Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 5 154299581 154299581 + Silent SNP A A G TCGA-OR-A5KP-01A-11D-A30A-10 TCGA-OR-A5KP-10A-01D-A30A-10 g.chr5:154299581A>G c.1545T>C c.(1543-1545)ctT>ctC p.L515L BLCA 5 154267890 154267890 + Silent SNP G G T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr5:154267890G>T c.4407C>A c.(4405-4407)ctC>ctA p.L1469L BLCA 5 154268890 154268890 + Missense_Mutation SNP C C G TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr5:154268890C>G c.4350G>C c.(4348-4350)gaG>gaC p.E1450D BLCA 5 154272068 154272068 + Silent SNP C C T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr5:154272068C>T c.3639G>A c.(3637-3639)ctG>ctA p.L1213L BLCA 5 154278781 154278781 + Missense_Mutation SNP C C G TCGA-XF-A9SK-01A-11D-A42E-08 TCGA-XF-A9SK-10A-01D-A42H-08 g.chr5:154278781C>G c.3104G>C c.(3103-3105)aGa>aCa p.R1035T BLCA 5 154284069 154284069 + Missense_Mutation SNP C C T TCGA-E7-A4IJ-01A-31D-A26M-08 TCGA-E7-A4IJ-10A-01D-A26K-08 g.chr5:154284069C>T c.2630G>A c.(2629-2631)aGa>aAa p.R877K BLCA 5 154284173 154284173 + Missense_Mutation SNP C C A TCGA-GU-A42Q-01A-11D-A23U-08 TCGA-GU-A42Q-10A-01D-A23U-08 g.chr5:154284173C>A c.2526G>T c.(2524-2526)aaG>aaT p.K842N BLCA 5 154287153 154287153 + Missense_Mutation SNP G G A TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr5:154287153G>A c.2393C>T c.(2392-2394)gCg>gTg p.A798V BLCA 5 154291355 154291355 + Missense_Mutation SNP G G A TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr5:154291355G>A c.2099C>T c.(2098-2100)tCa>tTa p.S700L BLCA 5 154292599 154292599 + Splice_Site SNP C C G TCGA-K4-AAQO-01A-11D-A38G-08 TCGA-K4-AAQO-10A-01D-A38J-08 g.chr5:154292599C>G c.e14-1 BLCA 5 154296709 154296709 + Silent SNP C C T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr5:154296709C>T c.1704G>A c.(1702-1704)ctG>ctA p.L568L BLCA 5 154296732 154296732 + Missense_Mutation SNP C C T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr5:154296732C>T c.1681G>A c.(1681-1683)Gaa>Aaa p.E561K BLCA 5 154307068 154307068 + Silent SNP C C T TCGA-GU-A42P-01A-11D-A23U-08 TCGA-GU-A42P-10A-01D-A23U-08 g.chr5:154307068C>T c.957G>A c.(955-957)cgG>cgA p.R319R BLCA 5 154308188 154308188 + Silent SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr5:154308188C>T c.813G>A c.(811-813)aaG>aaA p.K271K BLCA 5 154308191 154308191 + Silent SNP C C T TCGA-FD-A5BT-01A-11D-A26M-08 TCGA-FD-A5BT-10A-01D-A26K-08 g.chr5:154308191C>T c.810G>A c.(808-810)ctG>ctA p.L270L BRCA 5 154282237 154282237 + Splice_Site SNP C C A TCGA-BH-A0HY-01A-11W-A071-09 TCGA-BH-A0HY-10A-02W-A071-09 g.chr5:154282237C>A c.e20-1 BRCA 5 154284974 154284974 + Missense_Mutation SNP T T C TCGA-BH-A0B4-01A-11W-A019-09 TCGA-BH-A0B4-10A-01W-A021-09 g.chr5:154284974T>C c.2458A>G c.(2458-2460)Att>Gtt p.I820V BRCA 5 154304056 154304056 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr5:154304056A>C c.1352T>G c.(1351-1353)gTg>gGg p.V451G BRCA 5 154308089 154308089 + Missense_Mutation SNP A A C TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr5:154308089A>C c.912T>G c.(910-912)ttT>ttG p.F304L BRCA 5 154316741 154316741 + Silent SNP T T G TCGA-E2-A574-01A-11D-A29N-09 TCGA-E2-A574-10A-01D-A29N-09 g.chr5:154316741T>G c.171A>C c.(169-171)atA>atC p.I57I BRCA 5 154317530 154317530 + Missense_Mutation SNP C C T TCGA-A2-A0T6-01A-11D-A099-09 TCGA-A2-A0T6-10A-01D-A099-09 g.chr5:154317530C>T c.164G>A c.(163-165)cGa>cAa p.R55Q CESC 5 154272068 154272068 + Silent SNP C C T TCGA-C5-A1BK-01B-11D-A13W-08 TCGA-C5-A1BK-10A-01D-A13W-08 g.chr5:154272068C>T c.3639G>A c.(3637-3639)ctG>ctA p.L1213L CESC 5 154272083 154272083 + Silent SNP C C T TCGA-Q1-A73P-01A-11D-A32I-09 TCGA-Q1-A73P-10B-01D-A32I-09 g.chr5:154272083C>T c.3624G>A c.(3622-3624)ttG>ttA p.L1208L CESC 5 154278076 154278076 + Missense_Mutation SNP C C G TCGA-DG-A2KM-01A-11D-A17W-09 TCGA-DG-A2KM-10A-01D-A17W-09 g.chr5:154278076C>G c.3269G>C c.(3268-3270)aGa>aCa p.R1090T CESC 5 154280963 154280963 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr5:154280963G>A c.2950C>T c.(2950-2952)Cac>Tac p.H984Y CESC 5 154280965 154280965 + Missense_Mutation SNP G G C TCGA-EX-A69L-01A-11D-A32I-09 TCGA-EX-A69L-10A-01D-A32I-09 g.chr5:154280965G>C c.2948C>G c.(2947-2949)tCt>tGt p.S983C CESC 5 154317604 154317604 + Silent SNP G G A TCGA-Q1-A73P-01A-11D-A32I-09 TCGA-Q1-A73P-10B-01D-A32I-09 g.chr5:154317604G>A c.90C>T c.(88-90)ttC>ttT p.F30F CHOL 5 154270801 154270801 + Splice_Site SNP C C T TCGA-W5-AA2H-01A-31D-A417-09 TCGA-W5-AA2H-10A-01D-A41A-09 g.chr5:154270801C>T c.4262G>A c.(4261-4263)tGt>tAt p.C1421Y COAD 5 154267921 154267921 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:154267921T>C c.4376A>G c.(4375-4377)gAt>gGt p.D1459G COAD 5 154268966 154268966 + Missense_Mutation SNP T T C TCGA-AA-3549-01A-02W-0831-10 TCGA-AA-3549-10A-01W-0831-10 g.chr5:154268966T>C c.4274A>G c.(4273-4275)aAa>aGa p.K1425R COAD 5 154270969 154270969 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr5:154270969G>A c.4094C>T c.(4093-4095)gCc>gTc p.A1365V COAD 5 154271208 154271208 + Silent SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr5:154271208C>T c.3855G>A c.(3853-3855)ctG>ctA p.L1285L COAD 5 154271213 154271213 + Missense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr5:154271213G>A c.3850C>T c.(3850-3852)Cgt>Tgt p.R1284C COAD 5 154272043 154272043 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr5:154272043C>T c.3664G>A c.(3664-3666)Gag>Aag p.E1222K COAD 5 154272092 154272092 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr5:154272092G>A c.3615C>T c.(3613-3615)tgC>tgT p.C1205C COAD 5 154275815 154275815 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr5:154275815T>C c.3434A>G c.(3433-3435)tAc>tGc p.Y1145C COAD 5 154278000 154278000 + Splice_Site SNP C C A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr5:154278000C>A c.3345G>T c.(3343-3345)caG>caT p.Q1115H COAD 5 154280908 154280908 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr5:154280908T>C c.3005A>G c.(3004-3006)cAt>cGt p.H1002R COAD 5 154282108 154282108 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr5:154282108C>A c.2857G>T c.(2857-2859)Gca>Tca p.A953S COAD 5 154282719 154282719 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:154282719C>T c.2649G>A c.(2647-2649)gtG>gtA p.V883V COAD 5 154282722 154282722 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:154282722A>T c.2646T>A c.(2644-2646)gaT>gaA p.D882E COAD 5 154284103 154284103 + Missense_Mutation SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr5:154284103C>T c.2596G>A c.(2596-2598)Gac>Aac p.D866N COAD 5 154287275 154287275 + Silent SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr5:154287275C>T c.2271G>A c.(2269-2271)tcG>tcA p.S757S COAD 5 154287276 154287276 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:154287276G>T c.2270C>A c.(2269-2271)tCg>tAg p.S757* COAD 5 154287370 154287370 + Frame_Shift_Del DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr5:154287370delT c.2176delA c.(2176-2178)agtfs p.S726fs COAD 5 154296683 154296683 + Missense_Mutation SNP T T C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:154296683T>C c.1730A>G c.(1729-1731)cAt>cGt p.H577R COAD 5 154297547 154297547 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr5:154297547G>A c.1617C>T c.(1615-1617)caC>caT p.H539H COAD 5 154300942 154300942 + Missense_Mutation SNP T T C TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr5:154300942T>C c.1423A>G c.(1423-1425)Act>Gct p.T475A COAD 5 154307045 154307045 + Missense_Mutation SNP G G A TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr5:154307045G>A c.980C>T c.(979-981)tCa>tTa p.S327L COAD 5 154315505 154315505 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:154315505G>T c.405C>A c.(403-405)ttC>ttA p.F135L COAD 5 154315574 154315574 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr5:154315574T>C c.336A>G c.(334-336)atA>atG p.I112M COADREAD 5 154267921 154267921 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr5:154267921T>C c.4376A>G c.(4375-4377)gAt>gGt p.D1459G COADREAD 5 154268966 154268966 + Missense_Mutation SNP T T C TCGA-AA-3549-01A-02W-0831-10 TCGA-AA-3549-10A-01W-0831-10 g.chr5:154268966T>C c.4274A>G c.(4273-4275)aAa>aGa p.K1425R COADREAD 5 154270969 154270969 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr5:154270969G>A c.4094C>T c.(4093-4095)gCc>gTc p.A1365V COADREAD 5 154271208 154271208 + Silent SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr5:154271208C>T c.3855G>A c.(3853-3855)ctG>ctA p.L1285L COADREAD 5 154271213 154271213 + Missense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr5:154271213G>A c.3850C>T c.(3850-3852)Cgt>Tgt p.R1284C COADREAD 5 154272043 154272043 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr5:154272043C>T c.3664G>A c.(3664-3666)Gag>Aag p.E1222K COADREAD 5 154272092 154272092 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr5:154272092G>A c.3615C>T c.(3613-3615)tgC>tgT p.C1205C COADREAD 5 154275815 154275815 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr5:154275815T>C c.3434A>G c.(3433-3435)tAc>tGc p.Y1145C COADREAD 5 154278000 154278000 + Splice_Site SNP C C A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr5:154278000C>A c.3345G>T c.(3343-3345)caG>caT p.Q1115H COADREAD 5 154278135 154278135 + Silent SNP C C T TCGA-DC-6681-01A-11D-1826-10 TCGA-DC-6681-10A-01D-1826-10 g.chr5:154278135C>T c.3210G>A c.(3208-3210)acG>acA p.T1070T COADREAD 5 154280908 154280908 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr5:154280908T>C c.3005A>G c.(3004-3006)cAt>cGt p.H1002R COADREAD 5 154282108 154282108 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr5:154282108C>A c.2857G>T c.(2857-2859)Gca>Tca p.A953S COADREAD 5 154282719 154282719 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:154282719C>T c.2649G>A c.(2647-2649)gtG>gtA p.V883V COADREAD 5 154282722 154282722 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr5:154282722A>T c.2646T>A c.(2644-2646)gaT>gaA p.D882E COADREAD 5 154284103 154284103 + Missense_Mutation SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr5:154284103C>T c.2596G>A c.(2596-2598)Gac>Aac p.D866N COADREAD 5 154287187 154287187 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:154287187G>A c.2359C>T c.(2359-2361)Cgg>Tgg p.R787W COADREAD 5 154287275 154287275 + Silent SNP C C T TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr5:154287275C>T c.2271G>A c.(2269-2271)tcG>tcA p.S757S COADREAD 5 154287276 154287276 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:154287276G>T c.2270C>A c.(2269-2271)tCg>tAg p.S757* COADREAD 5 154287314 154287314 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr5:154287314C>T c.2232G>A c.(2230-2232)aaG>aaA p.K744K COADREAD 5 154287370 154287370 + Frame_Shift_Del DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr5:154287370delT c.2176delA c.(2176-2178)agtfs p.S726fs COADREAD 5 154296683 154296683 + Missense_Mutation SNP T T C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr5:154296683T>C c.1730A>G c.(1729-1731)cAt>cGt p.H577R COADREAD 5 154297547 154297547 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr5:154297547G>A c.1617C>T c.(1615-1617)caC>caT p.H539H COADREAD 5 154300942 154300942 + Missense_Mutation SNP T T C TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr5:154300942T>C c.1423A>G c.(1423-1425)Act>Gct p.T475A COADREAD 5 154307007 154307007 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:154307007A>C c.1018T>G c.(1018-1020)Tta>Gta p.L340V COADREAD 5 154307045 154307045 + Missense_Mutation SNP G G A TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr5:154307045G>A c.980C>T c.(979-981)tCa>tTa p.S327L COADREAD 5 154311118 154311118 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr5:154311118G>A c.681C>T c.(679-681)aaC>aaT p.N227N COADREAD 5 154315505 154315505 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:154315505G>T c.405C>A c.(403-405)ttC>ttA p.F135L COADREAD 5 154315574 154315574 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr5:154315574T>C c.336A>G c.(334-336)atA>atG p.I112M ESCA 5 154291332 154291332 + Missense_Mutation SNP G G A TCGA-Z6-A8JD-01A-11D-A36J-09 TCGA-Z6-A8JD-10A-01D-A36M-09 g.chr5:154291332G>A c.2122C>T c.(2122-2124)Cac>Tac p.H708Y GBM 5 154275813 154275813 + Missense_Mutation SNP G G C TCGA-32-4209-01A-01D-1353-08 TCGA-32-4209-10A-01D-1353-08 g.chr5:154275813G>C c.3436C>G c.(3436-3438)Cac>Gac p.H1146D GBM 5 154311130 154311130 + Silent SNP A A G TCGA-32-1986-01A-01D-1494-08 TCGA-32-1986-10A-01D-1494-08 g.chr5:154311130A>G c.669T>C c.(667-669)gcT>gcC p.A223A GBMLGG 5 154270897 154270897 + Missense_Mutation SNP T T C TCGA-CS-6667-01A-12D-2024-08 TCGA-CS-6667-10A-01D-2024-08 g.chr5:154270897T>C c.4166A>G c.(4165-4167)cAa>cGa p.Q1389R GBMLGG 5 154275813 154275813 + Missense_Mutation SNP G G C TCGA-32-4209-01A-01D-1353-08 TCGA-32-4209-10A-01D-1353-08 g.chr5:154275813G>C c.3436C>G c.(3436-3438)Cac>Gac p.H1146D GBMLGG 5 154307077 154307077 + Silent SNP A A G TCGA-CS-6666-01A-11D-1893-08 TCGA-CS-6666-10A-01D-1893-08 g.chr5:154307077A>G c.948T>C c.(946-948)tcT>tcC p.S316S GBMLGG 5 154311130 154311130 + Silent SNP A A G TCGA-32-1986-01A-01D-1494-08 TCGA-32-1986-10A-01D-1494-08 g.chr5:154311130A>G c.669T>C c.(667-669)gcT>gcC p.A223A GBMLGG 5 154315435 154315438 + Frame_Shift_Del DEL AAGT AAGT - TCGA-HT-7855-01A-11D-2395-08 TCGA-HT-7855-10A-01D-2396-08 g.chr5:154315435_154315438delAAGT c.472_475delACTT c.(472-477)acttgtfs p.TC158fs HNSC 5 154268973 154268973 + Missense_Mutation SNP C C T TCGA-IQ-A61I-01A-11D-A30E-08 TCGA-IQ-A61I-10A-01D-A30H-08 g.chr5:154268973C>T c.4267G>A c.(4267-4269)Gaa>Aaa p.E1423K HNSC 5 154271032 154271032 + Missense_Mutation SNP C C T TCGA-CV-A45R-01A-11D-A24D-08 TCGA-CV-A45R-10A-01D-A24F-08 g.chr5:154271032C>T c.4031G>A c.(4030-4032)aGa>aAa p.R1344K HNSC 5 154278159 154278159 + Missense_Mutation SNP C C A TCGA-CN-4738-01A-02D-1512-08 TCGA-CN-4738-10A-01D-1512-08 g.chr5:154278159C>A c.3186G>T c.(3184-3186)aaG>aaT p.K1062N HNSC 5 154278774 154278774 + Silent SNP G G A TCGA-H7-A6C5-01A-11D-A30E-08 TCGA-H7-A6C5-10A-01D-A30H-08 g.chr5:154278774G>A c.3111C>T c.(3109-3111)ggC>ggT p.G1037G HNSC 5 154287226 154287226 + Missense_Mutation SNP C C G TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chr5:154287226C>G c.2320G>C c.(2320-2322)Gag>Cag p.E774Q HNSC 5 154296703 154296703 + Silent SNP C C T TCGA-CV-6939-01A-11D-1912-08 TCGA-CV-6939-10A-01D-1912-08 g.chr5:154296703C>T c.1710G>A c.(1708-1710)ctG>ctA p.L570L HNSC 5 154305443 154305443 + Silent SNP G G T TCGA-CN-5373-01A-01D-1434-08 TCGA-CN-5373-10A-01D-1434-08 g.chr5:154305443G>T c.1272C>A c.(1270-1272)ggC>ggA p.G424G HNSC 5 154311746 154311746 + Nonsense_Mutation SNP G G A TCGA-BB-A6UM-01A-12D-A34J-08 TCGA-BB-A6UM-10A-01D-A34M-08 g.chr5:154311746G>A c.574C>T c.(574-576)Cga>Tga p.R192* KIPAN 5 154268882 154268882 + Splice_Site SNP T T C TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr5:154268882T>C c.4358A>G c.(4357-4359)aAg>aGg p.K1453R KIPAN 5 154270986 154270986 + Silent SNP G G A TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr5:154270986G>A c.4077C>T c.(4075-4077)ctC>ctT p.L1359L KIPAN 5 154271054 154271054 + Missense_Mutation SNP T T A TCGA-CJ-4870-01A-01D-1373-10 TCGA-CJ-4870-11A-01D-1373-10 g.chr5:154271054T>A c.4009A>T c.(4009-4011)Agg>Tgg p.R1337W KIPAN 5 154278063 154278063 + Silent SNP C C T TCGA-BP-4768-01A-01D-1366-10 TCGA-BP-4768-11A-01D-1366-10 g.chr5:154278063C>T c.3282G>A c.(3280-3282)gaG>gaA p.E1094E KIPAN 5 154278113 154278113 + Missense_Mutation SNP C C T TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr5:154278113C>T c.3232G>A c.(3232-3234)Gta>Ata p.V1078I KIPAN 5 154287300 154287300 + Frame_Shift_Del DEL A A - TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr5:154287300delA c.2246delT c.(2245-2247)ttgfs p.L749fs KIRC 5 154268882 154268882 + Splice_Site SNP T T C TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr5:154268882T>C c.4358A>G c.(4357-4359)aAg>aGg p.K1453R KIRC 5 154270986 154270986 + Silent SNP G G A TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr5:154270986G>A c.4077C>T c.(4075-4077)ctC>ctT p.L1359L KIRC 5 154271054 154271054 + Missense_Mutation SNP T T A TCGA-CJ-4870-01A-01D-1373-10 TCGA-CJ-4870-11A-01D-1373-10 g.chr5:154271054T>A c.4009A>T c.(4009-4011)Agg>Tgg p.R1337W KIRC 5 154278063 154278063 + Silent SNP C C T TCGA-BP-4768-01A-01D-1366-10 TCGA-BP-4768-11A-01D-1366-10 g.chr5:154278063C>T c.3282G>A c.(3280-3282)gaG>gaA p.E1094E KIRC 5 154287300 154287300 + Frame_Shift_Del DEL A A - TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr5:154287300delA c.2246delT c.(2245-2247)ttgfs p.L749fs KIRP 5 154278113 154278113 + Missense_Mutation SNP C C T TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr5:154278113C>T c.3232G>A c.(3232-3234)Gta>Ata p.V1078I LGG 5 154270897 154270897 + Missense_Mutation SNP T T C TCGA-CS-6667-01A-12D-2024-08 TCGA-CS-6667-10A-01D-2024-08 g.chr5:154270897T>C c.4166A>G c.(4165-4167)cAa>cGa p.Q1389R LGG 5 154307077 154307077 + Silent SNP A A G TCGA-CS-6666-01A-11D-1893-08 TCGA-CS-6666-10A-01D-1893-08 g.chr5:154307077A>G c.948T>C c.(946-948)tcT>tcC p.S316S LGG 5 154315435 154315438 + Frame_Shift_Del DEL AAGT AAGT - TCGA-HT-7855-01A-11D-2395-08 TCGA-HT-7855-10A-01D-2396-08 g.chr5:154315435_154315438delAAGT c.472_475delACTT c.(472-477)acttgtfs p.TC158fs LIHC 5 154287212 154287212 + Silent SNP T T C TCGA-CC-A7II-01A-11D-A33K-10 TCGA-CC-A7II-10A-01D-A33K-10 g.chr5:154287212T>C c.2334A>G c.(2332-2334)tcA>tcG p.S778S LIHC 5 154287223 154287223 + Missense_Mutation SNP T T C TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr5:154287223T>C c.2323A>G c.(2323-2325)Aat>Gat p.N775D LIHC 5 154311018 154311018 + Splice_Site SNP C C T TCGA-DD-A4NR-01A-11D-A30V-10 TCGA-DD-A4NR-10A-01D-A30V-10 g.chr5:154311018C>T c.781G>A c.(781-783)Ggg>Agg p.G261R LIHC 5 154311099 154311099 + Missense_Mutation SNP C C T TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr5:154311099C>T c.700G>A c.(700-702)Gct>Act p.A234T LIHC 5 154311736 154311736 + Missense_Mutation SNP T T C TCGA-DD-AAE3-01A-11D-A40R-10 TCGA-DD-AAE3-10A-01D-A40U-10 g.chr5:154311736T>C c.584A>G c.(583-585)gAt>gGt p.D195G LIHC 5 154311783 154311783 + Silent SNP A A G TCGA-CC-A7IH-01A-11D-A33K-10 TCGA-CC-A7IH-10A-01D-A33K-10 g.chr5:154311783A>G c.537T>C c.(535-537)atT>atC p.I179I LIHC 5 154317547 154317547 + Silent SNP T T C TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr5:154317547T>C c.147A>G c.(145-147)ccA>ccG p.P49P LUAD 5 154270801 154270801 + Splice_Site SNP C C A TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr5:154270801C>A c.4262G>T c.(4261-4263)tGt>tTt p.C1421F LUAD 5 154270922 154270922 + Silent SNP A A G TCGA-67-3772-01A-01W-0928-08 TCGA-67-3772-10A-01W-0928-08 g.chr5:154270922A>G c.4141T>C c.(4141-4143)Ttg>Ctg p.L1381L LUAD 5 154271039 154271039 + Missense_Mutation SNP C C G TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr5:154271039C>G c.4024G>C c.(4024-4026)Gac>Cac p.D1342H LUAD 5 154271093 154271093 + Missense_Mutation SNP C C T TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr5:154271093C>T c.3970G>A c.(3970-3972)Gaa>Aaa p.E1324K LUAD 5 154275708 154275708 + Missense_Mutation SNP G G T TCGA-44-A47A-01A-21D-A24D-08 TCGA-44-A47A-10A-01D-A24F-08 g.chr5:154275708G>T c.3541C>A c.(3541-3543)Cag>Aag p.Q1181K LUAD 5 154278851 154278851 + Nonsense_Mutation SNP T T A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr5:154278851T>A c.3034A>T c.(3034-3036)Aag>Tag p.K1012* LUAD 5 154292552 154292552 + Silent SNP G G A TCGA-97-7547-01A-11D-2036-08 TCGA-97-7547-10A-01D-2036-08 g.chr5:154292552G>A c.1902C>T c.(1900-1902)acC>acT p.T634T LUAD 5 154300914 154300914 + Missense_Mutation SNP G G A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr5:154300914G>A c.1451C>T c.(1450-1452)cCc>cTc p.P484L LUAD 5 154306962 154306962 + Missense_Mutation SNP T T C TCGA-69-7760-01A-11D-2167-08 TCGA-69-7760-10A-01D-2167-08 g.chr5:154306962T>C c.1063A>G c.(1063-1065)Aca>Gca p.T355A LUSC 5 154287306 154287306 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr5:154287306G>A c.2240C>T c.(2239-2241)cCc>cTc p.P747L LUSC 5 154308114 154308114 + Missense_Mutation SNP G G T TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr5:154308114G>T c.887C>A c.(886-888)cCa>cAa p.P296Q LUSC 5 154311721 154311721 + Missense_Mutation SNP G G C TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr5:154311721G>C c.599C>G c.(598-600)tCc>tGc p.S200C LUSC 5 154316660 154316660 + Silent SNP G G T TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr5:154316660G>T c.252C>A c.(250-252)acC>acA p.T84T LUSC 5 154317677 154317677 + Missense_Mutation SNP C C T TCGA-34-5928-01A-11D-1817-08 TCGA-34-5928-10A-01D-1817-08 g.chr5:154317677C>T c.17G>A c.(16-18)cGg>cAg p.R6Q OV 5 154278854 154278854 + Missense_Mutation SNP C C G TCGA-13-1409-01A-01W-0492-08 TCGA-13-1409-10A-01W-0493-08 g.chr5:154278854C>G c.3031G>C c.(3031-3033)Gcc>Ccc p.A1011P PAAD 5 154287370 154287370 + Frame_Shift_Del DEL T T - TCGA-HZ-8637-01A-11D-2396-08 TCGA-HZ-8637-10A-01D-2396-08 g.chr5:154287370delT c.2176delA c.(2176-2178)agtfs p.S726fs PAAD 5 154292538 154292538 + Missense_Mutation SNP G G A TCGA-2J-AAB1-01A-11D-A40W-08 TCGA-2J-AAB1-10A-01D-A40W-08 g.chr5:154292538G>A c.1916C>T c.(1915-1917)aCg>aTg p.T639M PAAD 5 154292538 154292538 + Missense_Mutation SNP G G A TCGA-3A-A9IB-01A-21D-A397-08 TCGA-3A-A9IB-10A-01D-A39A-08 g.chr5:154292538G>A c.1916C>T c.(1915-1917)aCg>aTg p.T639M PRAD 5 154270986 154270986 + Silent SNP G G C TCGA-KK-A6E4-01A-11D-A30E-08 TCGA-KK-A6E4-11A-11D-A30H-08 g.chr5:154270986G>C c.4077C>G c.(4075-4077)ctC>ctG p.L1359L READ 5 154278135 154278135 + Silent SNP C C T TCGA-DC-6681-01A-11D-1826-10 TCGA-DC-6681-10A-01D-1826-10 g.chr5:154278135C>T c.3210G>A c.(3208-3210)acG>acA p.T1070T READ 5 154287187 154287187 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:154287187G>A c.2359C>T c.(2359-2361)Cgg>Tgg p.R787W READ 5 154287314 154287314 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr5:154287314C>T c.2232G>A c.(2230-2232)aaG>aaA p.K744K READ 5 154307007 154307007 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:154307007A>C c.1018T>G c.(1018-1020)Tta>Gta p.L340V READ 5 154311118 154311118 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr5:154311118G>A c.681C>T c.(679-681)aaC>aaT p.N227N SARC 5 154282137 154282137 + Missense_Mutation SNP C C T TCGA-DX-A48O-01A-11D-A307-09 TCGA-DX-A48O-10A-01D-A307-09 g.chr5:154282137C>T c.2828G>A c.(2827-2829)gGg>gAg p.G943E SARC 5 154287187 154287187 + Missense_Mutation SNP G G A TCGA-DX-A8BU-01A-11D-A37C-09 TCGA-DX-A8BU-10A-01D-A37F-09 g.chr5:154287187G>A c.2359C>T c.(2359-2361)Cgg>Tgg p.R787W SARC 5 154305483 154305483 + Missense_Mutation SNP G G A TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr5:154305483G>A c.1232C>T c.(1231-1233)tCc>tTc p.S411F SKCM 5 154267830 154267830 + Silent SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr5:154267830G>A c.4467C>T c.(4465-4467)ctC>ctT p.L1489L SKCM 5 154270981 154270981 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr5:154270981G>A c.4082C>T c.(4081-4083)tCa>tTa p.S1361L SKCM 5 154271035 154271036 + Frame_Shift_Del DEL AA AA - TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr5:154271035_154271036delAA c.4027_4028delTT c.(4027-4029)ttgfs p.L1343fs SKCM 5 154271117 154271117 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:154271117G>A c.3946C>T c.(3946-3948)Cag>Tag p.Q1316* SKCM 5 154271173 154271173 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr5:154271173G>A c.3890C>T c.(3889-3891)cCa>cTa p.P1297L SKCM 5 154272026 154272026 + Silent SNP G G A TCGA-EE-A29N-06A-12D-A197-08 TCGA-EE-A29N-10A-01D-A199-08 g.chr5:154272026G>A c.3681C>T c.(3679-3681)ctC>ctT p.L1227L SKCM 5 154275824 154275824 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr5:154275824G>A c.3425C>T c.(3424-3426)tCc>tTc p.S1142F SKCM 5 154278121 154278121 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr5:154278121G>A c.3224C>T c.(3223-3225)gCt>gTt p.A1075V SKCM 5 154282156 154282156 + Nonsense_Mutation SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr5:154282156G>A c.2809C>T c.(2809-2811)Cag>Tag p.Q937* SKCM 5 154282694 154282694 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr5:154282694G>A c.2674C>T c.(2674-2676)Cat>Tat p.H892Y SKCM 5 154284151 154284151 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:154284151G>A c.2548C>T c.(2548-2550)Ccc>Tcc p.P850S SKCM 5 154284938 154284938 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:154284938G>A c.2494C>T c.(2494-2496)Cca>Tca p.P832S SKCM 5 154291305 154291305 + Missense_Mutation SNP G G A TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr5:154291305G>A c.2149C>T c.(2149-2151)Cat>Tat p.H717Y SKCM 5 154291320 154291320 + Missense_Mutation SNP T T A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr5:154291320T>A c.2134A>T c.(2134-2136)Act>Tct p.T712S SKCM 5 154296622 154296622 + Silent SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr5:154296622G>A c.1791C>T c.(1789-1791)agC>agT p.S597S SKCM 5 154307058 154307058 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr5:154307058G>A c.967C>T c.(967-969)Ctc>Ttc p.L323F SKCM 5 154308188 154308188 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr5:154308188C>T c.813G>A c.(811-813)aaG>aaA p.K271K SKCM 5 154311045 154311045 + Nonsense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr5:154311045G>A c.754C>T c.(754-756)Cga>Tga p.R252* SKCM 5 154311712 154311712 + Nonsense_Mutation SNP C C T TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr5:154311712C>T c.608G>A c.(607-609)tGg>tAg p.W203* SKCM 5 154311726 154311726 + Silent SNP G G A TCGA-EE-A29R-06A-11D-A197-08 TCGA-EE-A29R-10A-01D-A199-08 g.chr5:154311726G>A c.594C>T c.(592-594)atC>atT p.I198I SKCM 5 154316593 154316593 + Missense_Mutation SNP G G C TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr5:154316593G>C c.319C>G c.(319-321)Ctc>Gtc p.L107V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 5 154308136 154308136 single base substitution G A exon_variant AML-US 5 154308136 154308136 single base substitution G A missense_variant L289F 865C>T BLCA-CN 5 154320693 154320693 single base substitution A T upstream_gene_variant BLCA-US 5 154267890 154267890 single base substitution G T downstream_gene_variant BLCA-US 5 154267890 154267890 single base substitution G T synonymous_variant L1469L 4407C>A BLCA-US 5 154268890 154268890 single base substitution C G downstream_gene_variant BLCA-US 5 154268890 154268890 single base substitution C G missense_variant E1450D 4350G>C BLCA-US 5 154272068 154272068 single base substitution C T exon_variant BLCA-US 5 154272068 154272068 single base substitution C T synonymous_variant L1213L 3639G>A BLCA-US 5 154308188 154308188 single base substitution C T exon_variant BLCA-US 5 154308188 154308188 single base substitution C T synonymous_variant K271K 813G>A BOCA-FR 5 154317229 154317229 single base substitution C A intron_variant BRCA-EU 5 154262907 154262907 single base substitution A G downstream_gene_variant BRCA-EU 5 154263595 154263595 single base substitution C T downstream_gene_variant BRCA-EU 5 154264836 154264836 single base substitution C T downstream_gene_variant BRCA-EU 5 154265617 154265617 single base substitution C T downstream_gene_variant BRCA-EU 5 154266879 154266879 insertion of <=200bp - A downstream_gene_variant BRCA-EU 5 154267002 154267002 single base substitution C G 3_prime_UTR_variant BRCA-EU 5 154267002 154267002 single base substitution C G downstream_gene_variant BRCA-EU 5 154267065 154267065 single base substitution C T 3_prime_UTR_variant BRCA-EU 5 154267065 154267065 single base substitution C T downstream_gene_variant BRCA-EU 5 154267213 154267213 single base substitution C T 3_prime_UTR_variant BRCA-EU 5 154267213 154267213 single base substitution C T downstream_gene_variant BRCA-EU 5 154271222 154271222 single base substitution G T exon_variant BRCA-EU 5 154271222 154271222 single base substitution G T missense_variant L1281I 3841C>A BRCA-EU 5 154272155 154272155 single base substitution G T exon_variant BRCA-EU 5 154272155 154272155 single base substitution G T intron_variant BRCA-EU 5 154272192 154272192 single base substitution C T exon_variant BRCA-EU 5 154272192 154272192 single base substitution C T intron_variant BRCA-EU 5 154272783 154272783 single base substitution C T intron_variant BRCA-EU 5 154272783 154272783 single base substitution C T upstream_gene_variant BRCA-EU 5 154273724 154273724 single base substitution C G intron_variant BRCA-EU 5 154273724 154273724 single base substitution C G upstream_gene_variant BRCA-EU 5 154277059 154277059 deletion of <=200bp T - intron_variant BRCA-EU 5 154277059 154277059 deletion of <=200bp T - upstream_gene_variant BRCA-EU 5 154278839 154278839 single base substitution G T missense_variant R1016S 3046C>A BRCA-EU 5 154278858 154278858 single base substitution C T synonymous_variant A1009A 3027G>A BRCA-EU 5 154279506 154279506 single base substitution T C intron_variant BRCA-EU 5 154279980 154279980 single base substitution C T intron_variant BRCA-EU 5 154280506 154280506 single base substitution A C intron_variant BRCA-EU 5 154281681 154281681 single base substitution A T intron_variant BRCA-EU 5 154281748 154281748 single base substitution G C intron_variant BRCA-EU 5 154281763 154281763 single base substitution G T intron_variant BRCA-EU 5 154281909 154281909 single base substitution A C intron_variant BRCA-EU 5 154282560 154282560 single base substitution G A intron_variant BRCA-EU 5 154282764 154282764 single base substitution G C intron_variant BRCA-EU 5 154282940 154282940 single base substitution T C intron_variant BRCA-EU 5 154283046 154283046 deletion of <=200bp A - intron_variant BRCA-EU 5 154283386 154283386 deletion of <=200bp A - intron_variant BRCA-EU 5 154283386 154283386 single base substitution A T intron_variant BRCA-EU 5 154283396 154283396 single base substitution T A intron_variant BRCA-EU 5 154283653 154283653 insertion of <=200bp - T intron_variant BRCA-EU 5 154286068 154286068 deletion of <=200bp G - intron_variant BRCA-EU 5 154286134 154286134 single base substitution T A intron_variant BRCA-EU 5 154286309 154286309 single base substitution T C intron_variant BRCA-EU 5 154286878 154286878 single base substitution C T intron_variant BRCA-EU 5 154287807 154287807 single base substitution C G intron_variant BRCA-EU 5 154288475 154288475 single base substitution A G intron_variant BRCA-EU 5 154290720 154290720 single base substitution C G intron_variant BRCA-EU 5 154291224 154291224 single base substitution T C intron_variant BRCA-EU 5 154291820 154291820 single base substitution C T intron_variant BRCA-EU 5 154293824 154293824 single base substitution G A intron_variant BRCA-EU 5 154293938 154293938 single base substitution G A intron_variant BRCA-EU 5 154295289 154295289 single base substitution C G intron_variant BRCA-EU 5 154295381 154295381 single base substitution C A intron_variant BRCA-EU 5 154296047 154296047 deletion of <=200bp T - intron_variant BRCA-EU 5 154296720 154296720 single base substitution T C missense_variant I565V 1693A>G BRCA-EU 5 154299605 154299605 single base substitution G C synonymous_variant V507V 1521C>G BRCA-EU 5 154299848 154299851 deletion of <=200bp AAAA - intron_variant BRCA-EU 5 154300017 154300017 single base substitution A G intron_variant BRCA-EU 5 154300495 154300495 insertion of <=200bp - T intron_variant BRCA-EU 5 154301247 154301247 single base substitution C G intron_variant BRCA-EU 5 154302381 154302381 single base substitution C T downstream_gene_variant BRCA-EU 5 154302381 154302381 single base substitution C T intron_variant BRCA-EU 5 154305850 154305850 single base substitution G A downstream_gene_variant BRCA-EU 5 154305850 154305850 single base substitution G A intron_variant BRCA-EU 5 154307410 154307410 single base substitution G C intron_variant BRCA-EU 5 154310682 154310682 single base substitution A C intron_variant BRCA-EU 5 154312578 154312578 single base substitution C G intron_variant BRCA-EU 5 154312578 154312578 single base substitution C G upstream_gene_variant BRCA-EU 5 154313249 154313249 single base substitution T A intron_variant BRCA-EU 5 154313249 154313249 single base substitution T A upstream_gene_variant BRCA-EU 5 154313614 154313614 single base substitution C T intron_variant BRCA-EU 5 154313614 154313614 single base substitution C T upstream_gene_variant BRCA-EU 5 154315702 154315702 single base substitution C A intron_variant BRCA-EU 5 154315702 154315702 single base substitution C A upstream_gene_variant BRCA-EU 5 154316176 154316176 single base substitution G T intron_variant BRCA-EU 5 154316176 154316176 single base substitution G T upstream_gene_variant BRCA-EU 5 154316530 154316530 single base substitution G C intron_variant BRCA-EU 5 154317183 154317183 single base substitution C T intron_variant BRCA-EU 5 154317538 154317538 single base substitution G A synonymous_variant P52P 156C>T BRCA-EU 5 154317708 154317708 single base substitution A T 5_prime_UTR_variant BRCA-EU 5 154320598 154320598 single base substitution T G upstream_gene_variant BRCA-EU 5 154320642 154320642 single base substitution C T upstream_gene_variant BRCA-EU 5 154322697 154322697 deletion of <=200bp T - upstream_gene_variant BRCA-EU 5 154322704 154322704 single base substitution T C upstream_gene_variant BRCA-EU 5 154322730 154322730 single base substitution C T upstream_gene_variant BRCA-FR 5 154264836 154264836 single base substitution C T downstream_gene_variant BRCA-FR 5 154265617 154265617 single base substitution C T downstream_gene_variant BRCA-FR 5 154271222 154271222 single base substitution G T exon_variant BRCA-FR 5 154271222 154271222 single base substitution G T missense_variant L1281I 3841C>A BRCA-FR 5 154275266 154275266 single base substitution G A intron_variant BRCA-FR 5 154275266 154275266 single base substitution G A upstream_gene_variant BRCA-FR 5 154286878 154286878 single base substitution C T intron_variant BRCA-FR 5 154291820 154291820 single base substitution C T intron_variant BRCA-FR 5 154293474 154293474 single base substitution C T intron_variant BRCA-FR 5 154310716 154310716 single base substitution C T intron_variant BRCA-FR 5 154312578 154312578 single base substitution C G intron_variant BRCA-FR 5 154312578 154312578 single base substitution C G upstream_gene_variant BRCA-FR 5 154315869 154315869 single base substitution C T intron_variant BRCA-FR 5 154315869 154315869 single base substitution C T upstream_gene_variant BRCA-FR 5 154317708 154317708 single base substitution A T 5_prime_UTR_variant BRCA-FR 5 154320598 154320598 single base substitution T G upstream_gene_variant BRCA-KR 5 154267795 154267795 single base substitution C G downstream_gene_variant BRCA-KR 5 154267795 154267795 single base substitution C G missense_variant R1501T 4502G>C BRCA-UK 5 154263595 154263595 single base substitution C T downstream_gene_variant BRCA-UK 5 154267065 154267065 single base substitution C T 3_prime_UTR_variant BRCA-UK 5 154267065 154267065 single base substitution C T downstream_gene_variant BRCA-UK 5 154268847 154268847 single base substitution G A downstream_gene_variant BRCA-UK 5 154268847 154268847 single base substitution G A intron_variant BRCA-UK 5 154288475 154288475 single base substitution A G intron_variant BRCA-UK 5 154315515 154315515 single base substitution C T missense_variant G132E 395G>A BRCA-UK 5 154315515 154315515 single base substitution C T upstream_gene_variant BRCA-US 5 154284974 154284974 single base substitution T C missense_variant I820V 2458A>G BRCA-US 5 154304056 154304056 single base substitution A C downstream_gene_variant BRCA-US 5 154304056 154304056 single base substitution A C missense_variant V451G 1352T>G BRCA-US 5 154308089 154308089 single base substitution A C missense_variant F304L 912T>G BRCA-US 5 154308089 154308089 single base substitution A C splice_region_variant BRCA-US 5 154316741 154316741 single base substitution T G synonymous_variant I57I 171A>C BRCA-US 5 154317530 154317530 single base substitution C T missense_variant R55Q 164G>A BTCA-JP 5 154270854 154270854 single base substitution C A downstream_gene_variant BTCA-JP 5 154270854 154270854 single base substitution C A missense_variant K1403N 4209G>T BTCA-JP 5 154271004 154271004 single base substitution C T exon_variant BTCA-JP 5 154271004 154271004 single base substitution C T synonymous_variant L1353L 4059G>A BTCA-JP 5 154271883 154271883 single base substitution C T intron_variant BTCA-JP 5 154284028 154284028 single base substitution G A intron_variant BTCA-JP 5 154284154 154284154 single base substitution G A missense_variant L849F 2545C>T BTCA-JP 5 154299560 154299560 single base substitution G A synonymous_variant I522I 1566C>T BTCA-JP 5 154299746 154299746 single base substitution C T intron_variant BTCA-JP 5 154300913 154300913 deletion of <=200bp G - frameshift_variant P484 BTCA-JP 5 154304119 154304119 deletion of <=200bp A - downstream_gene_variant BTCA-JP 5 154304119 154304119 deletion of <=200bp A - splice_region_variant BTCA-JP 5 154308191 154308191 single base substitution C G exon_variant BTCA-JP 5 154308191 154308191 single base substitution C G synonymous_variant L270L 810G>C BTCA-JP 5 154311709 154311709 single base substitution C T missense_variant C204Y 611G>A BTCA-JP 5 154311709 154311709 single base substitution C T upstream_gene_variant CESC-US 5 154272068 154272068 single base substitution C T exon_variant CESC-US 5 154272068 154272068 single base substitution C T synonymous_variant L1213L 3639G>A CESC-US 5 154272083 154272083 single base substitution C T exon_variant CESC-US 5 154272083 154272083 single base substitution C T synonymous_variant L1208L 3624G>A CESC-US 5 154278076 154278076 single base substitution C G missense_variant R1090T 3269G>C CESC-US 5 154280963 154280963 single base substitution G A missense_variant H984Y 2950C>T CESC-US 5 154280965 154280965 single base substitution G C missense_variant S983C 2948C>G CESC-US 5 154317604 154317604 single base substitution G A synonymous_variant F30F 90C>T CLLE-ES 5 154290754 154290754 single base substitution A G intron_variant CLLE-ES 5 154291151 154291151 single base substitution C G intron_variant CLLE-ES 5 154299299 154299299 single base substitution T G intron_variant COAD-US 5 154270969 154270969 single base substitution G A downstream_gene_variant COAD-US 5 154270969 154270969 single base substitution G A missense_variant A1365V 4094C>T COAD-US 5 154271208 154271208 single base substitution C T exon_variant COAD-US 5 154271208 154271208 single base substitution C T synonymous_variant L1285L 3855G>A COAD-US 5 154272043 154272043 single base substitution C T exon_variant COAD-US 5 154272043 154272043 single base substitution C T missense_variant E1222K 3664G>A COAD-US 5 154272092 154272092 single base substitution G A exon_variant COAD-US 5 154272092 154272092 single base substitution G A synonymous_variant C1205C 3615C>T COAD-US 5 154275786 154275786 single base substitution G A missense_variant P1155S 3463C>T COAD-US 5 154275786 154275786 single base substitution G A upstream_gene_variant COAD-US 5 154275815 154275815 single base substitution T C missense_variant Y1145C 3434A>G COAD-US 5 154275815 154275815 single base substitution T C upstream_gene_variant COAD-US 5 154280908 154280908 single base substitution T C missense_variant H1002R 3005A>G COAD-US 5 154282235 154282235 single base substitution T C splice_region_variant COAD-US 5 154282719 154282719 single base substitution C T synonymous_variant V883V 2649G>A COAD-US 5 154282722 154282722 single base substitution A T missense_variant D882E 2646T>A COAD-US 5 154284109 154284109 insertion of <=200bp - A frameshift_variant H864L? COAD-US 5 154287275 154287275 single base substitution C T synonymous_variant S757S 2271G>A COAD-US 5 154287276 154287276 single base substitution G T stop_gained S757* 2270C>A COAD-US 5 154297547 154297547 single base substitution G A synonymous_variant H539H 1617C>T COAD-US 5 154307045 154307045 single base substitution G A exon_variant COAD-US 5 154307045 154307045 single base substitution G A missense_variant S327L 980C>T COAD-US 5 154311812 154311812 insertion of <=200bp - A splice_acceptor_variant COAD-US 5 154311812 154311812 insertion of <=200bp - A upstream_gene_variant COAD-US 5 154315505 154315505 single base substitution G T missense_variant F135L 405C>A COAD-US 5 154315505 154315505 single base substitution G T upstream_gene_variant COCA-CN 5 154267767 154267767 single base substitution A C 3_prime_UTR_variant COCA-CN 5 154267767 154267767 single base substitution A C downstream_gene_variant COCA-CN 5 154268862 154268862 single base substitution G T downstream_gene_variant COCA-CN 5 154268862 154268862 single base substitution G T intron_variant COCA-CN 5 154272044 154272044 single base substitution G A exon_variant COCA-CN 5 154272044 154272044 single base substitution G A synonymous_variant D1221D 3663C>T COCA-CN 5 154272048 154272048 single base substitution C A exon_variant COCA-CN 5 154272048 154272048 single base substitution C A missense_variant W1220L 3659G>T COCA-CN 5 154275238 154275238 single base substitution A T intron_variant COCA-CN 5 154275238 154275238 single base substitution A T upstream_gene_variant COCA-CN 5 154278225 154278225 single base substitution A C intron_variant COCA-CN 5 154282303 154282303 single base substitution G T intron_variant COCA-CN 5 154282629 154282629 single base substitution A T intron_variant COCA-CN 5 154284283 154284283 single base substitution C T intron_variant COCA-CN 5 154287017 154287017 single base substitution A G intron_variant COCA-CN 5 154287019 154287019 single base substitution C A intron_variant COCA-CN 5 154287272 154287272 single base substitution A C missense_variant I758M 2274T>G COCA-CN 5 154291257 154291257 single base substitution G T intron_variant COCA-CN 5 154296474 154296474 single base substitution A C intron_variant COCA-CN 5 154299655 154299657 deletion of <=200bp CTT - disruptive_inframe_deletion EG490G COCA-CN 5 154305158 154305158 single base substitution G A downstream_gene_variant COCA-CN 5 154305158 154305158 single base substitution G A intron_variant COCA-CN 5 154311150 154311150 single base substitution T C exon_variant COCA-CN 5 154311150 154311150 single base substitution T C intron_variant EOPC-DE 5 154318400 154318400 single base substitution T A upstream_gene_variant EOPC-DE 5 154318407 154318407 single base substitution G A upstream_gene_variant ESAD-UK 5 154263224 154263224 single base substitution G T downstream_gene_variant ESAD-UK 5 154263777 154263777 single base substitution C G downstream_gene_variant ESAD-UK 5 154264458 154264461 deletion of <=200bp CAAA - downstream_gene_variant ESAD-UK 5 154265268 154265268 single base substitution T C downstream_gene_variant ESAD-UK 5 154265770 154265770 single base substitution G A downstream_gene_variant ESAD-UK 5 154266175 154266175 single base substitution G A downstream_gene_variant ESAD-UK 5 154268120 154268120 single base substitution C G downstream_gene_variant ESAD-UK 5 154268120 154268120 single base substitution C G intron_variant ESAD-UK 5 154269970 154269970 single base substitution T G downstream_gene_variant ESAD-UK 5 154269970 154269970 single base substitution T G intron_variant ESAD-UK 5 154271060 154271060 single base substitution G T exon_variant ESAD-UK 5 154271060 154271060 single base substitution G T missense_variant P1335T 4003C>A ESAD-UK 5 154271173 154271173 single base substitution G A exon_variant ESAD-UK 5 154271173 154271173 single base substitution G A missense_variant P1297L 3890C>T ESAD-UK 5 154278113 154278113 single base substitution C T missense_variant V1078I 3232G>A ESAD-UK 5 154278125 154278125 single base substitution A C missense_variant L1074V 3220T>G ESAD-UK 5 154280132 154280132 single base substitution C G intron_variant ESAD-UK 5 154281355 154281355 single base substitution T C intron_variant ESAD-UK 5 154282144 154282144 single base substitution C T missense_variant E941K 2821G>A ESAD-UK 5 154283653 154283653 single base substitution T A intron_variant ESAD-UK 5 154284527 154284527 single base substitution C T intron_variant ESAD-UK 5 154288167 154288167 single base substitution T C intron_variant ESAD-UK 5 154290280 154290280 single base substitution A G intron_variant ESAD-UK 5 154290923 154290923 insertion of <=200bp - C intron_variant ESAD-UK 5 154291403 154291403 single base substitution C T missense_variant R684Q 2051G>A ESAD-UK 5 154295149 154295149 single base substitution G A intron_variant ESAD-UK 5 154297762 154297762 single base substitution A G intron_variant ESAD-UK 5 154297899 154297899 single base substitution A G intron_variant ESAD-UK 5 154298607 154298607 insertion of <=200bp - T intron_variant ESAD-UK 5 154301982 154301982 single base substitution C G downstream_gene_variant ESAD-UK 5 154301982 154301982 single base substitution C G intron_variant ESAD-UK 5 154302662 154302662 single base substitution G A downstream_gene_variant ESAD-UK 5 154302662 154302662 single base substitution G A intron_variant ESAD-UK 5 154303680 154303680 single base substitution G A downstream_gene_variant ESAD-UK 5 154303680 154303680 single base substitution G A intron_variant ESAD-UK 5 154306193 154306193 single base substitution G T downstream_gene_variant ESAD-UK 5 154306193 154306193 single base substitution G T intron_variant ESAD-UK 5 154308477 154308477 single base substitution C T intron_variant ESAD-UK 5 154309174 154309174 single base substitution A G intron_variant ESAD-UK 5 154309302 154309302 single base substitution C A intron_variant ESAD-UK 5 154311932 154311932 single base substitution G A intron_variant ESAD-UK 5 154311932 154311932 single base substitution G A upstream_gene_variant ESAD-UK 5 154318982 154318982 single base substitution C T upstream_gene_variant ESAD-UK 5 154322121 154322121 single base substitution C T upstream_gene_variant ESCA-CN 5 154291403 154291403 single base substitution C T missense_variant R684Q 2051G>A ESCA-CN 5 154310997 154310997 single base substitution C A intron_variant ESCA-CN 5 154311796 154311796 single base substitution A G missense_variant I175T 524T>C ESCA-CN 5 154311796 154311796 single base substitution A G upstream_gene_variant GBM-US 5 154275813 154275813 single base substitution G C missense_variant H1146D 3436C>G GBM-US 5 154275813 154275813 single base substitution G C upstream_gene_variant GBM-US 5 154311130 154311130 single base substitution A G exon_variant GBM-US 5 154311130 154311130 single base substitution A G synonymous_variant A223A 669T>C KIRC-US 5 154270986 154270986 single base substitution G A downstream_gene_variant KIRC-US 5 154270986 154270986 single base substitution G A synonymous_variant L1359L 4077C>T KIRC-US 5 154271054 154271054 single base substitution T A exon_variant KIRC-US 5 154271054 154271054 single base substitution T A missense_variant R1337W 4009A>T KIRC-US 5 154278063 154278063 single base substitution C T synonymous_variant E1094E 3282G>A KIRC-US 5 154287300 154287300 deletion of <=200bp A - frameshift_variant L749 KIRP-US 5 154278113 154278113 single base substitution C T missense_variant V1078I 3232G>A LAML-KR 5 154262244 154262244 single base substitution C T downstream_gene_variant LAML-KR 5 154285277 154285277 single base substitution G T intron_variant LGG-US 5 154270897 154270897 single base substitution T C downstream_gene_variant LGG-US 5 154270897 154270897 single base substitution T C missense_variant Q1389R 4166A>G LGG-US 5 154315435 154315438 deletion of <=200bp AAGT - frameshift_variant TC158 LGG-US 5 154315435 154315438 deletion of <=200bp AAGT - upstream_gene_variant LICA-CN 5 154282696 154282696 single base substitution A C missense_variant F891C 2672T>G LICA-CN 5 154284974 154284974 single base substitution T A missense_variant I820F 2458A>T LICA-CN 5 154311680 154311680 single base substitution T C missense_variant I214V 640A>G LICA-CN 5 154311680 154311680 single base substitution T C upstream_gene_variant LICA-FR 5 154272071 154272071 single base substitution C A exon_variant LICA-FR 5 154272071 154272071 single base substitution C A synonymous_variant V1212V 3636G>T LICA-FR 5 154278000 154278000 single base substitution C A missense_variant Q1115H 3345G>T LICA-FR 5 154279232 154279232 single base substitution G A intron_variant LICA-FR 5 154280060 154280060 single base substitution C A intron_variant LICA-FR 5 154287942 154287942 single base substitution T C intron_variant LICA-FR 5 154294121 154294121 single base substitution T G intron_variant LICA-FR 5 154297359 154297359 single base substitution G C intron_variant LICA-FR 5 154308040 154308040 single base substitution T C intron_variant LIHC-US 5 154287212 154287212 single base substitution T C synonymous_variant S778S 2334A>G LIHC-US 5 154287223 154287223 single base substitution T C missense_variant N775D 2323A>G LIHC-US 5 154311018 154311018 single base substitution C T missense_variant G261R 781G>A LIHC-US 5 154311018 154311018 single base substitution C T splice_region_variant LIHC-US 5 154311099 154311099 single base substitution C T exon_variant LIHC-US 5 154311099 154311099 single base substitution C T missense_variant A234T 700G>A LIHC-US 5 154311783 154311783 single base substitution A G synonymous_variant I179I 537T>C LIHC-US 5 154311783 154311783 single base substitution A G upstream_gene_variant LIHC-US 5 154317547 154317547 single base substitution T C synonymous_variant P49P 147A>G LINC-JP 5 154270335 154270335 single base substitution A G downstream_gene_variant LINC-JP 5 154270335 154270335 single base substitution A G intron_variant LINC-JP 5 154271883 154271883 single base substitution C T intron_variant LINC-JP 5 154282621 154282621 single base substitution T A intron_variant LINC-JP 5 154286134 154286134 single base substitution T A intron_variant LINC-JP 5 154296170 154296170 single base substitution C T intron_variant LINC-JP 5 154296265 154296265 single base substitution G A intron_variant LINC-JP 5 154306867 154306867 single base substitution G A downstream_gene_variant LINC-JP 5 154306867 154306867 single base substitution G A intron_variant LINC-JP 5 154308053 154308053 single base substitution T C intron_variant LINC-JP 5 154311068 154311068 single base substitution G C exon_variant LINC-JP 5 154311068 154311068 single base substitution G C missense_variant T244S 731C>G LINC-JP 5 154315577 154315577 single base substitution C G synonymous_variant T111T 333G>C LINC-JP 5 154315577 154315577 single base substitution C G upstream_gene_variant LIRI-JP 5 154262030 154262030 single base substitution T C downstream_gene_variant LIRI-JP 5 154263299 154263299 single base substitution C A downstream_gene_variant LIRI-JP 5 154265279 154265279 single base substitution A C downstream_gene_variant LIRI-JP 5 154265798 154265798 single base substitution C G downstream_gene_variant LIRI-JP 5 154272237 154272237 single base substitution T A intron_variant LIRI-JP 5 154272237 154272237 single base substitution T A upstream_gene_variant LIRI-JP 5 154273897 154273897 single base substitution T C intron_variant LIRI-JP 5 154273897 154273897 single base substitution T C upstream_gene_variant LIRI-JP 5 154274981 154274981 single base substitution T G intron_variant LIRI-JP 5 154274981 154274981 single base substitution T G upstream_gene_variant LIRI-JP 5 154277445 154277445 single base substitution C T intron_variant LIRI-JP 5 154278605 154278605 single base substitution A G intron_variant LIRI-JP 5 154280150 154280150 single base substitution A G intron_variant LIRI-JP 5 154287521 154287521 single base substitution T C intron_variant LIRI-JP 5 154290658 154290658 single base substitution T C intron_variant LIRI-JP 5 154293255 154293255 single base substitution T C intron_variant LIRI-JP 5 154296206 154296206 single base substitution C A intron_variant LIRI-JP 5 154299537 154299537 single base substitution T C missense_variant N530S 1589A>G LIRI-JP 5 154301806 154301806 single base substitution C T intron_variant LIRI-JP 5 154302156 154302156 single base substitution G A downstream_gene_variant LIRI-JP 5 154302156 154302156 single base substitution G A intron_variant LIRI-JP 5 154306357 154306357 single base substitution G A downstream_gene_variant LIRI-JP 5 154306357 154306357 single base substitution G A intron_variant LIRI-JP 5 154309576 154309576 single base substitution T C intron_variant LIRI-JP 5 154311816 154311816 single base substitution A T splice_region_variant LIRI-JP 5 154311816 154311816 single base substitution A T upstream_gene_variant LIRI-JP 5 154311836 154311836 single base substitution A G intron_variant LIRI-JP 5 154311836 154311836 single base substitution A G upstream_gene_variant LIRI-JP 5 154314127 154314127 single base substitution C G intron_variant LIRI-JP 5 154314127 154314127 single base substitution C G upstream_gene_variant LIRI-JP 5 154314347 154314347 single base substitution A G intron_variant LIRI-JP 5 154314347 154314347 single base substitution A G upstream_gene_variant LIRI-JP 5 154316076 154316076 single base substitution T C intron_variant LIRI-JP 5 154316076 154316076 single base substitution T C upstream_gene_variant LIRI-JP 5 154317591 154317591 single base substitution A T missense_variant S35T 103T>A LIRI-JP 5 154318384 154318384 single base substitution G A upstream_gene_variant LIRI-JP 5 154319713 154319713 single base substitution G A upstream_gene_variant LIRI-JP 5 154320384 154320384 single base substitution T C upstream_gene_variant LIRI-JP 5 154322513 154322513 single base substitution G T upstream_gene_variant LUSC-KR 5 154273799 154273799 single base substitution C A intron_variant LUSC-KR 5 154273799 154273799 single base substitution C A upstream_gene_variant LUSC-KR 5 154278306 154278306 single base substitution C G intron_variant LUSC-KR 5 154281680 154281680 single base substitution T A intron_variant LUSC-KR 5 154285842 154285842 single base substitution C A intron_variant LUSC-KR 5 154287017 154287017 single base substitution A G intron_variant LUSC-KR 5 154293959 154293959 single base substitution T C intron_variant LUSC-KR 5 154298138 154298138 single base substitution C A intron_variant LUSC-KR 5 154298139 154298139 single base substitution C A intron_variant LUSC-KR 5 154310798 154310798 single base substitution T A intron_variant LUSC-KR 5 154314032 154314032 single base substitution T A intron_variant LUSC-KR 5 154314032 154314032 single base substitution T A upstream_gene_variant LUSC-KR 5 154315354 154315354 single base substitution G A intron_variant LUSC-KR 5 154315354 154315354 single base substitution G A upstream_gene_variant LUSC-KR 5 154316775 154316775 single base substitution C A intron_variant LUSC-KR 5 154320125 154320125 single base substitution G A upstream_gene_variant LUSC-US 5 154287306 154287306 single base substitution G A missense_variant P747L 2240C>T LUSC-US 5 154308114 154308114 single base substitution G T exon_variant LUSC-US 5 154308114 154308114 single base substitution G T missense_variant P296Q 887C>A LUSC-US 5 154311721 154311721 single base substitution G C missense_variant S200C 599C>G LUSC-US 5 154311721 154311721 single base substitution G C upstream_gene_variant LUSC-US 5 154316660 154316660 single base substitution G T synonymous_variant T84T 252C>A LUSC-US 5 154317677 154317677 single base substitution C T missense_variant R6Q 17G>A MALY-DE 5 154265112 154265112 single base substitution T C downstream_gene_variant MALY-DE 5 154272902 154272902 single base substitution A G intron_variant MALY-DE 5 154272902 154272902 single base substitution A G upstream_gene_variant MALY-DE 5 154283653 154283653 single base substitution T A intron_variant MALY-DE 5 154287813 154287813 single base substitution T G intron_variant MALY-DE 5 154300655 154300655 single base substitution T C intron_variant MALY-DE 5 154322307 154322307 single base substitution T A upstream_gene_variant MELA-AU 5 154262148 154262148 single base substitution G A downstream_gene_variant MELA-AU 5 154262655 154262655 single base substitution G A downstream_gene_variant MELA-AU 5 154262714 154262714 single base substitution G A downstream_gene_variant MELA-AU 5 154262828 154262828 single base substitution G A downstream_gene_variant MELA-AU 5 154262872 154262872 single base substitution C G downstream_gene_variant MELA-AU 5 154263135 154263135 single base substitution G A downstream_gene_variant MELA-AU 5 154263243 154263243 single base substitution G A downstream_gene_variant MELA-AU 5 154264135 154264135 single base substitution G A downstream_gene_variant MELA-AU 5 154265556 154265556 single base substitution G A downstream_gene_variant MELA-AU 5 154265876 154265876 single base substitution G A downstream_gene_variant MELA-AU 5 154266359 154266359 single base substitution C T downstream_gene_variant MELA-AU 5 154267111 154267111 single base substitution G A 3_prime_UTR_variant MELA-AU 5 154267111 154267111 single base substitution G A downstream_gene_variant MELA-AU 5 154267832 154267832 single base substitution G A downstream_gene_variant MELA-AU 5 154267832 154267832 single base substitution G A missense_variant L1489F 4465C>T MELA-AU 5 154268467 154268467 single base substitution G A downstream_gene_variant MELA-AU 5 154268467 154268467 single base substitution G A intron_variant MELA-AU 5 154268507 154268507 single base substitution T A downstream_gene_variant MELA-AU 5 154268507 154268507 single base substitution T A intron_variant MELA-AU 5 154268509 154268509 single base substitution C T downstream_gene_variant MELA-AU 5 154268509 154268509 single base substitution C T intron_variant MELA-AU 5 154269765 154269765 single base substitution G A downstream_gene_variant MELA-AU 5 154269765 154269765 single base substitution G A intron_variant MELA-AU 5 154270427 154270427 single base substitution G A downstream_gene_variant MELA-AU 5 154270427 154270427 single base substitution G A intron_variant MELA-AU 5 154271160 154271160 single base substitution G A exon_variant MELA-AU 5 154271160 154271160 single base substitution G A synonymous_variant V1301V 3903C>T MELA-AU 5 154271730 154271730 single base substitution G A intron_variant MELA-AU 5 154272443 154272444 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154272443 154272444 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 5 154272586 154272587 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154272586 154272587 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 5 154272667 154272667 single base substitution A G intron_variant MELA-AU 5 154272667 154272667 single base substitution A G upstream_gene_variant MELA-AU 5 154272669 154272669 single base substitution C A intron_variant MELA-AU 5 154272669 154272669 single base substitution C A upstream_gene_variant MELA-AU 5 154272789 154272789 single base substitution G A intron_variant MELA-AU 5 154272789 154272789 single base substitution G A upstream_gene_variant MELA-AU 5 154272797 154272797 single base substitution G A intron_variant MELA-AU 5 154272797 154272797 single base substitution G A upstream_gene_variant MELA-AU 5 154272897 154272897 single base substitution G A intron_variant MELA-AU 5 154272897 154272897 single base substitution G A upstream_gene_variant MELA-AU 5 154272962 154272962 single base substitution G A intron_variant MELA-AU 5 154272962 154272962 single base substitution G A upstream_gene_variant MELA-AU 5 154273260 154273260 single base substitution C T intron_variant MELA-AU 5 154273260 154273260 single base substitution C T upstream_gene_variant MELA-AU 5 154273639 154273639 single base substitution G A intron_variant MELA-AU 5 154273639 154273639 single base substitution G A upstream_gene_variant MELA-AU 5 154274030 154274030 single base substitution A C intron_variant MELA-AU 5 154274030 154274030 single base substitution A C upstream_gene_variant MELA-AU 5 154274380 154274380 single base substitution T C intron_variant MELA-AU 5 154274380 154274380 single base substitution T C upstream_gene_variant MELA-AU 5 154274399 154274399 single base substitution G A intron_variant MELA-AU 5 154274399 154274399 single base substitution G A upstream_gene_variant MELA-AU 5 154274425 154274425 single base substitution C T intron_variant MELA-AU 5 154274425 154274425 single base substitution C T upstream_gene_variant MELA-AU 5 154274461 154274461 single base substitution C T intron_variant MELA-AU 5 154274461 154274461 single base substitution C T upstream_gene_variant MELA-AU 5 154274566 154274566 single base substitution G A intron_variant MELA-AU 5 154274566 154274566 single base substitution G A upstream_gene_variant MELA-AU 5 154274754 154274754 single base substitution T A intron_variant MELA-AU 5 154274754 154274754 single base substitution T A upstream_gene_variant MELA-AU 5 154275092 154275092 single base substitution G A intron_variant MELA-AU 5 154275092 154275092 single base substitution G A upstream_gene_variant MELA-AU 5 154276182 154276182 single base substitution T C intron_variant MELA-AU 5 154276182 154276182 single base substitution T C upstream_gene_variant MELA-AU 5 154276229 154276229 single base substitution G A intron_variant MELA-AU 5 154276229 154276229 single base substitution G A upstream_gene_variant MELA-AU 5 154276949 154276949 single base substitution T C intron_variant MELA-AU 5 154276949 154276949 single base substitution T C upstream_gene_variant MELA-AU 5 154277346 154277346 single base substitution G A intron_variant MELA-AU 5 154277443 154277444 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154277880 154277880 single base substitution G A intron_variant MELA-AU 5 154277949 154277949 single base substitution G A intron_variant MELA-AU 5 154279267 154279267 single base substitution C T intron_variant MELA-AU 5 154279285 154279285 single base substitution G A intron_variant MELA-AU 5 154279374 154279374 single base substitution G A intron_variant MELA-AU 5 154279416 154279416 single base substitution G A intron_variant MELA-AU 5 154279681 154279681 single base substitution G C intron_variant MELA-AU 5 154279869 154279869 single base substitution G A intron_variant MELA-AU 5 154280172 154280172 single base substitution G A intron_variant MELA-AU 5 154281304 154281304 single base substitution A T intron_variant MELA-AU 5 154281355 154281355 single base substitution T C intron_variant MELA-AU 5 154282883 154282883 single base substitution G A intron_variant MELA-AU 5 154283195 154283195 single base substitution G A intron_variant MELA-AU 5 154283361 154283361 single base substitution G A intron_variant MELA-AU 5 154283722 154283722 single base substitution G A intron_variant MELA-AU 5 154283735 154283735 single base substitution G A intron_variant MELA-AU 5 154283761 154283761 single base substitution C T intron_variant MELA-AU 5 154284795 154284795 single base substitution A C intron_variant MELA-AU 5 154285048 154285049 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154285876 154285876 single base substitution G A intron_variant MELA-AU 5 154285918 154285918 single base substitution G A intron_variant MELA-AU 5 154285921 154285921 single base substitution G A intron_variant MELA-AU 5 154286220 154286220 single base substitution G A intron_variant MELA-AU 5 154286584 154286584 deletion of <=200bp T - intron_variant MELA-AU 5 154286846 154286846 single base substitution G A intron_variant MELA-AU 5 154287905 154287905 single base substitution T A intron_variant MELA-AU 5 154288102 154288102 single base substitution C T intron_variant MELA-AU 5 154289458 154289458 single base substitution G A intron_variant MELA-AU 5 154289516 154289516 single base substitution G A intron_variant MELA-AU 5 154289759 154289759 single base substitution G A intron_variant MELA-AU 5 154290282 154290282 single base substitution G A intron_variant MELA-AU 5 154291049 154291049 single base substitution G A intron_variant MELA-AU 5 154291305 154291305 single base substitution G A missense_variant H717Y 2149C>T MELA-AU 5 154291370 154291370 single base substitution G A missense_variant P695L 2084C>T MELA-AU 5 154292073 154292073 single base substitution G A intron_variant MELA-AU 5 154292370 154292370 single base substitution G A intron_variant MELA-AU 5 154292612 154292612 single base substitution G A intron_variant MELA-AU 5 154292735 154292735 single base substitution G A intron_variant MELA-AU 5 154293629 154293630 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154294308 154294308 single base substitution A G intron_variant MELA-AU 5 154294482 154294482 single base substitution G A intron_variant MELA-AU 5 154294483 154294483 single base substitution G A intron_variant MELA-AU 5 154294669 154294669 single base substitution T C intron_variant MELA-AU 5 154295020 154295020 single base substitution C T intron_variant MELA-AU 5 154295021 154295021 single base substitution G A intron_variant MELA-AU 5 154295587 154295587 single base substitution G A intron_variant MELA-AU 5 154296006 154296006 single base substitution A C intron_variant MELA-AU 5 154296037 154296037 single base substitution G A intron_variant MELA-AU 5 154296504 154296504 single base substitution G A intron_variant MELA-AU 5 154297092 154297092 single base substitution G A intron_variant MELA-AU 5 154297359 154297359 single base substitution G A intron_variant MELA-AU 5 154298458 154298458 single base substitution G A intron_variant MELA-AU 5 154298638 154298638 single base substitution G A intron_variant MELA-AU 5 154298758 154298758 single base substitution G T intron_variant MELA-AU 5 154298919 154298919 single base substitution G A intron_variant MELA-AU 5 154299005 154299005 single base substitution G A intron_variant MELA-AU 5 154299099 154299099 single base substitution G A intron_variant MELA-AU 5 154299944 154299945 multiple base substitution (>=2bp and <=200bp) AG GA intron_variant MELA-AU 5 154301016 154301016 single base substitution G A intron_variant MELA-AU 5 154301162 154301162 single base substitution T A intron_variant MELA-AU 5 154301733 154301740 deletion of <=200bp TTTTTCTG - intron_variant MELA-AU 5 154301794 154301794 single base substitution C T intron_variant MELA-AU 5 154301973 154301973 single base substitution C T downstream_gene_variant MELA-AU 5 154301973 154301973 single base substitution C T intron_variant MELA-AU 5 154302073 154302073 single base substitution T A downstream_gene_variant MELA-AU 5 154302073 154302073 single base substitution T A intron_variant MELA-AU 5 154302632 154302632 single base substitution G A downstream_gene_variant MELA-AU 5 154302632 154302632 single base substitution G A intron_variant MELA-AU 5 154303124 154303124 single base substitution G A downstream_gene_variant MELA-AU 5 154303124 154303124 single base substitution G A intron_variant MELA-AU 5 154303679 154303680 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 5 154303679 154303680 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154303722 154303723 multiple base substitution (>=2bp and <=200bp) GG AC downstream_gene_variant MELA-AU 5 154303722 154303723 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 5 154303857 154303857 single base substitution G A downstream_gene_variant MELA-AU 5 154303857 154303857 single base substitution G A intron_variant MELA-AU 5 154304005 154304005 single base substitution G A downstream_gene_variant MELA-AU 5 154304005 154304005 single base substitution G A intron_variant MELA-AU 5 154304157 154304157 single base substitution G A downstream_gene_variant MELA-AU 5 154304157 154304157 single base substitution G A intron_variant MELA-AU 5 154304203 154304203 single base substitution G A downstream_gene_variant MELA-AU 5 154304203 154304203 single base substitution G A intron_variant MELA-AU 5 154304711 154304711 single base substitution G A downstream_gene_variant MELA-AU 5 154304711 154304711 single base substitution G A intron_variant MELA-AU 5 154304737 154304737 single base substitution G A downstream_gene_variant MELA-AU 5 154304737 154304737 single base substitution G A intron_variant MELA-AU 5 154304758 154304758 single base substitution T A downstream_gene_variant MELA-AU 5 154304758 154304758 single base substitution T A intron_variant MELA-AU 5 154304880 154304880 single base substitution G A downstream_gene_variant MELA-AU 5 154304880 154304880 single base substitution G A intron_variant MELA-AU 5 154305085 154305086 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 5 154305085 154305086 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154305207 154305207 single base substitution G A downstream_gene_variant MELA-AU 5 154305207 154305207 single base substitution G A intron_variant MELA-AU 5 154305367 154305367 single base substitution G A downstream_gene_variant MELA-AU 5 154305367 154305367 single base substitution G A intron_variant MELA-AU 5 154305672 154305672 single base substitution G A downstream_gene_variant MELA-AU 5 154305672 154305672 single base substitution G A intron_variant MELA-AU 5 154305815 154305815 single base substitution G A downstream_gene_variant MELA-AU 5 154305815 154305815 single base substitution G A intron_variant MELA-AU 5 154305989 154305989 single base substitution G A downstream_gene_variant MELA-AU 5 154305989 154305989 single base substitution G A intron_variant MELA-AU 5 154306893 154306893 single base substitution C T downstream_gene_variant MELA-AU 5 154306893 154306893 single base substitution C T intron_variant MELA-AU 5 154307825 154307825 single base substitution G A intron_variant MELA-AU 5 154308766 154308766 insertion of <=200bp - AG intron_variant MELA-AU 5 154309414 154309414 single base substitution G A intron_variant MELA-AU 5 154309477 154309477 single base substitution G A intron_variant MELA-AU 5 154310896 154310896 single base substitution A G intron_variant MELA-AU 5 154311002 154311002 single base substitution G A intron_variant MELA-AU 5 154311427 154311427 single base substitution G A intron_variant MELA-AU 5 154311427 154311427 single base substitution G A upstream_gene_variant MELA-AU 5 154311591 154311591 single base substitution G A intron_variant MELA-AU 5 154311591 154311591 single base substitution G A upstream_gene_variant MELA-AU 5 154312130 154312130 single base substitution G A intron_variant MELA-AU 5 154312130 154312130 single base substitution G A upstream_gene_variant MELA-AU 5 154312171 154312172 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154312171 154312172 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 5 154312395 154312395 single base substitution G A intron_variant MELA-AU 5 154312395 154312395 single base substitution G A upstream_gene_variant MELA-AU 5 154314902 154314902 single base substitution A G intron_variant MELA-AU 5 154314902 154314902 single base substitution A G upstream_gene_variant MELA-AU 5 154315314 154315314 single base substitution G A intron_variant MELA-AU 5 154315314 154315314 single base substitution G A upstream_gene_variant MELA-AU 5 154315555 154315555 single base substitution G A missense_variant P119S 355C>T MELA-AU 5 154315555 154315555 single base substitution G A upstream_gene_variant MELA-AU 5 154316031 154316031 single base substitution G A intron_variant MELA-AU 5 154316031 154316031 single base substitution G A upstream_gene_variant MELA-AU 5 154316878 154316879 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 154317690 154317690 single base substitution C T missense_variant G2R 4G>A MELA-AU 5 154317995 154317995 single base substitution C T upstream_gene_variant MELA-AU 5 154318471 154318471 single base substitution A T upstream_gene_variant MELA-AU 5 154318583 154318583 single base substitution C T upstream_gene_variant MELA-AU 5 154318915 154318915 single base substitution G A upstream_gene_variant MELA-AU 5 154318978 154318978 single base substitution C T upstream_gene_variant MELA-AU 5 154319105 154319105 single base substitution C T upstream_gene_variant MELA-AU 5 154319515 154319515 single base substitution A G upstream_gene_variant MELA-AU 5 154319604 154319604 single base substitution C T upstream_gene_variant MELA-AU 5 154319922 154319922 single base substitution G A upstream_gene_variant MELA-AU 5 154320255 154320255 single base substitution C T upstream_gene_variant MELA-AU 5 154320552 154320552 single base substitution G A upstream_gene_variant MELA-AU 5 154321055 154321055 single base substitution C T upstream_gene_variant MELA-AU 5 154321553 154321554 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 5 154321564 154321564 single base substitution C T upstream_gene_variant MELA-AU 5 154321804 154321804 single base substitution T C upstream_gene_variant MELA-AU 5 154321975 154321975 single base substitution C T upstream_gene_variant MELA-AU 5 154322621 154322621 single base substitution A T upstream_gene_variant ORCA-IN 5 154297154 154297154 single base substitution C A intron_variant ORCA-IN 5 154307225 154307225 single base substitution G C intron_variant OV-AU 5 154272343 154272343 single base substitution C T intron_variant OV-AU 5 154272343 154272343 single base substitution C T upstream_gene_variant OV-AU 5 154278473 154278473 single base substitution G A intron_variant OV-AU 5 154280030 154280030 single base substitution G C intron_variant OV-AU 5 154286161 154286161 single base substitution G T intron_variant OV-AU 5 154295456 154295456 single base substitution T C intron_variant OV-AU 5 154296571 154296571 single base substitution C T synonymous_variant L614L 1842G>A OV-AU 5 154300093 154300093 single base substitution C T intron_variant OV-AU 5 154306197 154306197 single base substitution C T downstream_gene_variant OV-AU 5 154306197 154306197 single base substitution C T intron_variant OV-AU 5 154307064 154307064 single base substitution A G exon_variant OV-AU 5 154307064 154307064 single base substitution A G missense_variant Y321H 961T>C OV-AU 5 154308488 154308488 single base substitution T A intron_variant OV-AU 5 154308788 154308788 single base substitution G C intron_variant OV-AU 5 154318854 154318854 single base substitution A C upstream_gene_variant OV-AU 5 154322370 154322370 single base substitution C T upstream_gene_variant PACA-AU 5 154266225 154266225 single base substitution G C downstream_gene_variant PACA-AU 5 154270309 154270309 single base substitution C A downstream_gene_variant PACA-AU 5 154270309 154270309 single base substitution C A intron_variant PACA-AU 5 154278972 154278972 single base substitution C G intron_variant PACA-AU 5 154281030 154281030 single base substitution C A missense_variant W961C 2883G>T PACA-AU 5 154288625 154288625 single base substitution C T intron_variant PACA-AU 5 154290238 154290238 single base substitution G C intron_variant PACA-AU 5 154292556 154292556 single base substitution C T missense_variant R633Q 1898G>A PACA-AU 5 154300863 154300863 single base substitution A T intron_variant PACA-AU 5 154302979 154302979 single base substitution T A downstream_gene_variant PACA-AU 5 154302979 154302979 single base substitution T A intron_variant PACA-AU 5 154304551 154304555 deletion of <=200bp AAAAC - downstream_gene_variant PACA-AU 5 154304551 154304555 deletion of <=200bp AAAAC - intron_variant PACA-AU 5 154307691 154307691 single base substitution C T intron_variant PACA-AU 5 154308151 154308151 single base substitution G A exon_variant PACA-AU 5 154308151 154308151 single base substitution G A missense_variant R284C 850C>T PACA-AU 5 154310363 154310363 single base substitution T C intron_variant PACA-AU 5 154313293 154313293 single base substitution C T intron_variant PACA-AU 5 154313293 154313293 single base substitution C T upstream_gene_variant PACA-AU 5 154318999 154318999 single base substitution C T upstream_gene_variant PACA-CA 5 154263536 154263536 single base substitution C T downstream_gene_variant PACA-CA 5 154268079 154268079 single base substitution C G downstream_gene_variant PACA-CA 5 154268079 154268079 single base substitution C G intron_variant PACA-CA 5 154271155 154271155 single base substitution A C exon_variant PACA-CA 5 154271155 154271155 single base substitution A C missense_variant V1303G 3908T>G PACA-CA 5 154271343 154271343 single base substitution T C intron_variant PACA-CA 5 154275524 154275524 single base substitution G A intron_variant PACA-CA 5 154275524 154275524 single base substitution G A upstream_gene_variant PACA-CA 5 154284432 154284432 deletion of <=200bp A - intron_variant PACA-CA 5 154284478 154284478 single base substitution C A intron_variant PACA-CA 5 154287626 154287626 single base substitution C T intron_variant PACA-CA 5 154288489 154288489 single base substitution G A intron_variant PACA-CA 5 154302342 154302342 single base substitution C T downstream_gene_variant PACA-CA 5 154302342 154302342 single base substitution C T intron_variant PACA-CA 5 154302894 154302894 single base substitution C T downstream_gene_variant PACA-CA 5 154302894 154302894 single base substitution C T intron_variant PACA-CA 5 154306467 154306467 single base substitution G A downstream_gene_variant PACA-CA 5 154306467 154306467 single base substitution G A intron_variant PACA-CA 5 154306622 154306622 insertion of <=200bp - C downstream_gene_variant PACA-CA 5 154306622 154306622 insertion of <=200bp - C intron_variant PACA-CA 5 154306883 154306883 single base substitution C T downstream_gene_variant PACA-CA 5 154306883 154306883 single base substitution C T intron_variant PACA-CA 5 154310397 154310397 deletion of <=200bp A - intron_variant PACA-CA 5 154312891 154312891 insertion of <=200bp - T intron_variant PACA-CA 5 154312891 154312891 insertion of <=200bp - T upstream_gene_variant PACA-CA 5 154313045 154313045 deletion of <=200bp A - intron_variant PACA-CA 5 154313045 154313045 deletion of <=200bp A - upstream_gene_variant PACA-CA 5 154314165 154314165 single base substitution C T intron_variant PACA-CA 5 154314165 154314165 single base substitution C T upstream_gene_variant PACA-CA 5 154316837 154316837 single base substitution C G intron_variant PACA-CA 5 154317530 154317530 single base substitution C G missense_variant R55P 164G>C PACA-CA 5 154317633 154317633 single base substitution C T missense_variant D21N 61G>A PACA-CA 5 154319610 154319610 single base substitution T C upstream_gene_variant PAEN-AU 5 154287220 154287220 single base substitution C T missense_variant G776S 2326G>A PAEN-AU 5 154288032 154288032 single base substitution C T intron_variant PAEN-AU 5 154298579 154298579 single base substitution C A intron_variant PAEN-IT 5 154270243 154270243 single base substitution G T downstream_gene_variant PAEN-IT 5 154270243 154270243 single base substitution G T intron_variant PBCA-DE 5 154278326 154278326 single base substitution C T intron_variant PBCA-DE 5 154280869 154280869 single base substitution G T intron_variant PBCA-DE 5 154283653 154283653 insertion of <=200bp - T intron_variant PBCA-DE 5 154296047 154296047 insertion of <=200bp - T intron_variant PBCA-DE 5 154296690 154296690 single base substitution G T missense_variant Q575K 1723C>A PRAD-UK 5 154318390 154318390 single base substitution C T upstream_gene_variant PRAD-US 5 154270986 154270986 single base substitution G C downstream_gene_variant PRAD-US 5 154270986 154270986 single base substitution G C synonymous_variant L1359L 4077C>G READ-US 5 154278135 154278135 single base substitution C T synonymous_variant T1070T 3210G>A READ-US 5 154287314 154287314 single base substitution C T synonymous_variant K744K 2232G>A RECA-EU 5 154267156 154267156 single base substitution A C 3_prime_UTR_variant RECA-EU 5 154267156 154267156 single base substitution A C downstream_gene_variant RECA-EU 5 154270129 154270129 single base substitution T C downstream_gene_variant RECA-EU 5 154270129 154270129 single base substitution T C intron_variant RECA-EU 5 154275217 154275217 single base substitution A T intron_variant RECA-EU 5 154275217 154275217 single base substitution A T upstream_gene_variant RECA-EU 5 154275383 154275383 single base substitution G A intron_variant RECA-EU 5 154275383 154275383 single base substitution G A upstream_gene_variant RECA-EU 5 154278607 154278607 single base substitution G A intron_variant RECA-EU 5 154283394 154283394 single base substitution A T intron_variant RECA-EU 5 154289649 154289649 single base substitution T A intron_variant RECA-EU 5 154291583 154291583 single base substitution G C intron_variant RECA-EU 5 154293668 154293668 single base substitution C A intron_variant RECA-EU 5 154318705 154318705 single base substitution C G upstream_gene_variant SKCA-BR 5 154265587 154265587 single base substitution T C downstream_gene_variant SKCA-BR 5 154268674 154268674 single base substitution G A downstream_gene_variant SKCA-BR 5 154268674 154268674 single base substitution G A intron_variant SKCA-BR 5 154270007 154270007 single base substitution A C downstream_gene_variant SKCA-BR 5 154270007 154270007 single base substitution A C intron_variant SKCA-BR 5 154270027 154270028 deletion of <=200bp AT - downstream_gene_variant SKCA-BR 5 154270027 154270028 deletion of <=200bp AT - intron_variant SKCA-BR 5 154271626 154271626 single base substitution T C intron_variant SKCA-BR 5 154271696 154271696 single base substitution T C intron_variant SKCA-BR 5 154272801 154272801 single base substitution T G intron_variant SKCA-BR 5 154272801 154272801 single base substitution T G upstream_gene_variant SKCA-BR 5 154272815 154272815 insertion of <=200bp - TA intron_variant SKCA-BR 5 154272815 154272815 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 5 154274895 154274895 insertion of <=200bp - GGA intron_variant SKCA-BR 5 154274895 154274895 insertion of <=200bp - GGA upstream_gene_variant SKCA-BR 5 154280477 154280477 single base substitution G A intron_variant SKCA-BR 5 154283931 154283931 single base substitution G A intron_variant SKCA-BR 5 154285260 154285260 insertion of <=200bp - GT intron_variant SKCA-BR 5 154285494 154285494 single base substitution A C intron_variant SKCA-BR 5 154285664 154285664 single base substitution T C intron_variant SKCA-BR 5 154293487 154293487 single base substitution G A intron_variant SKCA-BR 5 154304005 154304005 single base substitution G A downstream_gene_variant SKCA-BR 5 154304005 154304005 single base substitution G A intron_variant SKCA-BR 5 154304331 154304331 single base substitution C T downstream_gene_variant SKCA-BR 5 154304331 154304331 single base substitution C T intron_variant SKCA-BR 5 154306425 154306425 single base substitution G A downstream_gene_variant SKCA-BR 5 154306425 154306425 single base substitution G A intron_variant SKCA-BR 5 154308438 154308438 single base substitution G A intron_variant SKCA-BR 5 154310081 154310081 single base substitution G A intron_variant SKCA-BR 5 154317776 154317776 single base substitution T G upstream_gene_variant SKCA-BR 5 154318428 154318428 single base substitution T C upstream_gene_variant SKCA-BR 5 154322261 154322261 single base substitution C T upstream_gene_variant SKCA-BR 5 154322315 154322315 single base substitution C T upstream_gene_variant SKCM-US 5 154267830 154267830 single base substitution G A downstream_gene_variant SKCM-US 5 154267830 154267830 single base substitution G A synonymous_variant L1489L 4467C>T SKCM-US 5 154267904 154267904 single base substitution G A downstream_gene_variant SKCM-US 5 154267904 154267904 single base substitution G A missense_variant L1465F 4393C>T SKCM-US 5 154270981 154270981 single base substitution G A downstream_gene_variant SKCM-US 5 154270981 154270981 single base substitution G A missense_variant S1361L 4082C>T SKCM-US 5 154271035 154271036 deletion of <=200bp AA - exon_variant SKCM-US 5 154271035 154271036 deletion of <=200bp AA - frameshift_variant L1343 SKCM-US 5 154271117 154271117 single base substitution G A exon_variant SKCM-US 5 154271117 154271117 single base substitution G A stop_gained Q1316* 3946C>T SKCM-US 5 154271173 154271173 single base substitution G A exon_variant SKCM-US 5 154271173 154271173 single base substitution G A missense_variant P1297L 3890C>T SKCM-US 5 154272026 154272026 single base substitution G A exon_variant SKCM-US 5 154272026 154272026 single base substitution G A synonymous_variant L1227L 3681C>T SKCM-US 5 154275824 154275824 single base substitution G A missense_variant S1142F 3425C>T SKCM-US 5 154275824 154275824 single base substitution G A upstream_gene_variant SKCM-US 5 154278121 154278121 single base substitution G A missense_variant A1075V 3224C>T SKCM-US 5 154282156 154282156 single base substitution G A stop_gained Q937* 2809C>T SKCM-US 5 154282694 154282694 single base substitution G A missense_variant H892Y 2674C>T SKCM-US 5 154284151 154284151 single base substitution G A missense_variant P850S 2548C>T SKCM-US 5 154284938 154284938 single base substitution G A missense_variant P832S 2494C>T SKCM-US 5 154291305 154291305 single base substitution G A missense_variant H717Y 2149C>T SKCM-US 5 154291320 154291320 single base substitution T A missense_variant T712S 2134A>T SKCM-US 5 154292583 154292583 single base substitution G A missense_variant S624F 1871C>T SKCM-US 5 154296622 154296622 single base substitution G A synonymous_variant S597S 1791C>T SKCM-US 5 154307058 154307058 single base substitution G A exon_variant SKCM-US 5 154307058 154307058 single base substitution G A missense_variant L323F 967C>T SKCM-US 5 154308188 154308188 single base substitution C T exon_variant SKCM-US 5 154308188 154308188 single base substitution C T synonymous_variant K271K 813G>A SKCM-US 5 154311045 154311045 single base substitution G A exon_variant SKCM-US 5 154311045 154311045 single base substitution G A stop_gained R252* 754C>T SKCM-US 5 154311712 154311712 single base substitution C T stop_gained W203* 608G>A SKCM-US 5 154311712 154311712 single base substitution C T upstream_gene_variant SKCM-US 5 154311726 154311726 single base substitution G A synonymous_variant I198I 594C>T SKCM-US 5 154311726 154311726 single base substitution G A upstream_gene_variant SKCM-US 5 154316593 154316593 single base substitution G C missense_variant L107V 319C>G STAD-US 5 154272096 154272096 single base substitution A T exon_variant STAD-US 5 154272096 154272096 single base substitution A T missense_variant I1204N 3611T>A STAD-US 5 154281007 154281007 single base substitution G C missense_variant A969G 2906C>G STAD-US 5 154284949 154284949 single base substitution T C missense_variant K828R 2483A>G STAD-US 5 154284999 154284999 single base substitution T C synonymous_variant S811S 2433A>G STAD-US 5 154287325 154287325 single base substitution G A missense_variant P741S 2221C>T STAD-US 5 154287348 154287348 single base substitution C T missense_variant R733Q 2198G>A STAD-US 5 154304058 154304058 deletion of <=200bp T - downstream_gene_variant STAD-US 5 154304058 154304058 deletion of <=200bp T - frameshift_variant K450 STAD-US 5 154311781 154311781 single base substitution T C missense_variant D180G 539A>G STAD-US 5 154311781 154311781 single base substitution T C upstream_gene_variant THCA-SA 5 154267080 154267080 single base substitution T C 3_prime_UTR_variant THCA-SA 5 154267080 154267080 single base substitution T C downstream_gene_variant THCA-US 5 154280951 154280951 single base substitution T A missense_variant I988F 2962A>T THCA-US 5 154315560 154315560 single base substitution C A missense_variant W117L 350G>T THCA-US 5 154315560 154315560 single base substitution C A upstream_gene_variant UCEC-US 5 154267810 154267810 single base substitution G A downstream_gene_variant UCEC-US 5 154267810 154267810 single base substitution G A missense_variant T1496M 4487C>T UCEC-US 5 154271271 154271271 single base substitution G A exon_variant UCEC-US 5 154271271 154271271 single base substitution G A synonymous_variant D1264D 3792C>T UCEC-US 5 154278046 154278046 single base substitution T A missense_variant N1100I 3299A>T UCEC-US 5 154278114 154278114 single base substitution G A synonymous_variant I1077I 3231C>T UCEC-US 5 154278182 154278182 single base substitution C T missense_variant A1055T 3163G>A UCEC-US 5 154280932 154280932 single base substitution G A missense_variant A994V 2981C>T UCEC-US 5 154281030 154281030 single base substitution C T stop_gained W961* 2883G>A UCEC-US 5 154282160 154282160 single base substitution A C synonymous_variant V935V 2805T>G UCEC-US 5 154282708 154282708 single base substitution A T missense_variant V887D 2660T>A UCEC-US 5 154287153 154287153 single base substitution G A missense_variant A798V 2393C>T UCEC-US 5 154287276 154287276 single base substitution G A missense_variant S757L 2270C>T UCEC-US 5 154291388 154291388 single base substitution G A missense_variant A689V 2066C>T UCEC-US 5 154296573 154296573 single base substitution G T missense_variant L614M 1840C>A UCEC-US 5 154296726 154296726 single base substitution A C missense_variant F563V 1687T>G UCEC-US 5 154305458 154305458 single base substitution T G downstream_gene_variant UCEC-US 5 154305458 154305458 single base substitution T G missense_variant K419N 1257A>C UCEC-US 5 154308128 154308128 single base substitution C T exon_variant UCEC-US 5 154308128 154308128 single base substitution C T stop_gained W291* 873G>A UCEC-US 5 154308151 154308151 single base substitution G A exon_variant UCEC-US 5 154308151 154308151 single base substitution G A missense_variant R284C 850C>T UCEC-US 5 154311018 154311018 single base substitution C A missense_variant G261W 781G>T UCEC-US 5 154311018 154311018 single base substitution C A splice_region_variant UCEC-US 5 154316705 154316705 single base substitution G A synonymous_variant G69G 207C>T UCEC-US 5 154316719 154316719 single base substitution C T missense_variant E65K 193G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-G2-A3VY-01 COSM3776460 c.4350G>C p.E1450D Substitution - Missense 5:154889330-154889330 - PD5961a COSM5791427 c.3027G>A p.A1009A Substitution - coding silent 5:154899298-154899298 - 74 COSM4778184 c.2575T>C p.S859P Substitution - Missense 5:154904564-154904564 - TCGA-FW-A3R5-06 COSM3919427 c.2548C>T p.P850S Substitution - Missense 5:154904591-154904591 - 1946219 COSM1197701 c.827G>T p.G276V Substitution - Missense 5:154928614-154928614 - 2521243 COSM5716722 c.2576C>T p.S859F Substitution - Missense 5:154904563-154904563 - TCGA-EE-A2MS-06 COSM3612920 c.967C>T p.L323F Substitution - Missense 5:154927498-154927498 - TCGA-D9-A6EC-06 COSM3776462 c.813G>A p.K271K Substitution - coding silent 5:154928628-154928628 - TCGA-DY-A1DD-01 COSM1567816 c.2232G>A p.K744K Substitution - coding silent 5:154907754-154907754 - TCGA-BR-4361-01 COSM3853048 c.2906C>G p.A969G Substitution - Missense 5:154901447-154901447 - BCM711T COSM4956077 c.3636G>T p.V1212V Substitution - coding silent 5:154892511-154892511 - pfg019T COSM1642664 c.261C>T p.D87D Substitution - coding silent 5:154937091-154937091 - T14 COSM5344891 c.2367G>A p.P789P Substitution - coding silent 5:154907619-154907619 - PD13606a COSM5793783 c.3841C>A p.L1281I Substitution - Missense 5:154891662-154891662 - TCGA-BR-6452-01 COSM3853052 c.539A>G p.D180G Substitution - Missense 5:154932221-154932221 - TCGA-AA-A00N-01 COSM275283 c.4376A>G p.D1459G Substitution - Missense 5:154888361-154888361 - STC252 COSM4762939 c.3185A>G p.K1062R Substitution - Missense 5:154898600-154898600 - ESO-859 COSM1238974 c.594C>T p.I198I Substitution - coding silent 5:154932166-154932166 - YUDAB COSM1696637 c.1192G>A p.G398S Substitution - Missense 5:154925963-154925963 - sysucc-1163T COSM5459172 c.2274T>G p.I758M Substitution - Missense 5:154907712-154907712 - TCGA-CG-5721-01 COSM3853049 c.2483A>G p.K828R Substitution - Missense 5:154905389-154905389 - PD9702a COSM5772634 c.3046C>A p.R1016S Substitution - Missense 5:154899279-154899279 - HCC082T COSM5816321 c.2672T>G p.F891C Substitution - Missense 5:154903136-154903136 - PCA78-1 COSM5415735 c.3577A>T p.N1193Y Substitution - Missense 5:154896112-154896112 - TCGA-EX-A69L-01 COSM4854749 c.2948C>G p.S983C Substitution - Missense 5:154901405-154901405 - T3262 COSM4686769 c.3790delG p.D1264fs*40 Deletion - Frameshift 5:154891713-154891713 - BD114T COSM5503037 c.4209G>T p.K1403N Substitution - Missense 5:154891294-154891294 - S01864 COSM5671790 c.3624G>C p.L1208F Substitution - Missense 5:154892523-154892523 - PCSI_0127_Pa_P COSM3381169 c.61G>A p.D21N Substitution - Missense 5:154938073-154938073 - 587228 COSM1208098 c.826G>T p.G276C Substitution - Missense 5:154928615-154928615 - RK131_C01 COSM3702757 c.103T>A p.S35T Substitution - Missense 5:154938031-154938031 - LUAD_E01147 COSM390642 c.4085A>G p.E1362G Substitution - Missense 5:154891418-154891418 - 1_PRE-TREATMENT COSM1718942 c.2827G>A p.G943R Substitution - Missense 5:154902578-154902578 - TCGA-GN-A26C-01 COSM3612918 c.1871C>T p.S624F Substitution - Missense 5:154913023-154913023 - Pat_58_A COSM5867958 c.3434_3435AC>TT p.Y1145F Substitution - Missense 5:154896254-154896255 - 587342 COSM1208102 c.584A>G p.D195G Substitution - Missense 5:154932176-154932176 - LC_C20 COSM1186887 c.4396G>A p.V1466I Substitution - Missense 5:154888341-154888341 - 8061103 COSM3784673 c.1898G>A p.R633Q Substitution - Missense 5:154912996-154912996 - LUAD-LC15C COSM341972 c.2662G>C p.E888Q Substitution - Missense 5:154903146-154903146 - TARGET-20-PARENB-09A-02D COSM5487189 c.865C>T p.L289F Substitution - Missense 5:154928576-154928576 - 8051715 COSM4135455 c.2326G>A p.G776S Substitution - Missense 5:154907660-154907660 - AOCS-134-3-9 COSM4141589 c.1842G>A p.L614L Substitution - coding silent 5:154917011-154917011 - LP6005409-DNA_C02 COSM5952413 c.2821G>A p.E941K Substitution - Missense 5:154902584-154902584 - TCGA-BR-4362-01 COSM3853050 c.2433A>G p.S811S Substitution - coding silent 5:154905439-154905439 - LUAD-5V8LT COSM402723 c.2284G>A p.E762K Substitution - Missense 5:154907702-154907702 - TCGA-CS-6667-01 COSM3975348 c.4166A>G p.Q1389R Substitution - Missense 5:154891337-154891337 - TCGA-CJ-5676-01 COSM482400 c.4077C>T p.L1359L Substitution - coding silent 5:154891426-154891426 - 2328683 COSM4972079 c.1418T>C p.V473A Substitution - Missense 5:154921387-154921387 - LP6005409-DNA_B04 COSM3612911 c.3890C>T p.P1297L Substitution - Missense 5:154891613-154891613 - TCGA-AX-A0J0-01 COSM1064773 c.3231C>T p.I1077I Substitution - coding silent 5:154898554-154898554 - S01022 COSM5666061 c.3650T>C p.M1217T Substitution - Missense 5:154892497-154892497 - DN120FF COSM5793783 c.3841C>A p.L1281I Substitution - Missense 5:154891662-154891662 - HCC049T COSM5812041 c.640A>G p.I214V Substitution - Missense 5:154932120-154932120 - LUAD-S01404 COSM398828 c.3790G>A p.D1264N Substitution - Missense 5:154891713-154891713 - TCGA-DD-A4NR-01 COSM4941166 c.781G>A p.G261R Substitution - Missense 5:154931458-154931458 - I2L-P7-Tumor-Organoid COSM5356916 c.3040C>T p.R1014W Substitution - Missense 5:154899285-154899285 - TCGA-AY-6197-01 COSM1435451 c.3005A>G p.H1002R Substitution - Missense 5:154901348-154901348 - TCGA-B5-A11E-01 COSM1064769 c.3792C>T p.D1264D Substitution - coding silent 5:154891711-154891711 - TCGA-FW-A3R5-06 COSM3919428 c.2494C>T p.P832S Substitution - Missense 5:154905378-154905378 - TCGA-AM-5820-01 COSM3761061 c.3463C>T p.P1155S Substitution - Missense 5:154896226-154896226 - 587342 COSM1208101 c.2155C>T p.R719W Substitution - Missense 5:154911739-154911739 - AOCS-166-1-2 COSM4141590 c.961T>C p.Y321H Substitution - Missense 5:154927504-154927504 - Gp2D COSM3245793 c.1189A>G p.I397V Substitution - Missense 5:154925966-154925966 - C135 COSM4618490 c.3026C>T p.A1009V Substitution - Missense 5:154899299-154899299 - HCC2998 COSM3245762 c.2658T>A p.D886E Substitution - Missense 5:154903150-154903150 - PD4120a COSM161243 c.395G>A p.G132E Substitution - Missense 5:154935955-154935955 - Pat_41_B COSM5867959 c.2729G>A p.G910E Substitution - Missense 5:154902676-154902676 - TCGA-AP-A0LM-01 COSM1064767 c.4487C>T p.T1496M Substitution - Missense 5:154888250-154888250 - TCGA-B0-5098-01 COSM1496074 c.4358A>G p.K1453R Substitution - Missense 5:154889322-154889322 - TCGA-AP-A0LM-01 COSM1064806 c.193G>A p.E65K Substitution - Missense 5:154937159-154937159 - ESO-153 COSM1253180 c.3568T>C p.S1190P Substitution - Missense 5:154896121-154896121 - CSCC-27-T COSM4476032 c.2035C>T p.R679* Substitution - Nonsense 5:154911859-154911859 - TCGA-ER-A19F-06 COSM3612908 c.4467C>T p.L1489L Substitution - coding silent 5:154888270-154888270 - TCGA-CM-4746-01 COSM1435447 c.3855G>A p.L1285L Substitution - coding silent 5:154891648-154891648 - TCGA-DA-A1IC-06 COSM3612915 c.2809C>T p.Q937* Substitution - Nonsense 5:154902596-154902596 - 2492706 COSM5716722 c.2576C>T p.S859F Substitution - Missense 5:154904563-154904563 - T2225 COSM4686774 c.974G>T p.S325I Substitution - Missense 5:154927491-154927491 - TCGA-AX-A05S-01 COSM1064804 c.207C>T p.G69G Substitution - coding silent 5:154937145-154937145 - YUKAT COSM5402805 c.3455C>T p.T1152I Substitution - Missense 5:154896234-154896234 - CLL153 COSM1292061 c.34C>A p.P12T Substitution - Missense 5:154938100-154938100 - 61 COSM3245735 c.3977C>T p.T1326M Substitution - Missense 5:154891526-154891526 - RKO COSM3245794 c.1146A>G p.A382A Substitution - coding silent 5:154926009-154926009 - SW620 COSM3245796 c.950G>A p.W317* Substitution - Nonsense 5:154927515-154927515 - 587284 COSM1208100 c.601A>G p.I201V Substitution - Missense 5:154932159-154932159 - PDA_069 COSM5001619 c.4244G>T p.C1415F Substitution - Missense 5:154891259-154891259 - 587376 COSM1208103 c.1161C>A p.F387L Substitution - Missense 5:154925994-154925994 - TCGA-EE-A181-06 COSM3612911 c.3890C>T p.P1297L Substitution - Missense 5:154891613-154891613 - TCGA-D1-A176-01 COSM1064785 c.2395G>T p.V799F Substitution - Missense 5:154907591-154907591 - ME009T COSM223039 c.172G>A p.G58R Substitution - Missense 5:154937180-154937180 - TCGA-IA-A40U-01 COSM3994141 c.3232G>A p.V1078I Substitution - Missense 5:154898553-154898553 - TCGA-E2-A574-01 COSM3827519 c.171A>C p.I57I Substitution - coding silent 5:154937181-154937181 - CSCC-38-T COSM4504231 c.659C>T p.S220L Substitution - Missense 5:154932101-154932101 - BD57T COSM5510112 c.1294-5delT p.? Unknown 5:154924559-154924559 - HCC058T COSM5804704 c.2458A>T p.I820F Substitution - Missense 5:154905414-154905414 - TCGA-HJ-7597-01 COSM3853047 c.3611T>A p.I1204N Substitution - Missense 5:154892536-154892536 - TCGA-AZ-6598-01 COSM1435453 c.2649G>A p.V883V Substitution - coding silent 5:154903159-154903159 - LUAD-CHTN-MAD06-00668 COSM360117 c.1954G>C p.D652H Substitution - Missense 5:154912940-154912940 - ESCC-110T COSM3941207 c.524T>C p.I175T Substitution - Missense 5:154932236-154932236 - TCGA-AZ-6601-01 COSM1435448 c.3664G>A p.E1222K Substitution - Missense 5:154892483-154892483 - TCGA-D1-A101-01 COSM1064791 c.2066C>T p.A689V Substitution - Missense 5:154911828-154911828 - S02360 COSM5696225 c.389A>G p.E130G Substitution - Missense 5:154935961-154935961 - TCGA-EE-A2GC-06 COSM3612914 c.3224C>T p.A1075V Substitution - Missense 5:154898561-154898561 - TCGA-BS-A0UF-01 COSM1064797 c.1257A>C p.K419N Substitution - Missense 5:154925898-154925898 - TCGA-EE-A2MK-06 COSM3612917 c.2149C>T p.H717Y Substitution - Missense 5:154911745-154911745 - TCGA-FR-A3YN-06 COSM3612922 c.608G>A p.W203* Substitution - Nonsense 5:154932152-154932152 - TCGA-18-3409-01 COSM737121 c.2240C>T p.P747L Substitution - Missense 5:154907746-154907746 - PD7281a COSM3720078 c.3474G>A p.E1158E Substitution - coding silent 5:154896215-154896215 - TCGA-BS-A0UF-01 COSM1064777 c.2981C>T p.A994V Substitution - Missense 5:154901372-154901372 - TCGA-AD-5900-01 COSM1435459 c.1617C>T p.H539H Substitution - coding silent 5:154917987-154917987 - T2950 COSM4686775 c.575G>A p.R192Q Substitution - Missense 5:154932185-154932185 - RK148_C01 COSM1634082 c.1589A>G p.N530S Substitution - Missense 5:154919977-154919977 - 2237 COSM1644634 c.3838T>A p.F1280I Substitution - Missense 5:154891665-154891665 - KM12 COSM3245773 c.2196delA p.K732fs*18 Deletion - Frameshift 5:154907790-154907790 - TCGA-EB-A3XB-01 COSM3612909 c.4393C>T p.L1465F Substitution - Missense 5:154888344-154888344 - TCGA-BR-6452-01 COSM3853051 c.2221C>T p.P741S Substitution - Missense 5:154907765-154907765 - 61 COSM5014541 c.805T>A p.F269I Substitution - Missense 5:154928636-154928636 - TCGA-HU-8602-01 COSM3245772 c.2198G>A p.R733Q Substitution - Missense 5:154907788-154907788 - TCGA-D1-A103-01 COSM218833 c.850C>T p.R284C Substitution - Missense 5:154928591-154928591 - TCGA-EE-A29R-06 COSM1238974 c.594C>T p.I198I Substitution - coding silent 5:154932166-154932166 - TCGA-EE-A2MS-06 COSM3612921 c.754C>T p.R252* Substitution - Nonsense 5:154931485-154931485 - TCGA-BJ-A3PT-01 COSM3373758 c.350G>T p.W117L Substitution - Missense 5:154936000-154936000 - TCGA-BH-A0B4-01 COSM449171 c.2458A>G p.I820V Substitution - Missense 5:154905414-154905414 - TCGA-EE-A29M-06 COSM3612910 c.4082C>T p.S1361L Substitution - Missense 5:154891421-154891421 - TCGA-EE-A29M-06 COSM3612919 c.1791C>T p.S597S Substitution - coding silent 5:154917062-154917062 - TCGA-CA-6717-01 COSM1435462 c.405C>A p.F135L Substitution - Missense 5:154935945-154935945 - TCGA-UB-A7MB-01 COSM4931655 c.2323A>G p.N775D Substitution - Missense 5:154907663-154907663 - TCGA-ED-A4XI-01 COSM4913345 c.700G>A p.A234T Substitution - Missense 5:154931539-154931539 - T3152 COSM4686772 c.2176A>C p.S726R Substitution - Missense 5:154907810-154907810 - TCGA-BS-A0UF-01 COSM1064781 c.2805T>G p.V935V Substitution - coding silent 5:154902600-154902600 - TCGA-CA-6717-01 COSM1435456 c.2270C>A p.S757* Substitution - Nonsense 5:154907716-154907716 - 2492729 COSM5727851 c.1221G>A p.W407* Substitution - Nonsense 5:154925934-154925934 - RMS10_ COSM4985783 c.3793C>A p.H1265N Substitution - Missense 5:154891710-154891710 - KPOPBR-27-T COSM5965989 c.4502G>C p.R1501T Substitution - Missense 5:154888235-154888235 - MO_1012 COSM3853047 c.3611T>A p.I1204N Substitution - Missense 5:154892536-154892536 - ESCC_125 COSM5641172 c.3039C>A p.A1013A Substitution - coding silent 5:154899286-154899286 - PAPNNX COSM5004964 c.4317C>T p.T1439T Substitution - coding silent 5:154889363-154889363 - TCGA-F4-6856-01 COSM1435449 c.3615C>T p.C1205C Substitution - coding silent 5:154892532-154892532 - KYSE-450 COSM4439612 c.1086A>C p.K362N Substitution - Missense 5:154926069-154926069 - TCGA-EE-A29N-06 COSM3612912 c.3681C>T p.L1227L Substitution - coding silent 5:154892466-154892466 - LUAD_E00522 COSM353349 c.3439A>T p.T1147S Substitution - Missense 5:154896250-154896250 - TCGA-UB-A7MB-01 COSM4932553 c.147A>G p.P49P Substitution - coding silent 5:154937987-154937987 - sysucc-1317T COSM5450098 c.3659G>T p.W1220L Substitution - Missense 5:154892488-154892488 - TCGA-D1-A167-01 COSM1064783 c.2660T>A p.V887D Substitution - Missense 5:154903148-154903148 - TCGA-GN-A266-06 COSM3612916 c.2674C>T p.H892Y Substitution - Missense 5:154903134-154903134 - BCM711T COSM4956077 c.3636G>T p.V1212V Substitution - coding silent 5:154892511-154892511 - TCGA-G4-6309-01 COSM1435446 c.4094C>T p.A1365V Substitution - Missense 5:154891409-154891409 - NB-1056 COSM1285150 c.778C>T p.R260* Substitution - Nonsense 5:154931461-154931461 - HCC64T COSM1619893 c.731C>G p.T244S Substitution - Missense 5:154931508-154931508 - YUKAT COSM5402804 c.3718T>C p.F1240L Substitution - Missense 5:154892429-154892429 - TCGA-D5-5537-01 COSM5830089 c.510-3_510-2insT p.? Unknown 5:154932252-154932253 - BD183T COSM5508048 c.611G>A p.C204Y Substitution - Missense 5:154932149-154932149 - TCGA-AA-3549-01 COSM292180 c.4274A>G p.K1425R Substitution - Missense 5:154889406-154889406 - TCGA-BT-A3PH-01 COSM1310884 c.4407C>A p.L1469L Substitution - coding silent 5:154888330-154888330 - TCGA-32-4209-01 COSM3410033 c.3436C>G p.H1146D Substitution - Missense 5:154896253-154896253 - HF-23896 COSM1197701 c.827G>T p.G276V Substitution - Missense 5:154928614-154928614 - ESO-143 COSM1253179 c.2996A>C p.K999T Substitution - Missense 5:154901357-154901357 - 2492729 COSM5727850 c.2964C>T p.I988I Substitution - coding silent 5:154901389-154901389 - LP6007546-DNA_A01 COSM5439390 c.2051G>A p.R684Q Substitution - Missense 5:154911843-154911843 - TCGA-34-5928-01 COSM737117 c.17G>A p.R6Q Substitution - Missense 5:154938117-154938117 - TCGA-14-1037 COSM2155289 c.1270G>A p.G424S Substitution - Missense 5:154925885-154925885 - 169T COSM1725865 c.1962G>T p.R654S Substitution - Missense 5:154912932-154912932 - Pat_50_A COSM5867960 c.1373_1374CC>TT p.S458F Substitution - Missense 5:154924474-154924475 - TCGA-IR-A3LK-01 COSM4816587 c.2950C>T p.H984Y Substitution - Missense 5:154901403-154901403 - HCC64 COSM1619893 c.731C>G p.T244S Substitution - Missense 5:154931508-154931508 - BD124T COSM5491949 c.2545C>T p.L849F Substitution - Missense 5:154904594-154904594 - HT115 COSM3245775 c.2044C>T p.R682* Substitution - Nonsense 5:154911850-154911850 - TCGA-13-1409-01 COSM70882 c.3031G>C p.A1011P Substitution - Missense 5:154899294-154899294 - sysucc-966T COSM5487114 c.3663C>T p.D1221D Substitution - coding silent 5:154892484-154892484 - CRC-19T COSM5482385 c.1469_1471delAAG p.E490delE Deletion - In frame 5:154920095-154920097 - BN24T COSM1619894 c.333G>C p.T111T Substitution - coding silent 5:154936017-154936017 - TCGA-BJ-A0Z0-01 COSM3373757 c.2962A>T p.I988F Substitution - Missense 5:154901391-154901391 - Gp5D COSM3245793 c.1189A>G p.I397V Substitution - Missense 5:154925966-154925966 - HN_62854 COSM123342 c.589G>C p.E197Q Substitution - Missense 5:154932171-154932171 - TCGA-CC-A7II-01 COSM4937715 c.2334A>G p.S778S Substitution - coding silent 5:154907652-154907652 - BCM759T COSM206818 c.3345G>T p.Q1115H Substitution - Missense 5:154898440-154898440 - TCGA-BP-4768-01 COSM3365947 c.3282G>A p.E1094E Substitution - coding silent 5:154898503-154898503 - T55 COSM4686768 c.4003C>T p.P1335S Substitution - Missense 5:154891500-154891500 - TCGA-Q1-A73P-01 COSM4826011 c.90C>T p.F30F Substitution - coding silent 5:154938044-154938044 - LIM2551 COSM4644653 c.2987A>T p.E996V Substitution - Missense 5:154901366-154901366 - DU-145 COSM1672074 c.2120T>C p.V707A Substitution - Missense 5:154911774-154911774 - TCGA-AM-5820-01 COSM3761062 c.2730A>G p.G910G Substitution - coding silent 5:154902675-154902675 - pfg181T COSM4762938 c.3851G>A p.R1284H Substitution - Missense 5:154891652-154891652 - TCGA-DC-6681-01 COSM1567817 c.3210G>A p.T1070T Substitution - coding silent 5:154898575-154898575 - TCGA-EE-A3AC-06 COSM3612923 c.319C>G p.L107V Substitution - Missense 5:154937033-154937033 - TCGA-AP-A0LM-01 COSM1064787 c.2393C>T p.A798V Substitution - Missense 5:154907593-154907593 - 587332 COSM1208099 c.4348G>A p.E1450K Substitution - Missense 5:154889332-154889332 - TCGA-DK-A3X1-01 COSM3776461 c.3639G>A p.L1213L Substitution - coding silent 5:154892508-154892508 - TCGA-AX-A060-01 COSM1064765 c.4515C>A p.T1505T Substitution - coding silent 5:154888222-154888222 - TCGA-18-3414-01 COSM737118 c.252C>A p.T84T Substitution - coding silent 5:154937100-154937100 - TCGA-32-1986-01 COSM3410034 c.669T>C p.A223A Substitution - coding silent 5:154931570-154931570 - PD13762a COSM5770637 c.156C>T p.P52P Substitution - coding silent 5:154937978-154937978 - 2492705 COSM5716722 c.2576C>T p.S859F Substitution - Missense 5:154904563-154904563 - YUSCO COSM1696638 c.284A>T p.D95V Substitution - Missense 5:154937068-154937068 - pfg068T COSM4762939 c.3185A>G p.K1062R Substitution - Missense 5:154898600-154898600 - TCGA-C5-A1BK-01 COSM3776461 c.3639G>A p.L1213L Substitution - coding silent 5:154892508-154892508 - TCGA-AP-A051-01 COSM1064793 c.1840C>A p.L614M Substitution - Missense 5:154917013-154917013 - MBRep_T44 COSM215973 c.1723C>A p.Q575K Substitution - Missense 5:154917130-154917130 - EGC3 COSM1435446 c.4094C>T p.A1365V Substitution - Missense 5:154891409-154891409 - PCSI_0006_Pa_C COSM3786893 c.3908T>G p.V1303G Substitution - Missense 5:154891595-154891595 - TCGA-G4-6626-01 COSM1435460 c.980C>T p.S327L Substitution - Missense 5:154927485-154927485 - T3049 COSM1435459 c.1617C>T p.H539H Substitution - coding silent 5:154917987-154917987 - TCGA-D8-A1XQ-01 COSM3827518 c.912T>G p.F304L Substitution - Missense 5:154928529-154928529 - TCGA-AX-A060-01 COSM1064763 c.4517T>A p.F1506Y Substitution - Missense 5:154888220-154888220 - PD8617a COSM5769229 c.1693A>G p.I565V Substitution - Missense 5:154917160-154917160 - LB2518-MEL COSM23518 c.4351_4352delAG p.S1451fs*2 Deletion - Frameshift 5:154889328-154889329 - ESCC_BICR_013T COSM5439390 c.2051G>A p.R684Q Substitution - Missense 5:154911843-154911843 - A2 COSM5351171 c.1222A>C p.N408H Substitution - Missense 5:154925933-154925933 - 16 COSM3735700 c.2942C>T p.A981V Substitution - Missense 5:154901411-154901411 - T3204 COSM4686770 c.3148A>C p.T1050P Substitution - Missense 5:154898637-154898637 - TCGA-AP-A051-01 COSM1064775 c.3163G>A p.A1055T Substitution - Missense 5:154898622-154898622 - PCSI_0127_Pa_P COSM3381168 c.164G>C p.R55P Substitution - Missense 5:154937970-154937970 - BCM759T COSM206818 c.3345G>T p.Q1115H Substitution - Missense 5:154898440-154898440 - TCGA-AM-5820-01 COSM5134599 c.2589_2590insT p.H864fs*18 Insertion - Frameshift 5:154904549-154904550 - PTC-14C COSM4159669 c.2608C>A p.L870I Substitution - Missense 5:154904531-154904531 - TCGA-AX-A063-01 COSM1064799 c.873G>A p.W291* Substitution - Nonsense 5:154928568-154928568 - BD169T COSM5506103 c.1566C>T p.I522I Substitution - coding silent 5:154920000-154920000 - 260211 COSM3725734 c.995A>G p.N332S Substitution - Missense 5:154927470-154927470 - TCGA-Q1-A73P-01 COSM4826152 c.3624G>A p.L1208L Substitution - coding silent 5:154892523-154892523 - TCGA-A2-A0T6-01 COSM449173 c.164G>A p.R55Q Substitution - Missense 5:154937970-154937970 - 8067182 COSM3784672 c.2883G>T p.W961C Substitution - Missense 5:154901470-154901470 - TCGA-AP-A051-01 COSM1064802 c.781G>T p.G261W Substitution - Missense 5:154931458-154931458 - TCGA-G4-6586-01 COSM1435450 c.3434A>G p.Y1145C Substitution - Missense 5:154896255-154896255 - ICGC_0046 COSM218833 c.850C>T p.R284C Substitution - Missense 5:154928591-154928591 - ESCC_140 COSM5643422 c.214T>G p.F72V Substitution - Missense 5:154937138-154937138 - TCGA-B5-A11H-01 COSM1064771 c.3299A>T p.N1100I Substitution - Missense 5:154898486-154898486 - BN24 COSM1619894 c.333G>C p.T111T Substitution - coding silent 5:154936017-154936017 - MO_1232 COSM5552992 c.589G>T p.E197* Substitution - Nonsense 5:154932171-154932171 - TCGA-22-5473-01 COSM737119 c.599C>G p.S200C Substitution - Missense 5:154932161-154932161 - CSCC-44-T COSM4546299 c.3973G>T p.E1325* Substitution - Nonsense 5:154891530-154891530 - TCGA-AZ-6598-01 COSM1435454 c.2646T>A p.D882E Substitution - Missense 5:154903162-154903162 - TCGA-CM-4746-01 COSM1435455 c.2271G>A p.S757S Substitution - coding silent 5:154907715-154907715 - 1_RESISTANT COSM1718942 c.2827G>A p.G943R Substitution - Missense 5:154902578-154902578 - T3266 COSM4686771 c.3139_3140delTT p.L1047fs*7 Deletion - Frameshift 5:154898645-154898646 - TCGA-BP-4976-01 COSM1496073 c.1379A>G p.K460R Substitution - Missense 5:154924469-154924469 - LUAD-S01354 COSM385962 c.1275G>T p.V425V Substitution - coding silent 5:154925880-154925880 - TCGA-AX-A0J0-01 COSM1064789 c.2270C>T p.S757L Substitution - Missense 5:154907716-154907716 - RK081_C01 COSM3768254 c.510-6T>A p.? Unknown 5:154932256-154932256 - CSCC-29-T COSM4541715 c.3054G>A p.E1018E Substitution - coding silent 5:154899271-154899271 - YUKAT COSM5402806 c.3283C>T p.L1095L Substitution - coding silent 5:154898502-154898502 - SJHGG003_A COSM4968853 c.4305C>A p.T1435T Substitution - coding silent 5:154889375-154889375 - TCGA-B5-A0JY-01 COSM1064789 c.2270C>T p.S757L Substitution - Missense 5:154907716-154907716 - LP6005334-DNA_E03 COSM4412863 c.4003C>A p.P1335T Substitution - Missense 5:154891500-154891500 - TCGA-FW-A3R5-06 COSM3919426 c.3946C>T p.Q1316* Substitution - Nonsense 5:154891557-154891557 - BD114T COSM5503038 c.810G>C p.L270L Substitution - coding silent 5:154928631-154928631 - YUZINO COSM1542594 c.1451C>T p.P484L Substitution - Missense 5:154921354-154921354 - TCGA-AA-3715-01 COSM269236 c.336A>G p.I112M Substitution - Missense 5:154936014-154936014 - TCGA-AP-A056-01 COSM1064795 c.1687T>G p.F563V Substitution - Missense 5:154917166-154917166 - WA32 COSM239965 c.1857G>C p.E619D Substitution - Missense 5:154913037-154913037 - HCT15 COSM3245766 c.2506C>T p.P836S Substitution - Missense 5:154905366-154905366 - TCGA-D9-A6EC-06 COSM4404400 c.2134A>T p.T712S Substitution - Missense 5:154911760-154911760 - TCGA-CJ-4870-01 COSM3365946 c.4009A>T p.R1337W Substitution - Missense 5:154891494-154891494 - ICGC_MB12 COSM215973 c.1723C>A p.Q575K Substitution - Missense 5:154917130-154917130 - TCGA-AX-A0J1-01 COSM1064779 c.2883G>A p.W961* Substitution - Nonsense 5:154901470-154901470 - 2492704 COSM5716722 c.2576C>T p.S859F Substitution - Missense 5:154904563-154904563 - YUWIA COSM5402807 c.1131C>T p.S377S Substitution - coding silent 5:154926024-154926024 - TCGA-A3-3320-01 COSM1137290 c.3200C>T p.S1067L Substitution - Missense 5:154898585-154898585 - 12T COSM109084 c.2432C>T p.S811L Substitution - Missense 5:154905440-154905440 - 61 COSM5737393 c.4197T>A p.N1399K Substitution - Missense 5:154891306-154891306 - TCGA-KK-A6E4-01 COSM4876463 c.4077C>G p.L1359L Substitution - coding silent 5:154891426-154891426 - TCGA-EE-A2MT-06 COSM3612913 c.3425C>T p.S1142F Substitution - Missense 5:154896264-154896264 - S0021 COSM5884164 c.2969A>G p.K990R Substitution - Missense 5:154901384-154901384 - SWE-4B COSM1179574 c.969C>A p.L323L Substitution - coding silent 5:154927496-154927496 - LIM1899 COSM4640638 c.1108G>A p.E370K Substitution - Missense 5:154926047-154926047 - T3091 COSM4686773 c.1264delT p.W422fs*4 Deletion - Frameshift 5:154925891-154925891 - pfg181T COSM4765983 c.2177_2178insA p.S726fs*3 Insertion - Frameshift 5:154907808-154907809 - SNU-C4 COSM4653920 c.172G>T p.G58* Substitution - Nonsense 5:154937180-154937180 - S02286 COSM5685408 c.2850G>T p.V950V Substitution - coding silent 5:154902555-154902555 - TCGA-A8-A0A6-01 COSM3827517 c.1352T>G p.V451G Substitution - Missense 5:154924496-154924496 - SNU-C2B COSM3245727 c.4322C>T p.A1441V Substitution - Missense 5:154889358-154889358 - 8015764 COSM218833 c.850C>T p.R284C Substitution - Missense 5:154928591-154928591 - TCGA-66-2795-01 COSM737120 c.887C>A p.P296Q Substitution - Missense 5:154928554-154928554 - TCGA-DK-A2I4-01 COSM3776462 c.813G>A p.K271K Substitution - coding silent 5:154928628-154928628 - PT40 COSM1064789 c.2270C>T p.S757L Substitution - Missense 5:154907716-154907716 - TCGA-DG-A2KM-01 COSM4851688 c.3269G>C p.R1090T Substitution - Missense 5:154898516-154898516 - MedB-1 COSM5620869 c.4052G>A p.R1351Q Substitution - Missense 5:154891451-154891451 - YUSWI COSM1696636 c.1898_1899GG>AA p.R633Q Substitution - Missense 5:154912995-154912996 - TCGA-CC-A7IH-01 COSM4923858 c.537T>C p.I179I Substitution - coding silent 5:154932223-154932223 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.483921 5q33.2 607005

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AA - Frameshift p.L1343Efs*7 c.4027_4028delTT 5 154271035 CM A C Missense p.S388A c.1162T>G 5 154305553 CM A - Frameshift p.L749*fs*1 c.2246delT 5 154287300 RCCC A G IntronicSNV . c.662-6T>C 5 154311143 CM A G Missense p.S1190P c.3568T>C 5 154275681 ESCA A G Synonymous p.A223A c.669T>C 5 154311130 GBM A G Synonymous p.L1381L c.4141T>C 5 154270922 LUAD A G Synonymous p.S316S c.948T>C 5 154307077 LGG A - IntronicDeletion . c.510-29delT 5 154311839 ESCA A - IntronicDeletion . c.510-29delT 5 154311839 STAD C A Missense p.C1421F c.4262G>T 5 154270801 LUAD C A SpliceAcceptorSNV . c.2729-1G>T 5 154282237 BRCA CC TT SpliceAcceptorBlockSubstitution . c.782_783delinsAA 5 154308218 CM C G Missense p.A1011P c.3031G>C 5 154278854 OV C G Missense p.D1342H c.4024G>C 5 154271039 LUAD C G Missense p.E1138Q c.3412G>C 5 154275837 ALL C G Missense p.E164Q c.490G>C 5 154315420 BRCA C G Missense p.E197Q c.589G>C 5 154311731 HNSC C G Missense p.E774Q c.2320G>C 5 154287226 HNSC C G SpliceAcceptorSNV . c.3346-1G>C 5 154275904 CM C T Missense p.E1324K c.3970G>A 5 154271093 LUAD C T Missense p.G132E c.395G>A 5 154315515 BRCA C T Missense p.G58R c.172G>A 5 154316740 CM C T Missense p.R55Q c.164G>A 5 154317530 BRCA C T Missense p.R6Q c.17G>A 5 154317677 LUSC C T Nonsense p.W291* c.873G>A 5 154308128 UCEC C T Synonymous p.E1094E c.3282G>A 5 154278063 RCCC C T Synonymous p.K271K c.813G>A 5 154308188 BLCA C T Synonymous p.L570L c.1710G>A 5 154296703 HNSC G A Missense p.A1075V c.3224C>T 5 154278121 CM G A Missense p.A689V c.2066C>T 5 154291388 UCEC G A Missense p.H163Y c.487C>T 5 154315423 ALL G A Missense p.H717Y c.2149C>T 5 154291305 CM G A Missense p.H892Y c.2674C>T 5 154282694 CM G A Missense p.L323F c.967C>T 5 154307058 CM G A Missense p.P1297L c.3890C>T 5 154271173 CM G A Missense p.P376L c.1127C>T 5 154305588 CM G A Missense p.R284C c.850C>T 5 154308151 PAAD G A Missense p.S1142F c.3425C>T 5 154275824 CM G A Missense p.S1361L c.4082C>T 5 154270981 CM G A Missense p.S624F c.1871C>T 5 154292583 CM G A Nonsense p.Q937* c.2809C>T 5 154282156 CM G A Nonsense p.R252* c.754C>T 5 154311045 CM G A Synonymous p.D87D c.261C>T 5 154316651 STAD G A Synonymous p.G69G c.207C>T 5 154316705 UCEC G A Synonymous p.I198I c.594C>T 5 154311726 CM G A Synonymous p.L1022L c.3064C>T 5 154278821 CM G A Synonymous p.L1227L c.3681C>T 5 154272026 CM G A Synonymous p.L1359L c.4077C>T 5 154270986 RCCC G A Synonymous p.L1489L c.4467C>T 5 154267830 CM G A Synonymous p.P292P c.876C>T 5 154308125 CM G A Synonymous p.S1142S c.3426C>T 5 154275823 CM G A Synonymous p.S495S c.1485C>T 5 154299641 CM G A Synonymous p.S597S c.1791C>T 5 154296622 CM G C Missense p.H1146D c.3436C>G 5 154275813 GBM G C Missense p.L107V c.319C>G 5 154316593 CM G C Missense p.Q1368E c.4102C>G 5 154270961 HNSC G C Missense p.S200C c.599C>G 5 154311721 LUSC G C Synonymous p.L1359L c.4077C>G 5 154270986 PRAD G T Missense p.P12T c.34C>A 5 154317660 CLL G T Missense p.P296Q c.887C>A 5 154308114 LUSC G T Missense p.Q575K c.1723C>A 5 154296690 MB G T Synonymous p.G424G c.1272C>A 5 154305443 HNSC G T Synonymous p.L1469L c.4407C>A 5 154267890 BLCA G T Synonymous p.R633R c.1897C>A 5 154292557 STAD G T Synonymous p.T84T c.252C>A 5 154316660 LUSC T A Missense p.I988F c.2962A>T 5 154280951 THCA T A Missense p.N1100I c.3299A>T 5 154278046 UCEC T A Missense p.R1337W c.4009A>T 5 154271054 RCCC T C Missense p.I820V c.2458A>G 5 154284974 BRCA T C Missense p.K1425R c.4274A>G 5 154268966 COREAD T C Missense p.Q1389R c.4166A>G 5 154270897 LGG T C Synonymous p.L352L c.1056A>G 5 154306969 BRCA T G Missense p.K999T c.2996A>C 5 154280917 ESCA