C>T COAD-US 4 40103771 40103771 single base substitution C T upstream_gene_variant COAD-US 4 40104016 40104016 single base substitution C T 3_prime_UTR_variant COAD-US 4 40104016 40104016 single base substitution C T missense_variant S104L 311C>T COAD-US 4 40104016 40104016 single base substitution C T missense_variant S184L 551C>T COAD-US 4 40104016 40104016 single base substitution C T upstream_gene_variant COAD-US 4 40104739 40104739 deletion of <=200bp C - 3_prime_UTR_variant COAD-US 4 40104739 40104739 deletion of <=200bp C - downstream_gene_variant COAD-US 4 40104739 40104739 deletion of <=200bp C - frameshift_variant T425 COAD-US 4 40104739 40104739 deletion of <=200bp C - frameshift_variant T71 COAD-US 4 40113761 40113761 single base substitution A G 3_prime_UTR_variant COAD-US 4 40113761 40113761 single base substitution A G missense_variant Q165R 494A>G COAD-US 4 40113761 40113761 single base substitution A G missense_variant Q519R 1556A>G COAD-US 4 40122539 40122539 single base substitution A C 3_prime_UTR_variant COAD-US 4 40122539 40122539 single base substitution A C missense_variant Q582H 1746A>C COAD-US 4 40122539 40122539 single base substitution A C missense_variant Q936H 2808A>C COAD-US 4 40122652 40122652 single base substitution C T 3_prime_UTR_variant COAD-US 4 40122652 40122652 single base substitution C T missense_variant S620L 1859C>T COAD-US 4 40122652 40122652 single base substitution C T missense_variant S974L 2921C>T COAD-US 4 40122829 40122829 single base substitution T C 3_prime_UTR_variant COAD-US 4 40122829 40122829 single base substitution T C missense_variant I1033T 3098T>C COAD-US 4 40122829 40122829 single base substitution T C missense_variant I679T 2036T>C COAD-US 4 40123098 40123098 single base substitution A G 3_prime_UTR_variant COAD-US 4 40123098 40123098 single base substitution A G missense_variant S1123G 3367A>G COAD-US 4 40123098 40123098 single base substitution A G missense_variant S769G 2305A>G COAD-US 4 40123185 40123185 single base substitution C T 3_prime_UTR_variant COAD-US 4 40123185 40123185 single base substitution C T missense_variant P1152S 3454C>T COAD-US 4 40123185 40123185 single base substitution C T missense_variant P798S 2392C>T COAD-US 4 40123641 40123641 single base substitution T C 3_prime_UTR_variant COAD-US 4 40123641 40123641 single base substitution T C missense_variant Y1304H 3910T>C COAD-US 4 40123641 40123641 single base substitution T C missense_variant Y950H 2848T>C COAD-US 4 40127790 40127790 single base substitution C A 3_prime_UTR_variant COAD-US 4 40127790 40127790 single base substitution C A missense_variant P1102H 3305C>A COAD-US 4 40127790 40127790 single base substitution C A missense_variant P1456H 4367C>A COAD-US 4 40127795 40127795 insertion of <=200bp - A 3_prime_UTR_variant COAD-US 4 40127795 40127795 insertion of <=200bp - A frameshift_variant Q1104T? COAD-US 4 40127795 40127795 insertion of <=200bp - A frameshift_variant Q1458T? COAD-US 4 40146250 40146250 single base substitution A G splice_acceptor_variant COAD-US 4 40146318 40146318 single base substitution G A 3_prime_UTR_variant COAD-US 4 40146318 40146318 single base substitution G A missense_variant V1310I 3928G>A COAD-US 4 40146318 40146318 single base substitution G A missense_variant V1681I 5041G>A COAD-US 4 40155844 40155844 single base substitution T C 3_prime_UTR_variant COAD-US 4 40155844 40155844 single base substitution T C missense_variant V1396A 4187T>C COAD-US 4 40155844 40155844 single base substitution T C missense_variant V1767A 5300T>C COCA-CN 4 40061627 40061627 single base substitution C T intron_variant COCA-CN 4 40074127 40074127 single base substitution G A intron_variant COCA-CN 4 40094783 40094783 single base substitution T C intron_variant COCA-CN 4 40099029 40099029 single base substitution C T exon_variant COCA-CN 4 40099029 40099029 single base substitution C T intron_variant COCA-CN 4 40099029 40099029 single base substitution C T synonymous_variant V23V 69C>T COCA-CN 4 40101528 40101528 single base substitution G T intron_variant COCA-CN 4 40101528 40101528 single base substitution G T upstream_gene_variant COCA-CN 4 40101541 40101541 single base substitution A C intron_variant COCA-CN 4 40101541 40101541 single base substitution A C upstream_gene_variant COCA-CN 4 40101544 40101544 single base substitution T C intron_variant COCA-CN 4 40101544 40101544 single base substitution T C upstream_gene_variant COCA-CN 4 40103671 40103671 single base substitution G A intron_variant COCA-CN 4 40103671 40103671 single base substitution G A upstream_gene_variant COCA-CN 4 40108642 40108642 single base substitution G A downstream_gene_variant COCA-CN 4 40108642 40108642 single base substitution G A missense_variant R145H 434G>A COCA-CN 4 40108642 40108642 single base substitution G A missense_variant R499H 1496G>A COCA-CN 4 40108642 40108642 single base substitution G A splice_region_variant COCA-CN 4 40113709 40113709 single base substitution G T 3_prime_UTR_variant COCA-CN 4 40113709 40113709 single base substitution G T stop_gained E148* 442G>T COCA-CN 4 40113709 40113709 single base substitution G T stop_gained E502* 1504G>T COCA-CN 4 40115253 40115253 single base substitution C T intron_variant COCA-CN 4 40121713 40121713 single base substitution G T 3_prime_UTR_variant COCA-CN 4 40121713 40121713 single base substitution G T missense_variant R307I 920G>T COCA-CN 4 40121713 40121713 single base substitution G T missense_variant R661I 1982G>T COCA-CN 4 40121887 40121887 single base substitution C A 3_prime_UTR_variant COCA-CN 4 40121887 40121887 single base substitution C A missense_variant S365Y 1094C>A COCA-CN 4 40121887 40121887 single base substitution C A missense_variant S719Y 2156C>A COCA-CN 4 40123143 40123143 single base substitution T C 3_prime_UTR_variant COCA-CN 4 40123143 40123143 single base substitution T C missense_variant F1138L 3412T>C COCA-CN 4 40123143 40123143 single base substitution T C missense_variant F784L 2350T>C COCA-CN 4 40124679 40124679 single base substitution T G intron_variant COCA-CN 4 40133614 40133614 single base substitution T C intron_variant COCA-CN 4 40154660 40154660 single base substitution A T intron_variant COCA-CN 4 40155868 40155868 single base substitution C A 3_prime_UTR_variant COCA-CN 4 40155927 40155927 single base substitution T C 3_prime_UTR_variant EOPC-DE 4 40084801 40084801 single base substitution C T intron_variant ESAD-UK 4 40055921 40055921 single base substitution C T upstream_gene_variant ESAD-UK 4 40070597 40070597 single base substitution G A intron_variant ESAD-UK 4 40078232 40078232 single base substitution C A intron_variant ESAD-UK 4 40078642 40078642 single base substitution G A intron_variant ESAD-UK 4 40081383 40081383 single base substitution C G intron_variant ESAD-UK 4 40082672 40082672 deletion of <=200bp A - intron_variant ESAD-UK 4 40082839 40082839 deletion of <=200bp A - intron_variant ESAD-UK 4 40083220 40083220 single base substitution T G intron_variant ESAD-UK 4 40085294 40085294 single base substitution G A intron_variant ESAD-UK 4 40085705 40085705 single base substitution G T intron_variant ESAD-UK 4 40087325 40087325 single base substitution G A intron_variant ESAD-UK 4 40088905 40088905 single base substitution A T intron_variant ESAD-UK 4 40089246 40089246 single base substitution A C intron_variant ESAD-UK 4 40089366 40089366 deletion of <=200bp T - intron_variant ESAD-UK 4 40090567 40090567 insertion of <=200bp - T intron_variant ESAD-UK 4 40091364 40091364 single base substitution G A intron_variant ESAD-UK 4 40093326 40093326 single base substitution A T intron_variant ESAD-UK 4 40095414 40095414 single base substitution T A intron_variant ESAD-UK 4 40097781 40097781 single base substitution G A intron_variant ESAD-UK 4 40097921 40097921 single base substitution G A intron_variant ESAD-UK 4 40099975 40099975 insertion of <=200bp - T intron_variant ESAD-UK 4 40099975 40099975 insertion of <=200bp - T upstream_gene_variant ESAD-UK 4 40100184 40100184 single base substitution G T intron_variant ESAD-UK 4 40100184 40100184 single base substitution G T upstream_gene_variant ESAD-UK 4 40101235 40101235 single base substitution G A intron_variant ESAD-UK 4 40101235 40101235 single base substitution G A upstream_gene_variant ESAD-UK 4 40107375 40107375 single base substitution T A downstream_gene_variant ESAD-UK 4 40107375 40107375 single base substitution T A intron_variant ESAD-UK 4 40109173 40109173 single base substitution T G downstream_gene_variant ESAD-UK 4 40109173 40109173 single base substitution T G intron_variant ESAD-UK 4 40114332 40114332 single base substitution T G intron_variant ESAD-UK 4 40114652 40114652 deletion of <=200bp T - intron_variant ESAD-UK 4 40116514 40116514 single base substitution C G intron_variant ESAD-UK 4 40116614 40116614 single base substitution C T intron_variant ESAD-UK 4 40117093 40117093 single base substitution G A intron_variant ESAD-UK 4 40120615 40120615 single base substitution A C intron_variant ESAD-UK 4 40123489 40123489 single base substitution T G 3_prime_UTR_variant ESAD-UK 4 40123489 40123489 single base substitution T G missense_variant I1253S 3758T>G ESAD-UK 4 40123489 40123489 single base substitution T G missense_variant I899S 2696T>G ESAD-UK 4 40123669 40123669 single base substitution G C 3_prime_UTR_variant ESAD-UK 4 40123669 40123669 single base substitution G C missense_variant R1313T 3938G>C ESAD-UK 4 40123669 40123669 single base substitution G C missense_variant R959T 2876G>C ESAD-UK 4 40124582 40124582 single base substitution G T intron_variant ESAD-UK 4 40125558 40125558 single base substitution A T intron_variant ESAD-UK 4 40129344 40129344 single base substitution G A intron_variant ESAD-UK 4 40130636 40130636 deletion of <=200bp T - intron_variant ESAD-UK 4 40130949 40130949 single base substitution C T intron_variant ESAD-UK 4 40134667 40134667 single base substitution G T intron_variant ESAD-UK 4 40135996 40135996 insertion of <=200bp - G intron_variant ESAD-UK 4 40137806 40137806 single base substitution G A intron_variant ESAD-UK 4 40141587 40141587 single base substitution T G intron_variant ESAD-UK 4 40142211 40142211 deletion of <=200bp A - intron_variant ESAD-UK 4 40144243 40144243 single base substitution T G intron_variant ESAD-UK 4 40147348 40147348 single base substitution C T intron_variant ESAD-UK 4 40147740 40147740 single base substitution G A intron_variant ESAD-UK 4 40147809 40147809 deletion of <=200bp A - intron_variant ESAD-UK 4 40151304 40151304 single base substitution G T intron_variant ESAD-UK 4 40152175 40152175 single base substitution C G intron_variant ESAD-UK 4 40152297 40152297 single base substitution A G intron_variant ESAD-UK 4 40157444 40157444 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 4 40157444 40157444 deletion of <=200bp T - downstream_gene_variant ESAD-UK 4 40158194 40158194 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 4 40158194 40158194 deletion of <=200bp T - downstream_gene_variant ESAD-UK 4 40159591 40159591 single base substitution A G 3_prime_UTR_variant ESAD-UK 4 40159591 40159591 single base substitution A G downstream_gene_variant ESAD-UK 4 40163899 40163899 single base substitution A G downstream_gene_variant ESAD-UK 4 40164820 40164820 single base substitution G A downstream_gene_variant ESCA-CN 4 40099138 40099138 single base substitution G A exon_variant ESCA-CN 4 40099138 40099138 single base substitution G A intron_variant ESCA-CN 4 40099138 40099138 single base substitution G A missense_variant D60N 178G>A ESCA-CN 4 40103891 40103891 single base substitution G A 3_prime_UTR_variant ESCA-CN 4 40103891 40103891 single base substitution G A synonymous_variant L142L 426G>A ESCA-CN 4 40103891 40103891 single base substitution G A synonymous_variant L62L 186G>A ESCA-CN 4 40103891 40103891 single base substitution G A upstream_gene_variant ESCA-CN 4 40119435 40119435 single base substitution T A intron_variant ESCA-CN 4 40119573 40119573 single base substitution G A 3_prime_UTR_variant ESCA-CN 4 40119573 40119573 single base substitution G A missense_variant M229I 687G>A ESCA-CN 4 40119573 40119573 single base substitution G A missense_variant M583I 1749G>A ESCA-CN 4 40123791 40123791 single base substitution G T 3_prime_UTR_variant ESCA-CN 4 40123791 40123791 single base substitution G T missense_variant G1000W 2998G>T ESCA-CN 4 40123791 40123791 single base substitution G T missense_variant G1354W 4060G>T ESCA-CN 4 40144380 40144380 single base substitution G C 3_prime_UTR_variant ESCA-CN 4 40144380 40144380 single base substitution G C missense_variant E1254Q 3760G>C ESCA-CN 4 40144380 40144380 single base substitution G C missense_variant E1625Q 4873G>C GBM-US 4 40119548 40119548 single base substitution G A 3_prime_UTR_variant GBM-US 4 40119548 40119548 single base substitution G A missense_variant R221H 662G>A GBM-US 4 40119548 40119548 single base substitution G A missense_variant R575H 1724G>A GBM-US 4 40122570 40122570 single base substitution G T 3_prime_UTR_variant GBM-US 4 40122570 40122570 single base substitution G T stop_gained G593* 1777G>T GBM-US 4 40122570 40122570 single base substitution G T stop_gained G947* 2839G>T GBM-US 4 40127847 40127847 single base substitution C T 3_prime_UTR_variant GBM-US 4 40127847 40127847 single base substitution C T missense_variant S1121F 3362C>T GBM-US 4 40127847 40127847 single base substitution C T missense_variant S1475F 4424C>T KIRC-US 4 40121716 40121716 deletion of <=200bp G - 3_prime_UTR_variant KIRC-US 4 40121716 40121716 deletion of <=200bp G - frameshift_variant R308 KIRC-US 4 40121716 40121716 deletion of <=200bp G - frameshift_variant R662 KIRC-US 4 40122527 40122527 single base substitution C T 3_prime_UTR_variant KIRC-US 4 40122527 40122527 single base substitution C T synonymous_variant G578G 1734C>T KIRC-US 4 40122527 40122527 single base substitution C T synonymous_variant G932G 2796C>T KIRP-US 4 40103811 40103811 single base substitution A G 3_prime_UTR_variant KIRP-US 4 40103811 40103811 single base substitution A G missense_variant I116V 346A>G KIRP-US 4 40103811 40103811 single base substitution A G missense_variant I36V 106A>G KIRP-US 4 40103811 40103811 single base substitution A G upstream_gene_variant KIRP-US 4 40122682 40122682 single base substitution C G 3_prime_UTR_variant KIRP-US 4 40122682 40122682 single base substitution C G missense_variant P630R 1889C>G KIRP-US 4 40122682 40122682 single base substitution C G missense_variant P984R 2951C>G KIRP-US 4 40122970 40122970 deletion of <=200bp A - 3_prime_UTR_variant KIRP-US 4 40122970 40122970 deletion of <=200bp A - frameshift_variant E1080 KIRP-US 4 40122970 40122970 deletion of <=200bp A - frameshift_variant E726 LAML-KR 4 40053663 40053663 single base substitution A G upstream_gene_variant LAML-KR 4 40055056 40055056 single base substitution C A upstream_gene_variant LAML-KR 4 40080423 40080423 single base substitution C T intron_variant LAML-KR 4 40081059 40081059 single base substitution G T intron_variant LAML-KR 4 40094811 40094811 single base substitution G A intron_variant LAML-KR 4 40133614 40133614 single base substitution T C intron_variant LAML-KR 4 40148857 40148857 single base substitution T C intron_variant LAML-KR 4 40154594 40154594 single base substitution A G intron_variant LGG-US 4 40104251 40104251 insertion of <=200bp - A 3_prime_UTR_variant LGG-US 4 40104251 40104251 insertion of <=200bp - A downstream_gene_variant LGG-US 4 40104251 40104251 insertion of <=200bp - A frameshift_variant L262L? LGG-US 4 40104251 40104251 insertion of <=200bp - A upstream_gene_variant LICA-FR 4 40075889 40075889 insertion of <=200bp - TTAGTAGCGATGGGGTTTCACATATTGGTCAGGCTAG intron_variant LICA-FR 4 40099189 40099189 single base substitution G A intron_variant LICA-FR 4 40099189 40099189 single base substitution G A missense_variant V77I 229G>A LICA-FR 4 40099189 40099189 single base substitution G A splice_region_variant LICA-FR 4 40122370 40122370 single base substitution A G 3_prime_UTR_variant LICA-FR 4 40122370 40122370 single base substitution A G missense_variant N526S 1577A>G LICA-FR 4 40122370 40122370 single base substitution A G missense_variant N880S 2639A>G LICA-FR 4 40122951 40122951 single base substitution A G 3_prime_UTR_variant LICA-FR 4 40122951 40122951 single base substitution A G missense_variant K1074E 3220A>G LICA-FR 4 40122951 40122951 single base substitution A G missense_variant K720E 2158A>G LICA-FR 4 40123573 40123573 single base substitution C T 3_prime_UTR_variant LICA-FR 4 40123573 40123573 single base substitution C T missense_variant P1281L 3842C>T LICA-FR 4 40123573 40123573 single base substitution C T missense_variant P927L 2780C>T LICA-FR 4 40123919 40123919 single base substitution T C 3_prime_UTR_variant LICA-FR 4 40123919 40123919 single base substitution T C synonymous_variant G1042G 3126T>C LICA-FR 4 40123919 40123919 single base substitution T C synonymous_variant G1396G 4188T>C LICA-FR 4 40153989 40153989 single base substitution G A intron_variant LIHC-US 4 40103840 40103840 single base substitution T G 3_prime_UTR_variant LIHC-US 4 40103840 40103840 single base substitution T G missense_variant S125R 375T>G LIHC-US 4 40103840 40103840 single base substitution T G missense_variant S45R 135T>G LIHC-US 4 40103840 40103840 single base substitution T G upstream_gene_variant LIHC-US 4 40121838 40121838 single base substitution A G 3_prime_UTR_variant LIHC-US 4 40121838 40121838 single base substitution A G missense_variant I349V 1045A>G LIHC-US 4 40121838 40121838 single base substitution A G missense_variant I703V 2107A>G LINC-JP 4 40056856 40056856 single base substitution T C upstream_gene_variant LINC-JP 4 40059403 40059403 single base substitution T C intron_variant LINC-JP 4 40062083 40062083 single base substitution G A intron_variant LINC-JP 4 40069138 40069138 single base substitution C A intron_variant LINC-JP 4 40080303 40080303 single base substitution G A intron_variant LINC-JP 4 40081949 40081949 single base substitution C T intron_variant LINC-JP 4 40093582 40093582 single base substitution A T intron_variant LINC-JP 4 40095206 40095206 single base substitution T C intron_variant LINC-JP 4 40099030 40099030 single base substitution G T exon_variant LINC-JP 4 40099030 40099030 single base substitution G T intron_variant LINC-JP 4 40099030 40099030 single base substitution G T missense_variant V24L 70G>T LINC-JP 4 40100718 40100718 single base substitution C A intron_variant LINC-JP 4 40100718 40100718 single base substitution C A upstream_gene_variant LINC-JP 4 40102797 40102797 single base substitution G C intron_variant LINC-JP 4 40102797 40102797 single base substitution G C upstream_gene_variant LINC-JP 4 40121888 40121888 deletion of <=200bp T - 3_prime_UTR_variant LINC-JP 4 40121888 40121888 deletion of <=200bp T - frameshift_variant S365 LINC-JP 4 40121888 40121888 deletion of <=200bp T - frameshift_variant S719 LINC-JP 4 40139385 40139385 single base substitution T C intron_variant LINC-JP 4 40141139 40141139 single base substitution A G intron_variant LINC-JP 4 40151522 40151522 single base substitution G A intron_variant LINC-JP 4 40157768 40157768 single base substitution A G 3_prime_UTR_variant LINC-JP 4 40157768 40157768 single base substitution A G downstream_gene_variant LIRI-JP 4 40055992 40055992 single base substitution G A upstream_gene_variant LIRI-JP 4 40056214 40056214 deletion of <=200bp C - upstream_gene_variant LIRI-JP 4 40056217 40056218 deletion of <=200bp CA - upstream_gene_variant LIRI-JP 4 40058937 40058937 single base substitution G T intron_variant LIRI-JP 4 40059548 40059548 single base substitution T G intron_variant LIRI-JP 4 40062131 40062131 single base substitution C A intron_variant LIRI-JP 4 40064972 40064972 single base substitution C T intron_variant LIRI-JP 4 40065599 40065599 single base substitution G A intron_variant LIRI-JP 4 40068048 40068048 single base substitution C T intron_variant LIRI-JP 4 40074619 40074619 single base substitution G C intron_variant LIRI-JP 4 40075157 40075157 single base substitution G A 5_prime_UTR_variant LIRI-JP 4 40075816 40075816 single base substitution C G intron_variant LIRI-JP 4 40076546 40076546 single base substitution G T intron_variant LIRI-JP 4 40078520 40078520 single base substitution G T intron_variant LIRI-JP 4 40079868 40079868 single base substitution A G intron_variant LIRI-JP 4 40080852 40080852 single base substitution G C intron_variant LIRI-JP 4 40084204 40084204 single base substitution G C intron_variant LIRI-JP 4 40084610 40084610 single base substitution G T intron_variant LIRI-JP 4 40087608 40087608 single base substitution G A intron_variant LIRI-JP 4 40088741 40088741 single base substitution A G intron_variant LIRI-JP 4 40089564 40089564 single base substitution A T intron_variant LIRI-JP 4 40090107 40090107 single base substitution T C intron_variant LIRI-JP 4 40092161 40092161 single base substitution G A intron_variant LIRI-JP 4 40094529 40094529 single base substitution G T intron_variant LIRI-JP 4 40096200 40096200 single base substitution A T intron_variant LIRI-JP 4 40100391 40100391 single base substitution A G intron_variant LIRI-JP 4 40100391 40100391 single base substitution A G upstream_gene_variant LIRI-JP 4 40101165 40101165 single base substitution C T intron_variant LIRI-JP 4 40101165 40101165 single base substitution C T upstream_gene_variant LIRI-JP 4 40103070 40103070 single base substitution A G intron_variant LIRI-JP 4 40103070 40103070 single base substitution A G upstream_gene_variant LIRI-JP 4 40104041 40104041 single base substitution T C 3_prime_UTR_variant LIRI-JP 4 40104041 40104041 single base substitution T C synonymous_variant S112S 336T>C LIRI-JP 4 40104041 40104041 single base substitution T C synonymous_variant S192S 576T>C LIRI-JP 4 40104041 40104041 single base substitution T C upstream_gene_variant LIRI-JP 4 40106207 40106207 single base substitution A G downstream_gene_variant LIRI-JP 4 40106207 40106207 single base substitution A G intron_variant LIRI-JP 4 40107897 40107897 single base substitution G T downstream_gene_variant LIRI-JP 4 40107897 40107897 single base substitution G T intron_variant LIRI-JP 4 40108539 40108539 single base substitution C T 3_prime_UTR_variant LIRI-JP 4 40108539 40108539 single base substitution C T downstream_gene_variant LIRI-JP 4 40108539 40108539 single base substitution C T missense_variant P111S 331C>T LIRI-JP 4 40108539 40108539 single base substitution C T missense_variant P465S 1393C>T LIRI-JP 4 40108641 40108641 single base substitution C A 3_prime_UTR_variant LIRI-JP 4 40108641 40108641 single base substitution C A downstream_gene_variant LIRI-JP 4 40108641 40108641 single base substitution C A missense_variant R145S 433C>A LIRI-JP 4 40108641 40108641 single base substitution C A missense_variant R499S 1495C>A LIRI-JP 4 40109313 40109313 single base substitution A G intron_variant LIRI-JP 4 40109484 40109484 single base substitution A C intron_variant LIRI-JP 4 40110886 40110886 single base substitution A G intron_variant LIRI-JP 4 40113480 40113480 single base substitution C T intron_variant LIRI-JP 4 40116425 40116425 single base substitution T A intron_variant LIRI-JP 4 40116834 40116834 single base substitution A G intron_variant LIRI-JP 4 40117126 40117126 single base substitution A G intron_variant LIRI-JP 4 40119085 40119085 single base substitution T A intron_variant LIRI-JP 4 40122721 40122721 single base substitution A G 3_prime_UTR_variant LIRI-JP 4 40122721 40122721 single base substitution A G missense_variant E643G 1928A>G LIRI-JP 4 40122721 40122721 single base substitution A G missense_variant E997G 2990A>G LIRI-JP 4 40128883 40128883 single base substitution G T intron_variant LIRI-JP 4 40129896 40129896 single base substitution G A intron_variant LIRI-JP 4 40132157 40132157 single base substitution A G intron_variant LIRI-JP 4 40133605 40133605 single base substitution T G intron_variant LIRI-JP 4 40134176 40134176 single base substitution A G intron_variant LIRI-JP 4 40134299 40134299 single base substitution T C intron_variant LIRI-JP 4 40135031 40135031 single base substitution C G intron_variant LIRI-JP 4 40136159 40136159 single base substitution C T intron_variant LIRI-JP 4 40138468 40138468 single base substitution A G intron_variant LIRI-JP 4 40140655 40140655 single base substitution C T intron_variant LIRI-JP 4 40143927 40143927 single base substitution C T intron_variant LIRI-JP 4 40148033 40148033 single base substitution A G intron_variant LIRI-JP 4 40150118 40150118 single base substitution G T intron_variant LIRI-JP 4 40151675 40151675 single base substitution T A intron_variant LIRI-JP 4 40151992 40151992 single base substitution A C intron_variant LIRI-JP 4 40153163 40153163 single base substitution A T intron_variant LIRI-JP 4 40153447 40153447 single base substitution T G intron_variant LIRI-JP 4 40154783 40154783 single base substitution A G intron_variant LIRI-JP 4 40155328 40155328 single base substitution G T intron_variant LIRI-JP 4 40156529 40156529 single base substitution A C 3_prime_UTR_variant LIRI-JP 4 40156529 40156529 single base substitution A G 3_prime_UTR_variant LIRI-JP 4 40159426 40159426 single base substitution T A 3_prime_UTR_variant LIRI-JP 4 40159426 40159426 single base substitution T A downstream_gene_variant LIRI-JP 4 40159895 40159898 deletion of <=200bp ATTT - downstream_gene_variant LIRI-JP 4 40162857 40162857 single base substitution G A downstream_gene_variant LUSC-KR 4 40071231 40071231 single base substitution T A intron_variant LUSC-KR 4 40075187 40075187 single base substitution G A intron_variant LUSC-KR 4 40081059 40081059 single base substitution G T intron_variant LUSC-KR 4 40084841 40084841 single base substitution T C intron_variant LUSC-KR 4 40088417 40088417 single base substitution G T intron_variant LUSC-KR 4 40088877 40088877 single base substitution C T intron_variant LUSC-KR 4 40092641 40092641 single base substitution G T intron_variant LUSC-KR 4 40094811 40094811 single base substitution G A intron_variant LUSC-KR 4 40095075 40095075 single base substitution G T intron_variant LUSC-KR 4 40099541 40099541 single base substitution C T intron_variant LUSC-KR 4 40099541 40099541 single base substitution C T upstream_gene_variant LUSC-KR 4 40099938 40099938 single base substitution G C intron_variant LUSC-KR 4 40099938 40099938 single base substitution G C upstream_gene_variant LUSC-KR 4 40103767 40103767 single base substitution G T 3_prime_UTR_variant LUSC-KR 4 40103767 40103767 single base substitution G T missense_variant S101I 302G>T LUSC-KR 4 40103767 40103767 single base substitution G T missense_variant S21I 62G>T LUSC-KR 4 40103767 40103767 single base substitution G T upstream_gene_variant LUSC-KR 4 40110439 40110439 single base substitution A T intron_variant LUSC-KR 4 40115083 40115083 single base substitution G T 3_prime_UTR_variant LUSC-KR 4 40115083 40115083 single base substitution G T missense_variant R186L 557G>T LUSC-KR 4 40115083 40115083 single base substitution G T missense_variant R540L 1619G>T LUSC-KR 4 40115338 40115338 single base substitution A T intron_variant LUSC-KR 4 40119501 40119501 single base substitution T C 3_prime_UTR_variant LUSC-KR 4 40119501 40119501 single base substitution T C synonymous_variant H205H 615T>C LUSC-KR 4 40119501 40119501 single base substitution T C synonymous_variant H559H 1677T>C LUSC-KR 4 40127400 40127400 single base substitution C T intron_variant LUSC-KR 4 40131892 40131892 single base substitution T C intron_variant LUSC-KR 4 40133029 40133029 single base substitution C T intron_variant LUSC-KR 4 40133301 40133301 single base substitution G A intron_variant LUSC-KR 4 40133426 40133426 single base substitution G T 3_prime_UTR_variant LUSC-KR 4 40133426 40133426 single base substitution G T missense_variant R1157S 3471G>T LUSC-KR 4 40133426 40133426 single base substitution G T missense_variant R1511S 4533G>T LUSC-KR 4 40134335 40134335 single base substitution A G intron_variant LUSC-KR 4 40136994 40136994 single base substitution G A intron_variant LUSC-KR 4 40137021 40137021 single base substitution A G intron_variant LUSC-KR 4 40142307 40142307 single base substitution T C intron_variant LUSC-KR 4 40142430 40142430 single base substitution T C intron_variant LUSC-KR 4 40148528 40148528 single base substitution A T intron_variant LUSC-KR 4 40154233 40154233 single base substitution G A intron_variant LUSC-KR 4 40156098 40156098 single base substitution A C 3_prime_UTR_variant LUSC-KR 4 40156577 40156577 single base substitution G T 3_prime_UTR_variant LUSC-US 4 40099026 40099026 single base substitution T G exon_variant LUSC-US 4 40099026 40099026 single base substitution T G intron_variant LUSC-US 4 40099026 40099026 single base substitution T G synonymous_variant V22V 66T>G LUSC-US 4 40121557 40121557 single base substitution G T 3_prime_UTR_variant LUSC-US 4 40121557 40121557 single base substitution G T missense_variant R255I 764G>T LUSC-US 4 40121557 40121557 single base substitution G T missense_variant R609I 1826G>T LUSC-US 4 40121558 40121558 single base substitution A T 3_prime_UTR_variant LUSC-US 4 40121558 40121558 single base substitution A T missense_variant R255S 765A>T LUSC-US 4 40121558 40121558 single base substitution A T missense_variant R609S 1827A>T LUSC-US 4 40121773 40121773 single base substitution C A 3_prime_UTR_variant LUSC-US 4 40121773 40121773 single base substitution C A missense_variant P327Q 980C>A LUSC-US 4 40121773 40121773 single base substitution C A missense_variant P681Q 2042C>A LUSC-US 4 40122763 40122763 single base substitution T C 3_prime_UTR_variant LUSC-US 4 40122763 40122763 single base substitution T C missense_variant V1011A 3032T>C LUSC-US 4 40122763 40122763 single base substitution T C missense_variant V657A 1970T>C LUSC-US 4 40123254 40123254 single base substitution C A 3_prime_UTR_variant LUSC-US 4 40123254 40123254 single base substitution C A missense_variant P1175T 3523C>A LUSC-US 4 40123254 40123254 single base substitution C A missense_variant P821T 2461C>A LUSC-US 4 40123482 40123482 single base substitution C T 3_prime_UTR_variant LUSC-US 4 40123482 40123482 single base substitution C T missense_variant P1251S 3751C>T LUSC-US 4 40123482 40123482 single base substitution C T missense_variant P897S 2689C>T LUSC-US 4 40123493 40123493 single base substitution A G 3_prime_UTR_variant LUSC-US 4 40123493 40123493 single base substitution A G synonymous_variant L1254L 3762A>G LUSC-US 4 40123493 40123493 single base substitution A G synonymous_variant L900L 2700A>G MALY-DE 4 40057847 40057847 single base substitution G A upstream_gene_variant MALY-DE 4 40079274 40079274 single base substitution A G intron_variant MALY-DE 4 40087806 40087806 single base substitution A T intron_variant MALY-DE 4 40098602 40098602 single base substitution T A intron_variant MALY-DE 4 40101310 40101310 single base substitution T C intron_variant MALY-DE 4 40101310 40101310 single base substitution T C upstream_gene_variant MALY-DE 4 40104785 40104785 single base substitution A T 3_prime_UTR_variant MALY-DE 4 40104785 40104785 single base substitution A T downstream_gene_variant MALY-DE 4 40104785 40104785 single base substitution A T synonymous_variant L440L 1320A>T MALY-DE 4 40104785 40104785 single base substitution A T synonymous_variant L86L 258A>T MALY-DE 4 40108841 40108841 single base substitution C T downstream_gene_variant MALY-DE 4 40108841 40108841 single base substitution C T intron_variant MALY-DE 4 40114332 40114332 single base substitution T G intron_variant MALY-DE 4 40120336 40120336 single base substitution T G intron_variant MALY-DE 4 40123943 40123943 single base substitution A G intron_variant MALY-DE 4 40128835 40128835 insertion of <=200bp - T intron_variant MALY-DE 4 40154488 40154488 single base substitution A C 3_prime_UTR_variant MALY-DE 4 40154488 40154488 single base substitution A C synonymous_variant P1373P 4119A>C MALY-DE 4 40154488 40154488 single base substitution A C synonymous_variant P1744P 5232A>C MALY-DE 4 40154519 40154519 single base substitution T C 3_prime_UTR_variant MALY-DE 4 40154519 40154519 single base substitution T C missense_variant F1384L 4150T>C MALY-DE 4 40154519 40154519 single base substitution T C missense_variant F1755L 5263T>C MALY-DE 4 40160218 40160218 single base substitution G A downstream_gene_variant MELA-AU 4 40053647 40053648 multiple base substitution (>=2bp and <=200bp) TC CT upstream_gene_variant MELA-AU 4 40053850 40053850 single base substitution G A upstream_gene_variant MELA-AU 4 40054128 40054128 single base substitution T A upstream_gene_variant MELA-AU 4 40054167 40054167 single base substitution G A upstream_gene_variant MELA-AU 4 40054188 40054188 single base substitution G A upstream_gene_variant MELA-AU 4 40055202 40055202 single base substitution G A upstream_gene_variant MELA-AU 4 40055215 40055215 single base substitution C T upstream_gene_variant MELA-AU 4 40055713 40055713 single base substitution G A upstream_gene_variant MELA-AU 4 40055811 40055811 single base substitution C T upstream_gene_variant MELA-AU 4 40055983 40055983 single base substitution C T upstream_gene_variant MELA-AU 4 40056479 40056479 single base substitution G A upstream_gene_variant MELA-AU 4 40056533 40056533 single base substitution G A upstream_gene_variant MELA-AU 4 40059234 40059234 single base substitution C T intron_variant MELA-AU 4 40060029 40060029 single base substitution A G intron_variant MELA-AU 4 40060780 40060780 single base substitution C T intron_variant MELA-AU 4 40061187 40061187 single base substitution C T intron_variant MELA-AU 4 40061259 40061259 single base substitution C T intron_variant MELA-AU 4 40061776 40061776 single base substitution C T intron_variant MELA-AU 4 40062022 40062022 single base substitution G A intron_variant MELA-AU 4 40062599 40062599 single base substitution C T intron_variant MELA-AU 4 40062744 40062744 single base substitution T G intron_variant MELA-AU 4 40062961 40062961 single base substitution C T intron_variant MELA-AU 4 40063073 40063073 single base substitution C T intron_variant MELA-AU 4 40063075 40063075 single base substitution C T intron_variant MELA-AU 4 40063109 40063109 single base substitution C T intron_variant MELA-AU 4 40063378 40063378 single base substitution A C intron_variant MELA-AU 4 40064249 40064249 single base substitution C T intron_variant MELA-AU 4 40065344 40065344 single base substitution A G intron_variant MELA-AU 4 40065651 40065651 single base substitution C T intron_variant MELA-AU 4 40067614 40067614 single base substitution G A intron_variant MELA-AU 4 40067761 40067761 single base substitution G A intron_variant MELA-AU 4 40068229 40068229 single base substitution C T intron_variant MELA-AU 4 40069654 40069654 single base substitution C T intron_variant MELA-AU 4 40069915 40069915 single base substitution C T intron_variant MELA-AU 4 40070063 40070063 single base substitution T C intron_variant MELA-AU 4 40070064 40070064 single base substitution A G intron_variant MELA-AU 4 40070130 40070130 single base substitution C T intron_variant MELA-AU 4 40070201 40070201 single base substitution C T intron_variant MELA-AU 4 40070567 40070567 single base substitution C T intron_variant MELA-AU 4 40070775 40070775 single base substitution C T intron_variant MELA-AU 4 40071059 40071059 single base substitution C T intron_variant MELA-AU 4 40071804 40071804 single base substitution C T intron_variant MELA-AU 4 40072004 40072004 single base substitution C T intron_variant MELA-AU 4 40072278 40072278 single base substitution C T intron_variant MELA-AU 4 40072764 40072764 single base substitution C T intron_variant MELA-AU 4 40073312 40073312 single base substitution G A intron_variant MELA-AU 4 40073375 40073375 single base substitution G A intron_variant MELA-AU 4 40073382 40073382 single base substitution C T intron_variant MELA-AU 4 40073386 40073386 single base substitution A T intron_variant MELA-AU 4 40074231 40074231 single base substitution C G intron_variant MELA-AU 4 40074584 40074584 single base substitution C T intron_variant MELA-AU 4 40074965 40074965 single base substitution T C intron_variant MELA-AU 4 40075536 40075536 single base substitution C T intron_variant MELA-AU 4 40075634 40075634 single base substitution A G intron_variant MELA-AU 4 40075678 40075678 single base substitution C T intron_variant MELA-AU 4 40075740 40075740 single base substitution T C intron_variant MELA-AU 4 40075918 40075918 single base substitution C T intron_variant MELA-AU 4 40075952 40075952 single base substitution C T intron_variant MELA-AU 4 40076231 40076231 single base substitution G A intron_variant MELA-AU 4 40076238 40076238 single base substitution C T intron_variant MELA-AU 4 40076316 40076316 single base substitution C T intron_variant MELA-AU 4 40077216 40077216 single base substitution C T intron_variant MELA-AU 4 40077454 40077454 single base substitution T A intron_variant MELA-AU 4 40077642 40077642 single base substitution C T intron_variant MELA-AU 4 40077703 40077703 single base substitution C T intron_variant MELA-AU 4 40077978 40077978 single base substitution C T intron_variant MELA-AU 4 40078438 40078439 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 40079462 40079462 single base substitution C T intron_variant MELA-AU 4 40080393 40080393 single base substitution C T intron_variant MELA-AU 4 40081151 40081151 single base substitution C T intron_variant MELA-AU 4 40082243 40082243 single base substitution C T intron_variant MELA-AU 4 40082362 40082363 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 40082961 40082961 single base substitution C T intron_variant MELA-AU 4 40083123 40083123 single base substitution G A intron_variant MELA-AU 4 40083560 40083560 single base substitution C T intron_variant MELA-AU 4 40084194 40084194 single base substitution C A intron_variant MELA-AU 4 40084619 40084619 single base substitution C T intron_variant MELA-AU 4 40085665 40085665 single base substitution C T intron_variant MELA-AU 4 40085796 40085796 single base substitution C T intron_variant MELA-AU 4 40085820 40085820 single base substitution C T intron_variant MELA-AU 4 40086398 40086398 single base substitution G A intron_variant MELA-AU 4 40087285 40087285 single base substitution C A intron_variant MELA-AU 4 40088588 40088588 single base substitution C T intron_variant MELA-AU 4 40088838 40088838 single base substitution C T intron_variant MELA-AU 4 40089074 40089074 single base substitution C T intron_variant MELA-AU 4 40089777 40089777 single base substitution G A intron_variant MELA-AU 4 40090542 40090542 single base substitution C T intron_variant MELA-AU 4 40090811 40090811 single base substitution G A intron_variant MELA-AU 4 40090989 40090989 single base substitution C T intron_variant MELA-AU 4 40091192 40091192 single base substitution G A intron_variant MELA-AU 4 40091207 40091207 single base substitution C T intron_variant MELA-AU 4 40091371 40091371 single base substitution C T intron_variant MELA-AU 4 40091461 40091461 single base substitution C T intron_variant MELA-AU 4 40092017 40092017 single base substitution C T intron_variant MELA-AU 4 40092678 40092678 single base substitution C T intron_variant MELA-AU 4 40093379 40093380 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 40093942 40093942 single base substitution C T intron_variant MELA-AU 4 40094017 40094017 single base substitution C T intron_variant MELA-AU 4 40094305 40094305 single base substitution C T intron_variant MELA-AU 4 40094920 40094920 single base substitution C T intron_variant MELA-AU 4 40095819 40095819 single base substitution G A intron_variant MELA-AU 4 40096688 40096688 single base substitution G T intron_variant MELA-AU 4 40097027 40097027 single base substitution C T intron_variant MELA-AU 4 40097348 40097348 single base substitution C T intron_variant MELA-AU 4 40097918 40097918 single base substitution C T intron_variant MELA-AU 4 40100725 40100725 single base substitution G A intron_variant MELA-AU 4 40100725 40100725 single base substitution G A upstream_gene_variant MELA-AU 4 40100889 40100889 single base substitution T C intron_variant MELA-AU 4 40100889 40100889 single base substitution T C upstream_gene_variant MELA-AU 4 40101111 40101111 single base substitution C T intron_variant MELA-AU 4 40101111 40101111 single base substitution C T upstream_gene_variant MELA-AU 4 40101228 40101228 single base substitution A T intron_variant MELA-AU 4 40101228 40101228 single base substitution A T upstream_gene_variant MELA-AU 4 40101556 40101556 single base substitution C T intron_variant MELA-AU 4 40101556 40101556 single base substitution C T upstream_gene_variant MELA-AU 4 40101787 40101787 single base substitution C T intron_variant MELA-AU 4 40101787 40101787 single base substitution C T upstream_gene_variant MELA-AU 4 40102540 40102540 single base substitution C T intron_variant MELA-AU 4 40102540 40102540 single base substitution C T upstream_gene_variant MELA-AU 4 40102811 40102811 single base substitution C T intron_variant MELA-AU 4 40102811 40102811 single base substitution C T upstream_gene_variant MELA-AU 4 40102867 40102867 single base substitution C T intron_variant MELA-AU 4 40102867 40102867 single base substitution C T upstream_gene_variant MELA-AU 4 40103145 40103145 single base substitution C T intron_variant MELA-AU 4 40103145 40103145 single base substitution C T upstream_gene_variant MELA-AU 4 40103385 40103385 single base substitution C T intron_variant MELA-AU 4 40103385 40103385 single base substitution C T upstream_gene_variant MELA-AU 4 40103602 40103602 single base substitution C T intron_variant MELA-AU 4 40103602 40103602 single base substitution C T upstream_gene_variant MELA-AU 4 40104152 40104152 single base substitution G A 3_prime_UTR_variant MELA-AU 4 40104152 40104152 single base substitution G A synonymous_variant K149K 447G>A MELA-AU 4 40104152 40104152 single base substitution G A synonymous_variant K229K 687G>A MELA-AU 4 40104152 40104152 single base substitution G A upstream_gene_variant MELA-AU 4 40104313 40104313 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40104313 40104313 single base substitution C T downstream_gene_variant MELA-AU 4 40104313 40104313 single base substitution C T missense_variant P283L 848C>T MELA-AU 4 40104313 40104313 single base substitution C T upstream_gene_variant MELA-AU 4 40104500 40104500 single base substitution G A 3_prime_UTR_variant MELA-AU 4 40104500 40104500 single base substitution G A downstream_gene_variant MELA-AU 4 40104500 40104500 single base substitution G A synonymous_variant P345P 1035G>A MELA-AU 4 40104500 40104500 single base substitution G A upstream_gene_variant MELA-AU 4 40104546 40104546 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40104546 40104546 single base substitution C T downstream_gene_variant MELA-AU 4 40104546 40104546 single base substitution C T missense_variant P361S 1081C>T MELA-AU 4 40104546 40104546 single base substitution C T missense_variant P7S 19C>T MELA-AU 4 40105526 40105526 single base substitution C T downstream_gene_variant MELA-AU 4 40105526 40105526 single base substitution C T intron_variant MELA-AU 4 40105545 40105545 single base substitution C T downstream_gene_variant MELA-AU 4 40105545 40105545 single base substitution C T intron_variant MELA-AU 4 40105556 40105556 single base substitution C T downstream_gene_variant MELA-AU 4 40105556 40105556 single base substitution C T intron_variant MELA-AU 4 40105805 40105805 single base substitution C T downstream_gene_variant MELA-AU 4 40105805 40105805 single base substitution C T intron_variant MELA-AU 4 40106342 40106342 single base substitution C T downstream_gene_variant MELA-AU 4 40106342 40106342 single base substitution C T intron_variant MELA-AU 4 40106523 40106523 single base substitution C T downstream_gene_variant MELA-AU 4 40106523 40106523 single base substitution C T intron_variant MELA-AU 4 40106679 40106679 single base substitution C A downstream_gene_variant MELA-AU 4 40106679 40106679 single base substitution C A intron_variant MELA-AU 4 40106878 40106878 single base substitution G A downstream_gene_variant MELA-AU 4 40106878 40106878 single base substitution G A intron_variant MELA-AU 4 40106984 40106984 single base substitution C T downstream_gene_variant MELA-AU 4 40106984 40106984 single base substitution C T intron_variant MELA-AU 4 40106994 40106994 single base substitution T G downstream_gene_variant MELA-AU 4 40106994 40106994 single base substitution T G intron_variant MELA-AU 4 40107464 40107464 single base substitution C T downstream_gene_variant MELA-AU 4 40107464 40107464 single base substitution C T intron_variant MELA-AU 4 40108027 40108027 single base substitution C T downstream_gene_variant MELA-AU 4 40108027 40108027 single base substitution C T intron_variant MELA-AU 4 40108071 40108072 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 40108071 40108072 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 40108323 40108323 single base substitution C T downstream_gene_variant MELA-AU 4 40108323 40108323 single base substitution C T intron_variant MELA-AU 4 40108593 40108593 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40108593 40108593 single base substitution C T downstream_gene_variant MELA-AU 4 40108593 40108593 single base substitution C T stop_gained Q129* 385C>T MELA-AU 4 40108593 40108593 single base substitution C T stop_gained Q483* 1447C>T MELA-AU 4 40108932 40108932 single base substitution G A downstream_gene_variant MELA-AU 4 40108932 40108932 single base substitution G A intron_variant MELA-AU 4 40109022 40109022 single base substitution C T downstream_gene_variant MELA-AU 4 40109022 40109022 single base substitution C T intron_variant MELA-AU 4 40109481 40109481 single base substitution T A intron_variant MELA-AU 4 40110528 40110528 single base substitution C T intron_variant MELA-AU 4 40110546 40110546 single base substitution C T intron_variant MELA-AU 4 40111271 40111271 single base substitution G A intron_variant MELA-AU 4 40111592 40111592 single base substitution C T intron_variant MELA-AU 4 40111717 40111717 single base substitution T G intron_variant MELA-AU 4 40112006 40112006 single base substitution C T intron_variant MELA-AU 4 40112384 40112384 single base substitution C T intron_variant MELA-AU 4 40113180 40113180 single base substitution C T intron_variant MELA-AU 4 40113197 40113197 single base substitution C T intron_variant MELA-AU 4 40113975 40113975 single base substitution G A intron_variant MELA-AU 4 40114236 40114236 single base substitution C T intron_variant MELA-AU 4 40114308 40114308 single base substitution C T intron_variant MELA-AU 4 40114412 40114412 single base substitution C T intron_variant MELA-AU 4 40115376 40115376 single base substitution C T intron_variant MELA-AU 4 40115532 40115532 single base substitution C T intron_variant MELA-AU 4 40115937 40115937 single base substitution T A intron_variant MELA-AU 4 40116265 40116265 single base substitution T G intron_variant MELA-AU 4 40117134 40117134 single base substitution C T intron_variant MELA-AU 4 40117550 40117550 single base substitution C T intron_variant MELA-AU 4 40117633 40117633 single base substitution C G intron_variant MELA-AU 4 40118070 40118070 single base substitution C T intron_variant MELA-AU 4 40118311 40118311 single base substitution C T intron_variant MELA-AU 4 40118714 40118714 single base substitution C T intron_variant MELA-AU 4 40118844 40118844 single base substitution G A intron_variant MELA-AU 4 40118901 40118901 single base substitution C T intron_variant MELA-AU 4 40119091 40119091 single base substitution C T intron_variant MELA-AU 4 40119341 40119341 single base substitution C A intron_variant MELA-AU 4 40120832 40120832 single base substitution G A intron_variant MELA-AU 4 40121787 40121787 single base substitution T C 3_prime_UTR_variant MELA-AU 4 40121787 40121787 single base substitution T C missense_variant S332P 994T>C MELA-AU 4 40121787 40121787 single base substitution T C missense_variant S686P 2056T>C MELA-AU 4 40122167 40122167 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40122167 40122167 single base substitution C T synonymous_variant S458S 1374C>T MELA-AU 4 40122167 40122167 single base substitution C T synonymous_variant S812S 2436C>T MELA-AU 4 40122497 40122497 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40122497 40122497 single base substitution C T synonymous_variant S568S 1704C>T MELA-AU 4 40122497 40122497 single base substitution C T synonymous_variant S922S 2766C>T MELA-AU 4 40123039 40123039 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40123039 40123039 single base substitution C T missense_variant S1103L 3308C>T MELA-AU 4 40123039 40123039 single base substitution C T missense_variant S749L 2246C>T MELA-AU 4 40123437 40123437 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40123437 40123437 single base substitution C T missense_variant P1236S 3706C>T MELA-AU 4 40123437 40123437 single base substitution C T missense_variant P882S 2644C>T MELA-AU 4 40124105 40124105 single base substitution T G intron_variant MELA-AU 4 40124141 40124141 single base substitution G A intron_variant MELA-AU 4 40124727 40124727 single base substitution C T intron_variant MELA-AU 4 40125000 40125000 single base substitution A C intron_variant MELA-AU 4 40125635 40125635 single base substitution C T intron_variant MELA-AU 4 40125917 40125917 single base substitution T A intron_variant MELA-AU 4 40125985 40125985 single base substitution G A intron_variant MELA-AU 4 40126193 40126193 single base substitution C T intron_variant MELA-AU 4 40127298 40127298 single base substitution G A intron_variant MELA-AU 4 40127662 40127662 single base substitution C T intron_variant MELA-AU 4 40128250 40128250 single base substitution C T intron_variant MELA-AU 4 40128582 40128582 single base substitution T C intron_variant MELA-AU 4 40128988 40128988 single base substitution C T intron_variant MELA-AU 4 40129203 40129203 single base substitution C T intron_variant MELA-AU 4 40129401 40129401 single base substitution C T intron_variant MELA-AU 4 40129475 40129475 single base substitution G A intron_variant MELA-AU 4 40129735 40129735 single base substitution C T intron_variant MELA-AU 4 40130039 40130039 single base substitution C T intron_variant MELA-AU 4 40130676 40130676 single base substitution C T intron_variant MELA-AU 4 40131258 40131258 single base substitution C T intron_variant MELA-AU 4 40131333 40131333 single base substitution C T intron_variant MELA-AU 4 40131983 40131983 single base substitution C T intron_variant MELA-AU 4 40132243 40132243 single base substitution C T intron_variant MELA-AU 4 40132334 40132334 single base substitution T C intron_variant MELA-AU 4 40132534 40132534 single base substitution A G intron_variant MELA-AU 4 40132679 40132679 single base substitution C T intron_variant MELA-AU 4 40134002 40134002 single base substitution C T intron_variant MELA-AU 4 40134403 40134403 single base substitution C T intron_variant MELA-AU 4 40134514 40134514 single base substitution C T intron_variant MELA-AU 4 40134949 40134949 single base substitution C T intron_variant MELA-AU 4 40135066 40135066 single base substitution C T intron_variant MELA-AU 4 40135290 40135290 single base substitution T G intron_variant MELA-AU 4 40136005 40136005 single base substitution G C intron_variant MELA-AU 4 40136012 40136012 single base substitution C T intron_variant MELA-AU 4 40136429 40136429 single base substitution T A intron_variant MELA-AU 4 40136520 40136520 single base substitution C T intron_variant MELA-AU 4 40137356 40137356 single base substitution T C intron_variant MELA-AU 4 40137411 40137411 single base substitution T C intron_variant MELA-AU 4 40137460 40137460 single base substitution T C intron_variant MELA-AU 4 40140124 40140124 single base substitution C T intron_variant MELA-AU 4 40140231 40140231 single base substitution C T intron_variant MELA-AU 4 40140481 40140481 single base substitution C T intron_variant MELA-AU 4 40140549 40140549 single base substitution T G intron_variant MELA-AU 4 40140680 40140680 single base substitution T G intron_variant MELA-AU 4 40141109 40141109 single base substitution G A intron_variant MELA-AU 4 40141390 40141390 single base substitution C T intron_variant MELA-AU 4 40141542 40141542 single base substitution C T intron_variant MELA-AU 4 40141824 40141824 single base substitution T C intron_variant MELA-AU 4 40142235 40142235 single base substitution C T intron_variant MELA-AU 4 40142900 40142900 single base substitution C T intron_variant MELA-AU 4 40142976 40142976 single base substitution C T intron_variant MELA-AU 4 40143018 40143018 single base substitution C T intron_variant MELA-AU 4 40143218 40143218 single base substitution C T intron_variant MELA-AU 4 40143719 40143719 single base substitution C T intron_variant MELA-AU 4 40144172 40144172 single base substitution C T intron_variant MELA-AU 4 40144495 40144495 single base substitution C T intron_variant MELA-AU 4 40144506 40144506 single base substitution T C intron_variant MELA-AU 4 40145842 40145842 single base substitution C T intron_variant MELA-AU 4 40146153 40146153 single base substitution C T intron_variant MELA-AU 4 40146167 40146167 single base substitution C T intron_variant MELA-AU 4 40146228 40146228 single base substitution C T intron_variant MELA-AU 4 40146231 40146231 single base substitution G A intron_variant MELA-AU 4 40147093 40147093 single base substitution C T intron_variant MELA-AU 4 40147579 40147579 single base substitution C T intron_variant MELA-AU 4 40147915 40147915 single base substitution C T intron_variant MELA-AU 4 40149694 40149694 single base substitution C T intron_variant MELA-AU 4 40151223 40151223 single base substitution G A intron_variant MELA-AU 4 40151471 40151471 single base substitution C T intron_variant MELA-AU 4 40151682 40151682 single base substitution C T intron_variant MELA-AU 4 40152870 40152870 single base substitution G A intron_variant MELA-AU 4 40152881 40152881 single base substitution G A intron_variant MELA-AU 4 40153091 40153091 single base substitution C T intron_variant MELA-AU 4 40153280 40153280 single base substitution C T intron_variant MELA-AU 4 40154504 40154504 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40154504 40154504 single base substitution C T missense_variant L1379F 4135C>T MELA-AU 4 40154504 40154504 single base substitution C T missense_variant L1750F 5248C>T MELA-AU 4 40154836 40154836 single base substitution T A intron_variant MELA-AU 4 40155228 40155228 single base substitution C T intron_variant MELA-AU 4 40155555 40155555 single base substitution C T intron_variant MELA-AU 4 40155936 40155936 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40156382 40156382 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40157544 40157544 single base substitution G A 3_prime_UTR_variant MELA-AU 4 40157544 40157544 single base substitution G A downstream_gene_variant MELA-AU 4 40157663 40157663 single base substitution A T 3_prime_UTR_variant MELA-AU 4 40157663 40157663 single base substitution A T downstream_gene_variant MELA-AU 4 40157734 40157734 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40157734 40157734 single base substitution C T downstream_gene_variant MELA-AU 4 40158508 40158508 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40158508 40158508 single base substitution C T downstream_gene_variant MELA-AU 4 40158888 40158888 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40158888 40158888 single base substitution C T downstream_gene_variant MELA-AU 4 40158948 40158948 single base substitution A C 3_prime_UTR_variant MELA-AU 4 40158948 40158948 single base substitution A C downstream_gene_variant MELA-AU 4 40159519 40159519 single base substitution C T 3_prime_UTR_variant MELA-AU 4 40159519 40159519 single base substitution C T downstream_gene_variant MELA-AU 4 40159766 40159766 single base substitution A T 3_prime_UTR_variant MELA-AU 4 40159766 40159766 single base substitution A T downstream_gene_variant MELA-AU 4 40160119 40160119 single base substitution G C downstream_gene_variant MELA-AU 4 40160251 40160251 single base substitution C T downstream_gene_variant MELA-AU 4 40160316 40160316 single base substitution C T downstream_gene_variant MELA-AU 4 40161103 40161103 single base substitution C T downstream_gene_variant MELA-AU 4 40162520 40162520 single base substitution G A downstream_gene_variant MELA-AU 4 40162770 40162770 single base substitution C T downstream_gene_variant MELA-AU 4 40163744 40163744 single base substitution T G downstream_gene_variant MELA-AU 4 40164047 40164047 single base substitution C T downstream_gene_variant MELA-AU 4 40164450 40164450 single base substitution G A downstream_gene_variant ORCA-IN 4 40059485 40059485 single base substitution G A intron_variant ORCA-IN 4 40059541 40059541 single base substitution C G intron_variant ORCA-IN 4 40076072 40076072 single base substitution G A intron_variant ORCA-IN 4 40078350 40078350 single base substitution C T intron_variant ORCA-IN 4 40104312 40104312 single base substitution C T 3_prime_UTR_variant ORCA-IN 4 40104312 40104312 single base substitution C T downstream_gene_variant ORCA-IN 4 40104312 40104312 single base substitution C T missense_variant P283S 847C>T ORCA-IN 4 40104312 40104312 single base substitution C T upstream_gene_variant ORCA-IN 4 40138003 40138003 deletion of <=200bp T - intron_variant ORCA-IN 4 40150697 40150697 single base substitution A G intron_variant ORCA-IN 4 40153912 40153912 single base substitution C T intron_variant ORCA-IN 4 40155849 40155849 single base substitution C A 3_prime_UTR_variant ORCA-IN 4 40155849 40155849 single base substitution C A missense_variant L1398I 4192C>A ORCA-IN 4 40155849 40155849 single base substitution C A missense_variant L1769I 5305C>A OV-AU 4 40069486 40069486 single base substitution G C intron_variant OV-AU 4 40069697 40069697 single base substitution A G intron_variant OV-AU 4 40070904 40070904 single base substitution C G intron_variant OV-AU 4 40071687 40071687 single base substitution T C intron_variant OV-AU 4 40072573 40072573 single base substitution T A intron_variant OV-AU 4 40079655 40079655 single base substitution T C intron_variant OV-AU 4 40082839 40082839 single base substitution A T intron_variant OV-AU 4 40085837 40085837 single base substitution C A intron_variant OV-AU 4 40088457 40088457 single base substitution T A intron_variant OV-AU 4 40095613 40095613 single base substitution C T intron_variant OV-AU 4 40116347 40116347 single base substitution G T intron_variant OV-AU 4 40119923 40119923 single base substitution C G intron_variant OV-AU 4 40136465 40136465 single base substitution G T intron_variant OV-AU 4 40141304 40141304 single base substitution G C intron_variant OV-AU 4 40141439 40141439 single base substitution T C intron_variant OV-AU 4 40150819 40150819 single base substitution A C intron_variant OV-AU 4 40151863 40151863 single base substitution T C intron_variant OV-AU 4 40156273 40156273 single base substitution A G 3_prime_UTR_variant OV-AU 4 40159444 40159444 single base substitution A T 3_prime_UTR_variant OV-AU 4 40159444 40159444 single base substitution A T downstream_gene_variant OV-AU 4 40163118 40163118 single base substitution A T downstream_gene_variant OV-US 4 40124773 40124773 single base substitution G A 3_prime_UTR_variant OV-US 4 40124773 40124773 single base substitution G A missense_variant V1055I 3163G>A OV-US 4 40124773 40124773 single base substitution G A missense_variant V1409I 4225G>A PACA-AU 4 40063985 40063985 single base substitution C T intron_variant PACA-AU 4 40066610 40066610 single base substitution G A intron_variant PACA-AU 4 40081829 40081829 single base substitution T C intron_variant PACA-AU 4 40083689 40083689 single base substitution G A intron_variant PACA-AU 4 40085179 40085179 single base substitution C T intron_variant PACA-AU 4 40086796 40086796 single base substitution G T intron_variant PACA-AU 4 40088905 40088905 single base substitution A T intron_variant PACA-AU 4 40089669 40089669 single base substitution C T intron_variant PACA-AU 4 40092291 40092291 single base substitution G A intron_variant PACA-AU 4 40094920 40094920 single base substitution C T intron_variant PACA-AU 4 40097156 40097156 single base substitution T C intron_variant PACA-AU 4 40108079 40108079 single base substitution G A downstream_gene_variant PACA-AU 4 40108079 40108079 single base substitution G A intron_variant PACA-AU 4 40129070 40129070 single base substitution A C intron_variant PACA-AU 4 40133368 40133368 deletion of <=200bp T - intron_variant PACA-AU 4 40139351 40139351 single base substitution G T intron_variant PACA-AU 4 40145573 40145573 single base substitution C G intron_variant PACA-AU 4 40148186 40148186 single base substitution A G intron_variant PACA-AU 4 40150265 40150265 single base substitution T A intron_variant PACA-AU 4 40150525 40150525 single base substitution G A intron_variant PACA-AU 4 40153579 40153582 deletion of <=200bp ATTA - intron_variant PACA-AU 4 40164854 40164854 single base substitution G C downstream_gene_variant PACA-CA 4 40055814 40055814 single base substitution G T upstream_gene_variant PACA-CA 4 40059727 40059727 single base substitution T C intron_variant PACA-CA 4 40073524 40073524 single base substitution T C intron_variant PACA-CA 4 40080060 40080060 single base substitution T C intron_variant PACA-CA 4 40080989 40080989 single base substitution G A intron_variant PACA-CA 4 40082935 40082935 single base substitution A G intron_variant PACA-CA 4 40085776 40085781 deletion of <=200bp GCCCAG - intron_variant PACA-CA 4 40087520 40087520 single base substitution C T intron_variant PACA-CA 4 40090356 40090356 single base substitution T A intron_variant PACA-CA 4 40090843 40090843 single base substitution C A intron_variant PACA-CA 4 40094580 40094580 single base substitution A T intron_variant PACA-CA 4 40095276 40095276 single base substitution G T intron_variant PACA-CA 4 40097201 40097201 single base substitution A G intron_variant PACA-CA 4 40106071 40106071 single base substitution C T downstream_gene_variant PACA-CA 4 40106071 40106071 single base substitution C T intron_variant PACA-CA 4 40106306 40106306 single base substitution T C downstream_gene_variant PACA-CA 4 40106306 40106306 single base substitution T C intron_variant PACA-CA 4 40106380 40106380 single base substitution G C downstream_gene_variant PACA-CA 4 40106380 40106380 single base substitution G C intron_variant PACA-CA 4 40109711 40109711 single base substitution C A intron_variant PACA-CA 4 40113852 40113852 single base substitution T A intron_variant PACA-CA 4 40114191 40114191 single base substitution G A intron_variant PACA-CA 4 40115664 40115664 single base substitution G T intron_variant PACA-CA 4 40115713 40115713 single base substitution C A intron_variant PACA-CA 4 40120673 40120673 single base substitution C T intron_variant PACA-CA 4 40122873 40122873 single base substitution G A 3_prime_UTR_variant PACA-CA 4 40122873 40122873 single base substitution G A missense_variant G1048R 3142G>A PACA-CA 4 40122873 40122873 single base substitution G A missense_variant G694R 2080G>A PACA-CA 4 40129024 40129024 single base substitution G A intron_variant PACA-CA 4 40129442 40129442 single base substitution G A intron_variant PACA-CA 4 40134631 40134631 single base substitution G A intron_variant PACA-CA 4 40135236 40135236 single base substitution G A intron_variant PACA-CA 4 40138254 40138254 single base substitution C T intron_variant PACA-CA 4 40139301 40139301 single base substitution T C intron_variant PACA-CA 4 40140075 40140075 single base substitution G A intron_variant PACA-CA 4 40140076 40140076 single base substitution C A intron_variant PACA-CA 4 40142211 40142211 deletion of <=200bp A - intron_variant PACA-CA 4 40142864 40142864 single base substitution C T intron_variant PACA-CA 4 40147541 40147541 single base substitution G A intron_variant PACA-CA 4 40147774 40147774 single base substitution C T intron_variant PACA-CA 4 40149747 40149747 single base substitution C T intron_variant PACA-CA 4 40150657 40150657 single base substitution G A intron_variant PACA-CA 4 40152224 40152224 single base substitution G T intron_variant PACA-CA 4 40157030 40157030 single base substitution G A 3_prime_UTR_variant PACA-CA 4 40157030 40157030 single base substitution G A downstream_gene_variant PACA-CA 4 40157444 40157444 deletion of <=200bp T - 3_prime_UTR_variant PACA-CA 4 40157444 40157444 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 40158194 40158194 deletion of <=200bp T - 3_prime_UTR_variant PACA-CA 4 40158194 40158194 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 40164771 40164771 single base substitution C T downstream_gene_variant PAEN-AU 4 40144767 40144767 single base substitution A G intron_variant PAEN-AU 4 40159335 40159335 single base substitution T C 3_prime_UTR_variant PAEN-AU 4 40159335 40159335 single base substitution T C downstream_gene_variant PAEN-AU 4 40162016 40162016 single base substitution T C downstream_gene_variant PAEN-IT 4 40056140 40056140 single base substitution T C upstream_gene_variant PAEN-IT 4 40060562 40060562 single base substitution C T intron_variant PAEN-IT 4 40152988 40152988 single base substitution T G intron_variant PBCA-DE 4 40054260 40054260 insertion of <=200bp - T upstream_gene_variant PBCA-DE 4 40069322 40069322 single base substitution A G intron_variant PBCA-DE 4 40073152 40073152 single base substitution T G intron_variant PBCA-DE 4 40087911 40087911 single base substitution C T intron_variant PBCA-DE 4 40104549 40104549 single base substitution A G 3_prime_UTR_variant PBCA-DE 4 40104549 40104549 single base substitution A G downstream_gene_variant PBCA-DE 4 40104549 40104549 single base substitution A G missense_variant M362V 1084A>G PBCA-DE 4 40104549 40104549 single base substitution A G missense_variant M8V 22A>G PBCA-DE 4 40114321 40114321 single base substitution A C intron_variant PBCA-DE 4 40115582 40115582 single base substitution A G intron_variant PBCA-DE 4 40125462 40125462 single base substitution G T intron_variant PBCA-DE 4 40127403 40127403 single base substitution A T intron_variant PBCA-DE 4 40134634 40134634 single base substitution C T intron_variant PBCA-DE 4 40136198 40136198 single base substitution T G intron_variant PBCA-DE 4 40158807 40158807 single base substitution C T 3_prime_UTR_variant PBCA-DE 4 40158807 40158807 single base substitution C T downstream_gene_variant PBCA-DE 4 40159034 40159034 single base substitution A C 3_prime_UTR_variant PBCA-DE 4 40159034 40159034 single base substitution A C downstream_gene_variant PRAD-CA 4 40061627 40061627 single base substitution C T intron_variant PRAD-CA 4 40075057 40075057 single base substitution A G intron_variant PRAD-CA 4 40081947 40081947 single base substitution C T intron_variant PRAD-CA 4 40089855 40089855 single base substitution C T intron_variant PRAD-CA 4 40094579 40094579 single base substitution T A intron_variant PRAD-CA 4 40107682 40107682 single base substitution A G downstream_gene_variant PRAD-CA 4 40107682 40107682 single base substitution A G intron_variant PRAD-CA 4 40129472 40129472 single base substitution G A intron_variant PRAD-CA 4 40146599 40146599 single base substitution G A intron_variant PRAD-CA 4 40152576 40152576 single base substitution C A intron_variant PRAD-CA 4 40161734 40161734 single base substitution C G downstream_gene_variant PRAD-UK 4 40059358 40059359 deletion of <=200bp CA - intron_variant PRAD-UK 4 40080283 40080283 single base substitution C G intron_variant PRAD-UK 4 40090657 40090657 single base substitution A G intron_variant PRAD-UK 4 40094920 40094920 single base substitution C T intron_variant PRAD-UK 4 40100823 40100823 single base substitution G C intron_variant PRAD-UK 4 40100823 40100823 single base substitution G C upstream_gene_variant PRAD-UK 4 40103941 40103941 single base substitution A C 3_prime_UTR_variant PRAD-UK 4 40103941 40103941 single base substitution A C missense_variant D159A 476A>C PRAD-UK 4 40103941 40103941 single base substitution A C missense_variant D79A 236A>C PRAD-UK 4 40103941 40103941 single base substitution A C upstream_gene_variant PRAD-UK 4 40107372 40107372 single base substitution G C downstream_gene_variant PRAD-UK 4 40107372 40107372 single base substitution G C intron_variant PRAD-UK 4 40108111 40108111 single base substitution C A downstream_gene_variant PRAD-UK 4 40108111 40108111 single base substitution C A intron_variant PRAD-UK 4 40119920 40119920 single base substitution C G intron_variant PRAD-UK 4 40122995 40122995 single base substitution A G 3_prime_UTR_variant PRAD-UK 4 40122995 40122995 single base substitution A G synonymous_variant E1088E 3264A>G PRAD-UK 4 40122995 40122995 single base substitution A G synonymous_variant E734E 2202A>G PRAD-UK 4 40128635 40128635 single base substitution T G intron_variant PRAD-UK 4 40129441 40129441 single base substitution C T intron_variant PRAD-UK 4 40131755 40131755 single base substitution G T intron_variant PRAD-UK 4 40135519 40135519 single base substitution A G intron_variant PRAD-UK 4 40145447 40145447 single base substitution G A intron_variant PRAD-UK 4 40148974 40148974 deletion of <=200bp C - intron_variant PRAD-UK 4 40151794 40151794 single base substitution A T intron_variant PRAD-UK 4 40153281 40153281 single base substitution G T intron_variant PRAD-US 4 40119567 40119567 single base substitution A G 3_prime_UTR_variant PRAD-US 4 40119567 40119567 single base substitution A G missense_variant I227M 681A>G PRAD-US 4 40119567 40119567 single base substitution A G missense_variant I581M 1743A>G READ-US 4 40104077 40104077 single base substitution G T 3_prime_UTR_variant READ-US 4 40104077 40104077 single base substitution G T missense_variant E124D 372G>T READ-US 4 40104077 40104077 single base substitution G T missense_variant E204D 612G>T READ-US 4 40104077 40104077 single base substitution G T upstream_gene_variant READ-US 4 40104123 40104123 single base substitution G A 3_prime_UTR_variant READ-US 4 40104123 40104123 single base substitution G A missense_variant V140I 418G>A READ-US 4 40104123 40104123 single base substitution G A missense_variant V220I 658G>A READ-US 4 40104123 40104123 single base substitution G A upstream_gene_variant READ-US 4 40104571 40104571 single base substitution C T 3_prime_UTR_variant READ-US 4 40104571 40104571 single base substitution C T downstream_gene_variant READ-US 4 40104571 40104571 single base substitution C T missense_variant A15V 44C>T READ-US 4 40104571 40104571 single base substitution C T missense_variant A369V 1106C>T READ-US 4 40104789 40104789 single base substitution C A 3_prime_UTR_variant READ-US 4 40104789 40104789 single base substitution C A downstream_gene_variant READ-US 4 40104789 40104789 single base substitution C A missense_variant L442I 1324C>A READ-US 4 40104789 40104789 single base substitution C A missense_variant L88I 262C>A RECA-EU 4 40056328 40056328 single base substitution A T upstream_gene_variant RECA-EU 4 40066766 40066766 single base substitution A G intron_variant RECA-EU 4 40070097 40070097 single base substitution A C intron_variant RECA-EU 4 40070870 40070870 single base substitution C T intron_variant RECA-EU 4 40076833 40076833 single base substitution C T intron_variant RECA-EU 4 40098560 40098560 single base substitution C T intron_variant RECA-EU 4 40102925 40102925 single base substitution C T intron_variant RECA-EU 4 40102925 40102925 single base substitution C T upstream_gene_variant RECA-EU 4 40126544 40126544 single base substitution A T intron_variant RECA-EU 4 40133662 40133662 single base substitution T G intron_variant RECA-EU 4 40155552 40155552 single base substitution A T intron_variant RECA-EU 4 40157470 40157470 single base substitution C A 3_prime_UTR_variant RECA-EU 4 40157470 40157470 single base substitution C A downstream_gene_variant SKCA-BR 4 40055070 40055074 deletion of <=200bp TTTTC - upstream_gene_variant SKCA-BR 4 40055799 40055799 single base substitution A T upstream_gene_variant SKCA-BR 4 40058476 40058476 single base substitution T C 5_prime_UTR_variant SKCA-BR 4 40058476 40058476 single base substitution T C upstream_gene_variant SKCA-BR 4 40063141 40063141 single base substitution C T intron_variant SKCA-BR 4 40064182 40064182 insertion of <=200bp - CT intron_variant SKCA-BR 4 40064250 40064250 single base substitution C T intron_variant SKCA-BR 4 40076238 40076238 single base substitution C T intron_variant SKCA-BR 4 40078124 40078124 single base substitution T A intron_variant SKCA-BR 4 40079733 40079733 insertion of <=200bp - ATG intron_variant SKCA-BR 4 40081664 40081664 single base substitution C T intron_variant SKCA-BR 4 40081846 40081846 single base substitution C T intron_variant SKCA-BR 4 40082197 40082197 single base substitution T C intron_variant SKCA-BR 4 40086251 40086252 deletion of <=200bp AT - intron_variant SKCA-BR 4 40086268 40086268 single base substitution T C intron_variant SKCA-BR 4 40089473 40089473 single base substitution T A intron_variant SKCA-BR 4 40090122 40090122 insertion of <=200bp - GTT intron_variant SKCA-BR 4 40090745 40090745 single base substitution C T intron_variant SKCA-BR 4 40091557 40091557 single base substitution C T intron_variant SKCA-BR 4 40092476 40092476 single base substitution C T intron_variant SKCA-BR 4 40096926 40096926 single base substitution C T intron_variant SKCA-BR 4 40100836 40100836 single base substitution C T intron_variant SKCA-BR 4 40100836 40100836 single base substitution C T upstream_gene_variant SKCA-BR 4 40101532 40101532 single base substitution A C intron_variant SKCA-BR 4 40101532 40101532 single base substitution A C upstream_gene_variant SKCA-BR 4 40101538 40101538 single base substitution G C intron_variant SKCA-BR 4 40101538 40101538 single base substitution G C upstream_gene_variant SKCA-BR 4 40101541 40101541 single base substitution A C intron_variant SKCA-BR 4 40101541 40101541 single base substitution A C upstream_gene_variant SKCA-BR 4 40101553 40101553 single base substitution C T intron_variant SKCA-BR 4 40101553 40101553 single base substitution C T upstream_gene_variant SKCA-BR 4 40102989 40102989 single base substitution A G intron_variant SKCA-BR 4 40102989 40102989 single base substitution A G upstream_gene_variant SKCA-BR 4 40104516 40104516 single base substitution C T 3_prime_UTR_variant SKCA-BR 4 40104516 40104516 single base substitution C T downstream_gene_variant SKCA-BR 4 40104516 40104516 single base substitution C T missense_variant P351S 1051C>T SKCA-BR 4 40104516 40104516 single base substitution C T upstream_gene_variant SKCA-BR 4 40105399 40105399 single base substitution C T downstream_gene_variant SKCA-BR 4 40105399 40105399 single base substitution C T intron_variant SKCA-BR 4 40106649 40106649 single base substitution C T downstream_gene_variant SKCA-BR 4 40106649 40106649 single base substitution C T intron_variant SKCA-BR 4 40106655 40106655 single base substitution C T downstream_gene_variant SKCA-BR 4 40106655 40106655 single base substitution C T intron_variant SKCA-BR 4 40106716 40106716 single base substitution C T downstream_gene_variant SKCA-BR 4 40106716 40106716 single base substitution C T intron_variant SKCA-BR 4 40112585 40112585 single base substitution C T intron_variant SKCA-BR 4 40112625 40112625 single base substitution C T intron_variant SKCA-BR 4 40116366 40116369 deletion of <=200bp TTTC - intron_variant SKCA-BR 4 40120792 40120792 single base substitution C T intron_variant SKCA-BR 4 40121070 40121070 single base substitution G T intron_variant SKCA-BR 4 40127506 40127507 deletion of <=200bp CA - intron_variant SKCA-BR 4 40127525 40127527 deletion of <=200bp AAT - intron_variant SKCA-BR 4 40128123 40128123 single base substitution C T intron_variant SKCA-BR 4 40128961 40128961 single base substitution C T intron_variant SKCA-BR 4 40136308 40136308 single base substitution C T intron_variant SKCA-BR 4 40136523 40136527 deletion of <=200bp TTCTC - intron_variant SKCA-BR 4 40136756 40136756 single base substitution C T intron_variant SKCA-BR 4 40136863 40136863 single base substitution C T intron_variant SKCA-BR 4 40137963 40137967 deletion of <=200bp AATCT - intron_variant SKCA-BR 4 40137999 40137999 insertion of <=200bp - TATCTATC intron_variant SKCA-BR 4 40138226 40138226 single base substitution C T intron_variant SKCA-BR 4 40140403 40140403 single base substitution C T intron_variant SKCA-BR 4 40144980 40144980 single base substitution C T intron_variant SKCA-BR 4 40146646 40146646 single base substitution C T intron_variant SKCA-BR 4 40147024 40147024 single base substitution A T intron_variant SKCA-BR 4 40147037 40147037 single base substitution T G intron_variant SKCA-BR 4 40147915 40147915 single base substitution C T intron_variant SKCA-BR 4 40149805 40149805 single base substitution C T intron_variant SKCA-BR 4 40150211 40150211 single base substitution C T intron_variant SKCA-BR 4 40163182 40163182 single base substitution T G downstream_gene_variant SKCA-BR 4 40164516 40164516 single base substitution G A downstream_gene_variant SKCM-US 4 40098995 40098995 single base substitution C T exon_variant SKCM-US 4 40098995 40098995 single base substitution C T intron_variant SKCM-US 4 40098995 40098995 single base substitution C T missense_variant P12L 35C>T SKCM-US 4 40099190 40099190 single base substitution G A intron_variant SKCM-US 4 40099190 40099190 single base substitution G A splice_donor_variant SKCM-US 4 40104513 40104513 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40104513 40104513 single base substitution C T downstream_gene_variant SKCM-US 4 40104513 40104513 single base substitution C T missense_variant L350F 1048C>T SKCM-US 4 40104513 40104513 single base substitution C T upstream_gene_variant SKCM-US 4 40104546 40104546 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40104546 40104546 single base substitution C T downstream_gene_variant SKCM-US 4 40104546 40104546 single base substitution C T missense_variant P361S 1081C>T SKCM-US 4 40104546 40104546 single base substitution C T missense_variant P7S 19C>T SKCM-US 4 40104609 40104609 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40104609 40104609 single base substitution C T downstream_gene_variant SKCM-US 4 40104609 40104609 single base substitution C T missense_variant P28S 82C>T SKCM-US 4 40104609 40104609 single base substitution C T missense_variant P382S 1144C>T SKCM-US 4 40104657 40104657 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40104657 40104657 single base substitution C T downstream_gene_variant SKCM-US 4 40104657 40104657 single base substitution C T missense_variant P398S 1192C>T SKCM-US 4 40104657 40104657 single base substitution C T missense_variant P44S 130C>T SKCM-US 4 40104726 40104726 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40104726 40104726 single base substitution C T downstream_gene_variant SKCM-US 4 40104726 40104726 single base substitution C T stop_gained Q421* 1261C>T SKCM-US 4 40104726 40104726 single base substitution C T stop_gained Q67* 199C>T SKCM-US 4 40104765 40104765 single base substitution A C 3_prime_UTR_variant SKCM-US 4 40104765 40104765 single base substitution A C downstream_gene_variant SKCM-US 4 40104765 40104765 single base substitution A C missense_variant K434Q 1300A>C SKCM-US 4 40104765 40104765 single base substitution A C missense_variant K80Q 238A>C SKCM-US 4 40104811 40104811 single base substitution C G 3_prime_UTR_variant SKCM-US 4 40104811 40104811 single base substitution C G downstream_gene_variant SKCM-US 4 40104811 40104811 single base substitution C G missense_variant P449R 1346C>G SKCM-US 4 40104811 40104811 single base substitution C G missense_variant P95R 284C>G SKCM-US 4 40108641 40108641 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40108641 40108641 single base substitution C T downstream_gene_variant SKCM-US 4 40108641 40108641 single base substitution C T missense_variant R145C 433C>T SKCM-US 4 40108641 40108641 single base substitution C T missense_variant R499C 1495C>T SKCM-US 4 40115076 40115076 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40115076 40115076 single base substitution C T missense_variant L184F 550C>T SKCM-US 4 40115076 40115076 single base substitution C T missense_variant L538F 1612C>T SKCM-US 4 40119499 40119499 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40119499 40119499 single base substitution C T missense_variant H205Y 613C>T SKCM-US 4 40119499 40119499 single base substitution C T missense_variant H559Y 1675C>T SKCM-US 4 40121767 40121767 single base substitution A G 3_prime_UTR_variant SKCM-US 4 40121767 40121767 single base substitution A G missense_variant E325G 974A>G SKCM-US 4 40121767 40121767 single base substitution A G missense_variant E679G 2036A>G SKCM-US 4 40121902 40121902 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40121902 40121902 single base substitution C T missense_variant S370L 1109C>T SKCM-US 4 40121902 40121902 single base substitution C T missense_variant S724L 2171C>T SKCM-US 4 40121980 40121980 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40121980 40121980 single base substitution C T missense_variant S396F 1187C>T SKCM-US 4 40121980 40121980 single base substitution C T missense_variant S750F 2249C>T SKCM-US 4 40123006 40123006 single base substitution T C 3_prime_UTR_variant SKCM-US 4 40123006 40123006 single base substitution T C missense_variant L1092P 3275T>C SKCM-US 4 40123006 40123006 single base substitution T C missense_variant L738P 2213T>C SKCM-US 4 40123361 40123361 single base substitution T A 3_prime_UTR_variant SKCM-US 4 40123361 40123361 single base substitution T A synonymous_variant T1210T 3630T>A SKCM-US 4 40123361 40123361 single base substitution T A synonymous_variant T856T 2568T>A SKCM-US 4 40123395 40123395 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40123395 40123395 single base substitution C T missense_variant P1222S 3664C>T SKCM-US 4 40123395 40123395 single base substitution C T missense_variant P868S 2602C>T SKCM-US 4 40123586 40123586 single base substitution T A 3_prime_UTR_variant SKCM-US 4 40123586 40123586 single base substitution T A synonymous_variant S1285S 3855T>A SKCM-US 4 40123586 40123586 single base substitution T A synonymous_variant S931S 2793T>A SKCM-US 4 40123874 40123874 single base substitution C T 3_prime_UTR_variant SKCM-US 4 40123874 40123874 single base substitution C T synonymous_variant P1027P 3081C>T SKCM-US 4 40123874 40123874 single base substitution C T synonymous_variant P1381P 4143C>T SKCM-US 4 40133427 40133427 single base substitution G A 3_prime_UTR_variant SKCM-US 4 40133427 40133427 single base substitution G A missense_variant E1158K 3472G>A SKCM-US 4 40133427 40133427 single base substitution G A missense_variant E1512K 4534G>A STAD-US 4 40104250 40104253 deletion of <=200bp TCAA - 3_prime_UTR_variant STAD-US 4 40104250 40104253 deletion of <=200bp TCAA - downstream_gene_variant STAD-US 4 40104250 40104253 deletion of <=200bp TCAA - frameshift_variant LN262 STAD-US 4 40104250 40104253 deletion of <=200bp TCAA - upstream_gene_variant STAD-US 4 40104327 40104327 single base substitution G A 3_prime_UTR_variant STAD-US 4 40104327 40104327 single base substitution G A downstream_gene_variant STAD-US 4 40104327 40104327 single base substitution G A missense_variant A288T 862G>A STAD-US 4 40104327 40104327 single base substitution G A upstream_gene_variant STAD-US 4 40104430 40104430 single base substitution A G 3_prime_UTR_variant STAD-US 4 40104430 40104430 single base substitution A G downstream_gene_variant STAD-US 4 40104430 40104430 single base substitution A G missense_variant E322G 965A>G STAD-US 4 40104430 40104430 single base substitution A G upstream_gene_variant STAD-US 4 40108561 40108561 single base substitution C T 3_prime_UTR_variant STAD-US 4 40108561 40108561 single base substitution C T downstream_gene_variant STAD-US 4 40108561 40108561 single base substitution C T missense_variant T118I 353C>T STAD-US 4 40108561 40108561 single base substitution C T missense_variant T472I 1415C>T STAD-US 4 40115053 40115053 single base substitution C A missense_variant S176Y 527C>A STAD-US 4 40115053 40115053 single base substitution C A missense_variant S530Y 1589C>A STAD-US 4 40115053 40115053 single base substitution C A splice_region_variant STAD-US 4 40115104 40115104 single base substitution A C 3_prime_UTR_variant STAD-US 4 40115104 40115104 single base substitution A C missense_variant K193T 578A>C STAD-US 4 40115104 40115104 single base substitution A C missense_variant K547T 1640A>C STAD-US 4 40119490 40119490 single base substitution C T missense_variant R202C 604C>T STAD-US 4 40119490 40119490 single base substitution C T missense_variant R556C 1666C>T STAD-US 4 40119490 40119490 single base substitution C T splice_region_variant STAD-US 4 40121855 40121855 deletion of <=200bp A - 3_prime_UTR_variant STAD-US 4 40121855 40121855 deletion of <=200bp A - frameshift_variant V354 STAD-US 4 40121855 40121855 deletion of <=200bp A - frameshift_variant V708 STAD-US 4 40122019 40122019 single base substitution C T 3_prime_UTR_variant STAD-US 4 40122019 40122019 single base substitution C T missense_variant T409M 1226C>T STAD-US 4 40122019 40122019 single base substitution C T missense_variant T763M 2288C>T STAD-US 4 40122061 40122061 deletion of <=200bp A - 3_prime_UTR_variant STAD-US 4 40122061 40122061 deletion of <=200bp A - frameshift_variant E423 STAD-US 4 40122061 40122061 deletion of <=200bp A - frameshift_variant E777 STAD-US 4 40122482 40122482 single base substitution A G 3_prime_UTR_variant STAD-US 4 40122482 40122482 single base substitution A G synonymous_variant K563K 1689A>G STAD-US 4 40122482 40122482 single base substitution A G synonymous_variant K917K 2751A>G STAD-US 4 40123127 40123127 single base substitution A T 3_prime_UTR_variant STAD-US 4 40123127 40123127 single base substitution A T missense_variant L1132F 3396A>T STAD-US 4 40123127 40123127 single base substitution A T missense_variant L778F 2334A>T STAD-US 4 40127824 40127824 single base substitution A G 3_prime_UTR_variant STAD-US 4 40127824 40127824 single base substitution A G synonymous_variant K1113K 3339A>G STAD-US 4 40127824 40127824 single base substitution A G synonymous_variant K1467K 4401A>G STAD-US 4 40127935 40127935 single base substitution G A 3_prime_UTR_variant STAD-US 4 40127935 40127935 single base substitution G A synonymous_variant Q1150Q 3450G>A STAD-US 4 40127935 40127935 single base substitution G A synonymous_variant Q1504Q 4512G>A THCA-SA 4 40156098 40156098 single base substitution A C 3_prime_UTR_variant THCA-SA 4 40156577 40156577 single base substitution G T 3_prime_UTR_variant THCA-US 4 40113746 40113746 single base substitution A G 3_prime_UTR_variant THCA-US 4 40113746 40113746 single base substitution A G missense_variant D160G 479A>G THCA-US 4 40113746 40113746 single base substitution A G missense_variant D514G 1541A>G UCEC-US 4 40099126 40099126 single base substitution G T exon_variant UCEC-US 4 40099126 40099126 single base substitution G T intron_variant UCEC-US 4 40099126 40099126 single base substitution G T stop_gained E56* 166G>T UCEC-US 4 40103771 40103771 single base substitution C T 3_prime_UTR_variant UCEC-US 4 40103771 40103771 single base substitution C T synonymous_variant F102F 306C>T UCEC-US 4 40103771 40103771 single base substitution C T synonymous_variant F22F 66C>T UCEC-US 4 40103771 40103771 single base substitution C T upstream_gene_variant UCEC-US 4 40103821 40103821 single base substitution A G 3_prime_UTR_variant UCEC-US 4 40103821 40103821 single base substitution A G missense_variant K119R 356A>G UCEC-US 4 40103821 40103821 single base substitution A G missense_variant K39R 116A>G UCEC-US 4 40103821 40103821 single base substitution A G upstream_gene_variant UCEC-US 4 40103837 40103837 single base substitution G T 3_prime_UTR_variant UCEC-US 4 40103837 40103837 single base substitution G T missense_variant E124D 372G>T UCEC-US 4 40103837 40103837 single base substitution G T missense_variant E44D 132G>T UCEC-US 4 40103837 40103837 single base substitution G T upstream_gene_variant UCEC-US 4 40104192 40104192 single base substitution T C 3_prime_UTR_variant UCEC-US 4 40104192 40104192 single base substitution T C missense_variant S163P 487T>C UCEC-US 4 40104192 40104192 single base substitution T C missense_variant S243P 727T>C UCEC-US 4 40104192 40104192 single base substitution T C upstream_gene_variant UCEC-US 4 40122331 40122331 single base substitution A C 3_prime_UTR_variant UCEC-US 4 40122331 40122331 single base substitution A C missense_variant K513T 1538A>C UCEC-US 4 40122331 40122331 single base substitution A C missense_variant K867T 2600A>C UCEC-US 4 40122539 40122539 single base substitution A C 3_prime_UTR_variant UCEC-US 4 40122539 40122539 single base substitution A C missense_variant Q582H 1746A>C UCEC-US 4 40122539 40122539 single base substitution A C missense_variant Q936H 2808A>C UCEC-US 4 40122672 40122672 single base substitution A G 3_prime_UTR_variant UCEC-US 4 40122672 40122672 single base substitution A G missense_variant N627D 1879A>G UCEC-US 4 40122672 40122672 single base substitution A G missense_variant N981D 2941A>G UCEC-US 4 40122717 40122717 single base substitution G T 3_prime_UTR_variant UCEC-US 4 40122717 40122717 single base substitution G T missense_variant A642S 1924G>T UCEC-US 4 40122717 40122717 single base substitution G T missense_variant A996S 2986G>T UCEC-US 4 40122924 40122924 single base substitution G T 3_prime_UTR_variant UCEC-US 4 40122924 40122924 single base substitution G T missense_variant A1065S 3193G>T UCEC-US 4 40122924 40122924 single base substitution G T missense_variant A711S 2131G>T UCEC-US 4 40123257 40123257 single base substitution G A 3_prime_UTR_variant UCEC-US 4 40123257 40123257 single base substitution G A missense_variant V1176M 3526G>A UCEC-US 4 40123257 40123257 single base substitution G A missense_variant V822M 2464G>A UCEC-US 4 40123635 40123635 single base substitution G T 3_prime_UTR_variant UCEC-US 4 40123635 40123635 single base substitution G T stop_gained E1302* 3904G>T UCEC-US 4 40123635 40123635 single base substitution G T stop_gained E948* 2842G>T UCEC-US 4 40124796 40124796 single base substitution G A 3_prime_UTR_variant UCEC-US 4 40124796 40124796 single base substitution G A synonymous_variant A1062A 3186G>A UCEC-US 4 40124796 40124796 single base substitution G A synonymous_variant A1416A 4248G>A UCEC-US 4 40124821 40124821 single base substitution G T 3_prime_UTR_variant UCEC-US 4 40124821 40124821 single base substitution G T stop_gained E1071* 3211G>T UCEC-US 4 40124821 40124821 single base substitution G T stop_gained E1425* 4273G>T UCEC-US 4 40127829 40127829 single base substitution T C 3_prime_UTR_variant UCEC-US 4 40127829 40127829 single base substitution T C missense_variant L1115P 3344T>C UCEC-US 4 40127829 40127829 single base substitution T C missense_variant L1469P 4406T>C UCEC-US 4 40133420 40133420 single base substitution G T splice_acceptor_variant UCEC-US 4 40133540 40133540 single base substitution G T splice_donor_variant UCEC-US 4 40146282 40146282 single base substitution G A 3_prime_UTR_variant UCEC-US 4 40146282 40146282 single base substitution G A missense_variant A1298T 3892G>A UCEC-US 4 40146282 40146282 single base substitution G A missense_variant A1669T 5005G>A UCEC-US 4 40146308 40146308 single base substitution C A 3_prime_UTR_variant UCEC-US 4 40146308 40146308 single base substitution C A synonymous_variant I1306I 3918C>A UCEC-US 4 40146308 40146308 single base substitution C A synonymous_variant I1677I 5031C>A UCEC-US 4 40146329 40146329 single base substitution G A 3_prime_UTR_variant UCEC-US 4 40146329 40146329 single base substitution G A synonymous_variant S1313S 3939G>A UCEC-US 4 40146329 40146329 single base substitution G A synonymous_variant S1684S 5052G>A UCEC-US 4 40146335 40146335 single base substitution G A 3_prime_UTR_variant UCEC-US 4 40146335 40146335 single base substitution G A synonymous_variant L1315L 3945G>A UCEC-US 4 40146335 40146335 single base substitution G A synonymous_variant L1686L 5058G>A UCEC-US 4 40146336 40146336 single base substitution C T 3_prime_UTR_variant UCEC-US 4 40146336 40146336 single base substitution C T missense_variant P1316S 3946C>T UCEC-US 4 40146336 40146336 single base substitution C T missense_variant P1687S 5059C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-CA-6718-01 COSM1055297 c.2808A>C p.Q936H Substitution - Missense 4:40120919-40120919 + CSCC-60-T COSM4491919 c.3889C>T p.L1297F Substitution - Missense 4:40122000-40122000 + TCGA-BR-6452-01 COSM4124634 c.3396A>T p.L1132F Substitution - Missense 4:40121507-40121507 + TCGA-C8-A1HK-01 COSM1485956 c.2320T>C p.S774P Substitution - Missense 4:40120431-40120431 + 24 COSM4777628 c.1894T>C p.F632L Substitution - Missense 4:40120005-40120005 + LC_S11 COSM1186551 c.2456A>G p.Y819C Substitution - Missense 4:40120567-40120567 + TCGA-B5-A11N-01 COSM1055305 c.4406T>C p.L1469P Substitution - Missense 4:40126209-40126209 + TCGA-AN-A0FZ-01 COSM447845 c.935C>T p.T312I Substitution - Missense 4:40102780-40102780 + TCGA-AP-A059-01 COSM1055309 c.5031C>A p.I1677I Substitution - coding silent 4:40144688-40144688 + RK030_C01 COSM3702591 c.2990A>G p.E997G Substitution - Missense 4:40121101-40121101 + ZZUFHECRKL-G034T COSM5440284 c.4060G>T p.G1354W Substitution - Missense 4:40122171-40122171 + TCGA-BF-A3DL-01 COSM4904995 c.4534G>A p.E1512K Substitution - Missense 4:40131807-40131807 + LAU618 COSM232845 c.3431C>T p.S1144L Substitution - Missense 4:40121542-40121542 + LUAD-NYU259 COSM371907 c.3788G>T p.S1263I Substitution - Missense 4:40121899-40121899 + CSCC-19-T COSM4484059 c.2765C>T p.S922F Substitution - Missense 4:40120876-40120876 + TCGA-D1-A161-01 COSM1055293 c.356A>G p.K119R Substitution - Missense 4:40102201-40102201 + YUGASP COSM232845 c.3431C>T p.S1144L Substitution - Missense 4:40121542-40121542 + PT48 COSM5931514 c.2545G>A p.E849K Substitution - Missense 4:40120656-40120656 + HCC2218 COSM21725 c.847C>G p.P283A Substitution - Missense 4:40102692-40102692 + TCGA-BS-A0UV-01 COSM1055310 c.5052G>A p.S1684S Substitution - coding silent 4:40144709-40144709 + 2P3 COSM3733659 c.1582G>T p.A528S Substitution - Missense 4:40112167-40112167 + PCSI_0476_Pa_P_526 COSM5031375 c.3142G>A p.G1048R Substitution - Missense 4:40121253-40121253 + S00841 COSM317663 c.4964A>G p.Y1655C Substitution - Missense 4:40142851-40142851 + TCGA-BS-A0UF-01 COSM1055291 c.166G>T p.E56* Substitution - Nonsense 4:40097506-40097506 + RC-2 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + TCGA-D3-A3C7-06 COSM3603614 c.1495C>T p.R499C Substitution - Missense 4:40107021-40107021 + TCGA-DK-A1AC-01 COSM1310052 c.3523C>T p.P1175S Substitution - Missense 4:40121634-40121634 + ZZUFHECRKL-G075T COSM2846867 c.426G>A p.L142L Substitution - coding silent 4:40102271-40102271 + TCGA-AP-A051-01 COSM1055307 c.4646+1G>T p.? Unknown 4:40131920-40131920 + 226 COSM3730149 c.3120A>C p.K1040N Substitution - Missense 4:40121231-40121231 + LOVO COSM1429668 c.4942delA p.N1650fs*17 Deletion - Frameshift 4:40142829-40142829 + T3151 COSM4705318 c.4247C>T p.A1416V Substitution - Missense 4:40123175-40123175 + RK216_C01 COSM3767859 c.1393C>T p.P465S Substitution - Missense 4:40106919-40106919 + WA43-71 COSM240810 c.3271A>G p.N1091D Substitution - Missense 4:40121382-40121382 + BRC39 COSM5026139 c.4300G>C p.E1434Q Substitution - Missense 4:40124175-40124175 + TCGA-A2-A0EY-01 COSM447849 c.4384C>G p.Q1462E Substitution - Missense 4:40126187-40126187 + TCGA-GC-A3I6-01 COSM1310049 c.911G>A p.G304D Substitution - Missense 4:40102756-40102756 + TCGA-AZ-4315-01 COSM1429658 c.2921C>T p.S974L Substitution - Missense 4:40121032-40121032 + TCGA-EE-A2MS-06 COSM3603605 c.35C>T p.P12L Substitution - Missense 4:40097375-40097375 + CCK81 COSM2846865 c.353A>G p.E118G Substitution - Missense 4:40102198-40102198 + 61 COSM5736944 c.2395C>T p.Q799* Substitution - Nonsense 4:40120506-40120506 + TCGA-D1-A17Q-01 COSM1055294 c.372G>T p.E124D Substitution - Missense 4:40102217-40102217 + S0029 COSM5002945 c.1528C>T p.P510S Substitution - Missense 4:40112113-40112113 + TCGA-AP-A0LE-01 COSM1055311 c.5058G>A p.L1686L Substitution - coding silent 4:40144715-40144715 + T1154 COSM4705315 c.1618C>T p.R540W Substitution - Missense 4:40113462-40113462 + HF-11782 COSM1192918 c.2295delA p.A766fs*62 Deletion - Frameshift 4:40120406-40120406 + LAU165 COSM232847 c.4258C>T p.H1420Y Substitution - Missense 4:40123186-40123186 + TCGA-76-6193-01 COSM3409292 c.4424C>T p.S1475F Substitution - Missense 4:40126227-40126227 + TCGA-AA-A010-01 COSM283088 c.446C>T p.A149V Substitution - Missense 4:40102291-40102291 + RC-14 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + TCGA-CA-6717-01 COSM1429669 c.5041G>A p.V1681I Substitution - Missense 4:40144698-40144698 + ccRCC-83 COSM1662983 c.656C>A p.S219* Substitution - Nonsense 4:40102501-40102501 + 2521252 COSM5535182 c.1342C>T p.L448F Substitution - Missense 4:40103187-40103187 + RC-19 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + LUAD-D01603 COSM337892 c.2467C>T p.Q823* Substitution - Nonsense 4:40120578-40120578 + EGC8 COSM5060347 c.1955A>G p.Y652C Substitution - Missense 4:40120066-40120066 + TCGA-EE-A3AG-06 COSM3603613 c.1346C>G p.P449R Substitution - Missense 4:40103191-40103191 + TCGA-G3-A5SM-01 COSM4911236 c.375T>G p.S125R Substitution - Missense 4:40102220-40102220 + LIM1215 COSM379339 c.5222G>A p.R1741H Substitution - Missense 4:40152858-40152858 + Capan-1 COSM328140 c.2722C>T p.P908S Substitution - Missense 4:40120833-40120833 + TCGA-CM-6675-01 COSM1429656 c.1556A>G p.Q519R Substitution - Missense 4:40112141-40112141 + LUAD-S01357 COSM387425 c.2397G>A p.Q799Q Substitution - coding silent 4:40120508-40120508 + TCGA-CG-5721-01 COSM4124633 c.2751A>G p.K917K Substitution - coding silent 4:40120862-40120862 + DN1401F COSM5961083 c.4898G>C p.R1633T Substitution - Missense 4:40142785-40142785 + LB647-SCLC COSM13893 c.4691A>T p.E1564V Substitution - Missense 4:40136988-40136988 + RC-4 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + 587284 COSM1216564 c.4666G>A p.V1556M Substitution - Missense 4:40136963-40136963 + 2734_T COSM3946343 c.3043A>G p.T1015A Substitution - Missense 4:40121154-40121154 + TCGA-DK-A1AC-01 COSM1310048 c.441G>A p.Q147Q Substitution - coding silent 4:40102286-40102286 + TCGA-AN-A0FV-01 COSM447846 c.1096A>G p.M366V Substitution - Missense 4:40102941-40102941 + C086 COSM5535182 c.1342C>T p.L448F Substitution - Missense 4:40103187-40103187 + RMS112_ COSM4419577 c.4759A>G p.T1587A Substitution - Missense 4:40137056-40137056 + TCGA-DK-A3X1-01 COSM3775837 c.3985G>A p.E1329K Substitution - Missense 4:40122096-40122096 + LUAD-QJN9L COSM342724 c.1593G>A p.Q531Q Substitution - coding silent 4:40113437-40113437 + HCC2998 COSM2846897 c.2138A>C p.K713T Substitution - Missense 4:40120249-40120249 + TCGA-BR-4184-01 COSM4124626 c.862G>A p.A288T Substitution - Missense 4:40102707-40102707 + TCGA-BR-8680-01 COSM4124631 c.1666C>T p.R556C Substitution - Missense 4:40117870-40117870 + TCGA-ER-A193-06 COSM3603611 c.1261C>T p.Q421* Substitution - Nonsense 4:40103106-40103106 + LUAD-F00365 COSM340696 c.362C>T p.P121L Substitution - Missense 4:40102207-40102207 + ccRCC-93 COSM1662984 c.987C>G p.H329Q Substitution - Missense 4:40102832-40102832 + CHC892T COSM4796102 c.229G>A p.V77I Substitution - Missense 4:40097569-40097569 + ESCC_BICR_005T COSM5439165 c.1749G>A p.M583I Substitution - Missense 4:40117953-40117953 + HCC64T COSM1618806 c.4960T>A p.F1654I Substitution - Missense 4:40142847-40142847 + CSCC-31-T COSM4567612 c.4785_4785+1GG>AA p.? Unknown 4:40137082-40137083 + TCGA-BS-A0UJ-01 COSM1055295 c.727T>C p.S243P Substitution - Missense 4:40102572-40102572 + HCT116 COSM2846889 c.1757C>T p.S586L Substitution - Missense 4:40117961-40117961 + TCGA-BS-A0UV-01 COSM1055306 c.4528-1G>T p.? Unknown 4:40131800-40131800 + NCI-H1770 COSM14039 c.432C>T p.S144S Substitution - coding silent 4:40102277-40102277 + OSCC-GB_00880111 COSM4887995 c.847C>T p.P283S Substitution - Missense 4:40102692-40102692 + WA43-27 COSM240810 c.3271A>G p.N1091D Substitution - Missense 4:40121382-40121382 + TCGA-BS-A0UA-01 COSM1055301 c.3526G>A p.V1176M Substitution - Missense 4:40121637-40121637 + TCGA-BJ-A0Z0-01 COSM3373491 c.1541A>G p.D514G Substitution - Missense 4:40112126-40112126 + 19 COSM5746277 c.4550delA p.D1519fs*6 Deletion - Frameshift 4:40131823-40131823 + TCGA-FR-A3R1-01 COSM3603615 c.1612C>T p.L538F Substitution - Missense 4:40113456-40113456 + OSCC-GB_00540111 COSM4889545 c.5305C>A p.L1769I Substitution - Missense 4:40154229-40154229 + TCGA-FP-A4BF-01 COSM4124635 c.4401A>G p.K1467K Substitution - coding silent 4:40126204-40126204 + TCGA-DA-A3F3-06 COSM1694252 c.2171C>T p.S724L Substitution - Missense 4:40120282-40120282 + RC-3 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + TCGA-A5-A0GE-01 COSM1055308 c.5005G>A p.A1669T Substitution - Missense 4:40144662-40144662 + TCGA-AA-3510-01 COSM1055292 c.306C>T p.F102F Substitution - coding silent 4:40102151-40102151 + CSCC-30-T COSM4507560 c.74C>T p.S25F Substitution - Missense 4:40097414-40097414 + PS-286-4D COSM4423791 c.3152C>T p.P1051L Substitution - Missense 4:40121263-40121263 + TCGA-DK-A3IS-01 COSM1310051 c.2545G>C p.E849Q Substitution - Missense 4:40120656-40120656 + 587284 COSM1216563 c.3946A>T p.N1316Y Substitution - Missense 4:40122057-40122057 + RC-16 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + pfg181T COSM4753401 c.2777C>T p.A926V Substitution - Missense 4:40120888-40120888 + ODG4 COSM3409290 c.1724G>A p.R575H Substitution - Missense 4:40117928-40117928 + NCI-H1770 COSM14039 c.432C>T p.S144S Substitution - coding silent 4:40102277-40102277 + TCGA-EB-A3Y7-01 COSM3603617 c.2036A>G p.E679G Substitution - Missense 4:40120147-40120147 + 94 COSM5014416 c.943T>C p.S315P Substitution - Missense 4:40102788-40102788 + LB647-SCLC COSM13893 c.4691A>T p.E1564V Substitution - Missense 4:40136988-40136988 + PD3499a COSM30402 c.3838delT p.S1280fs*20 Deletion - Frameshift 4:40121948-40121948 + TCGA-LP-A4AV-01 COSM4825244 c.314C>G p.S105C Substitution - Missense 4:40102159-40102159 + TCGA-21-1078-01 COSM733495 c.3032T>C p.V1011A Substitution - Missense 4:40121143-40121143 + MO_1040 COSM5560162 c.2836C>T p.L946L Substitution - coding silent 4:40120947-40120947 + PTC-14C COSM4159063 c.1618C>A p.R540R Substitution - coding silent 4:40113462-40113462 + S00841 COSM317663 c.4964A>G p.Y1655C Substitution - Missense 4:40142851-40142851 + TCGA-BR-6458-01 COSM4124630 c.1640A>C p.K547T Substitution - Missense 4:40113484-40113484 + BCM325T COSM4799000 c.3842C>T p.P1281L Substitution - Missense 4:40121953-40121953 + TCGA-AZ-6598-01 COSM1429670 c.5300T>C p.V1767A Substitution - Missense 4:40154224-40154224 + TCGA-FS-A1ZM-06 COSM3603619 c.3275T>C p.L1092P Substitution - Missense 4:40121386-40121386 + TCGA-AG-A002-01 COSM262283 c.3139G>T p.D1047Y Substitution - Missense 4:40121250-40121250 + TCGA-IR-A3LK-01 COSM4817758 c.3085G>C p.E1029Q Substitution - Missense 4:40121196-40121196 + CHC892T COSM4796102 c.229G>A p.V77I Substitution - Missense 4:40097569-40097569 + TCGA-F5-6814-01 COSM3428498 c.1324C>A p.L442I Substitution - Missense 4:40103169-40103169 + S0029 COSM5884020 c.1529C>T p.P510L Substitution - Missense 4:40112114-40112114 + PD9761a COSM5776090 c.1632A>G p.T544T Substitution - coding silent 4:40113476-40113476 + NB07C COSM1236471 c.1729G>T p.V577F Substitution - Missense 4:40117933-40117933 + 2492723 COSM5720229 c.2409G>A p.R803R Substitution - coding silent 4:40120520-40120520 + PD8969a COSM5789318 c.4198+6G>A p.? Unknown 4:40122315-40122315 + HT115 COSM1055302 c.3904G>T p.E1302* Substitution - Nonsense 4:40122015-40122015 + TCGA-BR-4361-01 COSM4124627 c.965A>G p.E322G Substitution - Missense 4:40102810-40102810 + TCGA-36-2542-01 COSM1328527 c.4929T>A p.A1643A Substitution - coding silent 4:40142816-40142816 + CPCG0103-P8 COSM3396562 c.896G>T p.G299V Substitution - Missense 4:40102741-40102741 + TCGA-CK-5916-01 COSM1429664 c.4367C>A p.P1456H Substitution - Missense 4:40126170-40126170 + TCGA-LP-A4AV-01 COSM4825163 c.383C>T p.S128L Substitution - Missense 4:40102228-40102228 + 2492721 COSM5720229 c.2409G>A p.R803R Substitution - coding silent 4:40120520-40120520 + TCGA-AZ-4615-01 COSM3760626 c.4975-2A>G p.? Unknown 4:40144630-40144630 + cSCCP4 COSM138430 c.4295G>A p.R1432K Substitution - Missense 4:40124170-40124170 + 1N47-VS-1T47 COSM4976283 c.3353T>G p.I1118S Substitution - Missense 4:40121464-40121464 + PD5935a COSM5794065 c.325G>C p.V109L Substitution - Missense 4:40102170-40102170 + TCGA-AP-A054-01 COSM1055298 c.2941A>G p.N981D Substitution - Missense 4:40121052-40121052 + TCGA-06-0141-01 COSM3409291 c.2839G>T p.G947* Substitution - Nonsense 4:40120950-40120950 + NCI-H1770 COSM14039 c.432C>T p.S144S Substitution - coding silent 4:40102277-40102277 + TCGA-CM-6162-01 COSM1429660 c.3367A>G p.S1123G Substitution - Missense 4:40121478-40121478 + PD4937a COSM162779 c.4360G>C p.D1454H Substitution - Missense 4:40126163-40126163 + TCGA-A7-A13E-01 COSM3825829 c.4064A>G p.E1355G Substitution - Missense 4:40122175-40122175 + 61 COSM5736945 c.3127A>G p.T1043A Substitution - Missense 4:40121238-40121238 + TCGA-CG-4305-01 COSM4124632 c.2288C>T p.T763M Substitution - Missense 4:40120399-40120399 + HT115 COSM2846908 c.3303C>A p.S1101S Substitution - coding silent 4:40121414-40121414 + LB647-SCLC COSM13893 c.4691A>T p.E1564V Substitution - Missense 4:40136988-40136988 + Au3 COSM3603610 c.1192C>T p.P398S Substitution - Missense 4:40103037-40103037 + SNUH_G76_S1 COSM4419577 c.4759A>G p.T1587A Substitution - Missense 4:40137056-40137056 + CHEWS027 COSM1055303 c.4248G>A p.A1416A Substitution - coding silent 4:40123176-40123176 + TCGA-CG-4442-01 COSM4124628 c.1415C>T p.T472I Substitution - Missense 4:40106941-40106941 + 587376 COSM1216566 c.1428T>G p.F476L Substitution - Missense 4:40106954-40106954 + T3505 COSM4705319 c.5157C>T p.N1719N Substitution - coding silent 4:40152793-40152793 + tumor_4120193 COSM3927433 c.5232A>C p.P1744P Substitution - coding silent 4:40152868-40152868 + RK136_C01 COSM3767858 c.576T>C p.S192S Substitution - coding silent 4:40102421-40102421 + CHC796T COSM4954124 c.4188T>C p.G1396G Substitution - coding silent 4:40122299-40122299 + TCGA-AG-3742-01 COSM1567341 c.658G>A p.V220I Substitution - Missense 4:40102503-40102503 + 61 COSM5736943 c.2104C>T p.Q702* Substitution - Nonsense 4:40120215-40120215 + BD118T COSM5507457 c.2023G>T p.A675S Substitution - Missense 4:40120134-40120134 + TCGA-18-3406-01 COSM733497 c.1827A>T p.R609S Substitution - Missense 4:40119938-40119938 + C086 COSM587194 c.40C>T p.R14W Substitution - Missense 4:40097380-40097380 + CHC302T COSM3669278 c.2639A>G p.N880S Substitution - Missense 4:40120750-40120750 + LAU50_1 COSM232846 c.3751C>T p.P1251S Substitution - Missense 4:40121862-40121862 + CH-60-T2 COSM5651238 c.496C>T p.P166S Substitution - Missense 4:40102341-40102341 + TCGA-CA-6717-01 COSM1429662 c.3910T>C p.Y1304H Substitution - Missense 4:40122021-40122021 + TCGA-FW-A3R5-06 COSM3917752 c.3630T>A p.T1210T Substitution - coding silent 4:40121741-40121741 + LIM2405 COSM4642891 c.2124A>G p.V708V Substitution - coding silent 4:40120235-40120235 + Case4 COSM1579330 c.1274C>G p.T425S Substitution - Missense 4:40103119-40103119 + TCGA-D5-6538-01 COSM1429659 c.3098T>C p.I1033T Substitution - Missense 4:40121209-40121209 + ESO-114 COSM1258643 c.1299G>C p.K433N Substitution - Missense 4:40103144-40103144 + HCT15 COSM2846893 c.1863T>A p.N621K Substitution - Missense 4:40119974-40119974 + TCGA-EE-A29E-06 COSM3603616 c.1675C>T p.H559Y Substitution - Missense 4:40117879-40117879 + TCGA-ER-A194-01 COSM3603606 c.229+1G>A p.? Unknown 4:40097570-40097570 + ESCC-F81 COSM5048727 c.1813A>T p.S605C Substitution - Missense 4:40118017-40118017 + TCGA-AA-3819-01 COSM270955 c.359G>A p.R120H Substitution - Missense 4:40102204-40102204 + PD1582a COSM25639 c.3601_3602delTC p.S1201fs*11 Deletion - Frameshift 4:40121712-40121713 + TCGA-FD-A3NA-01 COSM1310054 c.4981C>G p.L1661V Substitution - Missense 4:40144638-40144638 + TCGA-27-2523-01 COSM3409290 c.1724G>A p.R575H Substitution - Missense 4:40117928-40117928 + LP6007401-DNA_A01 COSM5036070 c.3938G>C p.R1313T Substitution - Missense 4:40122049-40122049 + PDA_089 COSM5002945 c.1528C>T p.P510S Substitution - Missense 4:40112113-40112113 + Au4 COSM5604191 c.2056T>C p.S686P Substitution - Missense 4:40120167-40120167 + 74 COSM447847 c.1831G>A p.D611N Substitution - Missense 4:40119942-40119942 + TCGA-AC-A5XS-01 COSM5834840 c.2201_2203delAAG p.E735delE Deletion - In frame 4:40120312-40120314 + PT38 COSM5922407 c.944C>T p.S315F Substitution - Missense 4:40102789-40102789 + TCGA-EE-A3AE-06 COSM3603618 c.2249C>T p.S750F Substitution - Missense 4:40120360-40120360 + TCGA-F5-6814-01 COSM3428497 c.612G>T p.E204D Substitution - Missense 4:40102457-40102457 + pfg043T COSM4753406 c.4727T>G p.F1576C Substitution - Missense 4:40137024-40137024 + ESCC-D1 COSM5045137 c.2882A>G p.Q961R Substitution - Missense 4:40120993-40120993 + 0027_CRUK_PC_0027_T1_DNA COSM5422593 c.476A>C p.D159A Substitution - Missense 4:40102321-40102321 + S02294 COSM5688880 c.1279G>T p.V427F Substitution - Missense 4:40103124-40103124 + CHC205T COSM217310 c.3220A>G p.K1074E Substitution - Missense 4:40121331-40121331 + LUAD-E00897 COSM364618 c.1480G>C p.E494Q Substitution - Missense 4:40107006-40107006 + C086 COSM232845 c.3431C>T p.S1144L Substitution - Missense 4:40121542-40121542 + TCGA-EJ-7123-01 COSM3674178 c.1743A>G p.I581M Substitution - Missense 4:40117947-40117947 + TCGA-AG-3592-01 COSM5066740 c.1374-9C>A p.? Unknown 4:40106891-40106891 + LUAD-B01970 COSM356157 c.553A>C p.S185R Substitution - Missense 4:40102398-40102398 + 585208 COSM325902 c.3440G>T p.G1147V Substitution - Missense 4:40121551-40121551 + TCGA-BH-A203-01 COSM1485958 c.4859A>T p.D1620V Substitution - Missense 4:40142746-40142746 + 66 COSM5743022 c.2521C>T p.R841* Substitution - Nonsense 4:40120632-40120632 + SNU-C2B COSM2846887 c.1667G>A p.R556H Substitution - Missense 4:40117871-40117871 + 2492720 COSM5720229 c.2409G>A p.R803R Substitution - coding silent 4:40120520-40120520 + 1848_T COSM3946344 c.4062G>T p.G1354G Substitution - coding silent 4:40122173-40122173 + TCGA-EE-A183-06 COSM3603621 c.4143C>T p.P1381P Substitution - coding silent 4:40122254-40122254 + LUAD-RT-S01702 COSM379339 c.5222G>A p.R1741H Substitution - Missense 4:40152858-40152858 + DLD1 COSM2846893 c.1863T>A p.N621K Substitution - Missense 4:40119974-40119974 + CHEWS020 COSM4585078 c.2773delA p.T925fs*14 Deletion - Frameshift 4:40120884-40120884 + C086 COSM5535181 c.3974C>T p.S1325L Substitution - Missense 4:40122085-40122085 + TCGA-AP-A059-01 COSM1055304 c.4273G>T p.E1425* Substitution - Nonsense 4:40123201-40123201 + YUFARCI COSM1694252 c.2171C>T p.S724L Substitution - Missense 4:40120282-40120282 + PD24212a COSM5795436 c.4769A>G p.K1590R Substitution - Missense 4:40137066-40137066 + TCGA-BR-A4QL-01 COSM4124636 c.4512G>A p.Q1504Q Substitution - coding silent 4:40126315-40126315 + HCC2998 COSM1670956 c.475G>T p.D159Y Substitution - Missense 4:40102320-40102320 + PT13 COSM5895738 c.116C>T p.S39F Substitution - Missense 4:40097456-40097456 + PT53 COSM5941239 c.1195C>T p.P399S Substitution - Missense 4:40103040-40103040 + CSCC-11-T COSM4549907 c.4861G>T p.D1621Y Substitution - Missense 4:40142748-40142748 + J90_T COSM3946345 c.4533G>T p.R1511S Substitution - Missense 4:40131806-40131806 + S0083 COSM5884021 c.4690G>T p.E1564* Substitution - Nonsense 4:40136987-40136987 + J30_T COSM3946342 c.1619G>T p.R540L Substitution - Missense 4:40113463-40113463 + CCK81 COSM2846862 c.244G>A p.D82N Substitution - Missense 4:40102089-40102089 + HCC2218 COSM21725 c.847C>G p.P283A Substitution - Missense 4:40102692-40102692 + TCGA-B5-A11E-01 COSM1055297 c.2808A>C p.Q936H Substitution - Missense 4:40120919-40120919 + TCGA-DZ-6132-01 COSM3993667 c.2951C>G p.P984R Substitution - Missense 4:40121062-40121062 + TCGA-61-1738-01 COSM1328528 c.823G>A p.V275I Substitution - Missense 4:40102668-40102668 + T155 COSM1176735 c.837C>A p.F279L Substitution - Missense 4:40102682-40102682 + SNU-175 COSM1429658 c.2921C>T p.S974L Substitution - Missense 4:40121032-40121032 + TCGA-33-4566-01 COSM733496 c.2042C>A p.P681Q Substitution - Missense 4:40120153-40120153 + TCGA-EE-A2MD-06 COSM3603608 c.1081C>T p.P361S Substitution - Missense 4:40102926-40102926 + ESO-1748 COSM1258644 c.1758G>A p.S586S Substitution - coding silent 4:40117962-40117962 + TCGA-EE-A3AG-06 COSM3603607 c.1048C>T p.L350F Substitution - Missense 4:40102893-40102893 + RC-18 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + C008 COSM5523224 c.4735C>T p.Q1579* Substitution - Nonsense 4:40137032-40137032 + HCC2218 COSM21725 c.847C>G p.P283A Substitution - Missense 4:40102692-40102692 + TCGA-D1-A17Q-01 COSM1055312 c.5059C>T p.P1687S Substitution - Missense 4:40144716-40144716 + 587376 COSM1216567 c.2247A>C p.K749N Substitution - Missense 4:40120358-40120358 + TCGA-EI-6507-01 COSM1567340 c.1106C>T p.A369V Substitution - Missense 4:40102951-40102951 + S0087 COSM5884019 c.814T>A p.S272T Substitution - Missense 4:40102659-40102659 + TCGA-G4-6588-01 COSM1429665 c.4372_4373insA p.S1460fs*17 Insertion - Frameshift 4:40126175-40126176 + TCGA-GN-A263-01 COSM3603612 c.1300A>C p.K434Q Substitution - Missense 4:40103145-40103145 + pfg127T COSM1429668 c.4942delA p.N1650fs*17 Deletion - Frameshift 4:40142829-40142829 + 96 COSM5011272 c.371A>G p.E124G Substitution - Missense 4:40102216-40102216 + RC-T COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + TCGA-FJ-A3Z7-01 COSM3775836 c.3561C>T p.N1187N Substitution - coding silent 4:40121672-40121672 + sysucc-1370T COSM5471885 c.1496G>A p.R499H Substitution - Missense 4:40107022-40107022 + TCGA-D1-A0ZR-01 COSM1055303 c.4248G>A p.A1416A Substitution - coding silent 4:40123176-40123176 + CHC205T COSM217310 c.3220A>G p.K1074E Substitution - Missense 4:40121331-40121331 + TCGA-G7-6793-01 COSM3993666 c.346A>G p.I116V Substitution - Missense 4:40102191-40102191 + HCC134T COSM3746663 c.70G>T p.V24L Substitution - Missense 4:40097410-40097410 + CHC302T COSM3669278 c.2639A>G p.N880S Substitution - Missense 4:40120750-40120750 + TCGA-EB-A44N-01 COSM3603620 c.3664C>T p.P1222S Substitution - Missense 4:40121775-40121775 + TCGA-DM-A28C-01 COSM1429655 c.1274delC p.P426fs*6 Deletion - Frameshift 4:40103119-40103119 + TCGA-AR-A0TX-01 COSM447848 c.4277C>T p.S1426F Substitution - Missense 4:40123205-40123205 + TCGA-FR-A44A-06 COSM3917753 c.3855T>A p.S1285S Substitution - coding silent 4:40121966-40121966 + ESCC_BICR_040T COSM5430125 c.178G>A p.D60N Substitution - Missense 4:40097518-40097518 + TCGA-BR-4368-01 COSM4124629 c.1589C>A p.S530Y Substitution - Missense 4:40113433-40113433 + CHC796T COSM4954124 c.4188T>C p.G1396G Substitution - coding silent 4:40122299-40122299 + ESO-H01 COSM1258645 c.4459C>G p.Q1487E Substitution - Missense 4:40126262-40126262 + RKO COSM4614935 c.568_569insT p.S192fs*10 Insertion - Frameshift 4:40102413-40102414 + TCGA-AG-A002-01 COSM262284 c.3336G>T p.E1112D Substitution - Missense 4:40121447-40121447 + TCGA-D1-A103-01 COSM1055302 c.3904G>T p.E1302* Substitution - Nonsense 4:40122015-40122015 + TCGA-GC-A3RC-01 COSM3775835 c.3486T>C p.I1162I Substitution - coding silent 4:40121597-40121597 + STC232 COSM5060348 c.2124delA p.Y711fs*45 Deletion - Frameshift 4:40120235-40120235 + TCGA-DD-A3A0-01 COSM4934712 c.2107A>G p.I703V Substitution - Missense 4:40120218-40120218 + T3174 COSM4705317 c.3797delA p.N1268fs*2 Deletion - Frameshift 4:40121908-40121908 + BCM325T COSM4799000 c.3842C>T p.P1281L Substitution - Missense 4:40121953-40121953 + TCGA-A3-3346-01 COSM1495777 c.3632C>T p.P1211L Substitution - Missense 4:40121743-40121743 + TCGA-B6-A0IP-01 COSM447844 c.733C>A p.L245I Substitution - Missense 4:40102578-40102578 + TCGA-DK-A1AC-01 COSM1310053 c.4868G>A p.R1623K Substitution - Missense 4:40142755-40142755 + RKO COSM2846888 c.1682T>C p.V561A Substitution - Missense 4:40117886-40117886 + TCGA-GV-A3JZ-01 COSM1310050 c.1023G>A p.V341V Substitution - coding silent 4:40102868-40102868 + LUAD-CHTN-3090346 COSM357001 c.1855G>C p.E619Q Substitution - Missense 4:40119966-40119966 + LUAD_E00623 COSM354411 c.1112A>T p.D371V Substitution - Missense 4:40102957-40102957 + TCGA-BT-A2LB-01 COSM3775834 c.637A>C p.N213H Substitution - Missense 4:40102482-40102482 + KM12 COSM1429668 c.4942delA p.N1650fs*17 Deletion - Frameshift 4:40142829-40142829 + MOLT-4 COSM587194 c.40C>T p.R14W Substitution - Missense 4:40097380-40097380 + TCGA-66-2755-01 COSM733500 c.66T>G p.V22V Substitution - coding silent 4:40097406-40097406 + 2492722 COSM5720229 c.2409G>A p.R803R Substitution - coding silent 4:40120520-40120520 + TCGA-B0-5075-01 COSM481257 c.2796C>T p.G932G Substitution - coding silent 4:40120907-40120907 + 587376 COSM1216565 c.1426T>G p.F476V Substitution - Missense 4:40106952-40106952 + CSB5 COSM5026138 c.3609G>A p.Q1203Q Substitution - coding silent 4:40121720-40121720 + CSCC-44-T COSM4494660 c.4379C>T p.S1460L Substitution - Missense 4:40126182-40126182 + ME009T COSM222914 c.3982G>A p.E1328K Substitution - Missense 4:40122093-40122093 + TCGA-FS-A1Z3-06 COSM3603609 c.1144C>T p.P382S Substitution - Missense 4:40102989-40102989 + 0039_CRUK_PC_0039_T1_DNA COSM5421642 c.3264A>G p.E1088E Substitution - coding silent 4:40121375-40121375 + RC-8 COSM328562 c.1680G>T p.G560G Substitution - coding silent 4:40117884-40117884 + TCGA-AP-A0LM-01 COSM1055296 c.2600A>C p.K867T Substitution - Missense 4:40120711-40120711 + TCGA-24-0966-01 COSM75545 c.4225G>A p.V1409I Substitution - Missense 4:40123153-40123153 + TCGA-D8-A1JG-01 COSM1485955 c.2156C>A p.S719Y Substitution - Missense 4:40120267-40120267 + TCGA-FW-A3TU-06 COSM3603610 c.1192C>T p.P398S Substitution - Missense 4:40103037-40103037 + TCGA-DK-A2I6-01 COSM1310055 c.5115G>C p.L1705F Substitution - Missense 4:40144772-40144772 + RMS111_ COSM4419577 c.4759A>G p.T1587A Substitution - Missense 4:40137056-40137056 + SCMC_RM2_ COSM4419577 c.4759A>G p.T1587A Substitution - Missense 4:40137056-40137056 + TCGA-66-2789-01 COSM232846 c.3751C>T p.P1251S Substitution - Missense 4:40121862-40121862 + CHC205T COSM217310 c.3220A>G p.K1074E Substitution - Missense 4:40121331-40121331 + LUAD_E01147 COSM392816 c.4269_4270delGA p.W1423fs*1 Deletion - Frameshift 4:40123197-40123198 + ATL063 COSM5709233 c.1147G>A p.V383I Substitution - Missense 4:40102992-40102992 + HN_62318 COSM124652 c.3415G>A p.E1139K Substitution - Missense 4:40121526-40121526 + TCGA-37-3789-01 COSM733493 c.3762A>G p.L1254L Substitution - coding silent 4:40121873-40121873 + SNU-C2B COSM4615347 c.4941_4942insA p.N1650fs*14 Insertion - Frameshift 4:40142828-40142829 + T613 COSM2846874 c.719C>T p.P240L Substitution - Missense 4:40102564-40102564 + PT24_1 COSM4799000 c.3842C>T p.P1281L Substitution - Missense 4:40121953-40121953 + TCGA-85-6561-01 COSM733494 c.3523C>A p.P1175T Substitution - Missense 4:40121634-40121634 + TCGA-A3-3346-01 COSM1495776 c.3640C>T p.H1214Y Substitution - Missense 4:40121751-40121751 + YUPROST COSM1694251 c.34C>T p.P12S Substitution - Missense 4:40097374-40097374 + TCGA-18-3406-01 COSM733499 c.1826G>T p.R609I Substitution - Missense 4:40119937-40119937 + RK083_C01 COSM1633679 c.1495C>A p.R499S Substitution - Missense 4:40107021-40107021 + TCGA-EE-A2MU-06 COSM3603614 c.1495C>T p.R499C Substitution - Missense 4:40107021-40107021 + HCT8 COSM2846893 c.1863T>A p.N621K Substitution - Missense 4:40119974-40119974 + ICGC_MB58 COSM3670334 c.1084A>G p.M362V Substitution - Missense 4:40102929-40102929 + C125 COSM4616904 c.955C>T p.L319L Substitution - coding silent 4:40102800-40102800 + SH-1537 COSM5018497 c.307G>T p.V103F Substitution - Missense 4:40102152-40102152 + S01020 COSM5665231 c.4030G>A p.A1344T Substitution - Missense 4:40122141-40122141 + T44 COSM5344707 c.2600A>T p.K867I Substitution - Missense 4:40120711-40120711 + LIM2405 COSM4613624 c.2449delA p.K818fs*10 Deletion - Frameshift 4:40120560-40120560 + TCGA-AP-A059-01 COSM1055300 c.3193G>T p.A1065S Substitution - Missense 4:40121304-40121304 + HCC2218 COSM21725 c.847C>G p.P283A Substitution - Missense 4:40102692-40102692 + PD1582a COSM25639 c.3601_3602delTC p.S1201fs*11 Deletion - Frameshift 4:40121712-40121713 + sysucc-1163T COSM5459109 c.69C>T p.V23V Substitution - coding silent 4:40097409-40097409 + TCGA-AD-5900-01 COSM1429654 c.551C>T p.S184L Substitution - Missense 4:40102396-40102396 + 2T COSM3733659 c.1582G>T p.A528S Substitution - Missense 4:40112167-40112167 + T3152 COSM4705316 c.2531C>T p.P844L Substitution - Missense 4:40120642-40120642 + LUAD-YINHD COSM351021 c.1116C>T p.L372L Substitution - coding silent 4:40102961-40102961 + 54 COSM5734910 c.5002G>C p.E1668Q Substitution - Missense 4:40144659-40144659 + ESCC_BICR_013T COSM5439378 c.4873G>C p.E1625Q Substitution - Missense 4:40142760-40142760 + TCGA-AP-A056-01 COSM1055292 c.306C>T p.F102F Substitution - coding silent 4:40102151-40102151 + TCGA-BS-A0UF-01 COSM1055299 c.2986G>T p.A996S Substitution - Missense 4:40121097-40121097 + TCGA-CA-6717-01 COSM1429661 c.3454C>T p.P1152S Substitution - Missense 4:40121565-40121565 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.390856;Hs.391051;Hs.391083;Hs.391286;Hs.391327;Hs.391463 4p14

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.5310+675A>C 4 40156529 HC A C Missense p.K434Q c.1300A>C 4 40104765 CM A C Missense p.K547T c.1640A>C 4 40115104 STAD A C Missense p.N213H c.637A>C 4 40104102 BLCA A - Frameshift p.Y711Ifs*45 c.2127delA 4 40121855 STAD AGGGAG - IntronicDeletion . c.4786-544_4786-539delAGAGGG 4 40143745 CM A G Missense p.D514G c.1541A>G 4 40113746 THCA A G Missense p.D857G c.2570A>G 4 40122301 STAD A G Missense p.I912V c.2734A>G 4 40122465 HNSC A G Missense p.K1074E c.3220A>G 4 40122951 HC A G Missense p.K119R c.356A>G 4 40103821 UCEC A G Missense p.M362V c.1084A>G 4 40104549 MB A G Missense p.M366V c.1096A>G 4 40104561 BRCA A G Missense p.N981D c.2941A>G 4 40122672 UCEC A G Missense p.Y1655C c.4964A>G 4 40144471 SCLC A G Synonymous p.L1254L c.3762A>G 4 40123493 LUSC A T Missense p.D1620V c.4859A>T 4 40144366 BRCA A T Missense p.R609S c.1827A>T 4 40121558 LUSC C A Missense p.H533Q c.1599C>A 4 40115063 HNSC C A Missense p.L245I c.733C>A 4 40104198 BRCA C A Missense p.P1175T c.3523C>A 4 40123254 LUSC C A Missense p.P320H c.959C>A 4 40104424 CM C A Missense p.R499S c.1495C>A 4 40108641 HC C A Missense p.S530Y c.1589C>A 4 40115053 STAD C A Missense p.S719Y c.2156C>A 4 40121887 BRCA CG GT Missense p.P449R c.1346_1347delinsGT 4 40104811 CM C G Missense p.L1661V c.4981C>G 4 40146258 BLCA C G Missense p.P283A c.847C>G 4 40104312 BRCA C G Missense p.Q1462E c.4384C>G 4 40127807 BRCA C G Missense p.Q1487E c.4459C>G 4 40127882 ESCA C G Missense p.S206C c.617C>G 4 40104082 LUAD C T Missense p.L350F c.1048C>T 4 40104513 CM C T Missense p.P1251S c.3751C>T 4 40123482 LUSC C T Missense p.P12L c.35C>T 4 40098995 CM C T Missense p.P1394L c.4181C>T 4 40123912 CM C T Missense p.P361S c.1081C>T 4 40104546 CM C T Missense p.P681S c.2041C>T 4 40121772 CM C T Missense p.R14W c.40C>T 4 40099000 LUAD C T Missense p.R499C c.1495C>T 4 40108641 CM C T Missense p.S1475F c.4424C>T 4 40127847 GBM C T Missense p.S724L c.2171C>T 4 40121902 CM C T Missense p.S750F c.2249C>T 4 40121980 CM C T Missense p.S922F c.2765C>T 4 40122496 CM C T Missense p.S944F c.2831C>T 4 40122562 CM C T Missense p.T312I c.935C>T 4 40104400 BRCA C T Missense p.T763M c.2288C>T 4 40122019 STAD C T Nonsense p.Q421* c.1261C>T 4 40104726 CM C T Synonymous p.C274C c.822C>T 4 40104287 LUAD C T Synonymous p.G932G c.2796C>T 4 40122527 RCCC C T Synonymous p.N1537N c.4611C>T 4 40133504 CM C T Synonymous p.N222N c.666C>T 4 40104131 LUAD C T Synonymous p.P1381P c.4143C>T 4 40123874 CM G A Missense p.A1669T c.5005G>A 4 40146282 UCEC G A Missense p.E1139K c.3415G>A 4 40123146 HNSC G A Missense p.E1328K c.3982G>A 4 40123713 CM G A Missense p.E1512K c.4534G>A 4 40133427 CM G A Missense p.E955K c.2863G>A 4 40122594 HNSC G A Missense p.E955K c.2863G>A 4 40122594 MM G A Missense p.G304D c.911G>A 4 40104376 BLCA G A Missense p.G932D c.2795G>A 4 40122526 GBM G A Missense p.R120H c.359G>A 4 40103824 COREAD G A Missense p.R575H c.1724G>A 4 40119548 GBM G A Missense p.V1176M c.3526G>A 4 40123257 UCEC G A Missense p.V1409I c.4225G>A 4 40124773 OV G A SpliceDonorSNV . c.229+1G>A 4 40099190 CM G A Synonymous p.A1416A c.4248G>A 4 40124796 UCEC G A Synonymous p.E1170E c.3510G>A 4 40123241 CM G A Synonymous p.L1686L c.5058G>A 4 40146335 UCEC G A Synonymous p.Q1203Q c.3609G>A 4 40123340 BRCA G A Synonymous p.S1216S c.3648G>A 4 40123379 MM G A Synonymous p.S586S c.1758G>A 4 40119582 ESCA G A Synonymous p.V341V c.1023G>A 4 40104488 BLCA G C Missense p.D1454H c.4360G>C 4 40127783 BRCA G C Missense p.E1434Q c.4300G>C 4 40125795 BRCA G C Missense p.E849Q c.2545G>C 4 40122276 BLCA G C Missense p.K433N c.1299G>C 4 40104764 ESCA G C Missense p.L1705F c.5115G>C 4 40146392 BLCA G - Frameshift p.R662Kfs*4 c.1985delG 4 40121716 RCCC G T Missense p.G1147V c.3440G>T 4 40123171 SCLC G T Missense p.G378V c.1133G>T 4 40104598 LUAD G T Missense p.R555M c.1664G>T 4 40115128 LUAD G T Missense p.R609I c.1826G>T 4 40121557 LUSC G T Missense p.V577F c.1729G>T 4 40119553 NB G T Nonsense p.G450* c.1348G>T 4 40104813 CM G T Nonsense p.G947* c.2839G>T 4 40122570 GBM T A Missense p.H845Q c.2535T>A 4 40122266 BRCA T A Missense p.N1316K c.3948T>A 4 40123679 MM T C Missense p.L1092P c.3275T>C 4 40123006 CM T C Missense p.L1309P c.3926T>C 4 40123657 HNSC T C Missense p.S774P c.2320T>C 4 40122051 BRCA T C Missense p.V1011A c.3032T>C 4 40122763 LUSC T C Missense p.V284A c.851T>C 4 40104316 HNSC T G Missense p.L1472V c.4414T>G 4 40127837 LUAD T G Synonymous p.V22V c.66T>G 4 40099026 LUSC